<?xml version='1.0'?>
<Strains>
  <Strain>
    <RGD_ID>10000</RGD_ID>
    <STRAIN_SYMBOL>ACI/N</STRAIN_SYMBOL>
    <FULL_NAME>A X C 9935, Irish</FULL_NAME>
    <ORIGINATION>&lt;a href= http://www.rrrc.us/Strain/?x=142&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href= http://www.rrrc.us/Strain/?x=142&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery</AVAILABILITY>
    <RESEARCH_USE>spontaneous tumors; chronic renal disease; congenital malformations</RESEARCH_USE>
    <ALLELES>Tnfrsf1a</ALLELES>
    <ALLELE_RGD_IDS>621237</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00142</CITATION_ID>
    <DESCRIPTION>Curtiss and Dunning 1926 at the Columbia University Institute for Cancer Research. To Heston 1945 at F30, to National Institutes of Health 1950 at F41. Subsequent sublines from Dunning or NIH. Donated to RRRC from NIH Animal Genetic Resource Bank (NIHAGR)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10001</RGD_ID>
    <STRAIN_SYMBOL>AVN/Orl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Ctr de Selection et d'Elev d'Anim de Lab, Orleans, France.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10001</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10002</RGD_ID>
    <STRAIN_SYMBOL>BBDP/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10002</CITATION_ID>
    <DESCRIPTION>S. Bieg and coworkers (1998) generated a congenic line in which diabetes and lymphopenia are controlled solely by Iddm 1. This strain was generated by nine cycles of cross-intercross breeding of diabetes-prone DP with DR BB rats. Iddm 1 in the BioBreeding (BB) rat designates the genomic region on rat Chromosome (Chr) 4 that harbors the gene causing peripheral T cell lymphopenia (Lyp) and diabetes. The average age of onset of diabetes was 85 ± 53 days of age after the first and 67 ± 10 days of age after the 9th cycle.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10003</RGD_ID>
    <STRAIN_SYMBOL>BBDR/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>R. H. William Laboratory, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10003</CITATION_ID>
    <DESCRIPTION>S. Bieg and coworkers (1998) generated a congenic line in which diabetes and lymphopenia are controlled solely by Iddm 1. This strain was generated by nine cycles of cross-intercross breeding of diabetes-prone DP with DR BB rats. Iddm 1 in the BioBreeding (BB) rat designates the genomic region on rat Chromosome (Chr) 4 that harbors the gene causing peripheral T cell lymphopenia (Lyp) and diabetes. The average age of onset of diabetes was 85 +/- 53 days of age after the first and 67 +/- 10 days of age after the 9th cycle.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10004</RGD_ID>
    <STRAIN_SYMBOL>BC/CpbU</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Central Laboratory Animal Institute of Utrecht University, The Netherlands.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10004</CITATION_ID>
    <DESCRIPTION>Obtained from the Central Laboratory Animal Institute of Utrecht University, The Netherlands.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10005</RGD_ID>
    <STRAIN_SYMBOL>BDIX/Han</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10005</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10006</RGD_ID>
    <STRAIN_SYMBOL>BDVII/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, </ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10006</CITATION_ID>
    <DESCRIPTION>Druckrey from F2 offspring of a cross between BDVI and BDI with subsequent selection of brother-sister pairs for a  pink-eyed, yellow, blackhooded phenotype.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10008</RGD_ID>
    <STRAIN_SYMBOL>BN/SsNHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10008</CITATION_ID>
    <DESCRIPTION>Obtained by HSD from nucleus colony at NIH</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10009</RGD_ID>
    <STRAIN_SYMBOL>BP/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, </ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10009</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10010</RGD_ID>
    <STRAIN_SYMBOL>BUF/Pit</STRAIN_SYMBOL>
    <FULL_NAME>Buffalo</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10010</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10011</RGD_ID>
    <STRAIN_SYMBOL>COP/OlaHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10011</CITATION_ID>
    <DESCRIPTION>These are derived from the original colony which was developed by Dr. W.F. Dunning.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10012</RGD_ID>
    <STRAIN_SYMBOL>DA/PitN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00154</CITATION_ID>
    <DESCRIPTION>Unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10013</RGD_ID>
    <STRAIN_SYMBOL>DON/Melb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10013</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10014</RGD_ID>
    <STRAIN_SYMBOL>F344/Pit</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10014</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10015</RGD_ID>
    <STRAIN_SYMBOL>FHH/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Erasmus University-Rotterdam</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10015</CITATION_ID>
    <DESCRIPTION>An outbred stock of fawn hooded rats introduced into Europe by Tschopp in the early 1970s. Maintained as an outbred stock until the mid-1980s, then brother x sister mating initiated by A.P. Provoost to produce two strains designated FHH (also known as FHR) and FHL, which differ in hypertension and proteinuria. The colony was transferred to Erasmus University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10016</RGD_ID>
    <STRAIN_SYMBOL>GH/Omr</STRAIN_SYMBOL>
    <FULL_NAME>Genetically Hypertensive</FULL_NAME>
    <ORIGINATION>University of Otago Wellcome Med. Res. Inst, New Zealand.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10016</CITATION_ID>
    <DESCRIPTION>This colony was established from rats of Wistar origin. This is an hysterectomy-derived colony at the University of Otago, which  was established from the  Wellcome Institute colony at generation 79. These have been inbred for over 90 generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10017</RGD_ID>
    <STRAIN_SYMBOL>GK/KyoSwe</STRAIN_SYMBOL>
    <FULL_NAME>Goto Kakizaki</FULL_NAME>
    <ORIGINATION>Department of Molecular Medicine, Karolinska Hospital, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10017</CITATION_ID>
    <DESCRIPTION>Developed from outbred Wistar rats with selection for high glucose levels in and oral glucose tolerance test (Goto et al 1975).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10018</RGD_ID>
    <STRAIN_SYMBOL>IS/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>ishibashi rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=5 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=5 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Osteosis</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10018</CITATION_ID>
    <DESCRIPTION>Ishibashi rat is derived from a cross between a wild male and a Wistar female, with sib mating since 1975 at Azabu University, transferred to Kyoto University in 1978.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10019</RGD_ID>
    <STRAIN_SYMBOL>LE/Mol</STRAIN_SYMBOL>
    <FULL_NAME>Long Evans</FULL_NAME>
    <ORIGINATION>M &amp; B A/S, Denmark.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10019</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10020</RGD_ID>
    <STRAIN_SYMBOL>LEW/Pit</STRAIN_SYMBOL>
    <FULL_NAME>Lewis</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10020</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10021</RGD_ID>
    <STRAIN_SYMBOL>LH/Mav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratoire de Physiologie, 8 Avenue Rockfeller, 69373 Lyon Cedex 08, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10021</CITATION_ID>
    <DESCRIPTION>In 1969 outbred Sprague-Dawley rats were selected for high systolic blood pressure using an indirect plethysmographic technique in pre-warmed unrestrained conscious rats. Three pairs were originally selected, and selection was continued with brother x sister mating. Strain LN was maintained as a normotensive control, and LL as a hypotensive strain. (see Vincent et al 1984, and Vincent and Sassard, 1994 for reviews).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10022</RGD_ID>
    <STRAIN_SYMBOL>LN/Mav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratoire de Physiologie, 8 Avenue Rockfeller, 69373 Lyon Cedex 08, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10022</CITATION_ID>
    <DESCRIPTION>In 1969 outbred Sprague-Dawley rats were selected for high systolic blood pressure using an indirect plethysmographic technique in pre-warmed unrestrained conscious rats. Three pairs were originally selected, and selection was continued with brother x sister mating. Strain LN was maintained as a normotensive control, and LL as a hypotensive strain. (see Vincent et al 1984, and Vincent and Sassard, 1994 for reviews).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10023</RGD_ID>
    <STRAIN_SYMBOL>LOU/CHan</STRAIN_SYMBOL>
    <FULL_NAME>Louvain</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10023</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10024</RGD_ID>
    <STRAIN_SYMBOL>M520/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Animal Genetic Resource</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=168&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00168</CITATION_ID>
    <DESCRIPTION>To N 1951 from Heston at F51. Developed by Curtis at Columbia University Institute for Cancer Research, 1920; to Heston, 1949 at F49.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10025</RGD_ID>
    <STRAIN_SYMBOL>MHS/Gib</STRAIN_SYMBOL>
    <FULL_NAME>Milan Hypertensive Strain</FULL_NAME>
    <ORIGINATION>Department of Sciences and Biomedical Technologies, University of Milan, Milan, Italy</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10025</CITATION_ID>
    <DESCRIPTION>Outbred Wistar rats with brother x sister mating and selection for high systolic blood pressure</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10026</RGD_ID>
    <STRAIN_SYMBOL>MNR/N</STRAIN_SYMBOL>
    <FULL_NAME>Maudsely non-reactive</FULL_NAME>
    <ORIGINATION>NIH Animal Genetic Resource</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00174</CITATION_ID>
    <DESCRIPTION>To N 1964 at F18+? from Maas. Developed by Broadhurst, 1954, from a commercial stock, with selection for low defecation response in an open field. A number of parallel sublines are in existence; these differ at least at the agouti and the major histocompatibility loci.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10027</RGD_ID>
    <STRAIN_SYMBOL>MNRA/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Animal Genetic Resource</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10027</CITATION_ID>
    <DESCRIPTION>To Harrington in 1965 at F25 (Harrington 1981).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10028</RGD_ID>
    <STRAIN_SYMBOL>MNS/Gib</STRAIN_SYMBOL>
    <FULL_NAME>Milan Normotensive Strain</FULL_NAME>
    <ORIGINATION>Department of Sciences and Biomedical Technologies, University of Milan, Milan, Italy</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10028</CITATION_ID>
    <DESCRIPTION>Outbred Wistar rats with brother x sister mating and selection for low systolic blood pressure as a normotensive control for MHS.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10029</RGD_ID>
    <STRAIN_SYMBOL>MR/Pit</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10029</CITATION_ID>
    <DESCRIPTION>As for MNR except selection was for high defecation response in the open field. To Harrington in 1965 at F25 and to NIH in 1964 at F18+ (Hansen et al 1982).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10030</RGD_ID>
    <STRAIN_SYMBOL>NEDH/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Central Institute for Diabetes, Karlsburg, Germany.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10030</CITATION_ID>
    <DESCRIPTION>Inbred by S. Warren at New England Deaconess Hospital, from Slonaker colony (University of Chicago ca. 1928). To Simonsen Laboratories in 1985 via B. Hoffman, Veterans Administration Medical Center, Palo Alto, CA. To Mollegaard in 1987.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10031</RGD_ID>
    <STRAIN_SYMBOL>NP9</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10031</CITATION_ID>
    <DESCRIPTION>From Wistar</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10032</RGD_ID>
    <STRAIN_SYMBOL>ODU/N</STRAIN_SYMBOL>
    <FULL_NAME>Osaka Dental University</FULL_NAME>
    <ORIGINATION>NIH Animal Genetic Resource</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00176</CITATION_ID>
    <DESCRIPTION>From outbred Wistar Kyoto stock inbred by N Ito, Osaka Dental University. Selected for susceptibility to development of dental plaque (Ito et al 1975). To NIH in 1977 at F3 (Hansen et al 1982).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10033</RGD_ID>
    <STRAIN_SYMBOL>OKA/Wsl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Professor Herve Bazin, Universite de Louvain, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10033</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10034</RGD_ID>
    <STRAIN_SYMBOL>OM/Ztm</STRAIN_SYMBOL>
    <FULL_NAME>Osborne-Mendel</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10034</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10035</RGD_ID>
    <STRAIN_SYMBOL>P5C</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10035</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10036</RGD_ID>
    <STRAIN_SYMBOL>PVG/Pit</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10036</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10037</RGD_ID>
    <STRAIN_SYMBOL>SD/Rij</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan Rijswijk</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10037</CITATION_ID>
    <DESCRIPTION>From Sprague-Dawley stock of an unknown source to Hoechst, Frankfurt. To O. Haferkamp, University of Ulm, to ITRI-TNO Rijswijk, The Netherlands in 1972 (van Hooft 1990). Note that other sublines of "SD" rats (including SD/A, SD/Cpb, and SD/Waa) are known to differ among themselves, and from this strain (Bender et al 1984, Festing and Bender 1984).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10038</RGD_ID>
    <STRAIN_SYMBOL>SHR/OlaHsd</STRAIN_SYMBOL>
    <FULL_NAME>Spontaneously Hypertensive Rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>Harlan Sprague Dawley, Inc.</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10038</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10039</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/Riv</STRAIN_SYMBOL>
    <FULL_NAME>Spontaneously Hypertensive Rat, Stroke Prone</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10039</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10040</RGD_ID>
    <STRAIN_SYMBOL>SR/Jr</STRAIN_SYMBOL>
    <FULL_NAME>Salt Resistant</FULL_NAME>
    <ORIGINATION>Dr. John P. Rapp, Medical College of Ohio, USA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=56&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00056</CITATION_ID>
    <DESCRIPTION>Originated from a Sprague-Dawley outbred colony developed by LK Dahl, Brookhaven National Laboratories, Upton, New York, selected for resistance to salt-induced hypertension (Dahl et al 1962a,b).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10041</RGD_ID>
    <STRAIN_SYMBOL>SS/Jr</STRAIN_SYMBOL>
    <FULL_NAME>Salt Sensitive</FULL_NAME>
    <ORIGINATION>Dr. John P. Rapp, Medical College of Ohio, USA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=55&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Hmox1</ALLELES>
    <ALLELE_RGD_IDS>2806</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00055</CITATION_ID>
    <DESCRIPTION>Strain originated from a colony of Sprague-Dawley outbred rats developed by LK Dahl, Brookhaven National Laboratories, Upton, New York, selected for sensitivity to salt-induced hypertension (Dahl et al 1962a,b, Rapp 1982)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10042</RGD_ID>
    <STRAIN_SYMBOL>WAG/RijKyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=14 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=14 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10042</CITATION_ID>
    <DESCRIPTION>Rij &gt; Kyo (1979, F?, GF)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043</RGD_ID>
    <STRAIN_SYMBOL>WF/Pit</STRAIN_SYMBOL>
    <FULL_NAME>Wistar Furth</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10044</RGD_ID>
    <STRAIN_SYMBOL>WIST/Nhg</STRAIN_SYMBOL>
    <FULL_NAME>Wistar</FULL_NAME>
    <ORIGINATION>Gesellschaft f. Strahlen &amp; Umweltforschung, Munich, Germany.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ugt1a1|Abcd2</ALLELES>
    <ALLELE_RGD_IDS>3935|69244</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10044</CITATION_ID>
    <DESCRIPTION>From outbred Wistar stock in 1967.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045</RGD_ID>
    <STRAIN_SYMBOL>WN/N</STRAIN_SYMBOL>
    <FULL_NAME>Inbred Wistar; W/N</FULL_NAME>
    <ORIGINATION>NIH Animal Genetic Resource</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045</CITATION_ID>
    <DESCRIPTION>Heston in 1942 from Wistar stock of Nettleship, to National Institutes of Health in 1950 at F15.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10046</RGD_ID>
    <STRAIN_SYMBOL>WKY/OlaHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan Sprague Dawley, Inc.</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10046</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>10047</RGD_ID>
    <STRAIN_SYMBOL>WTC/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=18 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=18 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2018-01-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10047</CITATION_ID>
    <DESCRIPTION>WTC was established as a coisogenic strain (tm&lt;+/+&gt;) from TRM (F18) in 1988. A missense mutation (c. 1061 C&gt;T, p. A354V) in the hyperpolarization-activated cyclic nucleotide-gated 1 channel (Hcn1) gene (Ohno et al. 2015).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60984</RGD_ID>
    <STRAIN_SYMBOL>GH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60984</CITATION_ID>
    <DESCRIPTION>University of Otago Medical School from rats of Wistar origin  imported from England in 1930. Selection for high blood pressure started by Smirk in 1955. A number of sublines have been developed. Closely related to strain AS (Heslop and Phelan 1973).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60985</RGD_ID>
    <STRAIN_SYMBOL>BN</STRAIN_SYMBOL>
    <FULL_NAME>BN</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/index.html&gt;Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/index.html&gt;Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd36|Tnfrsf1a</ALLELES>
    <ALLELE_RGD_IDS>2301|621237</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60985</CITATION_ID>
    <DESCRIPTION>Billingham and Silvers 1958, from a brown mutation maintained by DH King and P Aptekman in a pen-bred colony (Billingham and Silvers 1959).  A plasma kininogen-deficient mutant strain (BN/Ka) has been described  in which release of heat-induced substance P is defective (Tang et al, 1994) and response to the hypertensive effects of deoxycorticosterone acetate salt is much faster than in normal BN rats (Majima et al, 1995a,b).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60986</RGD_ID>
    <STRAIN_SYMBOL>BUF/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60986</CITATION_ID>
    <DESCRIPTION>Heston 1946 from Buffalo stock of H. Morris. To NIH in 1950 at F10.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60987</RGD_ID>
    <STRAIN_SYMBOL>MHS/N</STRAIN_SYMBOL>
    <FULL_NAME>Milan Hypertensive Strain</FULL_NAME>
    <ORIGINATION>Department of Sciences and Biomedical Technologies, University of Milan, Milan, Italy</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Add1|Add2</ALLELES>
    <ALLELE_RGD_IDS>2041|2042</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00169</CITATION_ID>
    <DESCRIPTION>Milan Hypertensive Strain: Outbred Wistar rats with brother x sister mating and selection for high systolic blood pressure (Bianchi et al 1974, Barber et al, 1994).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60988</RGD_ID>
    <STRAIN_SYMBOL>LOU/M</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60988</CITATION_ID>
    <DESCRIPTION>Bazin and Beckers from rats of presumed Wistar origin kept at the Universite Catholique de Louvain. LOU/C was selected among 28 parallel sublines for its high incidence of plasmacytomas, and LOU/M for its low incidence. The two are histocomaptible. Histocompatible with LOU/C and maintained by selection of LOU/M males on the basis of acceptance of skin grafts  from LOU/C rats (Bazin 1977, Beckers and Bazin 1978).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60989</RGD_ID>
    <STRAIN_SYMBOL>BP</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60989</CITATION_ID>
    <DESCRIPTION>Strain selected for resistance to Walker 256 tumour.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60990</RGD_ID>
    <STRAIN_SYMBOL>LH/MavRrrc</STRAIN_SYMBOL>
    <FULL_NAME>Lyon Hypertensive</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=57&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=57&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2020-02-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00057</CITATION_ID>
    <DESCRIPTION>Lyon Hypertensive. In 1969 outbred Sprague-Dawley rats were selected for high systolic blood pressure using an indirect plethysmographic technique in pre-warmed, unrestrained, conscious rats. Three pairs were originally selected, and selection was continued with brother x sister mating. Strain LN was maintained as a normotensive control, and LL as a hypotensive strain. (see Vincent et al 1984, and Vincent and Sassard, 1994 for reviews).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60991</RGD_ID>
    <STRAIN_SYMBOL>LE</STRAIN_SYMBOL>
    <FULL_NAME>Long Evans</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60991</CITATION_ID>
    <DESCRIPTION>Dr. M. Sabourdy about 1960 from Long-Evans outbred stock. To Muhlbock, Amsterdam, and to Han in 1973. Note that other inbred strains independently derived  from Long Evans stock may differ because of the outbred origin (Festing and Bender, 1984).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60992</RGD_ID>
    <STRAIN_SYMBOL>MNS</STRAIN_SYMBOL>
    <FULL_NAME>Milan normotensive strain</FULL_NAME>
    <ORIGINATION>Department of Sciences and Biomedical Technologies, University of Milan, Milan, Italy</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60992</CITATION_ID>
    <DESCRIPTION>Outbred Wistar rats with brother x sister mating and selection for low systolic blood pressure as a normotensive control for MHS. (Bianchi et al 1974).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60993</RGD_ID>
    <STRAIN_SYMBOL>FHH</STRAIN_SYMBOL>
    <FULL_NAME>Fawn Hooded Hypertensive</FULL_NAME>
    <ORIGINATION>University of Colorado Health Science Center, Denver, Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60993</CITATION_ID>
    <DESCRIPTION>An outbred stock of fawn hooded rats introduced into Europe by Tschopp in the early 1970s. Maintained as an outbred stock until the mid-1980s, then brother x sister mating initiated by A.P. Provoost to produce two strains designated FHH (also known as FHR) and FHL, which differ in hypertension and proteinuria. The colony was transferred to Erasmus University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60994</RGD_ID>
    <STRAIN_SYMBOL>F344</STRAIN_SYMBOL>
    <FULL_NAME>Fischer</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60994</CITATION_ID>
    <DESCRIPTION>Curtiss and Dunning 1920 at Columbia University Institute for Cancer Research,To Heston 1949 (Billingham and Silvers 1959). To National Institutes of Health in 1951 (Hansen et al 1982). Subsequent sublines from Dunning or NIH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60995</RGD_ID>
    <STRAIN_SYMBOL>DRY</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Sankyo Co., Ltd., Tokyo, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60995</CITATION_ID>
    <DESCRIPTION>Recombinant inbred strain used as normotensive control in studies of hypertension.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60996</RGD_ID>
    <STRAIN_SYMBOL>DON</STRAIN_SYMBOL>
    <FULL_NAME>Donryu rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60996</CITATION_ID>
    <DESCRIPTION>R. Sato 1950 by inbreeding Japanese albino rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60997</RGD_ID>
    <STRAIN_SYMBOL>DA</STRAIN_SYMBOL>
    <FULL_NAME>DA</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ednrb|Tnfrsf1a</ALLELES>
    <ALLELE_RGD_IDS>2536|621237</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60997</CITATION_ID>
    <DESCRIPTION>Developed from stock of unstated origin by Dr. T.T. Odell, Jr. at Oak Ridge National Laboratory, Tennessee to F11, then by Dr. Darcy Wilson at the Wistar Institute, who named it DA because it expressed the 'd'  blood group allele of Joy Palm, and it is 'a' agouti in colour (Wilson 1965). Inbreeding was completed in about 1965. Although Palm and Black (1971) suggest it may be related to COP, there is no real evidence that this is the case.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60998</RGD_ID>
    <STRAIN_SYMBOL>COP</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60998</CITATION_ID>
    <DESCRIPTION>This  Copenhagen (COP) rat  was an inbred strain from Curtiss 1921 at Columbia University  Institute for Cancer Research.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>60999</RGD_ID>
    <STRAIN_SYMBOL>LEW</STRAIN_SYMBOL>
    <FULL_NAME>Lewis</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>Harlan Sprague Dawley Inc. Indianapolis, United States</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fgf2|Tnfrsf1a</ALLELES>
    <ALLELE_RGD_IDS>2609|621237</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_60999</CITATION_ID>
    <DESCRIPTION>Dr. Margaret Lewis from Wistar stock, to Aptekman and Bogden 1954 at F20, to Silvers in 1958 at F31. Subsequently distributed by Silvers. Used as the inbred partner for a number of congenic strains at the major histocompatibility complex (Stark and Kren 1969). A substrain with congenital hydrocephalus due to primary aqueductal stenosis has been described by Yamada et al, (1992)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61000</RGD_ID>
    <STRAIN_SYMBOL>SHR</STRAIN_SYMBOL>
    <FULL_NAME>Spontaneously Hypertensive Rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Agtr1b|Cd36|Ephx2</ALLELES>
    <ALLELE_RGD_IDS>2071|2301|620732</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61000</CITATION_ID>
    <DESCRIPTION>Okamoto 1963 from outbred Wistar Kyoto rats. Bred from a male with mild hypertension, mated with a female with high blood pressure. Brother x sister mating with continued selection for high blood pressure (Okamoto 1969, Okamoto et al 1972). A number of sublines have been developed with a tendency to develop cardiovascular lesions and stroke (see particularly SHRSP) (Nagaoka et al 1976), and hypercholesterolemia (Yamori 1984). For a recent review see Yamori, (1994).  However, there is no evidence for substrain differentiation among SHR stocks from the major commercial suppliers in the USA both respect to phenotype and DNA fingerprints (Blizard et al, 1991). Strain WKY, developed from the same base populations is sometimes used as a normotensive control, though its use as such must be questioned as it differs at many genetic marker loci (Festing and Bender 1984, and see also strain WKY). Stelzin et al (1992) found that SHR and WKY shared only 50% of their DNA fingerprint bands, whereas SS and SR shared about 80% of bands. Most authorities suggest that WKY alone is not a good control strain, and that for most comparative studies several normotensive strains should be used. There is an extensive literature on the characteristics of SHR. DeJong (1984) provides a useful comparative review of this and other hypertensive strains, and there are regular symposia on hypertensive rat strains (see J. Hypertension 4(suppl):S1-S541, 1986, and Jpn. Heart J. 28:567-648).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61001</RGD_ID>
    <STRAIN_SYMBOL>NEDH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61001</CITATION_ID>
    <DESCRIPTION>Inbred by S. Warren at New England Deaconess Hospital, from Slonaker colony (University of Chicago ca. 1928). To Simonsen Laboratories in 1985 via  B. Hoffman, Veterans Administration Medical Center, Palo Alto, CA. To Mollegaard in 1987.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61002</RGD_ID>
    <STRAIN_SYMBOL>BDIX</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61002</CITATION_ID>
    <DESCRIPTION>Druckrey from a cross between BDI and BDVIII with subsequent selection of  brother-sister pairs for agouti coat color and dark, pigmented eyes. NB. Druckrey 1937 from a yellow, pink-eyed strain. Inbred and reduced to one pair after World War II. Crosses with Wistar stock and subsequent inbreeding led to the development of BDII. According to Druckrey (1971), strains BDIII-BDX were then developed from a cross of a single BDI x BDII mating pair, with subsequent selection for coat colour alleles. However, the strains have four different RT1 haplotypes (d, v, l and e) rather than the two that would be expected from such a cross (Stark and Zeiss 1970). The strains can _not_ be regarded as a set of recombinant inbred strains as defined by Bailey (1971), although their definition by coat colour alleles makes the set easily identifiable , and should help (but not guarantee!) to ensure authenticity. According to Druckrey (1971), all strains have a low tumour incidence, with a median life-span of 700-950 days, depending on strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61003</RGD_ID>
    <STRAIN_SYMBOL>BC</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61003</CITATION_ID>
    <DESCRIPTION>Hagadoorn, Holland to CPB in 1949 at F15. To Utrecht in 1973.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61004</RGD_ID>
    <STRAIN_SYMBOL>WIST/Zihk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61004</CITATION_ID>
    <DESCRIPTION>From Wistar outbred stock in 1978.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61005</RGD_ID>
    <STRAIN_SYMBOL>OM/N</STRAIN_SYMBOL>
    <FULL_NAME>Osborne-Mendel</FULL_NAME>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61005</CITATION_ID>
    <DESCRIPTION>Heston 1946 from non-inbred Osborne-Mendel stock obtained from J White, to NIH at F10 (Hansen et al 1982).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61006</RGD_ID>
    <STRAIN_SYMBOL>PVG</STRAIN_SYMBOL>
    <FULL_NAME>PVG</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61006</CITATION_ID>
    <DESCRIPTION>Kings College of Household Science, to Lister Institute, to Virol, to Glaxo 1946. Inbred by Glaxo. A substrain PVG/cBkl, which is C6 complement deficient due, presumably, to a spontaneous mutation has been described. In good environmental conditions it is perfectly healthy (Leenaerts et al, 1994).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61007</RGD_ID>
    <STRAIN_SYMBOL>WF</STRAIN_SYMBOL>
    <FULL_NAME>Wistar Furth</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61007</CITATION_ID>
    <DESCRIPTION>J Furth 1945 from a commercial Wistar stock in an attempt to develop a high leukaemia rat strain. Strain carries a distinctive heteropycnotic Y chromosome which may be used as a cellular marker (Zieverink and Moloney 1965). A substrain carrying the fuzzy mutation, which arose spontaneously in WF has been used in research on dermal toxicity, and is described in more detail by Marit et al, (1995).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61008</RGD_ID>
    <STRAIN_SYMBOL>WAG</STRAIN_SYMBOL>
    <FULL_NAME>Wistar Albino Glaxo</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61008</CITATION_ID>
    <DESCRIPTION>AL Bacharach, Glaxo Ltd 1924 from Wistar stock. Note that the presence of different coat color alleles in some sublines implies that this strain may have become genetically contaminated at some time in the past. It is therefore important that the subline should be stated carefully in published work. WAG/Cpb clearly differs from other sublines at many loci (Festing and Bender 1984).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61009</RGD_ID>
    <STRAIN_SYMBOL>AVN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61009</CITATION_ID>
    <DESCRIPTION> Unknown. Keil University from O Stark, Charles University, Prague.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61010</RGD_ID>
    <STRAIN_SYMBOL>SHRSP</STRAIN_SYMBOL>
    <FULL_NAME>Spontaneously Hypertensive Rat, Stroke Prone</FULL_NAME>
    <ORIGINATION>Iffa Credo, L'arbresle, France, Max-Delbruck-Center for Molecular Medicine, Berlin-Buch</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61010</CITATION_ID>
    <DESCRIPTION>The A1-sb and A3 substrains of SHR which had been bred as parallel lines from F20 to F36 were crossed (?) and further inbred with selection of offspring of parents that died of stroke (Okamoto et al 1974, 1986, Yamori 1984). To NIH in 1976, and designated SHRSP/A3N. Pathophysiology reviewed by Volpe and Rubattu (1994).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61011</RGD_ID>
    <STRAIN_SYMBOL>BB/N</STRAIN_SYMBOL>
    <FULL_NAME>BioBreeding rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00144</CITATION_ID>
    <DESCRIPTION>Mutation causing diabetes mellitus in a closed colony of outbred Wistar rats at Bio-Breeding Labs, Ontario, Canada in 1974 (Chappel and Chappel 1983). To Worcester in 1977 where inbreeding began. Sublines of diabetic-prone and diabetic-resistant animals have been developed, and there are also subline differences in the incidence, age of onset, untreated survival time of diabetes, leucopenia and body weight gain which can be attributed to genetic factors (Kloting et al 1987). A detailed study of 24 inbred and two outbred lines of diabetes-prone and diabetes resistant BB rats using eight marker loci found substantial genetic variation among and some variation within some of the colonies. The 22 colonies which were apparently isogenic could be divided into four groups on the basis of the marker loci (Prins et al 1990).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61013</RGD_ID>
    <STRAIN_SYMBOL>E3</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61013</CITATION_ID>
    <DESCRIPTION>Kroning, Gottingen from rats of unknown origin selected for fawn hooded phenotype, to Hannover 1957 at F16. To Gottschewski in 1964, then back to Hannover in 1968.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61014</RGD_ID>
    <STRAIN_SYMBOL>OLETF</STRAIN_SYMBOL>
    <FULL_NAME>Otsuka Long-Evans Tokushima fatty</FULL_NAME>
    <ORIGINATION>Otsuka Research Institute, Tokushima, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61014</CITATION_ID>
    <DESCRIPTION>Developed by Kazuya Kawano, Otsuka Pharmaceutical Co., Tokushima, Japan from Long-Evans outbred stock in 1982. A rat with spontaneous polyurea, polyphagia and polydipsia was found in a colony of outbred Long Evans rats purchased from Charles River in 1982. Selective breeding for diabetes with brother x sister mating was subsequently started at the Tokushima Research Institute, Otsuka Pharmaceutical Co., Japan to develop this strain Otsuka Long-Evans Tokushima fatty (OLETF). A deletion of 6847 bases in length in the Cckar gene of the OLETF was identified compared to the wild type gene of  the LETO gene sequence'</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61015</RGD_ID>
    <STRAIN_SYMBOL>LN/MavRrrc</STRAIN_SYMBOL>
    <FULL_NAME>lyon normotensive</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=58&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=58&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00058</CITATION_ID>
    <DESCRIPTION>(taken from Lyon Hypertensive entry, see LH) In 1969 outbred Sprague-Dawley rats were selected for high systolic blood pressure using an indirect plethysmographic technique in pre-warmed unrestrained conscious rats. Three pairs were originally selected, and selection was continued with brother x sister mating. Strain LN was maintained as a normotensive control, and LL as a hypotensive strain. (see Vincent et al 1984, and Vincent and Sassard, 1994 for reviews).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61096</RGD_ID>
    <STRAIN_SYMBOL>SHR/NCruk</STRAIN_SYMBOL>
    <FULL_NAME>Spontaneously Hypertensive Rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://guide.labanimal.com/guide/companyd.jsp?b=1602&gt;Charles River Laboratories &lt;/a&gt; UK</ORIGINATION>
    <SOURCE>&lt;a href=http://guide.labanimal.com/guide/companyd.jsp?b=1602&gt;Charles River Laboratories &lt;/a&gt; UK</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61096</CITATION_ID>
    <DESCRIPTION>NIH derived strain maintained at the Charles River, United Kingdom.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61097</RGD_ID>
    <STRAIN_SYMBOL>WKY/NCruk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://guide.labanimal.com/guide/companyd.jsp?b=1602&gt;Charles River Laboratories &lt;/a&gt; UK</ORIGINATION>
    <SOURCE>&lt;a href=http://guide.labanimal.com/guide/companyd.jsp?b=1602&gt;Charles River Laboratories &lt;/a&gt; UK</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61097</CITATION_ID>
    <DESCRIPTION>NIH derived strain maintained at the Charles River, United Kingdom.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61098</RGD_ID>
    <STRAIN_SYMBOL>BXH/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61098</CITATION_ID>
    <DESCRIPTION>These recombinant inbred strains are derived from the (BN-&lt;i&gt;Lx&lt;/i&gt;/Cub, SHR/OlaIpcv x BN)F2 pairs and maintained at Czech Academy of Sciences, Prague, Czech Republic</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61099</RGD_ID>
    <STRAIN_SYMBOL>HXB/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology, Czech Academy of Sciences, Charles University, Prague</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61099</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/Ola and BN-Lx/Cub, this strain has been extensively genotyped in known genes as well as DNA markers, strain distribution patterns of 700+ alleles have been published.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61100</RGD_ID>
    <STRAIN_SYMBOL>SHR/Ola</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61100</CITATION_ID>
    <DESCRIPTION>Strain originated from an inbred SHR strain from Harlan UK Ltd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61103</RGD_ID>
    <STRAIN_SYMBOL>WKY</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd36|Nos3</ALLELES>
    <ALLELE_RGD_IDS>2301|3186</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61103</CITATION_ID>
    <DESCRIPTION>This strain was maintained at Medical College of Ohio, Toledo, Ohio</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61104</RGD_ID>
    <STRAIN_SYMBOL>LEW/NCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.geneticmodels.com/RM/rats/rats_a_c.html&gt;Charles River Laboratories USA &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.geneticmodels.com/RM/rats/rats_a_c.html&gt;Charles River Laboratories USA &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61104</CITATION_ID>
    <DESCRIPTION>Substrain of LEW obtained from Charles River, which was developed from Dr Margaret Lewis from Wistar stock in early 1950s. This came to Charles River from Tulane in 1970 at F34.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61105</RGD_ID>
    <STRAIN_SYMBOL>WKY/NHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.envigo.com/model/wky-nhsd?selctry=U.S.&amp;ctry=/&gt; Envigo&lt;/a</ORIGINATION>
    <SOURCE>&lt;a href =https://www.envigo.com/model/wky-nhsd?selctry=U.S.&amp;ctry=/&gt; Envigo&lt;/a</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61105</CITATION_ID>
    <DESCRIPTION>Derived from a nucleus colony obtained from the National Institutes of Health, Bethesda, Maryland. and maintained at  Harlan Indianapolis, Indiana U.S.A.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61106</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D8Mit5-D8Mgh6&lt;/i&gt;)/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="39106258" STOP_POS="39106363" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="30848154" STOP_POS="61290444" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="33558660" STOP_POS="65717592" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="33603024" STOP_POS="65467051" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="32203394" STOP_POS="64762616" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61106</CITATION_ID>
    <DESCRIPTION>A segment of chr. 8 is transferred from the normotensive BN-&lt;i&gt;Lx&lt;/i&gt;/Cub rat to the SHR/Ola.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61107</RGD_ID>
    <STRAIN_SYMBOL>BB/OK</STRAIN_SYMBOL>
    <FULL_NAME>BioBreeding rat</FULL_NAME>
    <ORIGINATION>Central Institute for Diabetes, Karlsburg, Germany</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=512&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Immunology</RESEARCH_USE>
    <ALLELES>Asns|Cav1|Cftr|Cyp51|Hgf|Met|Smo|Tac1|Stx1a|Cdk5</ALLELES>
    <ALLELE_RGD_IDS>2162|2280|2332|2481|2794|3082|3726|3807|69430|70514</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61107</CITATION_ID>
    <DESCRIPTION>This colony was established in 1983, these rats were originally from an outbred colony from Ottawa, Canada.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61109</RGD_ID>
    <STRAIN_SYMBOL>F344/NHsd</STRAIN_SYMBOL>
    <FULL_NAME>F344/NHsd</FULL_NAME>
    <ORIGINATION>&lt;a href =http://www.envigo.com/model/f344-nhsd/&gt;Envigo&lt;/a&gt;, &lt;a href =http://www.envigo.com/model/f344-nhsd-aged/&gt;Envigo aged&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =http://www.envigo.com/model/f344-nhsd/&gt;Envigo&lt;/a&gt;, &lt;a href =http://www.envigo.com/model/f344-nhsd-aged/&gt;Envigo aged&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61109</CITATION_ID>
    <DESCRIPTION>Strain originated from Curtiss and Dunning 1920 at Columbia University Institute for Cancer Research, To Heston 1949 (Billingham and Silvers 1959). To National Institutes of Health in 1951 (Hansen et al 1982). Subsequent sublines from Dunning or NIH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61110</RGD_ID>
    <STRAIN_SYMBOL>SHR/Mol</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Mollegaard Breeding Centre Ltd., Denmark</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61110</CITATION_ID>
    <DESCRIPTION>Spontaneously hypertensive rat, maintained at the Mollegaard breeding center, displays traits of hypertension but not to diabetes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61111</RGD_ID>
    <STRAIN_SYMBOL>DA/Slc</STRAIN_SYMBOL>
    <FULL_NAME>dark agouti</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=380 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=380 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61111</CITATION_ID>
    <DESCRIPTION>These were produced by from SD parents in 1984 by hysterectomy and fostering, then moved to Kumamoto University of Medicine in 1983.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61112</RGD_ID>
    <STRAIN_SYMBOL>13M</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory of Human Behavior and Metabolism, Rockefeller University</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61112</CITATION_ID>
    <DESCRIPTION>This is a Leprfa/Leprfa substrain derived from the Zucker rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61113</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;I&gt;Lx&lt;/I&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61113</CITATION_ID>
    <DESCRIPTION>These were derived by introgressing mutant Lx gene of the polydactylous rat onto the BN background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61114</RGD_ID>
    <STRAIN_SYMBOL>DA/Bkl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Bantin and Kingman, Fremont, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61114</CITATION_ID>
    <DESCRIPTION>Commercially available strain.  Maintained at the National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD, for production of DA background QTL monocongenic rats and experimental controls.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61115</RGD_ID>
    <STRAIN_SYMBOL>BN/SsN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61115</CITATION_ID>
    <DESCRIPTION>To N 1972 from Silvers at F34. Silvers began brother-sister matings with selection for histocompatibility in 1958 from a brown mutation in a stock of wild rats maintained by King in a penbred colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61116</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/A3</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Graduate School of Human and Environmental Studies, University of Kyoto, Kyoto, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61116</CITATION_ID>
    <DESCRIPTION>Derived from the a substrain of the SHR strain by selective inbreeding for stroke proneness.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61117</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Lx&lt;/i&gt;/Cub</STRAIN_SYMBOL>
    <FULL_NAME>Brown Norway with polydactyly-luxate</FULL_NAME>
    <ORIGINATION>Charles University, Department of Biology, Prague</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61117</CITATION_ID>
    <DESCRIPTION>These were derived by introgressing mutant Lx gene of the polydactylous (PD/Cub) rat onto the BN background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61118</RGD_ID>
    <STRAIN_SYMBOL>BUF/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=458 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=458 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer; Urology</RESEARCH_USE>
    <ALLELES>Bsis</ALLELES>
    <ALLELE_RGD_IDS>2221</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61118</CITATION_ID>
    <DESCRIPTION>Strain originated from Heston 1946 from Buffalo stock of H. Morris. To NIH in 1950 at F10.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61119</RGD_ID>
    <STRAIN_SYMBOL>WKY/NCrlCrlj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Charles River Laboratories Japan, &lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=477&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-05-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61119</CITATION_ID>
    <DESCRIPTION>Originated from outbred Wistar of Kyoto University. To NIH from Kyoto University in 1971 and sib mating has started. To Charles River Laboratories, Inc from NIH in 1974 at F11, and to Charles River Japan, Inc. in 1981 at F25. (May 27, 2010). Used as control strain for the SHR strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61498</RGD_ID>
    <STRAIN_SYMBOL>BN/NHsdMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61498</CITATION_ID>
    <DESCRIPTION>Inbred from a single pair of SsN line rats obtained from Harlan Sprague Dawley (Alabama colony). Maintained at the Medical College of Wisconsin since 1995. To confirm homozygosity, the strain was tested with 200 microsatellite markers (genome-wide scan at 20cM) all of which were homozygous for all regions tested (Cowley et al. 2000, Physiol. Genomics. 2:107-115). The genome of this BN strain is used as the rat reference assembly.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61499</RGD_ID>
    <STRAIN_SYMBOL>SS/JrHsdMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61499</CITATION_ID>
    <DESCRIPTION>Inbred from a congenic control group of Dahl S rats (SS/Ren) obtained from Dr. Theodore Kurtz (UCSF, CA) which were originally derived from the Harlan SS/Jr colony. Maintained at the Medical College of Wisconsin since 1991, this strain has undergone considerable marker-selected breeding to eliminate residual heterozygosity and genetic contamination. To confirm homozygosity, the strain was tested with 200 microsatellite markers (genome-wide scan at 20cM) all of which were homozygous for all regions tested (Cowley etal. 2000, Physiol. Genomics. 2:107-115).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>61517</RGD_ID>
    <STRAIN_SYMBOL>FHL/Eur</STRAIN_SYMBOL>
    <FULL_NAME>Fawn Hooded Low blood pressure</FULL_NAME>
    <ORIGINATION>Erasmus University-Rotterdam</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_61517</CITATION_ID>
    <DESCRIPTION>An outbred stock of fawn hooded rats introduced into Europe by Tschopp in the early 1970s. Maintained as an outbred stock until the mid-1980s, then brother x sister mating initiated by A.P. Provoost to produce two strains designated FHH (also known as FHR) and FHL, which differ in hypertension and proteinuria. The colony was transferred to Erasmus University. FHL rats do not develop hypertension or renal damage</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67934</RGD_ID>
    <STRAIN_SYMBOL>WOKA</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67934</CITATION_ID>
    <DESCRIPTION>Outbred Wistar BB rats from Biobreeding Laboratories, Ottawa, Canada in 1981 to Dr.I. Kloting, Dept. of Laboratory Animal Science, Inst. of Pathology, University of Greifswald,D-17495, Karlsburg, Germany. WOKA (originally designated WOK.1A) was developed by brother x sister mating from rats homozygous for RT1a, and WOKW (originally designatedWOK.1W) from rats homozygous for RT1U , a haplotype which pre-disposes to type I diabetes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67935</RGD_ID>
    <STRAIN_SYMBOL>WOKW</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Laboratory Animal Science, Inst. of Pathology, University of Greifswald,D-17495, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67935</CITATION_ID>
    <DESCRIPTION>Outbred Wistar BB rats from Biobreeding Laboratories, Ottawa, Canada in 1981 to Dr.I. Kloting, Dept. of Laboratory Animal Science, Inst. of Pathology, University of Greifswald,D-17495, Karlsburg, Germany. WOKA (originally designated WOK.1A) was developed by brother x sister mating from rats homozygous for RT1a, and WOKW (originally designated WOK.1W) from rats homozygous for RT1U , a haplotype which pre-disposes to type I diabetes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67936</RGD_ID>
    <STRAIN_SYMBOL>WR</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67936</CITATION_ID>
    <DESCRIPTION> Sykora, Rosice (Stark et al 1968b). No further infromation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67937</RGD_ID>
    <STRAIN_SYMBOL>WST</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67937</CITATION_ID>
    <DESCRIPTION> Strain WAG, Glaxo Research, Uxbridge, UK to Institute of Rheumatology, Warsaw in 1964. To Institute of Oncology, Warsaw 1964. To Institute of Occupational Medicine (Imp), Warsaw in 1965 (Pietrowicz 1986).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67938</RGD_ID>
    <STRAIN_SYMBOL>Y59</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67938</CITATION_ID>
    <DESCRIPTION> Strain developed in Zagreb, Jugoslavia.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67939</RGD_ID>
    <STRAIN_SYMBOL>YA/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00191</CITATION_ID>
    <DESCRIPTION>No further information.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67940</RGD_ID>
    <STRAIN_SYMBOL>YO</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67940</CITATION_ID>
    <DESCRIPTION> Fredrich Cancer Research Facility to Pit at F35. Genetic charactersitics given by Kunz et al (1987). Rapid elimination of Trichinella spiralis worms (2/12) (Bell, 1992)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67941</RGD_ID>
    <STRAIN_SYMBOL>Z61</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67941</CITATION_ID>
    <DESCRIPTION>Curtis 1920 at Columbia University Institute for Cancer Research. Susceptible to Cysticercus. Susceptible to oestrogen and 2-acetylaminofluorine-induced tumours.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67942</RGD_ID>
    <STRAIN_SYMBOL>ZI</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67942</CITATION_ID>
    <DESCRIPTION> A breeder in W Germany to Hannover in 1980, to Kyoto in 1983. Carries recessive autosomal gene zitter which causes spongiform encephalopathy of the central nervous system with tremors at 15 days of age as well as curley whiskers  and hair (Yamada et al 1989).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67943</RGD_ID>
    <STRAIN_SYMBOL>SHE/N-cp</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67943</CITATION_ID>
    <DESCRIPTION>Reference found in: Berdanier C. D., Pan J. S., Hartle D. K., and Michaelis O. E. 1993, Comparative Biochemistry and physiology B-Biochemistry &amp; Molecular Biology 106:87-94.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67945</RGD_ID>
    <STRAIN_SYMBOL>IS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67945</CITATION_ID>
    <DESCRIPTION>from a cross between a wild male and a Wistar female, with sib mating since 1968.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67948</RGD_ID>
    <STRAIN_SYMBOL>JC</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67948</CITATION_ID>
    <DESCRIPTION> LEW/Ss to Hall Institute, to CSIRO in Brisbane, Australia. Presumed genetic comtamination some time prior to 1980, and re-named JC. To Dr. T Fukumoto, Hamamatsu University School of Medicine in 1983. Genetic markers described by Adams et al (1984).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67957</RGD_ID>
    <STRAIN_SYMBOL>APR</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67957</CITATION_ID>
    <DESCRIPTION>Developed as strain MF by Holme and Piechuta (1979) by selective breeding of Sprague-Dawley outbred rats. Individuals were injected sub-cutaneously with egg albumin and B. pertussis vaccine i.p. then challenged with areosolised egg albumin after 14-18 days. Individuals within litters with the most severe symproms (longest duration of dyspnea) were selected and mated brother x sister. Later re-named APR (Apnea Prone Rat).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67958</RGD_ID>
    <STRAIN_SYMBOL>AS</STRAIN_SYMBOL>
    <FULL_NAME>Albino Surgery</FULL_NAME>
    <ORIGINATION>National Institute for Medical Research, Mill Hill, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67958</CITATION_ID>
    <DESCRIPTION>University of Otago from Wistar rats imported from England in 1930. May be subline of GH, with which it is histocompatible (Heslop and Phelan 1973).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67959</RGD_ID>
    <STRAIN_SYMBOL>AS2</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67959</CITATION_ID>
    <DESCRIPTION>Outbred rats at the University of Otago Medical School, to Dept. of Surgery 1963 at F22-24. Not histocompatible with AS (Heslop 1968).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67960</RGD_ID>
    <STRAIN_SYMBOL>AUG</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67960</CITATION_ID>
    <DESCRIPTION>Derived from one of the US August sublines in 1951 and distributed by the Chester Beatty Institute, Pollards Wood, England.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67962</RGD_ID>
    <STRAIN_SYMBOL>AN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67962</CITATION_ID>
    <DESCRIPTION>Outbred Wistar Imamichi strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67965</RGD_ID>
    <STRAIN_SYMBOL>AXC</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67965</CITATION_ID>
    <DESCRIPTION> A recombinant inbred of ACI and C. Curtiss and Dunning 1926 at the Columbia University Institute for Cancer Research. To Albert Segaloff of the Alton Ochsner Medical Foundation, New Orleans before 1956, to Southwestern Foundation for Biomedical Research in 1976.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67966</RGD_ID>
    <STRAIN_SYMBOL>B</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67966</CITATION_ID>
    <DESCRIPTION> Dr. P Swanson from Wistar stock now known to be King B strain, to Dempster at F43. To Harrington in 1971 at F85.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67967</RGD_ID>
    <STRAIN_SYMBOL>B/1N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67967</CITATION_ID>
    <DESCRIPTION>No further information.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67971</RGD_ID>
    <STRAIN_SYMBOL>BBZ</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67971</CITATION_ID>
    <DESCRIPTION>Strain developed by crossing BB/Wor rats, a lean model of type I diabetes mellitus with a Zucker fatty (fa ) rat of unstated genetic background, followed by sib mating with forced heterozygosity for the fatty gene. Thus in each generation there is a ratio of 3</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67974</RGD_ID>
    <STRAIN_SYMBOL>BDE</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67974</CITATION_ID>
    <DESCRIPTION>Zentralinstitut fur Versuchstierzucht, Hannover, from a cross between BDVII and E3, with selection for black hooded offspring.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67975</RGD_ID>
    <STRAIN_SYMBOL>BDI</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67975</CITATION_ID>
    <DESCRIPTION>Druckrey 1937 from a yellow, pink-eyed strain.  Inbred and reduced to one pair after World War II. Crosses with Wistar stock and subsequent inbreeding led to the development of BDII. According to Druckrey (1971), strains BDIII-BDX were then developed from a cross of a single BDI x BDII mating pair, with subsequent selection for coat colour alleles. However, the strains have four different RT1 haplotypes (d, v, l and e) rather than the two that would be expected from such a cross (Stark and Zeiss 1970). The strains can _not_ be regarded as a set of recombinant inbred strains as defined by Bailey (1971), although their definition by coat colour alleles makes the set easily identifiable , and should help (but not guarantee!) to ensure authenticity. According to Druckrey (1971), all strains have a low tumour incidence, with a median life-span of 700-950 days, depending on strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67976</RGD_ID>
    <STRAIN_SYMBOL>BDII</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67976</CITATION_ID>
    <DESCRIPTION>Druckrey 1937 from a yellow, pink-eyed strain.  Inbred and reduced to one pair after World War II. Crosses with Wistar stock and subsequent inbreeding led to the development of BDII. According to Druckrey (1971), strains BDIII-BDX were then developed from a cross of a single BDI x BDII mating pair, with subsequent selection for coat colour alleles. However, the strains have four different RT1 haplotypes (d, v, l and e) rather than the two that would be expected from such a cross (Stark and Zeiss 1970). The strains can not be regarded as a set of recombinant inbred strains as defined by Bailey (1971), although their definition by coat colour alleles makes the set easily identifiable , and should help (but not guarantee!) to ensure authenticity. According to Druckrey (1971), all strains have a low tumour incidence, with a median life-span of 700-950 days, depending on strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67977</RGD_ID>
    <STRAIN_SYMBOL>BDIII</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67977</CITATION_ID>
    <DESCRIPTION>Druckrey 1937 from a yellow, pink-eyed strain. Inbred and reduced to one pair after World War II. Crosses with Wistar stock and subsequent inbreeding led to the development of BDII. According to Druckrey (1971), strains BDIII-BDX were then developed from a cross of a single BDI x BDII mating pair, with subsequent selection for coat colour alleles. However, the strains have four different RT1 haplotypes (d, v, l and e) rather than the two that would be expected from such a cross (Stark and Zeiss 1970). The strains can _not_ be regarded as a set of recombinant inbred strains as defined by Bailey (1971), although their definition by coat colour alleles makes the set easily identifiable , and should help (but not guarantee!) to ensure authenticity. According to Druckrey (1971), all strains have a low tumour incidence, with a median life-span of 700-950 days, depending on strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67978</RGD_ID>
    <STRAIN_SYMBOL>BDIV</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67978</CITATION_ID>
    <DESCRIPTION>Druckrey 1937 from a yellow, pink-eyed strain. Inbred and reduced to one pair after World War II. Crosses with Wistar stock and subsequent inbreeding led to the development of BDII. According to Druckrey (1971), strains BDIII-BDX were then developed from a cross of a single BDI x BDII mating pair, with subsequent selection for coat colour alleles. However, the strains have four different RT1 haplotypes (d, v, l and e) rather than the two that would be expected from such a cross (Stark and Zeiss 1970). The strains can _not_ be regarded as a set of recombinant inbred strains as defined by Bailey (1971), although their definition by coat colour alleles makes the set easily identifiable, and should help (but not guarantee!) to ensure authenticity. According to Druckrey (1971), all strains have a low tumour incidence, with a median life-span of 700-950 days, depending on strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67981</RGD_ID>
    <STRAIN_SYMBOL>BDV</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67981</CITATION_ID>
    <DESCRIPTION>Druckrey 1937 from a yellow, pink-eyed strain. Inbred and reduced to one pair after World War II. Crosses with Wistar stock and subsequent inbreeding led to the development of BDII. According to Druckrey (1971), strains BDIII-BDX were then developed from a cross of a single BDI x BDII mating pair, with subsequent selection for coat colour alleles. However, the strains have four different RT1 haplotypes (d, v, l and e) rather than the two that would be expected from such a cross (Stark and Zeiss 1970). The strains can _not_ be regarded as a set of recombinant inbred strains as defined by Bailey (1971), although their definition by coat colour alleles makes the set easily identifiable , and should help (but not guarantee!) to ensure authenticity. According to Druckrey (1971), all strains have a low tumour incidence, with a median life-span of 700-950 days, depending on strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67983</RGD_ID>
    <STRAIN_SYMBOL>BDVI</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67983</CITATION_ID>
    <DESCRIPTION>Druckrey 1937 from a yellow, pink-eyed strain. Inbred and reduced to one pair after World War II. Crosses with Wistar stock and subsequent inbreeding led to the development of BDII. According to Druckrey (1971), strains BDIII-BDX were then developed from a cross of a single BDI x BDII mating pair, with subsequent selection for coat colour alleles. However, the strains have four different RT1 haplotypes (d, v, l and e) rather than the two that would be expected from such a cross (Stark and Zeiss 1970). The strains can _not_ be regarded as a set of recombinant inbred strains as defined by Bailey (1971), although their definition by coat colour alleles makes the set easily identifiable , and should help (but not guarantee!) to ensure authenticity. According to Druckrey (1971), all strains have a low tumour incidence, with a median life-span of 700-950 days, depending on strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67984</RGD_ID>
    <STRAIN_SYMBOL>BDVII</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67984</CITATION_ID>
    <DESCRIPTION>Druckrey 1937 from a yellow, pink-eyed strain. Inbred and reduced to one pair after World War II. Crosses with Wistar stock and subsequent inbreeding led to the development of BDII. According to Druckrey (1971), strains BDIII-BDX were then developed from a cross of a single BDI x BDII mating pair, with subsequent selection for coat colour alleles. However, the strains have four different RT1 haplotypes (d, v, l and e) rather than the two that would be expected from such a cross (Stark and Zeiss 1970). The strains can _not_ be regarded as a set of recombinant inbred strains as defined by Bailey (1971), although their definition by coat colour alleles makes the set easily identifiable , and should help (but not guarantee!) to ensure authenticity. According to Druckrey (1971), all strains have a low tumour incidence, with a median life-span of 700-950 days, depending on strain. Low secondary antibody response to polypeptide (T,G)-Pro-Lys (20/20) (Gunther et al 1976)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67986</RGD_ID>
    <STRAIN_SYMBOL>BDVIII</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67986</CITATION_ID>
    <DESCRIPTION>Druckrey 1937 from a yellow, pink-eyed strain. Inbred and reduced to one pair after World War II. Crosses with Wistar stock and subsequent inbreeding led to the development of BDII. According to Druckrey (1971), strains BDIII-BDX were then developed from a cross of a single BDI x BDII mating pair, with subsequent selection for coat colour alleles. However, the strains have four different RT1 haplotypes (d, v, l and e) rather than the two that would be expected from such a cross (Stark and Zeiss 1970). The strains can _not_ be regarded as a set of recombinant inbred strains as defined by Bailey (1971), although their definition by coat colour alleles makes the set easily identifiable , and should help (but not guarantee!) to ensure authenticity. According to Druckrey (1971), all strains have a low tumour incidence, with a median life-span of 700-950 days, depending on strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67987</RGD_ID>
    <STRAIN_SYMBOL>BDX</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lypd3</ALLELES>
    <ALLELE_RGD_IDS>69053</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67987</CITATION_ID>
    <DESCRIPTION>Druckrey 1937 from a yellow, pink-eyed strain. Inbred and reduced to one pair after World War II. Crosses with Wistar stock and subsequent inbreeding led to the development of BDII. According to Druckrey (1971), strains BDIII-BDX were then developed from a cross of a single BDI x BDII mating pair, with subsequent selection for coat colour alleles. However, the strains have four different RT1 haplotypes (d, v, l and e) rather than the two that would be expected from such a cross (Stark and Zeiss 1970). The strains can _not_ be regarded as a set of recombinant inbred strains as defined by Bailey (1971), although their definition by coat colour alleles makes the set easily identifiable , and should help (but not guarantee!) to ensure authenticity. According to Druckrey (1971), all strains have a low tumour incidence, with a median life-span of 700-950 days, depending on strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67988</RGD_ID>
    <STRAIN_SYMBOL>BEG</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67988</CITATION_ID>
    <DESCRIPTION>from a cross between SC and TE.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67989</RGD_ID>
    <STRAIN_SYMBOL>BH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67989</CITATION_ID>
    <DESCRIPTION> D. Wilson, University of Pennsylvania from unknown stock. To Dml, who transferred stock to University of Iowa in 1973. Dml to Won to Ztm in 1973.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67990</RGD_ID>
    <STRAIN_SYMBOL>BI</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67990</CITATION_ID>
    <DESCRIPTION> Formerly called B3, but now extinct. Slow elimination of \i Trichinella spiralis\i0  worms (11/12) (Bell, 1992)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67991</RGD_ID>
    <STRAIN_SYMBOL>BIL/1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67991</CITATION_ID>
    <DESCRIPTION>University of Pittsburgh from a mutation in a colony of unknown background held by the NIH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>67993</RGD_ID>
    <STRAIN_SYMBOL>BIL/2</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_67993</CITATION_ID>
    <DESCRIPTION>University of Pittsburgh from a mutation in a colony of unknown background held by the NIH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68000</RGD_ID>
    <STRAIN_SYMBOL>BIRMB</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68000</CITATION_ID>
    <DESCRIPTION>same as BIRMA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68001</RGD_ID>
    <STRAIN_SYMBOL>BLK/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Asip</ALLELES>
    <ALLELE_RGD_IDS>2003</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68001</CITATION_ID>
    <DESCRIPTION>This strain has an agouti mutation</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68007</RGD_ID>
    <STRAIN_SYMBOL>BROFO</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68007</CITATION_ID>
    <DESCRIPTION> Medical Biological Laboratory, Defence Research Organisation, The Netherlands. Large Wistar type of rat maintained in germ-free and SPF conditions.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68008</RGD_ID>
    <STRAIN_SYMBOL>BS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68008</CITATION_ID>
    <DESCRIPTION> University of Otago Medical School from a cross of wild rats x Wistar stock, with black phenotype backcrossed to the Wistar (Zeiss 1966).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68011</RGD_ID>
    <STRAIN_SYMBOL>C</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68011</CITATION_ID>
    <DESCRIPTION>No further information.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68012</RGD_ID>
    <STRAIN_SYMBOL>CAP</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68012</CITATION_ID>
    <DESCRIPTION> Polish Academy of Sciences, Krakow (Stark et al 1968a).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68013</RGD_ID>
    <STRAIN_SYMBOL>CAR/N</STRAIN_SYMBOL>
    <FULL_NAME>Hunt-Hoppert caries resistant; CA/R</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68013</CITATION_ID>
    <DESCRIPTION>Hunt 1937, developed for resistance to dental caries (Hunt et al 1955).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68014</RGD_ID>
    <STRAIN_SYMBOL>CAS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68014</CITATION_ID>
    <DESCRIPTION>Hunt 1937, developed for high incidence of dental caries.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68015</RGD_ID>
    <STRAIN_SYMBOL>CBH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68015</CITATION_ID>
    <DESCRIPTION>Woodruff, Edinburgh to Chester Beatty Inst., Fulham Road, to Chemical Defense Establishment, Porton in 1963. Then to Chester Beatty, Pollards Wood in 1966. To Olac in 1980 when the strain was re-named CBH (Chester Beatty Hooded).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68018</RGD_ID>
    <STRAIN_SYMBOL>CPB-WE</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68018</CITATION_ID>
    <DESCRIPTION>Wistar outbred rats inbred at the Central Institute for Breeding of Laboratory Animals, Zeist, The Netherlands.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68019</RGD_ID>
    <STRAIN_SYMBOL>CRDH</STRAIN_SYMBOL>
    <FULL_NAME>Cohen Rosenthal Diabetic Hypertensive</FULL_NAME>
    <ORIGINATION>Hebrew University Hospital and Hadassah-Hebrew Medical College, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68019</CITATION_ID>
    <DESCRIPTION> As Cohen Rosenthal Diabetic Hypertensive, from a cross between strains CDR and SHR followed by selection for high blood pressure and blood glucose levels following two-months of feeding a  copper-poor, high (74%) sucrose diet. Selected animals were brother x sister mated (Cohen et al, 1993, Rosenthal et al 1995).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68020</RGD_ID>
    <STRAIN_SYMBOL>CWS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68020</CITATION_ID>
    <DESCRIPTION>R Shoji from a cross of an outbred Jcl:SD rat with spontaneous cataract and WKAH inbred rats. Subsequent brother x sister mating with selecting for cataract resulted in all offspring from the 3rd. generation developing cataract accompanied by microphthalmia which can be observed from the day that the eyes open.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68022</RGD_ID>
    <STRAIN_SYMBOL>DB</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68022</CITATION_ID>
    <DESCRIPTION>No further information.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68023</RGD_ID>
    <STRAIN_SYMBOL>DEBR</STRAIN_SYMBOL>
    <FULL_NAME>Dundee experimental bald rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68023</CITATION_ID>
    <DESCRIPTION>The DEBR rats have been bred at the University of Dundee since  March 1984. The original crosses involved the inbred stock BDIX rats showing lesion and Wistar rat. The descendants of this cross resulted from full sib-matings.Two strains of DEBR rats are geing developed: the black-hooded and brown-hooded strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68026</RGD_ID>
    <STRAIN_SYMBOL>DSS/1N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00155</CITATION_ID>
    <DESCRIPTION>Three inbred strains developed from outbred Sprague-Dawley stock selected for sensitivity to sodium chloride-induced hypertension (Dahl et al. 1962a, b). Inbred by Iwai and then Hansen (N).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68027</RGD_ID>
    <STRAIN_SYMBOL>DSS/2N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00156</CITATION_ID>
    <DESCRIPTION>Three inbred strains developed from outbred Sprague-Dawley stock selected for sensitivity to sodium chloride-induced hypertension (Dahl et el 1962a, b). Inbred by Iwai and then Hansen (N).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68028</RGD_ID>
    <STRAIN_SYMBOL>DSS/3N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00157</CITATION_ID>
    <DESCRIPTION>Three inbred strains developed from outbred Sprague-Dawley stock selected for sensitivity to sodium chloride-induced hypertension (Dahl et el 1962a, b). Inbred by Iwai and then Hansen (N).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68029</RGD_ID>
    <STRAIN_SYMBOL>DXE-1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68029</CITATION_ID>
    <DESCRIPTION>Set of 4 recombinant inbred strains from a cross between DA and E3 (Central Institute, Hannover)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68031</RGD_ID>
    <STRAIN_SYMBOL>ET</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Taisho Pharmaceutical Co. Ltd</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68031</CITATION_ID>
    <DESCRIPTION> WKA strain obtained from Taisho Pharmaceutical Co. Ltd. Develops ectopic scrota in about 70% of males. The defect is controled by multiple genes, and the females are normal  (Ikadai et al 1988b).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68032</RGD_ID>
    <STRAIN_SYMBOL>EXBH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68032</CITATION_ID>
    <DESCRIPTION>Hannover as a recombinant inbred strain from a cross between E3 and BN. Developed as a coat colour testing stock. Low reproductive performance (Greenhouse et al 1990)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68034</RGD_ID>
    <STRAIN_SYMBOL>F6R</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68034</CITATION_ID>
    <DESCRIPTION>Mutation in an irradiated F344 strain obtained from the National Institute of Genetics, Misima, Japan. Carries chromosomal translocation (9:14) (Yosida et al 1985).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68035</RGD_ID>
    <STRAIN_SYMBOL>FCH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68035</CITATION_ID>
    <DESCRIPTION>Fice Combined Hyperlipidemic strain. Strain developed from outbred stock by selection for high serum cholesterol.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68036</RGD_ID>
    <STRAIN_SYMBOL>FH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rab38&lt;sup&gt;ru&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>1600311</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68036</CITATION_ID>
    <DESCRIPTION> Dodds, 1974 from an outbred stock developed by NRF Maier, University of Michigan, Ann Arbor, from a cross between German brown rats and white Lashley rats (Tschopp and Zucker 1972). Note that other inbred strains have been developed from the same outbred stock (see strains FHH and FHL), which may have different characteristics.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68038</RGD_ID>
    <STRAIN_SYMBOL>FHL</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68038</CITATION_ID>
    <DESCRIPTION>see FHH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68040</RGD_ID>
    <STRAIN_SYMBOL>FNL</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68040</CITATION_ID>
    <DESCRIPTION>Fice Normolipidemic strain. Developed as a control strain for FCH (see FCH).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68041</RGD_ID>
    <STRAIN_SYMBOL>G</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68041</CITATION_ID>
    <DESCRIPTION> Gorter, Holland to Hagedoorn, to CPB at F 35 (van Vliet 1977)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68042</RGD_ID>
    <STRAIN_SYMBOL>GEPR</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68042</CITATION_ID>
    <DESCRIPTION>Jobe, 1971 from outbred Sprague-Dawley stock. Selected for moderate susceptibility to audiogenic stimuli-induced seizures (Reigel et al 1986a).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68044</RGD_ID>
    <STRAIN_SYMBOL>GHA</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68044</CITATION_ID>
    <DESCRIPTION> The Queen Elizabeth Hospital, Woodville, S. Australia from mixed Wistar, LEW and coloured stock (Festing and Staats 1973).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68046</RGD_ID>
    <STRAIN_SYMBOL>HCS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68046</CITATION_ID>
    <DESCRIPTION>Harvard to Liverpool, UK in 1960.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68047</RGD_ID>
    <STRAIN_SYMBOL>HMT</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68047</CITATION_ID>
    <DESCRIPTION>Outbred Alderley Park (strain 1) inbred since 1964 as "Harwell Mouth Tumor".</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68048</RGD_ID>
    <STRAIN_SYMBOL>HS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68048</CITATION_ID>
    <DESCRIPTION> Probably from same Wistar x wild rat cross as BS (Zeiss 1966). Docile, fair reproduction. Approximately 12% hydrocephalus.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68049</RGD_ID>
    <STRAIN_SYMBOL>HXB-1-43/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Laboratory Animal Science, Faculty of Veterinary Medicine, Utrecht University, P.O. Box 80.166 NL-3508 TD Utrecht, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68049</CITATION_ID>
    <DESCRIPTION>Set of 17 recombinant inbred strains developed by Pravenec, Klir and Kren from a cross between SHR/OlaIpcv and BN.Lx/CubIpcv, and described by Pravenec et al (1988). Strains have now been typed at 500 loci and scanned for quantitative trait loci associated with blood pressure and heart weight (Pravenec et al, 1995). These recombinant inbred strains are derived from the (SHR/OlaIpcvx BN-Lx/Cub)F2 pairs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68050</RGD_ID>
    <STRAIN_SYMBOL>IIM</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68050</CITATION_ID>
    <DESCRIPTION>Set of nine strains bred as parallel strains from a single outbred colony maintained by B. Houssay in 1948. All strains were selected for large body weight and high fertility. One strain designated Beta IIM (RGD:40924649) derived from line 'b'  became obese with mild glucose intolerance and glycosurea in older obese rats (Calderari et al 1987). Alpha IIM (RGD:40924650) was used as a control  strain  in study.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68051</RGD_ID>
    <STRAIN_SYMBOL>INR/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00160</CITATION_ID>
    <DESCRIPTION>Harrington 1962 from a stock selected by CS Hall for low open field defaecation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68052</RGD_ID>
    <STRAIN_SYMBOL>IR</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68052</CITATION_ID>
    <DESCRIPTION>Harrington 1962 from a cross  of a Michigan and a Berlin stock (Harrington 1981).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68057</RGD_ID>
    <STRAIN_SYMBOL>K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68057</CITATION_ID>
    <DESCRIPTION> Dr. E. Matthies, Halle-Wittenberg 1958 from outbred Wistar stock.. Low spontaneous tumour incidence (less that 0.5%). Good breeding performance. Weight at 100 days 290g in males and 200g in females. Developed for resistance to a range of transplantable tumours (Matthies and Ponsold 1973).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68058</RGD_ID>
    <STRAIN_SYMBOL>KGH/PitN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00162</CITATION_ID>
    <DESCRIPTION>Kunz and Gill from outbred NEDH rats supplied by the Animal Research Center, Harvard University (Kunz and Gill 1974, Kunz et al 1974).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68059</RGD_ID>
    <STRAIN_SYMBOL>KIRBY-B</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68059</CITATION_ID>
    <DESCRIPTION> From a cross between black hooded and CFY outbred rats with selection for resistance to chronic respiratory disease. Litter size 8-12 (60% male), but only 4-5 weaned. Agile, but tame (Bertok 1980).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68060</RGD_ID>
    <STRAIN_SYMBOL>KX</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68060</CITATION_ID>
    <DESCRIPTION> developed from Slonaker colony, University of  Chicago about 1928. Sublines which carry gene \i ic\i0  (infantile ichthyosis) and colour genes C and H have also been developed (Knox 1977)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68061</RGD_ID>
    <STRAIN_SYMBOL>KYN/Hok</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=69 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=69 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68061</CITATION_ID>
    <DESCRIPTION>Makino, Hokkaido University 1960 from stock the carrying the</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68062</RGD_ID>
    <STRAIN_SYMBOL>LA/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68062</CITATION_ID>
    <DESCRIPTION>from a cross between ALB/N and a hooded stock of unknown origin (Hansen et al 1982).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68063</RGD_ID>
    <STRAIN_SYMBOL>LA/N-&lt;i&gt;cp&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68063</CITATION_ID>
    <DESCRIPTION>The corpulent (LA/N-cp) rat developed at the National Institutes of Health (NIH) is a  congenic strain initially derived by mating a male Koletsky rat that was heterozygous for the corpulent gene (cp/ +) to a female Lister Albany/NIH (LAIN) rat. The obese homozygous  (cp/cp) littermates developspontaneous insulin resistance, obesity, impaired glucose tolerance, hypertriglyceridemia and atherosclerosis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68065</RGD_ID>
    <STRAIN_SYMBOL>LEA</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68065</CITATION_ID>
    <DESCRIPTION> Hok from outbred Long Evans stock, selected for agouti coat colour (though Long Evans stock is usually fixed for non-agouti, hooded genes) (MC Yoshida, personal communication). Liver gangliosides are of the a-type (cf ACI,LEW &amp; BUF) (Kasai et al 1993)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68066</RGD_ID>
    <STRAIN_SYMBOL>LEC</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68066</CITATION_ID>
    <DESCRIPTION>In 1975, at the Center for Experimental Plants and Animals, Hokkaido University, Long Evans Cinnamon was derived originally from a closed colony of Long-Evans rats obtained from Kobe University in 1975.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68067</RGD_ID>
    <STRAIN_SYMBOL>LEJ/Hok</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=72  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=72  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68067</CITATION_ID>
    <DESCRIPTION>Hok 1956 from Pacific Farms, USA as an outbred stock (Sasaki, personal communication).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68068</RGD_ID>
    <STRAIN_SYMBOL>LEM</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ckb</ALLELES>
    <ALLELE_RGD_IDS>2357</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68068</CITATION_ID>
    <DESCRIPTION> Subline of LET, which was a cross between LEW and a Long-Evans stock developed by TH Yoshida. Carries an inversion of chromosome 1 (Yosida, 1980).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68069</RGD_ID>
    <STRAIN_SYMBOL>LEO</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68069</CITATION_ID>
    <DESCRIPTION> from National Institute of Genetics Misima, Japan. Control strain for LEM and LET, without chromosomal inversions (Yosida, 1980).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68070</RGD_ID>
    <STRAIN_SYMBOL>LEP</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68070</CITATION_ID>
    <DESCRIPTION> Charles University from cross of outbred animals, including a Long Evans stock (Brdicka, personal communication). Has an unusual esterase haplotype (Festing and Bender 1984)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68071</RGD_ID>
    <STRAIN_SYMBOL>LER/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00164</CITATION_ID>
    <DESCRIPTION>Originally designated Le-R and thought to be a mutation within LEW conferring resistance of experimental allergic encephalomyelitis (EAE) (Waxman et al, 1981, Driscoll et al 1985, Gasser et al, 1983). However, it now appears to have been an accidental genetic contamination by BUF/N rats (Goldmuntz et al, 1993),. See LEW, Immunology.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68072</RGD_ID>
    <STRAIN_SYMBOL>LET</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68072</CITATION_ID>
    <DESCRIPTION> from National Institute of Genetics, Misima, Japan. From a cross betrween LEW and LEJ. Homozygous for a 1</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68073</RGD_ID>
    <STRAIN_SYMBOL>LETL</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68073</CITATION_ID>
    <DESCRIPTION> A rat with spontaneous polyurea, polyphagia and polydipsia was found in a colony of outbred Long Evans rats purchased from Charles River in 1982. Selective breeding for diabetes with brother x sister mating was subsequently started at the Tokushima Research Institute, Otsuka Pharmaceutical Co., Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68074</RGD_ID>
    <STRAIN_SYMBOL>LETO</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68074</CITATION_ID>
    <DESCRIPTION>THe LETO was obtained by mating of Long-Evan rats in  Otsuka Pharmaceutical Co.The LETO has not shown the diabetic syndrome.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68077</RGD_ID>
    <STRAIN_SYMBOL>LL/MavRrrc</STRAIN_SYMBOL>
    <FULL_NAME>Lyon hypotensive</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=59&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=59&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00059</CITATION_ID>
    <DESCRIPTION>Lyon Low-Tensive. See LH</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68079</RGD_ID>
    <STRAIN_SYMBOL>LOU</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante' et de la Recherche Medicale, Bichat-Claude Bernard, Paris, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68079</CITATION_ID>
    <DESCRIPTION> Bazin and Beckers from rats of presumed Wistar origin kept at the Universite Catholique de Louvain. LOU/C was selected among 28 parallel sublines for its high incidence of plasmacytomas, and LOU/M for its low incidence. The two are histocomaptible (Bazin 1977, Bazin and Beckers 1978).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68082</RGD_ID>
    <STRAIN_SYMBOL>LUDW</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68082</CITATION_ID>
    <DESCRIPTION>Ludwig Wistar; Wistar stock to Ludwig Institute to Olac in 1979. Susceptible to tumour induction by MNU.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68083</RGD_ID>
    <STRAIN_SYMBOL>LXB</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68083</CITATION_ID>
    <DESCRIPTION> Set of 13 recombinant inbred strains from a cross between LEW and BN (Central Institute, Hannover)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68084</RGD_ID>
    <STRAIN_SYMBOL>M14</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68084</CITATION_ID>
    <DESCRIPTION> AB Chapman 1940 from Sprague-Dawley stock, with selection for low ovarian response to pregnant mare's serum.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68085</RGD_ID>
    <STRAIN_SYMBOL>M17</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68085</CITATION_ID>
    <DESCRIPTION>AB Chapman 1940 from Sprague-Dawley stock with selection for high ovarian response to pregnant mare's serum.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68086</RGD_ID>
    <STRAIN_SYMBOL>M520</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68086</CITATION_ID>
    <DESCRIPTION>Curtiss 1920, Columbia University Institute for Cancer Research, to Heston in 1949 at F49. To NIH in 1951 at F51 (Hansen et al 1982). A congenic strain lacking vasopressin due to the presence of the diabetes insipidus gene, di (from the Brattleboro rat) has been described (Colombo et al, 1992).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68087</RGD_ID>
    <STRAIN_SYMBOL>MAXX</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68087</CITATION_ID>
    <DESCRIPTION>From a cross of BNxLEW with subsequent inbreeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68088</RGD_ID>
    <STRAIN_SYMBOL>MF</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68088</CITATION_ID>
    <DESCRIPTION>Developed as strain MF by Holme and Piechuta (1979) by selective breeding of Sprague-Dawley outbred rats. Individuals were injected sub-cutaneously with egg albumin and B. pertussis vaccine i.p. then challenged with areosolised egg albumin after 14-18 days. Individuals within litters with the most severe symproms (longest duration of dyspnea) were selected and mated brother x sister. Later re-named APR (Apnea Prone Rat).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68091</RGD_ID>
    <STRAIN_SYMBOL>MLCS</STRAIN_SYMBOL>
    <FULL_NAME>Milan low-calpastatin strain</FULL_NAME>
    <ORIGINATION>Department of Sciences and Biomedical Technologies, University of Milan, Milan, Italy</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68091</CITATION_ID>
    <DESCRIPTION>From a cross between MHS and MNS followed by backcrossing to MNS with selection for low calpastatin activity.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68097</RGD_ID>
    <STRAIN_SYMBOL>MSUBL</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68097</CITATION_ID>
    <DESCRIPTION> Dr. Stroyeva, Institute of Developmental Biology, Moscow from a cross of wild rats x MSU microphthalmic rats obtained from Dr Brouman, Montana State University. Selected for high incidence of microphthalmia (Borodin 1977).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68098</RGD_ID>
    <STRAIN_SYMBOL>MW</STRAIN_SYMBOL>
    <FULL_NAME>Munich Wistar</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68098</CITATION_ID>
    <DESCRIPTION>Munich Wistar stock selected for superficial glomeruli and inbred by Harlan-Sprague-Dawley, now at F17 (1990). See also MWF and WMS.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68099</RGD_ID>
    <STRAIN_SYMBOL>MWF</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68099</CITATION_ID>
    <DESCRIPTION>From outbred Wistar rats selected for large numbers of superficial glomeruli.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68100</RGD_ID>
    <STRAIN_SYMBOL>NBL</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68100</CITATION_ID>
    <DESCRIPTION> Bogden in the mid-1970s from Noble (Nb) strain rats (brother x sister mated but not descended from a single pair, and therefore not necessarily isogenic). To Fredrich Cancer Research facility in 1978. Note that the strain name NBL was selected in 1989.  In the literature these rats are called Noble or Nb rats, usually without identifying whether the animals came from the non-isogenic colony of Dr. Noble or from the isogenic colony at the National Cancer Institute (Greenhouse et al 1990).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68103</RGD_ID>
    <STRAIN_SYMBOL>NER</STRAIN_SYMBOL>
    <FULL_NAME>noda epileptic rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68103</CITATION_ID>
    <DESCRIPTION>From Crj: Wistar rats purchased from Charles River Japan in July 1985. Developed by A. Noda, Tokyo University of Agriculture, Hokkaido,  from a cross of mutant rats with spontaneous tonic-clonic seizures (Noda et al. 1998).  Susceptible to seizures induced by pentylenetetrazol, tossing and transcorneal electric shock, but not tactile, photic or acoustic stimuli or transauricular electric shock.  No pathologic changes have been found in the CNS. The condition appears to be inherited as an autosomal recessive gene and is comparable to generalised tonic-clonic seizures in humans. Maintained by Has.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68104</RGD_ID>
    <STRAIN_SYMBOL>NIG-III/Hok</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=73  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=73  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68104</CITATION_ID>
    <DESCRIPTION>From a mating in 1956 between a wild rat trapped in Misima, Japan, and Castle's black rat. To Hokkaido in 1975. Work on characterisation of RT1 summarised by Natori (1987).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68106</RGD_ID>
    <STRAIN_SYMBOL>NSD/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68106</CITATION_ID>
    <DESCRIPTION>NIH, Bethesda, 1964 from a non-inbred (Sprague-Dawley) stock.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68107</RGD_ID>
    <STRAIN_SYMBOL>NZR</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68107</CITATION_ID>
    <DESCRIPTION>Subline of AS2 separated at F32.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68109</RGD_ID>
    <STRAIN_SYMBOL>ODUS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68109</CITATION_ID>
    <DESCRIPTION>As for ODU, but maintained at Osaka Dental University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68113</RGD_ID>
    <STRAIN_SYMBOL>OXYR/Nov</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68113</CITATION_ID>
    <DESCRIPTION>Developed in 1972 at the Institute of Cytology and Genetics, Russian Academy of Sciences (Novosibirsk)  by Professor R.I. Salganik from Wistar stock, in contrast to OXYS rat strain by selection for resistance to cataractogenic effect of galactose rich diet and brother-sister mating of highly resistant rats. In 1992, due to new findings, the symbol R was assigned to this strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68114</RGD_ID>
    <STRAIN_SYMBOL>OXYS/Nov</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68114</CITATION_ID>
    <DESCRIPTION>Developed in 1972 at the Institute of Cytology and Genetics, Russian Academy of Sciences (Novosibirsk) by Professor R.I. Salganik from Wistar stock by selection for susceptibility to cataractogenic effect of galactose-rich diet and brother-sister mating of highly susceptible rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68115</RGD_ID>
    <STRAIN_SYMBOL>P77PMC</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68115</CITATION_ID>
    <DESCRIPTION>Wistar rats from Beijing Medical College in 1977.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68116</RGD_ID>
    <STRAIN_SYMBOL>PA</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68116</CITATION_ID>
    <DESCRIPTION> King 1909 from Wistar Institute stock, to Aptekman in 1946 at F135, to Bogden 1958 at F155. The oldest inbred strain of rats. WKA is probably a parallel subline of this strain.  Vigorous (and vicious), healthy, good reproduction.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68117</RGD_ID>
    <STRAIN_SYMBOL>PETH/N</STRAIN_SYMBOL>
    <FULL_NAME>Royal College of Surgeons, RCS</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68117</CITATION_ID>
    <DESCRIPTION> Bourne 1938, to Sidman at F9N1, to NIH in 1966 at F9N1F18. Should probably be regarded as a subline of RCS.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68118</RGD_ID>
    <STRAIN_SYMBOL>PKD</STRAIN_SYMBOL>
    <FULL_NAME>PKD</FULL_NAME>
    <ORIGINATION>Central Institute for Laboratory Animal Breeding, Hanover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68118</CITATION_ID>
    <DESCRIPTION>Outbred Han:SPRD-cy/+ Sprague-Dawley rats from the Zentralinstitut furVersuchstierkunde, Hannover, Germany to Dr. Bettina Kranzlin, Mannheim, Germany. Brother xsister inbreeding started in 1991.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68119</RGD_ID>
    <STRAIN_SYMBOL>PSDO/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00178</CITATION_ID>
    <DESCRIPTION>Reserved symbol for strain in development now at F6 (NIH 1989).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68121</RGD_ID>
    <STRAIN_SYMBOL>R</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68121</CITATION_ID>
    <DESCRIPTION>Muhlbock from a Wistar stock in 1947. A  congenic strain with hyperbilirubinaemia and jaundice has been developed by Leyten et al (1986) by backcrossing the jaundice gene j (the Gunn rat) onto strain R.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68122</RGD_ID>
    <STRAIN_SYMBOL>RCS/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00180</CITATION_ID>
    <DESCRIPTION>Developed before 1965 by Sidman from stock obtained from Sorsby of the Royal College of Surgeons, London (Sidman and Pearlstein 1965). PETH is a presumed subline.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68123</RGD_ID>
    <STRAIN_SYMBOL>RHA/N</STRAIN_SYMBOL>
    <FULL_NAME>Roman high avoidance</FULL_NAME>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68123</CITATION_ID>
    <DESCRIPTION>Bignami selected for high avoidance conditioning with light as a conditioned stimulus and electric shock as the unconditioned stimulus (Bignami 1965). To NIH in 1968 where b x s mating was initiated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68124</RGD_ID>
    <STRAIN_SYMBOL>RII/1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68124</CITATION_ID>
    <DESCRIPTION> Tif from outbred Sprague-Dawley stock received from Ivanovas, Germany (Greenhouse et al 1991).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68125</RGD_ID>
    <STRAIN_SYMBOL>RII/2</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68125</CITATION_ID>
    <DESCRIPTION> From outbred Sprague-Dawley stock received from IFFA Credo, France has been brother x sister mated for 16 generations (Greenhouse et al 1991).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68126</RGD_ID>
    <STRAIN_SYMBOL>RLA/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68126</CITATION_ID>
    <DESCRIPTION>Bignami selected for high avoidance conditioning with light as a conditioned stimulus and electric shock as an unconditioned stimulus (Bignami 1965). This outbred stock to NIH in 1968 where brother x sister mating was initiated. See also RHA. Note that the original outbred stock and other independently-derived inbred strains may differ in characteristics. Behavioural characteristics described by Driscoll et al (1979) and Fumm and Battig (1979). See RHA for details of comparative studies involving both strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68127</RGD_ID>
    <STRAIN_SYMBOL>RP/AEurRij</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68127</CITATION_ID>
    <DESCRIPTION>Muhlbock, Amsterdam, 1947, from Wistar stock. To University of Leiden in 1958. To Erasmus University, Rotterdam in 1968. To Rijswick in 1982 (Greenhouse et al 1991).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68128</RGD_ID>
    <STRAIN_SYMBOL>S5B</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68128</CITATION_ID>
    <DESCRIPTION> Poiley 1955 from a cross of outbred NBR rats x Sprague-Dawley, with five generations of backcrossing of the albino gene followed by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68129</RGD_ID>
    <STRAIN_SYMBOL>SBH</STRAIN_SYMBOL>
    <FULL_NAME>Sabra hypertensive</FULL_NAME>
    <ORIGINATION>Barzilai Medical Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68129</CITATION_ID>
    <DESCRIPTION>Sabra Hypertensive Hebrew University Sabra outbred rats with brother x sister mating and selection for high blood pressure following unilateral nephrectomy and treatment with deoxycorticosterone and sodium chloride (Ben-Ishay et al 1981, Ben-Ishay 1984, Ben-Ishay and Yagli, 1994 who also reviews their characteristics).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68130</RGD_ID>
    <STRAIN_SYMBOL>SBN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68130</CITATION_ID>
    <DESCRIPTION> As for SBH, but selected for low blood pressure as a normotensive control strain for SBH. See SBH  (Ben-Ishay 1984).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68131</RGD_ID>
    <STRAIN_SYMBOL>SC</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68131</CITATION_ID>
    <DESCRIPTION> Outbred Wistar Imamichi. Has small eyes and cataract (Proc. 8th. ICLAS Symposium, Gustav Fischer Verlag pp353-360)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68133</RGD_ID>
    <STRAIN_SYMBOL>SDJ/Hok</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=74  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=74  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc2a2</ALLELES>
    <ALLELE_RGD_IDS>3705</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68133</CITATION_ID>
    <DESCRIPTION>Takeda Chemical Industries from Sprague-Dawley stock, to Hokkaido in 1966.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68134</RGD_ID>
    <STRAIN_SYMBOL>SDNK</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68134</CITATION_ID>
    <DESCRIPTION>Sprague-Dawley outbred rats inbred since 1967 by Dr. K Yasutomi, Nippon Inst. for Biological Sciences, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68136</RGD_ID>
    <STRAIN_SYMBOL>SEL</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68136</CITATION_ID>
    <DESCRIPTION>Dunning 1948. Probably extinct.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68137</RGD_ID>
    <STRAIN_SYMBOL>SHHF</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Grk2|Grk3</ALLELES>
    <ALLELE_RGD_IDS>2062|2063</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68137</CITATION_ID>
    <DESCRIPTION> JE Miller of GD Searle to Sylvia McCune in 1983. Corpulent gene (cp ) partially backcrossed to SHR/N, followed by brother x sister mating (with some exceptions). Originally designated SHR/N-cp, but re-named to avoid confusion with the strain described by Michaelis and Hansen (1990) which has been backcrossed to N14. Strain is maintained by matings of proven cp/+ heterozygotes, and in some cases  cp/cp  homozygous males have proved to be fertile.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68140</RGD_ID>
    <STRAIN_SYMBOL>SPRD/Hsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Harlan</ORIGINATION>
    <SOURCE>Harlan</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68140</CITATION_ID>
    <DESCRIPTION>Originated by the Sprague-Dawley Company, Madison, Wisconsin, in 1925 through a series of crosses begun with a single-hooded male and six albino females of unknown origin. Current Harlan colonies are direct descendants of this original colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68143</RGD_ID>
    <STRAIN_SYMBOL>TA</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68143</CITATION_ID>
    <DESCRIPTION>Outbred Wistar Imamichi.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68144</RGD_ID>
    <STRAIN_SYMBOL>TE</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68144</CITATION_ID>
    <DESCRIPTION>Outbred Wistar Imamichi rats. Males develop hydro-testes caused by sperm retention cysts in the efferent duct. This defect is caused by an autosomal dominant locus and two autosomal recessive loci. Females are normal (Ikadai et al 1987).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68145</RGD_ID>
    <STRAIN_SYMBOL>TF</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68145</CITATION_ID>
    <DESCRIPTION>From outbred Wistar Imamichi rats. Carries an autosomal recessive gene causing male pseudohermaphroditism due to defect of Leydig cells. Homozygous females are normal (Ikadai et al 1988).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68146</RGD_ID>
    <STRAIN_SYMBOL>THA</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68146</CITATION_ID>
    <DESCRIPTION> Developed from Jcl-Wistar stock by inbreeding with selection for a high rate of electric shock avoidance by lever pressing. The strain has good learning performance not only in the Sidman avoidance task, but also in two other tasks when compared with the Jcl-Wistar stock, though the sensitivity  of the strain to electric shocks or heat stress was less (Shigeta et al 1990).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68147</RGD_ID>
    <STRAIN_SYMBOL>THE/Utp</STRAIN_SYMBOL>
    <FULL_NAME>Tsukuba high-emotional rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=516 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=516 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68147</CITATION_ID>
    <DESCRIPTION>Wistar albino rats selected for low ambulation in a bright runway out of a dark starting box (high emotionality) (see also TLE).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68148</RGD_ID>
    <STRAIN_SYMBOL>TLE/Utp</STRAIN_SYMBOL>
    <FULL_NAME>Tsukuba low-emotional rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=515 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=515 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68148</CITATION_ID>
    <DESCRIPTION>Wistar albino rats selected for high ambulation in a bright runway out of a dark starting box (low emotionality) (see also THE).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68149</RGD_ID>
    <STRAIN_SYMBOL>TM</STRAIN_SYMBOL>
    <FULL_NAME>Tester Moriyama rat</FULL_NAME>
    <ORIGINATION>Institute of Laboratory Animals, Faculty of Medicine, Kyoto University, Kyoto, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68149</CITATION_ID>
    <DESCRIPTION> Shionogi Pharmaceutical Company to Kyoto in 1976. Has thrombocyte storage pool deficiency (J Yamada, personal communication).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68150</RGD_ID>
    <STRAIN_SYMBOL>TMB</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68150</CITATION_ID>
    <DESCRIPTION> PL Broadhurst from stock selected by Tryon for good maze learning performance. Although TMB and TS1 are derived from the same outbred stock, they were inbred independently and should be regarded as different inbred strains (Festing 1979b).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68151</RGD_ID>
    <STRAIN_SYMBOL>TMD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68151</CITATION_ID>
    <DESCRIPTION> PL Broadhurst from stock selected by Tryon for poor maze learning performance. Although TMD and TS3 are derived from the same outbred stock, they were inbred independently and should be regarded as different inbred strains (Festing 1979b).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68152</RGD_ID>
    <STRAIN_SYMBOL>TO/Hok</STRAIN_SYMBOL>
    <FULL_NAME>Tokyo rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=75 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=75 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68152</CITATION_ID>
    <DESCRIPTION>A breeder in Tokyo, Japan, to Hokkaido University in 1952 (Festing and Staats 1973). Resistant to the induction of EAU by interphotoreceptor retinol-binding protein (contrast WKAH, W/M, LEJ, LEW and BUF) (Sasamoto et al, 1994).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68154</RGD_ID>
    <STRAIN_SYMBOL>TOM</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68154</CITATION_ID>
    <DESCRIPTION> Toma Institute, Japan (Ikadai, personal communication, 1991)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68155</RGD_ID>
    <STRAIN_SYMBOL>TS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68155</CITATION_ID>
    <DESCRIPTION> WKA strain obtained from Taisho Pharmaceutical Co. Ltd. Develops ectopic scrota in about 70% of males. The defect is controled by multiple genes, and the females are normal  (Ikadai et al 1988b).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68156</RGD_ID>
    <STRAIN_SYMBOL>TS1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68156</CITATION_ID>
    <DESCRIPTION> Harrington, from stock selected by Tryon in 1929 for good maze learning performance (Harrington 1981). Although TMB and TS1 are derived from the same outbred stock, they were inbred independently and should be regarded as different inbred strains (Festing 1979b).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68157</RGD_ID>
    <STRAIN_SYMBOL>TS3/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00185</CITATION_ID>
    <DESCRIPTION>Harrington, from stock selected by Tryon for poor maze learning performance (Harrington 1981). Although TMD and TS3 are derived from the same outbred stock, they were inbred independently and should be regarded as different inbred strains (Festing 1979b).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68158</RGD_ID>
    <STRAIN_SYMBOL>TT</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68158</CITATION_ID>
    <DESCRIPTION> outbred Wistar Imamichi strain. Carries an autosomal recessive gene \i as\i0  causing an arrest of spermatogenesis at an early meiotic stage. Homozygous females have normal fertility (Ikadai, personal communication, 1991).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68160</RGD_ID>
    <STRAIN_SYMBOL>TU</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68160</CITATION_ID>
    <DESCRIPTION> From a cross of a wild male and Wistar Imamichi outbred rats. Small litter size with malformations of kidneys and vas deferens in about 20% of offspring (H Ikadai, personal communication, 1991)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68161</RGD_ID>
    <STRAIN_SYMBOL>TW</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68161</CITATION_ID>
    <DESCRIPTION> Wistar Imamichi outbred stock. Testicular hypoplasia (unilateral or bilateral) with aplasia of the epididymus and ductus deferens in about 50% of males. Female genital organs are normal (Ikadai et al 1985, Ajisawa et al 1985).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68162</RGD_ID>
    <STRAIN_SYMBOL>TX</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68162</CITATION_ID>
    <DESCRIPTION> From a cross between a wild male and Wistar Imamichi females (H Ikadai, personal communication, 1991)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68163</RGD_ID>
    <STRAIN_SYMBOL>U</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68163</CITATION_ID>
    <DESCRIPTION> Zootechnical Institute, Utrecht to the Netherlands Cancer Institute in 1958. To Erasmus University, Rotterdam, then to ITRI-TNO, Rijswijk, the Netherlands in 1960 (van Hooft 1990).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68164</RGD_ID>
    <STRAIN_SYMBOL>UChA</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Chile, Casilla, Chile</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68164</CITATION_ID>
    <DESCRIPTION> Wistar rats selected for low voluntary 10% ethanol consumption, with brother x sister mating. Initiated from ALKO Labs, Finland now established in 1947 at University of Chile.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68165</RGD_ID>
    <STRAIN_SYMBOL>UChB</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Chile, Casilla, Chile</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68165</CITATION_ID>
    <DESCRIPTION> Wistar rats selected for high voluntary 10% ethanol consumption, with brother x sister mating. Initiated from ALKO Labs, Finland now established in 1947 at University of Chile.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68166</RGD_ID>
    <STRAIN_SYMBOL>W/Hok</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68166</CITATION_ID>
    <DESCRIPTION> Wistar Institute to University of Tokyo, Japan in 1938. To Hokkaido in 1944. Inbred by Makino. Congenital cleft palate 0.5% (Shoji 1977).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68167</RGD_ID>
    <STRAIN_SYMBOL>W/Nhg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68167</CITATION_ID>
    <DESCRIPTION> Wistar rats from the Zentralinstitut fur Versuchstier, Hannover in 1964, inbred since 1973 in Neuherberg, Germany.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68168</RGD_ID>
    <STRAIN_SYMBOL>WA</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68168</CITATION_ID>
    <DESCRIPTION> St Thomas's Hospital, from outbred Wistar stock, to Laboratory Animals Centre in 1964 at F43 (Festing and Blackmore 1971). To Ola in 1983.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68169</RGD_ID>
    <STRAIN_SYMBOL>WAB</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68169</CITATION_ID>
    <DESCRIPTION> Boots Ltd., from same stock as WAG, but separated in 1926, prior to inbreeding. Benign thymoma in 23% of individuals over 2 years, with 50% incidence in castrated males and 57% in spayed females (Hinsull and Bellamy 1977).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68171</RGD_ID>
    <STRAIN_SYMBOL>WBB/1N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00186</CITATION_ID>
    <DESCRIPTION>No further information</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68172</RGD_ID>
    <STRAIN_SYMBOL>WBB/2N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00187</CITATION_ID>
    <DESCRIPTION>No further information.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68173</RGD_ID>
    <STRAIN_SYMBOL>WBN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68173</CITATION_ID>
    <DESCRIPTION> Wistar rats from the Institute of Experimental Gerontology, Basel brother x sister mated in the Institute of Pathology, University of Bonn since 1961. To the Instuitute of Medical Science, University of Tokyo in 1976, then to Shizuoka Laboratory Animals Center where they were hysterectomy-derived.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68174</RGD_ID>
    <STRAIN_SYMBOL>WCF</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68174</CITATION_ID>
    <DESCRIPTION> R Shoji, 1972 from a male rat of strain WKAH/Idr with clubfoot of the right hind foot.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68175</RGD_ID>
    <STRAIN_SYMBOL>WDF</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68175</CITATION_ID>
    <DESCRIPTION>Ikeda et al (1981) by backcrossing the fatty gene to F8 and later generations of outbred Wistar Kyoto rats being inbred by brother x sister mating. The aim was to develop a model of non-insulin-dependent diabetes mellitus.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68176</RGD_ID>
    <STRAIN_SYMBOL>WEC</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68176</CITATION_ID>
    <DESCRIPTION> Centraal Proefdierenbedrig TNO from an outcross involving strains B, WAG and others, followed by inbreeding (Festing 1979b). Formarly known as WE/Cpb. Hyporesponder to dietary cholesterol (van Zutphen, unpublished).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68177</RGD_ID>
    <STRAIN_SYMBOL>WEK</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68177</CITATION_ID>
    <DESCRIPTION> Centraal Proefdierenbedrig TNO 1958 to Utrecht in 1973. Formerly known as WEchoc. Hyporesponder to dietary cholesterol (van Zutphen, unpublished).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68178</RGD_ID>
    <STRAIN_SYMBOL>WELS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68178</CITATION_ID>
    <DESCRIPTION>Outbred wistar rats in 1976. Some biological details mainly on haematology and blood biochemistry given by Henize et al (1984)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68180</RGD_ID>
    <STRAIN_SYMBOL>WIN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68180</CITATION_ID>
    <DESCRIPTION>WI outbred rats inbred since 1980 as WIN (Wistar-Imamichi-Natori). Has a unique RT1.A haplotype (RT1.A s BlDl) (Natori et al 1986).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68183</RGD_ID>
    <STRAIN_SYMBOL>WKA</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68183</CITATION_ID>
    <DESCRIPTION> King 1909 from Wistar Institute stock to Aptekman in 1946 at F135, to Hokkaido University in 1953 at F148. To Pit at F205 (Kunz et al 1987). Probably genetically identical to PA. Slow elimination of  Trichinella spiralis  worms (12/12) (Bell, 1992)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68184</RGD_ID>
    <STRAIN_SYMBOL>WKAH/Hok</STRAIN_SYMBOL>
    <FULL_NAME>Wistar-King Aptekman Hokkaido</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=76 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=76 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68184</CITATION_ID>
    <DESCRIPTION>King 1909 from Wistar Institute stock to Aptekman in 1946 at F135, to Hokkaido University in 1953 at F148. Formerly called WKA, Probably gentically identical to PA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68185</RGD_ID>
    <STRAIN_SYMBOL>WKAM</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68185</CITATION_ID>
    <DESCRIPTION> King 1909 to Aptekman 1946 at F135 to Hok in 1953 at F148 to Ms in 1953 (precise number not known), to Jic in 1980 at F208, back to Ms in 1980 at F211, to Slc in 1986 at F228, back to Ms in 1987 at F230 (Greenhouse et al 1990). Formerly called WKA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68186</RGD_ID>
    <STRAIN_SYMBOL>WKHA/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00188</CITATION_ID>
    <DESCRIPTION>From a cross between SHR and WKY with selection for high spontaneous activity and low systolic blood pressure.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68187</RGD_ID>
    <STRAIN_SYMBOL>WKHT/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00189</CITATION_ID>
    <DESCRIPTION>From a cross between SHR and WKY, with selection for high blood pressureand low spontaneous activity (Hendley et al 1988, Knardahl and Hendley 1990, Hendley and Fan, 1992).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68188</RGD_ID>
    <STRAIN_SYMBOL>WKS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68188</CITATION_ID>
    <DESCRIPTION> National Institute of Genetics, Mishima, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>68189</RGD_ID>
    <STRAIN_SYMBOL>HTX/Hcj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pharmacology, University of Florida, Gainesville.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_68189</CITATION_ID>
    <DESCRIPTION>D. F. Kohn, Inst. of Comparative Medicine,Columbia University, to University of Florida 1992 at F30.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>69369</RGD_ID>
    <STRAIN_SYMBOL>SS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Brookhaven National Laboratories, Upton, New York</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_69369</CITATION_ID>
    <DESCRIPTION>From a colony of Sprague-Dawley outbred rats developed by LK Dahl, Brookhaven National Laboratories, Upton, New York, selected for sensitivity to salt-induced hypertension (Dahl et al 1962a,b, Rapp 1982). Also designated S/JR by Rapp (1984), who gives an extensive review of the characteristics of the strain, and Dahl S by Mollegard, Copenhagen. Note that the Dahl selected strain has been independently inbred at the NIH, and designated DSS/N. There is likely to be confusion among these colonies unless considerable care is taken with nomenclature. Stlezin et al (1992) found that SS and SR had about 80% of DNA fingerprint bands in common, compared with 50% between SHR and WKY. According to Ginn et al, (1993) analysis of RFLPs and microsatellites suggest that SR is a reasonably good control strain for SS, though crosses between SS and unrelated normotensive strains will be useful in identifying the loci responsible for salt-induced hypertension.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>69638</RGD_ID>
    <STRAIN_SYMBOL>BN/Ka</STRAIN_SYMBOL>
    <FULL_NAME>Brown Norway Katholiek (kininogen or kinin deficient)</FULL_NAME>
    <ORIGINATION>Kitasato University, Kanagawa, Japan.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_69638</CITATION_ID>
    <DESCRIPTION>Kitasato University, Kanagawa, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>69643</RGD_ID>
    <STRAIN_SYMBOL>F344/DuCrlCrlj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.japancorp.net/company_show.asp?compid=3463&gt;Charles River Laboratories Japan&lt;/a&gt;, &lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=537&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.japancorp.net/company_show.asp?compid=3463&gt;Charles River Laboratories Japan&lt;/a&gt;, &lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=537&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_69643</CITATION_ID>
    <DESCRIPTION>This strain originated in 1920 by Curtis then was with Dunning and then with Charles River Japan from 1976.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70410</RGD_ID>
    <STRAIN_SYMBOL>AA</STRAIN_SYMBOL>
    <FULL_NAME>Alko, Alcohol</FULL_NAME>
    <ORIGINATION>Research Laboratories of the State Alcohol Monopoly (Alko), Helsinki, Finland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70410</CITATION_ID>
    <DESCRIPTION>Wistar rats were outbred and selected for breeding animals that differ in their alcohol consumption. Marked difference between the strains and sex was visible by the eighth generation. After puberty the animals were isolated and given 10% alcohol as drink for 10 days, after which they had access to water and alcohol for 4 weeks. The quantity of fluid intake was measured daily. Fluid intake of animals varied greatly in animals consuming the same amount of alcohol per unit body weight, so alcohol intake was used as a phenotypic measure.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70411</RGD_ID>
    <STRAIN_SYMBOL>ANA</STRAIN_SYMBOL>
    <FULL_NAME>Alko, Non-Alcohol</FULL_NAME>
    <ORIGINATION>Research Laboratories of the State Alcohol Monopoly (Alko), Helsinki, Finland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70411</CITATION_ID>
    <DESCRIPTION>Wistar rats were outbred and selected for breeding animals that differ in their alcohol consumption. Marked difference between the strains and sex was visible by the eighth generation. After puberty the animals were isolated and given 10% alcohol as fluid for 10 days, then they had access to water and alcohol for 4 weeks. The quantity of fluid intake was measured daily, as fluid intake of animals varied greatly in animals consuming the same amount of alcohol per unit body weight. Therefore, alcohol intake was kept as a phenotypic measure.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70413</RGD_ID>
    <STRAIN_SYMBOL>WBB</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70413</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>70416</RGD_ID>
    <STRAIN_SYMBOL>ACH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70416</CITATION_ID>
    <DESCRIPTION>Curtiss and Dunning 1926 at Columbia University Institute for Cancer Research.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70417</RGD_ID>
    <STRAIN_SYMBOL>A28807/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00141</CITATION_ID>
    <DESCRIPTION>Curtis and Dunning in 1936 as a subline of A7322 derived from a half-brother x sister mating at F15. To NIH in 1977 at F25 (Hansen et al 1982).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70418</RGD_ID>
    <STRAIN_SYMBOL>A35322</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70418</CITATION_ID>
    <DESCRIPTION>Curtiss and Dunning 1942 from a mutation originating in an aunt x nephew cross at F27 of animals of strain A990.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70419</RGD_ID>
    <STRAIN_SYMBOL>A7322</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70419</CITATION_ID>
    <DESCRIPTION>Curtis 1925 at Columbia University Institute of Cancer Research. Spontaneous mammary tumours frequent. Resistant to Cysticercus.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70420</RGD_ID>
    <STRAIN_SYMBOL>A990</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70420</CITATION_ID>
    <DESCRIPTION>Curtiss 1921 at Columbia University Institute for Cancer Research.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70421</RGD_ID>
    <STRAIN_SYMBOL>AAW</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70421</CITATION_ID>
    <DESCRIPTION>Atomic Energy Commission, Melbourne (Adams et al 1984).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70422</RGD_ID>
    <STRAIN_SYMBOL>ABH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Nishimura, Hammatsu University School of Medicine, Japan.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70422</CITATION_ID>
    <DESCRIPTION>Yamada from a cross between BN and outbred Wistar stock, with selection for the above coat colour, as a stock for testing coat colour genes in albino strains (Yamada and Nakajima 1976). To Nishimura, Hammatsu University School of Medicine, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70423</RGD_ID>
    <STRAIN_SYMBOL>ACP</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70423</CITATION_ID>
    <DESCRIPTION>Dunning to National Cancer Institute 1967 at F54.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70424</RGD_ID>
    <STRAIN_SYMBOL>AGA</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70424</CITATION_ID>
    <DESCRIPTION>Nakic, Zagreb (Stark et al 1968b). Used for immunological studies.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70425</RGD_ID>
    <STRAIN_SYMBOL>AGUS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70425</CITATION_ID>
    <DESCRIPTION>Germ-free strain developed by Gustafsson from stock (Sprague-Dawley?) by hysterectomy derivation in 1948 at F10. To Laboratory Animals Centre, Carshalton 1968 at F26.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70426</RGD_ID>
    <STRAIN_SYMBOL>ALB/N</STRAIN_SYMBOL>
    <FULL_NAME>Albany</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70426</CITATION_ID>
    <DESCRIPTION>Wolf and Wright, Albany Medical College in an attempt to develop a strain with a high incidence of spontaneous tumours, to NIH in 1950. No inbreeding records prior to transfer.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70427</RGD_ID>
    <STRAIN_SYMBOL>AM</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70427</CITATION_ID>
    <DESCRIPTION>Torres, Rio de Janeiro, from outbred stock.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70428</RGD_ID>
    <STRAIN_SYMBOL>AMDIL</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70428</CITATION_ID>
    <DESCRIPTION>Torres, Rio de Janeiro, from outbred stock</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70429</RGD_ID>
    <STRAIN_SYMBOL>AO</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70429</CITATION_ID>
    <DESCRIPTION>From ARC Compton, probably as "WAG", to Gowans, Oxford 1957. Appears to differ from other WAG sublines in having A at the agouti locus. Resistant to the development of experimental allergic encephalomyelitis upon treatment with a myelin basic protein-specific T cell line derived from an F1 hybrid between resistant AO and susceptible DA strain rats. This resistance was not abrogated by deletion of host's leukocytes using sublethal irradiation and cytotoxi drugs (Mostaricastrojkovic et al, 1992). Susceptible (2/4) to ocular infection with herpes simplex virus. PVG was relatively resistant (Nicholls et al, 1994). Met-enkephalin decreased H2O2 production by macrophages (contrast DA) (Radulovic et al, 1995).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70440</RGD_ID>
    <STRAIN_SYMBOL>BIRMA</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70440</CITATION_ID>
    <DESCRIPTION>AM Mandl 1952 from Albino rats purchased from Birmingham market.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70446</RGD_ID>
    <STRAIN_SYMBOL>LIH/Lac</STRAIN_SYMBOL>
    <FULL_NAME>Liverpool Hooded</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70446</CITATION_ID>
    <DESCRIPTION>"Liverpool Hooded". Strain now probably extinct, but haematology described by Lovell et al (1981).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70447</RGD_ID>
    <STRAIN_SYMBOL>MNR</STRAIN_SYMBOL>
    <FULL_NAME>Maudsely non-reactive</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70447</CITATION_ID>
    <DESCRIPTION>PL Broadhurst, 1954, from a commercial Wistar stock with selection for low defecation response in an open field. To Harrington 1965 at F25 and to National Institutes of Health 1964 at F18+. The strain was apparently inbred as a number of parallel sublines which differ at the agouti locus and major histocompatibility complex (Hansen et al 1982).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70448</RGD_ID>
    <STRAIN_SYMBOL>MNRA</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00692</CITATION_ID>
    <DESCRIPTION>Substrain of MNR. To Harrington in 1965 at F25 (Harrington 1981).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70449</RGD_ID>
    <STRAIN_SYMBOL>MR/N</STRAIN_SYMBOL>
    <FULL_NAME>Maudsely reactive</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70449</CITATION_ID>
    <DESCRIPTION>Origin: as for MNR except selection was for high defecation response in the open field. To Harrington in 1965 at F25 and to NIH in 1964 at F18+ (Hansen et al 1982).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70450</RGD_ID>
    <STRAIN_SYMBOL>NBR</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70450</CITATION_ID>
    <DESCRIPTION>Poiley 1966 from heterogeneous stock</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70451</RGD_ID>
    <STRAIN_SYMBOL>OKA</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70451</CITATION_ID>
    <DESCRIPTION>From faculty of Medicine, Kyoto, Japan to Dr. J Roba, Machelen, Belgium 1970, to Dr. H Bazin 1971 (Bazin 1977). Should probably regarded as a subline of SHR, though skin grafts between OKA and SHR are rejected after 30-45 days.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70452</RGD_ID>
    <STRAIN_SYMBOL>OM</STRAIN_SYMBOL>
    <FULL_NAME>Osborne-Mendel</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70452</CITATION_ID>
    <DESCRIPTION>Heston 1946 from non-inbred Osborne-Mendel stock obtained from J White, to NIH at F10 (Hansen et al 1982).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70453</RGD_ID>
    <STRAIN_SYMBOL>SR</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70453</CITATION_ID>
    <DESCRIPTION>Rapp from a Sprague-Dawley outbred  colony developed by LK Dahl, Brookhaven National Laboratories, Upton, New York, selected for resistance to salt-induced hypertension  (Dahl et al 1962a,b). Also designated R/JR by Rapp (1984), and Dahl R by Mollegard, Copenhagen.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70454</RGD_ID>
    <STRAIN_SYMBOL>WKY/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://dvrnet.ors.od.nih.gov/ratcenter/index.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=190&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://dvrnet.ors.od.nih.gov/ratcenter/index.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=190&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2019-02-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00190</CITATION_ID>
    <DESCRIPTION>National Institutes of Health in 1971 from outbred Wistar stock from Kyoto School of Medicine. Inbred as a normotensive control strain for SHR (Hanesn et al 1973), though there is some controversy about the validity of such use (see Rapp 1987). Johnson et al (1992) found large genetic differences using restriction fragment length polymorphisms between WKY and SHR, comparable to the maximum divergence possible between unrelated humans. Also, breeding stock of ths strain was distributed before F20, possibly resulting in the emergence of a number of strains or substrains (Kurtz and Morris 1987, Kurtz et al 1989). It is therefore essential that subline codes are always used in designating this strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70455</RGD_ID>
    <STRAIN_SYMBOL>WKYO/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=17 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=17 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70455</CITATION_ID>
    <DESCRIPTION>Inbred in 1980 from outbred Wistar Kyoto rats. Highly sensitive to the development of experimental glomerulonephritis following injection of nephritogenic antigen from bovine renal basement membrane (1/10) (Naito et al, 1991).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70456</RGD_ID>
    <STRAIN_SYMBOL>WM</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70456</CITATION_ID>
    <DESCRIPTION>Wistar Institute to Tokyo University in 1938. To Hokkaido in 1944. To National Institute of Genetics, Mishima in 1951.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70457</RGD_ID>
    <STRAIN_SYMBOL>WMS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70457</CITATION_ID>
    <DESCRIPTION>Munich, Germany from Wistar stock selectively bred for superficial glomeruli. To Sim via Veterans Administration Medical Center, San Francisco, California in 1979 at which time inbreeding was begun. Good reproductive performance. Has superficial glomeruli and prominant elongated renal papilla. See also MW and MWF</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70458</RGD_ID>
    <STRAIN_SYMBOL>WN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70458</CITATION_ID>
    <DESCRIPTION>Heston in 1942 from Wistar stock of Nettleship, This WN is the parent to WN substrains maintained in other institutions.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70459</RGD_ID>
    <STRAIN_SYMBOL>ZDF</STRAIN_SYMBOL>
    <FULL_NAME>Vancouver diabetic fatty Zucker</FULL_NAME>
    <ORIGINATION>Animal Model Core Facility, University of California at Davis</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70459</CITATION_ID>
    <DESCRIPTION>"Zucker" fatty rats of undefined outbred background, inbred with selection for non-insulin-dependent diabetes mellitus by mating diabetic homozygous fatty males to heterozygous sisters (Peterson et al 1990b).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70508</RGD_ID>
    <STRAIN_SYMBOL>SD</STRAIN_SYMBOL>
    <FULL_NAME>Sprague-Dawley</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Aqp1|Brca1|Brca2|Crebbp|Cyp11b1|Drd1|Edn1|Esr1|Gabrb1|Htr1b|Nos1|Nppa|Nppb|Prlr|Sdc1|Sdc4|Gpc1|Alox15|E2f5|Slc15a1|Cnga1|E2f1</ALLELES>
    <ALLELE_RGD_IDS>2141|2218|2219|2401|2453|2518|2532|2581|2649|2846|3184|3193|3194|3407|3648|3650|61853|70493|621357|621736|621815|728892</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_70508</CITATION_ID>
    <DESCRIPTION>This strain was initiated by R. Dawley, Sprague-Dawley Company, Madison, Wisconsin in 1925. A hybrid hooded male of unknown origin was mated to a white female (Douredoure strain, probably Wistar) and subsequently to his white female offspring for 7 generations. All the current colonies are from this original stock.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>70509</RGD_ID>
    <STRAIN_SYMBOL>F344/NRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=158&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=158&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cdkn2a|Gfap|Tnfrsf1a</ALLELES>
    <ALLELE_RGD_IDS>2323|2679|621237</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00158</CITATION_ID>
    <DESCRIPTION>Curtiss and Dunning 1920 at Columbia University Institute for Cancer Research,To Heston 1949 (Billingham and Silvers 1959). To National Institutes of Health in 1951 (Hansen et al 1982). Subsequent sublines from Dunning or NIH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>625624</RGD_ID>
    <STRAIN_SYMBOL>LE&lt;i&gt;Tsc2&lt;sup&gt;Eker&lt;/sup&gt;&lt;/i&gt;/Hin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Experimental Pathology, Cancer Institute, Toshima-ku, Tokyo Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tsc2|Tsc2&lt;sup&gt;Eker&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>3908|12791989</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="14125679" STOP_POS="14160317" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="13621135" STOP_POS="13655773" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="13962006" STOP_POS="13996684" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="13778990" STOP_POS="13813725" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="13848210" STOP_POS="13883189" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_625624</CITATION_ID>
    <DESCRIPTION>Eker rat is derived from the Long-Evans strain that has a mutation in Tsc2 gene. Originally reported by R. Eker in 1954 at the Norwegian Radium Hospital, Oslo.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>625659</RGD_ID>
    <STRAIN_SYMBOL>DRH/Seac</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=111 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=111 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_625659</CITATION_ID>
    <DESCRIPTION>Established by inbreeding closed colony of Donryu rats ( purchased from SEAC Yoshitomi, Ltd. Fukuoka, Japan) for more than 20 generations, their diet continously contained a hepatocarcinogen 3</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>628372</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Mit34-D1Rat156&lt;/i&gt;)/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Animal Research Center of the Erasmus University, Rotterdam, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="234540191" STOP_POS="234540296" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="225126575" STOP_POS="225126682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="245529606" STOP_POS="245529710" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="252776360" STOP_POS="279213254" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="230963695" STOP_POS="253410500" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_628372</CITATION_ID>
    <DESCRIPTION>The Rf-1 region of chromosome 1 which is between the D1Mit34 and D1Rat156 is transferred from FHH to the genomic background of ACI.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>628486</RGD_ID>
    <STRAIN_SYMBOL>NER/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Noda epileptic rat, GMS</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=26 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=26 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_628486</CITATION_ID>
    <DESCRIPTION>Originated in a group of Crj:Wistar rats which were developed and maintained at the Research Institute for Animal Science in Biotechnology and Toxicology, Kanagawa, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>628525</RGD_ID>
    <STRAIN_SYMBOL>Ni/Hin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Clea Japan Inc. Shiga</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_628525</CITATION_ID>
    <DESCRIPTION>Found in the Sprague-Dawley (Jci:SD) in Japan. In these the Tsc2 gene is not mutated. In this rat strain mutation was identified as an insertion of a cytosine (C) in a C tract within exon 3 of Flcn . This germline mutation results in a frameshift and produces a stop codon 26 amino-acids downstream</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>628907</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-RT1&lt;sup&gt;n&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_628907</CITATION_ID>
    <DESCRIPTION>This strain is derived by transferring a segment from chr. 20 which contains the major histocompatibility complex of the BN-Lx strain onto SHR.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>628908</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D1Mit3-Igf2&lt;/i&gt;)/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Igf2|Sa|Scnn1b|Scnn1g</ALLELES>
    <ALLELE_RGD_IDS>2870|3616|3640|3641</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="153679879" STOP_POS="207261263" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="144267353" STOP_POS="197831802" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="156446196" STOP_POS="215839081" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="162692213" STOP_POS="222733868" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="146971846" STOP_POS="202915231" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_628908</CITATION_ID>
    <DESCRIPTION>Segment of chromosome 1 from the normotensive BN/Cr was transferred to SHR. After 10 generations of backcrossing to SHR, the differential segment was fixed with the flanking markers.These were maintained in the homozygous state by brother x sister mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>628909</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D13Arb5-Ren1&lt;/i&gt;)/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="6002008" STOP_POS="6002173" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="5994668" STOP_POS="62022792" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="9016742" STOP_POS="67207219" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="14281836" STOP_POS="72173144" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="25430110" STOP_POS="64281346" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_628909</CITATION_ID>
    <DESCRIPTION>Segment of chromosome 13 from the normotensive BN/Crl was transferred to SHR. After 10 generations of backcrossing to SHR, the differential segment was fixed with the flanking markers.These were maintained in the homozygous state by brother x sister mating. The size of the chromosome transferred is 2.5 cM with an additional 16 cM region of heterozygosity.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629459</RGD_ID>
    <STRAIN_SYMBOL>ZUC-&lt;i&gt;Lepr&lt;sup&gt;faSteJrpz-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology, Louisiana State University Medical Center, New Orleans, LA, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629459</CITATION_ID>
    <DESCRIPTION>Obtained from Louisiana Sate University Medical Center, New Orleans by the Department of Physiology.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629462</RGD_ID>
    <STRAIN_SYMBOL>ZUC-&lt;I&gt;Lepr&lt;/I&gt;&lt;sup&gt;faSte-/-&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of California Davis, Davis, CA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13432153</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116389200" STOP_POS="116389200" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120597857" STOP_POS="120597857" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00839</CITATION_ID>
    <DESCRIPTION>This recessive fatty Zucker rat carries a  mutation that occurred spontaneously in the 13M stock and was reported by Lois Zucker and Theodore Zucker in 1960. This was observed during genetic experiments related to coat color and body size.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629463</RGD_ID>
    <STRAIN_SYMBOL>ZUC-&lt;I&gt;Lepr&lt;/I&gt;&lt;sup&gt;+Ste&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of California Davis, Davis, CA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr</ALLELES>
    <ALLELE_RGD_IDS>3001</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116294409" STOP_POS="116477904" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120503475" STOP_POS="120682281" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629463</CITATION_ID>
    <DESCRIPTION>This is the littermate of  ZUC-LeprfaSte-/-. The fa mutation occurred spontaneously in the 13M stock and was reported by Lois Zucker and Theodore Zucker in 1960. This was observed during genetic experiments related to coat color and body size. These rats have lean phenotype.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629464</RGD_ID>
    <STRAIN_SYMBOL>ZUC-&lt;I&gt;Lepr&lt;/I&gt;&lt;sup&gt;fa&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13432153</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116389200" STOP_POS="116389200" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120597857" STOP_POS="120597857" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629464</CITATION_ID>
    <DESCRIPTION>This fatty zucker is derived from  Lois and Theodore Zucker colonies from which Research colonies were established at many institutions.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629465</RGD_ID>
    <STRAIN_SYMBOL>SHR/NCrlCrlj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles River Japan, &lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=478&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>Charles River Japan, &lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=478&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629465</CITATION_ID>
    <DESCRIPTION>NIH derived strain maintained at the Charles River, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629481</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D1Wox33-D1Got194&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Département de Physiologie et Pharmacologie Clinique, Faculté de Pharmacie, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="203293397" STOP_POS="203293528" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="221363524" STOP_POS="221363653" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="174300636" STOP_POS="228298222" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="224991853" STOP_POS="224991955" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="160754901" STOP_POS="208638156" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="198300754" STOP_POS="198300855" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629481</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a WKY chromosome 1 segment containing QTLs affecting blood pressure and salt sensitivity transferred to the SHR background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629482</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;i&gt;D1Wox19-D1Mit2&lt;/i&gt;)/Njs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Leicester, Leicester, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="142582180" STOP_POS="142582336" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="181133855" STOP_POS="181134010" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="197963658" STOP_POS="197963812" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="204942418" STOP_POS="204942572" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="134980526" STOP_POS="185691036" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629482</CITATION_ID>
    <DESCRIPTION>Fragment of the chromosome 1 derived from SHR and repeated backcross to WKY</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629484</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;tl&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Inflammatory Joint Diseases Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Csf1|Csf1&lt;sup&gt;tl&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>621063|12910954</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629484</CITATION_ID>
    <DESCRIPTION>The outbred stock of Osborne Mendel rats maintained at the Great lakes Naval Training Station in early 1970s had the tl mutation. These rats donot survive to breed so this mutation was transferred to the LEW/N background by a series of backcrosses of heterozygous carriers to LEW/N.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629485</RGD_ID>
    <STRAIN_SYMBOL>LE/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=265 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=265 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629485</CITATION_ID>
    <DESCRIPTION>The LE/Stm rats were introduced into Saitama Cancer Center Research Institute in 1969 from a closed colony of Long Evans rats maintained in the Ben May Laboratory for Cancer Research, University of Chicago. A mutant with red-eyed dilution was found in 1970 in the Long-Evans colony, and the mutation was fixed by selective mating. Thereafter, they were maintained by sister-brother mating more than F50.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629486</RGD_ID>
    <STRAIN_SYMBOL>PVG/OlaHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href =http://www.envigo.com/products-services/research-models-services/find-a-model/research-models/rats/inbred/pvg-inbred-rat/&gt; Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629486</CITATION_ID>
    <DESCRIPTION>black hooded, from A.R.C. Cambridge, United Kingdom; to Olac, United Kingdom, in 1979; to Harlan, United States, in 1992</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629487</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D1Wox19-D1Wox34&lt;/i&gt;)/Njs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Leicester, Leicester, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="174182140" STOP_POS="174182274" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="164747424" STOP_POS="181134010" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="175447029" STOP_POS="197963812" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="182435050" STOP_POS="204942572" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="168382195" STOP_POS="185691036" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629487</CITATION_ID>
    <DESCRIPTION>Fragment of the chromosome 1 derived from WKY and repeated backcross to SHR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629488</RGD_ID>
    <STRAIN_SYMBOL>SI-Tg(Ednrb)Ywa</STRAIN_SYMBOL>
    <FULL_NAME>transgenic spotting lethal</FULL_NAME>
    <ORIGINATION>University of Texas Southwestern Medical Center, Dallas, Texas</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ednrb|Ednrb&lt;sup&gt;sl&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2536|10755424</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629488</CITATION_ID>
    <DESCRIPTION>A 5.8 kb fragment of the human dopamine-beta-hydroxylase (DbH) promoter used directs rat Endrb expression in  sl animals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629489</RGD_ID>
    <STRAIN_SYMBOL>Eker-Tg(Tsc2)5Hin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Experimental Pathology, Cancer Institute, Toshima-ku, Tokyo, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tsc2</ALLELES>
    <ALLELE_RGD_IDS>3908</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629489</CITATION_ID>
    <DESCRIPTION>Wild type Tsc2 transgene was constructed from the Tsc2 cDNA from BN rat and was microinjected into single male pronuclei. Eggs were cultured and tranferred into female wistar which were mated with Eker rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629490</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-Aia1/1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="33724392" STOP_POS="33724594" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="2646395" STOP_POS="2666654" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="3151815" STOP_POS="3172069" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="5249981" STOP_POS="36993999" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="2790511" STOP_POS="32560683" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629490</CITATION_ID>
    <DESCRIPTION>genomic segments with region of interest from chr 20 were inserted to DA strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629491</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-Aia1/2</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="40471453" STOP_POS="86709840" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="39505275" STOP_POS="85379614" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="37685175" STOP_POS="86438507" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="37534124" STOP_POS="151090861" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="36592628" STOP_POS="85014222" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629491</CITATION_ID>
    <DESCRIPTION>genomic segments with region of interest from chr 4 were inserted to DA strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629492</RGD_ID>
    <STRAIN_SYMBOL>Sl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Animal Reproduction, Omiya, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ednrb|Ednrb&lt;sup&gt;sl&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2536|10755424</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629492</CITATION_ID>
    <DESCRIPTION>Natural mutation in the progeny of a Wistar-Imamichi female and a wild rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629493</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-Aia1/3</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="57664252" STOP_POS="57664389" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="56698790" STOP_POS="56698927" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="55375865" STOP_POS="55376001" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="55118586" STOP_POS="55118722" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="54879077" STOP_POS="54879214" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629493</CITATION_ID>
    <DESCRIPTION>genomic segments with region of interest from chr 4 were inserted to DA strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629494</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-Aia1/4</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="23948641" STOP_POS="23948818" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="23444813" STOP_POS="104060283" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="24483076" STOP_POS="107857673" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="24340447" STOP_POS="107484761" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="24006429" STOP_POS="24006612" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629494</CITATION_ID>
    <DESCRIPTION>genomic segments with region of interest from chr 10 were inserted to DA strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629495</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;Mt1pa-D1Rat57&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Freie Universitdt Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mt1-ps1</ALLELES>
    <ALLELE_RGD_IDS>3118</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="182852943" STOP_POS="190563849" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="173421600" STOP_POS="181133270" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="188794419" STOP_POS="197963072" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="195736433" STOP_POS="204941832" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="177313819" STOP_POS="185690396" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629495</CITATION_ID>
    <DESCRIPTION>Fragment of the chromosome 1 derived from SHRSP and repeated backcross to WKY</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629499</RGD_ID>
    <STRAIN_SYMBOL>BXS/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czechoslovak Academy of Sciences, Prague</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629499</CITATION_ID>
    <DESCRIPTION>These recombinant inbred strains are obtained by crossing normotensive BN-&lt;i&gt;Lx&lt;/i&gt;/Cub with hypertensive SHR/Ola progenitor strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629500</RGD_ID>
    <STRAIN_SYMBOL>LEXF/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Saitama Cancer Center Research Institute, 818 Komuro Saitama, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629500</CITATION_ID>
    <DESCRIPTION>Recombinant inbred strain derived from LE/Stm (derived from Ben May, Laboratory for Cancer Research, University of Chicago, Chicago IL) and F344/Stm (derived from F344/DuCrlj; Charles River Japan) and then maintained by brother-sister mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629501</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Ren2)27</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Genome Research, University of Edinburgh, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Agtr1b|Ace</ALLELES>
    <ALLELE_RGD_IDS>2071|2493</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629501</CITATION_ID>
    <DESCRIPTION>This is a hypertensive rat strain in which the mouse Ren2 renin gene along with its 5' and 3' flanking sequences were microinjected into fertilized eggs from a Hannover Sprague-Dawley (SD) background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629502</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;Il6-Npy&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MRC Clinical Centre, London, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il6|Npy</ALLELES>
    <ALLELE_RGD_IDS>2901|3197</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="5889999" STOP_POS="80219310" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="5214602" STOP_POS="78888495" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="3043231" STOP_POS="79565059" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="3095536" STOP_POS="144240956" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="456799" STOP_POS="78045187" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629502</CITATION_ID>
    <DESCRIPTION>This congenic carries a chromosome 4 segment derived from BN/Crl (Charles River) and repeated backcross to SHR/NCruk and selection for Il6 and Npy heterozygotes</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629503</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D19Rat57-D19Mit7&lt;/i&gt;)/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Agt</ALLELES>
    <ALLELE_RGD_IDS>2069</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="61215906" STOP_POS="61216120" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="44306955" STOP_POS="55283277" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="48798983" STOP_POS="60220581" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="59599823" STOP_POS="70892142" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="57234802" STOP_POS="57235101" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629503</CITATION_ID>
    <DESCRIPTION>The segment of chromosome 19 from BN/Crl was transferred onto the genetic background of SHR/Ola. After 8 generations of selective backcrossing the transferred segment had the Agt gene. This was fixed by intercrossing heterozygotes and maintained by by brother and sister mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629504</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;i&gt;D1Mit3-D1Rat57&lt;/i&gt;)/Iwai</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shiga University of Medical Science, Otsu, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="153679879" STOP_POS="182853101" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="144267353" STOP_POS="173421758" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="156446196" STOP_POS="188794576" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="162692213" STOP_POS="195736590" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="146971846" STOP_POS="177313977" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629504</CITATION_ID>
    <DESCRIPTION>Fragment of the chromosome 1 derived from SHR and repeated backcross to WKY</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629505</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mit11-D10M11Mit119&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="101848470" STOP_POS="101848683" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629505</CITATION_ID>
    <DESCRIPTION>fragment of the chromosome 10 derived from MNS and repeated backcross to SS/Jr</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629506</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;tl&lt;/i&gt;.BN-(&lt;i&gt;D2Arb16-D2Wox8&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Inflammatory Joint Diseases Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Csf1</ALLELES>
    <ALLELE_RGD_IDS>621063</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="207184039" STOP_POS="207184330" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="190602746" STOP_POS="204499414" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="205572952" STOP_POS="219581453" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="225003539" STOP_POS="237636701" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="198312439" STOP_POS="212776982" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629506</CITATION_ID>
    <DESCRIPTION>LEW.&lt;i&gt;tl&lt;/i&gt; carrier females were mated with BN/SsNHsd males to develop these congenic animals which has a 2.5 cM region of chr 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629509</RGD_ID>
    <STRAIN_SYMBOL>FHH/EurMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=293&gt;Rat Resource and Research Center&lt;/a&gt;, &lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00293</CITATION_ID>
    <DESCRIPTION>An outbred stock of fawn hooded rats introduced into Europe by Tschopp in the early 1970s. Maintained as an outbred stock until the mid-1980s, then brother x sister mating initiated by A.P. Provoost to produce two strains designated FHH (also known as FHR) and FHL, which differ in hypertension and proteinuria. The colony was transferred to Erasmus University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629510</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D12Arb13-D12Rat79&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="59796478" STOP_POS="59796643" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="2745212" STOP_POS="61985812" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="2761846" STOP_POS="61177004" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="2848113" STOP_POS="62229060" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629510</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629511</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 2&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629511</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629512</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 12&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629512</CITATION_ID>
    <DESCRIPTION>A cross of FHH and BN strains which results in a FHH genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629513</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 4&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629513</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629514</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 6&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629514</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629515</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 7&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629515</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629516</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 8&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629516</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629517</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr Y&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629517</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629518</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 9&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629518</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629519</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Mgh13-D13Mit4&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="33794096" STOP_POS="89333251" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="31241331" STOP_POS="86800898" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="36147533" STOP_POS="92916783" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="41256240" STOP_POS="97381801" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="90551150" STOP_POS="90551272" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629519</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629520</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629520</CITATION_ID>
    <DESCRIPTION>A cross of FHH and BN strains which results in a FHH genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629521</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 11&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629521</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629522</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 20&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629522</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629523</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629523</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629524</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 16&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629524</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629525</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 18&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629525</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629548</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D1Mit3-Igf2&lt;/i&gt;)/1lpcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629548</CITATION_ID>
    <DESCRIPTION>SHR.BN-(D1Mit3-Igf2)/1lpcv is a subline of SHR.BN-(D1Mit3-Igf2)/lpcv.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629578</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Rat130-D5Mco10&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="36460764" STOP_POS="166764498" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="31663789" STOP_POS="161481680" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="31926122" STOP_POS="168109659" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="36590997" STOP_POS="171686754" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="32701659" STOP_POS="168174140" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629578</CITATION_ID>
    <DESCRIPTION> A large segment of chr. 5 from LEW was inserted into Dahl salt-sensitive (SS/Jr) background, congenic substrains were developed by crossing SS.LEW to SS for 8 generations</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631158</RGD_ID>
    <STRAIN_SYMBOL>DXE1/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut Fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631158</CITATION_ID>
    <DESCRIPTION>DXE1/Ztm is a recombinant inbred strain produced from a cross between DA/Han and E3/Han rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631160</RGD_ID>
    <STRAIN_SYMBOL>DXE2/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut Fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631160</CITATION_ID>
    <DESCRIPTION>Is a recombinant inbred strain produced from a cross between DA/Han and E3/Han rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631161</RGD_ID>
    <STRAIN_SYMBOL>DXE3/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut Fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631161</CITATION_ID>
    <DESCRIPTION>Is a recombinant inbred strain produced from a cross between DA/Han and E3/Han rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631163</RGD_ID>
    <STRAIN_SYMBOL>LE/BluGill</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Illinois at Urbana-Champaign</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631163</CITATION_ID>
    <DESCRIPTION>This inbred colony from the University of Illinois at Urbana-Champaign was derived from Long Evans Outbred rats originally purchased from Blue Spruce Farms, Altamont, NY in the Fall of 1982. In order to reduce individual differences, Principal Investigator, Martha U. Gillette, PhD, initiated inbreeding (consecutive brother-sister matings). In March 1993, the colony reached generation #20, defined by the Institute for Animal Laboratory Research (ILAR) as the point during inbreeding at which the strain can officially be considered inbred. This inbred colony continues to be used by Dr. Gillette and her laboratory at the University of Illinois at Urbana-Champaign to research cell, molecular and integrative mechanisms in the brain's circadian clock.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631182</RGD_ID>
    <STRAIN_SYMBOL>DA/BklArbN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH, Arthritis and Rheumatism Branch, Bethesda MD</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00091</CITATION_ID>
    <DESCRIPTION>This is maintained in the NIH animal facility of the Inflammatory Joint Diseases Section, Arthritis and Rheumatism Branch, Bethesda MD by brother and sister breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631219</RGD_ID>
    <STRAIN_SYMBOL>SDT/Jcl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/en/products/diabetes/item_a0140&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/en/products/diabetes/item_a0140&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-04-23)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631219</CITATION_ID>
    <DESCRIPTION>Established from an outbred colony of Sprague-Dawley (purchased from  Charles River Japan)  in Torii Pharmaceutical Co. Ltd. This company was merged to CLEA Japan Inc. in 1998. This substrain was established in 1997. Rats with polyuria and glucosuria were bred for  20 generations of brother-sister mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631220</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mco1-D10Mco31&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="67241334" STOP_POS="81034014" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="66743655" STOP_POS="80537228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="69123603" STOP_POS="83411656" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="68786307" STOP_POS="83220224" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="69986912" STOP_POS="84284667" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631220</CITATION_ID>
    <DESCRIPTION>Strains SS/Jr and LEW were bred for F1 then backcrossed to S to give BC1, this was backcrossed to S to give BC2 and so on till BC5, BC5 was crossed to S to duplicate the recombinant segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631275</RGD_ID>
    <STRAIN_SYMBOL>WKY/Cfd</STRAIN_SYMBOL>
    <FULL_NAME>WKY/Cfd</FULL_NAME>
    <ORIGINATION>Experimental Cardiovascular Biology Laboratory, Institut de Recherches Cliniques de Montreal, 119 Pine Ave W, Montreal, Quebec CA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631275</CITATION_ID>
    <DESCRIPTION>Substrain of WKY/Cr parents from a colony maintained at the Institut de Recherches Cliniques de Montreal (IRCM), the colony was derived from WKY/Cr parents obtained from Charles River (St. Constant, Quebec CA)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631276</RGD_ID>
    <STRAIN_SYMBOL>WKHA/Cfd</STRAIN_SYMBOL>
    <FULL_NAME>WKHA/Cfd</FULL_NAME>
    <ORIGINATION>Experimental Cardiovascular Biology Laboratory, Institut de Recherches Cliniques de Montreal, 119 Pine Ave W, Montreal, Quebec CA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631276</CITATION_ID>
    <DESCRIPTION>Originated from a colony maintained at the Institut de Recherches Cliniques de Montreal (IRCM)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631278</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;I&gt;D2Rat13-D2Rat157&lt;/I&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Western Infirmary, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fst|Gstm1|Vcam1|S1pr1</ALLELES>
    <ALLELE_RGD_IDS>2633|2755|3952|61958</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="47856345" STOP_POS="205135428" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="46123260" STOP_POS="202447032" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="46537589" STOP_POS="217498710" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="65576721" STOP_POS="235592880" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="46542246" STOP_POS="210636169" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631278</CITATION_ID>
    <DESCRIPTION>Congenic strain created by introgressing the Fst-D2Mgh12 (expanded to D2Rat13-D2Rat157) region from Chromosome 2 of WKY/Gcrc into the SHRSP/Gcrc background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631279</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;I&gt;D2Rat13-D2Mit5&lt;/I&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Western Infirmary, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fst</ALLELES>
    <ALLELE_RGD_IDS>2633</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="47856345" STOP_POS="67845370" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="46123260" STOP_POS="66118463" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="46537589" STOP_POS="66828236" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="65576721" STOP_POS="86560306" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="46542246" STOP_POS="66680209" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631279</CITATION_ID>
    <DESCRIPTION>Congenic strain created by introgressing the Fst-D2Mit5 region from Chromosome 2 of WKY/Gcrc into the SHRSP/Gcrc background in the lab of Dr Anna Dominiczak, University of Glasgow.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631280</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D2Mit5-D2Mgh12&lt;/I&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Western Infirmary, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pklr</ALLELES>
    <ALLELE_RGD_IDS>3336</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="67845182" STOP_POS="176849637" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="66118275" STOP_POS="174551863" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="66828049" STOP_POS="188458034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="86560119" STOP_POS="207874394" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="66680022" STOP_POS="181223505" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631280</CITATION_ID>
    <DESCRIPTION>Congenic strain created by introgressing the D2Mit5-D2Mgh12 region from Chromosome 2 of SHRSP/Gcrc into the WKY/Gcrc background in the lab of Dr Anna Dominiczak, University of Glasgow.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631281</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;Fst-Pklr&lt;/I&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Western Infirmary, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fst|Pklr</ALLELES>
    <ALLELE_RGD_IDS>2633|3336</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="47856345" STOP_POS="176849637" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="46123260" STOP_POS="174551863" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="46537589" STOP_POS="188458034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="65576721" STOP_POS="207874394" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="46542246" STOP_POS="181223505" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631281</CITATION_ID>
    <DESCRIPTION>Congenic strain created by introgressing the Fst-Pklr region from Chromosome 2 of SHRSP/Gcrc into the WKY/Gcrc background in the lab of Dr Anna Dominiczak, University of Glasgow.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631282</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;I&gt;D10Arb20-D10Arb22&lt;/I&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="23948641" STOP_POS="23948818" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="23444813" STOP_POS="104060283" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="24483076" STOP_POS="107857673" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="24340447" STOP_POS="107484761" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="24006429" STOP_POS="24006612" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631282</CITATION_ID>
    <DESCRIPTION>This speed congenic strain contains an F344 chromsome 10 segment transferred to a DA background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631283</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;I&gt;D10Arb21-D10Arb22&lt;/I&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="14991535" STOP_POS="14991725" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="14487011" STOP_POS="104060283" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="14827894" STOP_POS="107857673" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="14644150" STOP_POS="107484761" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="14721135" STOP_POS="14721325" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631283</CITATION_ID>
    <DESCRIPTION>This congenic substrain contains an F344 chromosome 10 segment transferred to a DA background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631285</RGD_ID>
    <STRAIN_SYMBOL>IER/Ihr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Experimental Animals of Shiga University, Medical Science, Ohtsu, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=732&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Ophthalmology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631285</CITATION_ID>
    <DESCRIPTION>A mutant rat strain which is a useful model for human cataract.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631286</RGD_ID>
    <STRAIN_SYMBOL>WKY/Izm</STRAIN_SYMBOL>
    <FULL_NAME>Wistar-Kyoto</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=412 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=412 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631286</CITATION_ID>
    <DESCRIPTION>WKY strain from the Izumo colony</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631294</RGD_ID>
    <STRAIN_SYMBOL>F344.GK-(&lt;I&gt;D1Arb42a-D1Rat90&lt;/I&gt;)/Swe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp2c12</ALLELES>
    <ALLELE_RGD_IDS>2470</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="248619887" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="238699859" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="258709726" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="266156838" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="267110921" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631294</CITATION_ID>
    <DESCRIPTION>This congenic strain carries a GK chromosome 1 segment defined by markers D1Arb42a and D1Rat90 transferred to the F344 background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631571</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Uia8-D1Mco38&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="119295112" STOP_POS="119295313" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="110159449" STOP_POS="110159650" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="116680361" STOP_POS="116680557" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="117836211" STOP_POS="117836407" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="110818690" STOP_POS="110818887" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631571</CITATION_ID>
    <DESCRIPTION>Segment of chr 1 from Lewis which was obtained from Charles was introgressed into Dahl salt-sensitive strain which is an in-house colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631572</RGD_ID>
    <STRAIN_SYMBOL>SBH/Ygl</STRAIN_SYMBOL>
    <FULL_NAME>Sabra hypertension prone</FULL_NAME>
    <ORIGINATION>Ben Gurion University Barzilai Medical Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE>Available at the Barzilai University Medical Center in Ashkelon, Israel</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-07-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631572</CITATION_ID>
    <DESCRIPTION>Bred from the original SBH colony established by Ben-Ishay at the Hebrew University Medical Center in Jerusalem. The original colony was found to be partly outbred and display phenotypic variability. To purify the colony and establish phenotypic homogeneity breeding pairs from the original colony were transferred to Ben Gurion University Barzilai University Medical Center in Ashkelon, Israel in 1992 where renewed secondary breeding was performed - hence substrain designated with suffix/Ygl.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631573</RGD_ID>
    <STRAIN_SYMBOL>SBN/Ygl</STRAIN_SYMBOL>
    <FULL_NAME>Sabra hypertension resistant</FULL_NAME>
    <ORIGINATION>Ben Gurion University Barzilai Medical Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE>Available at the Barzilai University Medical Center in Ashkelon, Israel</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-07-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631573</CITATION_ID>
    <DESCRIPTION>Bred from the original SBN colony established by Ben-Ishay at the Hebrew University Medical Center in Jerusalem. The original colony had been bred for 20+ generations but was found to be partly outbred and display phenotypic variability. To purify the colony and establish phenotypic homogeneity breeding pairs from the original colony were transferred to Ben Gurion University Barzilai Medical Center in Ashkelon, Israel in 1992 where renewed secondary breeding was performed - hence substrain designated with suffix/Ygl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631574</RGD_ID>
    <STRAIN_SYMBOL>Wild/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Laboratory Animal Science, Greifswald, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>wild</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631574</CITATION_ID>
    <DESCRIPTION>Wild rats were captured in Rostock, Greifswald, in an industrial pig farm near Greifswald and some in a farm near Munich in Germany.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631576</RGD_ID>
    <STRAIN_SYMBOL>LEW/CrlCrlj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Charles River, Atsugi, Japan, &lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=776&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Immunology; Osteosis</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631576</CITATION_ID>
    <DESCRIPTION>Developed by Dr. Lewis from Wistar stock in the early 1950s. To CRL from Tulane in 1970 at F34.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631577</RGD_ID>
    <STRAIN_SYMBOL>SHR/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=411 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Funabashi Farm, Chiba, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=411 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Funabashi Farm, Chiba, Japan</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631577</CITATION_ID>
    <DESCRIPTION>Strain originated in 1963 from outbred Wistar Kyoto rats. Bred from a male with mild hypertension, mated with a female with high blood pressure. Brother x sister mating with continued selection for high blood pressure (Okamoto 1969, Okamoto et al 1972).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631578</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;I&gt;D2Rat171-D2Arb24&lt;/I&gt;)/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology, Czech Academy of Sciences, Prague 4, Czech Republic.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="114384617" STOP_POS="215381366" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="67703258" STOP_POS="67703293" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="112456140" STOP_POS="212696837" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="116075644" STOP_POS="228737869" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="135770850" STOP_POS="248088631" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="116874922" STOP_POS="221284686" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631578</CITATION_ID>
    <DESCRIPTION>This congenic strain carries a BN/Crl chromosome 2 segment transferred to the SHR/OlaIpcv background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631579</RGD_ID>
    <STRAIN_SYMBOL>LEW/OlaHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Harlan France</ORIGINATION>
    <SOURCE>Harlan France</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631579</CITATION_ID>
    <DESCRIPTION>Obtained from Harlan UK, and for this study kept at the Department of Laboratory Animal Science, Faculty of Veterinary Medicine, Utrecht University, Utrecht, the Netherlands.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631581</RGD_ID>
    <STRAIN_SYMBOL>LEW.1F</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631581</CITATION_ID>
    <DESCRIPTION>Originally derived by Dr. Hans J. Hedrich at Versuchstierzucht, Hannover, Germany by transgressing the RT1&lt;sup&gt;f&lt;/sup&gt; haplotype into the LEW stock</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631582</RGD_ID>
    <STRAIN_SYMBOL>SS.WKY-(&lt;i&gt;Mme-D2Wox18&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mme</ALLELES>
    <ALLELE_RGD_IDS>3098</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="149806826" STOP_POS="170653323" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="147686913" STOP_POS="168355276" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="153799203" STOP_POS="181987474" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="173193501" STOP_POS="201402094" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="153031724" STOP_POS="174727552" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631582</CITATION_ID>
    <DESCRIPTION>Fragment of the chromosome 2 from WKY was transferred to SS/Jr background and repeated backcross to SS/Jr</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631583</RGD_ID>
    <STRAIN_SYMBOL>SS.WKY-(&lt;i&gt;D2Mgh8-D2Mgh9&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631583</CITATION_ID>
    <DESCRIPTION>Fragment of the chromosome 2 from WKY was transferred to SS/Jr background and repeated backcross to SS/Jr</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631585</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D16Mit2-D16Rat12&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="387123" STOP_POS="4234333" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="380245" STOP_POS="4227730" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="1090054" STOP_POS="5098704" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="1084304" STOP_POS="5038806" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="350121" STOP_POS="4304517" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631585</CITATION_ID>
    <DESCRIPTION>This congenic strain carries a LEW/NCrlBR chromosome 16 segment transferred to the SS/Jr background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631586</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;I&gt;D10Mco14-D10Mit11&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="44093097" STOP_POS="98502431" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="43593509" STOP_POS="98003205" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="45157430" STOP_POS="101482600" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="44914976" STOP_POS="101157704" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="45105978" STOP_POS="102587587" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631586</CITATION_ID>
    <DESCRIPTION>This congenic strain is derived by introgressing a desired region of chr 10 from MNS to the SS/Jr recipient.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631587</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10M11Mit119-D10Mit11&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ace</ALLELES>
    <ALLELE_RGD_IDS>2493</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="67241334" STOP_POS="98502431" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="66743655" STOP_POS="98003205" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="69123603" STOP_POS="101482600" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="68786307" STOP_POS="101157704" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="69986912" STOP_POS="102587587" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631587</CITATION_ID>
    <DESCRIPTION>This congenic strain is derived by introgressing a desired region of chr 10 from MNS to the SS/Jr recipient.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631588</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mit11-Vamp2&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Vamp2</ALLELES>
    <ALLELE_RGD_IDS>3949</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="54292423" STOP_POS="54296657" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="53793581" STOP_POS="53797815" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="55675171" STOP_POS="55679405" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="55418231" STOP_POS="55422465" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="55848264" STOP_POS="101848683" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631588</CITATION_ID>
    <DESCRIPTION>Fragment of the chromosome 10 derived from MNS and repeated backcross to SS/Jr</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631589</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D1Wox34-D1Rat164&lt;/i&gt;)/Njs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. Cardiology, Univ of Leicester, Clinical Sciences Wing. Glenfield Hospital, Groby Rd, Leicester, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="174182140" STOP_POS="175967785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="164747424" STOP_POS="166533203" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="175447029" STOP_POS="177235302" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="182435050" STOP_POS="184213712" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="168382195" STOP_POS="170218440" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631589</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived by backcrossing congenic strain SHR.WKY-(&lt;I&gt;D1Wox19-D1Wox34&lt;/i&gt;) to SHR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631590</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D1Wox34-Sah&lt;/i&gt;)/Njs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. Cardiology, Univ of Leicester, Clinical Sciences Wing. Glenfield Hospital, Groby Rd, Leicester, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Acsm3</ALLELES>
    <ALLELE_RGD_IDS>62086</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="174182140" STOP_POS="183591328" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="164747424" STOP_POS="174159966" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="175447029" STOP_POS="189541233" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="182435050" STOP_POS="196475596" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="168382195" STOP_POS="178081751" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631590</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived by backcrossing congenic strain SHR.WKY-(&lt;I&gt;D1Wox19-D1Wox34&lt;/i&gt;) to SHR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631591</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;i&gt;D1Rat56-D1M7Mit206&lt;/i&gt;)/Njs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. Cardiology, Univ of Leicester, Clinical Sciences Wing. Glenfield Hospital, Groby Rd, Leicester, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="178547286" STOP_POS="178547434" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="169112897" STOP_POS="169113045" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="184419946" STOP_POS="184420093" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="191393321" STOP_POS="191393468" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="172926151" STOP_POS="172926455" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631591</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived by backcrossing congenic strain WKY.SHR-(&lt;I&gt;DWox19-D1Mit2&lt;/i&gt;) to WKY</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631592</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;i&gt;D1Rat236-D1M7Mit206&lt;/i&gt;)/Njs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. Cardiology, Univ of Leicester, Clinical Sciences Wing. Glenfield Hospital, Groby Rd, Leicester, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="152234464" STOP_POS="152234669" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="162891429" STOP_POS="162891633" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="169098399" STOP_POS="169098603" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="155183458" STOP_POS="155183662" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631592</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived by backcrossing congenic strain WKY.SHR-(&lt;I&gt;D1Wox19-D1Mit2&lt;/i&gt;) to WKY</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631593</RGD_ID>
    <STRAIN_SYMBOL>LEW/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hopital Purpan, Toulouse Cedex, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631593</CITATION_ID>
    <DESCRIPTION>Strain first obtained in 1987 from the Centre de Selection et d’Elevage d’Animaux de Laboratoire (CSEAL, Orl´eans, bred at Janvier breeding centre (Le Genest-Saint-Isle, France).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631594</RGD_ID>
    <STRAIN_SYMBOL>BN/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hopital Purpan, Toulouse Cedex, France; Centre D'Elevage R. Janvier, Route des Chenes-Secs  Le Genest-St-Isle, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631594</CITATION_ID>
    <DESCRIPTION>Strain first obtained in 1987 from the Centre de Selection et d?Elevage d?Animaux de Laboratoire (CSEAL, Orl´eans, bred at Janvier breeding centre (Le Genest-Saint-Isle, France).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631595</RGD_ID>
    <STRAIN_SYMBOL>LEW.1AV1.DA-(&lt;i&gt;D10Rat92-D10Rat135&lt;/i&gt;)/Ubc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Biomedical Center in Uppsala, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="75082967" STOP_POS="75083145" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="74585846" STOP_POS="104670812" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="77269759" STOP_POS="108540162" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="77132487" STOP_POS="108145987" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="78170416" STOP_POS="108776963" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631595</CITATION_ID>
    <DESCRIPTION>LEW.1AV1 x DA F1 was backcrossed to LEW.1AV1 for 9 generations with selection for the Oia3 locus using flanking markers, then F1N9F1 rats were used as founders for the Oia3 congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631596</RGD_ID>
    <STRAIN_SYMBOL>LEW.1AV1.DA-(&lt;i&gt;D10Rat92-D10Wox17&lt;/i&gt;)/Ubc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Biomedical Center in Uppsala, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="75082967" STOP_POS="75083145" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="74585846" STOP_POS="87055282" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="77269759" STOP_POS="90042115" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="77132487" STOP_POS="89831596" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="78170416" STOP_POS="91168491" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631596</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from intercrosses of the Oia3-congenic strain (LEW.1AV1.DA-(D10Rat20-D10Mgh1)x LEW.1AV1)F2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631597</RGD_ID>
    <STRAIN_SYMBOL>LEW.1AV1.DA-(&lt;i&gt;D10Wox17-D10Rat135&lt;/i&gt;)/Ubc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Biomedical Center in Uppsala, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="87055121" STOP_POS="104670812" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="90041957" STOP_POS="108540162" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="89831438" STOP_POS="108145987" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="91168332" STOP_POS="108776963" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631597</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from intercrosses of the Oia3 containing strain (LEW.1AV1.DA-(D10Rat20-D10Mgh1)x LEW.1AV1)F2</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631598</RGD_ID>
    <STRAIN_SYMBOL>LEW.1AV1.DA-(&lt;i&gt;D10Got154-D10Rat135&lt;/i&gt;)/Ubc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Biomedical Center in Uppsala, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="97010147" STOP_POS="104670812" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="100460820" STOP_POS="108540162" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="100150192" STOP_POS="108145987" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="101532360" STOP_POS="108776963" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631598</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from the Oia3 containing strain intercrosses of (LEW.1AV1.DA-(D10Rat20-D10Mgh1)x LEW.1AV1)F2</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631599</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=409 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=409 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension; Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631599</CITATION_ID>
    <DESCRIPTION>Strain has been maintained at Kyoto University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631600</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;Mt1pa-D1Rat200&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Freie Universitat Berlin, Berlin, Germany.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mt1-ps1</ALLELES>
    <ALLELE_RGD_IDS>3118</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="135021436" STOP_POS="190563849" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="125611501" STOP_POS="181133270" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="133076978" STOP_POS="197963072" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="134116233" STOP_POS="204941832" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="126938969" STOP_POS="185690396" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631600</CITATION_ID>
    <DESCRIPTION>Fragment of the chromosome 1 derived from SHRSP and repeated backcross to WKY</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631601</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;Asgr1-Vamp2&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck Center for Molecular Medicine, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Asgr1|Vamp2</ALLELES>
    <ALLELE_RGD_IDS>2160|3949</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="54292423" STOP_POS="55278323" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="53793581" STOP_POS="54779642" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="55675171" STOP_POS="56666086" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="55418231" STOP_POS="56411205" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="55848264" STOP_POS="56903173" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631601</CITATION_ID>
    <DESCRIPTION>Both the strains WKY and SHRSP were from University of Heidelberg, Heidelberg, Germany; The SHRSP was originated in 1974 from Okamoto and Aoki</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631602</RGD_ID>
    <STRAIN_SYMBOL>BN/Elh</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Surgery and Biochemistry, University of Otago</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631602</CITATION_ID>
    <DESCRIPTION>These rats were transferred in 1986, from University of Pittsburgh, at 35 generation to University of Otago, New Zealand and have been continuously inbred in a hysterectomy-derived barrier-sustained colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631603</RGD_ID>
    <STRAIN_SYMBOL>WKY/Snk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Animal Science and Toxicology Laboratories, Sankyo Co. Ltd., Shizuoka, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631603</CITATION_ID>
    <DESCRIPTION>The original WKY animals were bred at the Animal Science and Toxicology Laboratories in Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631604</RGD_ID>
    <STRAIN_SYMBOL>SHR/Snk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Animal Science and Toxicology Laboratories, Sankyo Co. Ltd., Shizuoka, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631604</CITATION_ID>
    <DESCRIPTION>The original WKY animals were bred at the Animal Science and Toxicology Laboratories in Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631605</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Arb9-D10Got101&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="73887148" STOP_POS="73887455" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="76420583" STOP_POS="76420889" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="65339106" STOP_POS="73694285" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="65068360" STOP_POS="77547622" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631605</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from an inbred SS/Jr strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631606</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Rat13-D10Mit11&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="93198590" STOP_POS="93198873" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="92698959" STOP_POS="92699242" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="95967019" STOP_POS="95967298" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="95701164" STOP_POS="95701443" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="97152234" STOP_POS="101848683" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631606</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from an inbred SS/Jr strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631607</RGD_ID>
    <STRAIN_SYMBOL>SS.WKY-(&lt;i&gt;D2N35-Mme&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mme</ALLELES>
    <ALLELE_RGD_IDS>3098</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="149806826" STOP_POS="221200119" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="147686913" STOP_POS="147803808" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="153799203" STOP_POS="153880910" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="173193501" STOP_POS="173278946" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="153031724" STOP_POS="153114515" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631607</CITATION_ID>
    <DESCRIPTION>Fragment of the chromosome 2 from WKY was transferred to SS/Jr background and repeated backcross to SS/Jr</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631610</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Rat39-D1Rat131&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="152402875" STOP_POS="152403053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="124668437" STOP_POS="142990467" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="132134307" STOP_POS="152871103" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="133172202" STOP_POS="159182239" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="125983422" STOP_POS="145648920" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631610</CITATION_ID>
    <DESCRIPTION>Segment of chr 1 from Lewis which is an in-house colony was introgressed into Dahl salt-sensitive strain which was obtained from Charles River.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631691</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/A3Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Institute, International Medical Center of Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631691</CITATION_ID>
    <DESCRIPTION>Substrain originates from the SHRSP/Izm strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631693</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;Shbg-Atp1b2&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Atp1b2|Shbg</ALLELES>
    <ALLELE_RGD_IDS>2171|3671</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="54817473" STOP_POS="54849162" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="54318698" STOP_POS="54350409" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="56205622" STOP_POS="56237354" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="55951260" STOP_POS="55983036" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="56418323" STOP_POS="56435654" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631693</CITATION_ID>
    <DESCRIPTION>This strain has the blood pressure locus from chr 10</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631694</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D1Rat200-D1Rat216&lt;/I&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="135021436" STOP_POS="135021676" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="125611501" STOP_POS="125611741" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="133076978" STOP_POS="133164521" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="134116233" STOP_POS="205161264" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="126938969" STOP_POS="185923619" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631694</CITATION_ID>
    <DESCRIPTION>This single chromosome 1 congenic strain was constructed by using the double congenic SHRSP strain WKY.SHRSP-(&lt;I&gt;D1Rat200-D1Rat216&lt;/I&gt;)(&lt;I&gt;Shbg-Atp1b2&lt;/I&gt;) as the donor strain to transfer the chromosome 1 Bp QTL to the WKY background while selecting against the chromosome 10 Bp QTL to retain only the chromosome 10 locus in strain WKY.SHRSP-(&lt;I&gt;D1Rat200-D1Rat216&lt;/I&gt;)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631695</RGD_ID>
    <STRAIN_SYMBOL>SS/JrRkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Benjamin Franklin Klinikum, Freie Universitat Berlin, Hindenburgdamm 30, 12203 Berlin, Germany.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631695</CITATION_ID>
    <DESCRIPTION>This inbred strain was derived from the inbred SS/Jr strain available from Harlan Sprague-Dawley (Indianapolis, Ind, US). The colony was established in 1997 at the Freie Universitat Berlin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631696</RGD_ID>
    <STRAIN_SYMBOL>SHR/FubRkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Freie Universitat Berlin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631696</CITATION_ID>
    <DESCRIPTION>Strain originated from an SHR/Fub strain obtained in 1997 at the Freie Universitat Berlin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631697</RGD_ID>
    <STRAIN_SYMBOL>BBDP/Hri</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hagedorn Research Institute, Gentofte, Denmark</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631697</CITATION_ID>
    <DESCRIPTION>This strain has been maintained by brother and sister mating for 40 generations. These originated from the Worcester colony from the rats that were sent from Ottawa to Worcester in 1977.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631698</RGD_ID>
    <STRAIN_SYMBOL>BN/Mol</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Mollegaard Breeding Centre Ltd., Denmark</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631698</CITATION_ID>
    <DESCRIPTION>This strain is maintained at the Mollegaard breeding center.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631699</RGD_ID>
    <STRAIN_SYMBOL>BB.SHR-(&lt;i&gt;D6Rat184-D6Rat101&lt;/i&gt;)/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Greifswald, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="122236101" STOP_POS="122236199" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="116506292" STOP_POS="130245370" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="121224054" STOP_POS="135658578" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="130448688" STOP_POS="144756005" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="121381065" STOP_POS="135964844" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631699</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from an inbred BB/OK strain crossed with diabetes-resistant SHR/Mol females.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631700</RGD_ID>
    <STRAIN_SYMBOL>BB.SHR-(&lt;i&gt;Gnal-D18Mit9&lt;/i&gt;)/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Laboratory Animal Science, University Greifswald, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gnal</ALLELES>
    <ALLELE_RGD_IDS>2715</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="62892257" STOP_POS="79484461" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="60622311" STOP_POS="77209844" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="62805406" STOP_POS="80696375" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="61991738" STOP_POS="79748387" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="63595606" STOP_POS="80370517" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631700</CITATION_ID>
    <DESCRIPTION>Diabetic BB/OK were crossed with male SHR/Mol and the resulting hybrids were backcrossed to BB/OK. Hybrids of each backross were analysed using microsatellite markers. After 7 backcrosses the animals were intercrossed and the ones which were homozygous to the SHR allele were selected. This fragment is 24cM long.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631703</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat207-D10Mgh1&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="86387341" STOP_POS="86387484" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="85887040" STOP_POS="85887185" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="88865454" STOP_POS="88865596" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="88662536" STOP_POS="88662678" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="89896421" STOP_POS="89896564" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631703</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from an inbred SS strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631844</RGD_ID>
    <STRAIN_SYMBOL>Iusm:HAD1</STRAIN_SYMBOL>
    <FULL_NAME>high-alcohol-drinking</FULL_NAME>
    <ORIGINATION>Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631844</CITATION_ID>
    <DESCRIPTION>These high-alcohol-drinking rats were developed by selective breeding from the heterogeneous N/N  (N:NIH) strain . 8 inbred rat strains were intercrossed for alcohol preference and consumption.Within-family selection and a rotational breeding design were employed to reduce inbreeding and to allow maintenance of non-inbred replicate lines. Replicate lines were independently selected for high alcohol drinking (HAD1 and HAD2).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631845</RGD_ID>
    <STRAIN_SYMBOL>Iusm:LAD1</STRAIN_SYMBOL>
    <FULL_NAME>low-alcohol-drinking</FULL_NAME>
    <ORIGINATION>Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631845</CITATION_ID>
    <DESCRIPTION>These low-alcohol-drinking were developed by selective breeding from the heterogeneous strain N:NIH (RGD:728185). 8 inbred rat strains were intercrossed for alcohol preference and consumption. Within-family selection and a rotational breeding design were employed to reduce inbreeding and to allow maintenance of non-inbred replicate lines. Replicate lines were independently selected for low alcohol drinking (LAD1 and LAD2).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631846</RGD_ID>
    <STRAIN_SYMBOL>F344.GK-(&lt;i&gt;D1Mgh10-D1Rat90&lt;/i&gt;)/Swe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Karolinska Institute</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="208479811" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="199050459" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="217054291" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="223910550" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="204280278" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631846</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from an inbred F344/Mcwi strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631847</RGD_ID>
    <STRAIN_SYMBOL>F344.GK-(&lt;i&gt;D1Mit7-D1Mgh25&lt;/i&gt;)/Swe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Karolinska Institute</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="238963877" STOP_POS="238964073" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="229550480" STOP_POS="229550676" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="250195095" STOP_POS="250195290" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="257430524" STOP_POS="262617374" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="235677487" STOP_POS="240980321" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631847</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from an inbred F344 strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631848</RGD_ID>
    <STRAIN_SYMBOL>SHR/OlaIpcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sbf1&lt;i&gt;&lt;sup&gt;m1Ipcv&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>10002755</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631848</CITATION_ID>
    <DESCRIPTION>These are descendents of SHR which were originally from National Institutes of Health. It has been maintained by brother x sister mating at the Czech Academy of Sciences for more than 15 years. A spontaneous recessive mutation in intron 37 (-1 of exon 38) of Sbf1 was identified in this strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634359</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Pas1-D5Uwm37&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="129163811" STOP_POS="129163982" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="26141669" STOP_POS="123935338" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="26251767" STOP_POS="128812854" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="30952629" STOP_POS="132652105" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="26938679" STOP_POS="130527490" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634359</CITATION_ID>
    <DESCRIPTION>WKY/NHsd rats, carrying a region for resistance to mammary tumors between D5Wox7 and D5Uwm37 on chromosome 5 were mated to WF/NHsd. Progeny were backcrossed to WF for 8-9 generations, selecting for Mcs5 region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634363</RGD_ID>
    <STRAIN_SYMBOL>LEW/NIcoCrlf</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Charles River, France</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634363</CITATION_ID>
    <DESCRIPTION>A substrain of LEW that was purchased from Charles River France and bred at Institut Francois Magendie, Bordeaux Cedax, France.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634364</RGD_ID>
    <STRAIN_SYMBOL>SHR/NIcoCrlf</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Charles River, France</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634364</CITATION_ID>
    <DESCRIPTION>A substrain of SHR that was purchased from Charles River France and bred at Institut Francois Magendie, Bordeaux Cedax, France.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634365</RGD_ID>
    <STRAIN_SYMBOL>SS/Hsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan, Indianapolis, Indiana</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634365</CITATION_ID>
    <DESCRIPTION>This strain carries the systolic blood pressure QTL BP143 and the cholesterol-related QTLs Scl14, Scl15, Scl16, Scl17 and Scl18.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634366</RGD_ID>
    <STRAIN_SYMBOL>SR/Hsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan, Indianapolis, Indiana</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634366</CITATION_ID>
    <DESCRIPTION>This strain carries the systolic blood pressure QTL BP143 and the cholesterol-related QTLs Scl14, Scl15, Scl16, Scl17 and Scl18.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634367</RGD_ID>
    <STRAIN_SYMBOL>BN/CrlCrlj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.japancorp.net/company_show.asp?compid=3463&gt;Charles River Laboratories Japan&lt;/a&gt;,&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=777&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.japancorp.net/company_show.asp?compid=3463&gt;Charles River Laboratories Japan&lt;/a&gt;,&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=777&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology; Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634367</CITATION_ID>
    <DESCRIPTION>1976's American River CHARUSU Radiobiology Institute (Netherlands) introduced. After the SPF, the cesarean CHARUSU River Japan again in 1990 (stock) was introduced.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634369</RGD_ID>
    <STRAIN_SYMBOL>WBN/KobSlc</STRAIN_SYMBOL>
    <FULL_NAME>wistar bonn/kobori</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=378 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=378 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Ophthalmology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634369</CITATION_ID>
    <DESCRIPTION>This strain carries the body weight QTLs Bw12 and Bw13, the chronic pancreatitis and diabetes melllitus QTL Cpdm1 and the pancreas inflammation QTL Pi1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634370</RGD_ID>
    <STRAIN_SYMBOL>F344.GK-(&lt;i&gt;D1Mgh10-D1Rat119&lt;/i&gt;)/Swe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Karolinska Institute</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="208479811" STOP_POS="208479939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="199050459" STOP_POS="236036450" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="217054291" STOP_POS="256949019" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="223910550" STOP_POS="264429516" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="204280278" STOP_POS="242586311" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634370</CITATION_ID>
    <DESCRIPTION>GK rats, containing a region for susceptibility to development of type 2 diabetes between D1Mgh10-D1Rat110 on chromosome 1 were mated with normoglycemic F344 rats. Progeny were backcrossd onto F344 for 10 generations. Heterozygous animals were intercrossed to establish the congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634372</RGD_ID>
    <STRAIN_SYMBOL>GHS</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine and Physiology, University of Rochester, Rochester, New York</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634372</CITATION_ID>
    <DESCRIPTION>SD rats were selectively bred for hypercalciuria through four generations to create the genetic hypercalciuric strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634373</RGD_ID>
    <STRAIN_SYMBOL>DA/ZtmRhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Biomedical Center, Lund University, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634373</CITATION_ID>
    <DESCRIPTION>DA rats originating from Zentralinstitut fur Versuchstierzucht, Hannover, Germany and kept at Lund University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634374</RGD_ID>
    <STRAIN_SYMBOL>E3/ZtmRhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Biomedical Center, Lund University, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634374</CITATION_ID>
    <DESCRIPTION>E3 rats originating from Zentralinstitut fur Versuchstierzucht, Hannover, Germany and kept at Lund University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634376</RGD_ID>
    <STRAIN_SYMBOL>LEA/Ncu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Nagoya City University Medical School, Nagoya, Aichi, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634376</CITATION_ID>
    <DESCRIPTION>These rats were established from a closed colony of Long-Evans.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634377</RGD_ID>
    <STRAIN_SYMBOL>BN/Sea</STRAIN_SYMBOL>
    <FULL_NAME>BN/Sea</FULL_NAME>
    <ORIGINATION>Sea Life Supply, Sand City, CA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.sealifesupply.com&gt;  Sea Life Supply &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634377</CITATION_ID>
    <DESCRIPTION>This inbred strain was obtained from Sea life Supply</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634380</RGD_ID>
    <STRAIN_SYMBOL>iP/Iusm</STRAIN_SYMBOL>
    <FULL_NAME>inbred alcohol-preferring</FULL_NAME>
    <ORIGINATION>Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Npy</ALLELES>
    <ALLELE_RGD_IDS>3197</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634380</CITATION_ID>
    <DESCRIPTION>These were inbred alcohol-preferring rats  developed from outbred alcohol-preferring rats (Iusm:P) at generation 30 at Indiana University for high-alcohol-preferring behavior. Inbred rats utilized for the development of alcohol-preferring, alcohol-nonpreferring  congenic strains were in the27th generation of inbreeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634381</RGD_ID>
    <STRAIN_SYMBOL>iNP/Iusm</STRAIN_SYMBOL>
    <FULL_NAME>alcohol-nonpreferring</FULL_NAME>
    <ORIGINATION>Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Npy</ALLELES>
    <ALLELE_RGD_IDS>3197</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634381</CITATION_ID>
    <DESCRIPTION>These were inbred alcohol-nonpreferring rats developed from outbred alcohol-nonpreferring rats (Iusm:NP) at generation 30 at Indiana University for high-alcohol-nonpreferring behavior. Inbred rats utilized for the development of alcohol-preferring, alcohol-nonpreferring congenic strains were in the27th generation of inbreeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634382</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D5Wox12-D5Wox20&lt;/i&gt;)/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="145274041" STOP_POS="145274255" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="139989554" STOP_POS="139989768" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="145726049" STOP_POS="145726262" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="149494416" STOP_POS="149494629" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="147065698" STOP_POS="147065912" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634382</CITATION_ID>
    <DESCRIPTION>This congenic strain carries a BN/Crl chromosome 5 segment transferred to the SHR/OlaIpcv background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>634743</RGD_ID>
    <STRAIN_SYMBOL>BIL</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_634743</CITATION_ID>
    <DESCRIPTION>University of Pittsburgh from a mutation in a colony of unknown background held by the NIH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>724569</RGD_ID>
    <STRAIN_SYMBOL>MWF/FubRkb</STRAIN_SYMBOL>
    <FULL_NAME>Munich Wistar Fromter</FULL_NAME>
    <ORIGINATION>Freie Universitdt Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_724569</CITATION_ID>
    <DESCRIPTION>The MWF/FubRkb strain was established in generation F45 in 1996 by further inbreeding of rats obtained from the original colony (MWF/Ztm).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>724570</RGD_ID>
    <STRAIN_SYMBOL>LEW/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Freie Universitdt Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_724570</CITATION_ID>
    <DESCRIPTION>The LEW/Rkb rats were obtained from M&amp;B, Bomholtvej, Denmark, and a colony of was established at at the Freie Universitdt (FU) Berlin, Benjamin Franklin Hospital, Germany.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>724571</RGD_ID>
    <STRAIN_SYMBOL>MITE/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory of Animal Reproduction, Nagoya University, Nagoya, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_724571</CITATION_ID>
    <DESCRIPTION>This strain was established from captured Japanese wild rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>724572</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Wox51-D10Rat27&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universiti de Montrial, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="73950209" STOP_POS="73950353" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="68011827" STOP_POS="73453136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="70428844" STOP_POS="75983805" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="70062921" STOP_POS="74127968" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="71294871" STOP_POS="77092169" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_724572</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 10 was transferred from LEW into the SS background. Two congenic strains, designated S.L4 and S.L5, that were previously shown to have trapped 2 BP QTLs, were used to derive congenic substrains. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>724573</RGD_ID>
    <STRAIN_SYMBOL>SS/JrTol</STRAIN_SYMBOL>
    <FULL_NAME>Dahl salt-sensitive (SS/Jr) rats</FULL_NAME>
    <ORIGINATION>Housed at the University of Toledo College of Medicine and Life Sciences.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-06-08)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_724573</CITATION_ID>
    <DESCRIPTION>In the 1960s, Dahl selectively bred rats for sensitivity (SS rats) to the hypertensive effect of high-salt diet.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>724574</RGD_ID>
    <STRAIN_SYMBOL>SHR/NHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.envigo.com/model/shr-nhsd/&gt;Envigo&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.envigo.com/model/shr-nhsd/&gt;Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_724574</CITATION_ID>
    <DESCRIPTION>SHR strain obtained from Harlan Sprague-Dawley (Indianapolis, IN)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>724575</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat17-D10Mgh1&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universiti de Montrial, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="91127270" STOP_POS="91127454" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="90627439" STOP_POS="90627625" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="93886117" STOP_POS="93886300" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="93641751" STOP_POS="93641934" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="95066219" STOP_POS="95066632" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_724575</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 10 was transferred from LEW into the SS background. Two congenic strains, designated S.L4 and S.L5, that were previously shown to have trapped 2 BP QTLs, were used to derive congenic substrains. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>724576</RGD_ID>
    <STRAIN_SYMBOL>KDP/Tky</STRAIN_SYMBOL>
    <FULL_NAME>Komeda diabetes-prone rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=15 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=15 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Immunology</RESEARCH_USE>
    <ALLELES>Cblb</ALLELES>
    <ALLELE_RGD_IDS>620535</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_724576</CITATION_ID>
    <DESCRIPTION>This is a diabetic-prone substrain of LETL where only diabetic males were used for the backcross.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>724577</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat27-Igfbp4&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universiti de Montrial, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Igfbp4</ALLELES>
    <ALLELE_RGD_IDS>2875</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="73950209" STOP_POS="84503487" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="73452992" STOP_POS="84007272" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="75983662" STOP_POS="86962563" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="74127825" STOP_POS="86759484" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="77091834" STOP_POS="87834315" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_724577</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 10 was transferred from LEW into the SS background. Two congenic strains, designated S.L4 and S.L5, that were previously shown to have trapped 2 BP QTLs, were used to derive congenic substrains. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728133</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;I&gt;RT1&lt;SUP&gt;n&lt;/SUP&gt;&lt;/I&gt;/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Center dElevage R. Janvier, France.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728133</CITATION_ID>
    <DESCRIPTION>This coisogenic strain was produced by selecting BN rats with the &lt;I&gt;RT1&lt;SUP&gt;n&lt;/SUP&gt;&lt;/I&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728134</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Rat35-D1Rat49&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="132889797" STOP_POS="132889942" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="123479780" STOP_POS="154464242" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="130917121" STOP_POS="165129939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="131958920" STOP_POS="171330794" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="124748920" STOP_POS="157498254" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728134</CITATION_ID>
    <DESCRIPTION>Inbred Salt-sensitive SS/Jr rats were mated to LEW/NCrl rats to create congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728135</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D5Uwm14-D5Uwm31&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio 43614</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="51799340" STOP_POS="51799632" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="47002982" STOP_POS="47003274" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="47842131" STOP_POS="47842422" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="52440414" STOP_POS="52440705" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="48908533" STOP_POS="48908825" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728135</CITATION_ID>
    <DESCRIPTION>S.LEW-D5Rat130/D5Mco10/Jr was selectively bred for 2 generation to fix the chromosome and then backcrossed with S strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728137</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D10Rat141-D10Mgh1&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="88900501" STOP_POS="88900737" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="36511450" STOP_POS="36511619" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="91548145" STOP_POS="91548388" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="40571888" STOP_POS="40572056" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="51402312" STOP_POS="51402480" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="38295381" STOP_POS="38295550" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728137</CITATION_ID>
    <DESCRIPTION>Strains SS/Jr and LEW were bred for F1 then backcrossed to S to give BC1, this was backcrossed to S to give BC2 and so on till BC5, BC5 was crossed to S to duplicate the recombinant segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728138</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;I&gt;Mme-Gca&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Atp1a1|Mme|Npr1</ALLELES>
    <ALLELE_RGD_IDS>2167|3098|3195</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="149806826" STOP_POS="178247591" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="147686913" STOP_POS="175950118" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="153799203" STOP_POS="189857032" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="173193501" STOP_POS="209287892" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="153031724" STOP_POS="182740242" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728138</CITATION_ID>
    <DESCRIPTION>Segments from Milan normotensive rat were inserted in thre homologous region of Dahl salt-sensitive</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728139</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D1Rat200-D1Rat216&lt;/I&gt;)(&lt;I&gt;Shbg-Atp1b2&lt;/I&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728139</CITATION_ID>
    <DESCRIPTION>This double congenic strain was constructed by using the SHRSP strain as a donor strain to transfer the chromosome 1 Bp QTL to the chromosome 10 congenic strain in a cross between SHRSP and WKY.SHRSP-(&lt;I&gt;Shbg-Atp1b2&lt;/I&gt;) to construct an F1 that was then backcrossed to the congenic WKY.SHRSP-(&lt;I&gt;Shbg-Atp1b2&lt;/I&gt;)  for more than 10 generations to construct the double congenic strain now homozygous for the SS Bp QTL alleles at both the chromosome 10 and chromosome 1 Bp QTLs</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728140</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D10Rat11-D10Mgh1&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="96620293" STOP_POS="96620484" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="36511450" STOP_POS="36511619" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="96120911" STOP_POS="96121100" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="99492217" STOP_POS="99492409" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="40571888" STOP_POS="40572056" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="99184058" STOP_POS="99184250" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="51402312" STOP_POS="51402480" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="100633512" STOP_POS="100633982" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="38295381" STOP_POS="38295550" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728140</CITATION_ID>
    <DESCRIPTION>Strains SS/Jr and LEW were bred for F1 then backcrossed to S to give BC1, this was backcrossed to S to give BC2 and so on till BC5, BC5 was crossed to S to duplicate the recombinant segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728142</RGD_ID>
    <STRAIN_SYMBOL>BN.SHR-(&lt;i&gt;Il6-Cd36&lt;/i&gt;)/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd36|Il6</ALLELES>
    <ALLELE_RGD_IDS>2301|2901</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="5889999" STOP_POS="18302142" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="5214602" STOP_POS="17410084" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="3043231" STOP_POS="14191498" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="3095536" STOP_POS="14166434" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="456799" STOP_POS="13554416" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728142</CITATION_ID>
    <DESCRIPTION>This congenic strain has a segment of chr 4 which was of SHR origin. The length of the differential segment is 10 cM and has a defective cd36 allele of SHR.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728143</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Mco38-D1Rat49&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="119295112" STOP_POS="119295313" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="110159449" STOP_POS="154464242" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="116680361" STOP_POS="165129939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="117836211" STOP_POS="171330794" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="110818690" STOP_POS="157498254" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728143</CITATION_ID>
    <DESCRIPTION>Inbred Salt-sensitive SS/Jr rats were mated to LEW/NCrl rats to create congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728144</RGD_ID>
    <STRAIN_SYMBOL>BN.PD-(&lt;I&gt;D8Rat39-D8Rat35&lt;/I&gt;)/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="70041301" STOP_POS="70041537" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="46358478" STOP_POS="46358654" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="50356432" STOP_POS="50356607" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="48981076" STOP_POS="65325374" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="49035642" STOP_POS="64617259" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728144</CITATION_ID>
    <DESCRIPTION>This congenic strain has a segment of chr 8 from the polydactylous PD/Cub by backcrossing to the BN/Cub. The length of the differential segment is 10-15 cM.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728145</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D5Rat130-D5Rat108&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio 43614</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="36460764" STOP_POS="133270832" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="31663789" STOP_POS="128034027" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="31926122" STOP_POS="133313852" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="36590997" STOP_POS="137108002" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="32701659" STOP_POS="134872385" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728145</CITATION_ID>
    <DESCRIPTION>S.LEW-D5Rat130/D5Mco10/Jr was selectively bred for 2 generation to fix the chromosome and then backcrossed with S strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728146</RGD_ID>
    <STRAIN_SYMBOL>F344.BN-(&lt;I&gt;D3Mgh13-D3Mgh7&lt;/I&gt;)/Dlw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Biological Sciences, Oakland University, Rochester, MI</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="132725794" STOP_POS="132725928" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="10549351" STOP_POS="112272465" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="5775856" STOP_POS="117288411" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="11139240" STOP_POS="123812293" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="112319451" STOP_POS="112319585" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728146</CITATION_ID>
    <DESCRIPTION>This congenic strain carries the BN Edpm3 QTL along with many BN chromosome 3 markers on an F344 background.  This strain is maintained at Oakland University, Rochester MN, USA</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728147</RGD_ID>
    <STRAIN_SYMBOL>BN.PD-(&lt;I&gt;D8Rat39-D8Rat35&lt;/I&gt;),SHR-(&lt;I&gt;D4Mgh2-Cd36&lt;/I&gt;),SHR-(&lt;I&gt;D20Wox3-D20Mgh5&lt;/I&gt;)/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728147</CITATION_ID>
    <DESCRIPTION>This is a triple congenic strain that has a differential segment of chr 8, major histocompatibility complex from chr 20 and a small segment of chr 4. The length of the differential segment on chr 20 is 20 cM and on chr 8 it is 15 cM.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728148</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D16Uia2-D16Rat12&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="387123" STOP_POS="4234333" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="380245" STOP_POS="4227730" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="1090054" STOP_POS="5098704" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="1084304" STOP_POS="5038806" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="350121" STOP_POS="4304517" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728148</CITATION_ID>
    <DESCRIPTION>Strains SS/Jr and LEW were bred for F1 then backcrossed to S to give BC1, this was backcrossed to S to give BC2 and so on till BC5, BC5 was crossed to S to duplicate the recombinant segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728151</RGD_ID>
    <STRAIN_SYMBOL>UPL/Ncc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hiroshima University, School of Medicine, Hiroshima, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728151</CITATION_ID>
    <DESCRIPTION>The UPL rat strain was founded as a mutant with cataracts in a SD/CrljRbrc rat colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728152</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Rat196-D1Mgh7&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="66009857" STOP_POS="115183752" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="57336763" STOP_POS="106047988" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="58354072" STOP_POS="113593716" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="59282428" STOP_POS="114601028" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="55083934" STOP_POS="106445306" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728152</CITATION_ID>
    <DESCRIPTION>Inbred Salt-sensitive SS/Jr rats were mated to LEW/NCrl rats to create congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728153</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Rat196-D1Rat49&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="66009857" STOP_POS="66010048" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="57336763" STOP_POS="154464242" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="58354072" STOP_POS="165129939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="59282428" STOP_POS="171330794" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="55083934" STOP_POS="157498254" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728153</CITATION_ID>
    <DESCRIPTION>Inbred Salt-sensitive SS/Jr rats were mated to LEW/NCrl rats to create congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728155</RGD_ID>
    <STRAIN_SYMBOL>BBDR.BBDP-(&lt;I&gt;D4Mit6-D4Mit7&lt;/I&gt;)/1Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="80216705" STOP_POS="80217004" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="76647384" STOP_POS="78886189" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="77307388" STOP_POS="79562753" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="141978848" STOP_POS="141979031" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="75732943" STOP_POS="75733127" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728155</CITATION_ID>
    <DESCRIPTION>This congenic strain was developed by cyclic cross-intercross breeding using diabetic prone and diabetic resistant BB rats. (DP x DR)F1 x DR cross intercross breeding was used to generate F2 lymphopenic rats. These were then genotyped for both the flanking markers of the Gimap5 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728156</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D5Mco34-D5Mco10&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio 43614</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="118637788" STOP_POS="166764498" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="161481433" STOP_POS="161481680" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="168109415" STOP_POS="168109659" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="171686510" STOP_POS="171686754" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="168173895" STOP_POS="168174140" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728156</CITATION_ID>
    <DESCRIPTION>SS.LEW-(&lt;i&gt;D5Rat130-D5Mco10&lt;/i&gt;)/Jr was selectively bred for 2 generation to fix the chromosome and then backcrossed with S strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728157</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D5Rat130-D5Mit19&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio 43614</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="36460764" STOP_POS="139038027" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="31663789" STOP_POS="133752767" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="31926122" STOP_POS="139102349" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="36590997" STOP_POS="142892672" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="32701659" STOP_POS="140744137" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728157</CITATION_ID>
    <DESCRIPTION>SS.LEW-(D5Rat130-D5Mco10)/Jr was selectively bred for 2 generation to fix the chromosome and then backcrossed with SS strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728158</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D5Uia4-D5Mco10&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio 43614</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="143075353" STOP_POS="166764498" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="137790781" STOP_POS="161481680" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="143523348" STOP_POS="168109659" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="147288554" STOP_POS="171686754" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="144865363" STOP_POS="168174140" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728158</CITATION_ID>
    <DESCRIPTION>SS.LEW-(D5Rat130-D5Mco10)/Jr was selectively bred for 2 generation to fix the chromosome and then backcrossed with SS strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728159</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Mco36-D1Rat49&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="132889797" STOP_POS="152919303" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="123479780" STOP_POS="143506731" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="130917121" STOP_POS="153834227" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="131958920" STOP_POS="160138947" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="124748920" STOP_POS="146189942" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728159</CITATION_ID>
    <DESCRIPTION>Inbred Salt-sensitive SS/Jr rats were mated to LEW/NCrlBR rats to create congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728161</RGD_ID>
    <STRAIN_SYMBOL>PD/Cub</STRAIN_SYMBOL>
    <FULL_NAME>polydactylous</FULL_NAME>
    <ORIGINATION>Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728161</CITATION_ID>
    <DESCRIPTION>Strain a highly inbred strain kept since 1969 at the Institute of Biology Medical Genetics, Charles University, Prague. Strain originated from Wistar rats exhibiting a spontaneous mutation which gave rise to the polydactyly-luxate syndrome.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728162</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Mco87-D1Rat71&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="152402875" STOP_POS="210707719" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="142990289" STOP_POS="201278233" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="152870926" STOP_POS="219232156" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="159182062" STOP_POS="226102807" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="145648742" STOP_POS="206567907" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728162</CITATION_ID>
    <DESCRIPTION>Inbred Salt-sensitive SS/Jr rats were mated to LEW/NCrlBR rats to create congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728163</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Uia2-D1Rat49&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="154464069" STOP_POS="154464242" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="165129767" STOP_POS="165129939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="171330622" STOP_POS="171330794" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="157497884" STOP_POS="157498254" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728163</CITATION_ID>
    <DESCRIPTION>Inbred Salt-sensitive SS/Jr rats were mated to LEW/NCrl rats to create congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728165</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Rat196-D1Mco36&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="66009857" STOP_POS="131244255" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="57336763" STOP_POS="121834139" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="58354072" STOP_POS="129209407" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="59282428" STOP_POS="130268180" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="55083934" STOP_POS="122992360" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728165</CITATION_ID>
    <DESCRIPTION>Segment of chr 1 from Lewis which is an in-house colony was introgressed into Dahl salt-sensitive strain which was obtained from Charles River.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728166</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D1Rat112-D1Wox29&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shimane Medical University, Izumo, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="132760429" STOP_POS="132760602" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="123350408" STOP_POS="201284693" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="130779148" STOP_POS="219238616" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="131822204" STOP_POS="226109267" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="124614679" STOP_POS="206574346" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728166</CITATION_ID>
    <DESCRIPTION>A segment from SHRSP/Izm was transferred on a WKY/Izm background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728167</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;Nos2-D10M11Mit119&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nos2</ALLELES>
    <ALLELE_RGD_IDS>3185</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="64313335" STOP_POS="64349221" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="63815308" STOP_POS="63851208" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="66188290" STOP_POS="66221621" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="65423626" STOP_POS="65456957" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="65036884" STOP_POS="65072453" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728167</CITATION_ID>
    <DESCRIPTION>Strains SS/Jr and LEW were bred for F1 then backcrossed to S to give BC1, this was backcrossed to S to give BC2 and so on till BC5, BC5 was crossed to S to duplicate the recombinant segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728168</RGD_ID>
    <STRAIN_SYMBOL>WOK</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Diabetes Research Center, Karlsberg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728168</CITATION_ID>
    <DESCRIPTION>The inbred Wistar-Ottowa-Karlsburg (WOK) rats were obtained from the Diabetes Research Center, Karlsburg, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728170</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;I&gt;Mme-D2Mit14&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Atp1a1|Mme</ALLELES>
    <ALLELE_RGD_IDS>2167|3098</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="149806826" STOP_POS="192287892" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="147686913" STOP_POS="189599348" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="153799203" STOP_POS="204585731" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="173193501" STOP_POS="224018437" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="153031724" STOP_POS="197256313" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728170</CITATION_ID>
    <DESCRIPTION>Segments from Milan normotensive rat were inserted in thre homologous region of Dahl salt-sensitive, the Atp1a1 gene was from the S strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728171</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;I&gt;RT1&lt;SUP&gt;1&lt;/SUP&gt;&lt;/I&gt;/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Center dElevage R. Janvier, France.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728171</CITATION_ID>
    <DESCRIPTION>This coisogenic strain was produced by selecting LEW rats with the &lt;I&gt;RT1&lt;SUP&gt;1&lt;/SUP&gt;&lt;/I&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728172</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;I&gt;D2Mit6-Adh1&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adh1c|Agtr1b|Atp1a1</ALLELES>
    <ALLELE_RGD_IDS>2044|2071|2167</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="78269809" STOP_POS="229482291" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="76539322" STOP_POS="226808892" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="78321410" STOP_POS="243562243" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="98037122" STOP_POS="262102977" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="77630629" STOP_POS="235811584" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728172</CITATION_ID>
    <DESCRIPTION>Segments from Milan normotensive rat were inserted in thre homologous region of Dahl salt-sensitive, the Atp1a1 gene was from MNS</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728183</RGD_ID>
    <STRAIN_SYMBOL>WF/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728183</CITATION_ID>
    <DESCRIPTION>To N in 1975 from NCI at F18. Developed by J. Furth in 1945 from a commercial Wistar stock, in an attempt to develop a strain with high incidence of leukemia.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728184</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/A3N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2020-04-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728184</CITATION_ID>
    <DESCRIPTION>To NIH in 1975 from Yamori at F36. SHR was isolated from Wistar Kyoto rats by Okamoto and Aoki in 1963. SHR was later separated into several sublines; the A3 subline was found to have a high incidence of cerebrovascular lesions. (517)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728185</RGD_ID>
    <STRAIN_SYMBOL>N:NIH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00237</CITATION_ID>
    <DESCRIPTION>Developed in 1979/80 from a series involving eight inbred strains of rats (BN/SsN, MAIN, BuF/N, M520/N, WN/N, ACI/N, WKY IN, and F344/N). The resulting colony consists of 60 breeding pairs. A circular pair mating system is used to maintain the colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728186</RGD_ID>
    <STRAIN_SYMBOL>LEW/SsN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728186</CITATION_ID>
    <DESCRIPTION>To N 1972 from Silvers at F37. Developed by Lewis from a Wistar stock; to Aptekman and Bogden, 1954, at F20; to Silvers 1958 at F31.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728187</RGD_ID>
    <STRAIN_SYMBOL>ACI/N-j</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728187</CITATION_ID>
    <DESCRIPTION>Strain originated from Curtiss and Dunning 1926 at the Columbia University Institute for Cancer Research. To Heston 1945 at F30, to National Institutes of Health 1950 at F41. Subsequent sublines from Dunning or NIH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728188</RGD_ID>
    <STRAIN_SYMBOL>LOU/MN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2020-09-04)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728188</CITATION_ID>
    <DESCRIPTION>To NIH in 1975 from Bazin. In 1970 Bazin and Beckers started breeding LOU rat ancestors from various stocks kept at Universite Catholique de Louvain (probably of Wis- tar origin); from 28 lines bred in parallel, LOU/M was selected for low immunocytoma incidence and LOU/C for high immunocytoma incidence.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728189</RGD_ID>
    <STRAIN_SYMBOL>SHR/N-&lt;I&gt;di&lt;/I&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728189</CITATION_ID>
    <DESCRIPTION>Autosomal recessive congenic strain originated from an inbred transfered to NIH in 1966 at F13 from Okamoto. Okamoto, Kyoto School of Medicine, 1963, from outbred Wistar Kyoto male with marked elevation of blood pressure mated to female with slightly elevated blood pressure; brother-sister mating with contin- ued selection for spontaneous hypertension.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728190</RGD_ID>
    <STRAIN_SYMBOL>RCS-&lt;I&gt;rdy-c&lt;/I&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Albino retinal dystrophy</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728190</CITATION_ID>
    <DESCRIPTION>This congenic strain is obtained from pink-eyed, tan-hooded RCS rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728191</RGD_ID>
    <STRAIN_SYMBOL>LOU/CN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728191</CITATION_ID>
    <DESCRIPTION>To N in 1976 from Bazin at F?. In 1970 Bazin and Beckers started breeding LOU rat ancestors from various stocks kept at Universite Catholique de Louvain (probably of Wis- tar origin); from 28 lines bred in parallel, LOU/C was selected for high immunocytoma incidence and LOU/M for low immunocytoma incidence. (045)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728192</RGD_ID>
    <STRAIN_SYMBOL>RCS-rdy-p</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728192</CITATION_ID>
    <DESCRIPTION>This congenic strain is obtained from pink-eyed, tan-hooded RCS rats. Retinal degeneration starts at about 3 weeks.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728193</RGD_ID>
    <STRAIN_SYMBOL>N:SD</STRAIN_SYMBOL>
    <FULL_NAME>Sprague-Dawley</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=239&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=239&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00239</CITATION_ID>
    <DESCRIPTION>To N 1945 from Sprague Dawley, Inc. Colony closed since then.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728194</RGD_ID>
    <STRAIN_SYMBOL>SHR/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728194</CITATION_ID>
    <DESCRIPTION>To N 1966 at F13 from Okamoto. Okamoto, Kyoto School of Medicine, 1963, from outbred Wistar Kyoto male with marked elevation of blood pressure mated to female with slightly elevated blood pressure; brother-sister mating with contin- ued selection for spontaneous hypertension.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728195</RGD_ID>
    <STRAIN_SYMBOL>SHR/N-&lt;i&gt;cp&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=231&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=231&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2021-01-20)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00231</CITATION_ID>
    <DESCRIPTION>The spontaneously hypertensive corpulent (SHR/N-cp) rat developed at the National Institutes of Health (NIH) is a  congenic strain in which obese homozygotes {cp/cp) are characterized by genetic obesity, mild hypertension, hyper-insulinemia, and glucose intolerance. This rat strain was initially derived by mating a male Koletsky rat that was heterozygous for the corpulent gene (cp/ +) to a female SHR ratof the Okamoto strain. A minimum of 12 backcrosses were carried out to eliminate the non-cp genes of the Ko-letsky strain. The obese (cp/cp) littermates develop glucosuria, proteinuria, and renal structural lesions resemblingdiabetic glomerulosclerosis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728196</RGD_ID>
    <STRAIN_SYMBOL>RHA/N-&lt;i&gt;j&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728196</CITATION_ID>
    <DESCRIPTION>Heterozygous Gunn rats were mated with RHA/N the heterzygous offsprings of this and each following generation was backcrossed with RHA/N to get these congenics.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728197</RGD_ID>
    <STRAIN_SYMBOL>RCS-rdy-+</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728197</CITATION_ID>
    <DESCRIPTION>This congenic strain is obtained from pink-eyed, tan-hooded RCS rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728198</RGD_ID>
    <STRAIN_SYMBOL>BHE/N</STRAIN_SYMBOL>
    <FULL_NAME>Bureau of Home Economics</FULL_NAME>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728198</CITATION_ID>
    <DESCRIPTION>To N in 1979 from Flow Laboratories. Closed colony since then. BHE was started in 1942 by the Agricultural Research Service. USDA from a cross between a black and white hooded strain from Pennsylvania State College and an albino Os- borne-Mendel (also called the Yale strain) strain from Columbia University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728199</RGD_ID>
    <STRAIN_SYMBOL>RHA</STRAIN_SYMBOL>
    <FULL_NAME>Roman high avoidance</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728199</CITATION_ID>
    <DESCRIPTION>Bignami selected for high avoidance conditioning with light as a conditioned stimulus and electric shock as the unconditioned stimulus (Bignami 1965).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728200</RGD_ID>
    <STRAIN_SYMBOL>ACI/N-&lt;I&gt;di&lt;/I&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728200</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from ACI/N inbred strain which came to National Institutes of Health in 1950 at F41.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728358</RGD_ID>
    <STRAIN_SYMBOL>SB</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>R. Kalman, Authority for Animal Facilities</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728358</CITATION_ID>
    <DESCRIPTION>This outbred Sabra strain has been bred in Hebrew University for 60 years.Its breeding scheme and origin is unclear.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728383</RGD_ID>
    <STRAIN_SYMBOL>UPL/Cas</STRAIN_SYMBOL>
    <FULL_NAME>Upjohn Pharmaceuticals Limited</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=472 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=472 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gja8&lt;sup&gt;m1Cas&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13524999</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728383</CITATION_ID>
    <DESCRIPTION>In 1989 spontaneous cataract was observed in Sprague-Dawley rats at the Upjohn Pharmaceuticals Limited. The progeny of affected female had cataract which was hereditary by brother-sister mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728384</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat24-Igfbp4&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universiti de Montrial, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Igfbp4</ALLELES>
    <ALLELE_RGD_IDS>2875</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="76128947" STOP_POS="84503487" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="75631887" STOP_POS="84007272" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="78343027" STOP_POS="86962563" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="78194957" STOP_POS="86759484" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="79229067" STOP_POS="87834315" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728384</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 10 was transferred from LEW into the SS background. Two congenic strains, designated S.L4 and S.L5, that were previously shown to have trapped 2 BP QTLs, were used to derive congenic substrains. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728385</RGD_ID>
    <STRAIN_SYMBOL>WF.COP-(&lt;i&gt;D2Rat2-D2M13Mit286&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison, Wisconsin, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="18227137" STOP_POS="18227305" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="16491740" STOP_POS="16491908" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="14237830" STOP_POS="14237997" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="14095321" STOP_POS="14095488" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="14747814" STOP_POS="14747981" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728385</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 was transferred from COP into the WF background. The recombinant congenic strain, line QQ, was derived from three Mcs1-congenic lines at various backcross generations and was produced at the N10 or N12 backcross generations by intercrossing heterozygous brother and sister pairs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728386</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat119-D10Rat133&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universiti de Montrial, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="52167681" STOP_POS="64939207" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="53273326" STOP_POS="64823355" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="53675361" STOP_POS="65668639" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728386</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 10 was transferred from LEW into the SS background. Two congenic strains, designated S.L4 and S.L5, that were previously shown to have trapped 2 BP QTLs, were used to derive congenic substrains. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728387</RGD_ID>
    <STRAIN_SYMBOL>WF.COP-(&lt;i&gt;D2Mit29-D2Uwm13&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison, Wisconsin, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="9623581" STOP_POS="15576367" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="7887772" STOP_POS="13840758" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="5417336" STOP_POS="11522696" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="5396621" STOP_POS="11387756" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="5601528" STOP_POS="11957973" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728387</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 was transferred from COP into the WF background. The recombinant congenic strain (line Q) was derived from three Mcs1-congenic lines at various backcross generations and was produced at the N10 or N12 backcross generations by intercrossing heterozygous brother and sister pairs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728388</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat119-D10Mgh1&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universiti de Montrial, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="52167681" STOP_POS="52167799" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="53273326" STOP_POS="53273444" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="53675361" STOP_POS="53675478" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728388</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 10 was transferred from LEW into the SS background. Two congenic strains, designated S.L4 and S.L5, that were previously shown to have trapped 2 BP QTLs, were used to derive congenic substrains. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728389</RGD_ID>
    <STRAIN_SYMBOL>WF.COP-(&lt;i&gt;D2Mit29-D2Rat201&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison, Wisconsin, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="9623581" STOP_POS="51390083" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="7887772" STOP_POS="49657252" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="5417336" STOP_POS="50260392" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="5396621" STOP_POS="68633866" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="5601528" STOP_POS="49691646" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728389</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 was transferred from COP into the WF background. Rats were genotyped using multiple microsatellite markers spanning 20-30 cM of the Mcs1 locus from D2Mit29 to D2Rat201 on the centromeric end of chromosome 2. The strain was produced at the N10 or N12 backcross generations by intercrossing heterozygous brother and sister pairs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728391</RGD_ID>
    <STRAIN_SYMBOL>WF.COP-(&lt;i&gt;D2Rat253-D2Uwm17&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison, Wisconsin, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="28294553" STOP_POS="28294742" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="26559817" STOP_POS="32374088" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="25012974" STOP_POS="31224929" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="44171519" STOP_POS="50382003" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="25663274" STOP_POS="32051637" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728391</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 was transferred from COP into the WF background. The recombinant congenic strain, line K, was derived from three Mcs1-congenic lines at various backcross generations and was produced at the N10 or N12 backcross generations by intercrossing heterozygous brother and sister pairs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728392</RGD_ID>
    <STRAIN_SYMBOL>RHA/N-&lt;I&gt;di&lt;/I&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Roman high avoidance-&lt;i&gt;di&lt;/i&gt; mutation</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ors.od.nih.gov/dirs/vrp/ratcenter/f_strainlist.html&gt;NIH Autoimmune Rat Model Repository and Development Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728392</CITATION_ID>
    <DESCRIPTION>Brattleboro rats were mated with RHA/N, the heterzygous offsprings of this and each following generation was backcrossed with RHA/N to get these congenics.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728393</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Got125-D10Rat120&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universiti de Montrial, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="83709133" STOP_POS="88632711" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="83212828" STOP_POS="88132643" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="86168841" STOP_POS="91270722" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="85965754" STOP_POS="91041690" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="86983905" STOP_POS="92373412" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728393</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 10 was transferred from LEW into the SS background. Two congenic strains, designated S.L4 and S.L5, that were previously shown to have trapped 2 BP QTLs, were used to derive congenic substrains. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728394</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat55-D10Rat13&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universiti de Montrial, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="93198590" STOP_POS="93198873" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="85160679" STOP_POS="92699242" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="88140923" STOP_POS="95967298" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="87933406" STOP_POS="95701443" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="89167104" STOP_POS="97152587" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728394</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 10 was transferred from LEW into the SS background. Two congenic strains, designated S.L4 and S.L5, that were previously shown to have trapped 2 BP QTLs, were used to derive congenic substrains. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728395</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat55-D10Rat120&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universiti de Montrial, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="88632460" STOP_POS="88632711" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="85160679" STOP_POS="88132643" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="88140923" STOP_POS="91270722" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="87933406" STOP_POS="91041690" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="89167104" STOP_POS="92373412" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728395</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 10 was transferred from LEW into the SS background. Two congenic strains, designated S.L4 and S.L5, that were previously shown to have trapped 2 BP QTLs, were used to derive congenic substrains. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>728396</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mco15-D10Mgh1&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universiti de Montrial, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="94495280" STOP_POS="94495492" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="93995749" STOP_POS="93995963" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="97308358" STOP_POS="97308569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="97028717" STOP_POS="97028928" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="98392296" STOP_POS="98392508" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_728396</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 10 was transferred from LEW into the SS background. Two congenic strains, designated S.L4 and S.L5, that were previously shown to have trapped 2 BP QTLs, were used to derive congenic substrains. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>731185</RGD_ID>
    <STRAIN_SYMBOL>MWF/Fub</STRAIN_SYMBOL>
    <FULL_NAME>Munich Wistar Fromter</FULL_NAME>
    <ORIGINATION>Charite University Medicine Berlin, Campus Benjamin Franklin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_731185</CITATION_ID>
    <DESCRIPTION>Munich Wistar Fromter rats were obtained from colonies at the Freie Universitat,  Benjamin Franklin Campus Berlin, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>731186</RGD_ID>
    <STRAIN_SYMBOL>SHR/Fub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charite University Medicine Berlin, Campus Benjamin Franklin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_731186</CITATION_ID>
    <DESCRIPTION>Spontaneously hypertensive rats were obtained from colonies at the Freie Universit?t,  Benjamin Franklin Campus Berlin, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>731187</RGD_ID>
    <STRAIN_SYMBOL>Iusm:HAD2</STRAIN_SYMBOL>
    <FULL_NAME>high-alcohol-drinking</FULL_NAME>
    <ORIGINATION>Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_731187</CITATION_ID>
    <DESCRIPTION>These were developed by selective breeding for alcohol preference and consumption from the heterogeneous N/N strain. 8 inbred rat strains were intercrossed. Within-family selection and a rotational breeding design were employed to reduce inbreeding and to allow maintenance of non-inbred replicate lines. Replicate lines were independently selected for high alcohol drinking (HAD1 and HAD2).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>731188</RGD_ID>
    <STRAIN_SYMBOL>Iusm:LAD2</STRAIN_SYMBOL>
    <FULL_NAME>low-alcohol-drinking</FULL_NAME>
    <ORIGINATION>Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_731188</CITATION_ID>
    <DESCRIPTION>These were developed by selective breeding for alcohol preference and consumption from the heterogeneous strain  N:NIH (RGD:728185). 8 inbred rat strains were intercrossed.Within-family selection and a rotational breeding design were employed to reduce inbreeding and to allow maintenance of non-inbred replicate lines. Replicate lines were independently selected for low alcohol drinking (LAD1 and LAD2).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>731189</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;Klk1-D1Rat116&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Gene Diagnostics and Therapeutics, International Medical Center of Japan, Toyama, Shinjuku-ku, Tokyo, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_731189</CITATION_ID>
    <DESCRIPTION>A segment of RNO1 (~70 cM in size) was transferred from WKY/Izm onto the genetic background of SHRSP/Izm by the speed congenic method.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>731190</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Rat211-D1Rat18&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="32879372" STOP_POS="51816258" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="31050840" STOP_POS="49268520" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="33667777" STOP_POS="49454378" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="35077728" STOP_POS="50297622" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="1147796" STOP_POS="1148037" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="43747374" STOP_POS="43747532" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_731190</CITATION_ID>
    <DESCRIPTION>A segment of chr 1 from Lewis which was obtained from Charles was introgressed into Dahl salt-sensitive strain which is an in-house colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>731191</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D2Rat14-D2Mgh12&lt;/i&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="44537979" STOP_POS="205135428" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="42804607" STOP_POS="202447032" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="42776916" STOP_POS="217498710" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="61825950" STOP_POS="235592880" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="210636008" STOP_POS="210636169" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_731191</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 containing blood pressure QTLs was transferred from WKY into SHRSP.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>731192</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D3Rat52-D3Rat130&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="38708931" STOP_POS="67641995" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="18311454" STOP_POS="47233430" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="14090411" STOP_POS="48562146" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="19410399" STOP_POS="55227748" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="14051872" STOP_POS="44551542" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_731192</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D3Rat52-D3Rat17&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>731193</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG-(&lt;i&gt;D4Rat141-D4Mgh11&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="149763204" STOP_POS="168870974" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="148090542" STOP_POS="167139601" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="146942075" STOP_POS="168047091" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="210231569" STOP_POS="230565226" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="151158666" STOP_POS="171204531" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_731193</CITATION_ID>
    <DESCRIPTION>PVG allele is introgressed into the DA rats. Recombinant strains were derived from these which were used in further studies.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>731194</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D3Chm64-D3Rat17&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="141508991" STOP_POS="141509147" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="54740735" STOP_POS="121056321" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="56217734" STOP_POS="127023997" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="62850379" STOP_POS="133513825" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="52127226" STOP_POS="121619110" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_731194</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D3Rat52-D3Rat17&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>731195</RGD_ID>
    <STRAIN_SYMBOL>DA.E3-(&lt;i&gt;D14Wox8-D14Rat64&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical Inflammation Research, BMC, University of Lund, Lund, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="17877762" STOP_POS="67831717" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="63618971" STOP_POS="63619178" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="67944692" STOP_POS="67944898" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="67969510" STOP_POS="67969716" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="68573958" STOP_POS="68574165" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_731195</CITATION_ID>
    <DESCRIPTION>The fragment of interest is transferred from arthritis resistant E3 strain to the susceptible DA strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734471</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mgh7-D1Mco41&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="115183611" STOP_POS="231346522" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="106047847" STOP_POS="221920075" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="113593576" STOP_POS="242177304" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="114600888" STOP_POS="249451438" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="106445165" STOP_POS="227693454" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734471</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain derived from SS.LEW-(&lt;i&gt;D1Mco2-D1Mco35&lt;/i&gt;)/Jr. A 71 cM fragment of LEW chr 1 was introgressed into SS background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734472</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco2-D1Wox6&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="65405637" STOP_POS="139442279" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="56732484" STOP_POS="56732668" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="57761120" STOP_POS="137787460" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="58687835" STOP_POS="138778112" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="131956599" STOP_POS="131956825" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734472</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain derived from SS.LEW-(&lt;i&gt;D1Mco2-D1Mco35&lt;/i&gt;)/Jr. A 40 cM fragment of LEW chr 1 was introgressed into SS background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734473</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D17Mco3-D17Mco10&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="23286123" STOP_POS="64246746" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="23080368" STOP_POS="59555289" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="22774867" STOP_POS="64946465" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="24748228" STOP_POS="66699053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="28967455" STOP_POS="70289318" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734473</CITATION_ID>
    <DESCRIPTION>SS rats were crossed with LEW and the F1 rats were backcrossed to SS. Heterozygous rats with the chromosomal region of interest were selected and backcrossed for the next generation. This was done for eight generations and then the heterozygous animals were intercrossed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734474</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mit9-D5Mco10&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="65089051" STOP_POS="166764498" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="60293434" STOP_POS="161481680" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="61612600" STOP_POS="168109659" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="66128197" STOP_POS="171686754" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="62555131" STOP_POS="168174140" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734474</CITATION_ID>
    <DESCRIPTION>SS rats were crossed with LEW and the F1 rats were backcrossed to SS. Heterozygous rats with the chromosomal region of interest were selected and backcrossed for the next generation. This was done for eight generations and then the heterozygous animals were intercrossed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734475</RGD_ID>
    <STRAIN_SYMBOL>DA/OlaHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =http://www.envigo.com//model/da-olahsd/&gt; inotiv&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =http://www.envigo.com//model/da-olahsd/&gt; inotiv&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734475</CITATION_ID>
    <DESCRIPTION>Odell at the Oak Ridge National Laboratory (USA) initiated the inbreeding of these rats which was completed at the Wistar Institute (USA) in 1965.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734476</RGD_ID>
    <STRAIN_SYMBOL>Crl:CD(SD)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734476</CITATION_ID>
    <DESCRIPTION>Originated in 1925 by Robert W. Dawley from a hybrid hooded male and a female Wistar rat. To CRL in 1950 from Sprague Dawley, Inc. Caesarean rederived in 1955 from original Charles River Sprague Dawley. colonies. In 1991, 8 colonies were selected to form the IGS Foundation Colony. Rederived into isolator foundation colony in 1997. IGS refers to animals bred using the CRL International Genetic Standard system.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734478</RGD_ID>
    <STRAIN_SYMBOL>F344/DuCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.criver.com/products-services/find-model/fischer-cdf-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/fischer-cdf-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734478</CITATION_ID>
    <DESCRIPTION>This colony was originated by mating F344 rats which were purchased from local breeder(Fischer) by M.R. Curtis, Columbia University Institute for Cancer Research, 1920. Dunning at Columbia inbred to form the strain starting in 1920. Dunning to CRL in 1960 at F68. Caesarean rederived in 1960.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734479</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco2-D1Rat49&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="65405637" STOP_POS="65405819" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="56732484" STOP_POS="154464242" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="57761120" STOP_POS="165129939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="58687835" STOP_POS="171330794" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="157497884" STOP_POS="157498254" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734479</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain derived from SS.LEW-(&lt;i&gt;D1Mco2-D1Mco35&lt;/i&gt;)/Jr. A 57 cM fragment of LEW chr 1 was introgressed into SS background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734480</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mit10-D10Mgh1&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="27023535" STOP_POS="98502431" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="26521957" STOP_POS="98003205" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="27237530" STOP_POS="101482600" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="27082535" STOP_POS="101157704" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="27184741" STOP_POS="102587587" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734480</CITATION_ID>
    <DESCRIPTION>SS rats were crossed with LEW and the F1 rats were backcrossed to SS. Heterozygous rats with the chromosomal region of interest were selected and backcrossed for the next generation. This was done for eight generations and then the heterozygous animals were intercrossed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734481</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco2-D1Mco35&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sa</ALLELES>
    <ALLELE_RGD_IDS>3616</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="65405637" STOP_POS="241329842" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="56732484" STOP_POS="231916666" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="57761120" STOP_POS="252708858" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="58687835" STOP_POS="259930393" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="238358625" STOP_POS="238358813" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734481</CITATION_ID>
    <DESCRIPTION>SS rats were crossed with LEW and the F1 rats were backcrossed to SS. Heterozygous rats with the chromosomal region of interest were selected and backcrossed for the next generation. This was done for eight generations and then the heterozygous animals were intercrossed. A 118 cM fragment of LEW chr 1 was introgressed into SS background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734482</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Rat45-D1Mco41&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sa</ALLELES>
    <ALLELE_RGD_IDS>3616</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="152919152" STOP_POS="231346522" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="143506580" STOP_POS="221920075" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="153834077" STOP_POS="242177304" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="160138797" STOP_POS="249451438" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="146189650" STOP_POS="227693454" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734482</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain derived from SS.LEW-(&lt;i&gt;D1Mco2-D1Mco35&lt;/i&gt;)/Jr. A 43 cM fragment of LEW chr 1 was introgressed into SS background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734483</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Rat42-D1Wox10&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="223964326" STOP_POS="223964440" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="133587283" STOP_POS="214537671" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="141381406" STOP_POS="236763528" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="142342107" STOP_POS="244066407" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="135418152" STOP_POS="220639653" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734483</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain derived from SS.LEW-(&lt;i&gt;D1Mco2-D1Mco35&lt;/i&gt;)/Jr. A 43 cM fragment of LEW chr 1 was introgressed into SS background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734526</RGD_ID>
    <STRAIN_SYMBOL>OLETF/Got</STRAIN_SYMBOL>
    <FULL_NAME>Otsuka Long Evans Tokushima</FULL_NAME>
    <ORIGINATION>Otsuka Pharmacuetical Company, 463-10 Kagasuno, Tokushima, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734526</CITATION_ID>
    <DESCRIPTION>Long Evans Charles River Canada introduced it to Otsuka Pharmaceutical Co. in 1982. This is selectively bred by oral glucose tolerance test of selective brother-sister mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734527</RGD_ID>
    <STRAIN_SYMBOL>OLETF.F344-(&lt;i&gt;D1Rat169-D1Rat459&lt;/i&gt;)/Got</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Otsuka Pharmacuetical Company, 463-10 Kagasuno, Tokushima, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="233480549" STOP_POS="270108840" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="224054293" STOP_POS="260122809" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="244401175" STOP_POS="282365384" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="251652807" STOP_POS="289700417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="229876870" STOP_POS="267593558" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734527</CITATION_ID>
    <DESCRIPTION>Female OLETF/Got rats were crossed with F344/DuCrlCrlj rats. The F1 were backcrossed to OLETF to produce the BC1. Selective males from BC1 were backcrossed to OLETF to produce successive congenic generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734528</RGD_ID>
    <STRAIN_SYMBOL>OLETF.BN-(&lt;i&gt;D1Rat76-D1Rat459&lt;/i&gt;)/Got</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Otsuka Pharmacuetical Company, 463-10 Kagasuno, Tokushima, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="270108630" STOP_POS="270108840" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="224569538" STOP_POS="260122809" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="244992467" STOP_POS="282365384" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="252243728" STOP_POS="289700417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="230411091" STOP_POS="267593558" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734528</CITATION_ID>
    <DESCRIPTION>Female OLETF/Got rats were crossed with male BN rats. The F1 were backcrossed to OLETF to produce the BC1. Selective males from BC1 were backcrossed to OLETF to produce successive congenic generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734531</RGD_ID>
    <STRAIN_SYMBOL>OLETF.F344-(&lt;i&gt;D1Rat306-D1Rat461&lt;/i&gt;)/Got</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Otsuka Pharmacuetical Company, 463-10 Kagasuno, Tokushima, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="258843780" STOP_POS="258843987" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="280850604" STOP_POS="280850810" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="268967725" STOP_POS="288207792" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="248583506" STOP_POS="266234812" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734531</CITATION_ID>
    <DESCRIPTION>Female OLETF/Got rats were crossed with F344/DuCrlj rats. The F1 were backcrossed to OLETF to produce the BC1. Selective males from BC1 were backcrossed to OLETF to produce successive congenic generations. Fourth generation backcrossed congenic animals were intercrossed to produce the F2 generation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734758</RGD_ID>
    <STRAIN_SYMBOL>DA/Ham</STRAIN_SYMBOL>
    <FULL_NAME>Dark-agouti</FULL_NAME>
    <ORIGINATION>Shizuoka Laboratory Animal Center Hamamatsu, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734758</CITATION_ID>
    <DESCRIPTION>Original DA rats purchased from Shizuoka Laboratory Animal Center (Hamamatsu, Japan).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734759</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME>Spontaneously hypertensive rat, stroke prone</FULL_NAME>
    <ORIGINATION>University of Glasgow, Western Infirmary, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734759</CITATION_ID>
    <DESCRIPTION>SHRSP strain is maintained at the University of Glasgow since December 1991. This colony is the result of the strain specific brother-sister mating of 13 SHRSP (6 males and 7 females of each) that were obtained from Dr D.F. Bohr (Department of Physiology, University of Michigan, Ann Arbor) where they had been maintained as inbred colonies for more than 15 years. Their breeding stocks were originally obtained from NIH</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734760</RGD_ID>
    <STRAIN_SYMBOL>WKY/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME>Wistar-Kyoto</FULL_NAME>
    <ORIGINATION>University of Glasgow, Western Infirmary, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734760</CITATION_ID>
    <DESCRIPTION>WKY strain is maintained at the University of Glasgow since December 1991. This colony is the result of the strain specific brother-sister mating of 13 WKY (6 males and 7 females of each) that were obtained from Dr D.F. Bohr (Department of Physiology, University of Michigan, Ann Arbor) where they had been maintained as inbred colonies for more than 15 years. Their breeding stocks were originally obtained from NIH</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>734761</RGD_ID>
    <STRAIN_SYMBOL>WF/Kga</STRAIN_SYMBOL>
    <FULL_NAME>Wistar-Furth</FULL_NAME>
    <ORIGINATION>Kagoshima University Dental School, Kagoshima, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_734761</CITATION_ID>
    <DESCRIPTION>Obtained from Hiroshima University (Hiroshima, Japan) and maintained by brother-sister matings for more than 90 generations in the laboratory of Dr M. Kitano (Kagoshima University Dental School, Kagoshima, Japan).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737657</RGD_ID>
    <STRAIN_SYMBOL>LEW.1AV1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Veterinary Institute, Uppsala, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00201</CITATION_ID>
    <DESCRIPTION>Originally derived by Dr. Hans J. Hedrich at Versuchstierzucht, Hannover, Germany by transgressing the MHC of DA/Han rats (AV1) into LEW/Han rats for 16 backcross generations. RT1&lt;sup&gt;av1&lt;/sup&gt; haplotype is a variant to the standard a- haplotype with the difference residing in the atypical MHC class I region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737658</RGD_ID>
    <STRAIN_SYMBOL>PVG.1AV1</STRAIN_SYMBOL>
    <FULL_NAME>Piebald-Virol-Glaxo</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>Harlan UK, Blackthorn, Bicester, UK</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737658</CITATION_ID>
    <DESCRIPTION>Originally derived by Dr. Hans J. Hendrich at Versuchstierzucht, Hannover, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737690</RGD_ID>
    <STRAIN_SYMBOL>F344/Crli</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Charles River, Calco, Italy</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737690</CITATION_ID>
    <DESCRIPTION>These animals were from Charles River Italia, Calco, LC, Italy</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737691</RGD_ID>
    <STRAIN_SYMBOL>BN/Crli</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://guide.labanimal.com/guide/companyd.jsp?b=9143&gt;Charles River Laboratories &lt;/a&gt; Italy</ORIGINATION>
    <SOURCE>&lt;a href=http://guide.labanimal.com/guide/companyd.jsp?b=9143&gt;Charles River Laboratories &lt;/a&gt; Italy</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737691</CITATION_ID>
    <DESCRIPTION>These animals were from Charles River Italia, Calco, LC, Italy</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737703</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(HLA-B*0702,B2M)120-4Trg&lt;sup&gt;Tg/Tg&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=42&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=42&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2020-07-08)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00042</CITATION_ID>
    <DESCRIPTION>Lewis from CRL were used as the background strain. This strain was made by pronuclear injection into Lewis embryos. The embryos were coinjected with DNA fragments containing the HLA-B*0702 human gene and the human beta-2-microglobulin gene.  Founder 120-4 was selected and carrier animals from this founder were mated and this strain was bred to homozygosity.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737857</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat155-D4Rat84&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="50490466" STOP_POS="182430611" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="49524674" STOP_POS="180699135" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="48053950" STOP_POS="182171018" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="47848402" STOP_POS="246313537" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="185398415" STOP_POS="185398530" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737857</CITATION_ID>
    <DESCRIPTION>Congenic strain derived from marker assisted selection for PVG.1AV1 chromsome 4 alleles on the DA recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737858</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat155-Spr&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Spr</ALLELES>
    <ALLELE_RGD_IDS>3753</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="50490466" STOP_POS="119233320" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="49524674" STOP_POS="117676292" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="48053950" STOP_POS="116916073" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="47848402" STOP_POS="181496612" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="119365578" STOP_POS="119369308" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737858</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from marker assisted selection for PVG.1AV1 chromsome 4 alleles on the DA recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737859</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Mgh17-D4Rat56&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="142701358" STOP_POS="142701544" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="114921280" STOP_POS="114921417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="113100978" STOP_POS="113247809" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="177782842" STOP_POS="204673386" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="116611031" STOP_POS="143663540" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737859</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from marker assisted selection for PVG.1AV1 chromsome 4 alleles on the DA recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737861</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat63-D4Rat203&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="154946424" STOP_POS="159799026" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="153274175" STOP_POS="158112799" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="152598827" STOP_POS="157826751" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="219683260" STOP_POS="224843794" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="156442644" STOP_POS="161435775" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737861</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from marker assisted selection for PVG.1AV1 chromsome 4 alleles on the DA recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737862</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D2Rat14-D2Mit5&lt;/i&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="44537979" STOP_POS="67845370" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="42804607" STOP_POS="66118463" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="42776916" STOP_POS="66828236" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="61825950" STOP_POS="86560306" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="66680022" STOP_POS="66680209" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737862</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 containing blood pressure QTLs was transferred from WKY into SHRSP.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737863</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D2Wox9-D2Mgh12&lt;/i&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gstm1</ALLELES>
    <ALLELE_RGD_IDS>2755</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="138595962" STOP_POS="205135428" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="136445150" STOP_POS="202447032" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="141583337" STOP_POS="217498710" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="161271919" STOP_POS="235592880" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="141259937" STOP_POS="210636169" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737863</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 containing blood pressure QTLs was transferred from WKY into SHRSP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737864</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D13Mit9-D13Mit1&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>J.P.Rapp, Dept. Physiol. &amp; Molecular Med, Medical College of Ohio, P.O. Box 10008, Toledo, OH 43699-0008, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="6002008" STOP_POS="55601132" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="5994668" STOP_POS="53050594" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="9016742" STOP_POS="58537177" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="14281836" STOP_POS="63533335" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="25430110" STOP_POS="55033994" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737864</CITATION_ID>
    <DESCRIPTION>Congenic strain developed by introgressing SR/Jr renin gene into the SS/Jr strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737865</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;D2Rat14-D2Mgh12&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="44537979" STOP_POS="205135428" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="42804607" STOP_POS="202447032" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="42776916" STOP_POS="217498710" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="61825950" STOP_POS="235592880" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="210636008" STOP_POS="210636169" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737865</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 which includes blood pressure QTLs was transferred from SHRSP into WKY.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737866</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D2Rat14-D2Mit5&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="44537979" STOP_POS="67845370" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="42804607" STOP_POS="66118463" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="42776916" STOP_POS="66828236" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="61825950" STOP_POS="86560306" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="66680022" STOP_POS="66680209" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737866</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 near blood pressure QTLs was transferred from SHRSP into WKY</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737867</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;D13N1-D13Mit1&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="6002008" STOP_POS="6002173" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="5994668" STOP_POS="37902821" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="9016742" STOP_POS="43785939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="14281836" STOP_POS="48881269" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="25430110" STOP_POS="38985930" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737867</CITATION_ID>
    <DESCRIPTION>Congenic substrain which has a chromosome 13 segment from congenic SS/Jr.SR/Jr-&lt;I&gt;Ren&lt;/i&gt; transferred to the SS/Jr recipient strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737868</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;Syt2-D13Mit1&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Syt2</ALLELES>
    <ALLELE_RGD_IDS>3804</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="6002008" STOP_POS="48749814" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="5994668" STOP_POS="46197976" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="9016742" STOP_POS="51577824" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="14281836" STOP_POS="56630530" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="25430110" STOP_POS="47699094" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737868</CITATION_ID>
    <DESCRIPTION>Congenic substrain which has a chromosome 13 segment from congenic SS/Jr.SR/Jr-&lt;I&gt;Ren&lt;/i&gt; transferred to the SS/Jr recipient strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737869</RGD_ID>
    <STRAIN_SYMBOL>OLETF.BN-(&lt;I&gt;D1Rat461-D1Rat459&lt;/I&gt;)/Got</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Otsuka Pharmacuetical Company, 463-10 Kagasuno, Tokushima, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="270108630" STOP_POS="270108840" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="258843780" STOP_POS="260122809" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="280850604" STOP_POS="282365384" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="288207586" STOP_POS="289700417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="266234605" STOP_POS="267593558" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737869</CITATION_ID>
    <DESCRIPTION>Female OLETF/Got rats were crossed with male BN rats. The fifth generation of congenic animals were used for a Niddm QTL linkage study.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737870</RGD_ID>
    <STRAIN_SYMBOL>DA.E3-(&lt;i&gt;D20Wox3-D20Mgh4&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Lund University, Lund, Sweden.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="6693321" STOP_POS="6693431" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="3621656" STOP_POS="6691706" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="4855475" STOP_POS="5875448" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="6935875" STOP_POS="7910747" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="3660646" STOP_POS="6880472" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737870</CITATION_ID>
    <DESCRIPTION>A fragment containing MHC region was introduced in DA by marker-assisted breeding and verified as pure congenic line after six generations of backcross to DA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737871</RGD_ID>
    <STRAIN_SYMBOL>DA.E3-(&lt;i&gt;D12Got46-D12Rat26&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Lund University, Lund, Sweden.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="28328887" STOP_POS="28329066" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="22297209" STOP_POS="22692658" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="25307118" STOP_POS="29014362" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="27316608" STOP_POS="30964880" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="23362298" STOP_POS="23845733" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737871</CITATION_ID>
    <DESCRIPTION>This congenic strain was obtained by the conventional backcross breeding to the parental DA strain with the negative selection of all known Pia QTLs and positive selection of microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737872</RGD_ID>
    <STRAIN_SYMBOL>DA.E3-(&lt;i&gt;D4Mit16-D4Mgh11&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Lund University, Lund, Sweden.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="129846244" STOP_POS="168870974" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="128289450" STOP_POS="167139601" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="127777294" STOP_POS="168047091" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="192286223" STOP_POS="230565226" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="130228504" STOP_POS="171204531" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737872</CITATION_ID>
    <DESCRIPTION>This congenic strain was obtained by the conventional backcross breeding to the parental DA strain with the negative selection of all known Pia QTLs and positive selection of microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737873</RGD_ID>
    <STRAIN_SYMBOL>DA.E3-(&lt;i&gt;D6Wox5-D6Rat90&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Lund University, Lund, Sweden.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="118366855" STOP_POS="118366949" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="112636280" STOP_POS="112636374" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="117355600" STOP_POS="117355693" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="126582753" STOP_POS="126582846" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="117361909" STOP_POS="117362003" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737873</CITATION_ID>
    <DESCRIPTION>This congenic strain was obtained by the conventional backcross breeding to the parental DA strain with the negative selection of all known Pia QTLs and positive selection of microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737885</RGD_ID>
    <STRAIN_SYMBOL>RHA/Kun</STRAIN_SYMBOL>
    <FULL_NAME>Roman high avoidance</FULL_NAME>
    <ORIGINATION>Dept of Laboratory Animal Science, Faculty of Veterinary Medicine, Utrecht University, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737885</CITATION_ID>
    <DESCRIPTION>Roman High Avoidance strain selectively bred for good two-way avoidance acquisition, maintained by Mr. F.G.J. Janssen at Katholieke Universiteit, The Netherlands</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737886</RGD_ID>
    <STRAIN_SYMBOL>BDX/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept of Biology, Charles University, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737886</CITATION_ID>
    <DESCRIPTION>Recombinant inbred substrain of BDX, maintained by Faculty of Veterinary Medicine, Utrecht University, The Netherlands</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737887</RGD_ID>
    <STRAIN_SYMBOL>AO/OlaHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =http://www.envigo.com/products-services/research-models-services/find-a-model/research-models/rats/inbred/ao-inbred-rat/&gt; Envigo&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =http://www.envigo.com/products-services/research-models-services/find-a-model/research-models/rats/inbred/ao-inbred-rat/&gt; Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737887</CITATION_ID>
    <DESCRIPTION>These rats were obtained from Harlan UK and maintained at the Dept. of Laboratory Animal Science, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737888</RGD_ID>
    <STRAIN_SYMBOL>LEW/NHsdCpb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan Sprague Dawley, Inc., Indianapolis, IN</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737888</CITATION_ID>
    <DESCRIPTION>These rats were obtained from Harlan UK and maintained at the Dept. of Laboratory Animal Science, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737889</RGD_ID>
    <STRAIN_SYMBOL>LEW/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737889</CITATION_ID>
    <DESCRIPTION>These rats were obtained from Harlan UK and maintained at the Dept. of Laboratory Animal Science, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737891</RGD_ID>
    <STRAIN_SYMBOL>Crl:SD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href =https://www.criver.com/products-services/find-model/sas-sprague-dawley-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;, Wilmington, MA</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737891</CITATION_ID>
    <DESCRIPTION>Sprague-Dawley stock initiated by R. Dawley in 1925; To SASCO from ARS/Sprague Dawley in 1979. To Charles River in 1996 now maintained by Charles River Laboratory.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737892</RGD_ID>
    <STRAIN_SYMBOL>ACI/SegHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =http://www.envigo.com/model/aci-seghsd/&gt; Envigo&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =http://www.envigo.com/model/aci-seghsd/&gt; Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Carcinogenesis; Estrogen-induced pituitary growth; Transplant immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737892</CITATION_ID>
    <DESCRIPTION>This substrain is derived by Albert Segaloff of the Alton Ochsner Medical Foundation in 1956, now maintained by Harlan Sprague-Dawley, Inc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737893</RGD_ID>
    <STRAIN_SYMBOL>F344/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737893</CITATION_ID>
    <DESCRIPTION>Substrain of Fischer rats maintained by Dr. H.J. Hedrich, Hannover</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737894</RGD_ID>
    <STRAIN_SYMBOL>LEW/Orl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut de Transgenose, Orleans, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737894</CITATION_ID>
    <DESCRIPTION>Substrain of Lewis rats, maintained in Orleans, France</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737895</RGD_ID>
    <STRAIN_SYMBOL>WKY/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737895</CITATION_ID>
    <DESCRIPTION>Substrain of WKY rats maintained by Dr. H.J. Hedrich, Hannover</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737896</RGD_ID>
    <STRAIN_SYMBOL>BN/Maas</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Erasmus MC, DR Rotterdam, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737896</CITATION_ID>
    <DESCRIPTION>Substrain of BN rats, maintained by Dr. Alex Maas, The Netherlands</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737897</RGD_ID>
    <STRAIN_SYMBOL>ACI/Kun</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Central Animal Laboratory, Katholieke Universiteit, Nijmegen, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737897</CITATION_ID>
    <DESCRIPTION>Substrain of ACl maintained by Mr. F.G.J. Janssen at Katholieke Universiteit, The Netherlands</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737898</RGD_ID>
    <STRAIN_SYMBOL>WOKA/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Diabetes, Division of Laboratory Animal Science, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737898</CITATION_ID>
    <DESCRIPTION>Substrain of WOKA, maintained by Dr. H. Bibergeil in Karlsburg, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737899</RGD_ID>
    <STRAIN_SYMBOL>BN/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept of Biology, Charles University, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737899</CITATION_ID>
    <DESCRIPTION>Recombinant inbred substrain of BN, maintained by Faculty of Veterinary Medicine, Utrecht University, The Netherlands</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737900</RGD_ID>
    <STRAIN_SYMBOL>WF/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737900</CITATION_ID>
    <DESCRIPTION>Recombinant inbred substrain of WF, from Utrecht University to Dr. H.J. Hedrich, Hannover, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737901</RGD_ID>
    <STRAIN_SYMBOL>LH/Ztu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737901</CITATION_ID>
    <DESCRIPTION>A substrain of LH</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737902</RGD_ID>
    <STRAIN_SYMBOL>BDIX/Orl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut de Transgenose, Orleans, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737902</CITATION_ID>
    <DESCRIPTION>Substrain of BDIX, now maintained in Orleans, France</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737903</RGD_ID>
    <STRAIN_SYMBOL>Hsd:SD</STRAIN_SYMBOL>
    <FULL_NAME>Sprague Dawley</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href =https://www.envigo.com/model/hsd-sprague-dawley-sd/&gt;Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737903</CITATION_ID>
    <DESCRIPTION>Originated by the Sprague-Dawley Company in 1925 through a series of crosses begun with a single-hooded male and six albino females of unknown origin. Current Harlan Laboratories' colonies are direct descendants of this original colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737904</RGD_ID>
    <STRAIN_SYMBOL>U/A</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Netherlands Cancer Institute, Amsterdam, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737904</CITATION_ID>
    <DESCRIPTION>Substrain of U, from Zootechnical Institute, Utrecht to The Netherlands Cancer Institute</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737905</RGD_ID>
    <STRAIN_SYMBOL>LEW/Maas</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Limburg, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737905</CITATION_ID>
    <DESCRIPTION>Strain originated from Dr. Margaret Lewis from Wistar stock, to Aptekman and Bogden 1954 at F20, to Silvers in 1958 at F31. Subsequently distributed by Silvers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737906</RGD_ID>
    <STRAIN_SYMBOL>MWF/Hsd</STRAIN_SYMBOL>
    <FULL_NAME>Munich Wistar Fromter</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>Harlan</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2020-04-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737906</CITATION_ID>
    <DESCRIPTION>Substrain of Munich Wistar stock, inbred by Harlan Sprague Dawley</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737907</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-&lt;i&gt;Inha&lt;/i&gt;/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>J.P. Rapp, Dept Physiology and Molec Med, Medical College of Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737907</CITATION_ID>
    <DESCRIPTION>A chromosome 9 segment that may contain an SR/Jr low blood pressure allele was transferred to the SS/Jr recipient strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737908</RGD_ID>
    <STRAIN_SYMBOL>WF/NHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.envigo.com/model/wf-nhsd/&gt; Envigo&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.envigo.com/model/wf-nhsd/&gt; Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2022-03-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737908</CITATION_ID>
    <DESCRIPTION>Substrain of Wistar Furth stock, inbred by National Institute of Health, Bethesda, MD and now available at Harlan Sprague Dawley.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737909</RGD_ID>
    <STRAIN_SYMBOL>R/A</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Netherlands Cancer Institute, Amsterdam, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737909</CITATION_ID>
    <DESCRIPTION>Substrain of R, from Wistar stock in 1947, to The Netherlands Cancer Institute</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737910</RGD_ID>
    <STRAIN_SYMBOL>ARISTORAT/Wsl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Experimental Immunology Unite Faculty of Medicine Clos Chapelle aux Champs, Universite de Louvain, Bruxelles Belgium</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737910</CITATION_ID>
    <DESCRIPTION>Substrain of ARISTORAT, from Dr. Herve Bazin in Bruxelles, Belgium</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737911</RGD_ID>
    <STRAIN_SYMBOL>BUF/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737911</CITATION_ID>
    <DESCRIPTION>Substrain of BUF, from Heston 1946 from Buffalo stock of H. Morris, to Dr. H.J. Hedrich, Hannover, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737912</RGD_ID>
    <STRAIN_SYMBOL>SS/JrIpcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737912</CITATION_ID>
    <DESCRIPTION>strain originated from Dr. John P. Rapp, Medical College of Ohio, USA</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737913</RGD_ID>
    <STRAIN_SYMBOL>E3/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737913</CITATION_ID>
    <DESCRIPTION>Substrain of E3, from Dr. H.J. Hedrich, Hannover, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737914</RGD_ID>
    <STRAIN_SYMBOL>SDL/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737914</CITATION_ID>
    <DESCRIPTION>Substrain of SDL</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737915</RGD_ID>
    <STRAIN_SYMBOL>R/AWa</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept of Genetics, Agricultural University, Wageningen, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737915</CITATION_ID>
    <DESCRIPTION>Substrain of R, from Muhlbock from a Wistar stock in 1947, to Leyton in 1986</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737916</RGD_ID>
    <STRAIN_SYMBOL>DZB/Gro</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Biology Kerklaan, University of Groningen, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737916</CITATION_ID>
    <DESCRIPTION>Substrain of DZB, to Dr. G.A. van Oortmerssen at University of Groningen</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737917</RGD_ID>
    <STRAIN_SYMBOL>WF/Mol</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Mollegaard Breeding Centre Ltd., Denmark</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737917</CITATION_ID>
    <DESCRIPTION>Substrain of Wistar Furth stock, from J Furth in 1945 to P Schjodtz, Denmark</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737918</RGD_ID>
    <STRAIN_SYMBOL>BN/Orl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut de Transgenose, Orleans, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737918</CITATION_ID>
    <DESCRIPTION>Substrain of BN, from Billingham and Silvers 1958, to JP Regnault in Orleans, France</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737919</RGD_ID>
    <STRAIN_SYMBOL>LEW/Han</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737919</CITATION_ID>
    <DESCRIPTION>Substrain of LEW, from Dr Margaret Lewis from Wistar stock in early 1950s, to HJ Hedrich, Hannover, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737920</RGD_ID>
    <STRAIN_SYMBOL>BH/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737920</CITATION_ID>
    <DESCRIPTION>Substrain of BH, black-hooded, from D Wilson at U of Penn, to DML at U of Iowa in 1973, to ZTM in 1973</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737921</RGD_ID>
    <STRAIN_SYMBOL>BDIV/lfz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737921</CITATION_ID>
    <DESCRIPTION>Substrain of BDIV, from cross between BDI and BDII single mating pair, with selection for coat color alleles (Druckrey 1971)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737922</RGD_ID>
    <STRAIN_SYMBOL>LEW/SsNHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.envigo.com/model/lew-lew-ssnhsd&gt; ENVIGO &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.envigo.com/model/lew-lew-ssnhsd&gt; ENVIGO &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737922</CITATION_ID>
    <DESCRIPTION>Inbreeding of the Lewis rat is begun by Dr. Margaret Lewis from a Wistar stock. In 1924, at F20 to Aptekmanm and Bogdon. In 1958, at F31 to Silvers, who distributed this strain. subsequently. LEW/SsNHsd rats were descended from a nucleus colony obtained from the National Institutes of Health, Bethesda, Maryland USA. Harlan became Envigo in 2015.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737923</RGD_ID>
    <STRAIN_SYMBOL>SHR/Maas</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Erasmus MC, DR Rotterdam, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737923</CITATION_ID>
    <DESCRIPTION>Substrain of SHR, spontaneously hypertensive rat, from Okamoto in 1963, to A Maas in The Netherlands</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737924</RGD_ID>
    <STRAIN_SYMBOL>WAG/Rij</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan Sprague Dawley, Indianapolis, IN</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737924</CITATION_ID>
    <DESCRIPTION>Substrain of WAG, from AL Bacharach, Glaxo Ltd from Wistar stock in 1924, from Rij to Kyoto in 1979</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737925</RGD_ID>
    <STRAIN_SYMBOL>BN/Gro</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Biology Kerklaan, University of Groningen, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737925</CITATION_ID>
    <DESCRIPTION>Substrain of BN, from Billingham and Silvers 1958, to U of Groningen</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737926</RGD_ID>
    <STRAIN_SYMBOL>F344/NCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.criver.com/products-services/find-model/fischer-sas-fisch-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/fischer-sas-fisch-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737926</CITATION_ID>
    <DESCRIPTION>Derived from NIH stock in 1992 by SASCO. To Charles River in 1996.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737927</RGD_ID>
    <STRAIN_SYMBOL>ALC/Colle</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737927</CITATION_ID>
    <DESCRIPTION>Substrain of ALC</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737928</RGD_ID>
    <STRAIN_SYMBOL>BN/NHsdCpb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan CPB, Harlan Sprague Dawley, Inc., Indianapolis, IN</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737928</CITATION_ID>
    <DESCRIPTION>Substrain of BN, from Billingham and Silvers 1958</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737929</RGD_ID>
    <STRAIN_SYMBOL>Crl:WI</STRAIN_SYMBOL>
    <FULL_NAME>Wistar rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737929</CITATION_ID>
    <DESCRIPTION>To Scientific Products Farm, Ltd. [predecessor of Charles River United Kingdom (CRUK)] in 1947 from Wistar Institute. To Charles River in 1975 from CRUK. This particular colony was selected because of a low incidence of hydronephrosis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737930</RGD_ID>
    <STRAIN_SYMBOL>LEW/Ztm</STRAIN_SYMBOL>
    <FULL_NAME>LEW/Ztm</FULL_NAME>
    <ORIGINATION>Tierlaboratorium der Medizinischen Hochschule Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ncf1</ALLELES>
    <ALLELE_RGD_IDS>61307</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737930</CITATION_ID>
    <DESCRIPTION>This inbred strain originated from LEW rats housed at the Tierlaboratorium der Medizinischen Hochschule Hannover, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737931</RGD_ID>
    <STRAIN_SYMBOL>GC/Kun</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737931</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>737932</RGD_ID>
    <STRAIN_SYMBOL>LEW/Crl</STRAIN_SYMBOL>
    <FULL_NAME>Lewis</FULL_NAME>
    <ORIGINATION>&lt;a href=https://www.criver.com/products-services/find-model/lewis-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/lewis-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737932</CITATION_ID>
    <DESCRIPTION>Developed by Dr. Lewis from Wistar stock in the early 1950s. To Charles River from Tulane in 1970 at F34.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737933</RGD_ID>
    <STRAIN_SYMBOL>SD/A</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Netherlands Cancer Institute, Amsterdam, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737933</CITATION_ID>
    <DESCRIPTION>Sprague-Dawley stock initiated by R. Dawley in 1925</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737934</RGD_ID>
    <STRAIN_SYMBOL>BN/RijKun</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Central Animal Laboratory, Katholieke Universiteit, Nijmegen, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737934</CITATION_ID>
    <DESCRIPTION>Substrain of BN, from Billingham and Silvers 1958, from Harlan Rijnswijk to Central Catholic University</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737935</RGD_ID>
    <STRAIN_SYMBOL>LEW/Nhg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Gesellschaft fur Strahlen- und Umweltforschung Munchen, Neurerberg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737935</CITATION_ID>
    <DESCRIPTION>Substrain of LEW, from Dr Margaret Lewis from Wistar stock in early 1950s, to Neuherberg, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737936</RGD_ID>
    <STRAIN_SYMBOL>SR/JrIpcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Baylor College of Medicine, Houston, TX</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737936</CITATION_ID>
    <DESCRIPTION>Substrain of SR, from a Sprague-Dawley outbred colony, selected for resistance to salt-induced hypertension (Dahl, 1962)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737937</RGD_ID>
    <STRAIN_SYMBOL>SDH/Ztu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737937</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737938</RGD_ID>
    <STRAIN_SYMBOL>AUG/OlaHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =http://www.envigo.com/products-services/research-models-services/find-a-model/research-models/rats/inbred/aug-inbred-rat/&gt; Envigo&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =http://www.envigo.com/products-services/research-models-services/find-a-model/research-models/rats/inbred/aug-inbred-rat/&gt; Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737938</CITATION_ID>
    <DESCRIPTION>Substrain of AUG, derived from US August substrains in 1951</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737939</RGD_ID>
    <STRAIN_SYMBOL>BBWB/Mol</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Mollegaard Breeding Centre Ltd., Denmark</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737939</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737940</RGD_ID>
    <STRAIN_SYMBOL>PAR/Wsl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Experimental Immunology Unite Faculty of Medicine Clos Chapelle aux Champs, Universite de Louvain, Bruxelles Belgium</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737940</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737941</RGD_ID>
    <STRAIN_SYMBOL>LEP/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dr. Vladimir Kren, Dept of Biology, Charles University, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737941</CITATION_ID>
    <DESCRIPTION>Substrain of LEP, from Charles University cross of outbred animals</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737942</RGD_ID>
    <STRAIN_SYMBOL>LE/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737942</CITATION_ID>
    <DESCRIPTION>Substrain of Long-Evans, from Dr. M Sabourdy in 1960, to Hannover in 1973</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737943</RGD_ID>
    <STRAIN_SYMBOL>R/AEurRij</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dr. Adam Goedde,</ORIGINATION>
    <SOURCE>Harlan Rijswijk, Harlan Sprague Dawley, Indianapolis, IN</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737943</CITATION_ID>
    <DESCRIPTION>Substrain of R, from Muhlbock from a Wistar stock in 1947, to Leyton in 1986</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737944</RGD_ID>
    <STRAIN_SYMBOL>BN/RijN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan Rijswijk, Harlan Sprague Dawley, Indianapolis, IN</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2023-12-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737944</CITATION_ID>
    <DESCRIPTION>Substrain of BN, from Billingham and Silvers 1958, from Harlan Rijnswijk</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737945</RGD_ID>
    <STRAIN_SYMBOL>BN/Han</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737945</CITATION_ID>
    <DESCRIPTION>Substrain of BN, from Billingham and Silvers 1958, from Harlan Rijnswijk to Dr. H.J. Hedrich, Hannover, Germany in 1973.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737946</RGD_ID>
    <STRAIN_SYMBOL>WAG/OlaHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan Sprague Dawley, Inc., Indianapolis, IN</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737946</CITATION_ID>
    <DESCRIPTION>Substrain of WAG, from AL Bacharach, Glaxo Ltd from Wistar stock in 1924, maintained at Harlan Sprague Dawley</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737947</RGD_ID>
    <STRAIN_SYMBOL>BDII/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737947</CITATION_ID>
    <DESCRIPTION>Substrain of BDII, from cross between BDI and outbred Wistar stock to form single mating pair, with selection for coat color alleles (Druckrey 1971)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737948</RGD_ID>
    <STRAIN_SYMBOL>BDE/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737948</CITATION_ID>
    <DESCRIPTION>Substrain of BDE, resulting from a cross between BDIV and E3, and selected for black hood coat color.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737949</RGD_ID>
    <STRAIN_SYMBOL>A2/Colle</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dr. RL Collins, The Jackson Laboratory, Bar Harbor, ME</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737949</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737950</RGD_ID>
    <STRAIN_SYMBOL>DA/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737950</CITATION_ID>
    <DESCRIPTION>Substrain of DA/OlaHsd, to Hannover after 1965</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737951</RGD_ID>
    <STRAIN_SYMBOL>CAP/Kuv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dr. HU Wottge, Universitat Kiel, Kiel, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737951</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737952</RGD_ID>
    <STRAIN_SYMBOL>ACI/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737952</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737953</RGD_ID>
    <STRAIN_SYMBOL>LEW/Gut</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737953</CITATION_ID>
    <DESCRIPTION>Substrain of LEW, from Dr Margaret Lewis from Wistar stock in early 1950s, to Dr. H.J. Hedrich, Hannover, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737954</RGD_ID>
    <STRAIN_SYMBOL>AS/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737954</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737955</RGD_ID>
    <STRAIN_SYMBOL>Hooded/Colle</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dr. RL Collins, The Jackson Laboratory, Bar Harbor, ME</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737955</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737956</RGD_ID>
    <STRAIN_SYMBOL>WF/Gut</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737956</CITATION_ID>
    <DESCRIPTION>substrain of Wistar Furth stock, from J Furth in 1945</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737957</RGD_ID>
    <STRAIN_SYMBOL>WOKW/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Diabetes, Division of Laboratory Animal Science, Karlsburg, Germany</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=513 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737957</CITATION_ID>
    <DESCRIPTION>Substrain of WOKW (originally designated WOK.W1), from outbred Wistar BB rats by brother x sister mating, selected for homozygosity for RT1U, a haplotype which predisposes to type I diabetes, to Karlsburg after 1991</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737958</RGD_ID>
    <STRAIN_SYMBOL>CHOC/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology, Czech Academy of Sciences, Charles University, Prague</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737958</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737959</RGD_ID>
    <STRAIN_SYMBOL>RNU/Mol</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Mollegaard Breeding Centre Ltd., Denmark</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737959</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737960</RGD_ID>
    <STRAIN_SYMBOL>Hsd:WI</STRAIN_SYMBOL>
    <FULL_NAME>Wistar</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href =https://www.envigo.com/model/hsd-wi/&gt;Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737960</CITATION_ID>
    <DESCRIPTION>These are descendants of rats from the Wistar Institute, Philadelphia, Pennsylvania that are now available from Harlan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737961</RGD_ID>
    <STRAIN_SYMBOL>SR/JrMol</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Mollegaard Breeding Centre Ltd., Denmark</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737961</CITATION_ID>
    <DESCRIPTION>Substrain of SR, from a Sprague-Dawley outbred colony, selected for resistance to salt-induced hypertension (Dahl, 1962), from Medical College of Ohio to Mollegaard</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737962</RGD_ID>
    <STRAIN_SYMBOL>SPRD/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737962</CITATION_ID>
    <DESCRIPTION>Substrain of SPRD, from outbred Sprague-Dawley rats at the Hannover facility, where inbreeding began in 1976</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737963</RGD_ID>
    <STRAIN_SYMBOL>LEW/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology, Czech Academy of Sciences, Charles University, Prague</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737963</CITATION_ID>
    <DESCRIPTION>Substrain of LEW, from Dr Margaret Lewis from Wistar stock in early 1950s, to Charles University in Prague</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737964</RGD_ID>
    <STRAIN_SYMBOL>BN/OlaHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737964</CITATION_ID>
    <DESCRIPTION>Substrain of BN, from Billingham and Silvers 1958, from Harlan Rijnswijk to Harlan UK and back to Indianapolis</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737965</RGD_ID>
    <STRAIN_SYMBOL>AGUS/OlaHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737965</CITATION_ID>
    <DESCRIPTION>Substrain of AGUS, germ-free strain selected by hysterectomy derivation, to Harlan Sprague Dawley after 1968</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737966</RGD_ID>
    <STRAIN_SYMBOL>LEW/Kuv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Universitat Kiel, Kiel, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737966</CITATION_ID>
    <DESCRIPTION>Substrain of LEW, from Dr Margaret Lewis from Wistar stock in early 1950s, to Kiel University in Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737967</RGD_ID>
    <STRAIN_SYMBOL>BS/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737967</CITATION_ID>
    <DESCRIPTION>Substrain of BS, developed at U of Otago Medical School from a cross of wild rats x Wistar (Zeiss 1966), to Hannover after it was inbred in 1988</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737968</RGD_ID>
    <STRAIN_SYMBOL>BN/Gut</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737968</CITATION_ID>
    <DESCRIPTION>Substrain of BN, from Billingham and Silvers 1958</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737969</RGD_ID>
    <STRAIN_SYMBOL>NAR/SaU</STRAIN_SYMBOL>
    <FULL_NAME>non-albumin rat</FULL_NAME>
    <ORIGINATION>Dept of Laboratory Animal Science, University of Utrecht, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737969</CITATION_ID>
    <DESCRIPTION>Substrain of NAR, non-albumin rat, from the National Bio Resource Project in Japan to Utrecht</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737970</RGD_ID>
    <STRAIN_SYMBOL>AMORAT/Wsl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Experimental Immunology Unite Faculty of Medicine Clos Chapelle aux Champs, Universite de Louvain, Bruxelles, Belgium</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737970</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737971</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/Rivm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Institute of Public Health and Environmental Protection, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737971</CITATION_ID>
    <DESCRIPTION>unknown</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>737972</RGD_ID>
    <STRAIN_SYMBOL>BN/Crl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_737972</CITATION_ID>
    <DESCRIPTION>Silvers and Billingham began brother x sister matings with selection for histocompatibility in 1958 from a brown mutation in a stock of wild rats maintained by King and Aptekman in a pen-bred colony of rats trapped from the wild in 1930 by King at the Wistar Institute. To Charles River from Radiobiology Institute, Netherlands in 1976.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>738038</RGD_ID>
    <STRAIN_SYMBOL>HEP</STRAIN_SYMBOL>
    <FULL_NAME>high ethanol preferring</FULL_NAME>
    <ORIGINATION>Institut Francois Magendie, rue Camille Saint-Saens, Bordeaux Cedex, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_738038</CITATION_ID>
    <DESCRIPTION>High ethanol preferring strain HEP from generations S6 and S7 of selection were obtained from Robert D. Myers, East Carolina University at Greenville, North Carolina, USA</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>738120</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(HLA-B*2705m1,B2M)133-1Trg&lt;sup&gt;Tg/Tg&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=43&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=43&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2018-11-20)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00043</CITATION_ID>
    <DESCRIPTION>This strain was made by pronuclear injection into Lewis embryos. The embryos were co-injected with DNA fragments containing the HLA-B*2705 human gene (human HLA-B27 gene  with Serine replacing Cys67)  and the human beta-2-microglobulin gene.  Founder 133-1 was selected and carrier animals from this founder were mated and bred to homozygosity.  The strain was transferred from Dr. Joel Taurog, University of Texas Southwestern Medical School in Dallas to the Rat Resource and Research Center in 2002.  The strain has been maintained by sibling mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>738122</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(UBC-EGFP)1BalRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=52&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=52&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-07-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00052</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein gene under the control of the human ubiquitin-C promoter with a the woodchuck hepatitis virus posttranscriptional regulatory element (WRE).  This transgenic strain was made by injecting the lentivirus vector containing the GFP construct (vector name FUGW) into SD rat embryos.  Animals that exhibited fluorescence of tails where then mated.  The colony was transferred from Carlos Lois, California Institute of Technology, Pasedena, California to the Rat Resource and Research Center in 2002.  This strain has been maintained by inter-breeding of carrier animals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1298093</RGD_ID>
    <STRAIN_SYMBOL>LEW/NHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.envigo.com/model/lew-ssnhsd/&gt;Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1298093</CITATION_ID>
    <DESCRIPTION>Descended from a nucleus colony obtained from the National Institutes of Health, Bethesda, Maryland. Maintained at  Harlan-Sprague Dawley (Indianapolis, Indiana) .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299868</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;D7Uia1-D7Mco7&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="103146217" STOP_POS="103146515" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="112429186" STOP_POS="112429483" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="112367543" STOP_POS="116100169" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="108875615" STOP_POS="113014423" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1299868</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived by crossing the congenic strain SS.SR-&lt;I&gt;Cyp11b1&lt;/I&gt;/Jr to SS/Jr to isolate which contains a smaller SR/Jr derived chromosome 7 segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299869</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;Cyp11b1&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1299869</CITATION_ID>
    <DESCRIPTION>Congenic strain which has a SR/Jr chromosome 7 segment containing Cyp11b1 transferred to the SS/Jr recipient strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299870</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D5Uia8-D5Rat108&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121056335" STOP_POS="133270832" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="128033842" STOP_POS="128034027" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="133313668" STOP_POS="133313852" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124025017" STOP_POS="137108002" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="121964356" STOP_POS="134872385" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1299870</CITATION_ID>
    <DESCRIPTION>SS.LEW-(&lt;I&gt;D5Rat130-D5Rat108&lt;/i&gt;)/Jr was selectively backcrossed with the SS strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299871</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;I&gt;D20Arb2-D20Arb8&lt;/I&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="2646395" STOP_POS="2666654" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="3151815" STOP_POS="3172069" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="5249981" STOP_POS="5270235" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="2790511" STOP_POS="2811567" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1299871</CITATION_ID>
    <DESCRIPTION>Region of interest was introgressed from F344/Hsd into DA/BklArb by eight to ten genotype guided backcrosses followed by minimum five intercrosses.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299872</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;I&gt;D8Arb15-D8Arb22&lt;/I&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="68133439" STOP_POS="119085047" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="73320439" STOP_POS="128033168" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="77653284" STOP_POS="127239929" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="71843628" STOP_POS="124310337" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1299872</CITATION_ID>
    <DESCRIPTION>Region of interest was introgressed from F344/Hsd into DA/BklArb by eight to ten genotype guided backcrosses followed by minimum five intercrosses.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299873</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D5Mco34-D5Rat108&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="118637788" STOP_POS="133270832" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="128033842" STOP_POS="128034027" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="133313668" STOP_POS="133313852" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="137107818" STOP_POS="137108002" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="134871897" STOP_POS="134872385" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1299873</CITATION_ID>
    <DESCRIPTION>SS.LEW-(&lt;I&gt;D5Rat130-D5Rat108&lt;/i&gt;)/Jr was selectively backcrossed with the SS strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299874</RGD_ID>
    <STRAIN_SYMBOL>OLETF.F344-(&lt;i&gt;D1Rat166-D1Rat90&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory of Animal Breeding and Genetics, Kyoto University, Kyoto, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=94 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="258334277" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="248393012" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="269279863" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="276721459" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="255026793" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1299874</CITATION_ID>
    <DESCRIPTION>Female OLETF were crossed with male F344 rats. The male F1 progeny were backcrossed with female F344 to produce the BC1. Five generations of backcross matings were made between selective males from the BC1 and F344 females to produce the new congenic strain. Sucessive generations were maintained by a standard brother-sister mating protocol.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299875</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;i&gt;D7Rat22-D7Mit2&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=679&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-19)</AVAILABILITY>
    <RESEARCH_USE>arthritis/autoimmunity studies</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="116294265" STOP_POS="116294546" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="126080176" STOP_POS="126080454" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="125794079" STOP_POS="125794357" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="76615341" STOP_POS="123191874" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00679</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing F344/NHsd into DA/BklArbNsi 9 times then brother-sister mating to maintain in the homozygous state</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299876</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D5Rat54-D5Rat108&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="125411329" STOP_POS="133270832" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="120182440" STOP_POS="128034027" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="124957483" STOP_POS="133313852" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="128816449" STOP_POS="137108002" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="126386030" STOP_POS="134872385" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1299876</CITATION_ID>
    <DESCRIPTION>SS.LEW-(&lt;I&gt;D5Rat130-D5Rat108&lt;/i&gt;)/Jr was selectively backcrossed with the SS strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299877</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;I&gt;D10Rat204-D10Arb22&lt;/I&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="104060133" STOP_POS="104060283" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="107857524" STOP_POS="107857673" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="94240348" STOP_POS="107484761" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="95695076" STOP_POS="95695218" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1299877</CITATION_ID>
    <DESCRIPTION>Region of interest was introgressed from F344/Hsd into DA/BklArb by eight to ten genotype guided backcrosses followed by minimum five intercrosses.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299878</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;I&gt;D4Arb30-D4Arb4&lt;/I&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="75939858" STOP_POS="75939996" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="151805502" STOP_POS="151805662" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="150682435" STOP_POS="150682594" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="216606296" STOP_POS="216606455" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="73972453" STOP_POS="154937227" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1299878</CITATION_ID>
    <DESCRIPTION>The DA/BklArbN strain came from Bantin &amp; Kingman and the F344/NHsd strain came from Harlan Sprague Dawley</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299879</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;D7Mco7-D7Wox19&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="106839225" STOP_POS="106839474" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="116249395" STOP_POS="116249643" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="116151764" STOP_POS="116152012" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="113044000" STOP_POS="113044249" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1299879</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived by crossing the congenic strain SS.SR-&lt;I&gt;Cyp11b1&lt;/I&gt;/Jr to SS/Jr to isolate which contains a smaller SR/Jr derived chromosome 7 segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299880</RGD_ID>
    <STRAIN_SYMBOL>F344.DA-(&lt;I&gt;D20Arb2-D20Arb8&lt;/I&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="2646395" STOP_POS="2666654" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="3151815" STOP_POS="3172069" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="5249981" STOP_POS="5270235" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="2790511" STOP_POS="2811567" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1299880</CITATION_ID>
    <DESCRIPTION>Region of interest was introgressed from DA/BklArb into F344/Hsd by eight to ten genotype guided backcrosses followed by minimum five intercrosses.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1299881</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D5Wox3-D5Rat108&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="99905133" STOP_POS="133270832" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="94858972" STOP_POS="128034027" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="97921932" STOP_POS="133313852" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="101964092" STOP_POS="137108002" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="99080786" STOP_POS="134872385" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1299881</CITATION_ID>
    <DESCRIPTION>SS.LEW-(&lt;I&gt;D5Rat130-D5Rat108&lt;/i&gt;)/Jr was selectively backcrossed with the SS strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1300432</RGD_ID>
    <STRAIN_SYMBOL>HAA/FDSC</STRAIN_SYMBOL>
    <FULL_NAME>Hatano High Avoidance</FULL_NAME>
    <ORIGINATION>Hatano Research Institute, Food and Drug Safety Center, Hadano, Kanagawa, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=496 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1300432</CITATION_ID>
    <DESCRIPTION>In 1985 two lines of Sprague-Dawley were selectively bred for their active shuttle-box avoidance task which is a device used for evaluating the effects of chemicals in pharmacological and toxicological studies and testing learning behavior of animals. These animals have a higher rate of avoidance response and showed little interindividual variation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1300433</RGD_ID>
    <STRAIN_SYMBOL>LAA/FDSC</STRAIN_SYMBOL>
    <FULL_NAME>Hatano Low Avoidance</FULL_NAME>
    <ORIGINATION>Hatano Reserch Institute, Food and Drug Safety Center, Hadano, Kanagawa, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=497 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1300433</CITATION_ID>
    <DESCRIPTION>In 1985 two lines of Sprague-Dawley were selectively bred for their active shuttle-box avoidance task which is a device used for evaluating the effects of chemicals in pharmacological and toxicological studies and testing learning behavior of animals. These animals have a lower rate of avoidance response and showed little interindividual variation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1300439</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(UBC-EGFP)2BalRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=65&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=65&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-07-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00065</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein gene under the control of the human ubiquitin-C promoter with a the woodchuck hepatitis virus posttranscriptional regulatory element (WRE).  This transgenic strain was made by injecting the lentivirus vector containing the GFP construct (vector name FUGW) into SD rat embryos.  Animals that exhibited fluorescence of tails where then mated.  The colony was transferred from Carlos Lois, California Institute of Technology, Pasedena, California to the Rat Resource and Research Center in 2002.  This strain has been maintained by backcrossing carrier males to SD stock females in order to segregate transgenes and maintain the SD background.  The strain now carries a single transgene which is located at chromosome 14q21.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302359</RGD_ID>
    <STRAIN_SYMBOL>HsdFcen:SD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Bioterio Central, Ciudad Universitaria, Costanera Norte Ciudad Aut?noma de Buenos Aires Buenos Aires, Argentina</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302359</CITATION_ID>
    <DESCRIPTION>These animals were originally bought from Harlan, Indianapolis, USA are have been bred at Bioterio Central since then.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302360</RGD_ID>
    <STRAIN_SYMBOL>W/HsdFcen</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Bioterio Central, Ciudad Universitaria, Costanera Norte Ciudad Aut?noma de Buenos Aires Buenos Aires, Argentina</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302360</CITATION_ID>
    <DESCRIPTION>These animals were originally bought from Harlan, Indianapolis, USA are have been bred at Bioterio Central since then.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302372</RGD_ID>
    <STRAIN_SYMBOL>SDDIO/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=44&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=44&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00044</CITATION_ID>
    <DESCRIPTION>This strain was made by inbreeding SD rats selected for an obese phenotype when fed a high fat diet.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302373</RGD_ID>
    <STRAIN_SYMBOL>SDDR/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=45&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=45&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00045</CITATION_ID>
    <DESCRIPTION>This strain was made by inbreeding SD rats selected for a lean phenotype when fed a high fat diet.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302377</RGD_ID>
    <STRAIN_SYMBOL>SPRD-&lt;i&gt;Anks6&lt;sup&gt;PKD&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=46&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=46&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-03-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Anks6&lt;sup&gt;PKD&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11534996</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="66112770" STOP_POS="66112770" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="61317180" STOP_POS="61317180" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="62650971" STOP_POS="62650971" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="67163440" STOP_POS="67204853" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="63633540" STOP_POS="63674953" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00046</CITATION_ID>
    <DESCRIPTION>From outbred Han:SPRD (Sprague-Dawley rats) from Zentralinstitut furVersuchstierkunde, Hannover.  This strains carries the Pkdr1 (Anks6) mutation that causes autosomal dominant polycystic kidney disease.  The strain was transferred from Dr. Jared Grantham, University of Kansas Medical Center to the Rat Resource and Research Center in 2002.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302416</RGD_ID>
    <STRAIN_SYMBOL>ACI.DA-(&lt;i&gt;D10Rat2-D10Rat19&lt;/i&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Genomics and Human Genetics, Manhasset, New York</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302416</CITATION_ID>
    <DESCRIPTION>A fragment from DA/OlaHsd rats is transferred to ACI/SegHsd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302597</RGD_ID>
    <STRAIN_SYMBOL>LEXF7C/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=232 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=232 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302597</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302598</RGD_ID>
    <STRAIN_SYMBOL>FXLE26/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=264 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=264 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302598</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302599</RGD_ID>
    <STRAIN_SYMBOL>WKY/Ta</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=419 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=419 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302599</CITATION_ID>
    <DESCRIPTION>This strain originated from Takeda Chemical Industries, Ltd., Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302600</RGD_ID>
    <STRAIN_SYMBOL>HTX/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>hydrocephalus texas</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=3 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=3 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302600</CITATION_ID>
    <DESCRIPTION>1981 by Kohn from institutional albino rats of unknown origin at University of Texas. From Juntendo University to Kyoto University in 1992.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302601</RGD_ID>
    <STRAIN_SYMBOL>FXLE23/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=261 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=261 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302601</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302602</RGD_ID>
    <STRAIN_SYMBOL>FXLE12/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=250 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=250 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302602</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302603</RGD_ID>
    <STRAIN_SYMBOL>FXLE25/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=263 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=263 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302603</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302604</RGD_ID>
    <STRAIN_SYMBOL>LEXF4/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=226 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=226 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302604</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302605</RGD_ID>
    <STRAIN_SYMBOL>LEXF2A/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=222 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=222 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302605</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302606</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/Ta</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=414 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=414 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302606</CITATION_ID>
    <DESCRIPTION>This strain originated from Takeda Chemical Industries, Ltd., Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302607</RGD_ID>
    <STRAIN_SYMBOL>FXLE21/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=259 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=259 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302607</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302608</RGD_ID>
    <STRAIN_SYMBOL>CXH6/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=506 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=506 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Metabolism; Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302608</CITATION_ID>
    <DESCRIPTION>Strain originated from the Institute for Animal Experimentation, University of Tokushima, Tokushima, Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302610</RGD_ID>
    <STRAIN_SYMBOL>KMI/Tky</STRAIN_SYMBOL>
    <FULL_NAME>miniature rat ishikawa</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=29 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=29 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Osteosis</RESEARCH_USE>
    <ALLELES>Prkg2</ALLELES>
    <ALLELE_RGD_IDS>3401</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302610</CITATION_ID>
    <DESCRIPTION>Miniature Rat Ishikawa derived from a breeding colony of Wistar rats at the Ishikawa Animal Laboratory (Saitama). Introduced to Tokyo Medical College.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302611</RGD_ID>
    <STRAIN_SYMBOL>FXLE24/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=262 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=262 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302611</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302612</RGD_ID>
    <STRAIN_SYMBOL>LEXF10C/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=238 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=238 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302612</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302613</RGD_ID>
    <STRAIN_SYMBOL>BN/fMaiHok</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=65  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=65  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302613</CITATION_ID>
    <DESCRIPTION>Kyoto University (Kyo)to Aichi Colony Institute (Idn)to Hokkaido University, Laboratory of Experimental Animal Science(Hok) 1976, F7 to Hokkaido University, Center for Experimental Plants &amp; Animals(Hok) 1982,F21</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302614</RGD_ID>
    <STRAIN_SYMBOL>WKY/NMna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=460 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=460 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302614</CITATION_ID>
    <DESCRIPTION>Inbred strain originated at Fujita Health University School of Medicine, Japan from a WKY/N strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302615</RGD_ID>
    <STRAIN_SYMBOL>FXLE14/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=252 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=252 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302615</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302616</RGD_ID>
    <STRAIN_SYMBOL>LEXF10B/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=237 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=237 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302616</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302617</RGD_ID>
    <STRAIN_SYMBOL>LEXF6B/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=228 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=228 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302617</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302618</RGD_ID>
    <STRAIN_SYMBOL>LEXF9/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=235 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=235 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302618</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302619</RGD_ID>
    <STRAIN_SYMBOL>FXLE16/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=254 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=254 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-16)</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302619</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302620</RGD_ID>
    <STRAIN_SYMBOL>SHR/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>spontaneous hypertension rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=9 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=9 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2021-11-12)</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302620</CITATION_ID>
    <DESCRIPTION>Okamoto 1963 from outbred Wistar Kyoto rats. Bred from a male with mild hypertension, mated with a female with high blood pressure. Brother x sister mating with continued selection for high blood pressure (Okamoto 1969, Okamoto et al 1972).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302621</RGD_ID>
    <STRAIN_SYMBOL>LEXF10A/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=236 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=236 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302621</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302622</RGD_ID>
    <STRAIN_SYMBOL>WF/Kop</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=510 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=510 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302622</CITATION_ID>
    <DESCRIPTION>Inbred originated from Kagoshima University, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302623</RGD_ID>
    <STRAIN_SYMBOL>TM/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>tester moriyama rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=10 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=10 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Hematology</RESEARCH_USE>
    <ALLELES>Rab38&lt;sup&gt;ru&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>1600311</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302623</CITATION_ID>
    <DESCRIPTION>Tester Moriyama rat derived from Long-Evans at Aichi Cancer Center, were transferred to Moriyama Mental Disease Hospital and Nagoya University. Inbred Line was established at Nagoya University. From Shionogi &amp; Co., Ltd. to Kyo in 1976 .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302624</RGD_ID>
    <STRAIN_SYMBOL>RICO/Ngs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=479 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=479 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension; Ophthalmology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302624</CITATION_ID>
    <DESCRIPTION>Strain originated at Division of Comparative Medicine, Center for Frontier Life Sciences, Nagasaki University, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302625</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D16Wox4-D16Rat13&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>National BioResource Project for the Rat in Japan</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="54876458" STOP_POS="54876610" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="48143982" STOP_POS="73187298" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="51339600" STOP_POS="78172206" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="51050772" STOP_POS="77759249" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="51452966" STOP_POS="77968799" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302625</CITATION_ID>
    <DESCRIPTION>Male OLETF was crossed with female F344. F1 were backcrossed to female F344 for 5 generations. Microsatellite-based genotyping was performed to select the best male that had the best OLETF donor genome. Once the region was fixed the resultant congenic strain was maintained by brother-sister mating.37.4 cM segment of the OLETF genome was transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302626</RGD_ID>
    <STRAIN_SYMBOL>BN.UPL-(&lt;I&gt;D2Rat134-D2Rat2&lt;/I&gt;)/Cas</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=473 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=473 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="18227137" STOP_POS="18227305" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="16491740" STOP_POS="183719262" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="14237830" STOP_POS="198298901" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="14095321" STOP_POS="217785884" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="14747814" STOP_POS="190963154" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302626</CITATION_ID>
    <DESCRIPTION>Strain originated from Hiroshima University, Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302627</RGD_ID>
    <STRAIN_SYMBOL>F344/NSlc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=379 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=379 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302627</CITATION_ID>
    <DESCRIPTION>Strain originated from Japan SLC, Inc, Shizuoka, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302628</RGD_ID>
    <STRAIN_SYMBOL>ACIS/Hok</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=63 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=63 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302628</CITATION_ID>
    <DESCRIPTION>Spontaneous mutation from ACI/Hok in 1981.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302629</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D1Rat49-D1Rat112&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=314 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=314 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302629</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from SHRSP to WKY.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302630</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;I&gt;D10Wox7-D10Wox6&lt;/I&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=77 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=77 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="99451733" STOP_POS="99451848" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="98952626" STOP_POS="98952741" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="102427604" STOP_POS="102427718" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="102101261" STOP_POS="102101375" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="103550924" STOP_POS="103551039" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302630</CITATION_ID>
    <DESCRIPTION>Microsatellite-based genotyping was performed to select the best male that had the best OLETF donor genome. Once the region was fixed the resultant congenic strain was maintained by brother-sister mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302631</RGD_ID>
    <STRAIN_SYMBOL>BN/SsNSlc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=371 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=371 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302631</CITATION_ID>
    <DESCRIPTION>Strain originated from Japan SLC, Inc, Shizuoka, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302632</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D1Smu11-D1Arb21&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=313 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=313 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302632</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from SHRSP to WKY.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302633</RGD_ID>
    <STRAIN_SYMBOL>FXLE20/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=258 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=258 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302633</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302634</RGD_ID>
    <STRAIN_SYMBOL>BB/WorTky</STRAIN_SYMBOL>
    <FULL_NAME>BioBreeding rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=30 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=30 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302634</CITATION_ID>
    <DESCRIPTION>Mutation causing diabetes mellitus in a closed colony of outbred Wistar rats at Bio-Breeding Labs, Ontario, Canada in 1974 (Chappel and Chappel 1983). To Worcester in 1977 where inbreeding began. Introduced to Tokyo Medical College in 1983.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302635</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D12Rat8-D12Rat16&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>National BioResource Project for the Rat in Japan</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="28415861" STOP_POS="36063091" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="22779459" STOP_POS="30427275" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="25799119" STOP_POS="34265075" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="27805580" STOP_POS="36160041" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="23934730" STOP_POS="31489223" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302635</CITATION_ID>
    <DESCRIPTION>Male OLETF was crossed with female F344. F1 were backcrossed to female F344 for 5 generations. Microsatellite-based genotyping was performed to select the best male that had the best OLETF donor genome. Once the region was fixed the resultant congenic strain was maintained by brother-sister mating.37.4 cM segment of the OLETF genome was transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302636</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D1Wox29-D1Arb21&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=318 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=318 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="132760429" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="123350408" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="130779148" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="131822204" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="124614679" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302636</CITATION_ID>
    <DESCRIPTION>This congenic strain contains an SHRSP/Izm chromsome 1 segment containing a blood pressure QTL transferred to a WKY/Izm background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302637</RGD_ID>
    <STRAIN_SYMBOL>LAA</STRAIN_SYMBOL>
    <FULL_NAME>Hatano Low Avoidance</FULL_NAME>
    <ORIGINATION>Hatano Reserch Institute, Food and Drug Safety Center, Hadano, Kanagawa, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302637</CITATION_ID>
    <DESCRIPTION>Strain originated from Hatano Research Institute, Food and Drug Safety Center, Kanagawa, Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302638</RGD_ID>
    <STRAIN_SYMBOL>LEXF11/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=239 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=239 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302638</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302639</RGD_ID>
    <STRAIN_SYMBOL>KHR/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>kaken hairless rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=4 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=4 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Dermatology</RESEARCH_USE>
    <ALLELES>Oca2</ALLELES>
    <ALLELE_RGD_IDS>2318412</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="116252026" STOP_POS="116581838" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="107116278" STOP_POS="107446093" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="114661970" STOP_POS="114987433" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="115683593" STOP_POS="115991040" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302639</CITATION_ID>
    <DESCRIPTION>Kaken hairless rat were detected by Kimura from Gunn</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302640</RGD_ID>
    <STRAIN_SYMBOL>ACI/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=501 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=501 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302640</CITATION_ID>
    <DESCRIPTION>Strain originated from The University of Tokushima, Tokushima, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302641</RGD_ID>
    <STRAIN_SYMBOL>LEXF1A/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=219 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=219 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302641</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302642</RGD_ID>
    <STRAIN_SYMBOL>LEA/Hkm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=495 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=495 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302642</CITATION_ID>
    <DESCRIPTION>Strain originated at the University of Tokushima, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302643</RGD_ID>
    <STRAIN_SYMBOL>ACI/NKyo</STRAIN_SYMBOL>
    <FULL_NAME>august copenhagen irish</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=6 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=6 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Reproduction</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302643</CITATION_ID>
    <DESCRIPTION>NIH (1988, F143) &gt; Kyo (F43)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302644</RGD_ID>
    <STRAIN_SYMBOL>CXA5/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=505 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=505 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Metabolism; Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302644</CITATION_ID>
    <DESCRIPTION>Strain originated at the University of Tokushima, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302645</RGD_ID>
    <STRAIN_SYMBOL>DMY/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>demyelination rat</FULL_NAME>
    <ORIGINATION>The Laboratory animal facilities of the Universitat Autonoma de Barcelona (Bellaterra Campus) in 1991 via Institute Pasteur, Paris</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=8 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2023-12-29)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Mrs2&lt;sup&gt;dmyKyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12793071</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302645</CITATION_ID>
    <DESCRIPTION>From a closed but not inbred colony of Sprague Dawley (SD) rats in the laboratory animal facilities of the Universitat Autonoma de Barcelona (Bellaterra Campus) in 1991. Via Institute Pasteur, Paris, to Kyoto University (1996).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302646</RGD_ID>
    <STRAIN_SYMBOL>LEXF2C/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=224 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=224 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302646</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302647</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D5Rat166-D5Rat90&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory of Animal Breeding and Genetics, Kyoto University, Sakyoku, Kyoto, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="136117763" STOP_POS="137976723" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="130881210" STOP_POS="132691399" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="136271682" STOP_POS="138128882" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="140063670" STOP_POS="141938308" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="137718909" STOP_POS="139664499" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302647</CITATION_ID>
    <DESCRIPTION>Male OLETF was crossed with female F344. F1 were backcrossed to female F344 for 5 generations. Microsatellite-based genotyping was performed to select the best male that had the best OLETF donor genome. Once the region was fixed the resultant congenic strain was maintained by brother-sister mating.37.4 cM segment of the OLETF genome was transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302648</RGD_ID>
    <STRAIN_SYMBOL>LEC/Hok</STRAIN_SYMBOL>
    <FULL_NAME>Long Evans Cinnamon</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=71 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=71 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2016-12-01)</AVAILABILITY>
    <RESEARCH_USE>Cancer; Immunology</RESEARCH_USE>
    <ALLELES>Atp7b&lt;sup&gt;hts&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11532742</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302648</CITATION_ID>
    <DESCRIPTION>At the Center for Experimental Plants and Animals, Hokkaido University, LEC, along with LEA, was established from a closed colony of Long-Evans rats obtained  from Kobe University in 1975. In 1984, within the LEC rats of their F24 generation, a rat exhibiting spontaneous hepatitis with severe jaundice was found (Yoshida, 1987). The LEC was available from Charles River Japan, Inc., Kanagawa, as of spring, 1991.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302649</RGD_ID>
    <STRAIN_SYMBOL>LEXF7B/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=231 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=231 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302649</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302650</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D9Mgh8-D9Rat15&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>National BioResource Project for the Rat in Japan</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="36840385" STOP_POS="65383934" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="41139089" STOP_POS="70686886" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="40808491" STOP_POS="71887966" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="33374546" STOP_POS="62634991" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302650</CITATION_ID>
    <DESCRIPTION>Male OLETF was crossed with female F344. F1 were backcrossed to female F344 for 5 generations. Microsatellite-based genotyping was performed to select the best male that had the best OLETF donor genome. Once the region was fixed the resultant congenic strain was maintained by brother-sister mating.37.4 cM segment of the OLETF genome was transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302651</RGD_ID>
    <STRAIN_SYMBOL>CXA1/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=504 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=504 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Metabolism; Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302651</CITATION_ID>
    <DESCRIPTION>Strain originated from the The University of Tokushima, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302652</RGD_ID>
    <STRAIN_SYMBOL>LEXF7A/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=230 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=230 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302652</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302653</RGD_ID>
    <STRAIN_SYMBOL>LEXF8A/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=233 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=233 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302653</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302654</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Mgh16-D7Mgh20&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=81 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=81 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="99900464" STOP_POS="99900612" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="98011396" STOP_POS="116294546" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="106995385" STOP_POS="126080454" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="106942155" STOP_POS="125794357" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="103612739" STOP_POS="123191874" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302654</CITATION_ID>
    <DESCRIPTION>Male OLETF was crossed with female F344. F1 were backcrossed to female F344 for 5 generations. Microsatellite-based genotyping was performed to select the best male that had the best OLETF donor genome. Once the region was fixed the resultant congenic strain was maintained by brother-sister mating.26.6 cM segment of the OLETF genome was transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302655</RGD_ID>
    <STRAIN_SYMBOL>TO/Hkm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=493 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=493 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302655</CITATION_ID>
    <DESCRIPTION>Strain originated from the Graduate School of Medicine, Hokkaido University, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302656</RGD_ID>
    <STRAIN_SYMBOL>LEA/Hok</STRAIN_SYMBOL>
    <FULL_NAME>Long Evans Agouti</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=70 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=70 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2016-12-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302656</CITATION_ID>
    <DESCRIPTION>Long Evans Agouti derived originally from an outbred Long Evans stock at Hokkaido University and selected for agouti coat colour . It is used as the control strain of the LEC rat, which is reported to exhibit several mutant phenotypes such as hepatic disorder (hts), blockage of the T cell differentiation (thid) and X-ray hypersensitivity (xhs1 and xhs2).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302657</RGD_ID>
    <STRAIN_SYMBOL>DOP/Nem</STRAIN_SYMBOL>
    <FULL_NAME>dilute-opisthotonus (dop)</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=151 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=151 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Myo5a</ALLELES>
    <ALLELE_RGD_IDS>3143</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302657</CITATION_ID>
    <DESCRIPTION>Founded from a breeding colony of Wistar by Ohno at Yagi Memorial Park in 1988. A congenic line BN-dop and an inbred line DOP-dop were established.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302658</RGD_ID>
    <STRAIN_SYMBOL>LEJ/Hkm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=494 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=494 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302658</CITATION_ID>
    <DESCRIPTION>Strain originated at the Graduate School of Medicine, Hokkaido University, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302659</RGD_ID>
    <STRAIN_SYMBOL>CXH5/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=508 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=508 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Metabolism; Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302659</CITATION_ID>
    <DESCRIPTION>Strain originated at the University of Tokushima, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302660</RGD_ID>
    <STRAIN_SYMBOL>RCS/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>royal college of surgeons rat</FULL_NAME>
    <ORIGINATION>Department of Ophthalmology &amp; Visual Sciences, Kyoto University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=27 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2023-12-29)</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology</RESEARCH_USE>
    <ALLELES>Mertk&lt;sup&gt;&lt;i&gt;rdy&lt;/i&gt;&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>40902839</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302660</CITATION_ID>
    <DESCRIPTION>From Department of Ophthalmology &amp; Visual Sciences, Kyoto University to Institute of Laboratory Animals (Kyo) in 1998.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302661</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=87 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=87 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="39507513" STOP_POS="39507682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="1217606" STOP_POS="39153750" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="2227825" STOP_POS="61783215" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="2222207" STOP_POS="61886417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="1764386" STOP_POS="41707592" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302661</CITATION_ID>
    <DESCRIPTION>Male OLETF was crossed with female F344. F1 were backcrossed to female F344 for 5 generations. Microsatellite-based genotyping was performed to select the best male that had the best OLETF donor genome. Once the region was fixed the resultant congenic strain was maintained by brother-sister mating.29.5 cM segment from the centromere of chr 14 of the OLETF genome was transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302662</RGD_ID>
    <STRAIN_SYMBOL>CXH2/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=509 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=509 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Metabolism; Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302662</CITATION_ID>
    <DESCRIPTION>Strain originated at the University of Tokushima, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302663</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D11Rat4-D11Rat1&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>National BioResource Project for the Rat in Japan</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="76295832" STOP_POS="95955328" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="62790342" STOP_POS="82450994" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="65352097" STOP_POS="86593596" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="66731054" STOP_POS="89693367" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="64573222" STOP_POS="84443333" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302663</CITATION_ID>
    <DESCRIPTION>Male OLETF was crossed with female F344. F1 were backcrossed to female F344 for 5 generations. Microsatellite-based genotyping was performed to select the best male that had the best OLETF donor genome. Once the region was fixed the resultant congenic strain was maintained by brother-sister mating.37.4 cM segment of the OLETF genome was transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302664</RGD_ID>
    <STRAIN_SYMBOL>WNA/Nshm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=149&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=149&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302664</CITATION_ID>
    <DESCRIPTION>Nagoya University, Agriculuture to Nagoya University, Medicine 1986 to Nagoya University, Institute of Laboratory Animal Research</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302665</RGD_ID>
    <STRAIN_SYMBOL>FXLE13/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=251 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=251 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302665</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302666</RGD_ID>
    <STRAIN_SYMBOL>LEXF1C/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=221 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=221 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302666</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302667</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D5Mgh5-D5Mgh23&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>National BioResource Project for the Rat in Japan</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="48523123" STOP_POS="115013661" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="43726656" STOP_POS="109897936" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="44404276" STOP_POS="114014945" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="49028773" STOP_POS="117961491" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="45499364" STOP_POS="115361927" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302667</CITATION_ID>
    <DESCRIPTION>Male OLETF was crossed with female F344. F1 were backcrossed to female F344 for 5 generations. Microsatellite-based genotyping was performed to select the best male that had the best OLETF donor genome. Once the region was fixed the resultant congenic strain was maintained by brother-sister mating.37.4 cM segment of the OLETF genome was transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302668</RGD_ID>
    <STRAIN_SYMBOL>IS-&lt;I&gt;Tlk&lt;/I&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>tail anomaly lethal kyoto</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=25 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=25 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Osteosis</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302668</CITATION_ID>
    <DESCRIPTION>Spontaneous mutation was found in IS/Kyo inbred (F10) at Kyoto University in 1988. Tlk(Tail anomaly Lethal Kyoto)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302669</RGD_ID>
    <STRAIN_SYMBOL>HAA</STRAIN_SYMBOL>
    <FULL_NAME>Hatano High Avoidance</FULL_NAME>
    <ORIGINATION>Hatano Research Institute, Food and Drug Safety Center, Hadano, Kanagawa, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302669</CITATION_ID>
    <DESCRIPTION>Strain originated at the Hatano Research Institute, Food and Drug Safety Center, Kanagawa, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302670</RGD_ID>
    <STRAIN_SYMBOL>ACI/NSlc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=381 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=381 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302670</CITATION_ID>
    <DESCRIPTION>Strain is from Japan SLC, Inc., Shizuoka, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302671</RGD_ID>
    <STRAIN_SYMBOL>WM/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=503 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=503 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302671</CITATION_ID>
    <DESCRIPTION>Strain is from the University of Tokushima, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302672</RGD_ID>
    <STRAIN_SYMBOL>W/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=13 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=13 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302672</CITATION_ID>
    <DESCRIPTION>Hok&gt;Hkm&gt;Kyo</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302673</RGD_ID>
    <STRAIN_SYMBOL>FXLE15/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=253 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=253 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302673</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302674</RGD_ID>
    <STRAIN_SYMBOL>VF/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>vacuole formation rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=21  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=21  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2020-11-10)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Dop1a&lt;sup&gt;vf&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419686</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302674</CITATION_ID>
    <DESCRIPTION>The vacuole formation (VF) rat is an autosomal recessive myelin mutant characterized by generalized tremor, hypomyelination, and periaxonal vacuole formation of the central nervous system (CNS).  A nonsense mutation in the dopey family member 1 (Dopey1)(Dop1a, RGD:1305534) was identified as the likely causative gene for the neurological disease phenotype of the VF rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302675</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D1Smu13-D1Smu11&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=319 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=319 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302675</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from SHRSP to WKY.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302676</RGD_ID>
    <STRAIN_SYMBOL>NER/Slc</STRAIN_SYMBOL>
    <FULL_NAME>noda epileptic rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=382 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=382 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302676</CITATION_ID>
    <DESCRIPTION>Strain is from Japan SLC, Inc. Shizuoka, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302677</RGD_ID>
    <STRAIN_SYMBOL>NIG-III/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=502 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=502 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302677</CITATION_ID>
    <DESCRIPTION>Strain is from the University of Tokushima, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302678</RGD_ID>
    <STRAIN_SYMBOL>NAR/Slc</STRAIN_SYMBOL>
    <FULL_NAME>non albumin rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=375 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=375 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Hematology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302678</CITATION_ID>
    <DESCRIPTION>Strain originated from Japan SLC, Inc, Shizuoka, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302679</RGD_ID>
    <STRAIN_SYMBOL>TRMR/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>tremor resistant</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=12 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=12 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Aspa</ALLELES>
    <ALLELE_RGD_IDS>621693</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302679</CITATION_ID>
    <DESCRIPTION>Tremor Rat which was found in a colony of outbred Wistar/Kyo in 1980 was separated to Tanabe Seiyaku Co., Ltd. in 1982. This strain is a substrain of TRM/Kyo and does not show tremor behavior. This strain carrying wild type Hcn1, is considered as segregating inbred strain of TRM.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302680</RGD_ID>
    <STRAIN_SYMBOL>SHR/Ta</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=418 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=418 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302680</CITATION_ID>
    <DESCRIPTION>Strain orginated at Takeda Chemical Industries, Ltd., Osaka, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302681</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D1Smu11-D1Rat112&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=325 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=325 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302681</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from SHRSP to WKY.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302682</RGD_ID>
    <STRAIN_SYMBOL>FXLE18/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=256 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=256 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302682</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302683</RGD_ID>
    <STRAIN_SYMBOL>FXLE22/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=260 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=260 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302683</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302684</RGD_ID>
    <STRAIN_SYMBOL>F344/NHok</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=68  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=68  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302684</CITATION_ID>
    <DESCRIPTION>Dwango-Heston-N(Jay) 1950-Hokkaido University, Faculty of Science(Mk) 1956-National Institute of Genetics(Ms) 1958-Hokkaido University, Laboratory of Experimental Animal Science(Hok) 1959, F68-Hokkaido University, Center for Experimental Plants &amp; Animals</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302685</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat8-D14Rat26&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=99 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=99 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="30674469" STOP_POS="69239554" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="30320092" STOP_POS="65026991" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="32593926" STOP_POS="69517234" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="32389647" STOP_POS="69559504" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="32584630" STOP_POS="70077314" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302685</CITATION_ID>
    <DESCRIPTION>Microsatellite-based genotyping was performed to select the best male that had the best OLETF donor genome. Once the region was fixed the resultant congenic strain was maintained by brother-sister mating. Comprises of a 18.5 cM transferred segment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302686</RGD_ID>
    <STRAIN_SYMBOL>F344/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=266 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=266 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302686</CITATION_ID>
    <DESCRIPTION>Derived from F344/DuCrlj rats that were purchased from Charles River Kanagawa, Japan. These are maintained by brother and sister mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302687</RGD_ID>
    <STRAIN_SYMBOL>WKAH/HkmSlc</STRAIN_SYMBOL>
    <FULL_NAME>Wistar King A, Hokkaido</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=376 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=376 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302687</CITATION_ID>
    <DESCRIPTION>Strain originated from Japan SLC, Inc., Shizuoka, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302688</RGD_ID>
    <STRAIN_SYMBOL>ACI/NMna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=461 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=461 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302688</CITATION_ID>
    <DESCRIPTION>This strain is derived from the ACI/NMs strain bred at the Fujita Health University School of Medicine, Aichi, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302689</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;Ntrk3-D1Smu13&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=320 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=320 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302689</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from SHRSP to WKY.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302690</RGD_ID>
    <STRAIN_SYMBOL>FXLE19/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=257 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=257 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302690</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302691</RGD_ID>
    <STRAIN_SYMBOL>ALB/Hok</STRAIN_SYMBOL>
    <FULL_NAME>Albany</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=64 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=64 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Dentistry</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302691</CITATION_ID>
    <DESCRIPTION>Albany, N.Y.(Wolf)?N(Jay)to Hokkaido University, Faculty of Science(Mk)to National Institute of Genetics(Ms) 1958?Hokkaido University, Laboratory of Experimental Animal Science(Hok) 1975, F48 to Hokkaido University, Center for Experimental Plants &amp; Animals(Hok)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302692</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D1Wox18-D1Rat44&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=323 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=323 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302692</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from SHRSP to WKY.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302693</RGD_ID>
    <STRAIN_SYMBOL>KZ-&lt;I&gt;Lepr&lt;/I&gt;&lt;sup&gt;faTky&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=32 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=32 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Metabolism</RESEARCH_USE>
    <ALLELES>Lepr</ALLELES>
    <ALLELE_RGD_IDS>3001</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302693</CITATION_ID>
    <DESCRIPTION>A inbred strain from Zucker-fatty rats which were introduced to Takeda Chemical Industries in 1980.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302694</RGD_ID>
    <STRAIN_SYMBOL>WKA/Seac</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=112 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=112 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302694</CITATION_ID>
    <DESCRIPTION>Wistar King &gt; Aptekman &gt; Hokkaido University 1953 &gt; Kyushu University 1955 &gt; Seac Yoshitomi, LTD. 1979</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302695</RGD_ID>
    <STRAIN_SYMBOL>SER/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>spontaneously epileptic rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=28 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=28 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Atrn|Aspa</ALLELES>
    <ALLELE_RGD_IDS>69063|621693</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302695</CITATION_ID>
    <DESCRIPTION>Spontaneously Epileptic Rat was developed as a double mutant by Serikawa by crossing zi rats (derived from SD), carrying an autosomal recessive attractin mutation with trm rats (derived from Kyo:Wistar), carrying a genomic deletion comprising Aspartate Ac</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302696</RGD_ID>
    <STRAIN_SYMBOL>FH/HamSlc</STRAIN_SYMBOL>
    <FULL_NAME>fawn hooded rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=384 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=384 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302696</CITATION_ID>
    <DESCRIPTION>Strain originated at Japan SLC, Inc., Shizuoka , Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302697</RGD_ID>
    <STRAIN_SYMBOL>KND/Tky</STRAIN_SYMBOL>
    <FULL_NAME>komeda non-diabetic rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=16 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=16 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302697</CITATION_ID>
    <DESCRIPTION>Komeda diabetes-prone rat developed by Komeda from Long-Evans Tokushima Lean (LETL) rat at Tokyo Medical College in 1996. Komeda non Diabetic Rats were established simultaneusely as controls.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302698</RGD_ID>
    <STRAIN_SYMBOL>SDR/Slc</STRAIN_SYMBOL>
    <FULL_NAME>Spontaneous dwarf rat</FULL_NAME>
    <ORIGINATION>Japan SLC, Inc</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=373 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=66&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-05-04)</AVAILABILITY>
    <RESEARCH_USE>Metabolism</RESEARCH_USE>
    <ALLELES>Gh1&lt;sup&gt;sdr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12880380</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00066</CITATION_ID>
    <DESCRIPTION>The G to A substitution at the end of the 3rd intron of the rat Growth hormone gene was identified as the cause of the dwarf phenotype. This spontaneous mutation affected the 3' splice/acceptor site. Judging from this point mutation, one would predict an abnormal splicing and a 1-base deletion in the GH mRNA. Strain is from Japan SLC, Inc., Shizuoka, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302699</RGD_ID>
    <STRAIN_SYMBOL>LEXF8D/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=234 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=234 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302699</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302700</RGD_ID>
    <STRAIN_SYMBOL>HOB/Snk</STRAIN_SYMBOL>
    <FULL_NAME>hobble rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=154 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=154 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Unc5c|Unc5c&lt;sup&gt;hob&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>735109|12802353</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302700</CITATION_ID>
    <DESCRIPTION>HOB rat was identified in the F344 congenic rats (N12F13) to which the coat color locus (C) of fatty rat has been transferred in Sankyo Co., Ltd.  Introduced to Kyoto University in 1999 at F13.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302701</RGD_ID>
    <STRAIN_SYMBOL>LEW/SsNSlc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=372 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=372 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2020-08-26)</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302701</CITATION_ID>
    <DESCRIPTION>Inbreeding of the Lewis rat is begun by Dr. Margaret Lewis from a Wistar stock. In 1924, at F20 to Aptekmanm and Bogdon. In 1958, at F31 to Silvers, who distributed this strain. subsequently. LEW/SsNSlc rats were descended from a  colony obtained from the National Institutes of Health, Bethesda, Maryland USA in 1994 to  Japan SLC, Inc.,Shizuoka, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302702</RGD_ID>
    <STRAIN_SYMBOL>TRM/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>tremor rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=11 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=11 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2018-01-03)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Aspa|Hcn1&lt;sup&gt;A354V&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>621693|13464319</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302702</CITATION_ID>
    <DESCRIPTION>In 1980, a spontaneous tremor mutant rat was found in the colony of Kyo:Wistar (Yamada, 1985). This disorder was found to be caused by an autosomal recessive gene and was designated tremor (tm). Deletion of Aspa gene was identified in the animal with no aspartoacylase activity in the brain and measurable level of activity in the kidney. TRM was established as a segregating inbred strain. In F18 progeny, a rat which did not have tm mutation was separated and established as a control strain of WTC (NBRP No.0020). (Dec 8, 2010)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302703</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D1Wox29-D1Rat112&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=315 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=315 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302703</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from SHRSP to WKY.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302704</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D1Wox29-D1Rat199&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=321 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=321 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302704</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from SHRSP to WKY.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302705</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D1Wox29-D1Smu13&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=322 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=322 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302705</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from SHRSP to WKY.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302706</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D5Rat32-D5Rat26&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>National BioResource Project for the Rat in Japan</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="137971639" STOP_POS="137971798" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="113558156" STOP_POS="132686472" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="117554114" STOP_POS="138123957" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="121495621" STOP_POS="141933383" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="119332868" STOP_POS="139659574" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302706</CITATION_ID>
    <DESCRIPTION>Male OLETF was crossed with female F344. F1 were backcrossed to female F344 for 5 generations. Microsatellite-based genotyping was performed to select the best male that had the best OLETF donor genome. Once the region was fixed the resultant congenic strain was maintained by brother-sister mating.37.4 cM segment of the OLETF genome was transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302707</RGD_ID>
    <STRAIN_SYMBOL>LEXF3/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=225 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=225 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302707</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302708</RGD_ID>
    <STRAIN_SYMBOL>FXLE17/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=255 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=255 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302708</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302709</RGD_ID>
    <STRAIN_SYMBOL>WKY/Hcm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=442 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=442 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302709</CITATION_ID>
    <DESCRIPTION>Strain is from the Hyogo College of Medicine, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302710</RGD_ID>
    <STRAIN_SYMBOL>LEXF2B/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=223 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=223 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302710</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302711</RGD_ID>
    <STRAIN_SYMBOL>ExHC/Seac</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=115 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=115 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302711</CITATION_ID>
    <DESCRIPTION>Isolated from Sprague-Dawley (SD/Jcl) rats by Imai and Matsumura by selection for high serum cholesterol under high cholesterol diet for 7 days (app. 250 mg/dl, normal 100 mg/dl) in 1973. Kyushu University &gt; Seac Yoshitomi, LTD. 1993</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302712</RGD_ID>
    <STRAIN_SYMBOL>ZIMY/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Zitter Masao Yamada</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=24 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=24 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2020-12-17)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Atrn</ALLELES>
    <ALLELE_RGD_IDS>69063</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302712</CITATION_ID>
    <DESCRIPTION>ZIMY was produced by crossing tremor (TRM) rat and zitter (ZI) rat at Kyoto University. zi/zi, tm&lt;+/+&gt;. ZIMY (Zitter Masao Yamada). This strain is homozygous for zi and wild-type for tm. ZIMY (Zitter Masao Yamada)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302713</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D8Rat58-D8Mgh17&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=90  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=90  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="27588221" STOP_POS="27588390" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="46008836" STOP_POS="46008974" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="50007641" STOP_POS="50007776" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="21850030" STOP_POS="48631820" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="19796514" STOP_POS="48675424" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302713</CITATION_ID>
    <DESCRIPTION>Male OLETF was crossed with female F344. F1 were backcrossed to female F344 for 5 generations. Microsatellite-based genotyping was performed to select the best male that had the best OLETF donor genome. Once the region was fixed the resultant congenic strain was maintained by brother-sister mating.37.4 cM segment of the OLETF genome was transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302714</RGD_ID>
    <STRAIN_SYMBOL>KZC/Tky</STRAIN_SYMBOL>
    <FULL_NAME>Komeda Zucker Creeping rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=20 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=20 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Reln</ALLELES>
    <ALLELE_RGD_IDS>3553</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302714</CITATION_ID>
    <DESCRIPTION>Komeda Zucker Creeping rat derived from a closed colony of the Zucker fatty rat by spontaniously mutation at Tokyo Medical College in 1983.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302715</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;I&gt;D1Wox18-D1Wox29&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=324 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=324 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302715</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from SHRSP to WKY.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302716</RGD_ID>
    <STRAIN_SYMBOL>OM/NSlc</STRAIN_SYMBOL>
    <FULL_NAME>Osborne-Mendel rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=385 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=385 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302716</CITATION_ID>
    <DESCRIPTION>The Instutite of Medical Science, The University of Tokyo to Slc (1985)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302717</RGD_ID>
    <STRAIN_SYMBOL>ACI/NHok</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=62  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=62  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302717</CITATION_ID>
    <DESCRIPTION>NIH to Tokyo Biochemical Research Institute(Tbi) to Hokkaido University, Laboratory of Experimental Animal Science(Hok) 1967, F87 to Hokkaido University, Center for Experimental Plants &amp; Animals(Hok) 1982, F135</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302718</RGD_ID>
    <STRAIN_SYMBOL>HWY/Slc</STRAIN_SYMBOL>
    <FULL_NAME>hairless wistar yagi</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=374 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=374 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Dermatology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302718</CITATION_ID>
    <DESCRIPTION>Strain is from Japan SLC, Inc., Shizuoka, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302719</RGD_ID>
    <STRAIN_SYMBOL>DON/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Donryu rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302719</CITATION_ID>
    <DESCRIPTION>Japanese albino rats &gt; R.Sato, Nippon Rat(1950) &gt; Kyo (1978, F64), formaly DONRYU/2</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302720</RGD_ID>
    <STRAIN_SYMBOL>CXH10/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=507 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=507 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Metabolism; Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302720</CITATION_ID>
    <DESCRIPTION>Strain is from the University of Tokushima, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302721</RGD_ID>
    <STRAIN_SYMBOL>LEC/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=80 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=80 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES>Atp7b&lt;sup&gt;hts&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11532742</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302721</CITATION_ID>
    <DESCRIPTION>Found in Long Evans strain at Kobe University &gt; Inbreeding at Hokkaido University &gt; Otsuka Pharmaceutical Co. &gt; The University of Tokushima 1989</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302722</RGD_ID>
    <STRAIN_SYMBOL>PVG/Seac</STRAIN_SYMBOL>
    <FULL_NAME>Piebald Virol Glaxo</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=113 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=113 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302722</CITATION_ID>
    <DESCRIPTION>Strain is from Seac Yoshitomi, LTD., Fukuoka, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302723</RGD_ID>
    <STRAIN_SYMBOL>LEXF5/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=227 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=227 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302723</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302724</RGD_ID>
    <STRAIN_SYMBOL>SHR/Hcm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=441 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=441 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302724</CITATION_ID>
    <DESCRIPTION>Strain is from the Hyogo College of Medicine, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302726</RGD_ID>
    <STRAIN_SYMBOL>ZI/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=23 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=23 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Atrn&lt;sup&gt;&lt;i&gt;zi&lt;/i&gt;&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>40902832</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302726</CITATION_ID>
    <DESCRIPTION>Zitter rat was detected in a Sprague Dawley colony (SD) in Hannover in 1978 by Rehm. 1983 introduced to Kyoto University and established ZI/Kyo.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302727</RGD_ID>
    <STRAIN_SYMBOL>SHRSR/Ta</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=416 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=416 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302727</CITATION_ID>
    <DESCRIPTION>Strain is from Takeda Chemical Industries, Ltd., Osaka, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302728</RGD_ID>
    <STRAIN_SYMBOL>MES/Slc</STRAIN_SYMBOL>
    <FULL_NAME>Matsumoto Eosinophilia Shinshu</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=383&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=383&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Hematology</RESEARCH_USE>
    <ALLELES>Cyba&lt;sup&gt;mesSdi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13209000</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302728</CITATION_ID>
    <DESCRIPTION>Derived frm one pregnant SPF SD rat from a closed colony of SD rats at Japan SLC. 3 males and 5 females offspring had high eosinophil count at 10 weeks of age, these were bred brother x sister mating to generate these rats. Institute of Experimental Animals, Shinshu University School of Medicine to Slc (1999)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302729</RGD_ID>
    <STRAIN_SYMBOL>LEA/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=79 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=79 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302729</CITATION_ID>
    <DESCRIPTION>Found in Long Evans strain at Kobe University; Inbreeding at Hokkaido University; Otsuka Pharmaceutical Co.; The University of Tokushima 1989</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302795</RGD_ID>
    <STRAIN_SYMBOL>HTG</STRAIN_SYMBOL>
    <FULL_NAME>Prague hypertriglyceridemic</FULL_NAME>
    <ORIGINATION>Institute of Physiology, Academy of Sciences Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302795</CITATION_ID>
    <DESCRIPTION>These were originally derived from a colony of Wistar rats. Animals with high plasma triglyceride levels were selected as breeding pair and their offsprings used for further breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1302921</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(NPHS2-HBEGF)Wig</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Division of Nephrology, Department of Internal Medicine, University of MIchigan, Ann Habor, Michigan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1302921</CITATION_ID>
    <DESCRIPTION>hDTR (HBEGF) cDNA was inserted at the 3' of the 2.5 kb human podocin (NPHS2) promoter. This transgenic construct was released by XbaI/HindIII digestion and injected into the pronuclei of fertilized eggs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1303393</RGD_ID>
    <STRAIN_SYMBOL>LEC/Ncu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Nagoya City University Medical School, Nagoya, Aichi, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1303393</CITATION_ID>
    <DESCRIPTION>These rats were established from a closed colony of Long-Evans.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1304487</RGD_ID>
    <STRAIN_SYMBOL>BBDR/Wor</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1304487</CITATION_ID>
    <DESCRIPTION>Diabetic resistant  BB rats. These are derived from a viral antibody free (VAF)colony which was maintained  at University of Massachusetts and is now at BRM.   In 1977, Butler et al. began inbreeding BB rats at the University of Massachusetts Medical Center (laboratory code Wor) with 300 breeders purchased from the Bio-Breeding Laboratories. In 1978, during inbreding, pathogen-free rodent barrier system was introduced and a strain disease resistant (DR) by  was established by selective breeding of   diabtes free progenies.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331811</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Rat32-D10Rat133&lt;/i&gt;)/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="64939013" STOP_POS="64939207" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="51779662" STOP_POS="51779830" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="53630865" STOP_POS="53631032" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="53381898" STOP_POS="64823355" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="53786347" STOP_POS="65668639" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331811</CITATION_ID>
    <DESCRIPTION>This congenic strain was derived from female LEW rats and male BN rats obtained from the Janvier breeding center, Le Genest-Saint-Isle, France. F1 offsprings were crossed with LEW females to transfer the desired locus to LEW background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331812</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Rat83-D10Rat133&lt;/i&gt;)/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="45893342" STOP_POS="64939207" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="45393829" STOP_POS="45394002" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="46955258" STOP_POS="46955430" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="46728252" STOP_POS="64823355" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="46860047" STOP_POS="65668639" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331812</CITATION_ID>
    <DESCRIPTION>This congenic strain was derived from female LEW rats and male BN rats obtained from the Janvier breeding center, Le Genest-Saint-Isle, France. F1 offsprings were crossed with LEW females to transfer the desired locus to LEW background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331813</RGD_ID>
    <STRAIN_SYMBOL>BN.GK-(&lt;i&gt;D8Rat29-D8Got130&lt;/i&gt;)/Ox</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="82872062" STOP_POS="82872307" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="89482236" STOP_POS="89482480" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="76345502" STOP_POS="89012772" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="74769551" STOP_POS="87069779" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331813</CITATION_ID>
    <DESCRIPTION>This congenic strain contains the Nidd/gk5 locus transferred onto the BN background. GK rats are from a colony in Paris (CNRS) obtained in 1995. BN rats were initially obtained from Charles River Laboratories, Margate, UK.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331814</RGD_ID>
    <STRAIN_SYMBOL>BN.GK-(&lt;i&gt;D8Got302-D8Got130&lt;/i&gt;)/Ox</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="45539309" STOP_POS="82872307" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="49533872" STOP_POS="89482480" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="48160321" STOP_POS="89012772" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="48185711" STOP_POS="87069779" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331814</CITATION_ID>
    <DESCRIPTION>This congenic strain contains the Nidd/gk5 locus transferred onto the BN background. GK rats are from a colony in Paris (CNRS) obtained in 1995. BN rats were initially obtained from Charles River Laboratories, Margate, UK.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331815</RGD_ID>
    <STRAIN_SYMBOL>LEW/Mol</STRAIN_SYMBOL>
    <FULL_NAME>LEW/Mol</FULL_NAME>
    <ORIGINATION>Mollegaard Breeding Center Ltd., Denmark</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ncf1</ALLELES>
    <ALLELE_RGD_IDS>61307</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331815</CITATION_ID>
    <DESCRIPTION>This substrain can be traced originally to Scripps Clinic, La Jolla, to University of Pennsylvania to Simonsen Laboratories in 1966, to Institute of Pathological Anatomy, University of Copenhagen, Denmark 1973. From University of Copenhagen to M&amp;B A/S  (Mollegaard Breeding Center Ltd., Denmark ) from 1977 to 2002. (now Taconic Europe)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331816</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D10Rat2-D10Rat29&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Neuroimmunology Unit, Center for Molecular Medicine, Stockholm, Sweden</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1117&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="66108698" STOP_POS="107556066" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="107057622" STOP_POS="107057807" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="67988035" STOP_POS="110992275" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="67642121" STOP_POS="110568670" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="68842878" STOP_POS="68843272" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331816</CITATION_ID>
    <DESCRIPTION>(DA x ACI) x DA backcross in the second generation transfered 40 cM of DNA from ACI to DA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331817</RGD_ID>
    <STRAIN_SYMBOL>BN.LEW-(&lt;i&gt;D10Rat32-D10Mgh4&lt;/i&gt;)/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="92869025" STOP_POS="92869129" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="51779662" STOP_POS="92369470" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="53630865" STOP_POS="95638337" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="53381898" STOP_POS="95372987" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="53786347" STOP_POS="96799937" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331817</CITATION_ID>
    <DESCRIPTION>This congenic strain was derived from female LEW rats and male BN rats obtained from the Janvier breeding center, Le Genest-Saint-Isle, France. F1 offsprings were crossed with BN males to transfer the desired locus to BN background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331818</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Rat43-D10Mco4&lt;/i&gt;)/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="23422121" STOP_POS="41242295" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="22918268" STOP_POS="40741723" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="22402817" STOP_POS="41976505" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="22266756" STOP_POS="41793199" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="23428127" STOP_POS="42042465" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331818</CITATION_ID>
    <DESCRIPTION>This congenic strain was derived from female LEW rats and male BN rats obtained from the Janvier breeding center, Le Genest-Saint-Isle, France. F1 offsprings were crossed with LEW females to transfer the desired locus to LEW background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331819</RGD_ID>
    <STRAIN_SYMBOL>F344/Eer</STRAIN_SYMBOL>
    <FULL_NAME>F344/Eer</FULL_NAME>
    <ORIGINATION>Dept. of Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, Chicago, Illinois</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331819</CITATION_ID>
    <DESCRIPTION>Inbred strain originated from animals purchased from Harlan Industries, Indianapolis, Indiana</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331820</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Got9-D10Rat2&lt;/i&gt;)/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="107555881" STOP_POS="107556066" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="5684047" STOP_POS="107057807" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="5760565" STOP_POS="110992275" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="4578252" STOP_POS="110568670" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="5641331" STOP_POS="5641541" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331820</CITATION_ID>
    <DESCRIPTION>This congenic strain was derived from female LEW rats and male BN rats obtained from the Janvier breeding center, Le Genest-Saint-Isle, France. F1 offsprings were crossed with LEW females to transfer the desired locus to LEW background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331821</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Wox26-D10Arb4&lt;/i&gt;)/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="30160864" STOP_POS="30161017" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="29659462" STOP_POS="45274336" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="30303447" STOP_POS="46835685" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="30131785" STOP_POS="46592053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="30343658" STOP_POS="46737218" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331821</CITATION_ID>
    <DESCRIPTION>This congenic strain was derived from female LEW rats and male BN rats obtained from the Janvier breeding center, Le Genest-Saint-Isle, France. F1 offsprings were crossed with LEW females to transfer the desired locus to LEW background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331822</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D10Rat2-D10Rat6&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Neuroimmunology Unit, Center for Molecular Medicine, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="107555881" STOP_POS="107556066" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="101435864" STOP_POS="107057807" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="105077900" STOP_POS="110992275" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="104746165" STOP_POS="110568670" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="106310811" STOP_POS="106310957" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331822</CITATION_ID>
    <DESCRIPTION>DA.ACI-(D10Rat2-D10Rat29) congenic rats were backcrossed to parental DA rats and progeny were intercrossed to obtain homozygous recombinations within the desired region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331823</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Rat43-D10Rat27&lt;/i&gt;)/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="23422121" STOP_POS="73950353" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="22918268" STOP_POS="73453136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="22402817" STOP_POS="75983805" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="22266756" STOP_POS="74127968" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="23428127" STOP_POS="77092169" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331823</CITATION_ID>
    <DESCRIPTION>This congenic strain was derived from female LEW rats and male BN rats obtained from the Janvier breeding center, Le Genest-Saint-Isle, France. F1 offsprings were crossed with LEW females to transfer the desired locus to LEW background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331824</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D10Rat219-D10Rat29&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Neuroimmunology Unit, Center for Molecular Medicine, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="66108698" STOP_POS="66108888" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="78306880" STOP_POS="78307017" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="67988035" STOP_POS="81042642" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="67642121" STOP_POS="80884595" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="68842878" STOP_POS="81986757" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331824</CITATION_ID>
    <DESCRIPTION>DA.ACI-(D10Rat2-D10Rat29) congenic rats were backcrossed to parental DA rats and progeny were intercrossed to obtain homozygous recombinations within the desired region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331826</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Mgh7-D10Rat27&lt;/i&gt;)/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="54597481" STOP_POS="73950353" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="54098674" STOP_POS="73453136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="55978483" STOP_POS="75983805" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="55720558" STOP_POS="74127968" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="56170962" STOP_POS="77092169" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331826</CITATION_ID>
    <DESCRIPTION>This congenic strain was derived from female LEW rats and male BN rats obtained from the Janvier breeding center, Le Genest-Saint-Isle, France. F1 offsprings were crossed with LEW females to transfer the desired locus to LEW background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331827</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D10Rat10-D10Rat142&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Neuroimmunology Unit, Center for Molecular Medicine, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="88207600" STOP_POS="95803900" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="91345679" STOP_POS="99171690" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="91113514" STOP_POS="98868127" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="92448353" STOP_POS="100301488" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331827</CITATION_ID>
    <DESCRIPTION>DA.ACI-(D10Rat2-D10Rat29) congenic rats were backcrossed to parental DA rats and progeny were intercrossed to obtain homozygous recombinations within the desired region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331828</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D10Rat12-D10Rat144&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Neuroimmunology Unit, Center for Molecular Medicine, L8:04, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="83035172" STOP_POS="95224503" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="82538790" STOP_POS="94725019" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="85487741" STOP_POS="98044833" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="85276455" STOP_POS="97759008" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="86290650" STOP_POS="99198997" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331828</CITATION_ID>
    <DESCRIPTION>DA.ACI-(D10Rat2-D10Rat29) congenic rats were backcrossed to parental DA rats and progeny were intercrossed to obtain homozygous recombinations within the desired region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331829</RGD_ID>
    <STRAIN_SYMBOL>BN.LEW-(&lt;i&gt;D9Got8-D9Got200&lt;/i&gt;)/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="1272993" STOP_POS="1273201" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="1185844" STOP_POS="4302019" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="2657610" STOP_POS="10706733" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="2597055" STOP_POS="9698468" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="3811425" STOP_POS="3811711" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331829</CITATION_ID>
    <DESCRIPTION>This congenic strain was derived from female LEW rats and male BN rats obtained from the Janvier breeding center, Le Genest-Saint-Isle, France. F1 offsprings were crossed with BN males to transfer the desired locus to BN background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331830</RGD_ID>
    <STRAIN_SYMBOL>F344.BN-(&lt;i&gt;D5Rat1-D5Mit5&lt;/i&gt;)/Dlw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Biological Sciences, Oakland University, Rochester, MI</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="39526924" STOP_POS="39527086" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="34730116" STOP_POS="104251008" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="35225432" STOP_POS="108092802" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="39876314" STOP_POS="112058005" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="35911094" STOP_POS="109163425" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331830</CITATION_ID>
    <DESCRIPTION>This congenic strain carries the BN Edpm5 QTL on an F344 background. This strain is maintained at Oakland University, Rochester, MI, USA</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331831</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Rat173-D10Rat133&lt;/i&gt;)/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="36745333" STOP_POS="64939207" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="36244402" STOP_POS="36244613" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="37435916" STOP_POS="37436126" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="37209026" STOP_POS="64823355" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="37505289" STOP_POS="65668639" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331831</CITATION_ID>
    <DESCRIPTION>This congenic strain was derived from female LEW rats and male BN rats obtained from the Janvier breeding center, Le Genest-Saint-Isle, France. F1 offsprings were crossed with LEW females to transfer the desired locus to LEW background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331832</RGD_ID>
    <STRAIN_SYMBOL>BN.LEW-(&lt;i&gt;D10Rat72-D10Arb4&lt;/i&gt;)/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="45274234" STOP_POS="45274336" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="46835584" STOP_POS="46835685" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="46591952" STOP_POS="46592053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="46737116" STOP_POS="46737218" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331832</CITATION_ID>
    <DESCRIPTION>This congenic strain was derived from female LEW rats and male BN rats obtained from the Janvier breeding center, Le Genest-Saint-Isle, France. F1 offsprings were crossed with BN males to transfer the desired locus to BN background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331833</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D10Rat15-D10Rat29&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Neuroimmunology Unit, Center for Molecular Medicine, L8:04, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="66108698" STOP_POS="66108888" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="92238327" STOP_POS="92238497" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="67988035" STOP_POS="95508221" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="67642121" STOP_POS="95243104" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="68842878" STOP_POS="96667338" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331833</CITATION_ID>
    <DESCRIPTION>DA.ACI-(D10Rat2-D10Rat29) congenic rats were backcrossed to parental DA rats and progeny were intercrossed to obtain homozygous recombinations within the desired region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331834</RGD_ID>
    <STRAIN_SYMBOL>BN.LEW-(&lt;i&gt;D10Rat100-D10Rat126&lt;/i&gt;)/Rj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="26292794" STOP_POS="26292937" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="25790546" STOP_POS="41482228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="26517020" STOP_POS="42716241" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="26363403" STOP_POS="42526523" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="26434477" STOP_POS="26434620" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331834</CITATION_ID>
    <DESCRIPTION>This congenic strain was derived from female LEW rats and male BN rats obtained from the Janvier breeding center, Le Genest-Saint-Isle, France. F1 offsprings were crossed with BN males to transfer the desired locus to BN background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1331836</RGD_ID>
    <STRAIN_SYMBOL>WKY/Eer</STRAIN_SYMBOL>
    <FULL_NAME>WKY/Eer</FULL_NAME>
    <ORIGINATION>Dept. of Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, Chicago, Illinois</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1331836</CITATION_ID>
    <DESCRIPTION>Inbred strain originated from animals purchased from Harlan Industries, Indianapolis, Indiana</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1354669</RGD_ID>
    <STRAIN_SYMBOL>BN/OrlIcoCrlf</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.geneticmodels.com/crfrance/services.html&gt;Charles River&lt;/a&gt; France</ORIGINATION>
    <SOURCE>&lt;a href=http://www.geneticmodels.com/crfrance/services.html&gt;Charles River&lt;/a&gt; France</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1354669</CITATION_ID>
    <DESCRIPTION>Strain selected by Silvers and Billingham in 1958 after cross-breeding of histocompatible animals from a colony of mutants. These animals were then maintained in closed colony by H.D. King and P. Aptekman at the National Institutes of Health (NIH) (Bethesda, MD, USA). The strain was obtained by Microbiological Associates, Inc., Department of Laboratory Animals, Walkersville, Maryland, USA in 1969 and introduced into CNRS/CSEAL in Orleans, France in 1988. It was then transferred to Charles River Laboratories France in 1991.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1354670</RGD_ID>
    <STRAIN_SYMBOL>F344/IcoCrlf</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.geneticmodels.com/crfrance/services.html&gt;Charles River&lt;/a&gt; France</ORIGINATION>
    <SOURCE>&lt;a href=http://www.geneticmodels.com/crfrance/services.html&gt;Charles River&lt;/a&gt; France</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1354670</CITATION_ID>
    <DESCRIPTION>These are inbred rats that were bought from Charles River, Les Oncins near Lyon, France.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357172</RGD_ID>
    <STRAIN_SYMBOL>WF.BBDR-(&lt;i&gt;D4Arb29-D4Rat44&lt;/i&gt;)/Wor</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Massachusetts Medical School, Worcerster, MA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="65495851" STOP_POS="65496104" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="64528739" STOP_POS="64528994" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="63537179" STOP_POS="63537431" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="63250011" STOP_POS="183837621" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="63276741" STOP_POS="121645621" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357172</CITATION_ID>
    <DESCRIPTION>This congenic was generated by the marker-assisted protocol where a segment of BBDR/Wor is transferred to WF background and the animals were screened using microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357173</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;Vamp2-D10M11Mit84&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Vamp2</ALLELES>
    <ALLELE_RGD_IDS>3949</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="54292423" STOP_POS="54296657" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="53793581" STOP_POS="53797815" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="55675171" STOP_POS="55679405" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="55418231" STOP_POS="55422465" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="55848264" STOP_POS="55852132" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357173</CITATION_ID>
    <DESCRIPTION>This congenic strain is derived by introgressing a desired region of chr 10 from MNS to the SS/Jr recipient.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357174</RGD_ID>
    <STRAIN_SYMBOL>BBDR.BBDP-(&lt;i&gt;D4Mit6-D4Mit24&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="76647384" STOP_POS="78882945" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="77307388" STOP_POS="79575658" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="141978848" STOP_POS="144249450" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="75732943" STOP_POS="78039637" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357174</CITATION_ID>
    <DESCRIPTION>S. Bieg and coworkers (1998) generated this congenic line in which diabetes and lymphopenia are controlled solely by Iddm 1. This strain was generated by nine cycles of cross-intercross breeding of diabetes-prone DP with DR BB rats. Iddm 1 in the BioBreeding (BB) rat designates the genomic region on rat Chromosome (Chr) 4 that harbors the gene causing peripheral T cell lymphopenia (Lyp) and diabetes. The average age of onset of diabetes  was 85 ÃÂ± 53 days of age after the first and   67 Â± 10 days of age after the 9th cycle. Lacks one C nucleotide at 478 position which causes a frameshift mutation in the ORF of exon 3 forming a significantly truncated protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357175</RGD_ID>
    <STRAIN_SYMBOL>F344.DR-(&lt;i&gt;D4Mit6-D4Mit24&lt;/i&gt;)-Tg(Gimap5)Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology, Medical College of Wisconsin, Milwaukee Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357175</CITATION_ID>
    <DESCRIPTION>Wild type allele of Gimap5 from BN was microinjected into the pronuclei of fertilized eggs from a T cell lymphopenic congenic strain F344.DR-(&lt;i&gt;D4Mit6-D4Mit24&lt;/i&gt;)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357176</RGD_ID>
    <STRAIN_SYMBOL>WF.BBDR-(&lt;i&gt;D4Arb29-D4Rat96&lt;/i&gt;)/Wor</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Massachusetts Medical School, Worcerster, MA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="65495851" STOP_POS="67576447" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="64528739" STOP_POS="66609456" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="63537179" STOP_POS="65577249" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="63250011" STOP_POS="65397196" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="63276741" STOP_POS="65434807" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357176</CITATION_ID>
    <DESCRIPTION>This congenic was generated by the marker-assisted protocol where a segment of BBDR/Wor is transferred to WF background and the animals were screened using microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357177</RGD_ID>
    <STRAIN_SYMBOL>F344.DR(DP)-(&lt;i&gt;D4Mit6-D4Mit24&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=82&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="76647384" STOP_POS="78882945" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="77307388" STOP_POS="79575658" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="141978848" STOP_POS="144249450" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="75732943" STOP_POS="78039637" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00082</CITATION_ID>
    <DESCRIPTION>The lymphopenia locus from BBDR.BBDP-(&lt;i&gt;D4Mit6-D4Mit24&lt;/i&gt;) was transferred onto F344 by marker assisted selection in five cycles of cross-intercross breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357178</RGD_ID>
    <STRAIN_SYMBOL>CD</STRAIN_SYMBOL>
    <FULL_NAME>Cohen diabetic rat</FULL_NAME>
    <ORIGINATION>Hebrew University Hospital and Hadassah-Hebrew Medical College, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357178</CITATION_ID>
    <DESCRIPTION>Originally developed by late professor A.M. Cohen in Israel nearly 40 years ago. These were genetically selected from the Hebrew University albino rats. When fed a copper-poor high-sucrose diet these develop impaired carbohydrate metabolism.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357179</RGD_ID>
    <STRAIN_SYMBOL>SS.WKY-(&lt;i&gt;D2N35-Mme&lt;/i&gt;),MNS-(&lt;i&gt;D10Mit11-D10M11Mit119&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357179</CITATION_ID>
    <DESCRIPTION>SS.WKY-(D2N35-Mme)/Mco and SS.MNS-(D10Mit11-D10M11Mit119)/Mco were crossed and the F&lt;sub&gt;1&lt;/sub&gt; were backcrossed to SS.WKY-(D2N35-Mme)/Mco. Rats that were homozygous on the chr 2 loci were selected and crossed with the ones that were homozygous on the chr 10 loci. This produced the double congenic strain which was maintained by brother-sister mating</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357180</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D8Chm14-D8Rat16&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Grik4</ALLELES>
    <ALLELE_RGD_IDS>2734</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="51802045" STOP_POS="103268530" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="42903043" STOP_POS="94388843" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="46804134" STOP_POS="101305168" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="45279673" STOP_POS="100781055" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="45510258" STOP_POS="98878889" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357180</CITATION_ID>
    <DESCRIPTION>Congenic strain produced from a SS/Jr strain and a LEW/CrlBR strain purchased from Charles Rivers, Quebec, Canada</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357181</RGD_ID>
    <STRAIN_SYMBOL>CDR/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hebrew University Hospital and Hadassah-Hebrew Medical College, Jerusalem, Israel; Israeli Rat Genome Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357181</CITATION_ID>
    <DESCRIPTION>Cohen rats that had an oral tolerance test with blood glucose levels &lt;180mg/dl were selected. More stringent criteria was set during the secondary inbreeding: rats with blood glucose levels &lt;140mg/dl were selected. Brother and sister mating was carried on for 10 additional generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357182</RGD_ID>
    <STRAIN_SYMBOL>Eker-Tg(Tsc2)28Hin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Experimental Pathology, Cancer Institute, Toshima-ku, Tokyo, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tsc2</ALLELES>
    <ALLELE_RGD_IDS>3908</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357182</CITATION_ID>
    <DESCRIPTION>Wild type Tsc2 transgene was constructed from the Tsc2 cDNA from BN rat and was microinjected into single male pronuclei. Eggs were cultured and tranferred into female wistar which were mated with Eker rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357183</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco10-Aldoc&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nos2</ALLELES>
    <ALLELE_RGD_IDS>3185</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="64313335" STOP_POS="64349221" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="6813971" STOP_POS="63851208" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="6908932" STOP_POS="66221621" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="5706467" STOP_POS="65456957" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="6849272" STOP_POS="65072453" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357183</CITATION_ID>
    <DESCRIPTION>This congenic strain is derived by introgressing a desired region of chr 10 from MNS to the SS/Jr recipient.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357184</RGD_ID>
    <STRAIN_SYMBOL>Crl:ZUC-&lt;I&gt;Lepr&lt;/I&gt;&lt;sup&gt;fa&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Zucker rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13432153</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357184</CITATION_ID>
    <DESCRIPTION>The obese and fatty condition appeared spontaneously in the 13M stock and was reported by Lois Zucker and Theodore Zucker in 1960 at the Laboratory of Comparative Pathology in Stow, Massachusetts. These came to Charles River in 1985 from a research colony maintained at a pharmaceutical company.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357185</RGD_ID>
    <STRAIN_SYMBOL>RHA.Gunn-&lt;i&gt;Ugt1a1&lt;/i&gt;&lt;sup&gt;j&lt;/sup&gt;/N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Developmental Pharmacology Branch, National Institute of Child Health and Human Development, National Institute of Health, Bethesda, MD, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357185</CITATION_ID>
    <DESCRIPTION>RHA/N rats were crossed with Gunn rats. F&lt;sub&gt;1&lt;/sub&gt; hybrids were intercrossed for 12 cycles while selecting for jaundice loci.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357186</RGD_ID>
    <STRAIN_SYMBOL>Gunn-&lt;i&gt;Ugt1a1&lt;/i&gt;&lt;sup&gt;j&lt;/sup&gt;/BluHsd</STRAIN_SYMBOL>
    <FULL_NAME>Gunn rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>Harlan</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ugt1a1&lt;sup&gt;j&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13432064</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="96249143" STOP_POS="96256264" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="88805660" STOP_POS="88805660" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="95300017" STOP_POS="95300017" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="94982916" STOP_POS="94990037" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="87091241" STOP_POS="87098362" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357186</CITATION_ID>
    <DESCRIPTION>This mutation was first observed in normal Wistar albino rats in  a breeding colony at Cannaught Laboratories in 1934. Jaundice was evident at birth or shortly after and was persistant throughout life.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357187</RGD_ID>
    <STRAIN_SYMBOL>WF.BBDR-(&lt;i&gt;D4Rat16-D4Got39&lt;/i&gt;)/Wor</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Massachusetts Medical School, Worcerster, MA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="58432133" STOP_POS="58432232" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="57101077" STOP_POS="57101175" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="56868238" STOP_POS="56868336" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="56704868" STOP_POS="56704967" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357187</CITATION_ID>
    <DESCRIPTION>This congenic was generated by the marker-assisted protocol where a segment of BBDR/Wor is transferred to WF background and the animals were screened using microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357189</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D8Rat56-D8Rat51&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="8462195" STOP_POS="28243068" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="9531047" STOP_POS="30918267" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="9505886" STOP_POS="30947391" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="8294860" STOP_POS="29559867" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357189</CITATION_ID>
    <DESCRIPTION>Congenic strain produced from a SS/Jr strain and a LEW/CrlBR strain purchased from Charles Rivers, Quebec, Canada</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357190</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;I&gt;Adh1-D2Mit5&lt;/I&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adh1c</ALLELES>
    <ALLELE_RGD_IDS>2044</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="229470703" STOP_POS="229482291" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="226797303" STOP_POS="226808892" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="243550655" STOP_POS="243562243" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="262090818" STOP_POS="262102977" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="235799396" STOP_POS="235811584" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357190</CITATION_ID>
    <DESCRIPTION>This congenic strain contains an MNS chromosome 2 segment transferred to an SS/Jr background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357191</RGD_ID>
    <STRAIN_SYMBOL>CDS/Ygl</STRAIN_SYMBOL>
    <FULL_NAME>Cohen diabetic-sensitive rat</FULL_NAME>
    <ORIGINATION>Hebrew University Hospital and Hadassah-Hebrew Medical College, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357191</CITATION_ID>
    <DESCRIPTION>Cohen rats that had an oral tolerance test with blood glucose levels &gt;180mg/dl were selected. More stringent criteria was set during the secondary inbreeding: rats with blood glucose levels &gt;230mg/dl were selected. Brother and sister mating was carried on for 10 additional generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357192</RGD_ID>
    <STRAIN_SYMBOL>WF.BBDR-(&lt;i&gt;D4Got39-D4Rat44&lt;/i&gt;)/Wor</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Massachusetts Medical School, Worcerster, MA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="58432133" STOP_POS="58432232" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="57101077" STOP_POS="57101175" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="56868238" STOP_POS="183837621" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="56704868" STOP_POS="121645621" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357192</CITATION_ID>
    <DESCRIPTION>This congenic was generated by the marker-assisted protocol where a segment of BBDR/Wor is transferred to WF background and the animals were screened using microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357193</RGD_ID>
    <STRAIN_SYMBOL>WF.BBDR-(&lt;i&gt;D4Got51-D4Rat44&lt;/i&gt;)/Wor</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Massachusetts Medical School, Worcerster, MA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="71241724" STOP_POS="71241930" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="71744558" STOP_POS="71744763" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="136548956" STOP_POS="183837621" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="70123187" STOP_POS="121645621" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357193</CITATION_ID>
    <DESCRIPTION>This congenic was generated by the marker-assisted protocol where a segment of BBDR/Wor is transferred to WF background and the animals were screened using microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357194</RGD_ID>
    <STRAIN_SYMBOL>WF.BBDR-(&lt;i&gt;D4Rat96-D4Rat44&lt;/i&gt;)/Wor</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Massachusetts Medical School, Worcerster, MA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="67576349" STOP_POS="67576447" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="66609358" STOP_POS="66609456" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="65577152" STOP_POS="65577249" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="65397099" STOP_POS="183837621" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="65434709" STOP_POS="121645621" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357194</CITATION_ID>
    <DESCRIPTION>This congenic was generated by the marker-assisted protocol where a segment of BBDR/Wor is transferred to WF background and the animals were screened using microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357195</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;Aldoc-D10Mco1&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nos2</ALLELES>
    <ALLELE_RGD_IDS>3185</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="61843496" STOP_POS="61843633" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="61345276" STOP_POS="61345413" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="64648175" STOP_POS="64648311" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="63366082" STOP_POS="63366218" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="67677924" STOP_POS="67678060" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357195</CITATION_ID>
    <DESCRIPTION>This congenic strain is derived by introgressing a desired region of chr 10 from MNS to the SS/Jr recipient.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357196</RGD_ID>
    <STRAIN_SYMBOL>WF.BBDR-(&lt;i&gt;D4Arb29-D4Rat265&lt;/i&gt;)/Wor</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Massachusetts Medical School, Worcerster, MA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="65495851" STOP_POS="84338055" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="64528739" STOP_POS="83007655" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="63537179" STOP_POS="84053053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="63250011" STOP_POS="148715224" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="63276741" STOP_POS="82266081" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357196</CITATION_ID>
    <DESCRIPTION>This congenic was generated by the marker-assisted protocol where a segment of BBDR/Wor is transferred to WF background and the animals were screened using microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357345</RGD_ID>
    <STRAIN_SYMBOL>DA/K</STRAIN_SYMBOL>
    <FULL_NAME>Dark Agouti/Karlsburg</FULL_NAME>
    <ORIGINATION>Dept. of Laboratory Animal Science, Inst. of Pathology, University of Greifswald,D-17495, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357345</CITATION_ID>
    <DESCRIPTION>Dark agouti rats which were bred and housed in Dept. of Laboratory Animal Science, Karlsburg, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357346</RGD_ID>
    <STRAIN_SYMBOL>BB.SHR-(&lt;i&gt;D4Mit6-Spr&lt;/i&gt;)/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Laboratory Animal Science, Inst of Pathophysiology, University of Greifswald, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Npy|Spr</ALLELES>
    <ALLELE_RGD_IDS>3197|3753</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="119229447" STOP_POS="119233320" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="76647384" STOP_POS="117676292" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="77307388" STOP_POS="116916073" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="141978848" STOP_POS="181496612" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="75732943" STOP_POS="119369308" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357346</CITATION_ID>
    <DESCRIPTION>BB/OK lymphopenic rats were crossed with non-lymphopenic, spontaneously hypertensive SHR/Mol rats.  Rats heterzygous for D4Mit6, Npy, and Spr and homozygous for BB alleles were selected.  After 5 backcross generations, rats were intercrossed.  Rats homozygous at SHR loci of interest were selected.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357417</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Npy)400Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357417</CITATION_ID>
    <DESCRIPTION>14.5 kb lambda clone of the rat Npy gene was subcloned with a polylinker that had NotI and EcoRI restriction sites. This transgene that was released by NotI digestion contained ~5kb 5'and ~1kb 3' and was injected into the pronuclei of fertilized SD rats. Founders were mated with SD females. F1 animals were mated with SD females till line 400 hemizygous animals were developed that had 5 copies of the Npy gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357953</RGD_ID>
    <STRAIN_SYMBOL>WAG/RijHfr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Envigo (Harlan France)</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357953</CITATION_ID>
    <DESCRIPTION>Substrain of WAG, from AL Bacharach, Glaxo Ltd from Wistar stock in 1924, from Rij to Envigo (Harlan France)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357954</RGD_ID>
    <STRAIN_SYMBOL>F344/NHfr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan France</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357954</CITATION_ID>
    <DESCRIPTION>Strain originated from Curtiss and Dunning 1920 at Columbia University Institute for Cancer Research, To Heston 1949 (Billingham and Silvers 1959). To National Institutes of Health in 1951 (Hansen et al 1982), Supplied by Harlan, France.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357955</RGD_ID>
    <STRAIN_SYMBOL>WF/NHfr</STRAIN_SYMBOL>
    <FULL_NAME>Wistar-Furth</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>Harlan France</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357955</CITATION_ID>
    <DESCRIPTION>Substrain of Wistar Furth stock, inbred by National Institute of Health, Bethesda, MD and now available at Harlan, France.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357957</RGD_ID>
    <STRAIN_SYMBOL>LEW/HanHfr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.envigo.com/model/lew-han-hsd&gt; ENVIGO France &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.envigo.com/model/lew-han-hsd&gt; ENVIGO France &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>The LEW/HanHsd is very susceptible to the induction of EAE, while the LEW/SsNHsd is not susceptible to the induction of EAE</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357957</CITATION_ID>
    <DESCRIPTION>Inbreeding of the Lewis rat is begun by Dr. Margaret Lewis from a Wistar stock. In 1924, at F20 to Aptekmanm and Bogdon. In 1958, at F31 to Silvers, who distributed this strain.  subsequently. To Central Institute for Laboratory Animal Breeding, Hannover, in 1973 at F58. In 1994, to Harlan Netherlands through acquisition of Central Institute for Laboratory Animal Breeding. Harlan became Envigo in 2015</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357958</RGD_ID>
    <STRAIN_SYMBOL>BN/RijHfr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan France</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357958</CITATION_ID>
    <DESCRIPTION>Substrain of BN, from Billingham and Silvers 1958, from Harlan Rijnswijk, supplied by Harlan France.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357959</RGD_ID>
    <STRAIN_SYMBOL>FHH.BN-(&lt;i&gt;D1Hmgc14-D1Hmgc15&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology, Medical College of Wisconsin, Milwaukee Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ctsc|Grm5|Nox4|Rab38|Tyr</ALLELES>
    <ALLELE_RGD_IDS>2445|2746|620600|628752|1589755</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="140879679" STOP_POS="142314355" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="150775310" STOP_POS="152202960" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157084760" STOP_POS="158516775" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357959</CITATION_ID>
    <DESCRIPTION>The Rf-2 region of chromosome 1 is transferred from BN to the genomic background of FHH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357960</RGD_ID>
    <STRAIN_SYMBOL>LE/CpbHfr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Envigo (Harlan France)</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357960</CITATION_ID>
    <DESCRIPTION>Substrain of LE which was bred at Harlan CPB now at Harlan France.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357974</RGD_ID>
    <STRAIN_SYMBOL>BB.SHR-(&lt;i&gt;D4Got41-Gimap5&lt;/i&gt;)/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Laboratory Animal Science, University of Greifswald, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gimap5</ALLELES>
    <ALLELE_RGD_IDS>628871</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="79025151" STOP_POS="79031917" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="61697658" STOP_POS="77701025" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="60439127" STOP_POS="78386683" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="60179409" STOP_POS="143073003" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="60262965" STOP_POS="76843214" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357974</CITATION_ID>
    <DESCRIPTION>Originated from BB.SHR-(&lt;i&gt;D4Got41-Tacr1&lt;/i&gt;) rats crossed with BB/OK rats to create a congenic substrain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357975</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco4-D1Rat18&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="30866622" STOP_POS="51816258" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="29038037" STOP_POS="49268520" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="31647701" STOP_POS="49454378" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="33073397" STOP_POS="50297622" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="29841428" STOP_POS="43747532" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357975</CITATION_ID>
    <DESCRIPTION>This strain was constructed from the progenitor strain SS.LEW-(&lt;i&gt;D1Uia8-D1Rat18&lt;/i&gt;)/Mco by crossing the progenitor strain to SS rats to get F&lt;sub&gt;1&lt;/sub&gt; followed by F&lt;sub&gt;1&lt;/sub&gt; X F&lt;sub&gt;1&lt;/sub&gt; intercross to get F&lt;sub&gt;2&lt;/sub&gt; which was screened for the desired recombinants.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357976</RGD_ID>
    <STRAIN_SYMBOL>BB.SHR-(&lt;i&gt;D4Got41-D4Rat171&lt;/i&gt;)/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Laboratory Animal Science, University of Greifswald, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="89547115" STOP_POS="89547365" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="61697658" STOP_POS="88217207" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="60439127" STOP_POS="89342035" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="60179409" STOP_POS="154162556" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="60262965" STOP_POS="87996003" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357976</CITATION_ID>
    <DESCRIPTION>Originated from BB.SHR-(&lt;i&gt;D4Got41-Tacr1&lt;/i&gt;) rats crossed with BB/OK rats to create a congenic substrain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357977</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco8-D1Rat213&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="41570983" STOP_POS="90905414" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="81777564" STOP_POS="81777720" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="83282659" STOP_POS="83282814" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="84537073" STOP_POS="84537228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="7947583" STOP_POS="7947744" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="32329137" STOP_POS="81548909" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357977</CITATION_ID>
    <DESCRIPTION>This strain was constructed from the progenitor strain SS.LEW-(&lt;i&gt;D1Uia8-D1Rat18&lt;/i&gt;)/Mco by crossing the progenitor strain to SS rats to get F&lt;sub&gt;1&lt;/sub&gt; followed by F&lt;sub&gt;1&lt;/sub&gt; X F&lt;sub&gt;1&lt;/sub&gt; intercross to get F&lt;sub&gt;2&lt;/sub&gt; which was screened for the desired recombinants.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357978</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Mit6-D2Rat303&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de L'Universite de Montreal (CHUM), Montreal, Quebec,Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="78269809" STOP_POS="78269996" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="76539322" STOP_POS="127460910" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="78321410" STOP_POS="135646395" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="98037122" STOP_POS="155130826" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="77630629" STOP_POS="131522430" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357978</CITATION_ID>
    <DESCRIPTION>Congenic strain was created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Mit6-Adh1&lt;/i&gt;)/Lt strain into the parental Dahl Salt-sensitive (SS) strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357979</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;Mme-D2Rat131&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de L'Universite de Montreal (CHUM), Montreal, Quebec,Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mme</ALLELES>
    <ALLELE_RGD_IDS>3098</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="149806826" STOP_POS="149957381" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="147686913" STOP_POS="172711135" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="153799203" STOP_POS="186612024" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="173193501" STOP_POS="206015340" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="153031724" STOP_POS="179302663" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357979</CITATION_ID>
    <DESCRIPTION>Congenic strain was created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Mit6-Adh1&lt;/i&gt;)/Lt strain into the parental Dahl Salt-sensitive (SS) strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357980</RGD_ID>
    <STRAIN_SYMBOL>BB.SHR-(&lt;i&gt;D4Got41-Tacr1&lt;/i&gt;)/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Laboratory Animal Science, University of Greifswald, Karlsburg, Germany</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=514 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Metabolism</RESEARCH_USE>
    <ALLELES>Tacr1</ALLELES>
    <ALLELE_RGD_IDS>3811</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="116478617" STOP_POS="116647492" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="61697658" STOP_POS="115089733" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="60439127" STOP_POS="113416139" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="60179409" STOP_POS="178095041" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="60262965" STOP_POS="116780394" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357980</CITATION_ID>
    <DESCRIPTION>Congenic BB.LL rats were established as speed-congenics by cross of BB/OK and SHR/Mol rats and repeated backcrossing onto BB/OK rats and marker-aided selection in 1997.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357981</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D3Mco21-D3Rat17&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="90755164" STOP_POS="141509147" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="70348525" STOP_POS="121056321" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="72672290" STOP_POS="127023997" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="79183926" STOP_POS="133513825" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="68499987" STOP_POS="121619110" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357981</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D3Rat52-D3Rat17&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357982</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D3Rat52-D3Chm63&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="38708931" STOP_POS="38709087" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="18311454" STOP_POS="53781346" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="14090411" STOP_POS="55245509" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="19410399" STOP_POS="61857467" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="14051872" STOP_POS="51161895" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357982</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D3Rat52-D3Rat17&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357983</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco75-D1Rat18&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="51816100" STOP_POS="51816258" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="32765502" STOP_POS="49268520" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="35406399" STOP_POS="49454378" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="36805624" STOP_POS="50297622" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="43747374" STOP_POS="43747532" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="2897342" STOP_POS="2897591" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357983</CITATION_ID>
    <DESCRIPTION>This strain was constructed from the progenitor strain SS.LEW-(&lt;i&gt;D1Uia8-D1Rat18&lt;/i&gt;)/Mco by crossing the progenitor strain to SS rats to get F&lt;sub&gt;1&lt;/sub&gt; followed by F&lt;sub&gt;1&lt;/sub&gt; X F&lt;sub&gt;1&lt;/sub&gt; intercross to get F&lt;sub&gt;2&lt;/sub&gt; which was screened for the desired recombinants.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357984</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Mit6-D2Rat166&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de L'Universite de Montreal (CHUM), Montreal, Quebec,Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="78269809" STOP_POS="142786220" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="76539322" STOP_POS="140636154" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="78321410" STOP_POS="145903673" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="98037122" STOP_POS="165313939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="77630629" STOP_POS="145701148" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357984</CITATION_ID>
    <DESCRIPTION>Congenic strain was created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Mit6-Adh1&lt;/i&gt;)/Lt strain into the parental Dahl Salt-sensitive (SS) strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357985</RGD_ID>
    <STRAIN_SYMBOL>LOU/Ins</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>INSERM, C.H.U. Bichat-Claude Bernard, Paris, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357985</CITATION_ID>
    <DESCRIPTION>originated from Universite Catholique de Louvain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357986</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Uia8-D1Rat211&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="32879372" STOP_POS="32879613" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="31050840" STOP_POS="31051081" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="33667777" STOP_POS="33668017" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="35077728" STOP_POS="35077968" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="1147796" STOP_POS="1148037" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357986</CITATION_ID>
    <DESCRIPTION>This strain was constructed from the progenitor strain SS.LEW-(&lt;i&gt;D1Uia8-D1Rat18&lt;/i&gt;)/Mco by crossing the progenitor strain to SS rats to get F&lt;sub&gt;1&lt;/sub&gt; followed by F&lt;sub&gt;1&lt;/sub&gt; X F&lt;sub&gt;1&lt;/sub&gt; intercross to get F&lt;sub&gt;2&lt;/sub&gt; which was screened for the desired recombinants.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357987</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Uia8-D1Rat18&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="51816100" STOP_POS="51816258" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="49268362" STOP_POS="49268520" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="49454221" STOP_POS="49454378" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="50297465" STOP_POS="50297622" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="43747374" STOP_POS="43747532" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357987</CITATION_ID>
    <DESCRIPTION>A 17 cM segment of chr 1 from Lewis which was obtained from Charles was introgressed into Dahl salt-sensitive strain which is an in-house colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357988</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D3Rat52-D3Rat17&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="38708931" STOP_POS="141509147" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="18311454" STOP_POS="121056321" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="14090411" STOP_POS="127023997" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="19410399" STOP_POS="133513825" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="14051872" STOP_POS="121619110" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357988</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 3 was transferred from LEW into the SS background. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1357994</RGD_ID>
    <STRAIN_SYMBOL>SHR/NCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2020-01-23)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1357994</CITATION_ID>
    <DESCRIPTION>To Charles River from NIH in 1973 at F32. To N 1966 at F13 from Okamoto. Okamoto, Kyoto School of Medicine, 1963, from outbred Wistar Kyoto male with marked elevation of blood pressure mated to female with slightly elevated blood pressure; brother-sister mating with continued selection for spontaneous hypertension.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358112</RGD_ID>
    <STRAIN_SYMBOL>WKY/NCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.criver.com/products-services/find-model/wistar-kyoto-wky-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/wistar-kyoto-wky-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358112</CITATION_ID>
    <DESCRIPTION>Outbred Wistar stock from Kyoto School of Medicine to NIH in 1971, to Charles River in 1974 from NIH at F11</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358114</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 5&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358114</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358150</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D16Rat12-D16Chm23&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="387123" STOP_POS="387234" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="88524" STOP_POS="380356" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="756352" STOP_POS="1090164" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="751266" STOP_POS="1084414" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="42656" STOP_POS="350232" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358150</CITATION_ID>
    <DESCRIPTION>This congenic strain originated from a SS/Jr parental strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358151</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 8&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358151</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 8 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358152</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 14&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358152</CITATION_ID>
    <DESCRIPTION>A SS genomic background with a BN chromosome 14 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358153</RGD_ID>
    <STRAIN_SYMBOL>COP/CrCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358153</CITATION_ID>
    <DESCRIPTION>Inbred strain is from Curtis in 1921 at Columbia University Institute for Cancer Research. To National Cancer Institute Animal Production Program (Cr). To Charles River from the National Cancer Institute in 1998.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358154</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 3&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358154</CITATION_ID>
    <DESCRIPTION>A SS genomic background with a BN chromosome 3 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358155</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat119-D10Mgh1&lt;/i&gt;)(&lt;i&gt;D16Rat21-D16Rat112&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358155</CITATION_ID>
    <DESCRIPTION>This double congenic strain was constructed by using the SS/Jr strain as a donor strain to transfer regions (&lt;i&gt;D10Rat119-D10Mgh1&lt;/i&gt;)and (&lt;i&gt;D16Rat21-D16Rat112&lt;/i&gt;) from the LEW strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358156</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Rat183-D2Chm113&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de L'Universite de Montreal (CHUM), Montreal, Quebec,Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="139096736" STOP_POS="140708949" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="144313532" STOP_POS="145975996" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="163731761" STOP_POS="165386311" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="144136724" STOP_POS="145774334" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358156</CITATION_ID>
    <DESCRIPTION>Congenic strain was created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Mit6-D2Rat166&lt;/i&gt;)/Lt strain into the parental Dahl Salt-sensitive (SS) strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358157</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 7&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358157</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 7 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358158</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 16&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358158</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 16 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358159</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 6&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358159</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 6 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358160</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D8Rat163-D8Rat81&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="30188867" STOP_POS="119698120" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="32888352" STOP_POS="128653291" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="32911182" STOP_POS="127854519" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="31508524" STOP_POS="124926877" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358160</CITATION_ID>
    <DESCRIPTION>A SS genomic background with a majority BN chromosome 8 introgressed. The segment of chromosome 8 that caries the BN extends from D8Rat163-D8Rat81.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358161</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D16Rat38-D16Chm66&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="2995225" STOP_POS="8336378" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="3439525" STOP_POS="9316554" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="3405986" STOP_POS="11276947" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="3080748" STOP_POS="8612621" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358161</CITATION_ID>
    <DESCRIPTION>This congenic strain originated from a SS/Jr parental strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358162</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358162</CITATION_ID>
    <DESCRIPTION>A SS genomic background with a BN chromosome 12 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358163</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 15&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358163</CITATION_ID>
    <DESCRIPTION>A SS genomic background with a BN chromosome 15 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358164</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 17&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358164</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 17 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358165</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm51-D2Rat341&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de L'Universite de Montreal (CHUM), Montreal, Quebec,Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="152400438" STOP_POS="152400642" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="146368688" STOP_POS="150090572" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="152460836" STOP_POS="157650873" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="171854997" STOP_POS="177018102" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="151616735" STOP_POS="155664303" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358165</CITATION_ID>
    <DESCRIPTION>Congenic strain was created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Mit6-D2Rat166&lt;/i&gt;)/Ayd strain into the parental Dahl Salt-sensitive (SS) strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358166</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D16Mit3-D16Rat112&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="117469" STOP_POS="50968773" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="110590" STOP_POS="44236047" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="778415" STOP_POS="47346612" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="773329" STOP_POS="47069744" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="64718" STOP_POS="47434384" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358166</CITATION_ID>
    <DESCRIPTION>This congenic strain originated from a SS/Jr parental strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358167</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Wox27-Adh1&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de L'Universite de Montreal (CHUM), Montreal, Quebec,Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adh1c</ALLELES>
    <ALLELE_RGD_IDS>2044</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="197040544" STOP_POS="229482291" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="194352314" STOP_POS="226808892" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="209489455" STOP_POS="243562243" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="228956554" STOP_POS="262102977" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="202186267" STOP_POS="235811584" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358167</CITATION_ID>
    <DESCRIPTION>Congenic strain was created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Mit6-Adh1&lt;/i&gt;)/Lt strain into the parental Dahl Salt-sensitive (SS) strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358168</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D16Mit2-D16Chm23&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="4234212" STOP_POS="4234333" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="88524" STOP_POS="4227730" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="756352" STOP_POS="5098704" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="751266" STOP_POS="5038806" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="42656" STOP_POS="4304517" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358168</CITATION_ID>
    <DESCRIPTION>This congenic strain originated from a SS/Jr parental strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358169</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm25-D2Rat131&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de L'Universite de Montreal (CHUM), Montreal, Quebec,Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="166144095" STOP_POS="172711135" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="179779225" STOP_POS="186612024" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="199188066" STOP_POS="206015340" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="172459883" STOP_POS="179302663" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358169</CITATION_ID>
    <DESCRIPTION>Congenic strain was created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Chm90-D2Wox37&lt;/i&gt;)/Lt strain into the parental Dahl Salt-sensitive (SS) strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358170</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 5&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358170</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 5 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358171</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 17&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358171</CITATION_ID>
    <DESCRIPTION>A SS genomic background with a BN chromosome 17 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358172</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm25-Fgg&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de L'Universite de Montreal (CHUM), Montreal, Quebec,Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fgg</ALLELES>
    <ALLELE_RGD_IDS>2613</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="170652929" STOP_POS="170660372" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="166144095" STOP_POS="168362325" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="179779225" STOP_POS="181994523" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="199188066" STOP_POS="201409143" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="172459883" STOP_POS="174734594" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358172</CITATION_ID>
    <DESCRIPTION>Congenic strain was created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Mit6-Adh1&lt;/i&gt;)/Lt strain into the parental Dahl Salt-sensitive (SS) strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358173</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 11&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358173</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 11 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358174</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 19&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=601&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-05-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00601</CITATION_ID>
    <DESCRIPTION>A SS genomic background with a BN chromosome 19 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358175</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 20&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358175</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 20 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358176</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 18&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358176</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 18 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358177</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm25-D2Mit14&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de L'Universite de Montreal (CHUM), Montreal, Quebec,Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="192287802" STOP_POS="192287892" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="166144095" STOP_POS="189599348" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="179779225" STOP_POS="204585731" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="199188066" STOP_POS="224018437" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="172459883" STOP_POS="197256313" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358177</CITATION_ID>
    <DESCRIPTION>Congenic strain was created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Mit6-Adh1&lt;/i&gt;)/Lt strain into the parental Dahl Salt-sensitive (SS) strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358178</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 10&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358178</CITATION_ID>
    <DESCRIPTION>A SS genomic background with a BN chromosome 10 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358179</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358179</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 13 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358180</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 19&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=581&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-05-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00581</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 19 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358258</RGD_ID>
    <STRAIN_SYMBOL>RCS/LavRrrc</STRAIN_SYMBOL>
    <FULL_NAME>royal college of surgeons rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=314&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=314&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2018-11-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00314</CITATION_ID>
    <DESCRIPTION>Originally developed before 1965 by Sidman from stock obtained from Sorsby of the Royal College of Surgeons, London. Then to University of California- San Francisco, School of Medicine, deposited to Rat Resource &amp; Research Center.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358259</RGD_ID>
    <STRAIN_SYMBOL>RCS-&lt;i&gt;p&lt;/i&gt;&lt;sup&gt;+&lt;/sup&gt;/LavRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=315&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=315&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2018-11-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00315</CITATION_ID>
    <DESCRIPTION>This strain has homozygous wild type at the pink eye (p+) locus and homozygous for a deletion in the Mertk gene. Developed by intercrossing (brother x sister) two black-eyed p/+ rats from the RCS-p/+ strain. The black-eyed animals were tested for homozygous p locus and then backcrossed to the parental strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358277</RGD_ID>
    <STRAIN_SYMBOL>RCS-&lt;I&gt;rdy&lt;/I&gt;&lt;sup&gt;+&lt;/sup&gt;/LavRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=317&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=317&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2018-07-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00317</CITATION_ID>
    <DESCRIPTION>Developed by crossing an inbred RCS (rdy/rdy) with a cesarian developed Fischer (+/+) rat (from Charles River). The normal rats(+/rdy) were backcrossed to the RCS and the procedure repeated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358278</RGD_ID>
    <STRAIN_SYMBOL>RCS-&lt;i&gt;rdy&lt;/I&gt;&lt;sup&gt;+&lt;/sup&gt;&lt;I&gt;p&lt;/I&gt;&lt;sup&gt;+&lt;/sup&gt;/LavRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=316&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=316&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2021-02-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00316</CITATION_ID>
    <DESCRIPTION>Developed by crossing a pink-eyed control(RCS-rdy&lt;sup&gt;+&lt;/sup&gt;/Lav  x black-eyed dystrophic(RCS-p&lt;sup&gt;+&lt;/sup&gt;/Lav) The F12 progeny was backcrossed to RCS-rdy&lt;sup&gt;+&lt;/sup&gt;/Lav. The strain is pigmented (p+) congenic control strain (rdy+, wild-type at the retinal dystrophy locus) for the pigmented RCS-p+ dystrophic (rdy-) strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358298</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Rho*P23H)1LavRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;,&lt;a href=http://www.rrrc.us/Strain/?x=639&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;,&lt;a href=http://www.rrrc.us/Strain/?x=639&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-05-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rho</ALLELES>
    <ALLELE_RGD_IDS>11239</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00639</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries a copy of mouse Rhodopsin gene with a proline to histidine substitution at codon 23 (c.68C&gt;A).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358299</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Rho*P23H)2Lav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358299</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries a copy of mouse Rhodopsin gene with a proline to histidine substitution at codon 23 (c.68C&gt;A).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358300</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Rho*P23H)3Lav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;,&lt;a href=http://www.rrrc.us/Strain/?x=641&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;,&lt;a href=http://www.rrrc.us/Strain/?x=641&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00641</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries a copy of mouse Rhodopsin gene with a proline to histidine substitution at codon 23 (c.68C&gt;A).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358302</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Rho*S334X)3Lav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=643&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=643&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00643</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries a mouse rhodopsin gene that bears a termination codon at residue 334, which encodes a C-terminal truncated opsin protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358303</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Rho*S334X)4Lav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;,&lt;a href=http:///www.rrrc.us/Strain/?x=645&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;,&lt;a href=http:///www.rrrc.us/Strain/?x=645&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00645</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries a mouse rhodopsin gene that bears a termination codon at residue 334, which encodes a C-terminal truncated opsin protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358304</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Rho*S334X)5Lav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358304</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries a mouse rhodopsin gene that bears a termination codon at residue 334, which encodes a C-terminal truncated opsin protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358305</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Rho*S334X)7Lav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358305</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries a mouse rhodopsin gene that bears a termination codon at residue 334, which encodes a C-terminal truncated opsin protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358306</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Rho*S334X)9Lav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358306</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries a mouse rhodopsin gene that bears a termination codon at residue 334, which encodes a C-terminal truncated opsin protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358632</RGD_ID>
    <STRAIN_SYMBOL>MR/Har</STRAIN_SYMBOL>
    <FULL_NAME>Maudsely reactive</FULL_NAME>
    <ORIGINATION>Center for Developmental and Health Genetics, Pennsylvania State University, Pennsylvania. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=691&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2019-02-20)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00691</CITATION_ID>
    <DESCRIPTION>This strain has been selected for high open-field defecation (a test of emotional reactivity). The underlying genetic basis for this phenotype is not known. Originally selected by Broadhurst in 1954 for high open-field defacation (OFD) response in an open field. By Broadhurst to Harrington at the University of Northern Iowa at generation 25 in 1965.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358633</RGD_ID>
    <STRAIN_SYMBOL>MNRA/Har</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Developmental and Health Genetics, Pennsylvania State University, Pennsylvania</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358633</CITATION_ID>
    <DESCRIPTION>Originally selected by Broadhurst in 1954 for low open-field defacation (OFD) response in an open field. By Broadhurst to Harrington at the University of Northern Iowa at generation 25 in 1965.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358918</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Plp1&lt;sup&gt;md&lt;/sup&gt;&lt;/i&gt;/Nya</STRAIN_SYMBOL>
    <FULL_NAME>W-&lt;i&gt;Plp1&lt;/i&gt;&lt;sup&gt;md&lt;/sup&gt;</FULL_NAME>
    <ORIGINATION>Division of Laboratories and Research, New York State Department of Health, Albany, New York</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Plp1|Plp1&lt;i&gt;&lt;sup&gt;md&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>3354|12802346</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="104933921" STOP_POS="104993317" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="100195051" STOP_POS="100195051" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="107505372" STOP_POS="107505372" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="107379831" STOP_POS="107394881" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="124488627" STOP_POS="124503639" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358918</CITATION_ID>
    <DESCRIPTION>Wistar rats were received in 1957 from Walter Reed Army Medical Center. In 1977, three ofsprings exhibited body tremor. Two of these had hydrocephalus and the brain of the third was normal. The mother rat and four of its clinically mormal youngs along with three adult males were breed as nuclear breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358919</RGD_ID>
    <STRAIN_SYMBOL>F344/Seac</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>SEAC Yoshitomi Co., Fukuoka, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358919</CITATION_ID>
    <DESCRIPTION>Inbred strain originated from F344 rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358921</RGD_ID>
    <STRAIN_SYMBOL>WF.DA-(&lt;i&gt;D19Mit1-D19Mit6&lt;/i&gt;)/Kop</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=521&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES>Nqo1</ALLELES>
    <ALLELE_RGD_IDS>2503</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="41722546" STOP_POS="41722671" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="24817978" STOP_POS="39654489" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="24455726" STOP_POS="43907843" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="35433730" STOP_POS="54715514" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="26536747" STOP_POS="41612881" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358921</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from a parental DA/Slc strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358922</RGD_ID>
    <STRAIN_SYMBOL>BB.WOKW-(&lt;i&gt;D4Got41-Fabp1&lt;/i&gt;)/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Laboratory Animal Science, Medical Faculty, University of Greifswald, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fabp1</ALLELES>
    <ALLELE_RGD_IDS>2590</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="104744302" STOP_POS="104753119" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="61697658" STOP_POS="103194791" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="60439127" STOP_POS="99066957" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="60179409" STOP_POS="163844105" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="60262965" STOP_POS="104415981" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358922</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from a BB/OK parental strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358923</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Mbp&lt;sup&gt;md&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mbp|Mbp&lt;sup&gt;md&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>3054|12802351</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="78130652" STOP_POS="78241174" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="75855878" STOP_POS="75966404" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="79326738" STOP_POS="79437310" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="78385304" STOP_POS="78504226" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="78943608" STOP_POS="79057329" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358923</CITATION_ID>
    <DESCRIPTION>A spontaneous tremor rat was originated from in-house breeding colony , after purchased from Charles River Laboratory 12 years earlier, at McMaster University Central Animal Facility, Hamilton, Ontario, Canada. 10-12 days old rats had tremors that were followed by ataxia, hind limb paresis, episodes of immobility, and seizures by 5-14 weeks.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358989</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;I&gt;D2Rat174-D2Rat28&lt;/I&gt;)(&lt;I&gt;D2Rat161-D2Rat185&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept Pharmacology, Univ. of California San Diego, La Jolla, CA  USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358989</CITATION_ID>
    <DESCRIPTION>This congenic substrain was contructed by repeated backcrossing of congenic strain WKY.SHR-(&lt;i&gt;D2Rat174-D2Rat185&lt;/i&gt;) to parental strain WKY/NCrl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358990</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;i&gt;D10Mit9-D10Rat24&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Shore-Long Island Jewish Research Institute,350 Community Drive - Manhasset, NY 11030</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="76128947" STOP_POS="76129113" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="31224026" STOP_POS="75632053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="31919397" STOP_POS="78343192" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="31740635" STOP_POS="78195122" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="31931622" STOP_POS="79229233" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358990</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing DA/BklArbNsi and F344/Hsd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358991</RGD_ID>
    <STRAIN_SYMBOL>F344.HTX-(&lt;i&gt;D11Rat4-D11Arb4&lt;/i&gt;)/Hcj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pharmacology, University of Florida, Gainesville</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="76295832" STOP_POS="76295999" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="62790342" STOP_POS="66422377" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="65352097" STOP_POS="69649936" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="66731054" STOP_POS="72739915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="64573222" STOP_POS="68235010" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358991</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from F344/NHsd parental strain bred to HTX/Hcj</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358992</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;I&gt;D2Rat40-D2Rat50&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept Pharmacology, Univ. of California San Diego, La Jolla, CA  USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="159440760" STOP_POS="195313808" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="157142078" STOP_POS="192625452" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="169852670" STOP_POS="207612467" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="189197858" STOP_POS="227035367" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="163154227" STOP_POS="200390471" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358992</CITATION_ID>
    <DESCRIPTION>Congenic strains were constructed by repeated backcross of an (SHR/NCrl x WKY/NCrl)F1 to the SHR/NCrl recipient strain with selection for chromosome 2 markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358993</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;I&gt;D2Rat161-D2Rat185&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept Pharmacology, Univ. of California San Diego, La Jolla, CA  USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="231732847" STOP_POS="231733024" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="114837527" STOP_POS="229059787" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="118446646" STOP_POS="245893748" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="138120195" STOP_POS="264423808" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="118264490" STOP_POS="238140155" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358993</CITATION_ID>
    <DESCRIPTION>This congenic substrain was contructed by repeated backcrossing of congenic strain WKY.SHR-(&lt;i&gt;D2Rat174-D2Rat185&lt;/i&gt;) to parental strain WKY/NCrl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358994</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;I&gt;D2Rat161-D2Rat241&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept Pharmacology, Univ. of California San Diego, La Jolla, CA  USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="212145319" STOP_POS="212145502" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="114837527" STOP_POS="114837675" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="118446646" STOP_POS="118446793" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="138120195" STOP_POS="242993417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="118264490" STOP_POS="217985582" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358994</CITATION_ID>
    <DESCRIPTION>This congenic substrain was constructed by repeated backcrossing the congenic strain SHR.WKY-(&lt;I&gt;D2Rat10-D2Mgh13&lt;/I&gt;) congenic strain to the parental strain SHR/NCrl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358995</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D1Rat166-D1Rat90&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory of Animal Breeding and Genetics, Kyoto University, Sakyoku, Kyoto, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="258334277" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="248393012" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="269279863" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="276721459" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="255026793" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358995</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from backcrossing parental F344/Crlj and OLETF/Otk animals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358996</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;I&gt;D2Rat10-D2Mgh13&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept Pharmacology, Univ. of California San Diego, La Jolla, CA  USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="37756937" STOP_POS="238161384" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="36023184" STOP_POS="235501121" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="34967269" STOP_POS="252466565" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="54092967" STOP_POS="270992875" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="35874553" STOP_POS="244809764" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358996</CITATION_ID>
    <DESCRIPTION>This congenic strain carries a WKY/NCrl chromosome 2 segment transferred to a SHR/NCrl background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358997</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;I&gt;D2Rat241-D2Rat185&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept Pharmacology, Univ. of California San Diego, La Jolla, CA  USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="212145319" STOP_POS="231733024" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="229059610" STOP_POS="229059787" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="245893572" STOP_POS="245893748" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="242993235" STOP_POS="264423808" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="217985399" STOP_POS="238140155" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358997</CITATION_ID>
    <DESCRIPTION>This congenic substrain was contructed by repeated backcrossing of congenic strain WKY.SHR-(&lt;i&gt;D2Rat174-D2Rat185&lt;/i&gt;)/NCrl to parental strain WKY/NCrl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358998</RGD_ID>
    <STRAIN_SYMBOL>BUF/NHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Harlan</ORIGINATION>
    <SOURCE>Harlan</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358998</CITATION_ID>
    <DESCRIPTION>Heston 1946 from Buffalo stock of H. Morris. To NIH in 1950 at F10. These were bought from Harlan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1358999</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;I&gt;D2Rat174-D2Rat28&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept Pharmacology, Univ. of California San Diego, La Jolla, CA  USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="61471959" STOP_POS="61472143" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="59744817" STOP_POS="104815148" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="60746052" STOP_POS="107083569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="83930202" STOP_POS="126824737" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="60124623" STOP_POS="107574826" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1358999</CITATION_ID>
    <DESCRIPTION>This congenic substrain was contructed by repeated backcrossing of congenic strain WKY.SHR-(&lt;i&gt;D2Rat174-D2Rat185&lt;/i&gt;) to parental strain WKY/NCrl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1359000</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;i&gt;D10Arb27-D10Rat6&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Shore-Long Island Jewish Research Institute,350 Community Drive - Manhasset, NY 11030</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="65927233" STOP_POS="101436010" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="68305037" STOP_POS="105078045" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="67971352" STOP_POS="104746310" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="69160380" STOP_POS="106310957" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1359000</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing DA/BklArbNsi and F344/Hsd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1359001</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;I&gt;D2Rat42-D2Rat139&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept Pharmacology, Univ. of California San Diego, La Jolla, CA  USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="226164337" STOP_POS="226164486" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="174110900" STOP_POS="223490532" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="188013923" STOP_POS="240243929" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="207416346" STOP_POS="258769070" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="180768203" STOP_POS="232533087" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1359001</CITATION_ID>
    <DESCRIPTION>Congenic strains were constructed by repeated backcross of an (SHR/NCrl x WKY/NCrl)F1 to the WKY/Crl recipient strain with selection for chromosome 2 SHR markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1359002</RGD_ID>
    <STRAIN_SYMBOL>NTac:WKY</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.taconic.com/anmodels/wky.htm&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1359002</CITATION_ID>
    <DESCRIPTION>The Taconic Wistar Kyoto rat was received from the NIH Animal Genetic Resource in 1974 at F10. The NIH-stock was obtained in 1971 as non-inbred Wistar stock from the Kyoto School of Medicine. Cesarean derived in 1982, Taconic's WKY is randomly bred in a closed colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1359003</RGD_ID>
    <STRAIN_SYMBOL>LEW/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1359003</CITATION_ID>
    <DESCRIPTION>This strain is maintained by Dr. J Rapp at the Medical College of Ohio (Toledo), USA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1359004</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;i&gt;D10Mit9-D10Rat11&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Shore-Long Island Jewish Research Institute,350 Community Drive - Manhasset, NY 11030</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="96620293" STOP_POS="96620484" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="31224026" STOP_POS="96121100" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="31919397" STOP_POS="99492409" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="31740635" STOP_POS="99184250" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="31931622" STOP_POS="100633982" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1359004</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing DA/BklArbNsi and F344/Hsd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1359005</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;I&gt;D2Rat15-D2Rat50&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept Pharmacology, Univ. of California San Diego, La Jolla, CA  USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="48870940" STOP_POS="195313808" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="47137898" STOP_POS="192625452" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="47783949" STOP_POS="207612467" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="66171293" STOP_POS="227035367" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="46251938" STOP_POS="200390471" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1359005</CITATION_ID>
    <DESCRIPTION>This congenic substrain was constructed by repeated backcrossing the congenic strain SHR.WKY-(&lt;I&gt;D2Rat10-D2Mgh13&lt;/I&gt;) to parental strain SHR/NCrl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1359006</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;I&gt;D2Rat27-D2Rat243&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept Pharmacology, Univ. of California San Diego, La Jolla, CA  USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="96266720" STOP_POS="215404472" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="94359407" STOP_POS="212719943" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="96556622" STOP_POS="228759752" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="116297660" STOP_POS="248110514" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="96481750" STOP_POS="221307793" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1359006</CITATION_ID>
    <DESCRIPTION>This congenic substrain was contructed by repeated backcrossing of congenic strain WKY.SHR-(&lt;i&gt;D2Rat174-D2Rat185&lt;/i&gt;)/NCrl to parental strain WKY/NCrl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1359007</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;I&gt;D2Rat174-D2Rat62&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept Pharmacology, Univ. of California San Diego, La Jolla, CA  USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="61471959" STOP_POS="61472143" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="59744817" STOP_POS="219753474" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="60746052" STOP_POS="236318668" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="83930202" STOP_POS="254867363" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="60124623" STOP_POS="228664122" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1359007</CITATION_ID>
    <DESCRIPTION>This congenic substrain was contructed by repeated backcrossing of congenic strain WKY.SHR-(&lt;i&gt;D2Rat174-D2Rat185&lt;/i&gt;)/NCrl to parental strain WKY/NCrl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1359008</RGD_ID>
    <STRAIN_SYMBOL>F344.HTX-(&lt;i&gt;D11Rat4-D11Arb4&lt;/i&gt;)(&lt;i&gt;D17Rat23-D17Rat154&lt;/i&gt;)/Hcj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pharmacology, University of Florida, Gainesville</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1359008</CITATION_ID>
    <DESCRIPTION>Double congenic strain originated from a cross between single congenic strains F344.HTX-(&lt;i&gt;D11Rat4-D11Arb4&lt;/i&gt;)/Hcj and F344.HTX-(&lt;i&gt;D17Rat23-D17Rat154&lt;/i&gt;)/Hcj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1359009</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;I&gt;D2Rat174-D2Rat185&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept Pharmacology, Univ. of California San Diego, La Jolla, CA  USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="61471959" STOP_POS="231733024" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="59744817" STOP_POS="229059787" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="60746052" STOP_POS="245893748" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="83930202" STOP_POS="264423808" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="60124623" STOP_POS="238140155" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1359009</CITATION_ID>
    <DESCRIPTION>Congenic strains were constructed by repeated backcross of an (SHR/NCrl x WKY/NCrl)F1 to the WKY/Crl recipient strain with selection for chromosome 2 SHR markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1359010</RGD_ID>
    <STRAIN_SYMBOL>WF.BBDR-ART2&lt;SUP&gt;a&lt;/SUP&gt;/Wor</STRAIN_SYMBOL>
    <FULL_NAME>Wistar Furth</FULL_NAME>
    <ORIGINATION>University of Massachusetts Medical School,Department of Pathology 55 Lake Avenue Worcester, MA 01605</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1359010</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing WF strain to BBDR strain which are RT1 &lt;SUP&gt;u/u&lt;/SUP&gt; , ART2&lt;SUP&gt;a&lt;/SUP&gt;.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1547865</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 3&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1547865</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 3 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1547866</RGD_ID>
    <STRAIN_SYMBOL>F344/Jcl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/en/products/outbred/item_a0470&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/en/products/outbred/item_a0470&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-04-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1547866</CITATION_ID>
    <DESCRIPTION>Inbred strain originated from F344</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1547867</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 4&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1547867</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 4 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1547868</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 2&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1547868</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 2 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1547869</RGD_ID>
    <STRAIN_SYMBOL>ACI/Eur</STRAIN_SYMBOL>
    <FULL_NAME>August x Copenhagen Irish</FULL_NAME>
    <ORIGINATION>Department of Pediatric Surery, Erasmus Medical Center, Rotterdam, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1547869</CITATION_ID>
    <DESCRIPTION>Curtiss and Dunning 1926 at the Columbia University Institute for Cancer Research. To Heston 1945 at F30, to National Institutes of Health 1950 at F41. Subsequent sublines from Dunning or NIH</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1547870</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 14&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1547870</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 14 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1547871</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Rat324-D1Rat156&lt;/i&gt;)/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pediatric Surgery, Erasmus Medical Center, Rotterdam, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="223506828" STOP_POS="223507030" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="243853559" STOP_POS="243853760" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="251109240" STOP_POS="279213254" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="229301063" STOP_POS="253410500" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1547871</CITATION_ID>
    <DESCRIPTION>Congenic strain created from backcrossing ACI/Eur and FHH/Eur parental strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1547872</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr X&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME>FHH-Chr X&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</FULL_NAME>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1547872</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome X introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1547873</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 15&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1547873</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 15 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1547874</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr Y&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME>FHH-Chr Y&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</FULL_NAME>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1547874</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome Y introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1547875</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D17Rat117-D17Arb5&lt;/i&gt;)(&lt;i&gt;D17Rat180-D17Rat51&lt;/i&gt;)/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pediatric Surgery, Erasmus Medical Center, Rotterdam, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="25188284" STOP_POS="25188477" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="24982652" STOP_POS="58691962" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="25609692" STOP_POS="65831023" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="27537443" STOP_POS="67580933" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="31007408" STOP_POS="69257442" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1547875</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from backcrossing ACI/Eur and FHH/Eur parental strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1547876</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 10&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1547876</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 10 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549794</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D2Rat199-D2Mco17&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre Hospitalier de l'Universite de Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="42977386" STOP_POS="42977529" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="154786975" STOP_POS="154787045" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="46603085" STOP_POS="46603120" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="41243963" STOP_POS="74997963" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="41179255" STOP_POS="75896315" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="154125111" STOP_POS="154125180" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="60242455" STOP_POS="95618891" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="221211532" STOP_POS="221211601" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="157987925" STOP_POS="157987994" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="41032071" STOP_POS="76020140" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549794</CITATION_ID>
    <DESCRIPTION>Congenic strain was created from a SS/Jr parental strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549795</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D2Rat199-D2Rat143&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre Hospitalier de l'Universite de Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="42977386" STOP_POS="105448034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="41243963" STOP_POS="103519040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="41179255" STOP_POS="106156987" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="60242455" STOP_POS="125885146" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="41032071" STOP_POS="106236206" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549795</CITATION_ID>
    <DESCRIPTION>Congenic strain was created from a SS/Jr parental strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549796</RGD_ID>
    <STRAIN_SYMBOL>BN/2Hok</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=67 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=67 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549796</CITATION_ID>
    <DESCRIPTION>Transferred from Hokkaido University, Chromosome Research Unit, 1987 F16</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549797</RGD_ID>
    <STRAIN_SYMBOL>BUF.ACI-(&lt;i&gt;D16Rat31-D16Arb1&lt;/i&gt;)/Ncc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=171 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=171 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="8089205" STOP_POS="84186211" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="8082906" STOP_POS="8083107" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="9055590" STOP_POS="9055792" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="11019972" STOP_POS="11020174" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="8340080" STOP_POS="8340453" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549797</CITATION_ID>
    <DESCRIPTION>This congenic strain in the BUF background that has homozygous ACI chr16 was developed by the speed congenic method.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549798</RGD_ID>
    <STRAIN_SYMBOL>BB.PVG-&lt;i&gt;RT1&lt;/i&gt;&lt;sup&gt;u/a&lt;/sup&gt;/Tky</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=31 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=31 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549798</CITATION_ID>
    <DESCRIPTION>A congenic strain with the genetic background of the BB/WorTky strain (RT1.B&lt;sup&gt;u&lt;/sup&gt;,D&lt;sup&gt;u&lt;/sup&gt; ) onto which the MHC locus of PVG.R23 strain (RT1.B&lt;a&gt;,D&lt;a&gt;) has been transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549799</RGD_ID>
    <STRAIN_SYMBOL>BB.SHR-&lt;i&gt;(D6Rat184-D6Rat3)&lt;/i&gt;/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=517 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=517 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="122236101" STOP_POS="122236199" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="116506292" STOP_POS="138922889" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="121224054" STOP_POS="145868598" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="130448688" STOP_POS="154782041" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="121381065" STOP_POS="145279536" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549799</CITATION_ID>
    <DESCRIPTION>Congenic BB.6S rats were established by cross of BB/OK and SHR/Mol rats and repeated backcrossing onto BB/OK rats in 2000.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549800</RGD_ID>
    <STRAIN_SYMBOL>BN/KunKtsSlc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>This strain is no longer available from NBRP-Rat (June 2022).</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2022-06-09)</AVAILABILITY>
    <RESEARCH_USE>Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549800</CITATION_ID>
    <DESCRIPTION>Kitasato University School of Medicine to Slc (2001)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549801</RGD_ID>
    <STRAIN_SYMBOL>BN/Seac</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Seac Yoshitomi, LTD, Fukuoka, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=421&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Behavior; Ophthalmology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549801</CITATION_ID>
    <DESCRIPTION>Seac Yoshitomi, LTD, Fukuoka, Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549802</RGD_ID>
    <STRAIN_SYMBOL>BN/1Hok</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=66 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=66 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549802</CITATION_ID>
    <DESCRIPTION>Transferred from Hokkaido University, Chromosome Research Unit, 1987 F15</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549803</RGD_ID>
    <STRAIN_SYMBOL>ACI-&lt;i&gt;Lyst&lt;/i&gt;&lt;sup&gt;bg-Kyo&lt;/sup&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=7 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=7 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Hematology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549803</CITATION_ID>
    <DESCRIPTION>Spontaneous mutation from ACI/NKyo inbred at Kyoto University in 1999.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549804</RGD_ID>
    <STRAIN_SYMBOL>BUF/NacJcl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Carcinogenesis Division, National Cancer Center Research Institute, Chuo-ku, Tokyo, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549804</CITATION_ID>
    <DESCRIPTION>CLEA Japan, Inc., Tokyo Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549805</RGD_ID>
    <STRAIN_SYMBOL>BUF.Cg-&lt;i&gt;Foxn1&lt;/i&gt;&lt;sup&gt;rnu&lt;/sup&gt;/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=459 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=459 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Urology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549805</CITATION_ID>
    <DESCRIPTION>BUF/Mna, NN1H-Rnu/Rnu</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549806</RGD_ID>
    <STRAIN_SYMBOL>BUF.ACI-(&lt;i&gt;D3Rat56-D3Rat83&lt;/i&gt;)/Ncc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Carcinogenesis Division, National Cancer Center Research Institute, Chuo-ku, Tokyo, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=167&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="28625339" STOP_POS="28625536" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="8227194" STOP_POS="45391731" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="2631421" STOP_POS="46996487" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="2612834" STOP_POS="52104192" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="3577905" STOP_POS="42635088" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549806</CITATION_ID>
    <DESCRIPTION>This strain was produced by speed congenic methods in which several generations of backcrossing were carried out in order to transfer the ACI chromosome 3 region into the BUF/Nac background recipient strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549808</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;Prlr-D2Rat143&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre Hospitalier de l'Universite de Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prlr</ALLELES>
    <ALLELE_RGD_IDS>3407</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="60861391" STOP_POS="105448034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="59134147" STOP_POS="103519040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="60131410" STOP_POS="106156987" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="84360850" STOP_POS="125885146" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="59507966" STOP_POS="106236206" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549808</CITATION_ID>
    <DESCRIPTION>Congenic strain was created from a SS/Jr parental strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549809</RGD_ID>
    <STRAIN_SYMBOL>BN/KtsSlc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>This strain is no longer available from NBRP-Rat (June 2022).</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2022-06-09)</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549809</CITATION_ID>
    <DESCRIPTION>Kitasato University School of Medicine to Slc (2002)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549810</RGD_ID>
    <STRAIN_SYMBOL>AI/Msik</STRAIN_SYMBOL>
    <FULL_NAME>amelogenesis imperfecta rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=443 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=443 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Dentistry</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549810</CITATION_ID>
    <DESCRIPTION>This strain is originated from female rats showing white incisors of an SD rat colony purchased from Charles River Japan, Inc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549811</RGD_ID>
    <STRAIN_SYMBOL>ACI/NJcl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Carcinogenesis Division, National Cancer Center Research Institute, Chuo-ku, Tokyo, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=546&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549811</CITATION_ID>
    <DESCRIPTION>ACI/N rats that were purchased from CLEA Japan, Inc., Tokyo Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1549813</RGD_ID>
    <STRAIN_SYMBOL>F344.ACI-&lt;i&gt;Lmx1a&lt;sup&gt;qc&lt;/sup&gt;&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Laboratory Animals at Kyoto University, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=2&amp;StrainsDir=Asc&amp;StrainsPageSize=20&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2020-11-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Apoa2|Selp|Lmx1a</ALLELES>
    <ALLELE_RGD_IDS>2131|3656|1304784</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="79009379" STOP_POS="86178819" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="76476229" STOP_POS="83646358" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="82428914" STOP_POS="89598805" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="87308435" STOP_POS="94225670" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="79886614" STOP_POS="87116372" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1549813</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrosses between ACI/Pas and F344/NSlc strains. The short-tail mutation, âqueue courteâ in French (with qc as a symbol), occurred spontaneously in 1994, in the ACI/Pas inbred strain of rat maintained at the Institute Pasteur (Paris, France), and was kept segregating in this stock. Since importation into the Institute of Laboratory Animals at Kyoto University, it has been maintained as a congenic strain F344.ACI-qc using F344/NSlc as an inbred partner.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1554301</RGD_ID>
    <STRAIN_SYMBOL>WKHA/Bord</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Universite Victor Segalen Bordeaux 2, Bordeaux cedex, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1554301</CITATION_ID>
    <DESCRIPTION>Strain was originated from WHHA/Edh at the University of Vermont College of Medicine</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1554302</RGD_ID>
    <STRAIN_SYMBOL>HOB-&lt;I&gt;Unc5c&lt;sup&gt;hob&lt;/sup&gt;&lt;/I&gt;/Snk</STRAIN_SYMBOL>
    <FULL_NAME>hobble rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=545 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=545 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Unc5c|Unc5c&lt;sup&gt;hob&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>735109|12802353</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="233141456" STOP_POS="233141457" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="230468188" STOP_POS="230468189" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="247330560" STOP_POS="247330561" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="265573406" STOP_POS="265926229" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="239365109" STOP_POS="239721231" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1554302</CITATION_ID>
    <DESCRIPTION>Homozygous hobble rats that were taken from the inbred hobble rat colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1554303</RGD_ID>
    <STRAIN_SYMBOL>CVD/Opu</STRAIN_SYMBOL>
    <FULL_NAME>Cerebellar vermis defect rat</FULL_NAME>
    <ORIGINATION>Department of Veterinary Pathology, Osaka Prefecture University, Sakai, Osaka, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Unc5c</ALLELES>
    <ALLELE_RGD_IDS>735109</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1554303</CITATION_ID>
    <DESCRIPTION>Originated from a colony of Lewis rats that were spontaneously ataxic. Maintained by brother-sister mating with phenotypically normal littermates.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1554304</RGD_ID>
    <STRAIN_SYMBOL>GAERS/Mave</STRAIN_SYMBOL>
    <FULL_NAME>Genetic Absence Epilepsy Rats from Strasbourg</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=557 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=557 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1554304</CITATION_ID>
    <DESCRIPTION>30% of the Wistar rats from the initial breeding colony in Strasbourg had spontaneous spike and wave discharges (SWDs) which were bilateral and synchronous over the cerebral cortex. Breeders with SWDs were selected and used for breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1554305</RGD_ID>
    <STRAIN_SYMBOL>DA-Tg(CAG-lacZ)30Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=531 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=531 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00295</CITATION_ID>
    <DESCRIPTION>lacZ cDNA was inserted in the EcoRI site of the pCAGGS expression vector. This DNA was microinjected into the DA/Crlj. The expression of the transgene was determined by beta-gal staining.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1554306</RGD_ID>
    <STRAIN_SYMBOL>GK/Slc</STRAIN_SYMBOL>
    <FULL_NAME>Goto Kakizaki Rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=377 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=377 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1554306</CITATION_ID>
    <DESCRIPTION>Spontaneous mutant GK rat which were obtained from Japan SLC, Inc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1554307</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(LAC3)Ys</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>YS New Technology Institute, Tochigi, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1554307</CITATION_ID>
    <DESCRIPTION>These transgenic rats are produced by the intracytoplasmic sperm injection (ICSI) using a Piezo-driven micromanipulator. This tranasgenic line carries a single copy of 210 kb YAC gene that codes for human lactalbumin and thymidine kinase.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1554308</RGD_ID>
    <STRAIN_SYMBOL>Gunn-&lt;i&gt;Ugt1a1&lt;sup&gt;j&lt;/i&gt;&lt;/sup&gt;/Slc</STRAIN_SYMBOL>
    <FULL_NAME>Gunn</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=370 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=370 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Metabolism</RESEARCH_USE>
    <ALLELES>Ugt1a1&lt;sup&gt;j&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13432064</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1554308</CITATION_ID>
    <DESCRIPTION>Segregated inbred Gunn rat which were obtained from Japan SLC, Inc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1554309</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(CAG-GFP)184Ys</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=525 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=259&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=525 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=259&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00259</CITATION_ID>
    <DESCRIPTION>These transgenic rats are produced by the intracytoplasmic sperm injection (ICSI) using a Piezo-driven micromanipulator.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1554310</RGD_ID>
    <STRAIN_SYMBOL>DA-Tg(CAG-lacZ)19Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=530 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=294&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=530 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=294&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00294</CITATION_ID>
    <DESCRIPTION>lacZ cDNA was inserted in the EcoRI site of the pCAGGS expression vector. This DNA was microinjected into the DA/Crlj. The expression of the transgene was determined by beta-gal staining.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1556748</RGD_ID>
    <STRAIN_SYMBOL>F344/Snk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medicinal Safety Research Laboratories, Sankyo Co. Ltd., Shizuoka, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1556748</CITATION_ID>
    <DESCRIPTION>Medicinal Safety Research Laboratories, Sankyo Co. Ltd., Shizuoka, Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1558660</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Gene Diagonostics and Therapeutics, Research Institute, International Medical Center of Japan, Tokyo, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1558660</CITATION_ID>
    <DESCRIPTION>Substrain of SHRSP rats maintained at International Medical Center of Japan, Tokyo</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1558661</RGD_ID>
    <STRAIN_SYMBOL>WKY/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Gene Diagonostics and Therapeutics, Research Institute, International Medical Center of Japan, Tokyo, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1558661</CITATION_ID>
    <DESCRIPTION>Substrain of WKY rats maintained at International Medical Center of Japan, Tokyo</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1558662</RGD_ID>
    <STRAIN_SYMBOL>SHR/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Gene Diagonostics and Therapeutics, Research Institute, International Medical Center of Japan, Tokyo, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1558662</CITATION_ID>
    <DESCRIPTION>Substrain of SHR rats maintained at International Medical Center of Japan, Tokyo</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559030</RGD_ID>
    <STRAIN_SYMBOL>LEC-Tg(ATP7B)Tohm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=457 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=457 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559030</CITATION_ID>
    <DESCRIPTION>A 4.5 kb fragment of human ATP7B cDNA was blunt-end ligated into the pCXN2 vector that contained the CAG promoter to generate pCXN2ATP7B which was microinjected into the pronuclei of LEC/Crlj. The transgenic founders were identified by the PCR analysis of the tail-DNA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559031</RGD_ID>
    <STRAIN_SYMBOL>NE/Mave</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=558 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=558 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559031</CITATION_ID>
    <DESCRIPTION>The control strain of GAERS, free of any spontaneous spike and wave discharges.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559032</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D17Rat65-D17Chm2&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hosp Univ Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="87387778" STOP_POS="87388164" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="70973784" STOP_POS="82479847" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="74823053" STOP_POS="86731080" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="76483116" STOP_POS="88435496" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="82247891" STOP_POS="93930006" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559032</CITATION_ID>
    <DESCRIPTION>This congenic substrain contains a LEW/Crlc chromosome 17 segment transferred to the SS/Jr recipient strain; derived by crossing congenic strain SS.LEW-(&lt;I&gt;D17Rat65-Prl&lt;/i&gt;) with SS/Jr, F2 animals were screened with D17Rat65 and Prl to identify regions with crossovers within this chromosome 17 segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559033</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D17Rat65-Prl&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hosp Univ Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prl</ALLELES>
    <ALLELE_RGD_IDS>3403</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="38287355" STOP_POS="87388164" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="37859999" STOP_POS="82479847" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="39814236" STOP_POS="86731080" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="41720751" STOP_POS="88435496" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="44699101" STOP_POS="93930006" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559033</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a  LEW/Crlc chromosome 17 segment transferred to the SS/Jr recipient strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559034</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D17Chm14-D17Rat97&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hosp Univ Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="67019466" STOP_POS="67019705" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="62109333" STOP_POS="68784138" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="58467778" STOP_POS="72580782" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="60264084" STOP_POS="74265481" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="73041111" STOP_POS="80182186" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559034</CITATION_ID>
    <DESCRIPTION>This congenic substrain contains a LEW/CrlBR chromosome 17 segment transferred to the SS/Jr recipient strain; derived by crossing congenic strain SS.LEW-(&lt;I&gt;D17Rat65-Prl&lt;/i&gt;) with SS/Jr, F2 animals were screened with D17Rat65 and Prl to identify regions with crossovers within this chromosome 17 segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559035</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D17Chm14-D17Rat181&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hosp Univ Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="32104761" STOP_POS="32104921" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="31896010" STOP_POS="68784138" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="33208959" STOP_POS="72580782" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="35100574" STOP_POS="74265481" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="38257211" STOP_POS="80182186" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559035</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a LEW/Crlc chromosome 17 segment transferred to the SS/Jr recipient strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559036</RGD_ID>
    <STRAIN_SYMBOL>LEW/Jms</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=192 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=54&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=192 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=54&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2019-02-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00054</CITATION_ID>
    <DESCRIPTION>Lewis rats from Tokyo Medical Insitute to Seiwa Institute of Experimental Animals, Hydrocephalus was found the rats at F27 in 1980, these were sent to Dr. Yasutaka Noda at Center for Animal Experiments, Kurume University, The hydrocephalus rat strains have been maintained out by selective breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559037</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D17Chm9-D17Rat97&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hosp Univ Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="67019466" STOP_POS="67019705" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="62109333" STOP_POS="71774817" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="58467778" STOP_POS="75705622" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="60264084" STOP_POS="77361330" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="73041111" STOP_POS="83074398" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559037</CITATION_ID>
    <DESCRIPTION>This congenic substrain contains a LEW/Crlc chromosome 17 segment transferred to the SS/Jr recipient strain; derived by crossing congenic strain SS.LEW-(&lt;I&gt;D17Rat65-Prl&lt;/i&gt;) with SS/Jr, F2 animals were screened with D17Rat65 and Prl to identify regions with crossovers within this chromosome 17 segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559039</RGD_ID>
    <STRAIN_SYMBOL>ODS/Shi</STRAIN_SYMBOL>
    <FULL_NAME>Osteogenic disorder Shionogi</FULL_NAME>
    <ORIGINATION>Shionogi &amp; Co., Ltd. Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559039</CITATION_ID>
    <DESCRIPTION>Dr. Susumu Makino and his colleagues found several animals that had gait abnormalities among Wistar rats maintained at Shionogi Co. They named these animals osteogenic disorder (OD) rats because they exhibited prominent bone and joint abnormalities and systemic bleeding. Subsequent studies revealed that these symptoms were derived from an ascorbic acid (vitamin C) deficiency arising from defective gulonolactone oxidase (GLO) activity. This characteristic was confirmed to be the result of a mutation involving the autosomal single recessive gene od. Scurvy due to L-gulonolactone oxidase deficincy; phenotype normalizes if supplied with ascorbic acid 300mg/kg/d. od/od rats are more susceptible to dental caries as compared with +/+ rats, in only amoun parous females.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559040</RGD_ID>
    <STRAIN_SYMBOL>MD/Tama</STRAIN_SYMBOL>
    <FULL_NAME>myelin deficient rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=248 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=248 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559040</CITATION_ID>
    <DESCRIPTION>X-linked mutant of the Wistar rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559041</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/Ngsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=303 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=303 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Cardio Hypertension; Osteosis</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559041</CITATION_ID>
    <DESCRIPTION>Substrain of SHRSP developed by Prof. Okamoto at Kinki University, Japan in 1980.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559042</RGD_ID>
    <STRAIN_SYMBOL>SHR/Nig</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=286 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=286 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension; Pharmacology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559042</CITATION_ID>
    <DESCRIPTION>Originated in the SHR given from Prof. Okamoto at Kinki University, Japan in 1976.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559043</RGD_ID>
    <STRAIN_SYMBOL>MV/Opu</STRAIN_SYMBOL>
    <FULL_NAME>myelin vacuolation rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=187 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=187 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Atrn&lt;sup&gt;&lt;i&gt;mv&lt;/i&gt;&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>40902835</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559043</CITATION_ID>
    <DESCRIPTION>The myelin vacuolation rats showing body tremor were found in an outbred colony of Sprague-Dawley rats at Osaka Osaka Prefecture University in 1999.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559044</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D3Mco19-D3Mco5&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Edn3</ALLELES>
    <ALLELE_RGD_IDS>2534</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="166291690" STOP_POS="186012944" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="21089863" STOP_POS="21090040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="145871677" STOP_POS="145871858" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="153327515" STOP_POS="153327695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="27206010" STOP_POS="27206186" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="27325365" STOP_POS="27325541" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="158391833" STOP_POS="183008351" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="23312460" STOP_POS="23312636" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="147799021" STOP_POS="167653069" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559044</CITATION_ID>
    <DESCRIPTION>A region of chr 3 which contains the Edn3 gene was introgressed into the SS rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559045</RGD_ID>
    <STRAIN_SYMBOL>LEW/Crlc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Charles River Laboratories, La Salle, Quebec, Canada</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559045</CITATION_ID>
    <DESCRIPTION>LEW substrain obtained from Charles River Laboratories, La Salle, Quebec, Canada</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559046</RGD_ID>
    <STRAIN_SYMBOL>SHR-Chr Y&lt;sup&gt;W&lt;/sup&gt;/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=518 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=518 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559046</CITATION_ID>
    <DESCRIPTION>Consomic SHR rats were established by crossing of SHR females and one wild rat male captured in northern part of Germany. Male hybrids were repeatedly backcrossed onto SHR females replacing the chromosome Y of SHR/Mol by that of wild rats in 1996.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559047</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/Ezo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=357 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=357 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559047</CITATION_ID>
    <DESCRIPTION>Substrain of SHRSP maintained at Hokkaido University School of Medicine, Sapporo, Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1559048</RGD_ID>
    <STRAIN_SYMBOL>SHR.ODS-&lt;i&gt;Gulo&lt;sup&gt;od&lt;/sup&gt;&lt;/i&gt;/Shi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=114 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=114 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension; Osteosis</RESEARCH_USE>
    <ALLELES>Gulo</ALLELES>
    <ALLELE_RGD_IDS>620701</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1559048</CITATION_ID>
    <DESCRIPTION>A congenic strain developed from a recipient, SHR and a donor, ODS. The first generation was backcrossed to SHR and these rats were genotyped and the heterozygous rats were backcrossed to SHR to generate the congenics. Introduced to Nagoya University in 1995.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566430</RGD_ID>
    <STRAIN_SYMBOL>SimTac:LE</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.taconic.com/anmodels/longev.htm&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566430</CITATION_ID>
    <DESCRIPTION>Taconic Long Evans rats originated with Drs. Long and Evans in 1915 by a cross of several Wistar Institute white females with a wild grey male. Rederived in 1975 by Simonsen Laboratories from stock obtained from the University of California at Berkeley in 1949. Derived by Taconic in August 1998. Like all Taconic outbred rats, a monogamous mating system is used to maximize the heterozygosity of the stock.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566431</RGD_ID>
    <STRAIN_SYMBOL>BN/MolTac</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.taconic.com/anmodels/BN.htm&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566431</CITATION_ID>
    <DESCRIPTION>The BN/MolTac arrived at M&amp;B A/S in 1993 at F90 from the Zentralinstitut f?r Versuchstierzucht, Hannover, Germany (Han). It was rederived at Taconic, USA in 2003.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566432</RGD_ID>
    <STRAIN_SYMBOL>WKY/NMolTac</STRAIN_SYMBOL>
    <FULL_NAME>Wistar Kyoto</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.taconic.com/anmodels/wkyn1.htm&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566432</CITATION_ID>
    <DESCRIPTION>The inbred Wistar Kyoto rat was received at Taconic from M&amp;B A/S in 1998 at F61. M&amp;B (formerly Mollegaard) received the strain from the NIH Animal Genetic Resource in 1975 at F13. The NIH-stock was obtained in 1971 as non-inbred Wistar stock from the Kyoto School of Medicine. Cesarean derived in 1999, Taconics Foundation Colony of inbred WKYs is maintained in a plastic-film gnotbiotic isolator. Breeders from the FC are regularly transferred to Taconics WKY Production Colony which is maintained in an MPF Barrier Unit.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566433</RGD_ID>
    <STRAIN_SYMBOL>HanTac:WH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.taconic.com/anmodels/whgalas.htm&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566433</CITATION_ID>
    <DESCRIPTION>In 1989 RCC Ltd. of Switzerland obtained 156 breeding pairs of Wistar Hannovers from Dr. Willy Heine, Zentralinstitut f?r Versuchstierzucht (ZfV), Hannover, Germany. The stock was hysterectomy derived at RCC in 1989. Genetic drift in RCC?s colony of Wistar Hannovers is minimized through the use of the Poiley rotational breeding system and revitalization of the stock with cryopreserved embryos (most recent revitalization completed in 1998).Each Member of GALAS obtained in excess of fifty (50) Wistar Hannover breeders from RCC in late 1998. The line was cesarean derived in 1999 and Taconic replaced its former WH stock with the GALAS Wistar Hannover rat in June 2000.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566434</RGD_ID>
    <STRAIN_SYMBOL>NTac:SHR</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.taconic.com/anmodels/sponthyp.htm&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566434</CITATION_ID>
    <DESCRIPTION>Taconics original SHR breeding stock was obtained in 1972 at F35 from the NIH Animal Genetic Resource. The NIH colony was established with rats from Okamoto in 1966 at F13 (Okamoto, Kyoto School of Medicine, from Wistar Kyoto outbred stock). Cesarean derived in 1984, Taconics SHR is randomly bred in a closed colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566437</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr X&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566437</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566438</RGD_ID>
    <STRAIN_SYMBOL>DA/MolTac</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.taconic.com/anmodels/DA.htm&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566438</CITATION_ID>
    <DESCRIPTION>Developed at the Agricultural Research Council, Institute of Animal Physiology, Cambridge, UK; it then went to the Centralinstitut f?r Versuchstierzucht, Hannover, Germany (Han). From Han to M&amp;B in 1990. Inbreeding F + 17 (February 2000). Rederived at Taconic, USA in 2004.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566439</RGD_ID>
    <STRAIN_SYMBOL>F344/NTac</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.taconic.com/anmodels/F344.htm&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566439</CITATION_ID>
    <DESCRIPTION>Axenic breeders were obtained at F143 by Taconic in 1984 from the NIH Animal Genetic Resource. Origin of the strain is as follows: to NIH in 1951 from Heston; to Heston in 1949 from Curtis, Columbia University Institute for Cancer Research. To preserve genetic continuity, Taconics F344 foundation colony is maintained in gnotobiotic isolators and the strain is periodically reestablished with breeding pairs from NIH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566440</RGD_ID>
    <STRAIN_SYMBOL>NTac:SD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.taconic.com/rat-model/sprague-dawley&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566440</CITATION_ID>
    <DESCRIPTION>Taconic SD rats were first obtained in 1970 from the NIH Animal Genetic Resource. The NIH stock originated from Sprague Dawley, Inc. in 1945 and has since been maintained as an outbred closed colony. To maintain genetic continuity with the SDN:SD strain of NIH, Taconic continually receives axenic breeder stock from the NIH Animal Genetic Resource for systematic introduction into Taconics production colonies.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566443</RGD_ID>
    <STRAIN_SYMBOL>LEW/MolTac</STRAIN_SYMBOL>
    <FULL_NAME>Lewis</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.taconic.com/anmodels/Lewis_rat.htm&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566443</CITATION_ID>
    <DESCRIPTION>Scripps Clinic, La Jolla, California to the University of Pennsylvania; to Simonsen Laboratories in 1966 at F20; to the Institute of Pathological Anatomy, University of Copenhagen, Denmark in 1973 at F28. The Lewis rat was obtained from the University of Copenhagen by M&amp;B in 1977, and was received at Taconic, USA in 2002, where it was rederived.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566444</RGD_ID>
    <STRAIN_SYMBOL>MolTac:SD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.taconic.com/anmodels/SDMOL_rat.htm&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566444</CITATION_ID>
    <DESCRIPTION>The SD Hannover was developed at the National Institutes of Health, Bethesda, USA. It later went to the Zentralinstitut fur Versuchstierzucht, Hannover, Germany (Han) and was received by M&amp;B A/S in 1993.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566445</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;I&gt;D5Mgh17-D5Rat205&lt;/I&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Genetics, Cell Biology and Anatomy, University Of Nebraska Medical Center, Omaha, Nebraska</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="19327036" STOP_POS="160071397" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="14529225" STOP_POS="14529436" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="14408903" STOP_POS="14409113" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="19190627" STOP_POS="19190837" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="14730738" STOP_POS="14730949" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566445</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 5 transferred to the ACI/SegHsd strain background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566447</RGD_ID>
    <STRAIN_SYMBOL>GK/MolTac</STRAIN_SYMBOL>
    <FULL_NAME>Goto-Kakizaki</FULL_NAME>
    <ORIGINATION>&lt;a href=https://www.taconic.com/rat-model/goto-kakizaki&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.taconic.com/rat-model/goto-kakizaki&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566447</CITATION_ID>
    <DESCRIPTION>The Goto-Kakizaki inbred model was developed by Tohoku University in 1975. Aarhus University Hospital in Denmark received stock in 1994. M&amp;B A/S (now Taconic Europe) received stock from Aarhus in 1997. The rats were derived by embryo transfer in 2005 at Taconic US.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566448</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 9&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566448</CITATION_ID>
    <DESCRIPTION>A FHH genomic background with a BN chromosome 9 introgressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566453</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(HIV-LacZ)AngRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=49&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=49&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00049</CITATION_ID>
    <DESCRIPTION>Fertilized eggs were microinjected with 300-500 copies of DNA per egg which comprised of an insert (5,230 bp) containing U3R region, the lacZ gene and the SV 40 polyadenylation signal which was excised from the bacterial plasmid.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566454</RGD_ID>
    <STRAIN_SYMBOL>BDIV/Zte</STRAIN_SYMBOL>
    <FULL_NAME>BDIV/Zte</FULL_NAME>
    <ORIGINATION>Institute of Cell Biology (Cancer Research) of Duisburg-Essen University Medical School, Essen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566454</CITATION_ID>
    <DESCRIPTION>derived from Berlin-Druckrey strain BDIV</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566455</RGD_ID>
    <STRAIN_SYMBOL>HTX/HcjRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=50&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=50&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00050</CITATION_ID>
    <DESCRIPTION>Available at RRRC;these were originally bred by D. F. Kohn, Inst. of Comparative Medicine,Columbia University, New York. Then housed at University of Florida 1992 at F30.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566456</RGD_ID>
    <STRAIN_SYMBOL>BDIX/Zte</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cell Biology (Cancer Research) of Duisburg-Essen University Medical School, Essen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566456</CITATION_ID>
    <DESCRIPTION>derived from Berlin-Druckrey strain BDIX</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566457</RGD_ID>
    <STRAIN_SYMBOL>SPRD</STRAIN_SYMBOL>
    <FULL_NAME>Sprague-Dawley</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566457</CITATION_ID>
    <DESCRIPTION>From outbred Han:SPRD (Sprague-Dawley) rats. Dominant pelage mutation designatedcurly-3 (Cu3) occured in 1975 at the Gesellschaft fur Strahlenforschung, Dortmund, Germany.Mutant animals returned to Hannover where inbreeding begun in 1976 (Greenhouse et al 1990).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566458</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(ROSA26-ALPP)EpsRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=48&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=48&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-07-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>ALPP</ALLELES>
    <ALLELE_RGD_IDS>1314395</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00048</CITATION_ID>
    <DESCRIPTION>F344 embryos were microinjected with R26-hPAP trangene which comprises of 0.8 kb genomic sequence of ROSA 26 promoter fused to human placental alkaline phosphatase (hPAP, ALPP).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566459</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(ROSA26-EGFP)Eps</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pathobiological Sciences, University of Wisconsin-Madison, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1566459</CITATION_ID>
    <DESCRIPTION>F344 embryos were microinjected with R26-EGFP trangene which comprises of 0.8 kb genomic sequence of ROSA 26 promoter fused to enhanced green fluorescent protein (EGFP).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1566460</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(ICAM2-CD55)AngRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=51&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=51&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2025-11-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>CD55</ALLELES>
    <ALLELE_RGD_IDS>737499</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00051</CITATION_ID>
    <DESCRIPTION>Embryos were microinjected with DNA containing the human CD55 (DAF, decay-acceletating factor) gene under control of the human ICAM2 promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578692</RGD_ID>
    <STRAIN_SYMBOL>BN.LEW-(&lt;i&gt;D10Rat32-D10Rat116&lt;/i&gt;)/Ciml</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="52699004" STOP_POS="52699134" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="51779662" STOP_POS="52200160" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="53630865" STOP_POS="54057745" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="53381898" STOP_POS="53807373" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="53786347" STOP_POS="54220239" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578692</CITATION_ID>
    <DESCRIPTION>Congenic strain was bred from BN.LEW-(&lt;i&gt;D10Mco17-D10Mco14&lt;/i&gt;)/Ciml backcrossed to BN/Rj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578693</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Mco17-D10Rat221&lt;/i&gt;)/Ciml</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="44093097" STOP_POS="44093499" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="43593509" STOP_POS="43593911" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="45157430" STOP_POS="45157831" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="44914976" STOP_POS="44915377" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="45105978" STOP_POS="45106380" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578693</CITATION_ID>
    <DESCRIPTION>Congenic strain created from parental LEW/Rj and BN/Rj strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578694</RGD_ID>
    <STRAIN_SYMBOL>AT</STRAIN_SYMBOL>
    <FULL_NAME>Alcohol-Tolerant</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=76&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=76&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00076</CITATION_ID>
    <DESCRIPTION>The parents of the base stock were produced by crossbreeding female AA of the F22 generation of Wistar origin with Helsinki Zoo male albinos. AT rats are selectively bred  at ALKO in Finland for ethanol-induced ataxia on the inclined plane. These were moved 1998 to University of Colorado.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578695</RGD_ID>
    <STRAIN_SYMBOL>SHA/BruRrrc</STRAIN_SYMBOL>
    <FULL_NAME>Syracuse High Avoidance</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=68&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=68&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00068</CITATION_ID>
    <DESCRIPTION>Selective breeding of Long-Evans in active two-way shuttle box for high avoidance resulted in these SHA rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578696</RGD_ID>
    <STRAIN_SYMBOL>LAS1</STRAIN_SYMBOL>
    <FULL_NAME>Low Alcohol Sensitive strain 1</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=80&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=80&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00080</CITATION_ID>
    <DESCRIPTION>Selectively bred for 24 generations for low sensitivity to ethanol then inbred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578697</RGD_ID>
    <STRAIN_SYMBOL>BN.LEW-(&lt;i&gt;D10Rat32-D10Rat31&lt;/i&gt;)/Ciml</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="52110562" STOP_POS="52110694" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="51611529" STOP_POS="51779830" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="53465198" STOP_POS="53631032" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="53216481" STOP_POS="53382065" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="53616237" STOP_POS="53786515" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578697</CITATION_ID>
    <DESCRIPTION>Congenic strain was bred from BN.LEW-(&lt;i&gt;D10Rat32-D10Rat221&lt;/i&gt;)/Ciml backcrossed to BN/Rj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578698</RGD_ID>
    <STRAIN_SYMBOL>LAS2</STRAIN_SYMBOL>
    <FULL_NAME>Low Alcohol Sensitive strain 2</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=81&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=81&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00081</CITATION_ID>
    <DESCRIPTION>Selectively bred for 24 generations for low hypnotic response to high dose ethanol, then inbred</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578699</RGD_ID>
    <STRAIN_SYMBOL>BG</STRAIN_SYMBOL>
    <FULL_NAME>anemic Belgrade</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=72&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00072</CITATION_ID>
    <DESCRIPTION>These are descendants of the original Belgrade colony which was obtained by K. Kellar Centers forDisease Control and Prevention, Atlanta, GA. These were backcrossed with Harlan Sprague-Dawley Wistar and then amintained as a closed colony in Buffalo, NY.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578700</RGD_ID>
    <STRAIN_SYMBOL>HAS1</STRAIN_SYMBOL>
    <FULL_NAME>High Alcohol Sensitive strain 1</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=77&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=77&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00077</CITATION_ID>
    <DESCRIPTION>Selectively bred for high sensitivity for ethanol hypnosis for 24 generations then inbred</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578701</RGD_ID>
    <STRAIN_SYMBOL>HAS2</STRAIN_SYMBOL>
    <FULL_NAME>High Alcohol Sensitive strain 2</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=79&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=79&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00079</CITATION_ID>
    <DESCRIPTION>Selectively bred for high ethanol sensitivity for 24 generations, then inbred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578702</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Rat32-D10Rat133&lt;/i&gt;)/Ciml</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="64939013" STOP_POS="64939207" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="51779662" STOP_POS="51779830" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="53630865" STOP_POS="53631032" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="53381898" STOP_POS="64823355" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="53786347" STOP_POS="65668639" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578702</CITATION_ID>
    <DESCRIPTION>Congenic strain created from parental LEW/Rj and BN/Rj strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578703</RGD_ID>
    <STRAIN_SYMBOL>SLA/BruRrrc</STRAIN_SYMBOL>
    <FULL_NAME>Syracuse Low Avoidance</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=69&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=69&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00069</CITATION_ID>
    <DESCRIPTION>Selective breeding of Long-Evans in active two-way shuttle box for low avoidance resulted in these SLA rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578704</RGD_ID>
    <STRAIN_SYMBOL>WLP</STRAIN_SYMBOL>
    <FULL_NAME>Warsaw Low Prefering</FULL_NAME>
    <ORIGINATION>Department of Pharmacology and Physiology of the Nervous System, Institute of Psychiatry and Neurology, Sobieskiego 9, Warszawa, Poland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578704</CITATION_ID>
    <DESCRIPTION>These were bred from albino stock of Wistar rats as lines that had low ethanol preference.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578705</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Arb4-D10Rat133&lt;/i&gt;)/Ciml</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="64939013" STOP_POS="64939207" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="45274234" STOP_POS="45274336" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="46835584" STOP_POS="46835685" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="46591952" STOP_POS="64823355" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="46737116" STOP_POS="65668639" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578705</CITATION_ID>
    <DESCRIPTION>Congenic strain created from parental LEW/Rj and BN/Rj strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578706</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Mco17-D10Mco14&lt;/i&gt;)/Ciml</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="44093097" STOP_POS="44093499" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="43593509" STOP_POS="43593911" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="45157430" STOP_POS="45157831" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="44914976" STOP_POS="44915377" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="45105978" STOP_POS="45106380" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578706</CITATION_ID>
    <DESCRIPTION>Congenic strain created from parental LEW/Rj and BN/Rj strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578708</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Mgh7-D10Rat221&lt;/i&gt;)/Ciml</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="54597481" STOP_POS="54597696" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="54098674" STOP_POS="54098889" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="55978483" STOP_POS="55978697" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="55720558" STOP_POS="55720772" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="56170962" STOP_POS="56171177" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578708</CITATION_ID>
    <DESCRIPTION>Congenic strain created from parental LEW/Rj and BN/Rj strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578709</RGD_ID>
    <STRAIN_SYMBOL>IA</STRAIN_SYMBOL>
    <FULL_NAME>incisor absent</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=64&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=64&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00064</CITATION_ID>
    <DESCRIPTION>These rats have incisors and molars formed embryogically but are unable to erupt as no openings in the alveolar bone was created by selective resoption.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578710</RGD_ID>
    <STRAIN_SYMBOL>LEW.1AR1-&lt;I&gt;iddm&lt;/I&gt;/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute for Laboratory Animal Science, Hannover Medical School, Hanover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dock8&lt;sup&gt;m1Ztm&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13830868</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578710</CITATION_ID>
    <DESCRIPTION>arose through a spontaneous mutation in a congenic Lewis strain with a defined MHC haplotype (RT1.A&lt;SUP&gt;a&lt;/sup&gt;B/D&lt;SUP&gt;u&lt;/sup&gt;C&lt;SUP&gt;u&lt;/sup&gt;) in the intra-MHC recombinant inbred strain LEW.1AR1; mutation was discovered in Fx + 13 of the LEW.1AR1 and has been maintained as a separate strain since</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578711</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D10Mco17-D10Rat133&lt;/i&gt;)/Ciml</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="44093097" STOP_POS="64939207" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="43593509" STOP_POS="43593911" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="45157430" STOP_POS="45157831" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="44914976" STOP_POS="64823355" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="45105978" STOP_POS="65668639" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578711</CITATION_ID>
    <DESCRIPTION>Congenic strain created from parental LEW/Rj and BN/Rj strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578712</RGD_ID>
    <STRAIN_SYMBOL>BN.LEW-(&lt;i&gt;D10Mco17-D10Mco14&lt;/i&gt;)/Ciml</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="44093097" STOP_POS="44093499" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="43593509" STOP_POS="43593911" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="45157430" STOP_POS="45157831" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="44914976" STOP_POS="44915377" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="45105978" STOP_POS="45106380" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578712</CITATION_ID>
    <DESCRIPTION>Congenic strain created from parental LEW/Rj and BN/Rj strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578713</RGD_ID>
    <STRAIN_SYMBOL>BN/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute for Laboratory Animal Science, Hannover Medical School, Hanover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578713</CITATION_ID>
    <DESCRIPTION>substrain of BN</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578714</RGD_ID>
    <STRAIN_SYMBOL>BN.LEW-(&lt;i&gt;D10Mco17-D10Rat80&lt;/i&gt;)/Ciml</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="44093097" STOP_POS="59876693" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="43593509" STOP_POS="59378278" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="45157430" STOP_POS="61300905" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="44914976" STOP_POS="61030524" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="45105978" STOP_POS="61798393" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578714</CITATION_ID>
    <DESCRIPTION>Congenic strain created from parental LEW/Rj and BN/Rj strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578715</RGD_ID>
    <STRAIN_SYMBOL>ANT</STRAIN_SYMBOL>
    <FULL_NAME>Alcohol-Nontolerant</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=78&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=78&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gabra6</ALLELES>
    <ALLELE_RGD_IDS>61861</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00078</CITATION_ID>
    <DESCRIPTION>The parents of the base stock were produced by crossbreeding female AA of the F22 generation of Wistar origin with Helsinki Zoo male albinos. AT rats are selectively bred  at ALKO in Finland for ethanol-induced ataxia on the inclined plane. These were moved 1998 to University of Colorado.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578716</RGD_ID>
    <STRAIN_SYMBOL>LEW.1AR1/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute for Laboratory Animal Science, Hannover Medical School, Hanover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578716</CITATION_ID>
    <DESCRIPTION>Lewis strain containing MHC haplotype &lt;i&gt;RT1.A&lt;SUP&gt;a&lt;/sup&gt;B/D&lt;SUP&gt;u&lt;/sup&gt;C&lt;SUP&gt;u&lt;/sup&gt;&lt;/i&gt;</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1578717</RGD_ID>
    <STRAIN_SYMBOL>WHP</STRAIN_SYMBOL>
    <FULL_NAME>Warsaw High Prefering</FULL_NAME>
    <ORIGINATION>Department of Pharmacology and Physiology of the Nervous System, Institute of Psychiatry and Neurology, Sobieskiego 9, Warszawa, Poland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1578717</CITATION_ID>
    <DESCRIPTION>These were bred from albino stock of Wistar rats as lines that had ethanol preference.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579677</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Madd&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Madd&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578796</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="97570141" STOP_POS="97613688" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="77114330" STOP_POS="77157865" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="79960301" STOP_POS="80003023" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="86669054" STOP_POS="86711776" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="75498321" STOP_POS="75541073" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579677</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. G120R mutation is generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579678</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D3Wox2-D3Rat59&lt;/i&gt;)/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pediatric Surgery, Erasmus Medical Center, Rotterdam, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="69571327" STOP_POS="69571486" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="49162911" STOP_POS="161299569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="50533100" STOP_POS="170534769" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="57173123" STOP_POS="176609927" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="46419462" STOP_POS="163443738" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579678</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from backcrossing ACI/Eur and FHH/Eur parental strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579680</RGD_ID>
    <STRAIN_SYMBOL>Wild/Tku</STRAIN_SYMBOL>
    <FULL_NAME>Wild</FULL_NAME>
    <ORIGINATION>Caught in Tokyo</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>wild</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579680</CITATION_ID>
    <DESCRIPTION>These rats were caught wild in Tokyo, Japan, used for experiments and then sacrificed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579681</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Birc3&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Birc3&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578788</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="13285702" STOP_POS="13313329" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="5000844" STOP_POS="5028470" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="6048590" STOP_POS="6076828" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="6047454" STOP_POS="6075236" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="4682202" STOP_POS="4696856" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579681</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations.W76G mutation is generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579682</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Tlr4&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=411&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tlr4&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578785</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="85161247" STOP_POS="85174882" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="80145867" STOP_POS="80159501" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="82587424" STOP_POS="82601056" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="86690670" STOP_POS="86704302" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="83564100" STOP_POS="83577735" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00411</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. V489A mutation is generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579683</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Ghsr&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=405&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ghsr&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578794</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="112200211" STOP_POS="112200211" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="110271542" STOP_POS="110271542" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="113069938" STOP_POS="113069938" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="132784207" STOP_POS="132789319" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="113269623" STOP_POS="113272999" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00405</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. codon CAG/TAG mutation is generated which changes the AA Q343Stop.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579684</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Slc8a2&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=404&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc8a2&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578786</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="85944752" STOP_POS="85982900" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="76816583" STOP_POS="76852928" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="78029555" STOP_POS="78054042" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="79296259" STOP_POS="79320746" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="76473938" STOP_POS="76498624" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00404</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. Y213Stop mutation is generated from the codon change TAT/TAA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579685</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Tgfbr2&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=400&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tgfbr2&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578782</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="124672677" STOP_POS="124761741" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="115794537" STOP_POS="115883615" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="124310288" STOP_POS="124399345" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="123585765" STOP_POS="123671209" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="120593595" STOP_POS="120680453" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00400</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. E311K mutation is generated from the codon change GAG/AAG.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579686</RGD_ID>
    <STRAIN_SYMBOL>GH/OmrMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579686</CITATION_ID>
    <DESCRIPTION>This colony was established from rats of Wistar origin. This is an hysterectomy-derived colony at the University of Otago, which was established from the Wellcome Institute colony at generation 79. These have been inbred for over 90 generations. These were given to Dr. Howard Jacob in 1999 and have been bred in Medical College of Wisconsin since then.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579687</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Proc&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=410&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Proc&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578790</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="24038596" STOP_POS="24049061" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="23764367" STOP_POS="23774816" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="24918402" STOP_POS="24928822" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="24633206" STOP_POS="24643623" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="24563368" STOP_POS="24573715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00410</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. L312P mutation is generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579688</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Tgfbr2&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tgfbr2&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578800</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="124672677" STOP_POS="124761741" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="115794537" STOP_POS="115883615" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="124310288" STOP_POS="124399345" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="123585765" STOP_POS="123671209" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="120593595" STOP_POS="120680453" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579688</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. T289M mutation is generated from the codon change ACG/ATG.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579689</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;F10&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=401&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>F10&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578783</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="83170973" STOP_POS="83190280" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="76468834" STOP_POS="76488141" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="81803169" STOP_POS="81822476" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="81288536" STOP_POS="81307842" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="81327237" STOP_POS="81346544" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00401</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. V453G mutation is generated from the codon change GTC/GGC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579690</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Slc27a5&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc27a5&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578799</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="82688742" STOP_POS="82699335" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="73616556" STOP_POS="73627149" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="65576599" STOP_POS="65587192" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="66387832" STOP_POS="66398425" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="72924630" STOP_POS="72935223" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579690</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. K196Stop is generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579691</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D11Mgh3-D11Rat31&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="21646456" STOP_POS="21646608" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="8200022" STOP_POS="66422316" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="6673351" STOP_POS="69649875" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="10373455" STOP_POS="72739854" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="8176272" STOP_POS="68234949" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579691</CITATION_ID>
    <DESCRIPTION>Congenic strain from the parental SS/Jr and SHR/NHsd inbred strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579692</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Lcat&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=402&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lcat&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578793</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="50744598" STOP_POS="50748064" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="33834748" STOP_POS="33838214" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="37913333" STOP_POS="37916799" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="48780364" STOP_POS="48783830" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="35781507" STOP_POS="35784966" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00402</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. H353L mutation is generated from the codon change CAC/CTC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579693</RGD_ID>
    <STRAIN_SYMBOL>T2DN/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology, Medical College of Wisconsin, Milwaukee Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579693</CITATION_ID>
    <DESCRIPTION>Generated by crossing GK/Swe with female FHH/EurMcwi. During the F1 studies, the GK/Swe started to die out. In order to preserve the GK strain, single male GK was serially crossed to the ongoing GK-FHH cross. This resulted in rapid fixation of the original GK genome except for mitochondrial DNA. In the sixth generation male and female T2DN were intercrossed and strict b x s mating was maintained.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579694</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Egln3&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=409&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Egln3&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578781</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="77385549" STOP_POS="77411015" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="71650297" STOP_POS="71675766" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="75050329" STOP_POS="75075795" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="84592894" STOP_POS="84618360" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="74451038" STOP_POS="74476506" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00409</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations.  E60G mutation is generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579695</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Rat298-D1Rat90&lt;/i&gt;)/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pediatric Surgery, Erasmus Medical Center, Rotterdam, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="229359117" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="219932573" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="240017117" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="247303036" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="225625031" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579695</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from backcrossing ACI/Eur and FHH/Eur parental strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579696</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D6Wox13-D6Rat84&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="39571146" STOP_POS="136550638" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="130729205" STOP_POS="130729475" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="136142742" STOP_POS="136143011" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="144273721" STOP_POS="144273990" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="136451997" STOP_POS="136452267" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579696</CITATION_ID>
    <DESCRIPTION>Congenic strain from the parental SS/Jr and SHR/NHsd inbred strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579697</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D13Rat63-D13Mit1&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="6002008" STOP_POS="6002173" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="5994668" STOP_POS="77046890" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="9016742" STOP_POS="82995671" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="14281836" STOP_POS="87877411" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="25430110" STOP_POS="80482429" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579697</CITATION_ID>
    <DESCRIPTION>Congenic strain from the parental SS/Jr and SHR/NHsd inbred strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579698</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Adra1a&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=408&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adra1a&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578792</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="45005648" STOP_POS="45111416" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="40830125" STOP_POS="40935902" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="43296997" STOP_POS="43398314" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="48197628" STOP_POS="48297316" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="46173429" STOP_POS="46263198" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00408</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. G393V mutation is generated on rat Adra1a.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579699</RGD_ID>
    <STRAIN_SYMBOL>WKY.WKHA-(&lt;I&gt;D5Rat45-D5Rat245&lt;/I&gt;)/Cfd</STRAIN_SYMBOL>
    <FULL_NAME>WKY.WKHA-(&lt;I&gt;D5Rat45-D5Rat245&lt;/I&gt;)/Cfd</FULL_NAME>
    <ORIGINATION>Experimental Cardiovascular Biology Laboratory, Institut de Recherches Cliniques de Montreal, 119 Pine Ave W, Montreal, Quebec CA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="167181623" STOP_POS="167181764" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="152630083" STOP_POS="152630236" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="158854038" STOP_POS="158854190" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="162571275" STOP_POS="162571427" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="159265355" STOP_POS="159265706" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579699</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of WKHA/Cfd chromosome 5 transferred to the WKY/Cfd strain background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579700</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Rat475-D1Rat90&lt;/i&gt;)(&lt;i&gt;D3Rat84-D3Rat59&lt;/i&gt;)/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pediatric Surgery, Erasmus Medical Center, Rotterdam, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579700</CITATION_ID>
    <DESCRIPTION>Double congenic strain from backcross of ACI.FHH-(&lt;i&gt;D1Rat298-D1Rat90&lt;/i&gt;)/Eur and ACI.FHH-(&lt;i&gt;D3Wox2-D3Rat59&lt;/i&gt;)/Eur.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579701</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Nos1&lt;sup&gt;m1&lt;/i&gt;Mcwi&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nos1&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578795</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="44276011" STOP_POS="44456371" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="38615111" STOP_POS="38795492" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="44214949" STOP_POS="44405530" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="46049288" STOP_POS="46209569" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="39812500" STOP_POS="39869484" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579701</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. L72Stop mutation is generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579702</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Wox16-D9Rat64&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="98538372" STOP_POS="98538577" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="25268044" STOP_POS="91090963" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="29075079" STOP_POS="97647719" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="27914255" STOP_POS="97338238" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="21667066" STOP_POS="21667256" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579702</CITATION_ID>
    <DESCRIPTION>Congenic strain from the parental SS/Jr and SHR/NHsd inbred strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579703</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D2Rat61-D2Mco18&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="80396034" STOP_POS="220931416" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="78665619" STOP_POS="78665763" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="79924734" STOP_POS="79925127" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="68865414" STOP_POS="80632096" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="88594475" STOP_POS="100298539" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="79796833" STOP_POS="227150249" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579703</CITATION_ID>
    <DESCRIPTION>Congenic strain from the parental SS/Jr and SHR/NHsd inbred strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579704</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Agtr1b&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Rat Resource &amp; Research Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-11-29)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Agtr1b&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578784</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="104774005" STOP_POS="104849262" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="102844969" STOP_POS="102920232" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="105149020" STOP_POS="105224335" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="124879262" STOP_POS="124954378" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="105503269" STOP_POS="105602591" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579704</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females.  The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. A 3bp deletion generates a mutation at TTC (del251F)of rat Agtr1b.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579705</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Nr0b2&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=403&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nr0b2&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578798</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="151063160" STOP_POS="151066475" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="145779294" STOP_POS="145782609" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="151776004" STOP_POS="151779319" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="155465275" STOP_POS="155468590" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="151524685" STOP_POS="151528000" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00403</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. G96R mutation is generated from the codon change GGC/CGC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579706</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Nr4a1&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nr4a1&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578791</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="134263716" STOP_POS="134263716" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="132384969" STOP_POS="132384969" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="142915889" STOP_POS="142915889" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="140700242" STOP_POS="140721073" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="140012807" STOP_POS="140020590" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579706</CITATION_ID>
    <DESCRIPTION>Male founders (FHH/EurMcwi) were injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups were genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. Y130Stop mutation was generated from the codon change TAC/TAA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579707</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Adipoq&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=407&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adipoq&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578797</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="91226524" STOP_POS="91240244" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="77721912" STOP_POS="77735644" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="81330845" STOP_POS="81344488" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="84363940" STOP_POS="84382663" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="79908291" STOP_POS="79911065" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00407</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations.  I164N mutation is generated in rat Adipoq.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579708</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Des&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Des&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578801</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="84299626" STOP_POS="84307344" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="76850979" STOP_POS="76858695" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="82556574" STOP_POS="82564288" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="82325835" STOP_POS="82333549" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="74637783" STOP_POS="74645499" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579708</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. S25T mutation is generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579709</RGD_ID>
    <STRAIN_SYMBOL>Wild/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME>Wild</FULL_NAME>
    <ORIGINATION>Caught in Milwaukee Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>wild</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579709</CITATION_ID>
    <DESCRIPTION>These rats were caught wild in Milwaukee, used for experiments and then sacrificed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579710</RGD_ID>
    <STRAIN_SYMBOL>GK/Far</STRAIN_SYMBOL>
    <FULL_NAME>Goto-Kakizaki</FULL_NAME>
    <ORIGINATION>James A. Haley Veterans Hospital, Tampa Florida</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579710</CITATION_ID>
    <DESCRIPTION>Generated by selective brother x sister breeding of 18 non-diabetic Jcl:Wistar rats which were glucose intolerant on oral glucose tolerant tests. This colony is from F36 generation of the Japanese colony provided by Drs. Suzuki and Toyota of Tokoku University , Sendai Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579711</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Adipoq&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=406&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adipoq&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578787</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="91226524" STOP_POS="91240244" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="77721912" STOP_POS="77735644" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="81330845" STOP_POS="81344488" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="84363940" STOP_POS="84382663" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="79908291" STOP_POS="79911065" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00406</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations.Y162C mutation is generated on rat Adipoq.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579712</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Klf6&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Klf6&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1578789</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="69449483" STOP_POS="69458478" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="64539456" STOP_POS="64548451" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="67887939" STOP_POS="67945052" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="69616967" STOP_POS="69674031" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="75578498" STOP_POS="75585072" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579712</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. V135G mutation is generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579894</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat204-D10Rat9&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="90904245" STOP_POS="95604677" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="90404397" STOP_POS="90404618" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="93662786" STOP_POS="93663006" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="93421499" STOP_POS="93421719" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="94837236" STOP_POS="99588446" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579894</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Rat119-D10Mgh1&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579895</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Bdkrb2&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bdkrb2&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1579889</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="130237055" STOP_POS="130267205" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="124472317" STOP_POS="124502497" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="129399468" STOP_POS="129429676" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="138615812" STOP_POS="138622272" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="129744781" STOP_POS="129748851" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579895</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females.  The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. I214T mutation is generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579896</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D2Rat18-D2Chm277&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre Hospitalier de l'Universite de Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="41125789" STOP_POS="56532139" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="41063439" STOP_POS="56736627" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="60126669" STOP_POS="76472773" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="40912197" STOP_POS="56722286" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579896</CITATION_ID>
    <DESCRIPTION>Congenic strain was created from a SS/Jr parental strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579897</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Rat69-D9Mco14&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Cardiovascular Genomics, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="76821248" STOP_POS="76821368" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="69371595" STOP_POS="76650886" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="74858383" STOP_POS="82356286" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="74640722" STOP_POS="82125547" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="66679876" STOP_POS="74437140" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579897</CITATION_ID>
    <DESCRIPTION>A congenic strain derived from the progenitor strains SS and SR.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579898</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Chm128-D10Chm121&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="67232398" STOP_POS="68082614" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="69638898" STOP_POS="70499629" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="69272915" STOP_POS="71014829" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="70486334" STOP_POS="71365656" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579898</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Wox51-D10Rat27&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579899</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Rat130-D5Rat31&lt;/i&gt;)/JrMcwi</STRAIN_SYMBOL>
    <FULL_NAME>SS.LEW-(&lt;i&gt;D5Rat130-D5Rat31&lt;/i&gt;)/JrMcwi</FULL_NAME>
    <ORIGINATION>Department of Physiology, Medical College of Wisconsin, Milwaukee</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="36460764" STOP_POS="36460903" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="31663789" STOP_POS="133011550" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="31926122" STOP_POS="138454239" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="36590997" STOP_POS="142265366" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="32701659" STOP_POS="139996194" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579899</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a LEW chromosome 5 segment transferred to the Dahl salt sensitive background. The strain was originally developed by Drs. Rapp and M. R. Garrett at the Medical University of Ohio and has also been maintained by brother-sister mating at the Medical College of Wisconsin for more than 20 generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579900</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Rat89-Resp18&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Resp18</ALLELES>
    <ALLELE_RGD_IDS>3555</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="82150867" STOP_POS="84220186" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="74701668" STOP_POS="76771824" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="80400409" STOP_POS="82477136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="80172493" STOP_POS="82246695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="72257996" STOP_POS="74558151" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579900</CITATION_ID>
    <DESCRIPTION>Congenic strain was created by backcrossing SR strain  into the parental Dahl Salt-sensitive (SS) strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579901</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Chm224-D10Chm6&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="72508825" STOP_POS="72509024" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="75001953" STOP_POS="76556637" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="75100237" STOP_POS="76438561" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="74705355" STOP_POS="76000447" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579901</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Wox51-D10Rat27&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579902</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Rat130-D5Rat108&lt;/i&gt;)/JrMcwi</STRAIN_SYMBOL>
    <FULL_NAME>SS.LEW-(&lt;i&gt;D5Rat130-D5Rat108&lt;/i&gt;)/JrMcwi</FULL_NAME>
    <ORIGINATION>Department of Physiology, Medical College of Wisconsin, Milwaukee</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="36460764" STOP_POS="133270832" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="31663789" STOP_POS="128034027" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="31926122" STOP_POS="133313852" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="36590997" STOP_POS="137108002" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="32701659" STOP_POS="134872385" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579902</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a LEW chromosome 5 segment transferred to the Dahl salt sensitive background.  The strain was originally developed by Drs. Rapp and M. R. Garrett at the Medical University of Ohio and has also been maintained by brother-sister mating at the Medical College of Wisconsin for more than 20 generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579903</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="93198590" STOP_POS="96620484" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="92698959" STOP_POS="96121100" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="95967019" STOP_POS="99492409" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="95701164" STOP_POS="99184250" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="97152234" STOP_POS="100633982" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579903</CITATION_ID>
    <DESCRIPTION>A congenic substrain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Rat119-D10Mgh1&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579904</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mgh11-D9Mco33&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Cardiovascular Genomics, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="83709133" STOP_POS="83709383" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="83212828" STOP_POS="83213078" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="86168841" STOP_POS="86169090" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="85965754" STOP_POS="85966003" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="86983905" STOP_POS="86984155" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579904</CITATION_ID>
    <DESCRIPTION>A congenic strain derived from the progenitor strains SS and SR.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579905</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Rat89-D9Mco27&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Cardiovascular Genomics, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="82150867" STOP_POS="82151090" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="73473293" STOP_POS="73473492" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="72976092" STOP_POS="72976291" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="74701668" STOP_POS="74701891" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="80400409" STOP_POS="80400631" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="75505821" STOP_POS="75506019" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="80172493" STOP_POS="80172715" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="74600366" STOP_POS="74600564" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="76477677" STOP_POS="76477875" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="72257996" STOP_POS="72258219" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579905</CITATION_ID>
    <DESCRIPTION>Congenic strain derived from parental strains SS and SR.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579906</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Adipoq&lt;sup&gt;m3Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=414&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adipoq&lt;i&gt;&lt;sup&gt;m3Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1579887</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="91226524" STOP_POS="91240244" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="77721912" STOP_POS="77735644" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="81330845" STOP_POS="81344488" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="84363940" STOP_POS="84382663" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="79908291" STOP_POS="79911065" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00414</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. L119P mutation is generated from the codon change CTG/CCG of rat Adipoq.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579907</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Chm128-D10Chm169&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="67232398" STOP_POS="67400546" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="69638898" STOP_POS="69809020" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="69272915" STOP_POS="69442411" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="70486334" STOP_POS="70654393" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579907</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Wox51-D10Rat27&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579908</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mco95-Resp18&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Cardiovascular Genomics, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Resp18</ALLELES>
    <ALLELE_RGD_IDS>3555</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="84213844" STOP_POS="84220186" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="75403227" STOP_POS="76771824" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="81100315" STOP_POS="82477136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="80867159" STOP_POS="82246695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="74551809" STOP_POS="74558151" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579908</CITATION_ID>
    <DESCRIPTION>A congenic strain derived from the progenitor strains SS and SR.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579909</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Fgl2&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fgl2&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1579885</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="14602762" STOP_POS="14608405" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="13710566" STOP_POS="13716207" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="10323598" STOP_POS="10329241" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="10315666" STOP_POS="10321309" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="9176333" STOP_POS="9181976" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579909</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females.  The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. A301S mutation is generated from the codon change GCA/TCA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579910</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Ccr2&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=399&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ccr2&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1579888</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="132611883" STOP_POS="132619106" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="123734465" STOP_POS="123742483" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="128892784" STOP_POS="128893905" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00399</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females.  The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. N117S mutation is generated from the codon change AAT/AGT.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579911</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Rat130-D5Rat72&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME>SS.LEW-(&lt;i&gt;D5Rat130-D5Rat72&lt;/i&gt;)/Mcwi</FULL_NAME>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="36460764" STOP_POS="120088957" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="31663789" STOP_POS="114973531" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="31926122" STOP_POS="119125145" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="36590997" STOP_POS="123028200" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="32701659" STOP_POS="120983466" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579911</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a LEW chromosome 5 segment transferred to the Dahl salt sensitive background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579912</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;F10&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=412&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>F10&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1579886</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="83170973" STOP_POS="83190280" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="76468834" STOP_POS="76488141" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="81803169" STOP_POS="81822476" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="81288536" STOP_POS="81307842" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="81327237" STOP_POS="81346544" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00412</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. C388 Stop mutation is generated from the codon change TGC/TGA</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579913</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Chm224-D10Chm222&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="73473293" STOP_POS="73473492" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="72976092" STOP_POS="72976291" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="75505821" STOP_POS="75506019" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="74600366" STOP_POS="76309841" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="74705355" STOP_POS="76477875" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579913</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Wox51-D10Rat27&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1579914</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mco30-D10Got92&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="73887148" STOP_POS="74372232" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="76420583" STOP_POS="77055888" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="73693979" STOP_POS="76919627" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="77547289" STOP_POS="77956387" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1579914</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Rat27-Igfbp4&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1580542</RGD_ID>
    <STRAIN_SYMBOL>PCK-&lt;i&gt;Pkhd1&lt;sup&gt;pck&lt;/i&gt;&lt;/sup&gt;/CrljCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/products-services/find-model/pck-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/products-services/find-model/pck-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pkhd1&lt;sup&gt;pck&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11535943</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1580542</CITATION_ID>
    <DESCRIPTION>This model of polycystic kidney disease showing both kidney and liver involvement was identified in a colony of CD rats from the Charles River Japan production facility. The identification of the Pkhd1 gene mutation was reported by Harris and associates in 2002. This autosomal recessive Pkhd1 gene mutation is a model of human autosomal-recessive polycystic kidney disease (ARPKD).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581616</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D15Rat23-D15Rat71&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME>DA.ACI-(&lt;i&gt;D15Rat23-D15Rat71&lt;/i&gt;)/Kini</FULL_NAME>
    <ORIGINATION>Center for Molecular Medicine, Department of Clinical Neuroscience, Neuroimmunology Unit, Karolinska Institutet, SE-17176 Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="84744662" STOP_POS="84744859" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="76003569" STOP_POS="78330139" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="83647062" STOP_POS="86002030" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="87155990" STOP_POS="89768452" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="83040937" STOP_POS="85456512" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581616</CITATION_ID>
    <DESCRIPTION>This congenic strain contains an ACI chromosome 15 segment transferred to the DA background strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581617</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Ubc-eGFP-RNAi:Dazl)16-13Gar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Texas Southwestern Medical Center, Dallas Texas</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581617</CITATION_ID>
    <DESCRIPTION>This transgenic strain was made by injecting the lentivirus vector into SD rat embryos. Founders were identified by PCR and then bred with wild-type SD rats. The vectors are derived from pLL3.7 and contains GFP and short hairpain RNA (shRNA)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581618</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max - Delbruck - Center for Molecular Medicine, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581618</CITATION_ID>
    <DESCRIPTION>This SHRSP colony as obtained from the original Japanese stock from Okamoto and Aoki in 1974 and is propagated by strict inbreeding. Now this colony is maintained at University of Heidelberg, Heidelburg, Germany.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581619</RGD_ID>
    <STRAIN_SYMBOL>BN.PD-(&lt;i&gt;D8Rat39-D8Rat35&lt;/i&gt;),SHR-(&lt;i&gt;D2Mit4-D2Rat28&lt;/i&gt;),SHR-(&lt;i&gt;D2Rat103-D2Rat107&lt;/i&gt;)/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581619</CITATION_ID>
    <DESCRIPTION>This triple congenic strain has two segments of chr 2 spanning 53 Mb(centromeric segment) and 92 Mb (telomeric segment) from SHR and a differential segment of chr 8 of PD/Cub introgressed into BN-&lt;i&gt;Lx&lt;/i&gt;.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581620</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mco61-D9Mco27&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Cardiovascular Genomics, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581620</CITATION_ID>
    <DESCRIPTION>A congenic strain derived from the progenitor strains SS and SR.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581621</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D15Rat6-D15Rat48&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME>DA.ACI-(&lt;i&gt;D15Rat6-D15Rat48&lt;/i&gt;)/Kini</FULL_NAME>
    <ORIGINATION>Center for Molecular Medicine, Department of Clinical Neuroscience, Neuroimmunology Unit, Karolinska Institutet, SE-17176 Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="61710951" STOP_POS="61711157" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="28030665" STOP_POS="55302115" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="33219101" STOP_POS="62301382" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="37103190" STOP_POS="65959514" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="32638412" STOP_POS="61161186" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581621</CITATION_ID>
    <DESCRIPTION>This congenic strain contains an ACI chromosome 15 segment transferred to the DA background strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581622</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Ubc-eGFP-RNAi:Dazl)17-9GarRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Texas Southwestern Medical Center, Dallas, Texas</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=318&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-08-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00318</CITATION_ID>
    <DESCRIPTION>This transgenic strain was made by injecting the lentivirus vector into SD rat embryos. Founders were identified by PCR and then bred with wild-type SD rats. The vectors are derived from pLL3.7 and contains GFP and short hairpain RNA (shRNA)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581623</RGD_ID>
    <STRAIN_SYMBOL>LA/Humd</STRAIN_SYMBOL>
    <FULL_NAME>low autotomy</FULL_NAME>
    <ORIGINATION>Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581623</CITATION_ID>
    <DESCRIPTION>Low Autotomy segregation line derived from Sabra (Wistar derived) outbred stock. Males and females of low autotomy scores were coupled randomly. After each generation pairs were randomly selected from the available offspring from different litters.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581624</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Lipe&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lipe&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1581495</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="90093433" STOP_POS="90112117" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="80965612" STOP_POS="80984313" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="82248031" STOP_POS="82266727" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="83511504" STOP_POS="83530200" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="80663791" STOP_POS="80682480" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581624</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. L347P mutation is generated from the codon change CTA/CCA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581625</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Hand1&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Hand1&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1581493</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="42507117" STOP_POS="42509684" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="42006646" STOP_POS="42009213" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="43250729" STOP_POS="43253296" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="43050068" STOP_POS="43052635" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="43423366" STOP_POS="43425933" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581625</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. S109G mutation is generated from the codon change AGC/GGC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581626</RGD_ID>
    <STRAIN_SYMBOL>FHL/EurMcwi</STRAIN_SYMBOL>
    <FULL_NAME>Fawn Hooded Low blood pressure</FULL_NAME>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581626</CITATION_ID>
    <DESCRIPTION>The low blood pressure colony was transferred from Erasmus University to Medical College of Wisconsin, Milwaukee, USA. FHL rats do not develop hypertension or renal damage.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581627</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm66-D5Uwm67&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="69927283" STOP_POS="76370048" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="71940894" STOP_POS="78777811" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="76105513" STOP_POS="82897734" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="73080117" STOP_POS="79919776" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581627</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Wox7-D5Uwm37&lt;/i&gt;).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581628</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D15Rat6-D15Rat13&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME>DA.ACI-(&lt;i&gt;D15Rat 6-D15Rat13&lt;/i&gt;)/Kini</FULL_NAME>
    <ORIGINATION>Center for Molecular Medicine, Department of Clinical Neuroscience, Neuroimmunology Unit, Karolinska Institutet, SE-17176 Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="42868433" STOP_POS="42868608" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="28030665" STOP_POS="38692741" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="33219101" STOP_POS="47814460" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="37103190" STOP_POS="51565184" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="32638412" STOP_POS="43772355" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581628</CITATION_ID>
    <DESCRIPTION>This congenic strain contains an ACI chromosome 15 segment transferred to the DA background strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581629</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Wox8-D5Uwm62&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="9895285" STOP_POS="9895442" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="5112159" STOP_POS="58973694" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="4525738" STOP_POS="60225339" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="4498411" STOP_POS="64739489" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="4291144" STOP_POS="61238981" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581629</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Wox7-D5Uwm37&lt;/i&gt;).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581630</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm63-D5Uwm64&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="60360575" STOP_POS="60360793" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="55564549" STOP_POS="60051321" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="56733010" STOP_POS="61370302" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="61271852" STOP_POS="65886550" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="57848236" STOP_POS="62299211" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581630</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Wox7-D5Uwm37&lt;/i&gt;).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581631</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm61-D5Uwm37&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="129163811" STOP_POS="129163982" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="80813116" STOP_POS="123935338" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="83268986" STOP_POS="128812854" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="87362775" STOP_POS="132652105" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="84434303" STOP_POS="130527490" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581631</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Wox7-D5Uwm37&lt;/i&gt;).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581632</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm65-D5Uwm60&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="63190890" STOP_POS="72943679" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="68395096" STOP_POS="75274687" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="72838045" STOP_POS="79426001" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="65553185" STOP_POS="76159022" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581632</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(D5Wox7-D5Uwm37).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581633</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D15Rat6-D15Rat71&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME>DA.ACI-(&lt;i&gt;D15Rat6-D15Rat71&lt;/i&gt;)/Kini</FULL_NAME>
    <ORIGINATION>Center for Molecular Medicine, Department of Clinical Neuroscience, Neuroimmunology Unit, Karolinska Institutet, SE-17176 Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="84744662" STOP_POS="84744859" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="28030665" STOP_POS="78330139" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="33219101" STOP_POS="86002030" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="37103190" STOP_POS="89768452" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="32638412" STOP_POS="85456512" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581633</CITATION_ID>
    <DESCRIPTION>This congenic strain contains an ACI chromosome 15 segment transferred to the DA background strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581634</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Adora2a&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adora2a&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1581476</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="13315270" STOP_POS="13332802" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="13315848" STOP_POS="13333386" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="14265251" STOP_POS="14282873" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="16449385" STOP_POS="16466147" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="13815719" STOP_POS="13834131" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581634</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. C249S mutation is generated from the codon change TGT/AGT of rat Adora2a.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581635</RGD_ID>
    <STRAIN_SYMBOL>WKY/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max - Delbruck - Center for Molecular Medicine, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581635</CITATION_ID>
    <DESCRIPTION>This WKY colony was obtained from the Japanese colony in 1974. Now this is maintained at University of Heidelberg, Heidelburg, Germany.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581636</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Cebpe&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cebpe&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1581494</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="32139716" STOP_POS="32141476" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="28169711" STOP_POS="28171471" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="33356119" STOP_POS="33357517" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="37241081" STOP_POS="37242479" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="32787946" STOP_POS="32789344" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581636</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. E37G mutation is generated from the codon change GAG/GGG.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581637</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Has1&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Has1&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1581477</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="67366460" STOP_POS="67378686" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="58693411" STOP_POS="58705653" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="59720612" STOP_POS="59732409" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="60640270" STOP_POS="60652067" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="56503365" STOP_POS="56516133" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581637</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. F55L mutation is generated from the codon change TTT/TTG.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581638</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D15Rat126-D15Rat71&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME>DA.ACI-(&lt;i&gt;D15Rat126-D15Rat71&lt;/i&gt;)/Kini</FULL_NAME>
    <ORIGINATION>Center for Molecular Medicine, Department of Clinical Neuroscience, Neuroimmunology Unit, Karolinska Institutet, SE-17176 Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="81856510" STOP_POS="84744859" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="75448637" STOP_POS="78330139" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="83094829" STOP_POS="86002030" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="86610850" STOP_POS="89768452" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="85456315" STOP_POS="85456512" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581638</CITATION_ID>
    <DESCRIPTION>This congenic strain contains an ACI chromosome 15 segment transferred to the DA background strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581639</RGD_ID>
    <STRAIN_SYMBOL>HAn/Humd</STRAIN_SYMBOL>
    <FULL_NAME>high autotomy new</FULL_NAME>
    <ORIGINATION>Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581639</CITATION_ID>
    <DESCRIPTION>Males and females of high autotomy scores from HA/Humd were coupled randomly. After each generation pairs were randomly selected from the available offspring from different litters.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581640</RGD_ID>
    <STRAIN_SYMBOL>HA/Humd</STRAIN_SYMBOL>
    <FULL_NAME>high autotomy</FULL_NAME>
    <ORIGINATION>Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581640</CITATION_ID>
    <DESCRIPTION>High Autotomy segregation line derived from Sabra (Wistar derived) outbred stock. Males and females of high autotomy scores were coupled randomly. After each generation pairs were randomly selected from the available offspring from different litters.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581641</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="74047272" STOP_POS="90450412" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="76401130" STOP_POS="93273395" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="80544432" STOP_POS="97315322" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="77277626" STOP_POS="94516069" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581641</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Wox7-D5Uwm37&lt;/i&gt;).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581642</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Ccr4&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ccr4&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1581492</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="123054505" STOP_POS="123060244" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="114176291" STOP_POS="114182033" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="122530152" STOP_POS="122535959" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="121843005" STOP_POS="121848545" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="118883148" STOP_POS="118884230" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581642</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. I133V mutation is generated from the codon change ATA/GTA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581643</RGD_ID>
    <STRAIN_SYMBOL>LAn/Humd</STRAIN_SYMBOL>
    <FULL_NAME>low autotomy new</FULL_NAME>
    <ORIGINATION>Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581643</CITATION_ID>
    <DESCRIPTION>Males and females of low autotomy scores from LA/Humd were coupled randomly. After each generation pairs were randomly selected from the available offspring from different litters.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581644</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Htr1a&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=413&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Htr1a&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1581496</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="38427169" STOP_POS="38431733" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="36693462" STOP_POS="36698026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="36246628" STOP_POS="36247896" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="55362662" STOP_POS="55363930" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="36434518" STOP_POS="36435786" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00413</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. C266Y mutation is generated from the codon change TGT/TAT.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1581645</RGD_ID>
    <STRAIN_SYMBOL>LL/Mav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratoire de Physiologie, 8 Avenue Rockfeller, 69373 Lyon Cedex 08, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1581645</CITATION_ID>
    <DESCRIPTION>In 1969 outbred Sprague-Dawley rats were selected for high systolic blood pressure using an indirect plethysmographic technique in pre-warmed unrestrained conscious rats. Three pairs were originally selected, and selection was continued with brother x sister mating. Strain LN was maintained as a normotensive control, and LL as a hypotensive strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1582184</RGD_ID>
    <STRAIN_SYMBOL>SR/JrHsd</STRAIN_SYMBOL>
    <FULL_NAME>Dahl Salt-Resistant</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href =http://www.envigo.com/products-services/research-models-services/models/research-models/rats/inbred/dahl-salt-sensitive-resistant-(rapp)-inbred-rat/sr-jrhsd/&gt;inotiv&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1582184</CITATION_ID>
    <DESCRIPTION>Substrain of Dahl SR, from a Sprague-Dawley outbred colony, selected for resistance to salt-induced hypertension (Dahl, 1962), from Dr. John P. Rapp, Medical College of Ohio, Toledo,Ohio; to Harlan in 1986.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1582185</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D3Mco36-D3Got166&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="163556062" STOP_POS="168974694" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="172850273" STOP_POS="177366660" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="178896560" STOP_POS="181074971" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="166484910" STOP_POS="171009778" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1582185</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D3Mco19-D3Mco5&lt;/i&gt;)/Jr rats were crossed with SS to yield F1, these heterozygous rats were intercrossed to obtain F2 which were screened to identify the SR-rat derived region, these were then crossed with SS to duplicate the recombinant chromosome</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1582186</RGD_ID>
    <STRAIN_SYMBOL>FHH.FHH.1&lt;sup&gt;BN&lt;/sup&gt;-(&lt;i&gt;D1Rat183-D1Rat76&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="138793931" STOP_POS="138794173" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="129384185" STOP_POS="224569684" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="137083889" STOP_POS="244992610" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="138077032" STOP_POS="252243871" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="131123181" STOP_POS="230411453" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1582186</CITATION_ID>
    <DESCRIPTION>FHH-1&lt;sup&gt;BN&lt;/sup&gt;/Mcwi was backcrossed with FHH/EurMcwi to generate these rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1582187</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D3Mco24-D3Got130&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="184014001" STOP_POS="184014201" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="147739514" STOP_POS="163596045" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="155586270" STOP_POS="172890235" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="160026579" STOP_POS="178936339" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="149822571" STOP_POS="166525892" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1582187</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D3Mco19-D3Mco5&lt;/i&gt;)/Jr rats were crossed with SS to yield F1, these heterozygous rats were intercrossed to obtain F2 which were screened to identify the SR-rat derived region, these were then crossed with SS to duplicate the recombinant chromosome</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1582188</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D3Mco36-D3Mco46&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=660&gt;Rat Resource and Research Center&lt;/a&gt;,</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="167003822" STOP_POS="168974694" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="175283587" STOP_POS="177366660" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="181074759" STOP_POS="181830490" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="168983202" STOP_POS="171009778" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00660</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D3Mco19-D3Mco5&lt;/i&gt;)/Jr rats were crossed with SS to yield F1, these heterozygous rats were intercrossed to obtain F2 which were screened to identify the SR-rat derived region, these were then crossed with SS to duplicate the recombinant chromosome</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1582189</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D3Mco39-D3Got130&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="147739514" STOP_POS="167914627" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="155586270" STOP_POS="176305870" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="160026579" STOP_POS="180014700" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="149822571" STOP_POS="149823173" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1582189</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D3Mco19-D3Mco5&lt;/i&gt;)/Jr rats were crossed with SS to yield F1, these heterozygous rats were intercrossed to obtain F2 which were screened to identify the SR-rat derived region, these were then crossed with SS to duplicate the recombinant chromosome</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1582190</RGD_ID>
    <STRAIN_SYMBOL>SS/JrHsd</STRAIN_SYMBOL>
    <FULL_NAME>Dahl Salt-Sensitive</FULL_NAME>
    <ORIGINATION>&lt;a href =http://www.envigo.com/products-services/research-models-services/models/research-models/rats/inbred/dahl-salt-sensitive-resistant-(rapp)-inbred-rat/ss-jrhsd/&gt;Envigo&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =http://www.envigo.com/products-services/research-models-services/models/research-models/rats/inbred/dahl-salt-sensitive-resistant-(rapp)-inbred-rat/ss-jrhsd/&gt;Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1582190</CITATION_ID>
    <DESCRIPTION>Substrain of Dahl SS, from a Sprague-Dawley outbred colony, selected for sensitivity to salt-induced hypertension (Dahl, 1962), from Dr. John P. Rapp, Medical College of Ohio, Toledo,Ohio; to Harlan in 1986.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1582191</RGD_ID>
    <STRAIN_SYMBOL>FHH.FHH.1&lt;sup&gt;BN&lt;/sup&gt;-(&lt;i&gt;D1Rat287-D1Rat84&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="194786607" STOP_POS="262285541" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="185356336" STOP_POS="252280168" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="201358068" STOP_POS="273987019" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="208389496" STOP_POS="281400240" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="190114247" STOP_POS="259322833" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1582191</CITATION_ID>
    <DESCRIPTION>FHH-1&lt;sup&gt;BN&lt;/sup&gt;/Mcwi was backcrossed with FHH/EurMcwi to generate these rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1582192</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D3Mco36-D3Got159&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="168974481" STOP_POS="168974694" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="177366448" STOP_POS="177366660" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="181074759" STOP_POS="181074971" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="162807724" STOP_POS="171009778" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1582192</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D3Mco19-D3Mco5&lt;/i&gt;)/Jr rats were crossed with SS to yield F1, these heterozygous rats were intercrossed to obtain F2 which were screened to identify the SR-rat derived region, these were then crossed with SS to duplicate the recombinant chromosome</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1582193</RGD_ID>
    <STRAIN_SYMBOL>FHH.FHH.1&lt;sup&gt;BN&lt;/sup&gt;-(&lt;i&gt;D1Mgh13-D1Rat89&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="255849111" STOP_POS="255849249" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="245907761" STOP_POS="257976495" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="266793821" STOP_POS="279986079" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="274224224" STOP_POS="287349830" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="252340389" STOP_POS="265343617" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1582193</CITATION_ID>
    <DESCRIPTION>FHH-1&lt;sup&gt;BN&lt;/sup&gt;/Mcwi was backcrossed with FHH/EurMcwi to generate these rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1582194</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D3Mco78-D3Got130&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="147739514" STOP_POS="161994638" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="155586270" STOP_POS="171277347" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="160026579" STOP_POS="177341735" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="149822571" STOP_POS="164079729" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1582194</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D3Mco19-D3Mco5&lt;/i&gt;)/Jr rats were crossed with SS to yield F1, these heterozygous rats were intercrossed to obtain F2 which were screened to identify the SR-rat derived region, these were then crossed with SS to duplicate the recombinant chromosome</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1582195</RGD_ID>
    <STRAIN_SYMBOL>FHH.FHH.1&lt;sup&gt;BN&lt;/sup&gt;-(&lt;i&gt;D1Rat173F6B-D1Rat84&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="262285369" STOP_POS="262285541" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="252279996" STOP_POS="252280168" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="273986848" STOP_POS="273987019" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="281400069" STOP_POS="281400240" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="259322503" STOP_POS="259322833" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1582195</CITATION_ID>
    <DESCRIPTION>FHH-1&lt;sup&gt;BN&lt;/sup&gt;/Mcwi was backcrossed with FHH/EurMcwi to generate these rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1582196</RGD_ID>
    <STRAIN_SYMBOL>FHH.FHH.1&lt;sup&gt;BN&lt;/sup&gt;-(&lt;i&gt;D1Rat234-D1Rat265&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="90664883" STOP_POS="90665040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="94364073" STOP_POS="94364229" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="95453405" STOP_POS="95453561" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="41225047" STOP_POS="90449243" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1582196</CITATION_ID>
    <DESCRIPTION>FHH-1&lt;sup&gt;BN&lt;/sup&gt;/Mcwi was backcrossed with FHH/EurMcwi to generate these rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1598797</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D10Got124-D10Rat187&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, University of Wisconsin, Madison Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="85565469" STOP_POS="106428971" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="88544136" STOP_POS="110355174" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="88338460" STOP_POS="109941891" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="89575059" STOP_POS="110385665" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1598797</CITATION_ID>
    <DESCRIPTION>WKY/NHsd females were bred with WF/NHsd males to generate F1 males which were backcrossed with WF/NHsd females. This contains 24.7 Mb region of Mcs7 QTL.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1598798</RGD_ID>
    <STRAIN_SYMBOL>BBDP/WorN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Dev Ctr</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2021-02-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00092</CITATION_ID>
    <DESCRIPTION>Diabetes prone BB rats maintained in NIH. Developed from a closed colony of outbred wistar rats which spontaneously developed autoimmune diabetes mellitus at the Bio-Breeding Laboratories, Ontario. University of Massachusetts Medical Center started inbreeding these in 1977. In 1983 NIH established a reference colony from this inbred colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1598799</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Rat384-D1Rat452&lt;/i&gt;)(&lt;i&gt;D17Rat61-D1Arb5&lt;/i&gt;)(&lt;i&gt;D17Rat51&lt;/i&gt;)/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pediatric Surgery, Erasmus Medical Center, Rotterdam, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1598799</CITATION_ID>
    <DESCRIPTION>Triple congenic strain which was generated using the speed congenic strategy by backcrossing ACI/Eur and FHH/Eur parental strains. Rf1 QTL region of chr 1 and Rf5 QTL region of chr 17 are introgressed in this strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1598800</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Rat384-D1Rat156&lt;/i&gt;)/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pediatric Surgery, Erasmus Medical Center, Rotterdam, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="232817100" STOP_POS="232817248" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="223390805" STOP_POS="223390953" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="243737319" STOP_POS="243737466" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="250993318" STOP_POS="279213254" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="229184432" STOP_POS="253410500" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1598800</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing ACI/Eur and FHH/Eur parental strains. Rf1 QTL region of chr 1 is introgressed in this strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1598801</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Mit18-D1Mit8&lt;/i&gt;)(&lt;i&gt;D14Mit11-D14Hmgc14b&lt;/i&gt;)(&lt;i&gt;D14Rat65-D14Rat90&lt;/i&gt;)/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pediatric Surgery, Erasmus Medical Center, Rotterdam, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1598801</CITATION_ID>
    <DESCRIPTION>Triple congenic strain which was generated using the speed congenic strategy by backcrossing ACI/Eur and FHH/Eur parental strains. Rf1 QTL region of chr 1 and Rf4 QTL region of chr 14 are introgressed in this strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1598802</RGD_ID>
    <STRAIN_SYMBOL>BBDR/WorN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Dev Ctr</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2021-02-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00094</CITATION_ID>
    <DESCRIPTION>Diabetes resistant BB rats maintained in NIH. Developed from a closed colony of outbred wistar rats which spontaneously developed autoimmune diabetes mellitus at the Bio-Breeding Laboratories, Ontario. University of Massachusetts Medical Center started inbreeding these in 1977. In 1983 NIH established a reference colony from this inbred colony. These were derived from DP rats in the fifth generation</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1598803</RGD_ID>
    <STRAIN_SYMBOL>BBNB/WorN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Dev Ctr.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=93&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2020-02-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00093</CITATION_ID>
    <DESCRIPTION>Developed from a closed colony of outbred wistar rats which spontaneously developed autoimmune diabetes mellitus at the Bio-Breeding Laboratories, Ontario. University of Massachusetts Medical Center started inbreeding these in 1977. In 1983 NIH established a reference colony from this inbred colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1598804</RGD_ID>
    <STRAIN_SYMBOL>WKY.GHS-(&lt;i&gt;D1Rat32-D1Mit32&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine and Physiology, University of Rochester, Rochester New York</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="244113147" STOP_POS="244113296" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="195598053" STOP_POS="265002735" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="202649657" STOP_POS="272443364" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="112148733" STOP_POS="250430505" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1598804</CITATION_ID>
    <DESCRIPTION>GHS females were crossed with WKY males and the heterozygous males were backcrossed to WKY females for 10 generations this resulted in introgressing a 100 cM region of chr 1 which contained the Hc1 QTL</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599674</RGD_ID>
    <STRAIN_SYMBOL>BBDP.WF-(&lt;i&gt;D8Rat59-D8Sunn1467&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine and Immunology, University of Toronto, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="123815688" STOP_POS="123815899" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="133272922" STOP_POS="133273132" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="115112735" STOP_POS="132425312" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="112242639" STOP_POS="128970675" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599674</CITATION_ID>
    <DESCRIPTION>WF RT7.2 allele was introgressed onto the genetic background of BBDP rats and these were crossed with BBDP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599675</RGD_ID>
    <STRAIN_SYMBOL>BBDP.WF-(&lt;i&gt;D13Rat124-D13Mgh5&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine and Immunology, University of Toronto, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ptprc</ALLELES>
    <ALLELE_RGD_IDS>3451</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="47780418" STOP_POS="47780650" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45228358" STOP_POS="61058078" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50609228" STOP_POS="66204630" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55662705" STOP_POS="71178960" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="46721037" STOP_POS="63301552" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599675</CITATION_ID>
    <DESCRIPTION>The BBDP/WorSunn rats were crossed with inbred WF rats (that share the same MHC haplotype as BBDP/WorSunn rats but differ at the CD45 allele) obtained from Charles River. Introgression of the WF CD45 (RT7.2) allele into BBDP/WorSunn was performed by phenotypic selection of backcross breeders for &gt;10 generations, followed by intercrossing. This led to WF RT7.2 allele introgressed onto the genetic background of BBDP rats and also called BBDP/WorSunn.WF-CD45 inbred line.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599755</RGD_ID>
    <STRAIN_SYMBOL>F344.BN-(&lt;i&gt;D16Mit5-D16Rat75&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Biomedical Sciences, Division of Experimental Pathology and Oncology, University of Sassari, Sassari, Italy</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="16278184" STOP_POS="27244292" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="22477482" STOP_POS="22477621" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="24228228" STOP_POS="24228366" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="24112631" STOP_POS="24112769" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="24131965" STOP_POS="24132402" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599755</CITATION_ID>
    <DESCRIPTION>BN/Crli was crossed with F344/Crli, F1 animals were backcrossed with F344 females three times to get ~25 cM region which corresponds to Hcs4 segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599756</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Has2&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Has2&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1599566</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="90002929" STOP_POS="90028933" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="88113326" STOP_POS="88139337" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="96438046" STOP_POS="96464049" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="97055458" STOP_POS="97081461" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="93230135" STOP_POS="93256139" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599756</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. Y344Stop mutation is generated from the codon change TAT/TAA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599757</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Adora2a&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adora2a&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1599561</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="13315270" STOP_POS="13332802" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="13315848" STOP_POS="13333386" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="14265251" STOP_POS="14282873" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="16449385" STOP_POS="16466147" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="13815719" STOP_POS="13834131" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599757</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations.  Q310L mutation is generated from the codon change CAG/CTG of rat Adora2a.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599758</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sod3&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=415&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sod3&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1599567</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="62824092" STOP_POS="62824092" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="58611331" STOP_POS="58611331" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="60959816" STOP_POS="60959816" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="61071304" STOP_POS="61083776" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="63381447" STOP_POS="63387180" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00415</CITATION_ID>
    <DESCRIPTION>Male founders were injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups were genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. The E124D mutation was generated from the codon change GAG/GAT.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599759</RGD_ID>
    <STRAIN_SYMBOL>GRY/Idr</STRAIN_SYMBOL>
    <FULL_NAME>groggy rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=498&amp;StrainsDir=Asc&amp;s_Strainname=GRY&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Graduate School of Medicine, Kyoto University Institute of Laboratory Animals, Kyoto Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=498&amp;StrainsDir=Asc&amp;s_Strainname=GRY&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Graduate School of Medicine, Kyoto University Institute of Laboratory Animals, Kyoto Japan</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Cacna1a&lt;sup&gt;gry&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12880382</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599759</CITATION_ID>
    <DESCRIPTION>Groggy (gry) mutation was found in wistar rats at the Institute for Developmental Research, Aichi, in 1991. These were moved from the Institute for Developmental Research, Aichi Human Service Center to Institute of Laboratory Animals, Graduate School of Medicine, Kyoto University , Kyoto in September 2003.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599760</RGD_ID>
    <STRAIN_SYMBOL>SPRD.WKY-(&lt;i&gt;D18Wox8-D18Rat44&lt;/i&gt;)/Ibmm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Universite Libre de Bruxelles, Institut de Biologie et de Medecine Moleculaires, Gosselies, Belgium</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="19553532" STOP_POS="85493247" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="19278901" STOP_POS="83218561" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="20285758" STOP_POS="87080053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="20030289" STOP_POS="86114102" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="19892650" STOP_POS="86863412" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599760</CITATION_ID>
    <DESCRIPTION>SPRD/HanZtm were crossed with WKY/Han and F1 males were backcrossed with SPRD/HanZtm. Heterozygous carriers were bred to SPRD/HanZtm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599761</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Lcat&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lcat&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1599570</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="50744598" STOP_POS="50748064" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="33834748" STOP_POS="33838214" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="37913333" STOP_POS="37916799" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="48780364" STOP_POS="48783830" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="35781507" STOP_POS="35784966" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599761</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. D359E mutation is generated from the codon change GAC/GAG.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599762</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Bdkrb2&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bdkrb2&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1599568</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="130237055" STOP_POS="130267205" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="124472317" STOP_POS="124502497" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="129399468" STOP_POS="129429676" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="138615812" STOP_POS="138622272" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="129744781" STOP_POS="129748851" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599762</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. E178V mutation is generated from the codon change GAA/GTA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599763</RGD_ID>
    <STRAIN_SYMBOL>SPRD.WKY-(&lt;i&gt;D5Rat190-D5Rat114&lt;/i&gt;)/Ibmm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Universite Libre de Bruxelles, Institut de Biologie et de Medecine Moleculaires, Gosselies, Belgium</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="29109097" STOP_POS="29109277" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="24978084" STOP_POS="24978263" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599763</CITATION_ID>
    <DESCRIPTION>SPRD/HanZtm were crossed with WKY/Han and F1 males were backcrossed with SPRD/HanZtm. Heterozygous carriers were bred to SPRD/HanZtm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599764</RGD_ID>
    <STRAIN_SYMBOL>COP.DA-(&lt;I&gt;D16Rat12-D16Rat90&lt;/I&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo College of Medicine, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="387123" STOP_POS="387234" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="380245" STOP_POS="80345693" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="1090054" STOP_POS="86162972" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="1084304" STOP_POS="85597057" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="350121" STOP_POS="85734479" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599764</CITATION_ID>
    <DESCRIPTION>Male COP/OlaHsd were crossed with female DA/OlaHsd then the F1 males were backcrossed to COP females. Male progeny containing the fewest number of DA-alleles were backcrossed to female COP. These males were backcrossed to female COP.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599765</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Klf4&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Klf4&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1599559</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="75074107" STOP_POS="75079182" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="70278843" STOP_POS="70283751" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="72283311" STOP_POS="72287669" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="76447643" STOP_POS="76452001" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="73446928" STOP_POS="73451286" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599765</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. I150N mutation is generated from the codon change ATC/AAC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599766</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Hps6&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Hps6&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1599564</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="254802250" STOP_POS="254804859" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="244853256" STOP_POS="244855865" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="265761818" STOP_POS="265764427" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="273191755" STOP_POS="273194364" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="251226344" STOP_POS="251228953" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599766</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. L67R mutation is generated from the codon change CTG/CGG.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599767</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Htr1a&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Htr1a&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1599562</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="38427169" STOP_POS="38431733" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="36693462" STOP_POS="36698026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="36246628" STOP_POS="36247896" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="55362662" STOP_POS="55363930" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="36434518" STOP_POS="36435786" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599767</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. G76R mutation is generated from the codon change GGC/CGC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599768</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Klf4&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Klf4&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1599569</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="75074107" STOP_POS="75079182" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="70278843" STOP_POS="70283751" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="72283311" STOP_POS="72287669" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="76447643" STOP_POS="76452001" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="73446928" STOP_POS="73451286" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599768</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. V243I mutation is generated from the codon change GTC/ATC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1599769</RGD_ID>
    <STRAIN_SYMBOL>COP.DA-(&lt;I&gt;D3Rat233-D3Mgh14&lt;/I&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo College of Medicine, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="138829436" STOP_POS="138829559" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="118376416" STOP_POS="118376539" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="123700322" STOP_POS="123700444" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="130198712" STOP_POS="130198834" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="118863100" STOP_POS="118863223" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1599769</CITATION_ID>
    <DESCRIPTION>Male COP/OlaHsd were crossed with female DA/OlaHsd then the F1 males were backcrossed to COP females. Male progeny containing the fewest number of DA-alleles were backcrossed to female COP. These males were backcrossed to female COP.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1600337</RGD_ID>
    <STRAIN_SYMBOL>F344.GK-(&lt;i&gt;D1Mgh14-D1Rat90&lt;/i&gt;)/Swe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="266453608" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="256448513" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="278228767" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="285604773" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="263698966" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1600337</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain derived by intercrossing female F344/Crl and male F344.GK-(&lt;I&gt;D1Arb42a-D1Rat90&lt;/I&gt;)/Swe. F2 progeny carried the homozygous GK/Swe genome in different segments. These were then maintained by bxs breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1600338</RGD_ID>
    <STRAIN_SYMBOL>SHR.F344-(&lt;i&gt;D12Mgh5-D12Mgh6&lt;/i&gt;)/Snk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medicinal Safety Research Laboratories, Sankyo Co. Ltd., Shizuoka, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="33700432" STOP_POS="46784661" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="28064433" STOP_POS="28064557" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="31723565" STOP_POS="31723688" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="33647399" STOP_POS="33647522" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="29130180" STOP_POS="42387195" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1600338</CITATION_ID>
    <DESCRIPTION>Segment of chr 12 was introgressed from normotensive F344/Snk into SHR/Snk by the speed congenic technique</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1600339</RGD_ID>
    <STRAIN_SYMBOL>BN.GK-(&lt;i&gt;D1Wox18-D1Got254&lt;/i&gt;)/Ox</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="103780943" STOP_POS="267096252" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="94644435" STOP_POS="257091168" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="100133276" STOP_POS="278978026" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="101198387" STOP_POS="286341689" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="94626541" STOP_POS="264367394" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1600339</CITATION_ID>
    <DESCRIPTION>This congenic strain is derived from GK rats which were from a colony in Paris (CNRS) obtained in 1995. BN rats were initially obtained from Charles River Laboratories, Margate, UK.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1600340</RGD_ID>
    <STRAIN_SYMBOL>DA/BklArbNsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Feinstein Institute for Medical Research at North Shore-LIJ, Manhasset, NY</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=693&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00693</CITATION_ID>
    <DESCRIPTION>Originally purchased from Bantin and Kingman, Fremont, California, maintained at the National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH. This was then transferred to Feinstein Institute for Medical Research at North Shore-LIJ, which was formerly known as North Shore-LIJ Research Institute, NSI.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1600341</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(Ren2)27/Jmul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Wake Forest University School of Medicine, Winston-Salem, North Carolina</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1600341</CITATION_ID>
    <DESCRIPTION>This is a transgenic hypertensive rat strain, the mouse Ren2, renin gene is microinjected into fertilized eggs of LEW/Crl rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1600342</RGD_ID>
    <STRAIN_SYMBOL>F344.GK-(&lt;i&gt;D1Got250-D1Rat90&lt;/i&gt;)/Swe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="262086049" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="252080660" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="273787505" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="281200731" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="259168938" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1600342</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain derived by intercrossing female F344/Crl and male F344.GK-(&lt;I&gt;D1Arb42a-D1Rat90&lt;/I&gt;)/Swe. F2 progeny carried the homozygous GK/Swe genome in different segments. These were then maintained by bxs breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1600343</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;I&gt;D1Wox29-D1Arb21&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=480&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=480&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="132760429" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="123350408" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="130779148" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="131822204" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="124614679" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1600343</CITATION_ID>
    <DESCRIPTION>This congenic strain contains an WKY/Izm chromsome 1 segment containing a blood pressure QTL transferred to a SHRSP/Izm background by using speed congenic strategy</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1600344</RGD_ID>
    <STRAIN_SYMBOL>F344.GK-(&lt;i&gt;D1Rat175-D1Rat90&lt;/i&gt;)/Swe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="269633753" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="259647732" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="281795624" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="289137107" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="267110921" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1600344</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain derived by intercrossing female F344/Crl and male F344.GK-(&lt;I&gt;D1Arb42a-D1Rat90&lt;/I&gt;)/Swe. F2 progeny carried the homozygous GK/Swe genome in different segments. These were then maintained by bxs breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1600345</RGD_ID>
    <STRAIN_SYMBOL>F344.GK-(&lt;i&gt;D1Rat83-D1Rat376&lt;/i&gt;)/Swe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="245700955" STOP_POS="245701099" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="266587077" STOP_POS="266587220" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="274017004" STOP_POS="274017147" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="252133623" STOP_POS="252133935" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1600345</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain derived by intercrossing female F344/Crl and male F344.GK-(&lt;I&gt;D1Arb42a-D1Rat90&lt;/I&gt;)/Swe. F2 progeny carried the homozygous GK/Swe genome in different segments. These were then maintained by bxs breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1600346</RGD_ID>
    <STRAIN_SYMBOL>F344.GK-(&lt;i&gt;D1Swe4-D1Rat85&lt;/i&gt;)/Swe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="261731585" STOP_POS="261731717" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="248746112" STOP_POS="251790570" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="269633949" STOP_POS="273433763" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="277075545" STOP_POS="280845045" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="255386328" STOP_POS="258599658" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1600346</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain derived by intercrossing female F344/Crl and male F344.GK-(&lt;I&gt;D1Arb42a-D1Rat90&lt;/I&gt;)/Swe. F2 progeny carried the homozygous GK/Swe genome in different segments. These were then maintained by bxs breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1600490</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 1&lt;sup&gt;BN&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1600490</CITATION_ID>
    <DESCRIPTION>A cross of SS and BN strains which results in a SS genomic background with a BN chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1625284</RGD_ID>
    <STRAIN_SYMBOL>Wild1/Hubr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hubrecht Laboratory, Utrecht, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>wild</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1625284</CITATION_ID>
    <DESCRIPTION>This rat was caught in the canals of Utrecht, The Netherlands and sacrificed for DNA isolation</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1626207</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Adora2a&lt;sup&gt;m3Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adora2a&lt;i&gt;&lt;sup&gt;m3Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642070</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="13315270" STOP_POS="13332802" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="13315848" STOP_POS="13333386" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="14265251" STOP_POS="14282873" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="16449385" STOP_POS="16466147" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="13815719" STOP_POS="13834131" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1626207</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. E207K mutation is generated from the codon change GAG/AAG of rat Adora2a.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1626210</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Lipe&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lipe&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642169</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="90093433" STOP_POS="90112117" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="80965612" STOP_POS="80984313" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="82248031" STOP_POS="82266727" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="83511504" STOP_POS="83530200" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="80663791" STOP_POS="80682480" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1626210</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. Q52L mutation is generated from the codon change CTG/CAG.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1626211</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cpf2&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1626211</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1626213</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Oxtr&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Oxtr&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642173</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="147154374" STOP_POS="147171723" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="145598549" STOP_POS="145614674" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="144399326" STOP_POS="144417598" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="207701360" STOP_POS="207717840" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="148314089" STOP_POS="148326797" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1626213</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. F225Y mutation is generated from the codon change TTC/TAC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1626214</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Slc27a5&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc27a5&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642170</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="82688742" STOP_POS="82699335" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="73616556" STOP_POS="73627149" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="65576599" STOP_POS="65587192" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="66387832" STOP_POS="66398425" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="72924630" STOP_POS="72935223" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1626214</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. K160E mutation is generated from the codon change AAA/GAA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641831</RGD_ID>
    <STRAIN_SYMBOL>MWF-Chr 6&lt;sup&gt;SHR&lt;/sup&gt;/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Clinical Pharmacology and Toxicology, Charite-Universitatsmedizin Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641831</CITATION_ID>
    <DESCRIPTION>MWF/FubRkb male was crossed with female SHR/FubRkb to get F1 animals which in turn were backcrossed with female MWF/FubRkb to preserve the Y chromosome, this was repeated for 7 generations, tested by sequential marker-assisted backcrossing</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641849</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mit1-D10Mgh1&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="91417685" STOP_POS="91417879" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="93929621" STOP_POS="93929812" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="95368898" STOP_POS="95369088" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641849</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Mit10-D10Mgh1&lt;/i&gt;/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641850</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D1Got158-D1Got161&lt;/i&gt;)/Njs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Cardiovascular Sciences , University of Leicester, Glenfield Hospital, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Spon1</ALLELES>
    <ALLELE_RGD_IDS>619918</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="165908744" STOP_POS="165908902" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="176611942" STOP_POS="176612099" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="183593063" STOP_POS="183593220" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="169571535" STOP_POS="169571693" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641850</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SHR.WKY-(&lt;i&gt;D1Wox34-D1Rat164&lt;/i&gt;)/Njs to SHR to get F2 which were again crossed with SHR to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641851</RGD_ID>
    <STRAIN_SYMBOL>SHR.PD-(&lt;I&gt;D8Rat42-D8Arb23&lt;/I&gt;)/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Zbtb16|Zbtb16&lt;sup&gt;Lx&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>727921|12910834</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="57329182" STOP_POS="57329297" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="48432652" STOP_POS="49868959" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="52446316" STOP_POS="53840120" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="51046971" STOP_POS="52459221" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="51376771" STOP_POS="52822796" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641851</CITATION_ID>
    <DESCRIPTION>A differential segment of chr 8 from PD/Cub is introgressed onto the genetic background of SHR/OlaIpcv by narrowing down the segment in SHR-&lt;i&gt;Lx&lt;/i&gt; strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641852</RGD_ID>
    <STRAIN_SYMBOL>WF.BBDR-(&lt;i&gt;D4Got48-D4Got43&lt;/i&gt;)/Wor</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Massachusetts Medical School, Worcerster, MA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="67767242" STOP_POS="67767468" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="66800270" STOP_POS="69276226" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="65776688" STOP_POS="68645203" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="65594194" STOP_POS="133430955" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="65628995" STOP_POS="68036772" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641852</CITATION_ID>
    <DESCRIPTION>This congenic substrain was generated by the marker-assisted protocol where a segment of WF.BBDR-(&lt;i&gt;D4Rat96-D4Rat44&lt;/i&gt;)/Wor were transferred to WF background and the animals were screened using microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641853</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mco38-D10Mgh1&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="65339106" STOP_POS="66856515" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="65068360" STOP_POS="65122086" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641853</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Mit10-D10Mgh1&lt;/i&gt;/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641854</RGD_ID>
    <STRAIN_SYMBOL>HAS.LAS-(&lt;i&gt;D5Rat70-D5Rat37&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pharmaceutical Sciences, University of Colorado at Denver, Denver, Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="39985948" STOP_POS="39986213" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="35189153" STOP_POS="141643988" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="35788756" STOP_POS="147487820" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="40446731" STOP_POS="151220567" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="36386126" STOP_POS="148460381" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641854</CITATION_ID>
    <DESCRIPTION>HAS1 (RGD:1578700) and LAS1(RGD:1578696) rats were reciprocally mated to produce an F1 generation. Congenics were bred by backcrossing F1 male to HAS1 and the offsprings were genotyped,</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641855</RGD_ID>
    <STRAIN_SYMBOL>BBDP.WF-(&lt;i&gt;D8Rat73-D8Rat20&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine and Immunology, University of Toronto, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="97432569" STOP_POS="99388414" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="88552647" STOP_POS="90508589" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="95257972" STOP_POS="97339444" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="94761016" STOP_POS="96840283" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="92863340" STOP_POS="94870319" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641855</CITATION_ID>
    <DESCRIPTION>WF RT7.2 allele was introgressed onto the genetic background of BBDP rats and these were crossed with BBDP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641856</RGD_ID>
    <STRAIN_SYMBOL>P.NP-(&lt;i&gt;D4Rat119-D4Rat55&lt;/i&gt;)/Iusm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="65060960" STOP_POS="127749483" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="126192368" STOP_POS="126192555" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="62947687" STOP_POS="125671711" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="190188458" STOP_POS="190188644" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="62832008" STOP_POS="127941994" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641856</CITATION_ID>
    <DESCRIPTION>iP and iNP rats were backcrossed to get F1 animals which were further backcrossed to P rats for 10 generations, this was followed by intercross to generate the congenic strains, these animals were selected by marker-assisted selection</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641857</RGD_ID>
    <STRAIN_SYMBOL>BBDP.WF-(&lt;i&gt;D8Rat16-D8Sunn1467&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine and Immunology, University of Toronto, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="103268360" STOP_POS="103268530" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="94388671" STOP_POS="123815899" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="101304999" STOP_POS="133273132" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="100780886" STOP_POS="132425312" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="98878516" STOP_POS="128970675" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641857</CITATION_ID>
    <DESCRIPTION>WF RT7.2 allele was introgressed onto the genetic background of BBDP rats and these were crossed with BBDP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641858</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D1Rat420-D1Rat278&lt;/i&gt;)/Njs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Cardiovascular Sciences, University of Leicester, Glenfield Hospital, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="173745165" STOP_POS="173745308" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="164310419" STOP_POS="165279420" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="174905726" STOP_POS="175980872" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="181904343" STOP_POS="182965674" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="167931247" STOP_POS="168930831" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641858</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SHR.WKY-(&lt;i&gt;D1Wox34-D1Rat164&lt;/i&gt;)/Njs to SHR to get F2 which were again crossed with SHR to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641859</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Bra1-D10Mit11&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="101848470" STOP_POS="101848683" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641859</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10M11Mit119-D10Mit11&lt;/i&gt;/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641860</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco62-D10Mit1&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="91417685" STOP_POS="91417879" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="70763267" STOP_POS="93929812" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="72063231" STOP_POS="95369088" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641860</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10M11Mit119-D10Mit11&lt;/i&gt;/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641861</RGD_ID>
    <STRAIN_SYMBOL>HAS.LAS-(&lt;i&gt;D2Rat53-D2Rat138&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pharmaceutical Sciences, University of Colorado at Denver, Denver, Colorado</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=729&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="198834824" STOP_POS="223841096" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="196146703" STOP_POS="221167075" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="211301116" STOP_POS="237742948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="230770662" STOP_POS="256283467" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="204077549" STOP_POS="230157845" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00729</CITATION_ID>
    <DESCRIPTION>HAS1 (RGD:1578700) and LAS1(RGD:1578696) rats were reciprocally mated to produce an F1 generation. Congenics were bred by backcrossing F1 male to HAS1 and the offsprings were genotyped,</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641862</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Apc&lt;sup&gt;Pirc&lt;/i&gt;&lt;/sup&gt;/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin-Madison, Madison, Wisconsin</ORIGINATION>
    <SOURCE>A substrain with F344/NHsd background is deposit at &lt;a href=http://www.rrrc.us/Strain/?x=782&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-07-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Apc&lt;sup&gt;Pirc&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>1554322</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="26190901" STOP_POS="26190901" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="25916744" STOP_POS="25916744" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="27100213" STOP_POS="27100213" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="26725560" STOP_POS="26820837" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="26732147" STOP_POS="26790383" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00782</CITATION_ID>
    <DESCRIPTION>Male F344/NTac rats were injected with ENU (N-ethyl-N-nitrosourea) and then bred. Phenotypically variant pups were screened. A to T transversion at nucleotide 3409 of the coding sequence. (AAG.TAG) Amino acid 1137 (K.Xam)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641863</RGD_ID>
    <STRAIN_SYMBOL>SHR.PD-(&lt;I&gt;D8Mgh9-D8Rat149&lt;/I&gt;)/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Zbtb16|Zbtb16&lt;sup&gt;Lx&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>727921|12910834</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="55523877" STOP_POS="55524028" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="59716199" STOP_POS="59716349" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="58297648" STOP_POS="58297798" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="58692901" STOP_POS="58693265" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641863</CITATION_ID>
    <DESCRIPTION>A differential segment of chr 8 from PD/Cub is introgressed onto the genetic background of SHR/OlaIpcv.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641864</RGD_ID>
    <STRAIN_SYMBOL>WF/CrCrli</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://guide.labanimal.com/guide/companyd.jsp?b=9143&gt;Charles River Laboratories &lt;/a&gt; Italy</ORIGINATION>
    <SOURCE>&lt;a href=http://guide.labanimal.com/guide/companyd.jsp?b=9143&gt;Charles River Laboratories &lt;/a&gt; Italy</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641864</CITATION_ID>
    <DESCRIPTION>J. Furth in 1945 from a commercial Wistar stock in an attempt to develop a high leukemia rat strain. To Charles River in 1998 from the National Cancer Institute.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641865</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Brca2&lt;sup&gt;m1Uwm&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin-Madison, Madison, Wisconsin</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=286&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2016-12-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Brca2&lt;i&gt;&lt;sup&gt;m1Uwm&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>728326</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="4895092" STOP_POS="4939340" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="74070" STOP_POS="74070" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="518257" STOP_POS="518257" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="490733" STOP_POS="535090" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="4282952" STOP_POS="4323693" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00286</CITATION_ID>
    <DESCRIPTION>9 week-old male rats were injected with ENU (N-ethyl-N-nitrosourea) and then bred. Phenotypically variant pups were visually identified and screened. Nonsense transversion mutation at nucleotide T4254 that converted TAT (tyrosine) to TAA (stop codon).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641866</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mit10-D10Rat24&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="27023535" STOP_POS="76129113" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="26521957" STOP_POS="75632053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="27237530" STOP_POS="78343192" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="27082535" STOP_POS="78195122" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="27184741" STOP_POS="79229233" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641866</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Mit10-D10Mgh1&lt;/i&gt;/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641867</RGD_ID>
    <STRAIN_SYMBOL>Iusm:P</STRAIN_SYMBOL>
    <FULL_NAME>alcohol-preferring</FULL_NAME>
    <ORIGINATION>Indiana Alcohol Research Center  at the Indiana University School of Medicine</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Snca</ALLELES>
    <ALLELE_RGD_IDS>3729</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641867</CITATION_ID>
    <DESCRIPTION>These were developed at Indiana University for alcohol-preferring behavior through bidirectional selective breeding of Wistar rats from the Walter Reed Army Institute of Research, Washington, DC. A single pair of rats with high preference and another pair with low preference were mated to develop this preference line (P) and non-preference line (Iusm:NP, RGD:1641873).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641868</RGD_ID>
    <STRAIN_SYMBOL>WF.BBDR-(&lt;i&gt;D4Rat93-D4Rat228&lt;/i&gt;)/Wor</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Massachusetts Medical School, Worcerster, MA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tcrb</ALLELES>
    <ALLELE_RGD_IDS>3834</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="68653456" STOP_POS="68653663" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="67663300" STOP_POS="67663504" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="67470286" STOP_POS="67470490" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="67390393" STOP_POS="67390598" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641868</CITATION_ID>
    <DESCRIPTION>This congenic substrain was generated by the marker-assisted protocol where a segment of WF.BBDR-(&lt;i&gt;D4Rat96-D4Rat44&lt;/i&gt;)/Wor were transferred to WF background and the animals were screened using microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641869</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco31-D10Mit11&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="81033760" STOP_POS="81034014" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="80536974" STOP_POS="80537228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="83411403" STOP_POS="83411656" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="83219971" STOP_POS="83220224" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="84284413" STOP_POS="101848683" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641869</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10M11Mit119-D10Mit11&lt;/i&gt;/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641870</RGD_ID>
    <STRAIN_SYMBOL>BBDP.WF-(&lt;i&gt;D8Rat73-D8Rat121&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine and Immunology, University of Toronto, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="97432569" STOP_POS="122879301" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="88552647" STOP_POS="88552853" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="95257972" STOP_POS="95258175" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="94761016" STOP_POS="121648073" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="92863340" STOP_POS="118705380" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641870</CITATION_ID>
    <DESCRIPTION>WF RT7.2 allele was introgressed onto the genetic background of BBDP rats and these were crossed with BBDP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641871</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco62-D10Mco31&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="81033760" STOP_POS="81034014" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="80536974" STOP_POS="80537228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="83411403" STOP_POS="83411656" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="70763267" STOP_POS="83220224" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="72063231" STOP_POS="84284667" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641871</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10M11Mit119-D10Mit11&lt;/i&gt;/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641872</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mco38-D10Mco41&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="82553677" STOP_POS="82553948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="82057244" STOP_POS="82057515" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="85007626" STOP_POS="85007896" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="65339106" STOP_POS="84798381" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="65068360" STOP_POS="85793448" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641872</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Mit10-D10Mgh1&lt;/i&gt;/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641873</RGD_ID>
    <STRAIN_SYMBOL>Iusm:NP</STRAIN_SYMBOL>
    <FULL_NAME>alcohol-nonpreferring</FULL_NAME>
    <ORIGINATION>Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Snca</ALLELES>
    <ALLELE_RGD_IDS>3729</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641873</CITATION_ID>
    <DESCRIPTION>These were developed at Indiana University for alcohol-preferring behavior through bidirectional selective breeding of Wistar rats from the Walter Reed Army Institute of Research, Washington, DC. A single pair of rats with high preference and another pair with low preference were mated to develop a preference line (Iusm:P, RGD:1641867) and this non-preference line (Iusm:NP).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641874</RGD_ID>
    <STRAIN_SYMBOL>BBDP.WF-(&lt;i&gt;D8Rat73-D8Rat90&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine and Immunology, University of Toronto, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="97432569" STOP_POS="119450610" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="88552647" STOP_POS="110572221" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="95257972" STOP_POS="118862813" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="94761016" STOP_POS="118204000" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="92863340" STOP_POS="114974688" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641874</CITATION_ID>
    <DESCRIPTION>WF RT7.2 allele was introgressed onto the genetic background of BBDP rats and these were crossed with BBDP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641875</RGD_ID>
    <STRAIN_SYMBOL>SHR-Chr Y&lt;sup&gt;BN&lt;/sup&gt;/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641875</CITATION_ID>
    <DESCRIPTION>BN-&lt;i&gt;Lx&lt;/i&gt;/Cub males were crosssed with SHR/OlaIpcv females to get F1 animals, the hybrid animals were backcrossed with female SHR/OlaIpcv for 8 generations</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641876</RGD_ID>
    <STRAIN_SYMBOL>BBDP.WF-(&lt;i&gt;D8Rat73-D8Sunn1467&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine and Immunology, University of Toronto, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="97432569" STOP_POS="97432773" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="88552647" STOP_POS="123815899" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="95257972" STOP_POS="133273132" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="94761016" STOP_POS="132425312" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="92863340" STOP_POS="128970675" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641876</CITATION_ID>
    <DESCRIPTION>WF RT7.2 allele was introgressed onto the genetic background of BBDP rats and these were crossed with BBDP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641877</RGD_ID>
    <STRAIN_SYMBOL>NP.P-(&lt;i&gt;D4Rat119-D4Rat55&lt;/i&gt;)/Iusm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Akr1b1|Npy|Snca|Grid2|Dgki|Zfp212|Ppm1k|Sos1|Baiap1</ALLELES>
    <ALLELE_RGD_IDS>2092|3197|3729|68368|735049|1307836|1308501|1310949|1311418</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="65060960" STOP_POS="127749483" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="126192368" STOP_POS="126192555" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="62947687" STOP_POS="125671711" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="190188458" STOP_POS="190188644" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="62832008" STOP_POS="127941994" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641877</CITATION_ID>
    <DESCRIPTION>Male iP and female iNP rats were crossed to get F1 animals which were further backcrossed to iNP rats for 10 generations, this was followed by intercross to generate the congenic strains, these animals were selected by marker-assisted selection</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641878</RGD_ID>
    <STRAIN_SYMBOL>WF.BBDR-(&lt;i&gt;Clcn1-D4Rat228&lt;/i&gt;)/Wor</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Massachusetts Medical School, Worcerster, MA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Clcn1</ALLELES>
    <ALLELE_RGD_IDS>2360</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="72138739" STOP_POS="72168113" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="71171949" STOP_POS="71201483" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="71674218" STOP_POS="71704318" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="136479719" STOP_POS="136509472" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="70052319" STOP_POS="70081449" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641878</CITATION_ID>
    <DESCRIPTION>This congenic substrain was generated by the marker-assisted protocol where a segment of WF.BBDR-(&lt;i&gt;D4Rat96-D4Rat44&lt;/i&gt;)/Wor were transferred to WF background and the animals were screened using microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641879</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 19&lt;sup&gt;SHR&lt;/sup&gt;/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Clinical Pharmacology and Toxicology, Charite-Universitatsmedizin Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1641879</CITATION_ID>
    <DESCRIPTION>SS/JrRkb male was crossed with female SHR/FubRkb to get F1 animals which in turn were backcrossed with female SS/JrRkb to preserve the Y chromosome, this was repeated for 7 generations, tested by sequential marker-assisted backcrossing</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1641880</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Brca1&lt;sup&gt;m1Uwm&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin-Madison, Madison, Wisconsin</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=285&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2016-12-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Brca1|Brca1&lt;i&gt;&lt;sup&gt;m1Uwm&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>2218|728298</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="86919758" STOP_POS="86919758" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="86419516" STOP_POS="86419516" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="89396896" STOP_POS="89396896" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="89192653" STOP_POS="89252760" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="90513630" STOP_POS="90572676" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00285</CITATION_ID>
    <DESCRIPTION>9 week-old male rats were injected with ENU (N-ethyl-N-nitrosourea) and then bred. Phenotypically variant pups were visually identified and screened. mutation from A to G at the exon 21/22 border causes a frameshift and premature stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642017</RGD_ID>
    <STRAIN_SYMBOL>BBDR/WorBrm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.biomere.com/type1diabetes.php&gt;Biomedical Research Models, Inc.&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.biomere.com/type1diabetes.php&gt;Biomedical Research Models, Inc.&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642017</CITATION_ID>
    <DESCRIPTION>Diabetes resistant BB rats maintained in BRM. This strain has been maintained by brother and sister mating for 40 generations. These originated from the Worcester colony from the rats that were sent from Ottawa to Worcester in 1977. These are derived from a viral antibody free (VAF)colony which was maintained at University of Massachusetts and is now at Biomedical Research Models, Inc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642018</RGD_ID>
    <STRAIN_SYMBOL>BBDP/WorBrm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.biomere.com/type1diabetes.php&gt;Biomedical Research Models, Inc.&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.biomere.com/type1diabetes.php&gt;Biomedical Research Models, Inc.&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642018</CITATION_ID>
    <DESCRIPTION>This strain has been maintained by brother and sister mating for 40 generations. These originated from the Worcester colony from the rats that were sent from Ottawa to Worcester in 1977. Biomedical Research Models, Inc. got these from Worcester.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642036</RGD_ID>
    <STRAIN_SYMBOL>SHR/OlaIpcv-mt&lt;sup&gt;BN/Crl&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>conplastic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642036</CITATION_ID>
    <DESCRIPTION>Mitochodrial genome of SHR/OlaIpcv was selectively replaced by BN/Crl to create this conplastic strain using the supersonic breeding strategy; these have the mitochondrial genome of BN/Crl on SHR/OlaIpcv nuclear genetic background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642269</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Birc3&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Birc3&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642178</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="13285702" STOP_POS="13313329" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="5000844" STOP_POS="5028470" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="6048590" STOP_POS="6076828" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="6047454" STOP_POS="6075236" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="4682202" STOP_POS="4696856" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642269</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. K170E mutation is generated from the codon change AAG/GAG.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642270</RGD_ID>
    <STRAIN_SYMBOL>BN-Lcat&lt;i&gt;&lt;sup&gt;m3Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=397&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lcat&lt;i&gt;&lt;sup&gt;m3Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642175</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="50744598" STOP_POS="50748064" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="33834748" STOP_POS="33838214" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="37913333" STOP_POS="37916799" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="48780364" STOP_POS="48783830" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="35781507" STOP_POS="35784966" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00397</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. H316N mutation is generated from the codon change CAC/AAC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642271</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Klf4&lt;sup&gt;m3Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=417&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Klf4&lt;i&gt;&lt;sup&gt;m3Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642179</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="75074107" STOP_POS="75079182" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="70278843" STOP_POS="70283751" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="72283311" STOP_POS="72287669" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="76447643" STOP_POS="76452001" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="73446928" STOP_POS="73451286" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00417</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. H344L mutation is generated from the codon change CAT/CTT.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642272</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mco84-D10Got93&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="67502108" STOP_POS="69424978" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="69910832" STOP_POS="71870652" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="69542746" STOP_POS="71779712" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="70757255" STOP_POS="72827158" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642272</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Rat29-D10Got93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642273</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Thbd&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Thbd&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642182</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="156316526" STOP_POS="156320178" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="135863366" STOP_POS="135867018" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="142748673" STOP_POS="142752325" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="149159895" STOP_POS="149163547" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="137158955" STOP_POS="137162607" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642273</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. N256K mutation is generated from the codon change AAC/AAA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642274</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Has1&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Has1&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642171</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="67366460" STOP_POS="67378686" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="58693411" STOP_POS="58705653" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="59720612" STOP_POS="59732409" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="60640270" STOP_POS="60652067" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="56503365" STOP_POS="56516133" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642274</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. V155L mutation is generated from the codon change GTC/CTC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642275</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat29-D10Mco88&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="66108698" STOP_POS="66108888" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="68230134" STOP_POS="68230352" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="67988035" STOP_POS="70647306" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="67642121" STOP_POS="71109330" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="68842878" STOP_POS="71513333" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642275</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Rat29-D10Got93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642276</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcna5&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=418&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcna5&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642177</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="161040853" STOP_POS="161044311" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="159354689" STOP_POS="159358173" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="159077195" STOP_POS="159079003" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="226075051" STOP_POS="226076859" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="162896283" STOP_POS="162898091" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00418</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. N152K mutation is generated from the codon change AAT/AAA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642277</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cpt2&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=416&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cpt2&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642174</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="127893450" STOP_POS="127911347" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="122664677" STOP_POS="122682126" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="127505646" STOP_POS="127523016" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="131353542" STOP_POS="131370821" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="129007685" STOP_POS="129025501" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00416</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. F475L mutation is generated from the codon change TTC/CTC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642278</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ghsr&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ghsr&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642180</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="112196158" STOP_POS="112201666" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="110268489" STOP_POS="110271865" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="113065953" STOP_POS="113071265" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="132784207" STOP_POS="132789319" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="113269623" STOP_POS="113272999" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642278</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. S342P mutation is generated from the codon change TCC/CCC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642279</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Arb9-D10Rat161&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="63719161" STOP_POS="93608131" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="63221094" STOP_POS="63221223" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="65590122" STOP_POS="65590250" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="66048908" STOP_POS="96133217" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="64308668" STOP_POS="97589703" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642279</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Arb9-D10Got101&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642281</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Podxl&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Podxl&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642176</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="61102434" STOP_POS="61149131" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="60135124" STOP_POS="60181829" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="58829049" STOP_POS="58893353" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="58581513" STOP_POS="58645671" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="58611904" STOP_POS="58658598" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642281</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. T154A mutation is generated from the codon change ACA/GCA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642282</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cacna1g&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cacna1g&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642168</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="79851886" STOP_POS="79919926" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="79354998" STOP_POS="79422960" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="82129071" STOP_POS="82197828" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="81950594" STOP_POS="82017885" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="83043636" STOP_POS="83112886" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642282</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. S490T mutation is generated from the codon change TCT/ACT.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642283</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat29-D10Got93&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="66108698" STOP_POS="66108888" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="69424852" STOP_POS="69424978" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="67988035" STOP_POS="71870652" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="67642121" STOP_POS="71779712" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="68842878" STOP_POS="72827158" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642283</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Arb9-D10Got101&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642284</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Fgl2&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fgl2&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642181</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="14602762" STOP_POS="14608405" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="13710566" STOP_POS="13716207" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="10323598" STOP_POS="10329241" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="10315666" STOP_POS="10321309" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="9176333" STOP_POS="9181976" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642284</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. K129N mutation is generated from the codon change AAG/AAT.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642285</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Arb9-D10Rat57&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="63719161" STOP_POS="71480133" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="63221094" STOP_POS="70982751" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="65590122" STOP_POS="73582866" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="66048908" STOP_POS="73484175" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="64308668" STOP_POS="74388696" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642285</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Arb9-D10Got101&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642287</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Arb9-D10Mco84&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="63719161" STOP_POS="63719290" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="63221094" STOP_POS="67502273" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="65590122" STOP_POS="69910996" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="66048908" STOP_POS="69542910" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="64308668" STOP_POS="70757419" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642287</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Arb9-D10Got101&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642288</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mco89-D10Got101&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="69282350" STOP_POS="74676620" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="71727774" STOP_POS="77360263" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="71638135" STOP_POS="77223025" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="72684998" STOP_POS="78262332" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642288</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Arb9-D10Got101&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642289</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Serpina5&lt;sup&gt;m1Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Serpina5&lt;i&gt;&lt;sup&gt;m1Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642167</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="128774006" STOP_POS="128793187" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="123009224" STOP_POS="123028412" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="127753152" STOP_POS="127772403" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="136972583" STOP_POS="136990812" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="128156901" STOP_POS="128161334" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642289</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. H24R mutation is generated from the codon change CAT/CGT.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642362</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Has1&lt;sup&gt;m3Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Has1&lt;i&gt;&lt;sup&gt;m3Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642359</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="67366460" STOP_POS="67378686" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="58693411" STOP_POS="58705653" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="59720612" STOP_POS="59732409" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="60640270" STOP_POS="60652067" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="56503365" STOP_POS="56516133" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642362</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. D167D mutation is generated from the codon change GAT/GAC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642363</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Fgl2&lt;sup&gt;m3Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fgl2&lt;i&gt;&lt;sup&gt;m3Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642355</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="14602762" STOP_POS="14608405" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="13710566" STOP_POS="13716207" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="10323598" STOP_POS="10329241" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="10315666" STOP_POS="10321309" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="9176333" STOP_POS="9181976" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642363</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. N353H mutation is generated from the codon change AAT/CAT.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642364</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ghsr&lt;sup&gt;m3Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=421&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ghsr&lt;i&gt;&lt;sup&gt;m3Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642357</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="112196158" STOP_POS="112201666" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="110268489" STOP_POS="110271865" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="113065953" STOP_POS="113071265" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="132784207" STOP_POS="132789319" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="113269623" STOP_POS="113272999" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00421</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations.  N26K mutation is generated from the codon change AAC/AAA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642365</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Fgl2&lt;sup&gt;m4Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=420&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fgl2&lt;i&gt;&lt;sup&gt;m4Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642354</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="14602762" STOP_POS="14608405" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="13710566" STOP_POS="13716207" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="10323598" STOP_POS="10329241" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="10315666" STOP_POS="10321309" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="9176333" STOP_POS="9181976" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00420</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. H338P mutation is generated from the codon change CAT/CCT.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642366</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Lcat&lt;sup&gt;m4Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Rat Resource &amp; Research Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lcat&lt;i&gt;&lt;sup&gt;m4Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642358</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="50744598" STOP_POS="50748064" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="33834748" STOP_POS="33838214" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="37913333" STOP_POS="37916799" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="48780364" STOP_POS="48783830" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="35781507" STOP_POS="35784966" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642366</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. Y336N mutation is generated from the codon change TAT/AAT.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642367</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Ccr2&lt;sup&gt;m2Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ccr2&lt;i&gt;&lt;sup&gt;m2Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642356</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="132611883" STOP_POS="132619106" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="123734465" STOP_POS="123742483" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="128892784" STOP_POS="128893905" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642367</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. I99T mutation is generated from the codon change ATC/ACC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642439</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Lcat&lt;sup&gt;m5Mcwi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=419&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lcat&lt;i&gt;&lt;sup&gt;m5Mcwi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>1642438</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="50744598" STOP_POS="50748064" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="33834748" STOP_POS="33838214" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="37913333" STOP_POS="37916799" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="48780364" STOP_POS="48783830" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="35781507" STOP_POS="35784966" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00419</CITATION_ID>
    <DESCRIPTION>Male founders are injected with ENU (N-ethyl-N-nitrosourea) and harem bred to females. The pups are genetically screened using the TILLING assay (an enzyme-based heteroduplex cleavage assay) as well as nucleotide sequencing to identify and characterize target genes possessing ENU-induced mutations. Y297Stop mutation is generated from the codon change TAC/TAA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642689</RGD_ID>
    <STRAIN_SYMBOL>BN.OLETF-(&lt;i&gt;D1Rat169-D1Rat90&lt;/i&gt;)/Got</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Otsuka Pharmacuetical Company, Tokushima, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prlhr</ALLELES>
    <ALLELE_RGD_IDS>71037</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="233480549" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="224054293" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="244401175" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="251652807" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="229876870" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642689</CITATION_ID>
    <DESCRIPTION>OLETF/Got females were crossed with BN/Crlj to produce F&lt;sub&gt;1&lt;/sub&gt; which were backcrossed to BN/Crlj, animals with Dmo1 locus (~28.8 cM) were genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642690</RGD_ID>
    <STRAIN_SYMBOL>LA-&lt;i&gt;cp&lt;/i&gt;/NJcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Surgery, University of Alberta, Edmonton, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642690</CITATION_ID>
    <DESCRIPTION>Originated from a cross between ALB/N and a hooded stock of unknown origin; maintained at University of Alberta.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642968</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mco84-D10Rat58&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="68282569" STOP_POS="68282731" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="67502108" STOP_POS="67785171" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="69910832" STOP_POS="70202084" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="69542746" STOP_POS="70966782" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="70757255" STOP_POS="71067824" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642968</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Mco84-D10Got93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642969</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mco84-D10Mco134&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="67502108" STOP_POS="67502273" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="69910832" STOP_POS="69910996" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="69542746" STOP_POS="69542910" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="70757255" STOP_POS="70757419" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642969</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Mco84-D10Got93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642970</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mco113-D10Got93&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="69424852" STOP_POS="69424978" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="71870527" STOP_POS="71870652" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="71779587" STOP_POS="71779712" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="72827032" STOP_POS="72827158" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642970</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Mco84-D10Got93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642971</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mco84-D10Mco129&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="67502108" STOP_POS="67502273" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="69910832" STOP_POS="69910996" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="69542746" STOP_POS="69542910" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="70757255" STOP_POS="70757419" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642971</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Mco84-D10Got93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642972</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mco84-D10Mco143&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="67502108" STOP_POS="67502273" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="69910832" STOP_POS="69910996" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="69542746" STOP_POS="69542910" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="70757255" STOP_POS="70757419" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642972</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.LEW-(&lt;i&gt;D10Mco84-D10Got93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642989</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(CAG-EGFP)1Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-04-04)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642989</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein gene drived by ubiquitous CAG promoter. This vector contains long terminal repeats with self-inactivating mutation, a central polypurine tract of HIV-1, a human cytomegalovirus and a composite intron from rabbit beta-globin. This transgenic strain was made by injecting the lentivirus vector containing the eGFP construct (lentiviral-CAG-eGFP) into SS rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642990</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-EGFP)63Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642990</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein gene drived by ubiquitous CAG promoter. This vector contains long terminal repeats with self-inactivating mutation, a central polypurine tract of HIV-1, a human cytomegalovirus and a composite intron from rabbit beta-globin. This transgenic strain was made by injecting the lentivirus vector containing the eGFP construct (lentiviral-CAG-eGFP) into SD rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642991</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(CAG-eGFP)18Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642991</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein gene drived by ubiquitous CAG promoter. This vector contains long terminal repeats with self-inactivating mutation, a central polypurine tract of HIV-1, a human cytomegalovirus and a composite intron from rabbit beta-globin. This transgenic strain was made by injecting the lentivirus vector containing the eGFP construct (lentiviral-CAG-eGFP) into SS rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642992</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(CAG-EGFP)28Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642992</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein gene drived by ubiquitous CAG promoter. This vector contains long terminal repeats with self-inactivating mutation, a central polypurine tract of HIV-1, a human cytomegalovirus and a composite intron from rabbit beta-globin. This transgenic strain was made by injecting the lentivirus vector containing the eGFP construct (lentiviral-CAG-eGFP) into SS rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642993</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-EGFP)97Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642993</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein gene drived by ubiquitous CAG promoter. This vector contains long terminal repeats with self-inactivating mutation, a central polypurine tract of HIV-1, a human cytomegalovirus and a composite intron from rabbit beta-globin. This transgenic strain was made by injecting the lentivirus vector containing the eGFP construct (lentiviral-CAG-eGFP) into SD rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642994</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(CAG-EGFP)43Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642994</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein gene drived by ubiquitous CAG promoter. This vector contains long terminal repeats with self-inactivating mutation, a central polypurine tract of HIV-1, a human cytomegalovirus and a composite intron from rabbit beta-globin. This transgenic strain was made by injecting the lentivirus vector containing the eGFP construct (lentiviral-CAG-eGFP) into SS rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642995</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(CAG-eGFP)10Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642995</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein gene drived by ubiquitous CAG promoter. This vector contains long terminal repeats with self-inactivating mutation, a central polypurine tract of HIV-1, a human cytomegalovirus and a composite intron from rabbit beta-globin. This transgenic strain was made by injecting the lentivirus vector containing the eGFP construct (lentiviral-CAG-eGFP) into SS rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642996</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(CAG-EGFP)2Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642996</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein gene drived by ubiquitous CAG promoter. This vector contains long terminal repeats with self-inactivating mutation, a central polypurine tract of HIV-1, a human cytomegalovirus and a composite intron from rabbit beta-globin. This transgenic strain was made by injecting the lentivirus vector containing the eGFP construct (lentiviral-CAG-eGFP) into SS rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1642997</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(CAG-EGFP)23Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1642997</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein gene drived by ubiquitous CAG promoter. This vector contains long terminal repeats with self-inactivating mutation, a central polypurine tract of HIV-1, a human cytomegalovirus and a composite intron from rabbit beta-globin. This transgenic strain was made by injecting the lentivirus vector containing the eGFP construct (lentiviral-CAG-eGFP) into SS rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1643001</RGD_ID>
    <STRAIN_SYMBOL>FH/Unc</STRAIN_SYMBOL>
    <FULL_NAME>Fawn-hooded</FULL_NAME>
    <ORIGINATION>Department of Psychiatry, University of North Carolina, Chapel Hill, North Carolina</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1643001</CITATION_ID>
    <DESCRIPTION>A substrain of fawn hooded rat, maintained at Universtiy of North Carolina, Chapel Hill</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1643002</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D1Rat420-D1Got161&lt;/i&gt;)/Njs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. Cardiology, Univ of Leicester, Clinical Sciences Wing. Glenfield Hospital, Groby Rd, Leicester, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Spon1</ALLELES>
    <ALLELE_RGD_IDS>619918</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="173745165" STOP_POS="173745308" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="164310419" STOP_POS="164310563" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="174905726" STOP_POS="174905869" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="181904343" STOP_POS="181904486" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="167931247" STOP_POS="167931390" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1643002</CITATION_ID>
    <DESCRIPTION>Fragment of the chromosome 1 derived from WKY and repeated backcross to SHR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1643007</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D12Wox12-D12Rat53&lt;/i&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="25247593" STOP_POS="48489416" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="19610889" STOP_POS="42828880" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="22650721" STOP_POS="48598906" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="24663002" STOP_POS="50380790" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="20932555" STOP_POS="43863270" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1643007</CITATION_ID>
    <DESCRIPTION>ACI/SegHsd and DA/OlaHsd were crossed to get F&lt;sub&gt;2&lt;/sub&gt; animals which were backcrossed with DA/OlaHsd and the progeny genotyped then backcrossed with DA/OlaHsd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>1643010</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Rat18-D7Mit2&lt;/i&gt;)(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Tokushima Graduate School, Kuramato-cho, Tokushima, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_1643010</CITATION_ID>
    <DESCRIPTION>double congenic strain generated by intercrossing F344.OLETF-(&lt;i&gt;D7Rat18-D7Mit2&lt;/i&gt;)/Tj and F344.OLETF-(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;)/Tj and F&lt;sub&gt;2&lt;/sub&gt; rats screened for homozygosity</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2289819</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco62-D10Got99&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="72964095" STOP_POS="72964216" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="75493824" STOP_POS="75493944" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="70763267" STOP_POS="74612561" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="72063231" STOP_POS="76465800" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2289819</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10M11Mit119-D10Mit11&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2289820</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco30-D10Got91&lt;/i&gt;)/1Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="73887148" STOP_POS="73887455" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="76420583" STOP_POS="77211758" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="73693979" STOP_POS="77074440" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="77547289" STOP_POS="78112169" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2289820</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10Mco30-D10Mco31&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2289821</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco30-D10Got91&lt;/i&gt;)/3Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="73887148" STOP_POS="73887455" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="76420583" STOP_POS="77211758" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="73693979" STOP_POS="77074440" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="77547289" STOP_POS="78112169" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2289821</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10Mco30-D10Mco31&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2289822</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco30-D10Got112&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="76743133" STOP_POS="76743260" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="73887148" STOP_POS="76246212" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="76420583" STOP_POS="78970405" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="73693979" STOP_POS="78816367" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="77547289" STOP_POS="79857935" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2289822</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10Mco30-D10Mco31&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2289823</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco62-D10Mco30&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="73887148" STOP_POS="73887455" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="76420583" STOP_POS="76420889" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="70763267" STOP_POS="73694285" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="72063231" STOP_POS="77547622" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2289823</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10M11Mit119-D10Mit11&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2289824</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco30-D10Got101&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="73887148" STOP_POS="74676620" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="76420583" STOP_POS="77360263" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="73693979" STOP_POS="77223025" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="77547289" STOP_POS="78262332" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2289824</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10Mco30-D10Mco31&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2289825</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Rat24-D10Mco31&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="76128947" STOP_POS="81034014" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="75631887" STOP_POS="80537228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="78343027" STOP_POS="83411656" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="78194957" STOP_POS="83220224" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="79229067" STOP_POS="84284667" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2289825</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10Mco62-D10Mco31&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2289826</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco30-D10Got91&lt;/i&gt;)/2Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="73887148" STOP_POS="73887455" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="76420583" STOP_POS="77211758" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="73693979" STOP_POS="77074440" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="77547289" STOP_POS="78112169" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2289826</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10Mco30-D10Mco31&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2289827</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco30-D10Mco31&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="81033760" STOP_POS="81034014" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="73887148" STOP_POS="80537228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="76420583" STOP_POS="83411656" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="73693979" STOP_POS="83220224" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="77547289" STOP_POS="84284667" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2289827</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10Mco62-D10Mco31&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2289913</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Rat13-D10Rat12&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="93198590" STOP_POS="95224503" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="92698959" STOP_POS="94725019" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="95967019" STOP_POS="98044833" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="95701164" STOP_POS="97759008" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="97152234" STOP_POS="99198997" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2289913</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10Rat13-D10Mit11&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2289916</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco15-D10Mit11&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="94495280" STOP_POS="94495492" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="93995749" STOP_POS="93995963" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="97308358" STOP_POS="97308569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="97028717" STOP_POS="97028928" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="98392296" STOP_POS="101848683" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2289916</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10Rat13-D10Mit11&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2289917</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D10Mco70-D10Mit11&lt;/i&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="97335332" STOP_POS="97335592" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="96836006" STOP_POS="96836268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="100287441" STOP_POS="100287699" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="99976910" STOP_POS="99977168" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="101355656" STOP_POS="101848683" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2289917</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.MNS-(&lt;i&gt;D10Rat13-D10Mit11&lt;/i&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290056</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Elmod3&lt;sup&gt;Tn(sb-T2/Bart3)2.42Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=423&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Elmod3&lt;sup&gt;Tn(sb-T2/Bart3)2.42Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290055</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="106172819" STOP_POS="106211286" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="104614665" STOP_POS="104653122" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="100422256" STOP_POS="100465152" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="165192607" STOP_POS="165237016" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="105866419" STOP_POS="106099850" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00423</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into  the 4&lt;sup&gt;th&lt;/sup&gt; intron of the Rbed1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290057</RGD_ID>
    <STRAIN_SYMBOL>F344-TgTn(T2/Bart3)1Ceb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290057</CITATION_ID>
    <DESCRIPTION>The Sleeping Beauty transposon construct, T2/Bart3 consists of inverted terminal repeats separated by a gene trap cassette. The gene trap cassette consists of two splice acceptors, one from adenovirus and one from the mouse Hox9a gene, situated in opposite orientations. Each splice acceptor is followed by stop codons in each reading frame and a polyadenylation signal. Furthermore, the T2/Bart3 transposon harbors a mouse tyrosinase minigene which rescues the phenotype of albino rats, but demonstrates position effect variegated expression.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290064</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Trpc4&lt;sup&gt;Tn(sb-T2/Bart3)2.192Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=344&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpc4&lt;sup&gt;Tn(sb-T2/Bart3)2.192Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290060</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="140457841" STOP_POS="140629556" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="138307676" STOP_POS="138476856" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="143433102" STOP_POS="143605757" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="163115873" STOP_POS="163282223" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="143350286" STOP_POS="143485716" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00344</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Trpc4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290065</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;CA338503&lt;sup&gt;Tn(sb-T2/Bart3)2.196Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>CA338503&lt;sup&gt;Tn(sb-T2/Bart3)2.196Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290059</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290065</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD: 2290163)  and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290066</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Nell1&lt;sup&gt;Tn(sb-T2/Bart3)2.195Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nell1&lt;sup&gt;Tn(sb-T2/Bart3)2.195Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290061</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="108845462" STOP_POS="109709858" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="99709305" STOP_POS="100573872" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="105348577" STOP_POS="106218970" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="106397933" STOP_POS="107260905" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="99805922" STOP_POS="100758002" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290066</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the second intron of the Nell1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290067</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;BI285226&lt;sup&gt;Tn(sb-T2/Bart3)2.193Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>BI285226&lt;sup&gt;Tn(sb-T2/Bart3)2.193Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290062</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290067</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290078</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Myo9a&lt;sup&gt;Tn(sb-T2/Bart3)2.186Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=385&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Myo9a&lt;sup&gt;Tn(sb-T2/Bart3)2.186Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290068</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="69044853" STOP_POS="69248094" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="60149234" STOP_POS="60352330" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="64573248" STOP_POS="64777607" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="64335907" STOP_POS="64534890" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="63578001" STOP_POS="63783813" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00385</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 8th intron of the Myo9a gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290079</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;BI285226&lt;sup&gt;Tn(sb-T2/Bart3)2.194Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>BI285226&lt;sup&gt;Tn(sb-T2/Bart3)2.194Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290069</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290079</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290080</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;BI284938&lt;sup&gt;Tn(sb-T2/Bart3)2.187Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>BI284938&lt;sup&gt;Tn(sb-T2/Bart3)2.187Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290074</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290080</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290081</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;BI284934&lt;sup&gt;Tn(sb-T2/Bart3)2.185Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=367&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>BI284934&lt;sup&gt;Tn(sb-T2/Bart3)2.185Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290072</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00367</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290082</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Brinp3&lt;sup&gt;Tn(sb-T2/Bart3)2.189Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=425&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Brinp3&lt;sup&gt;Tn(sb-T2/Bart3)2.189Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290071</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="60964127" STOP_POS="61397044" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="58413883" STOP_POS="58846828" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="63526486" STOP_POS="63959390" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="68507826" STOP_POS="68938032" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="60584348" STOP_POS="61024196" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00425</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 7th intron of the Brinp3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290083</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Slc24a3&lt;sup&gt;Tn(sb-T2/Bart3)2.188Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc24a3&lt;sup&gt;Tn(sb-T2/Bart3)2.188Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290073</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="153005418" STOP_POS="153504497" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="132552119" STOP_POS="133051192" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="139333942" STOP_POS="139835728" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="145760074" STOP_POS="146259491" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="133734890" STOP_POS="134249326" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290083</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 3rd intron of the Slc24a3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290100</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Entpd6&lt;sup&gt;Tn(sb-T2/Bart3)2.174Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Entpd6&lt;sup&gt;Tn(sb-T2/Bart3)2.174Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290086</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="160036055" STOP_POS="160058580" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="139575659" STOP_POS="139598163" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="146546424" STOP_POS="146568828" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="152905464" STOP_POS="152927857" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="141385480" STOP_POS="141407860" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290100</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1&lt;sup&gt;st&lt;/sup&gt; intron of the Entpd6 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290101</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;CB706876&lt;sup&gt;Tn(sb-T2/Bart3)2.181Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>CB706876&lt;sup&gt;Tn(sb-T2/Bart3)2.181Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290092</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290101</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290102</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Klhl13&lt;sup&gt;Tn(sb-T2/Bart3)2.176Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Klhl13&lt;sup&gt;Tn(sb-T2/Bart3)2.176Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290085</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="118747298" STOP_POS="118912279" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="113942309" STOP_POS="114107299" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="121578965" STOP_POS="121735014" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="121716856" STOP_POS="121876640" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="10344050" STOP_POS="10424665" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290102</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Klhl13 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290103</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Nrg1&lt;sup&gt;Tn(sb-T2/Bart3)2.183Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=343&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nrg1&lt;sup&gt;Tn(sb-T2/Bart3)2.183Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290090</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="65954084" STOP_POS="67007484" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="59250658" STOP_POS="60304519" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="62969573" STOP_POS="64065063" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="62632432" STOP_POS="63718738" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="63937796" STOP_POS="64126183" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00343</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb and F344-Tg(PGK2-sb11)Ceb. This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Nrg1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290104</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Cadm2&lt;sup&gt;Tn(sb-T2/Bart3)2.180Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cadm2&lt;sup&gt;Tn(sb-T2/Bart3)2.180Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290088</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="17994856" STOP_POS="18971895" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="4548367" STOP_POS="5525420" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="4175078" STOP_POS="4397335" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="7871257" STOP_POS="8090100" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="4273771" STOP_POS="5330393" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290104</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the Cadm2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290105</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Sptbn4&lt;sup&gt;Tn(sb-T2/Bart3)2.179Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sptbn4&lt;sup&gt;Tn(sb-T2/Bart3)2.179Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290097</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="91778379" STOP_POS="91865970" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="82650750" STOP_POS="82738345" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="84168494" STOP_POS="84254679" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="85379609" STOP_POS="85467354" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="82436626" STOP_POS="82523827" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290105</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 17th intron of the Sptbn4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290106</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;BQ195794&lt;sup&gt;Tn(sb-T2/Bart3)2.182Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>BQ195794&lt;sup&gt;Tn(sb-T2/Bart3)2.182Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290070</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290106</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290107</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Cyss&lt;sup&gt;Tn(sb-T2/Bart3)2.173Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyss&lt;sup&gt;Tn(sb-T2/Bart3)2.173Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290095</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="157892660" STOP_POS="157897265" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="137432049" STOP_POS="137436654" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="144427430" STOP_POS="144431768" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="150801395" STOP_POS="150805733" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="138826625" STOP_POS="138830963" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290107</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1&lt;sup&gt;st&lt;/sup&gt; intron of the Cyss gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290108</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;LOC290071&lt;sup&gt;Tn(sb-T2/Bart3)2.170Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=338&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>LOC290071&lt;sup&gt;Tn(sb-T2/Bart3)2.170Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290089</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="30634899" STOP_POS="32273880" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00338</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into  the 2nd intron of the LOC290071 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290109</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;CA338503&lt;sup&gt;Tn(sb-T2/Bart3)2.168Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>CA338503&lt;sup&gt;Tn(sb-T2/Bart3)2.168Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290087</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290109</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290110</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Lims1&lt;sup&gt;Tn(sb-T2/Bart3)2.169Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=362&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lims1&lt;sup&gt;Tn(sb-T2/Bart3)2.169Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290096</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="26851364" STOP_POS="26961607" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="26309833" STOP_POS="26418511" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="27895981" STOP_POS="28004767" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="29715580" STOP_POS="29824252" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="37349188" STOP_POS="37397427" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00362</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the Lims1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290111</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Cst3&lt;sup&gt;Tn(sb-T2/Bart3)2.172Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cst3&lt;sup&gt;Tn(sb-T2/Bart3)2.172Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290093</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="156790061" STOP_POS="156794116" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="136336923" STOP_POS="136340796" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="143219671" STOP_POS="143223544" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="149628692" STOP_POS="149632565" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="137650903" STOP_POS="137654776" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290111</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1&lt;sup&gt;st&lt;/sup&gt; intron of the Cst3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290112</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;CA338503&lt;sup&gt;Tn(sb-T2/Bart3)2.175Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>CA338503&lt;sup&gt;Tn(sb-T2/Bart3)2.175Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290094</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290112</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290113</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Fam19a2&lt;sup&gt;Tn(sb-T2/Bart3)2.184Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=387&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fam19a2&lt;sup&gt;Tn(sb-T2/Bart3)2.184Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290098</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="60827985" STOP_POS="61303873" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="58942598" STOP_POS="59418640" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="66017066" STOP_POS="66496690" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="66221368" STOP_POS="66695803" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="63388665" STOP_POS="63566226" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00387</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the Fam19a2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290114</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Slc24a3&lt;sup&gt;Tn(sb-T2/Bart3)2.178Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc24a3&lt;sup&gt;Tn(sb-T2/Bart3)2.178Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290091</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="153005418" STOP_POS="153504497" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="132552119" STOP_POS="133051192" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="139333942" STOP_POS="139835728" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="145760074" STOP_POS="146259491" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="133734890" STOP_POS="134249326" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290114</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Slc24a3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290135</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Chsy1&lt;sup&gt;Tn(sb-T2/Bart3)2.165Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=337&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Chsy1&lt;sup&gt;Tn(sb-T2/Bart3)2.165Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290123</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="129100088" STOP_POS="129161167" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="119689626" STOP_POS="119750711" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="127010587" STOP_POS="127071570" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="128095353" STOP_POS="128156041" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="120539002" STOP_POS="120600102" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00337</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2&lt;sup&gt;nd&lt;/sup&gt; intron of the Chsy1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290136</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Slc24a4&lt;sup&gt;Tn(sb-T2/Bart3)2.145Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc24a4&lt;sup&gt;Tn(sb-T2/Bart3)2.145Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290127</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="127044470" STOP_POS="127184684" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="121279590" STOP_POS="121419811" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="126015799" STOP_POS="126158727" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="135226112" STOP_POS="135364945" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="126403837" STOP_POS="126538501" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290136</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2&lt;sup&gt;nd&lt;/sup&gt; intron of the Slc24a4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290137</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;BF522453&lt;sup&gt;Tn(sb-T2/Bart3)2.166Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=361&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>BF522453&lt;sup&gt;Tn(sb-T2/Bart3)2.166Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290126</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00361</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290138</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Glis1&lt;sup&gt;Tn(sb-T2/Bart3)2.149Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-12-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Glis1&lt;sup&gt;Tn(sb-T2/Bart3)2.149Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290128</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="127450934" STOP_POS="127640929" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="122222155" STOP_POS="122412141" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="127043344" STOP_POS="127233395" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="130891667" STOP_POS="131081696" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="128736183" STOP_POS="128739369" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00332</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the Glis1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290139</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;AW527406&lt;sup&gt;Tn(sb-T2/Bart3)2.156Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>AW527406&lt;sup&gt;Tn(sb-T2/Bart3)2.156Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290122</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290139</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290140</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;BI285110&lt;sup&gt;Tn(sb-T2/Bart3)2.167Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>BI285110&lt;sup&gt;Tn(sb-T2/Bart3)2.167Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290115</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290140</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290141</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Abat&lt;sup&gt;Tn(sb-T2/Bart3)2.163Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA, Transposagen.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=381&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-11)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abat&lt;sup&gt;Tn(sb-T2/Bart3)2.163Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290121</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="7503351" STOP_POS="7599474" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="6996688" STOP_POS="7092835" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="7093406" STOP_POS="7200439" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="5894187" STOP_POS="6002068" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="7040725" STOP_POS="7137154" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00381</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Abat gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290142</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;LOC681893&lt;sup&gt;Tn(sb-T2/Bart3)2.161Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>LOC681893&lt;sup&gt;Tn(sb-T2/Bart3)2.161Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290118</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290142</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into  the LOC681893 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290143</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Napb&lt;sup&gt;Tn(sb-T2/Bart3)2.162Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=335&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Napb&lt;sup&gt;Tn(sb-T2/Bart3)2.162Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290116</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="156585394" STOP_POS="156632418" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="136132248" STOP_POS="136179280" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="143017571" STOP_POS="143063904" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="149431212" STOP_POS="149473190" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="137447072" STOP_POS="137490500" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00335</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the Napb gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290144</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Adgrl3&lt;sup&gt;Tn(sb-T2/Bart3)2.151Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=334&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adgrl3&lt;sup&gt;Tn(sb-T2/Bart3)2.151Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290129</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="26690891" STOP_POS="27458132" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="26336320" STOP_POS="27104060" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="28362176" STOP_POS="29226085" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="28183727" STOP_POS="29040121" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="28385112" STOP_POS="28854677" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00334</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 7th intron of the Adgrl3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290145</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;BI284938&lt;sup&gt;Tn(sb-T2/Bart3)2.155Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>BI284938&lt;sup&gt;Tn(sb-T2/Bart3)2.155Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290120</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290145</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290146</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Plce1&lt;sup&gt;Tn(sb-T2/Bart3)2.146Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=380&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Plce1&lt;sup&gt;Tn(sb-T2/Bart3)2.146Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290125</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="245655855" STOP_POS="245964966" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="236243445" STOP_POS="236552571" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="257156023" STOP_POS="257465440" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="264652842" STOP_POS="264956664" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="242794858" STOP_POS="243103437" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00380</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Plce1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290147</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Sptlc3&lt;sup&gt;Tn(sb-T2/Bart3)2.147Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=331&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sptlc3&lt;sup&gt;Tn(sb-T2/Bart3)2.147Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290124</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="147301570" STOP_POS="147431696" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="126847878" STOP_POS="126978010" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="132560437" STOP_POS="132689313" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="139023075" STOP_POS="139151792" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="127691668" STOP_POS="127825206" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00331</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 6&lt;sup&gt;th&lt;/sup&gt; intron of the Sptlc3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290148</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Map2k5&lt;sup&gt;Tn(sb-T2/Bart3)2.150Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-12-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Map2k5&lt;sup&gt;Tn(sb-T2/Bart3)2.150Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290117</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="72520616" STOP_POS="72748395" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="63625220" STOP_POS="63852090" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="68055976" STOP_POS="68282656" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="67784868" STOP_POS="68010809" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="67313472" STOP_POS="67542723" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00333</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 17th intron of the Map2k5 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290159</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Spetex-2H&lt;sup&gt;Tn(sb-T2/Bart3)2.136Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Spetex-2H&lt;sup&gt;Tn(sb-T2/Bart3)2.136Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290150</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="5539869" STOP_POS="5543019" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="5180002" STOP_POS="5186910" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290159</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Spetex-2H gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290160</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Rph3a&lt;sup&gt;Tn(sb-T2/Bart3)2.104Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=326&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rph3a&lt;sup&gt;Tn(sb-T2/Bart3)2.104Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290154</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="41203004" STOP_POS="41279536" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="35542389" STOP_POS="35618901" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="41073296" STOP_POS="41149799" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="42938832" STOP_POS="43014142" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="36678613" STOP_POS="36753316" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00326</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 15th intron of the Rph3a gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290161</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Tmco1&lt;sup&gt;Tn(sb-T2/Bart3)2.135Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tmco1&lt;sup&gt;Tn(sb-T2/Bart3)2.135Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290156</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="81993172" STOP_POS="82016496" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="79460229" STOP_POS="79483557" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="85465015" STOP_POS="85559113" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="90108152" STOP_POS="90202246" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="82971926" STOP_POS="82995262" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00328</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 6th intron of the Tmco1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290162</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Inpp4b&lt;sup&gt;Tn(sb-T2/Bart3)2.143Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=379&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Inpp4b&lt;sup&gt;Tn(sb-T2/Bart3)2.143Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290149</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="42824710" STOP_POS="43575039" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="25920189" STOP_POS="26670085" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="29592889" STOP_POS="30341528" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="40508684" STOP_POS="41132035" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="27722430" STOP_POS="28363639" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00379</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Inpp4b gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290163</RGD_ID>
    <STRAIN_SYMBOL>F344-TgTn(T2/Bart3)2Ceb</STRAIN_SYMBOL>
    <FULL_NAME>transposon sleeping beauty</FULL_NAME>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-11-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290163</CITATION_ID>
    <DESCRIPTION>The Sleeping Beauty transposon construct, T2/Bart3 consists of inverted terminal repeats separated by a gene trap cassette. The gene trap cassette consists of two splice acceptors, one from Adenovirus and one from the mouse Hox9a gene, situated in opposite orientations. Each splice acceptor is followed by stop codons in each reading frame and a polyadenylation signal. Furthermore, the T2/Bart3 transposon harbors a mouse tyrosinase minigene which rescues the phenotype of albino rats, but demonstrates position effect variegated expression.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290164</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Syne1&lt;sup&gt;Tn(sb-T2/Bart3)2.68Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=325&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2024-04-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Syne1&lt;sup&gt;Tn(sb-T2/Bart3)2.68Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290153</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="43917640" STOP_POS="44388802" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="41512146" STOP_POS="41983382" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="41608287" STOP_POS="42086662" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="42947742" STOP_POS="43158478" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="35803552" STOP_POS="36269628" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00325</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 109&lt;sup&gt;th&lt;/sup&gt; intron of the Syne1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290165</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ntm&lt;sup&gt;Tn(sb-T2/Bart3)2.130Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ntm&lt;sup&gt;Tn(sb-T2/Bart3)2.130Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290157</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="35634929" STOP_POS="36625081" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="27376582" STOP_POS="28366604" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="30039332" STOP_POS="31041755" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="30073163" STOP_POS="31070882" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="28587019" STOP_POS="29019888" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00327</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 3th intron of the Ntm gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290166</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Plcb3&lt;sup&gt;Tn(sb-T2/Bart3)2.69Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=424&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Plcb3&lt;sup&gt;Tn(sb-T2/Bart3)2.69Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290155</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="213572499" STOP_POS="213589585" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="204143257" STOP_POS="204160384" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="222207887" STOP_POS="222224993" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="229198739" STOP_POS="229215831" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="209628425" STOP_POS="209643694" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00424</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 18th exon of the Plcb3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290167</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Dlg1&lt;sup&gt;Tn(sb-T2/Bart3)2.133Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dlg1&lt;sup&gt;Tn(sb-T2/Bart3)2.133Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290152</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="82416853" STOP_POS="82607797" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="68911883" STOP_POS="69103230" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="72164566" STOP_POS="72378895" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="75239783" STOP_POS="75454358" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="70735283" STOP_POS="70930374" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290167</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into  the 6&lt;sup&gt;th&lt;/sup&gt; intron of the Dlg1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290168</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Pde5a&lt;sup&gt;Tn(sb-T2/Bart3)2.144Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pde5a&lt;sup&gt;Tn(sb-T2/Bart3)2.144Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290151</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="213542822" STOP_POS="213687638" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="210858515" STOP_POS="211003480" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="226899604" STOP_POS="227044916" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="246260843" STOP_POS="246406296" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="219410394" STOP_POS="219550910" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00330</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). The trap construct targeted to the 4th intron of the Pde5a gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290169</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(PGK2-sb11)Ceb</STRAIN_SYMBOL>
    <FULL_NAME>Sleeping beauty transposase transgenic</FULL_NAME>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-11-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290169</CITATION_ID>
    <DESCRIPTION>sb11 cDNA linked to human PGK2 promoter was used.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290170</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Cd226&lt;sup&gt;Tn(sb-T2/Bart3)2.141Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=329&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd226&lt;sup&gt;Tn(sb-T2/Bart3)2.141Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290158</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="84723330" STOP_POS="84819836" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="82449924" STOP_POS="82545107" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="86299392" STOP_POS="86394772" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="85337942" STOP_POS="85433295" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="86064574" STOP_POS="86157909" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00329</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 3&lt;sup&gt;rd&lt;/sup&gt; intron of the Cd226 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290171</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;LOC681893&lt;sup&gt;Tn(sb-T2/Bart3)2.159Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>LOC681893&lt;sup&gt;Tn(sb-T2/Bart3)2.159Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2290119</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290171</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the LOC681893 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290186</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(SOD1*G93A)39</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Neuroscience, Tohoku University Graduate School of Medicine, Sendai, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>SOD1</ALLELES>
    <ALLELE_RGD_IDS>730855</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290186</CITATION_ID>
    <DESCRIPTION>SD rats were microinjected with a linear 11.5 kb EcoRI-BamH1 fragment containing the coding sequence and promoter region of human SOD1 gene with G93A mutation</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290187</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(SOD1*H46R)4</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Neuroscience, Tohoku University Graduate School of Medicine, Sendai, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>SOD1</ALLELES>
    <ALLELE_RGD_IDS>730855</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290187</CITATION_ID>
    <DESCRIPTION>SD rats were microinjected with a linear NdeI-Xba1 fragment containing the coding sequence and promoter region of human SOD1 gene with H46R mutation</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290272</RGD_ID>
    <STRAIN_SYMBOL>SS/JrNgs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=798&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=798&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290272</CITATION_ID>
    <DESCRIPTION>strain from Disease Model Cooperative Research Association Kyoto, Japan now maintained at Nagasaki University School of Medicine, Nagasaki Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290273</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-&lt;i&gt;(D1Mgh5-D1Wox10)(D9Rat83-D9Mit6)&lt;/i&gt;/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=785&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=785&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290273</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from WKY to SHRSP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290274</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-&lt;i&gt;(D15Rat2-D15Rat94)&lt;/i&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=795&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=795&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="10355054" STOP_POS="69625966" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="11605245" STOP_POS="77072316" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="15643978" STOP_POS="80627247" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="11832728" STOP_POS="76115762" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290274</CITATION_ID>
    <DESCRIPTION>This congenic strain was established from WKY purchased from Japan SLC, Inc. and SHRSP at the Research Institute International Medical Center of Japan in 2001. The rats which have the heterozygous consomic segment were established in 2004, and were bred homozygous in 2005.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290275</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-&lt;i&gt;(D3Tkyo7-D3Rat1)&lt;/i&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=786&amp;StrainsPage=20&amp;StrainsDir=Asc&gt;National Bio Resource Project&lt;/a&gt; Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=786&amp;StrainsPage=20&amp;StrainsDir=Asc&gt;National Bio Resource Project&lt;/a&gt; Japan</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="168026691" STOP_POS="168026850" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="176417943" STOP_POS="176418101" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="180127863" STOP_POS="180128021" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="170016252" STOP_POS="170016653" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290275</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from WKY to SHRSP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290276</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-&lt;i&gt;(D3Mgh16-D3Mgh15)&lt;/i&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=787&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=787&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="138728542" STOP_POS="138728660" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="10778704" STOP_POS="118275626" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="6000748" STOP_POS="123599709" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="11361699" STOP_POS="130099054" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="6373335" STOP_POS="118757096" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290276</CITATION_ID>
    <DESCRIPTION>This congenic strain was established from WKY purchased from Japan SLC, Inc. and SHRSP at the Research Institute International Medical Center of Japan in 2001. The rats which have the heterozygous consomic segment were established in 2004, and were bred homozygous in 2005.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290277</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-&lt;i&gt;(D3Rat227-D3Rat166)&lt;/i&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=783&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=783&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="122654702" STOP_POS="122654872" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="43827364" STOP_POS="102200699" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="45406058" STOP_POS="106900596" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="50522686" STOP_POS="113470358" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="41054012" STOP_POS="101359980" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290277</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from WKY to SHRSP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290278</RGD_ID>
    <STRAIN_SYMBOL>SR/JrNgs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=799&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=799&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290278</CITATION_ID>
    <DESCRIPTION>strain from Disease Model Cooperative Research Association Kyoto, Japan now maintained at Nagasaki University School of Medicine, Nagasaki Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290279</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-&lt;i&gt;(D15Rat68-D15Rat106)&lt;/i&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=796&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=796&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="62893434" STOP_POS="104695021" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="56484420" STOP_POS="98288169" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="63498932" STOP_POS="106550657" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="67139660" STOP_POS="109944957" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="62521452" STOP_POS="106177917" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290279</CITATION_ID>
    <DESCRIPTION>This congenic strain was established from WKY purchased from Japan SLC, Inc. and SHRSP at the Research Institute International Medical Center of Japan in 2001. The rats which have the heterozygous consomic segment were established in 2004, and were bred homozygous in 2005.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290280</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-&lt;i&gt;(D3Mgh16-D3Rat110)&lt;/i&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=780&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=780&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="10778704" STOP_POS="10778823" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="6000748" STOP_POS="47155284" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="11361699" STOP_POS="53824856" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="6373335" STOP_POS="42729760" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290280</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from WKY to SHRSP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290281</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-&lt;i&gt;(D3Rat227-D3Rat1)&lt;/i&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=794&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=794&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="43827364" STOP_POS="168026850" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="45406058" STOP_POS="176418101" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="50522686" STOP_POS="180128021" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="41054012" STOP_POS="170016653" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290281</CITATION_ID>
    <DESCRIPTION>This congenic strain was established from WKY purchased from Japan SLC, Inc. and SHRSP at the Research Institute International Medical Center of Japan in 2001. The rats which have the heterozygous consomic segment were established in 2004, and were bred homozygous in 2005.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290282</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-&lt;i&gt;(D1Mgh5-D1Rat71)(D13Tkyo1-D13Rat51)&lt;/i&gt;/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=784&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=784&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290282</CITATION_ID>
    <DESCRIPTION>The desired fragment is transferred from WKY to SHRSP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290298</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(Thy1-MAPT)318</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Axon-Neuroscience GmbH, Vienna, Austria</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>MAPT</ALLELES>
    <ALLELE_RGD_IDS>736496</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290298</CITATION_ID>
    <DESCRIPTION>SHR embryos were microinjected with mouse Thy1 promoter and cDNA coding for human tau protein truncated at amino acid positions 151-391</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290299</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(Thy1-MAPT)72</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Axon-Neuroscience GmbH, Vienna, Austria</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>MAPT</ALLELES>
    <ALLELE_RGD_IDS>736496</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290299</CITATION_ID>
    <DESCRIPTION>SHR embryos were microinjected with mouse Thy1 promoter and cDNA coding for human tau protein truncated at amino acid positions 151-391</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290311</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(SOD1*G93A)26Dwc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Ludwig Institute of Cancer Research, University of California at San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>SOD1</ALLELES>
    <ALLELE_RGD_IDS>730855</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290311</CITATION_ID>
    <DESCRIPTION>SD rats were microinjected with a linear 12 kb EcoRI-BamH1 fragment containing the coding sequence and promoter region of human SOD1 gene with G93A mutation</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290386</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Wld&lt;sup&gt;s&lt;/sup&gt;)23Cole</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Cologne, Cologne, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290386</CITATION_ID>
    <DESCRIPTION>SD rats were microinjected with a mouse Wld&lt;sup&gt;s&lt;/sup&gt; with a Ube4b-derived domain with A46R and M60T amino acid changes</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290387</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(UbC-APPswe)6590</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>APP</ALLELES>
    <ALLELE_RGD_IDS>736021</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290387</CITATION_ID>
    <DESCRIPTION>SD embryos were microinjected with a DNA construct containing a UbC promoter and human APPswe gene containing the Swedish APP670/671 mutation</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290391</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Wld&lt;sup&gt;s&lt;/sup&gt;)79Cole</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Cologne, Cologne, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2290391</CITATION_ID>
    <DESCRIPTION>SD rats were microinjected with a mouse Wld&lt;sup&gt;s&lt;/sup&gt; with a Ube4b-derived domain with A46R and M60T amino acid changes</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2290429</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(ApoC3-CETP)53Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Massachusetts. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=310&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00310</CITATION_ID>
    <DESCRIPTION>SS/JrHsd embryos were microinjected with 1.57 kb human CETP cDNA construct into pSV-SPORT1 with human ApoC3 promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2291840</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Dzank1&lt;sup&gt;Tn(sb-T2/Bart3)2.164Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PGA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-10-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dzank1&lt;sup&gt;Tn(sb-T2/Bart3)2.164Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2291839</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="152309228" STOP_POS="152361548" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="131855890" STOP_POS="131908217" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="138624517" STOP_POS="138684530" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="145054445" STOP_POS="145114445" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="133021912" STOP_POS="133073987" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2291840</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into  the Dzank1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292168</RGD_ID>
    <STRAIN_SYMBOL>ISIAH</STRAIN_SYMBOL>
    <FULL_NAME>Inherited stress-induced arterial hypertension</FULL_NAME>
    <ORIGINATION>Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292168</CITATION_ID>
    <DESCRIPTION>Selected from an outbred population of Wistar rats at the Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia, for increased response of blood pressure (systolic) which was induced by restraining the animals in a cylindrical wire mess that caused a mild emotional stress</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292384</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Chm167-D10Chm257&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="67833077" STOP_POS="67833322" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="67335465" STOP_POS="68083956" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="69742043" STOP_POS="70500971" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="69375493" STOP_POS="71016171" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="70589279" STOP_POS="71366998" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292384</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Chm128-D10Chm182&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292385</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Mco30-D10Got107&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="73887148" STOP_POS="75121215" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="76420583" STOP_POS="77803328" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="73693979" STOP_POS="77664589" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="77547289" STOP_POS="78712717" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292385</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Rat27-Igfbp4&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292386</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Chm155-D10Rat127&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="83959399" STOP_POS="96051775" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="83463114" STOP_POS="95552352" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="86418952" STOP_POS="98888676" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="86214887" STOP_POS="98591695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="87272312" STOP_POS="100040883" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292386</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Rat27-Igfbp4&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292387</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Chm224-D10Chm259&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="71831756" STOP_POS="71831983" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="74325927" STOP_POS="74326153" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="75776633" STOP_POS="76309841" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="74705355" STOP_POS="75291923" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292387</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Chm224-D10Chm6&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292388</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Chm246-D10Chm257&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="67979320" STOP_POS="68083956" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="70396378" STOP_POS="70500971" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="70027256" STOP_POS="71016171" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="71262405" STOP_POS="71366998" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292388</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Chm128-D10Chm182&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292389</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Chm10-D10Chm14&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="92348201" STOP_POS="94759977" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="95617075" STOP_POS="98079438" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="95351725" STOP_POS="97793613" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="96778676" STOP_POS="99233951" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292389</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Rat13-D10Rat11&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292390</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="72716561" STOP_POS="72716804" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="72219294" STOP_POS="72590339" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="74712046" STOP_POS="75083773" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="75018615" STOP_POS="75388855" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="75706467" STOP_POS="76081753" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292390</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Chm224-D10Chm6&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292451</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Stxbp5l&lt;sup&gt;Tn(sb-T2/Bart3)2.202Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=386&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Stxbp5l&lt;sup&gt;Tn(sb-T2/Bart3)2.202Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2292450</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="76838839" STOP_POS="77167852" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="63334667" STOP_POS="63654270" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="66246624" STOP_POS="66566331" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="69337663" STOP_POS="69661463" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="65129572" STOP_POS="65455115" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00386</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the Stxbp5l gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292452</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Syndig1&lt;sup&gt;Tn(sb-T2/Bart3)2.171Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=342&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Syndig1&lt;sup&gt;Tn(sb-T2/Bart3)2.171Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2292449</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="158491474" STOP_POS="158695174" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="138030995" STOP_POS="138234646" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="145031427" STOP_POS="145199273" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="151405855" STOP_POS="151571801" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="139434170" STOP_POS="139834916" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00342</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the Syndig1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292453</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;BE329202&lt;sup&gt;Tn(sb-T2/Bart3)2.198Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=345&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>BE329202&lt;sup&gt;Tn(sb-T2/Bart3)2.198Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2292448</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00345</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292454</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;RGD1564304&lt;sup&gt;Tn(sb-T2/Bart3)2.201Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>RGD1564304&lt;sup&gt;Tn(sb-T2/Bart3)2.201Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2292447</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292454</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the RGD1564304 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292459</RGD_ID>
    <STRAIN_SYMBOL>WF.LEW-&lt;i&gt;RVFV&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=208&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=208&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2019-11-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00208</CITATION_ID>
    <DESCRIPTION>This rat strain was developed by classical breeding technique inserting the gene for resistance to lethal RVFV infection from the LEW rat strain into the genetic background of the WF rat strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292526</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(Atp1a1)48Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=281&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=281&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2019-05-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00281</CITATION_ID>
    <DESCRIPTION>SS/Jr rats were microinjected with rat alpha1 Na,K-ATPase promoter (-1288) 5 flanking regulatory region isolated from Sprague Dawley genomic library); transgene cDNA: Dahl R alpha1 Na,K-ATPase</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292527</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(RA1V9)64Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=308&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=308&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00308</CITATION_ID>
    <DESCRIPTION>Dahl Sensitive rats were microinjected with AngII/AVP receptor gene and SV40 PolyA signal.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292528</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(APPswe)Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=283&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=283&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00283</CITATION_ID>
    <DESCRIPTION>F344 embryos were microinjected with a DNA construct containing human amyloid precursor protein with Swedish variant (APPswe; K670N/M671L) under control of platelet-derived growth factor-B (PDGF-b promoter) as a promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292529</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg((ROSA)26Sor-luc)11Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=299&gt;Rat Resource and Research Center&lt;/a&gt;, &lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=649&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=299&gt;Rat Resource and Research Center&lt;/a&gt;, &lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=649&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-08-08)</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00299</CITATION_ID>
    <DESCRIPTION>LEW/Crlj were microinjected with luciferase cDNA with ROSA26 promoter in the NcoI and XbaI site</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292530</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Pou5f1-Dsred)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=320&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=320&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00320</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries a random insertion of a construct containing mouse Oct 4 promoter and DsRed. This results in DsRed expression in germ and early embryonic cells.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292531</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Pou5f1-EGFP)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=319&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=319&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2018-04-23)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00319</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries a random insertion of a construct containing mouse promoter Pou5f1 to drive the expression of EGFP.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292532</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(betaCTF-l45F)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=277&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=277&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00277</CITATION_ID>
    <DESCRIPTION>F344 embryos were microinjected with human beta-C-terminal fragment of the amyloid protein</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292564</RGD_ID>
    <STRAIN_SYMBOL>ACI.COP-(&lt;i&gt;D6Rat80-D6Rat146&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Genetics, Cell Biology and Anatomy, University Of Nebraska Medical Center, Omaha, Nebraska</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="8052979" STOP_POS="27729050" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="2299357" STOP_POS="2299495" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="16100120" STOP_POS="16100257" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="26052697" STOP_POS="26052834" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="16302145" STOP_POS="16302283" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292564</CITATION_ID>
    <DESCRIPTION>Female COP/CrCrl and male ACI/SegHsd were crossed to get F&lt;sub&gt;1&lt;/sub&gt; progeny which were in turn backcrossed with female ACI/SegHsd; the offsprings were genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292565</RGD_ID>
    <STRAIN_SYMBOL>ACI.COP-(&lt;i&gt;D3Mgh16-D3Rat119&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Genetics, Cell Biology and Anatomy, University Of Nebraska Medical Center, Omaha, Nebraska</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="10778704" STOP_POS="55223816" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="6000748" STOP_POS="56715367" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="11361699" STOP_POS="63334520" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="6373335" STOP_POS="52643538" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292565</CITATION_ID>
    <DESCRIPTION>Female COP/CrCrl and male ACI/SegHsd were crossed to get F&lt;sub&gt;1&lt;/sub&gt; progeny which were in turn backcrossed with female ACI/SegHsd; the offsprings were genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292566</RGD_ID>
    <STRAIN_SYMBOL>ACI.COP-(&lt;i&gt;D3Rat130-D3Rat114&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Genetics, Cell Biology and Anatomy, University Of Nebraska Medical Center, Omaha, Nebraska</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="67641776" STOP_POS="167835660" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="47233211" STOP_POS="147415807" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="48561928" STOP_POS="155263151" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="55227530" STOP_POS="160347840" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="44551252" STOP_POS="149496698" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292566</CITATION_ID>
    <DESCRIPTION>Female COP/CrCrl and male ACI/SegHsd were crossed to get F&lt;sub&gt;1&lt;/sub&gt; progeny which were in turn backcrossed with female ACI/SegHsd; the offsprings were genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292567</RGD_ID>
    <STRAIN_SYMBOL>ACI.COP-(&lt;i&gt;D10Mgh20-D10Rat4&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Genetics, Cell Biology and Anatomy, University Of Nebraska Medical Center, Omaha, Nebraska</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="102134116" STOP_POS="102134272" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="105875105" STOP_POS="105875260" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="53376677" STOP_POS="105533612" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="53781126" STOP_POS="107033716" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292567</CITATION_ID>
    <DESCRIPTION>Female COP/CrCrl and male ACI/SegHsd were crossed to get F&lt;sub&gt;1&lt;/sub&gt; progeny which were in turn backcrossed with female ACI/SegHsd; the offsprings were genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292647</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Mco36-D1Rat106&lt;/I&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="131243790" STOP_POS="146594089" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="121833674" STOP_POS="137184926" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="129208943" STOP_POS="145354344" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="130267716" STOP_POS="146282094" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="122991895" STOP_POS="139471673" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292647</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing the progenitor strain SS.LEW-(&lt;I&gt;D1Mco36-D1Rat49&lt;/I&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292648</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Mco36-D1Mco77&lt;/I&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="131243790" STOP_POS="150719020" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="121833674" STOP_POS="121834139" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="129208943" STOP_POS="129209407" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="130267716" STOP_POS="130268180" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="122991895" STOP_POS="122992360" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292648</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing the progenitor strain SS.LEW-(&lt;I&gt;D1Mco36-D1Rat49&lt;/I&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292649</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Mco36-D1Rat131&lt;/I&gt;)/1Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="131243790" STOP_POS="152403053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="121833674" STOP_POS="142990467" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="129208943" STOP_POS="152871103" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="130267716" STOP_POS="159182239" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="122991895" STOP_POS="145648920" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292649</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing the progenitor strain SS.LEW-(&lt;I&gt;D1Mco36-D1Rat49&lt;/I&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292650</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Mco36-D1Rat131&lt;/I&gt;)/2Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="131243790" STOP_POS="152403053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="121833674" STOP_POS="142990467" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="129208943" STOP_POS="152871103" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="130267716" STOP_POS="159182239" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="122991895" STOP_POS="145648920" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292650</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing the progenitor strain SS.LEW-(&lt;I&gt;D1Mco36-D1Rat49&lt;/I&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292651</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Mco99-D1Rat49&lt;/I&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="145665383" STOP_POS="145665597" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="154464069" STOP_POS="154464242" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="165129767" STOP_POS="165129939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="171330622" STOP_POS="171330794" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="157497884" STOP_POS="157498254" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292651</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing the progenitor strain SS.LEW-(&lt;I&gt;D1Mco36-D1Rat49&lt;/I&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292652</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D1Mco85-D1Rat49&lt;/I&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="154464069" STOP_POS="154464242" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="165129767" STOP_POS="165129939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="171330622" STOP_POS="171330794" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="157497884" STOP_POS="157498254" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292652</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing the progenitor strain SS.LEW-(&lt;I&gt;D1Mco36-D1Rat49&lt;/I&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2292653</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco36-D1Mco101&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="131243790" STOP_POS="131244255" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="97146283" STOP_POS="121834139" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102658741" STOP_POS="129209407" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103735751" STOP_POS="130268180" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="97174943" STOP_POS="122992360" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2292653</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing the progenitor strain SS.LEW-(&lt;I&gt;D1Mco36-D1Rat49&lt;/I&gt;)/Jr to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2293012</RGD_ID>
    <STRAIN_SYMBOL>ACI.BBDP-(&lt;i&gt;RT1&lt;sup&gt;u&lt;/sup&gt;&lt;/i&gt;)(&lt;i&gt;Gimap5&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Sunnybrook Research Institute, Toronto, Ontario, Canada.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=788&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00788</CITATION_ID>
    <DESCRIPTION>2 BBDP regions [Iddm1(RT1u) and Iddm2(Gimap5)] were introgressed into the ACI/SegHsd background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2293120</RGD_ID>
    <STRAIN_SYMBOL>LOU.BN-(&lt;i&gt;D10Mgh1-D10Mgh14&lt;/i&gt;)/Ins</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Cardiovascular Physiopathology, INSERM, Montpellier, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ace</ALLELES>
    <ALLELE_RGD_IDS>2493</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="64653474" STOP_POS="64653589" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="64155469" STOP_POS="64155584" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="66539729" STOP_POS="66539843" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="65109232" STOP_POS="65109346" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="65379850" STOP_POS="65379965" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2293120</CITATION_ID>
    <DESCRIPTION>segment of chr 10 from BN which contained the Ace gene was introgressed into the genetic background of LOU</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2293143</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat20-D13Rat127&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ren</ALLELES>
    <ALLELE_RGD_IDS>3554</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="39814726" STOP_POS="39814866" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="37262092" STOP_POS="53383120" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="17996178" STOP_POS="42155682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="23200281" STOP_POS="47267192" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="38329089" STOP_POS="55373537" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2293143</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2293144</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat91-D13Rat179&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="47969805" STOP_POS="47969993" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45417753" STOP_POS="58498119" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50799478" STOP_POS="63611529" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55853015" STOP_POS="68592209" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="46911975" STOP_POS="60669696" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2293144</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2293145</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc64-RN34_13048990782&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ren</ALLELES>
    <ALLELE_RGD_IDS>3554</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="50392759" STOP_POS="50392939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="47841075" STOP_POS="47841255" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="43763752" STOP_POS="43763948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="49102205" STOP_POS="49102400" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="53264698" STOP_POS="53264877" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="54170894" STOP_POS="54171089" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="58314588" STOP_POS="58314767" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="49428397" STOP_POS="49428577" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="48990782" STOP_POS="48990782" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="45215472" STOP_POS="45215667" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2293145</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-Chr 13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2293146</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat20-D13Got22&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="39814726" STOP_POS="39814866" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="93541170" STOP_POS="93542503" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="37262092" STOP_POS="37262232" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="42155543" STOP_POS="49720682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="96601805" STOP_POS="96603137" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="47267053" STOP_POS="54791605" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="100631702" STOP_POS="100633034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="38329089" STOP_POS="45828716" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="97701780" STOP_POS="97703112" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2293146</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2293354</RGD_ID>
    <STRAIN_SYMBOL>LEW.WKY-(&lt;i&gt;D16Rat88-D16Rat40&lt;/i&gt;)/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Imperial College, London, UK</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=708&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="839086" STOP_POS="63437135" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="832236" STOP_POS="56733837" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="1550187" STOP_POS="60316851" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="1534408" STOP_POS="59992088" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="819225" STOP_POS="60432230" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00708</CITATION_ID>
    <DESCRIPTION>segment of interest of chr 16 from WKY/NCrl was introgressed into LEW/SsNHsd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2293355</RGD_ID>
    <STRAIN_SYMBOL>WKY.LEW-(&lt;i&gt;D16Rat88-D16Rat40&lt;/i&gt;)/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Imperial College, London, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="839086" STOP_POS="63437135" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="832236" STOP_POS="56733837" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="1550187" STOP_POS="60316851" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="1534408" STOP_POS="59992088" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="819225" STOP_POS="60432230" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00706</CITATION_ID>
    <DESCRIPTION>22.6 cM segment of chr 16 from LEW/SsNHsd was introgressed into WKY/NCrl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2293729</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Gja8&lt;/i&gt;&lt;sup&gt;m1-/-Cub&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Biology, Charles University in Prague, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gja8&lt;sup&gt;m1Cub&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12791992</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="187179668" STOP_POS="187181284" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="184492360" STOP_POS="184492360" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="199052374" STOP_POS="199052374" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="218536831" STOP_POS="218538447" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2293729</CITATION_ID>
    <DESCRIPTION>This strain is a coisogenic mutant derived from SHR/OlaIpcv where a mutation is observed in the NH&lt;sub&gt;2&lt;/sub&gt;-terminal cytosolic domain of Cx50, L7Q</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2293761</RGD_ID>
    <STRAIN_SYMBOL>LH-Chr 17&lt;sup&gt;BN&lt;/sup&gt;/Mav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratoire de Physiologie, Lyon Cedex , France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2293761</CITATION_ID>
    <DESCRIPTION>Chr 17 from BN/NHsdMcwi was introgressed onto the genetic background of LH/Mav and then genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2293770</RGD_ID>
    <STRAIN_SYMBOL>SHHF/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2293770</CITATION_ID>
    <DESCRIPTION>Initial breeders were from the original colony of S.A. McCune, University of Colorado, Boulder. These are maintained under strict breeding</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2293832</RGD_ID>
    <STRAIN_SYMBOL>LOU.BN-(&lt;i&gt;D6Rat128-D6Rat115&lt;/i&gt;)/Ins</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>INSERM, Paris, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="79427077" STOP_POS="117568932" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="73691999" STOP_POS="111838254" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="77111071" STOP_POS="116576287" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="86645162" STOP_POS="125802733" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="76613351" STOP_POS="116550459" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2293832</CITATION_ID>
    <DESCRIPTION>segment of interest from chr 6 of BN/Rj was introgressed on LOU/Ins by performing 8 backcrosses followed by 1 intercross</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2298494</RGD_ID>
    <STRAIN_SYMBOL>Kini:DA,PVG-G10</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>advanced_intercross_line</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2298494</CITATION_ID>
    <DESCRIPTION>Two breeding pairs from inbred DA/Han and PVG.1AV1 that share the RT.1AV1 MHC haplotype were bred to create F&lt;sub&gt;1&lt;/sub&gt; generation, 7 couples of F&lt;sub&gt;1&lt;/sub&gt; with DA/Han and PVG.1AV1 females founders generated F&lt;sub&gt;2&lt;/sub&gt;. F&lt;sub&gt;3&lt;/sub&gt; generation originated from breeding 50 random couples</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2298498</RGD_ID>
    <STRAIN_SYMBOL>W/Gaox</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Urology, Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2298498</CITATION_ID>
    <DESCRIPTION>Generated by selective breeding of a spontaneously mutant male from the inbred colony of Wistar rats at the Animal Research Center of Guangzhou Traditional Chinese Medicine University</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2298772</RGD_ID>
    <STRAIN_SYMBOL>WF&lt;sup&gt;fzHsd&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Fuzzy rat</FULL_NAME>
    <ORIGINATION>Tulane University to Skin and Cancer Hospital, Temple University, Philadelphia</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=340&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2023-12-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00340</CITATION_ID>
    <DESCRIPTION>Sparse fuzzy hair animals with Wistar Furth background found at Tulane University to Skin and Cancer Hospital, Temple University, Philadelphia to Harlan (1987)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299122</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Tasp1&lt;sup&gt;Tn(sb-T2/Bart3)2.219Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tasp1&lt;sup&gt;Tn(sb-T2/Bart3)2.219Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299101</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="147630092" STOP_POS="147861710" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="127176416" STOP_POS="127408039" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="132888785" STOP_POS="133131213" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="139347611" STOP_POS="139588372" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="128002479" STOP_POS="128228127" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2299122</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Tasp1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299123</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;AW921689&lt;sup&gt;Tn(sb-T2/Bart3)2.209Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>AW921689&lt;sup&gt;Tn(sb-T2/Bart3)2.209Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299108</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2299123</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299124</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ubqln4&lt;sup&gt;Tn(sb-T2/Bart3)2.230Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=350&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ubqln4&lt;sup&gt;Tn(sb-T2/Bart3)2.230Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299109</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="176310524" STOP_POS="176325724" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="174012726" STOP_POS="174028062" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="187915701" STOP_POS="187931035" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="207318101" STOP_POS="207333435" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="180669525" STOP_POS="180684724" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00350</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 4th intron of the Ubqln4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299125</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ccdc85a&lt;sup&gt;Tn(sb-T2/Bart3)2.248Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=356&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ccdc85a&lt;sup&gt;Tn(sb-T2/Bart3)2.248Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299113</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="106327580" STOP_POS="106560205" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="102126574" STOP_POS="102359207" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="112719482" STOP_POS="112900724" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="112609601" STOP_POS="112636341" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="109197317" STOP_POS="109434306" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00356</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Ccdc85a gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299126</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Kcnip4&lt;sup&gt;Tn(sb-T2/Bart3)2.225Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=348&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnip4&lt;sup&gt;Tn(sb-T2/Bart3)2.225Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299100</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="65593297" STOP_POS="66743994" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="61380699" STOP_POS="62531399" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="65549362" STOP_POS="66749181" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="65635533" STOP_POS="66780362" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="66284290" STOP_POS="67452628" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00348</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Kcnip4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299127</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Eva1a&lt;sup&gt;Tn(sb-T2/Bart3)2.233Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Eva1a&lt;sup&gt;Tn(sb-T2/Bart3)2.233Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299094</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="116151595" STOP_POS="116200827" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="114593773" STOP_POS="114643011" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="112714023" STOP_POS="112823659" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="177461600" STOP_POS="177511382" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="116280880" STOP_POS="116330122" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2299127</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into  the 1st intron of the Eva1a gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299128</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Lama2&lt;sup&gt;Tn(sb-T2/Bart3)2.2013Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=432&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2024-04-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lama2&lt;sup&gt;Tn(sb-T2/Bart3)2.2013Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299103</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="19492126" STOP_POS="20140056" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="17672675" STOP_POS="18320641" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="18491264" STOP_POS="19143486" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="20002787" STOP_POS="20647256" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="18203466" STOP_POS="18885462" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00432</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 38th intron of the Lama2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299129</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Lrrc4c&lt;sup&gt;Tn(sb-T2/Bart3)2.224Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrrc4c&lt;sup&gt;Tn(sb-T2/Bart3)2.224Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299107</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="102760152" STOP_POS="104139222" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="82305495" STOP_POS="83684039" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="85421169" STOP_POS="86821783" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="92119546" STOP_POS="93502229" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="80921606" STOP_POS="82413671" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2299129</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Lrrc4c gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299130</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ada&lt;sup&gt;Tn(sb-T2/Bart3)2.237Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=426&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ada&lt;sup&gt;Tn(sb-T2/Bart3)2.237Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299093</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="172818174" STOP_POS="172842283" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="152398745" STOP_POS="152422854" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="160115840" STOP_POS="160139947" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="166306001" STOP_POS="166330108" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="154636530" STOP_POS="154660637" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00426</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 7th intron of the Ada gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299131</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Grk1&lt;sup&gt;Tn(sb-T2/Bart3)2.234Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=388&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Grk1&lt;sup&gt;Tn(sb-T2/Bart3)2.234Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299115</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="82821184" STOP_POS="82837971" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="76122501" STOP_POS="76135792" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="81153489" STOP_POS="81165442" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="80641991" STOP_POS="80657693" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="80979323" STOP_POS="80991796" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00388</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into  the 3rd intron of the Grk1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299132</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Cadm1&lt;sup&gt;Tn(sb-T2/Bart3)2.229Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cadm1&lt;sup&gt;Tn(sb-T2/Bart3)2.229Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299116</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="56744374" STOP_POS="57075264" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="47847836" STOP_POS="48178703" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="51858906" STOP_POS="52200591" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="50460752" STOP_POS="50796128" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="50765645" STOP_POS="51108962" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2299132</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Cadm1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299133</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Rap1gds1&lt;sup&gt;Tn(sb-T2/Bart3)2.251Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=357&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rap1gds1&lt;sup&gt;Tn(sb-T2/Bart3)2.251Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299098</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="230173713" STOP_POS="230318555" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="227500366" STOP_POS="227645213" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="244258550" STOP_POS="244370983" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="262787595" STOP_POS="262899803" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="236522381" STOP_POS="236638692" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00357</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 9th intron of the Rap1gds1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299134</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ppapdc1a&lt;sup&gt;Tn(sb-T2/Bart3)2.207Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=347&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ppapdc1a&lt;sup&gt;Tn(sb-T2/Bart3)2.207Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299105</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="193260181" STOP_POS="193389659" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="183829794" STOP_POS="183959319" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="202432366" STOP_POS="202560628" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="209449940" STOP_POS="209577459" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="188518590" STOP_POS="188643804" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00347</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 6th intron of the Ppapdc1a gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299135</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Mgat4c&lt;sup&gt;Tn(sb-T2/Bart3)2.244Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=354&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mgat4c&lt;sup&gt;Tn(sb-T2/Bart3)2.244Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299106</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="38596117" STOP_POS="39361103" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="36709564" STOP_POS="37485810" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="43249369" STOP_POS="44024278" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="43829446" STOP_POS="44052611" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="40171454" STOP_POS="40383441" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00354</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Mgat4c gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299136</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Snph&lt;sup&gt;Tn(sb-T2/Bart3)2.214Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Snph&lt;sup&gt;Tn(sb-T2/Bart3)2.214Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299117</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="160558929" STOP_POS="160603636" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="140098540" STOP_POS="140139342" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="147102394" STOP_POS="147143576" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="153455882" STOP_POS="153496985" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="141921547" STOP_POS="141961697" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2299136</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 3rd intron of the Snph gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299137</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Erbb4&lt;sup&gt;Tn(sb-T2/Bart3)2.208Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=383&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Erbb4&lt;sup&gt;Tn(sb-T2/Bart3)2.208Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299110</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="76973386" STOP_POS="78045633" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="69523733" STOP_POS="70596743" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="75021790" STOP_POS="76178936" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="74804287" STOP_POS="75310350" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="66843898" STOP_POS="67967970" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00383</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Erbb4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299138</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Nrxn2&lt;sup&gt;Tn(sb-T2/Bart3)2.250Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=449&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nrxn2&lt;sup&gt;Tn(sb-T2/Bart3)2.250Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299118</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="213155673" STOP_POS="213271526" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="203726420" STOP_POS="203842301" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="221792191" STOP_POS="221908047" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="228789462" STOP_POS="228899340" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="209211740" STOP_POS="209318064" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00449</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 16th intron of the Nrxn2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299139</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Dnhd1&lt;sup&gt;Tn(sb-T2/Bart3)2.243Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dnhd1&lt;sup&gt;Tn(sb-T2/Bart3)2.243Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299114</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="169402615" STOP_POS="169486684" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="159990785" STOP_POS="160077990" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="170473792" STOP_POS="170570220" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="177487073" STOP_POS="177576072" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="163380065" STOP_POS="163467261" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2299139</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into  the 3rd intron of the Dnhd1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299140</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Dcc&lt;sup&gt;Tn(sb-T2/Bart3)2.205Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=384&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dcc&lt;sup&gt;Tn(sb-T2/Bart3)2.205Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2298938</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="67144272" STOP_POS="68248159" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="64868987" STOP_POS="65972783" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="66518213" STOP_POS="67629801" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="65688901" STOP_POS="66793126" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="68026795" STOP_POS="69140741" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00384</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Dcc gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299141</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ppp2r2b&lt;sup&gt;Tn(sb-T2/Bart3)2.239Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ppp2r2b&lt;sup&gt;Tn(sb-T2/Bart3)2.239Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299104</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="34904686" STOP_POS="35357299" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="34653716" STOP_POS="35080889" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="36985709" STOP_POS="37421383" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="36647298" STOP_POS="37076455" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="35865837" STOP_POS="36318308" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2299141</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 6th intron of the Ppp2r2b gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299142</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Inpp4b&lt;sup&gt;Tn(sb-T2/Bart3)2.232Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Inpp4b&lt;sup&gt;Tn(sb-T2/Bart3)2.232Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299095</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="42824710" STOP_POS="43575039" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="25920189" STOP_POS="26670085" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="29592889" STOP_POS="30341528" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="40508684" STOP_POS="41132035" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="27722430" STOP_POS="28363639" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2299142</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Inpp4b gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299143</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Kif16b&lt;sup&gt;Tn(sb-T2/Bart3)2.200Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=346&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kif16b&lt;sup&gt;Tn(sb-T2/Bart3)2.200Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299111</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="150428233" STOP_POS="150707755" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="129974692" STOP_POS="130254194" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="136596621" STOP_POS="136936809" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="143103727" STOP_POS="143381598" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="130967515" STOP_POS="131250402" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00346</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 11th intron of the Kif16b gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299144</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Trdn&lt;sup&gt;Tn(sb-T2/Bart3)2.238Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=368&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trdn&lt;sup&gt;Tn(sb-T2/Bart3)2.238Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299099</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="25774765" STOP_POS="26230069" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="23955651" STOP_POS="24410494" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="25403390" STOP_POS="25787664" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="26865461" STOP_POS="27248423" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="24514752" STOP_POS="24925948" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00368</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 9th intron of the Trdn gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299145</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Rprd1a&lt;sup&gt;Tn(sb-T2/Bart3)2.247Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rprd1a&lt;sup&gt;Tn(sb-T2/Bart3)2.247Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299096</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="16066169" STOP_POS="16114102" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="15791418" STOP_POS="15839338" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="16450160" STOP_POS="16497913" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="16209135" STOP_POS="16256883" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="16283291" STOP_POS="16328357" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2299145</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Rprd1a gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299146</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ptpre&lt;sup&gt;Tn(sb-T2/Bart3)236Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ptpre&lt;sup&gt;Tn(sb-T2/Bart3)236Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299097</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="199774195" STOP_POS="199924646" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="190344331" STOP_POS="190494815" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="207820719" STOP_POS="207987123" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="214818446" STOP_POS="214920034" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="195263489" STOP_POS="195303249" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2299146</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Ptpre gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299147</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Prr5l&lt;sup&gt;Tn(sb-T2/Bart3)2.228Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=349&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prr5l&lt;sup&gt;Tn(sb-T2/Bart3)2.228Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299112</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108458107" STOP_POS="108628552" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="88001951" STOP_POS="88173532" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91290207" STOP_POS="91461208" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97950297" STOP_POS="98119477" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86868129" STOP_POS="86948468" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00349</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Prr5l gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2299148</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Immp1l&lt;sup&gt;Tn(sb-T2/Bart3)2.246Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=355&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Immp1l&lt;sup&gt;Tn(sb-T2/Bart3)2.246Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2299102</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="112840015" STOP_POS="112904297" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="92385329" STOP_POS="92449559" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="95955126" STOP_POS="96024316" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="102575250" STOP_POS="102646194" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="91408864" STOP_POS="91436603" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00355</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 3rd intron of the Immp1l gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2300018</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.ZUC-(&lt;i&gt;D5Rat4-D5Rat36&lt;/i&gt;)/IzmDmcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Mukogawa Women's University, Nishinomiya, Hyogo Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=735&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2300018</CITATION_ID>
    <DESCRIPTION>Selective back cross breeding was done with SHRSP/Izm and Zucker fatty rats for 12 generations to introduce Lepr locus of chr 5 from Zucker fatty rats into SHRSP/Izm</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2300195</RGD_ID>
    <STRAIN_SYMBOL>EHC.BN-(&lt;i&gt;D14Rat43-D14Rat132&lt;/i&gt;)/Kyu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Kyushu University, Fukuoka, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="77914838" STOP_POS="104348525" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="100147356" STOP_POS="100147478" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="78446303" STOP_POS="110402569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="78419915" STOP_POS="110102984" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="79256324" STOP_POS="107101727" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2300195</CITATION_ID>
    <DESCRIPTION>EHC/Seac and BN/Seac were crossed to get F&lt;sub&gt;1&lt;/sub&gt; progeny which were in turn backcrossed with EHC/Seac and genotyped. Animals with completely replaced background were identified and mated to get homozygous congenics</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2300215</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D10Mgh3-D10Rat85&lt;/i&gt;)/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="47993234" STOP_POS="96099902" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="47494000" STOP_POS="95600487" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="49239646" STOP_POS="98939361" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="49018990" STOP_POS="98640289" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="48994688" STOP_POS="100090454" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2300215</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from SHR.BN-(&lt;i&gt;D10Mgh3-Srebf1&lt;/i&gt;)/Ipcv</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2300216</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(PEPCK-SREBF1)1Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>SREBF1</ALLELES>
    <ALLELE_RGD_IDS>69473</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2300216</CITATION_ID>
    <DESCRIPTION>SHR/OlaIpcv zygotes were microinjected with a construct containing rat PEPCK promoter fused to truncated human cDNA encoding SREBF1 (SREBP-1c isoform) and human growth hormone poly-A signal</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2300217</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D10Mgh3-Srebf1&lt;/i&gt;)/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Srebf1</ALLELES>
    <ALLELE_RGD_IDS>69423</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="45507152" STOP_POS="96099902" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="45007637" STOP_POS="95600487" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="46570996" STOP_POS="98939361" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="46326015" STOP_POS="98640289" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="46461684" STOP_POS="100090454" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2300217</CITATION_ID>
    <DESCRIPTION>53.7Mbp segment of chr 10 including Srebf1 gene from BN/Crl was introgressed into the SHR/OlaIpcv background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301079</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Lrrc7&lt;sup&gt;Tn(sb-T2/Bart3)2.253Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=360&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrrc7&lt;sup&gt;Tn(sb-T2/Bart3)2.253Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2301078</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="249792441" STOP_POS="250294267" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="247146616" STOP_POS="247634945" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="264910594" STOP_POS="265300860" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="283549882" STOP_POS="283934360" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="256228792" STOP_POS="256644029" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00360</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Lrrc7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301080</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Lrrc4c&lt;sup&gt;Tn(sb-T2/Bart3)2.254Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=359&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrrc4c&lt;sup&gt;Tn(sb-T2/Bart3)2.254Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2301076</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="102760152" STOP_POS="104139222" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="82305495" STOP_POS="83684039" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="85421169" STOP_POS="86821783" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="92119546" STOP_POS="93502229" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="80921606" STOP_POS="82413671" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00359</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 5th intron of the Lrrc4c gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301081</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Mmel1&lt;sup&gt;Tn(sb-T2/Bart3)2.255Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=358&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mmel1&lt;sup&gt;Tn(sb-T2/Bart3)2.255Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2301077</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="170713602" STOP_POS="170744058" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="165431278" STOP_POS="165461716" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="172273450" STOP_POS="172303905" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="175729143" STOP_POS="175759868" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="171675007" STOP_POS="171703353" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00358</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Mmel1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301246</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D3Rat61-D3Wox1&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="186555022" STOP_POS="186555229" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="145925360" STOP_POS="166177555" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="153381237" STOP_POS="174632112" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="158115782" STOP_POS="182470017" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="147852788" STOP_POS="168149595" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301246</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 3 was transferred from LEW/Crlc into the SS/Jr background. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301247</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D16Got3-D16Rat112&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="117469" STOP_POS="117710" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="110590" STOP_POS="3447332" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="778415" STOP_POS="4203372" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="773329" STOP_POS="4149422" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="64718" STOP_POS="3531727" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301247</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D16Mit2-D16Chm23&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301248</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D3Got33-D3Chm68&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="47769862" STOP_POS="62962984" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="49115270" STOP_POS="64892832" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="55769295" STOP_POS="71451283" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="45100293" STOP_POS="60708929" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301248</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D3Rat52-D3Rat17&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301249</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D18Rat30-D18Chm29&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="5584537" STOP_POS="11796356" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="5825946" STOP_POS="15691464" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="5795276" STOP_POS="15461904" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="5682011" STOP_POS="12249935" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301249</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 3 was transferred from LEW/Clrc into the SS/Jr background. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301315</RGD_ID>
    <STRAIN_SYMBOL>LE/Orl</STRAIN_SYMBOL>
    <FULL_NAME>Long-Evans/Cryptorchid</FULL_NAME>
    <ORIGINATION>Centre Nationale de la Researche Scientifique, Orleans, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301315</CITATION_ID>
    <DESCRIPTION>Obtained from Centre Nationale de la Researche Scientifique, Orleans, France</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301330</RGD_ID>
    <STRAIN_SYMBOL>KH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>International Foundation for the Study of Rat Genetics and Rodent Pest Control (INTROGEN) Oklahoma City, Oklahoma</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301330</CITATION_ID>
    <DESCRIPTION>Develped at the International Foundation for the Study of Rat Genetics and Rodent Pest Control (INTROGENE) Oklahoma City, Oklahoma</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301367</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;I&gt;D2Mit5-D2Rat133&lt;/I&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Western Infirmary, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="67845182" STOP_POS="166850800" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="66118275" STOP_POS="164552628" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="66828049" STOP_POS="178177553" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="86560119" STOP_POS="197513270" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="66680022" STOP_POS="170817807" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301367</CITATION_ID>
    <DESCRIPTION>Congenic substrain generated by crossing SHRSP.WKY-(&lt;I&gt;D2Rat13-D2Rat157&lt;/I&gt;)/Gcrc males with SHRSP/Gcrc females then intercrossed to fix the small congenic fragment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301368</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;I&gt;D2Wox15-D2Rat133&lt;/I&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Western Infirmary, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="166850605" STOP_POS="166850800" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="164552433" STOP_POS="164552628" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="178177359" STOP_POS="178177553" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="197513076" STOP_POS="197513270" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="170817613" STOP_POS="170817807" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301368</CITATION_ID>
    <DESCRIPTION>Congenic substrain generated by crossing SHRSP.WKY-(&lt;I&gt;D2Rat13-D2Rat157&lt;/I&gt;)/Gcrc males with SHRSP/Gcrc females then intercrossed to fix the small congenic fragment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301369</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;I&gt;D2Rat132-D2Rat53&lt;/I&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Western Infirmary, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="191345805" STOP_POS="198834962" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="188657176" STOP_POS="196146841" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="203613889" STOP_POS="211301253" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="223058573" STOP_POS="230770799" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="196277776" STOP_POS="204077687" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301369</CITATION_ID>
    <DESCRIPTION>Congenic substrain generated by crossing SHRSP.WKY-(&lt;I&gt;D2Rat13-D2Rat157&lt;/I&gt;)/Gcrc males with SHRSP/Gcrc females then intercrossed to fix the small congenic fragment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301370</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;I&gt;D2Wox9-D2Rat231&lt;/I&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Western Infirmary, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="138595962" STOP_POS="185737596" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="136445150" STOP_POS="183048631" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="141583337" STOP_POS="196645063" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="161271919" STOP_POS="216143762" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="141259937" STOP_POS="190384899" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301370</CITATION_ID>
    <DESCRIPTION>Congenic substrain generated by crossing SHRSP.WKY-(&lt;I&gt;D2Rat13-D2Rat157&lt;/I&gt;)/Gcrc males with SHRSP/Gcrc females then intercrossed to fix the small congenic fragment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301371</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;I&gt;D2Mit21-D2Rat157&lt;/I&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Western Infirmary, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gstm1|Vcam1|S1pr1</ALLELES>
    <ALLELE_RGD_IDS>2755|3952|61958</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="210956252" STOP_POS="210956469" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="209270725" STOP_POS="241761983" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="182724363" STOP_POS="216711836" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301371</CITATION_ID>
    <DESCRIPTION>Congenic substrain generated by crossing SHRSP.WKY-(&lt;I&gt;D2Rat13-D2Rat157&lt;/I&gt;)/Gcrc males with SHRSP/Gcrc females then intercrossed to fix the small congenic fragment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301381</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D18Chm41-D18Rat92&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="29804982" STOP_POS="51515008" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="31109532" STOP_POS="53083766" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="30797572" STOP_POS="52299753" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="30891173" STOP_POS="53898282" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301381</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301382</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D18Chm91-D18Rat67&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="12205066" STOP_POS="23012468" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="15274408" STOP_POS="24147513" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="15053338" STOP_POS="23867696" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="12677191" STOP_POS="23780206" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301382</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301383</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D18Chm31-D18Rat55&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="52539763" STOP_POS="52539863" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="2745212" STOP_POS="54108474" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="2761846" STOP_POS="53346447" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="2848113" STOP_POS="54856651" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301383</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301384</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D18Chm41-D18Rat45&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="76330583" STOP_POS="76330704" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="29804982" STOP_POS="74055742" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="31109532" STOP_POS="77212332" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="30797572" STOP_POS="76318715" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="30891173" STOP_POS="77511190" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301384</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301385</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D18Rat29-D18Rat55&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="13804626" STOP_POS="13804786" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="13529795" STOP_POS="52539863" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="13257458" STOP_POS="54108474" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="13042236" STOP_POS="53346447" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="13904295" STOP_POS="54856651" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301385</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301386</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D18Rat61-D18Rat45&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="61075796" STOP_POS="76330704" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="58805687" STOP_POS="74055742" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="60971508" STOP_POS="77212332" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="60167906" STOP_POS="76318715" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="61571526" STOP_POS="77511190" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301386</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301387</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D18Rat67-D18Rat55&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="23012321" STOP_POS="52539863" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="24147367" STOP_POS="54108474" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="23867550" STOP_POS="53346447" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="23779885" STOP_POS="54856651" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301387</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301388</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;I&gt;D18Chm56-D18Rat55&lt;/I&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="46969392" STOP_POS="52539863" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="48499359" STOP_POS="54108474" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="47711090" STOP_POS="53346447" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="49014933" STOP_POS="54856651" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301388</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301700</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Spata13&lt;sup&gt;Tn(sb-T2/Bart3)2.267Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=373&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Spata13&lt;sup&gt;Tn(sb-T2/Bart3)2.267Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2301697</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="38954585" STOP_POS="39083752" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="34778479" STOP_POS="34907645" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="40937652" STOP_POS="41066645" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="44749770" STOP_POS="44878760" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="39722469" STOP_POS="39849214" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00373</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Spata13 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301701</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ptpra&lt;sup&gt;Tn(sb-T2/Bart3)2.261Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=370&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ptpra&lt;sup&gt;Tn(sb-T2/Bart3)2.261Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2301698</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="138103261" STOP_POS="138212835" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="117650146" STOP_POS="117759744" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="122976066" STOP_POS="123084585" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="129475237" STOP_POS="129582992" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="118061713" STOP_POS="118171300" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00370</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 5th intron of the Ptpra gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301702</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Sf4&lt;sup&gt;Tn(sb-T2/Bart3)2.264Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=371&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sf4&lt;sup&gt;Tn(sb-T2/Bart3)2.264Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2301696</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="19386588" STOP_POS="19417460" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="19352659" STOP_POS="19383533" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="21100923" STOP_POS="21131795" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="20950430" STOP_POS="21047301" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="19835921" STOP_POS="19866795" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00371</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 4th intron of the Sf4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301937</RGD_ID>
    <STRAIN_SYMBOL>BN.GH-(&lt;i&gt;D18Rat41-D18Mgh4&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="56594589" STOP_POS="76477940" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="118921813" STOP_POS="118921891" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="58476128" STOP_POS="79948741" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="57699045" STOP_POS="79012652" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="59279066" STOP_POS="79585133" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301937</CITATION_ID>
    <DESCRIPTION>Male GH/Omr were intercrossed with female BN/Elh then F1 male offspring was backcrossed to female BN/Elh, marker-assisted selection strategy was used to select the males who were backcrossed to BN for 10 generations</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301938</RGD_ID>
    <STRAIN_SYMBOL>BN.GH-(&lt;i&gt;D6Mit12-D6Rat15&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="20509999" STOP_POS="20510098" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="100873387" STOP_POS="100873560" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="104890044" STOP_POS="104890216" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="2916444" STOP_POS="113050815" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="3158401" STOP_POS="105011726" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301938</CITATION_ID>
    <DESCRIPTION>Male GH/Omr were intercrossed with female BN/Elh then F1 male offspring was backcrossed to female BN/Elh, marker-assisted selection strategy was used to select the males who were backcrossed to BN for 10 generations</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301939</RGD_ID>
    <STRAIN_SYMBOL>BN.GH-(&lt;i&gt;D2Rat22-D2Mgh11&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="70189772" STOP_POS="70189885" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="68462860" STOP_POS="189039377" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="69243686" STOP_POS="204022555" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="88968735" STOP_POS="223460027" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="69302718" STOP_POS="69303085" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301939</CITATION_ID>
    <DESCRIPTION>Male GH/Omr were intercrossed with female BN/Elh then F1 male offspring was backcrossed to female BN/Elh, marker-assisted selection strategy was used to select the males who were backcrossed to BN for 10 generations</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301986</RGD_ID>
    <STRAIN_SYMBOL>BN.GH-(&lt;i&gt;D2Rat22-D2Mgh11&lt;/i&gt;)(&lt;i&gt;D18Rat41-D18Mgh4&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301986</CITATION_ID>
    <DESCRIPTION>desired segments from chr 2 and 18 from GH/Omr were introgressed in BN/Elh background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301987</RGD_ID>
    <STRAIN_SYMBOL>BN.GH-(&lt;i&gt;D2Rat22-D2Mgh11&lt;/i&gt;)(&lt;i&gt;D6Mit12-D6Rat15&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301987</CITATION_ID>
    <DESCRIPTION>desired segments from chr 2 and 6 from GH/Omr were introgressed in BN/Elh background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301988</RGD_ID>
    <STRAIN_SYMBOL>BN.GH-(&lt;i&gt;D6Mit12-D6Rat15&lt;/i&gt;)(&lt;i&gt;D18Rat41-D18Mgh4&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301988</CITATION_ID>
    <DESCRIPTION>desired segments from chr 6 and 18 from GH/Omr were introgressed in BN/Elh background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2301989</RGD_ID>
    <STRAIN_SYMBOL>BN.GH-(&lt;i&gt;D2Rat22-D2Mgh11&lt;/i&gt;)(&lt;i&gt;D6Mit12-D6Rat15&lt;/i&gt;)(&lt;i&gt;D18Rat41-D18Mgh4&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2301989</CITATION_ID>
    <DESCRIPTION>desired segments from chr 2, 6 and 18 from GH/Omr were introgressed in BN/Elh background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302067</RGD_ID>
    <STRAIN_SYMBOL>F344/DuCrlSwe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Biomedical Center, Lund University, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302067</CITATION_ID>
    <DESCRIPTION>Substrain of Fischer rats maintained at Malmo, Sweden</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302080</RGD_ID>
    <STRAIN_SYMBOL>Rhd:F344,GK-G21</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Biomedical Center, Lund University, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>advanced_intercross_line</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302080</CITATION_ID>
    <DESCRIPTION>GK/Swe and F344/Swe were bred to create F&lt;sub&gt;1&lt;/sub&gt; generation, couples of F&lt;sub&gt;1&lt;/sub&gt; with GK/Swe and F344/Swe females founders generated F&lt;sub&gt;2&lt;/sub&gt;. F&lt;sub&gt;3&lt;/sub&gt; generation originated from breeding random couples which were intercrossed to get further generations</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302081</RGD_ID>
    <STRAIN_SYMBOL>DA.E3-(&lt;i&gt;D11Got79-D11Wox5&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Lund University, Lund, Sweden.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="93543559" STOP_POS="93543650" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="80039141" STOP_POS="83440803" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="83727048" STOP_POS="87444587" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="86800287" STOP_POS="90495881" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="82238710" STOP_POS="85432136" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302081</CITATION_ID>
    <DESCRIPTION>This congenic strain was obtained by the conventional backcross breeding to the parental DA/ZtmRhd strain with positive selection of microsatellite markers. The region corresponding with he production of RF-Igl ambda  antibodies was mapped to a narrower region 'D11Got79-D11Rat50.'</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302106</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;I&gt;D1Rat44-D1Arb21&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=485&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=485&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="160283901" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="150872626" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="161493758" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="167707459" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="153754139" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302106</CITATION_ID>
    <DESCRIPTION>SHRSP.WKY-(&lt;I&gt;Klk1-D1Rat116&lt;/I&gt;)/Izm was backcrossed with SHRSP/Izm, resulting F&lt;sub&gt;1&lt;/sub&gt; were intercrossed to obtain F&lt;sub&gt;2&lt;/sub&gt; recombinant individuals were selected by marker assisted selection</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302108</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;I&gt;D1Mgh5-D1Wox29&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=446&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=446&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="132760602" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="123350581" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="130779320" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="131822376" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="124614852" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302108</CITATION_ID>
    <DESCRIPTION>SHRSP.WKY-(&lt;I&gt;Klk1-D1Rat116&lt;/I&gt;)/Izm was backcrossed with SHRSP/Izm, resulting F&lt;sub&gt;1&lt;/sub&gt; were intercrossed to obtain F&lt;sub&gt;2&lt;/sub&gt; recombinant individuals were selected by marker assisted selection</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302109</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;I&gt;D1Mgh5-D1Rat44&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=444&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=444&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="160284012" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="150872737" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="161493868" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="167707569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="153754250" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302109</CITATION_ID>
    <DESCRIPTION>SHRSP.WKY-(&lt;I&gt;Klk1-D1Rat116&lt;/I&gt;)/Izm was backcrossed with SHRSP/Izm, resulting F&lt;sub&gt;1&lt;/sub&gt; were intercrossed to obtain F&lt;sub&gt;2&lt;/sub&gt; recombinant individuals were selected by marker assisted selection</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302110</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;I&gt;Apbb1-D1Arb21&lt;/I&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=488&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=488&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES>Apbb1</ALLELES>
    <ALLELE_RGD_IDS>2122</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="169308719" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="159896889" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="170387625" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="177393531" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="163282918" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302110</CITATION_ID>
    <DESCRIPTION>SHRSP.WKY-(&lt;I&gt;Klk1-D1Rat116&lt;/I&gt;)/Izm was backcrossed with SHRSP/Izm, resulting F&lt;sub&gt;1&lt;/sub&gt; were intercrossed to obtain F&lt;sub&gt;2&lt;/sub&gt; recombinant individuals were selected by marker assisted selection</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302132</RGD_ID>
    <STRAIN_SYMBOL>SHRSP-Tg(Tagln-ACE2)6918Bdr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin-Buch, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tagln|ACE2</ALLELES>
    <ALLELE_RGD_IDS>3723|1347174</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302132</CITATION_ID>
    <DESCRIPTION>Trangenic line generated by microinjecting 2.8 kb fragment of smooth muscle 22 alpha promoter and cDNA for human ACE2 gene into SHRSP embryos</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302141</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(Cyp1a1-Ren2)10Jmul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Edinburgh Medical School, Edinburgh, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp1a1|Ren2</ALLELES>
    <ALLELE_RGD_IDS>2458|1622375</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302141</CITATION_ID>
    <DESCRIPTION>Generated by using cytochrome P-450 promoter, rat Cyp1a1 to drive mouse Ren2 gene expression. The integration site was on Y chromosome as suggested by Southern blot analysis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302148</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(EEF1A1-Cd36)10Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd36</ALLELES>
    <ALLELE_RGD_IDS>2301</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302148</CITATION_ID>
    <DESCRIPTION>Generated by microinjecting SHR/OlaIpcv zygotes with wild type Cd36 DNA from WKY cloned into Invitrogen pEF1/V5-HisA vector (with human EEF1A1 promoter)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302149</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(EEF1A1-Cd36)19Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd36</ALLELES>
    <ALLELE_RGD_IDS>2301</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302149</CITATION_ID>
    <DESCRIPTION>Generated by microinjecting SHR/OlaIpcv zygotes with wild type Cd36 DNA from WKY cloned into Invitrogen pEF1/V5-HisA vector (with human EEF1A1 promoter)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302150</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(EEF1A1-Cd36)93Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd36</ALLELES>
    <ALLELE_RGD_IDS>2301</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302150</CITATION_ID>
    <DESCRIPTION>Generated by microinjecting SHR/OlaIpcv zygotes with wild type Cd36 DNA from WKY cloned into Invitrogen pEF1/V5-HisA vector (with human EEF1A1 promoter).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302151</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(EEF1A1-Cd36)106Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd36</ALLELES>
    <ALLELE_RGD_IDS>2301</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302151</CITATION_ID>
    <DESCRIPTION>Generated by microinjecting SHR/OlaIpcv zygotes with wild type Cd36 DNA from WKY cloned into Invitrogen pEF1/V5-HisA vector (with human EEF1A1 promoter)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302279</RGD_ID>
    <STRAIN_SYMBOL>F344.SDT-(&lt;i&gt;D3Wox9-D3Arb20&lt;/i&gt;)/Kbe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Kobe University School of Medicine, Chuo-ku, Kobe, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="50436913" STOP_POS="50437042" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="51821710" STOP_POS="51821836" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="58456360" STOP_POS="58456486" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="47722501" STOP_POS="47722628" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302279</CITATION_ID>
    <DESCRIPTION>Female F344/NSlc were crossed with male SDT/CrljJcl, then female F&lt;sub&gt;1&lt;/sub&gt; were backcrossed to male F344/NSlc; male and female heterozygous carriers were backcrossed to male F344/NSlc, desired region was checked by SSLP markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302387</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D2Mit12-D2Mgh29&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Shore-Long Island Jewish Research Institute,350 Community Drive - Manhasset, NY 11030.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=667&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-18)</AVAILABILITY>
    <RESEARCH_USE>arthritis/autoimmunity studies</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="170656145" STOP_POS="221089121" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="168358098" STOP_POS="218414891" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="181990297" STOP_POS="235290110" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="74640967" STOP_POS="201405160" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="174730375" STOP_POS="227310008" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00667</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing DA/BklArbNsi and ACI/SegHsd which resulted in introgressing a 52.6 Mb from ACI into DA/BklArbNsi</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302649</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Nsun4&lt;sup&gt;Tn(sb-T2/Bart3)2.286Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=435&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nsun4&lt;sup&gt;Tn(sb-T2/Bart3)2.286Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302645</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="134749024" STOP_POS="134773630" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="129511224" STOP_POS="129532498" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="134885377" STOP_POS="134905492" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="138152068" STOP_POS="138689234" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="136277224" STOP_POS="136297339" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00435</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 3rd intron of the Nsun4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302650</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Enox1&lt;sup&gt;Tn(sb-T2/Bart3)2.282Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=470&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Enox1&lt;sup&gt;Tn(sb-T2/Bart3)2.282Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302641</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="58924519" STOP_POS="59488919" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="52517833" STOP_POS="53079752" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="59331134" STOP_POS="59884512" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="63013519" STOP_POS="63564418" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="58555747" STOP_POS="58762870" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00470</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into   the 6th intron of the Enox1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302651</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Klra1&lt;sup&gt;Tn(sb-T2/Bart3)2.279Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=431&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Klra1&lt;sup&gt;Tn(sb-T2/Bart3)2.279Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302638</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="166604723" STOP_POS="166717294" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="164873735" STOP_POS="164985429" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="165426365" STOP_POS="165460140" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="227986994" STOP_POS="228022556" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="168892865" STOP_POS="168928286" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00431</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Klra1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302652</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Pde4d&lt;sup&gt;Tn(sb-T2/Bart3)2.285Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=436&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pde4d&lt;sup&gt;Tn(sb-T2/Bart3)2.285Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302644</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="41748337" STOP_POS="43262567" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="40014933" STOP_POS="41529190" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="40219999" STOP_POS="41468551" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="59292847" STOP_POS="60521358" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="40196097" STOP_POS="41311012" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00436</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Pde4d gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302653</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Mov10&lt;sup&gt;Tn(sb-T2/Bart3)2.281Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=377&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mov10&lt;sup&gt;Tn(sb-T2/Bart3)2.281Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302647</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="194982014" STOP_POS="195003513" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="192292041" STOP_POS="192315142" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="207277088" STOP_POS="207301245" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="226696252" STOP_POS="226717551" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="200053185" STOP_POS="200075536" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00377</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 18th intron of the Mov10 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302654</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Csmd3&lt;sup&gt;Tn(sb-T2/Bart3)2.288Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=390&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Csmd3&lt;sup&gt;Tn(sb-T2/Bart3)2.288Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302637</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="80637341" STOP_POS="81956469" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="78747322" STOP_POS="80066466" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="86695703" STOP_POS="88072106" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="86689912" STOP_POS="87802035" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="83586771" STOP_POS="84932392" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00390</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 23rd intron of the Csmd3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302655</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Tmtc2&lt;sup&gt;Tn(sb-T2/Bart3)2.276Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=376&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tmtc2&lt;sup&gt;Tn(sb-T2/Bart3)2.276Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302646</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="42280746" STOP_POS="42695651" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="40392377" STOP_POS="40806685" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="47179596" STOP_POS="47586777" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="47197110" STOP_POS="47603261" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="43667983" STOP_POS="44133854" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00376</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Tmtc2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302656</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Casp7&lt;sup&gt;Tn(sb-T2/Bart3)2.280Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Casp7&lt;sup&gt;Tn(sb-T2/Bart3)2.280Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302642</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="265442647" STOP_POS="265481938" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="255437438" STOP_POS="255476737" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="277190557" STOP_POS="277242779" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="284572208" STOP_POS="284623736" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="262689300" STOP_POS="262721591" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302656</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Casp7 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302657</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Orc3&lt;sup&gt;Tn(sb-T2/Bart3)2.275Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=375&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2024-04-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Orc3&lt;sup&gt;Tn(sb-T2/Bart3)2.275Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302648</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="53923264" STOP_POS="53977869" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="49123758" STOP_POS="49181552" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="50019159" STOP_POS="50075533" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="54588113" STOP_POS="54644440" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="51172243" STOP_POS="51226644" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00375</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 4th intron of the Orc3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302658</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Bbx&lt;sup&gt;Tn(sb-T2/Bart3)2.291Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=428&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bbx&lt;sup&gt;Tn(sb-T2/Bart3)2.291Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302640</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="63850034" STOP_POS="64097700" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="50381249" STOP_POS="50628934" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="52983286" STOP_POS="53228557" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="56153038" STOP_POS="56397255" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="51655446" STOP_POS="51799132" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00428</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Bbx gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302659</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Snx25&lt;sup&gt;Tn(sb-T2/Bart3)2.270Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=374&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Snx25&lt;sup&gt;Tn(sb-T2/Bart3)2.270Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302636</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="52867102" STOP_POS="52971028" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="46134552" STOP_POS="46238471" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="49328958" STOP_POS="49432415" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="49051539" STOP_POS="49159381" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="49415658" STOP_POS="49518663" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00374</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 5th intron of the Snx25 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302660</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Nectin1&lt;sup&gt;Tn(sb-T2/Bart3)2.284Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=378&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nectin1&lt;sup&gt;Tn(sb-T2/Bart3)2.284Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302639</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="52998662" STOP_POS="53061745" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="44101776" STOP_POS="44164863" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="48094233" STOP_POS="48198499" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="46714981" STOP_POS="46777484" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="46739657" STOP_POS="46799051" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00378</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 5th intron of the Pvrl1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302661</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Gramd1b&lt;sup&gt;Tn(sb-T2/Bart3)2.287Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=389&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gramd1b&lt;sup&gt;Tn(sb-T2/Bart3)2.287Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302635</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="49551642" STOP_POS="49790965" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="40654492" STOP_POS="40893869" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="44160634" STOP_POS="44399110" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="61200537" STOP_POS="61378124" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="43260379" STOP_POS="43429258" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00389</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into  the 1st intron of the Gramd1b gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302662</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Slc7a11&lt;sup&gt;Tn(sb-T2/Bart3)2.266Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=372&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc7a11&lt;sup&gt;Tn(sb-T2/Bart3)2.266Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2302643</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="136532912" STOP_POS="136668560" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="134382002" STOP_POS="134517622" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="139453774" STOP_POS="139528479" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="158930294" STOP_POS="159004937" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="139241142" STOP_POS="139317101" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00372</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 6th intron of the Slc7a11 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302666</RGD_ID>
    <STRAIN_SYMBOL>Scr:sP</STRAIN_SYMBOL>
    <FULL_NAME>Sardinian alcohol-preferring rats</FULL_NAME>
    <ORIGINATION>The Scripps Research Institute, LaJolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302666</CITATION_ID>
    <DESCRIPTION>sP/Scr rats are derived from the selectively bred Sardinian alcohol-preferring rats (sP). This colony began with founders obtained after 32 generations of selective breeding for ethanol preference from Wistar stock by Prof. G.L. Gessa (University of Cagliari). Since receipt, this substrain has been maintained at the Scripps Institute for 24 generations of intra-line, unselected breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302984</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat151-D13Rat197&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="64375743" STOP_POS="64375941" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="61825626" STOP_POS="61825824" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="66971778" STOP_POS="66971975" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="71941043" STOP_POS="87516988" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="64083138" STOP_POS="80109632" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302984</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-Chr 13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302985</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat111-D13Got22&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="43736327" STOP_POS="43736554" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="30395351" STOP_POS="30395471" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="41184022" STOP_POS="41184251" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="93541170" STOP_POS="93542503" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="49720575" STOP_POS="49720682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="46444570" STOP_POS="46444796" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="35301263" STOP_POS="35301382" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="96601805" STOP_POS="96603137" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="54791498" STOP_POS="54791605" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="51509286" STOP_POS="51509512" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="40421740" STOP_POS="40421859" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="100631702" STOP_POS="100633034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="32030139" STOP_POS="32030259" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="42627610" STOP_POS="42627837" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="45828608" STOP_POS="45828716" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="97701780" STOP_POS="97703112" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302985</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302986</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat88-D13Rat91&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="43736327" STOP_POS="47969993" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="41184022" STOP_POS="45417941" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="46444570" STOP_POS="50799665" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="51509286" STOP_POS="55853202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="42627610" STOP_POS="46912163" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302986</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302987</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat7-D13Rat60&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="12285517" STOP_POS="23516549" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="11766535" STOP_POS="23001904" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="14279081" STOP_POS="26919398" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="19518130" STOP_POS="32069874" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="1084268" STOP_POS="13053933" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302987</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302989</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat57-D13Rat192&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="98253807" STOP_POS="98254003" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="95722244" STOP_POS="95722440" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="104392076" STOP_POS="104392271" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="87516787" STOP_POS="109040616" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="80109432" STOP_POS="100133413" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302989</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302994</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat127-D13Rat61&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="53382878" STOP_POS="61058159" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="17996178" STOP_POS="66204711" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="23200281" STOP_POS="71179041" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="55373161" STOP_POS="63301678" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302994</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302995</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat115-D13Rat101&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="50392759" STOP_POS="50392939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="34778619" STOP_POS="47841255" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="39639775" STOP_POS="53264877" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="44763184" STOP_POS="58314767" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="35719010" STOP_POS="49428577" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302995</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302996</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat7-D13Rat88&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="12285517" STOP_POS="39814866" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="11766535" STOP_POS="37262232" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="14279081" STOP_POS="42155682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="19518130" STOP_POS="47267192" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="1084268" STOP_POS="38329229" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302996</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302997</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat91-D13Got45&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="45990077" STOP_POS="45990211" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="43437904" STOP_POS="61058159" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="48776655" STOP_POS="66204711" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="53846466" STOP_POS="71179041" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="44872181" STOP_POS="63301678" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302997</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2302999</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat178-D13Got45&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="58031414" STOP_POS="64375941" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="55481090" STOP_POS="61825824" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="60528276" STOP_POS="66971975" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="65516837" STOP_POS="71941240" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="57566232" STOP_POS="64083335" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2302999</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303000</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat123-D13Rat150&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="45990077" STOP_POS="58031541" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="43437904" STOP_POS="55481217" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="48776655" STOP_POS="60528402" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="53846466" STOP_POS="65516963" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="44872181" STOP_POS="57566359" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303000</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303001</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat111-D13Rat127&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="50392759" STOP_POS="50392939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="30395351" STOP_POS="47841255" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="35301263" STOP_POS="53264877" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="40421740" STOP_POS="58314767" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="32030139" STOP_POS="49428577" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303001</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303002</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat123-D13Rat197&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="43736327" STOP_POS="43736554" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="41184022" STOP_POS="73485113" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="46444570" STOP_POS="79034003" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="51509286" STOP_POS="83929327" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="42627610" STOP_POS="76779489" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303002</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303003</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat7-D13Rat127&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="12285517" STOP_POS="50392939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="11766535" STOP_POS="47841255" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="14279081" STOP_POS="53264877" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="19518130" STOP_POS="58314767" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="1084268" STOP_POS="49428577" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303003</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303004</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat115-D13Rat61&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="67451461" STOP_POS="67451625" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="61057931" STOP_POS="64901750" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="66204484" STOP_POS="70172216" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="71178814" STOP_POS="75143303" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="63301384" STOP_POS="67752598" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303004</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303005</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat127-D13Rat77&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="58380103" STOP_POS="58380254" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="53382878" STOP_POS="55829942" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="17996178" STOP_POS="60876578" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="23200281" STOP_POS="65861506" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="55373161" STOP_POS="57922038" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303005</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303006</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat101-D13Rat46&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="47354258" STOP_POS="47354444" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="69535761" STOP_POS="69535887" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="75026588" STOP_POS="75026713" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55560677" STOP_POS="79943775" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="46269934" STOP_POS="72638941" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303006</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303007</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat127-D13Rat46&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="53382878" STOP_POS="69535887" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="17996178" STOP_POS="75026713" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="23200281" STOP_POS="79943775" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="55373161" STOP_POS="72638941" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303007</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303008</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat61-D13GRat197&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="61057931" STOP_POS="73485113" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="66204484" STOP_POS="79034003" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="71178814" STOP_POS="83929327" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="63301384" STOP_POS="76779489" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303008</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303009</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat183-D13Rat192&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="98253807" STOP_POS="98254003" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="74023918" STOP_POS="95722440" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="79567081" STOP_POS="104392271" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="84460970" STOP_POS="109040616" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="77336098" STOP_POS="100133413" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303009</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303010</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Got51-D13Rat192&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="98253807" STOP_POS="98254003" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="66706825" STOP_POS="95722440" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="72031440" STOP_POS="104392271" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="76974692" STOP_POS="109040616" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="69494047" STOP_POS="100133413" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303010</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303011</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Got51-D13Rat57&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="66706825" STOP_POS="66707096" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="72031440" STOP_POS="72031708" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="76974692" STOP_POS="87516988" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="69494047" STOP_POS="80109632" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303011</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303099</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Kcnh7&lt;sup&gt;Tn(sb-T2/Bart3)2.295Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=430&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnh7&lt;sup&gt;Tn(sb-T2/Bart3)2.295Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2303095</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="67737900" STOP_POS="68230950" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="47329338" STOP_POS="47822122" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="48662450" STOP_POS="49168716" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="55325680" STOP_POS="55822973" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="44657361" STOP_POS="45153509" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00430</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 8th intron of the Kcnh7 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303100</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Slc16a12&lt;sup&gt;Tn(sb-T2/Bart3)2.298Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=438&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc16a12&lt;sup&gt;Tn(sb-T2/Bart3)2.298Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2303097</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="241597165" STOP_POS="241674821" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="232184004" STOP_POS="232262170" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="252976071" STOP_POS="253054500" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="260197556" STOP_POS="260275962" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="238643040" STOP_POS="238665699" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00438</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Slc16a12 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303101</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Kcnab1&lt;sup&gt;Tn(sb-T2/Bart3)2.300Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=471&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnab1&lt;sup&gt;Tn(sb-T2/Bart3)2.300Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2303094</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="151446975" STOP_POS="151913636" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="149137025" STOP_POS="149603540" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="155555798" STOP_POS="156011438" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="174966379" STOP_POS="175400010" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="154837841" STOP_POS="155145882" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00471</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Kcnab1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303102</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Dnah11&lt;sup&gt;Tn(sb-T2/Bart3)2.293Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=429&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2024-04-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dnah11&lt;sup&gt;Tn(sb-T2/Bart3)2.293Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2303098</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="144982130" STOP_POS="145298523" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="138839175" STOP_POS="139155554" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="145784893" STOP_POS="146099212" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="154698519" STOP_POS="155011384" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="145190931" STOP_POS="145516859" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00429</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into  the 25th intron of the Dnah11 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303103</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Pebp4&lt;sup&gt;Tn(sb-T2/Bart3)2.299Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=455&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pebp4&lt;sup&gt;Tn(sb-T2/Bart3)2.299Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2303096</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="51328127" STOP_POS="51543920" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="44920946" STOP_POS="45134188" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="51528587" STOP_POS="51740626" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="55252902" STOP_POS="55466149" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="50225405" STOP_POS="50460627" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00455</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Pebp4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303116</RGD_ID>
    <STRAIN_SYMBOL>SPRD.WKY-(&lt;i&gt;D10Rat91-D10Rat135&lt;/i&gt;)/Ibmm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Universite Libre de Bruxelles, Institut de Biologie et de Medecine Moleculaires, Gosselies, Belgium</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="9658275" STOP_POS="104670812" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="9841807" STOP_POS="108540162" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="8619955" STOP_POS="108145987" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="9762188" STOP_POS="108776963" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303116</CITATION_ID>
    <DESCRIPTION>SPRD/HanZtm were crossed with WKY/HanZtm and F1 males were backcrossed with SPRD/HanZtm. Heterozygous carriers were bred to SPRD/HanZtm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303117</RGD_ID>
    <STRAIN_SYMBOL>SPRD.WKY-(&lt;i&gt;D5Rat190-D5Rat114&lt;/i&gt;)(&lt;i&gt;D18Rat102-D18Rat44&lt;/i&gt;)/Ibmm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Universite Libre de Bruxelles, Institut de Biologie et de Medecine Moleculaires, Gosselies, Belgium</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303117</CITATION_ID>
    <DESCRIPTION>Double congenic strain generated by intercrossing SPRD.WKY-(&lt;i&gt;D5Rat190-D5Rat114&lt;/i&gt;)/Ibmm and SPRD.WKY-(&lt;i&gt;D18Rat102-D18Rat44&lt;/i&gt;)/Ibmm; F&lt;sub&gt;1&lt;/sub&gt; animals were intercrossed and F&lt;sub&gt;2&lt;/sub&gt; screened for heterozygousity by markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303148</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Wox16-D9Rat76&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="29695268" STOP_POS="44458488" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="22198773" STOP_POS="36962591" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="25819185" STOP_POS="41261265" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="24681016" STOP_POS="40929956" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="18476042" STOP_POS="33497026" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303148</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Wox16-D9Rat64&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303149</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Wox16-D9Mco73&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="29695268" STOP_POS="29695440" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="22198773" STOP_POS="50687400" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="25819185" STOP_POS="55627498" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="24681016" STOP_POS="55323208" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="18476042" STOP_POS="47764357" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303149</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Wox16-D9Rat64&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303150</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco74-D9Rat64&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="28806563" STOP_POS="92491790" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="32677807" STOP_POS="99041268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="31484855" STOP_POS="98715585" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="25174989" STOP_POS="91131755" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303150</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Wox16-D9Rat64&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303151</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Wox16-D9Mco77&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="29695268" STOP_POS="64271691" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="22198773" STOP_POS="56777289" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="25819185" STOP_POS="64491201" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="24681016" STOP_POS="64294638" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="18476042" STOP_POS="54083264" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303151</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Wox16-D9Rat64&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303152</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco72-D9Mco93&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="47902208" STOP_POS="91616855" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="52686874" STOP_POS="98164303" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52352690" STOP_POS="97845437" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="44842118" STOP_POS="90249887" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303152</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Wox16-D9Rat64&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303153</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Rat7-D9Mco93&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="86720043" STOP_POS="86720295" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="79271511" STOP_POS="91616855" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="83686153" STOP_POS="98164303" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="83451810" STOP_POS="97845437" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="77170797" STOP_POS="90249887" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303153</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Wox16-D9Rat64&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303154</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Wox16-D9Mco85&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="29695268" STOP_POS="29695440" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="22198773" STOP_POS="78595166" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="25819185" STOP_POS="82890620" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="24681016" STOP_POS="82659881" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="18476042" STOP_POS="76456066" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303154</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Wox16-D9Rat64&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303504</RGD_ID>
    <STRAIN_SYMBOL>LEW/JmsNgs</STRAIN_SYMBOL>
    <FULL_NAME>congenital hydrocephalus rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=192 &gt; National BioResource Project for the Rat in Japan&lt;/a</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=192 &gt; National BioResource Project for the Rat in Japan&lt;/a</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Ophthalmology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303504</CITATION_ID>
    <DESCRIPTION>Lewis rats from Tokyo Medical Insitute to Seiwa Institute of Experimental Animals, Hydrocephalus was found the rats at F27 in 1980, these were sent to Dr. Yasutaka Noda at Center for Animal Experiments, Kurume University, The hydrocephalus rat strains have been maintained out by selective breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303610</RGD_ID>
    <STRAIN_SYMBOL>SD/HsdCwr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Case Western Reserve University School of Medicine, Cleveland, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303610</CITATION_ID>
    <DESCRIPTION>derived from SD/Hsd by cousin-cousin mating for more than 20 generations</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303611</RGD_ID>
    <STRAIN_SYMBOL>BN/HsdMcwiCwr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Case Western Reserve University School of Medicine, Cleveland, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303611</CITATION_ID>
    <DESCRIPTION>derived from BN/NHsdMcwi colony directly from Medical College of Wisconsin by brother-sister mating</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303640</RGD_ID>
    <STRAIN_SYMBOL>WAG/RijCmcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Medical Countermeasures Against Radiological Terrorism, Medical College of Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303640</CITATION_ID>
    <DESCRIPTION>Substrain of WAG/Rij, separated from the Rijswijk colony in about 1975, now maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303739</RGD_ID>
    <STRAIN_SYMBOL>RDW/UmeSlc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>This strain is no longer available from NBRP-Rat (June 2022).</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2022-06-09)</AVAILABILITY>
    <RESEARCH_USE>Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303739</CITATION_ID>
    <DESCRIPTION>From Tohoku University to Slc (1999)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303759</RGD_ID>
    <STRAIN_SYMBOL>WT/Jtt</STRAIN_SYMBOL>
    <FULL_NAME>whitish teeth rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=476 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=476 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Dentistry</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303759</CITATION_ID>
    <DESCRIPTION>In 2001, abnormal incisors that had deteriorated and had a whitish chalk-like appearance were unexpectedly discovered in one male rat among Sprague-Dawley [Crj:CD(SD)IGS] rats (Masuyama, 2005). After that, this mutant phenotype was maintained by sib-mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303761</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-EGFP)4Osb</STRAIN_SYMBOL>
    <FULL_NAME>Green rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=559&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=559&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303761</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries the enhanced green fluorescent protein (EGFP) gene driven by ubiquitous CAG promoter. This transgenic strain was established by Japan SLC, Inc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303779</RGD_ID>
    <STRAIN_SYMBOL>OLETF-Chr 14&lt;sup&gt;F344&lt;/sup&gt;/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=500 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=500 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303779</CITATION_ID>
    <DESCRIPTION>Chromosome 14 from F344 is introgressed in OLETF background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303784</RGD_ID>
    <STRAIN_SYMBOL>SHR-Chr 4&lt;sup&gt;WKY&lt;/sup&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=606&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=606&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303784</CITATION_ID>
    <DESCRIPTION>Chromosome 3 from WKY is introgressed into the genomic background of SHR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303785</RGD_ID>
    <STRAIN_SYMBOL>SHRSP-Chr 3&lt;sup&gt;WKY&lt;/sup&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=605&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=605&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303785</CITATION_ID>
    <DESCRIPTION>Chromosome 3 from WKY is introgressed into the genomic background of SHRSP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303792</RGD_ID>
    <STRAIN_SYMBOL>WTC.ZI-&lt;i&gt;Atrn&lt;sup&gt;zi&lt;/sup&gt;&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=22&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=22&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Atrn&lt;sup&gt;&lt;i&gt;zi&lt;/i&gt;&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>40902832</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303792</CITATION_ID>
    <DESCRIPTION>Zitter rat was detected in a Sprague Dawley colony (SD) in Hannover in 1978 by Rehm. 1983 introduced to Kyoto University and established ZI/Kyo. A second zi allele carrying line with WTC backgrund was established at Kyoto University</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303793</RGD_ID>
    <STRAIN_SYMBOL>WTC.DMY-&lt;i&gt;dmy&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=19&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=19&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303793</CITATION_ID>
    <DESCRIPTION>Congenic strain derived by transferring dmy locus from DMY/Kyo on WTC/Kyo background at Kyoto University</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303971</RGD_ID>
    <STRAIN_SYMBOL>OLETF.F344-(&lt;i&gt;D7Mgh16-D7Mgh20&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=82&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=82&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="93145728" STOP_POS="93145964" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="91256311" STOP_POS="91256547" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="100004559" STOP_POS="100004794" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="100584458" STOP_POS="100584693" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="96491967" STOP_POS="96492203" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303971</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1999. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303972</RGD_ID>
    <STRAIN_SYMBOL>BN-Chr 13&lt;sup&gt;SS&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303972</CITATION_ID>
    <DESCRIPTION>A cross of BN and SS strains which results in a BN genomic background with a SS chromosome introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303973</RGD_ID>
    <STRAIN_SYMBOL>OLETF.F344-(&lt;i&gt;D10Wox7-D10Wox6&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=78&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=78&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="99451733" STOP_POS="99451848" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="98952626" STOP_POS="98952741" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="102427604" STOP_POS="102427718" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="102101261" STOP_POS="102101375" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="103550924" STOP_POS="103551039" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303973</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1999-2000. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303976</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Cyp7b1&lt;sup&gt;Tn(sb-T2/Bart3)2.306Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=472&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp7b1&lt;sup&gt;Tn(sb-T2/Bart3)2.306Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2303974</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="102419011" STOP_POS="102586047" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="100502791" STOP_POS="100669713" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="102701903" STOP_POS="102871257" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="122442002" STOP_POS="122610354" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="103102679" STOP_POS="103271273" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00472</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Cyp7b1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303977</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ano3&lt;sup&gt;Tn(sb-T2/Bart3)2.307Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=477&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ano3&lt;sup&gt;Tn(sb-T2/Bart3)2.307Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2303975</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="117690242" STOP_POS="118004695" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="97235671" STOP_POS="97550090" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="101843516" STOP_POS="102203368" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="108441370" STOP_POS="108751911" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="96123925" STOP_POS="96237157" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00477</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Tmem16c gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303978</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Mgh16-D7Mgh20&lt;/i&gt;)(&lt;i&gt;D14Rat8-D14Rat26&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=83&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=83&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303978</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303979</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Mgh16-D7Mgh20&lt;/i&gt;)(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=84&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=84&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303979</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303986</RGD_ID>
    <STRAIN_SYMBOL>WKAH.LEC-&lt;i&gt;Atp7b&lt;sup&gt;hts&lt;/sup&gt;&lt;/i&gt;/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=106&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=106&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2021-02-11)</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES>Atp7b&lt;sup&gt;hts&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11532742</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="76654725" STOP_POS="76726092" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="69952286" STOP_POS="70024404" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="74865516" STOP_POS="74944935" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="74495179" STOP_POS="74575822" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="74607988" STOP_POS="74680080" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303986</CITATION_ID>
    <DESCRIPTION>A congenic strain produced by 8 generation backcrosses to WKAH strain in 1989.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303987</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D17Mgh4-Edn1&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=104&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=104&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES>Edn1</ALLELES>
    <ALLELE_RGD_IDS>2532</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="22660799" STOP_POS="49497050" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="22454924" STOP_POS="22460812" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="22136814" STOP_POS="22143745" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="24117499" STOP_POS="24124188" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="28303886" STOP_POS="28309775" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303987</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303988</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;)(&lt;i&gt;D8Rat54-D8Mgh17&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=88&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=88&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303988</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303989</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D9Mgh8-D9Mit2&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=96&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=96&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="73930789" STOP_POS="73930979" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="36840385" STOP_POS="66437242" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="41139089" STOP_POS="71771476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="40808491" STOP_POS="70797404" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="33374546" STOP_POS="63705951" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303989</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303990</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D1Mit20-D1Mgh26&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=92&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=92&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="172711200" STOP_POS="172711337" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="188051098" STOP_POS="188051234" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="100372156" STOP_POS="194998184" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="94356875" STOP_POS="176616212" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303990</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303991</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Rat31-D7Rat35&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=103 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=103 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="20057232" STOP_POS="20057375" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="18169505" STOP_POS="26029351" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="24175337" STOP_POS="32258115" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="24326613" STOP_POS="32338830" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="20307479" STOP_POS="28488710" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303991</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303992</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D5Mgh29-D5Mgh22&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=102 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=102 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="156289283" STOP_POS="156289444" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="151005994" STOP_POS="151006154" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="157212263" STOP_POS="157212422" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="160953624" STOP_POS="160953783" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="157584332" STOP_POS="157584492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303992</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303993</RGD_ID>
    <STRAIN_SYMBOL>OLETF.F344-(&lt;i&gt;D9Mgh8-D9Mit2&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=97 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=97 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="73930789" STOP_POS="73930979" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="36840385" STOP_POS="66437242" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="41139089" STOP_POS="71771476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="40808491" STOP_POS="70797404" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="33374546" STOP_POS="63705951" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303993</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1999. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303994</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D5Mgh4-D5Rat21&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=95&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=95&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="38207390" STOP_POS="100158356" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="95112065" STOP_POS="95112231" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="98224053" STOP_POS="98224216" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="102264251" STOP_POS="102264414" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="99344678" STOP_POS="99344842" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303994</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303995</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D8Rat54-D8Mgh17&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=90&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=90&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="27588221" STOP_POS="27588390" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="69349194" STOP_POS="69349344" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="74917593" STOP_POS="80840067" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="21850030" STOP_POS="79245063" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="19796514" STOP_POS="73102155" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303995</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303996</RGD_ID>
    <STRAIN_SYMBOL>F344.Cg-&lt;i&gt;Foxn1&lt;sup&gt;rnu&lt;/sup&gt;&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=541&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=541&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Immunology; Cancer</RESEARCH_USE>
    <ALLELES>Foxn1</ALLELES>
    <ALLELE_RGD_IDS>3970</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="63749461" STOP_POS="63778468" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="63251400" STOP_POS="63273710" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="65621142" STOP_POS="65634666" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="66004940" STOP_POS="66030134" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="64243323" STOP_POS="64256847" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303996</CITATION_ID>
    <DESCRIPTION>This congenic strain was established as a strain with the genetic background of F344/N onto which a segment from the nude rat containing the &lt;i&gt;Foxn1&lt;sup&gt;rnu&lt;/sup&gt;&lt;/i&gt; was transferred. Originally, hairless mutant (&lt;i&gt;rnu&lt;/i&gt;) was observed in a colony of outbred hooded rats maintained at the Rowett Research Institute in Scotland. Backcrossing started at Central Institute for Experimental Animals in 1979 and thereafter the subline was transported to the Institute of Laboratory Animals Graduate School of Medicine, Kyoto University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303997</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Mgh8-D7Mgh16&lt;/i&gt;)(&lt;i&gt;D14Rat23-D14Rat26&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=86&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=86&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303997</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303998</RGD_ID>
    <STRAIN_SYMBOL>WKAH.LEC-&lt;i&gt;Ptprk&lt;sup&gt;thid&lt;/sup&gt;&lt;/i&gt;/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=107&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=107&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES>Ptprk</ALLELES>
    <ALLELE_RGD_IDS>619706</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="18557091" STOP_POS="19056297" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="16738896" STOP_POS="17236687" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="17445052" STOP_POS="18058266" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="18602550" STOP_POS="19574958" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="17328563" STOP_POS="17752200" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303998</CITATION_ID>
    <DESCRIPTION>A congenic strain produced by 8 generation backcrosses to WKAH strain in 1989.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2303999</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat8-D14Rat26&lt;/i&gt;)(&lt;i&gt;D14Rat18-D14Rat22&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=100&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=100&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2303999</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304000</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D12Wox5-D12Rat21&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=98 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=98 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="18749469" STOP_POS="48428269" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="13635523" STOP_POS="42767729" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="15714609" STOP_POS="48536609" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="17721341" STOP_POS="50319569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="43801711" STOP_POS="43801909" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304000</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304001</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;)(&lt;i&gt;D14Rat8-D14Rat26&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=89&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=89&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304001</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304002</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D11Mgh4-D11Mgh1&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=91&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=91&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="73308315" STOP_POS="96071021" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="59802622" STOP_POS="82566702" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="62653194" STOP_POS="86714631" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="65784365" STOP_POS="89808503" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="61504311" STOP_POS="84560241" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304002</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304003</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D16Rat19-D16Rat13&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=101 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=101 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="31951520" STOP_POS="73187298" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="35307110" STOP_POS="78172206" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="35126908" STOP_POS="77759249" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="35339929" STOP_POS="77968799" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304003</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304004</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Mit2-D7Mgh16&lt;/i&gt;)(&lt;i&gt;D14Rat23-D14Rat26&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=85&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=85&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304004</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304016</RGD_ID>
    <STRAIN_SYMBOL>BUF.ACI-(&lt;i&gt;D4Rat192-D4Rat66&lt;/i&gt;)/Ncc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=165&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=165&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="157704599" STOP_POS="157704722" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="157417581" STOP_POS="157417703" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="224435359" STOP_POS="224435481" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="161023350" STOP_POS="161023765" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304016</CITATION_ID>
    <DESCRIPTION>This congenic strain in the BUF background that had homozygous ACI chr 4 was developed by speed congenic method.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304017</RGD_ID>
    <STRAIN_SYMBOL>F344.CVD-&lt;i&gt;Unc5c&lt;sup&gt;cvd&lt;/sup&gt;&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=153&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=153&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-04-05)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Unc5c|Unc5c&lt;sup&gt;cvd&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>735109|12802355</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="232854352" STOP_POS="233208482" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="230489880" STOP_POS="230489880" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="247352390" STOP_POS="247352390" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="265573406" STOP_POS="265926229" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="239365109" STOP_POS="239721231" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304017</CITATION_ID>
    <DESCRIPTION>CVD ( Cerebellar vermis defect) rat originated from spontanious mutation of LEW inbred at Osaka Prefecture University in 1992. A mutation in Unc5c has been identified in CVD rats.  A congenic strain was produced by backcrossing CVD to F344/NSlc strain at Kyoto University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304018</RGD_ID>
    <STRAIN_SYMBOL>BUF.ACI-(&lt;i&gt;D4Rat226-D4Rat109&lt;/i&gt;)/Ncc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=166&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=166&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="63804922" STOP_POS="116959332" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="62837725" STOP_POS="115401611" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="61612433" STOP_POS="113728420" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="61331785" STOP_POS="178404466" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="61542056" STOP_POS="117094107" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304018</CITATION_ID>
    <DESCRIPTION>This congenic strain in the BUF background that had homozygous ACI chr 4 was developed by speed congenic method.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304019</RGD_ID>
    <STRAIN_SYMBOL>BUF.ACI-(&lt;i&gt;D15Rat68-D15Rat29&lt;/i&gt;)/Ncc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=168&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=168&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="62893434" STOP_POS="106778366" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="56484420" STOP_POS="56484560" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="63498932" STOP_POS="63499071" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="67139660" STOP_POS="67139799" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="62521452" STOP_POS="108387411" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304019</CITATION_ID>
    <DESCRIPTION>This congenic strain in the BUF background that had homozygous ACI chr 15 was developed by speed congenic method.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304020</RGD_ID>
    <STRAIN_SYMBOL>ACI.BUF-(&lt;i&gt;D15Rat97-D15Rat29&lt;/i&gt;)/Ncc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=169&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=169&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="106778197" STOP_POS="106778366" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="71477067" STOP_POS="71477291" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="79033484" STOP_POS="79033707" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="82573157" STOP_POS="82573380" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="78048029" STOP_POS="108387411" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304020</CITATION_ID>
    <DESCRIPTION>This congenic strain in the ACI background that had homozygous BUF/Nac chr 15 was developed by speed congenic method.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304037</RGD_ID>
    <STRAIN_SYMBOL>DDI/Ddia</STRAIN_SYMBOL>
    <FULL_NAME>dokkyo diabetes insipidus rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=282&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=282&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Metabolism; Urology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304037</CITATION_ID>
    <DESCRIPTION>Strain developed at Dokkyo University, School of Medicine, Tochigi, Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304038</RGD_ID>
    <STRAIN_SYMBOL>OP/Jtt</STRAIN_SYMBOL>
    <FULL_NAME>Opacitas</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=181&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=181&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304038</CITATION_ID>
    <DESCRIPTION>Maintained in sib mating between opacitas rats (heterozygoutes) and normal rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304039</RGD_ID>
    <STRAIN_SYMBOL>WIC-&lt;i&gt;Tg&lt;sup&gt;rdw&lt;/sup&gt;&lt;/i&gt;/Kts</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>School of Medicine, Kitasato University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=193&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-04-21)</AVAILABILITY>
    <RESEARCH_USE>Metabolism</RESEARCH_USE>
    <ALLELES>Tg&lt;sup&gt;rdw&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12879860</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="100307349" STOP_POS="100492246" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="98517376" STOP_POS="98517376" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="107567063" STOP_POS="107567063" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="107399165" STOP_POS="107602400" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="104035776" STOP_POS="104220754" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304039</CITATION_ID>
    <DESCRIPTION>Established from a closed colony of Wistar-Imamichi (WIC) rats as a spontaneous mutant exhibiting congenital dwarfism (rdw), is inherited as an autosomal recessive. This strain has a spontaneous missense mutation, G2320R, in the thyroglobul gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304040</RGD_ID>
    <STRAIN_SYMBOL>F344.OP-&lt;i&gt;Op&lt;/i&gt;/Jtt</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=182&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=182&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304040</CITATION_ID>
    <DESCRIPTION>Opacitas rats (heterozygtes) are backcorssed with F344/DuCrj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304041</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-Rgn)Slc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=389&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=389&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Osteosis</RESEARCH_USE>
    <ALLELES>Rgn</ALLELES>
    <ALLELE_RGD_IDS>3560</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304041</CITATION_ID>
    <DESCRIPTION>Transgenic srain derived by injecting SD rats with a vector containing ubiquitous CAG promoter and the rat Rgn gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304045</RGD_ID>
    <STRAIN_SYMBOL>F344.ZUC-&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt;(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=392&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=392&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="39507513" STOP_POS="39507682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="1217606" STOP_POS="39153750" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="2227825" STOP_POS="61783215" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="2222207" STOP_POS="61886417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="1764386" STOP_POS="41707592" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304045</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 2002. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304046</RGD_ID>
    <STRAIN_SYMBOL>F344.ZUC-(&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt;)(&lt;i&gt;D7Rat16-D7Mgh20&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=391&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=391&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="102920123" STOP_POS="102920263" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="112204378" STOP_POS="112204517" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="112143411" STOP_POS="112143550" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="108647236" STOP_POS="108647376" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304046</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 2002. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304047</RGD_ID>
    <STRAIN_SYMBOL>F344.ZUC-&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt;/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=390&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=390&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES>Lepr|Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>3001|13432153</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304047</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 2001. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304050</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat23-D14Rat55&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=396 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=396 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="26011016" STOP_POS="26011237" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="1217606" STOP_POS="25656577" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="2227825" STOP_POS="27686562" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="2222207" STOP_POS="27510976" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="1764386" STOP_POS="27571792" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304050</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304051</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat8-D14Rat12&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=399 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=399 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="30674469" STOP_POS="39507682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="30320092" STOP_POS="39153750" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="32593926" STOP_POS="61783215" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="32389647" STOP_POS="61886417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="32584630" STOP_POS="41707592" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304051</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304052</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat55-D14Rat12&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=400 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=400 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="26011016" STOP_POS="39507682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="25656356" STOP_POS="39153750" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="27686342" STOP_POS="61783215" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="27510756" STOP_POS="61886417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="27571487" STOP_POS="41707592" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304052</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304053</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat23-D14Rat5&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=394 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=394 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="10581196" STOP_POS="10581346" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="1217606" STOP_POS="10277166" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="2227825" STOP_POS="11926177" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="2222207" STOP_POS="11868597" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="1764386" STOP_POS="11589751" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304053</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304054</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat23-D14Rat10&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=397 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=397 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="31238080" STOP_POS="31238250" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="1217606" STOP_POS="30883947" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="2227825" STOP_POS="33163485" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="2222207" STOP_POS="32957654" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="1764386" STOP_POS="33157602" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304054</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304055</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Wox1-D14Rat12&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=404&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=404&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="9119913" STOP_POS="39507682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="39153581" STOP_POS="39153750" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="61783047" STOP_POS="61783215" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="61886249" STOP_POS="61886417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="41707423" STOP_POS="41707592" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304055</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304056</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat23-D14Wox14&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=395 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=395 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="1217606" STOP_POS="1217776" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="2227825" STOP_POS="22009966" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="2222207" STOP_POS="21925011" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="1764386" STOP_POS="21885861" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304056</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304057</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat12&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=398 &gt; National BioResource Project for the Rat in Japan&lt;/a</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=398 &gt; National BioResource Project for the Rat in Japan&lt;/a</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="39507513" STOP_POS="39507682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="39153581" STOP_POS="39153750" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="61783047" STOP_POS="61783215" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="61886249" STOP_POS="61886417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="41707423" STOP_POS="41707592" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304057</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304058</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat143-D14Rat12&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=402&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=402&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="18496705" STOP_POS="39507682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="18212584" STOP_POS="39153750" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="19847829" STOP_POS="61783215" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="19754557" STOP_POS="61886417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="19738306" STOP_POS="41707592" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304058</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304059</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat5-D14Rat12&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=403&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=403&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="10581196" STOP_POS="39507682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="10277016" STOP_POS="39153750" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="11926028" STOP_POS="61783215" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="11868448" STOP_POS="61886417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="11589293" STOP_POS="41707592" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304059</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304060</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Wox14-D14Rat12&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=401&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=401&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="39507513" STOP_POS="39507682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="39153581" STOP_POS="39153750" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="22009849" STOP_POS="61783215" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="21924894" STOP_POS="61886417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="21885743" STOP_POS="41707592" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304060</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1998. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304061</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat23&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=393 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=393 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="1217606" STOP_POS="1217776" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="2227825" STOP_POS="2227992" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="2222207" STOP_POS="2222374" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="1764386" STOP_POS="1764554" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304061</CITATION_ID>
    <DESCRIPTION>Established as speed congenics (5 generations, microsatellite marker) at the University of Tokushima School of Medicine, Institute for Animal Experimentation in 1999. Afterwards, maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304063</RGD_ID>
    <STRAIN_SYMBOL>KDP-Tg(H2Kd-Cblb)2Nyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=451&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=451&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Immunology</RESEARCH_USE>
    <ALLELES>Cblb</ALLELES>
    <ALLELE_RGD_IDS>620535</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304063</CITATION_ID>
    <DESCRIPTION>Homozygous Cblb rats are usually infertile in both sexes and are therefore maintained by crossing heterozygous individuals (segregating inbred strain).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304064</RGD_ID>
    <STRAIN_SYMBOL>KDP-Tg(H2Kd-Cblb)1Nyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=450&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=450&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Immunology</RESEARCH_USE>
    <ALLELES>Cblb</ALLELES>
    <ALLELE_RGD_IDS>620535</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304064</CITATION_ID>
    <DESCRIPTION>Homozygous Cblb rats are usually infertile in both sexes and are therefore maintained by crossing heterozygous individuals (segregating inbred strain).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304065</RGD_ID>
    <STRAIN_SYMBOL>KDP-Tg(INS-Cblb)1Nyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=452&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=452&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Immunology</RESEARCH_USE>
    <ALLELES>Cblb</ALLELES>
    <ALLELE_RGD_IDS>620535</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304065</CITATION_ID>
    <DESCRIPTION>Homozygous Cblb rats are usually infertile in both sexes and are therefore maintained by crossing heterozygous individuals (segregating inbred strain).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304066</RGD_ID>
    <STRAIN_SYMBOL>KDP-Tg(CAG-Cblb)1Nyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=453&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=453&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cblb</ALLELES>
    <ALLELE_RGD_IDS>620535</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304066</CITATION_ID>
    <DESCRIPTION>Homozygous Cblb rats are usually infertile in both sexes and are therefore maintained by crossing heterozygous individuals (segregating inbred strain).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304074</RGD_ID>
    <STRAIN_SYMBOL>WKY.BUF-&lt;i&gt;Tsr1d&lt;/i&gt;/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=465&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=465&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304074</CITATION_ID>
    <DESCRIPTION>This congenic strain was established as a strain with the genetic background of WKY onto which a segment from the BUF/Mna containing the thymus susceptible gene of rat-1, Tsr-1 (on chr.7) has been transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304075</RGD_ID>
    <STRAIN_SYMBOL>ACI.BUF-&lt;i&gt;Pur1&lt;/i&gt;/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=467&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=467&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Urology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304075</CITATION_ID>
    <DESCRIPTION>This congenic strain was established as a strain with the genetic background of ACI onto which a segment from the BUF/Mna containing the proteinuria-susceptible gene, Pur1 (on chr.13) has been transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304076</RGD_ID>
    <STRAIN_SYMBOL>WKY.BUF-&lt;i&gt;Thym1, Thym2&lt;/i&gt;/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=464&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=464&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2018-03-14)</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304076</CITATION_ID>
    <DESCRIPTION>This double congenic strain was established as a strain with the genetic background of WKY onto which a segment from the BUF/Mna containing the thymus enlargement, Ten1 (Thym1) (on chr.1) and Ten2 (Thym2)(on chr. 13) has been transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304077</RGD_ID>
    <STRAIN_SYMBOL>WKY.BUF-&lt;i&gt;Pur1s&lt;/i&gt;/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=462&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=462&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Urology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304077</CITATION_ID>
    <DESCRIPTION>This congenic strain was established as a strain with the genetic background of WKY onto which a segment from the BUF/Mna containing the proteinuria-susceptible locus, on chr.13 has been transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304078</RGD_ID>
    <STRAIN_SYMBOL>ACI.BUF-&lt;i&gt;Ten1&lt;/i&gt;/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=468&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=468&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304078</CITATION_ID>
    <DESCRIPTION>This congenic strain was established as a strain with the genetic background of ACI onto which a segment from the BUF/Mna containing the thymus enlargement, Ten1 (on chr.1) has been transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304079</RGD_ID>
    <STRAIN_SYMBOL>WKY.BUF-&lt;i&gt;Ten1&lt;/i&gt;/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=471&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=471&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304079</CITATION_ID>
    <DESCRIPTION>This congenic strain was established as a strain with the genetic background of WKY onto which a segment from the BUF/Mna containing the thymus enlargement, Ten1 (on chr.1) has been transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304080</RGD_ID>
    <STRAIN_SYMBOL>ACI.BUF-&lt;i&gt;Aftm1&lt;/i&gt;/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=469&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=469&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304080</CITATION_ID>
    <DESCRIPTION>This congenic strain was established as a strain with the genetic background of ACI onto which a segment from the BUF/Mna has been transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304081</RGD_ID>
    <STRAIN_SYMBOL>WKY.BUF-&lt;i&gt;Pur1w&lt;/i&gt;/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=463&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=463&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Urology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304081</CITATION_ID>
    <DESCRIPTION>This congenic strain was established as a strain with the genetic background of WKY onto which a segment from the BUF/Mna containing the proteinuria-susceptible locus, on chr.13 has been transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304082</RGD_ID>
    <STRAIN_SYMBOL>WKY.BUF-&lt;i&gt;Ten2&lt;/i&gt;/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=466&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=466&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Urology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304082</CITATION_ID>
    <DESCRIPTION>This congenic strain was established as a strain with the genetic background of WKY onto which a segment from the BUF/Mna containing the thymus enlargement, Ten2 (on chr.13) has been transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304083</RGD_ID>
    <STRAIN_SYMBOL>ACI.BUF-&lt;i&gt;Ten2&lt;/i&gt;/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=470&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=470&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304083</CITATION_ID>
    <DESCRIPTION>This congenic strain was established as a strain with the genetic background of ACI onto which a segment from the BUF/Mna containing the thymus enlargement, Ten2 (on chr.13) has been transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304093</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Rat106-D1Arb21&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=484 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=484 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="146593951" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="137184788" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="145140412" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="146068162" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="139471535" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304093</CITATION_ID>
    <DESCRIPTION>Developed by the depositor</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304094</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Smu12-D1Rat44&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=447 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=447 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="160283901" STOP_POS="160284012" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="150872626" STOP_POS="150872737" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="161493758" STOP_POS="161493868" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="167707459" STOP_POS="167707569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="153754139" STOP_POS="153754250" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304094</CITATION_ID>
    <DESCRIPTION>This is a congenic strain developed by the depositor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304095</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Plcb2-WGA-EGFP)F1Abek</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=455 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=455 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304095</CITATION_ID>
    <DESCRIPTION>This is a transgenic strain developed by the depositor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304096</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Rat49-D1Arb21&lt;/i&gt;)/1Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=486 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=486 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="191848691" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="154464069" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="165129767" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="171330622" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="157497884" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304096</CITATION_ID>
    <DESCRIPTION>Developed by the depositor</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304097</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Rat49-D1Arb21&lt;/i&gt;)/2Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=448&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=448&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="191848691" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="154464069" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="165129767" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="171330622" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="157497884" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304097</CITATION_ID>
    <DESCRIPTION>This is a congenic strain developed by the depositor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304098</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Smu13-D1Arb21&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=487 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=487 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="191848691" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="182418219" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="199254518" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="206276946" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="187092235" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304098</CITATION_ID>
    <DESCRIPTION>Developed by the depositor</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304099</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Smu12-D1Arb21&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=482 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=482 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="191848691" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="182418219" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="199254518" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="206276946" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="187092235" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304099</CITATION_ID>
    <DESCRIPTION>This is a congenic strain developed by the depositor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304100</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Rat39-D1Arb21&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=481 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=481 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="191848691" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="124668437" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="132134307" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="133172202" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="125983422" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304100</CITATION_ID>
    <DESCRIPTION>This is a congenic strain developed by the depositor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304101</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Rat43-D1Arb21&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=483 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=483 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="146080545" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="182418219" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="144634295" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="206276946" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="187092235" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304101</CITATION_ID>
    <DESCRIPTION>This is a congenic strain developed by the depositor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304102</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Mgh5-D1Rat106&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=445&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=445&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="146594089" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="137184926" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="145354344" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="146282094" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="139471673" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304102</CITATION_ID>
    <DESCRIPTION>This is a congenic strain developed by the depositor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304104</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Plcb2-WGA-EGFP)M1Abek</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=456&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=456&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304104</CITATION_ID>
    <DESCRIPTION>This is a transgenic strain developed by the depositor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304120</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/2Ta</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=417&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=417&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304120</CITATION_ID>
    <DESCRIPTION>Kyo &gt; Ta (1972)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304121</RGD_ID>
    <STRAIN_SYMBOL>DA.WF-(&lt;i&gt;D1Mit1-D1Mit3&lt;/i&gt;)/Kop</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=522&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=522&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="153679879" STOP_POS="153680016" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="144267353" STOP_POS="144267916" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="156446196" STOP_POS="156446783" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="162692213" STOP_POS="162692800" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="146971846" STOP_POS="146971983" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304121</CITATION_ID>
    <DESCRIPTION>This congenic strain in the DA background by introgressing a segment from WF</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304122</RGD_ID>
    <STRAIN_SYMBOL>DA.WF-(&lt;i&gt;D1Mgh21-D1Mgh10&lt;/i&gt;)(&lt;i&gt;D4Mit11-Nos3&lt;/i&gt;)/Kop</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=523&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=523&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304122</CITATION_ID>
    <DESCRIPTION>This congenic strain in the DA background by introgressing a segment from WF</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304123</RGD_ID>
    <STRAIN_SYMBOL>DA.WF-(&lt;i&gt;D4Mit11-Nos3&lt;/i&gt;)/Kop</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=524&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=524&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES>Nos3</ALLELES>
    <ALLELE_RGD_IDS>3186</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="11686088" STOP_POS="92690793" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="10793834" STOP_POS="91360801" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="7321908" STOP_POS="92484312" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="7333272" STOP_POS="157291359" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="6158847" STOP_POS="91330856" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304123</CITATION_ID>
    <DESCRIPTION>This congenic strain in the DA background by introgressing a segment from WF</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304124</RGD_ID>
    <STRAIN_SYMBOL>DA.WF-(&lt;i&gt;D1Mgh21-D1Mgh10&lt;/i&gt;)(&lt;i&gt;D4Mit11-Nos3&lt;/i&gt;)(&lt;i&gt;D1Mit1-D1Mit3&lt;/i&gt;)/Kop</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=520&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=520&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304124</CITATION_ID>
    <DESCRIPTION>This congenic strain in the DA background by introgressing a segment from WF</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304125</RGD_ID>
    <STRAIN_SYMBOL>DRH.F344-(&lt;i&gt;D1Mgh8-D1Mgh12&lt;/i&gt;)/Shigm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=492&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=492&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University, Japan</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="162548015" STOP_POS="162548132" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="153136852" STOP_POS="153136969" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="163796316" STOP_POS="163796432" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="169999389" STOP_POS="270717037" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="156124624" STOP_POS="247322277" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304125</CITATION_ID>
    <DESCRIPTION>desired fragment from F344 was introgressed into DRH background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304200</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(CAG-ABO*A)32Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=535 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=535 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Hematology</RESEARCH_USE>
    <ALLELES>Abo3</ALLELES>
    <ALLELE_RGD_IDS>628609</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304200</CITATION_ID>
    <DESCRIPTION>This transgenic strain expresses the transferase A of the ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase ) driven by the CAG promoter established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304201</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Galntl6&lt;sup&gt;Tn(sb-T2/Bart3)2.311McwiRrrc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=450&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Galntl6&lt;sup&gt;Tn(sb-T2/Bart3)2.311Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2304194</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="36203674" STOP_POS="37454709" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="31192880" STOP_POS="32443979" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="34551052" STOP_POS="35803840" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="34380195" STOP_POS="35619972" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="34557663" STOP_POS="35853849" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00450</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 4th intron of the Galntl6 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304202</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;RGD1565323&lt;sup&gt;Tn(sb-T2/Bart3)2.312Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=437&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>RGD1565323&lt;sup&gt;Tn(sb-T2/Bart3)2.312Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2304193</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="31870462" STOP_POS="31887579" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="31661713" STOP_POS="31678816" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="32973695" STOP_POS="32990440" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="34865901" STOP_POS="34882646" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="38022396" STOP_POS="38039975" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00437</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of RGD1565323.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304203</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(CAG-DsRed2/GFP)1Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=532&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=532&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304203</CITATION_ID>
    <DESCRIPTION>DsRed2/GFP double-reporter transgenic rat driven under a ubiquitous CAG promoter. In this system, DsRed2 expression was replaced with GFP expression after Cre recombinase-mediated excision established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304204</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(CAG-ABO*B)13Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=527&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=527&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Hematology</RESEARCH_USE>
    <ALLELES>Abo3</ALLELES>
    <ALLELE_RGD_IDS>628609</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304204</CITATION_ID>
    <DESCRIPTION>This transgenic strain expresses the transferase B of the ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase ) driven by the CAG promoter established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304205</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Alb-DsRed2)34Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=528&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=528&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304205</CITATION_ID>
    <DESCRIPTION>This transgenic strain expresses the DsRed2 (DsRed: red fluorescent protein) liver-specific under the direction of the mouse albumin enhancer/promoter established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304206</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(CAG-DsRed2/GFP)15Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=533&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=300&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=533&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=300&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00300</CITATION_ID>
    <DESCRIPTION>DsRed2/GFP double-reporter transgenic rat driven under a ubiquitous CAG promoter. In this system, DsRed2 expression was replaced with GFP expression after Cre recombinase-mediated excision established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304207</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Lzic&lt;sup&gt;Tn(sb-T2/Bart3)2.309Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=434&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lzic&lt;sup&gt;Tn(sb-T2/Bart3)2.309Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2304196</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="165211359" STOP_POS="165224569" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="159928260" STOP_POS="159941512" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="166430305" STOP_POS="166443485" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="170076617" STOP_POS="170089776" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="166567412" STOP_POS="166579423" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00434</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 6th intron of the Lzic gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304208</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Rapgef4&lt;sup&gt;Tn(sb-T2/Bart3)2.314Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=479&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rapgef4&lt;sup&gt;Tn(sb-T2/Bart3)2.314Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2304197</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="77217024" STOP_POS="77509933" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="56809388" STOP_POS="57101332" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="58632338" STOP_POS="58925127" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="65122705" STOP_POS="65409814" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="54396312" STOP_POS="54717148" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00479</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 11th intron of the Rapgef4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304209</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Rorb&lt;sup&gt;Tn(sb-T2/Bart3)2.304Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rorb&lt;sup&gt;Tn(sb-T2/Bart3)2.304Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2304199</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="225790216" STOP_POS="225970973" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="216363629" STOP_POS="216544390" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="234252757" STOP_POS="234442597" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="241354340" STOP_POS="241541103" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="222545682" STOP_POS="222726307" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304209</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Rorb gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304210</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Alb-DsRed2)42Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=529&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=260&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=529&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=260&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00260</CITATION_ID>
    <DESCRIPTION>This transgenic strain expresses the DsRed2 (DsRed: red fluorescent protein) liver-specific under the direction of the mouse albumin enhancer/promoter established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304211</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(CAG-cre)81Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=534&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=301&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=534&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=301&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2018-07-16)</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00301</CITATION_ID>
    <DESCRIPTION>This strain expresses the cre recombinase ubiquitously driven by CAG promoter. The majority of expression of the transgene is detected in the skeletal muscles established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304212</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;RGD1563503&lt;sup&gt;Tn(sb-T2/Bart3)2.313Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=453&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>RGD1563503&lt;sup&gt;Tn(sb-T2/Bart3)2.313Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2304198</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="15526295" STOP_POS="15527253" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="17584757" STOP_POS="17585688" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="21066144" STOP_POS="21067040" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00453</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 6th intron of RGD1563503.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304213</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;P3h3&lt;sup&gt;Tn(sb-T2/Bart3)2.310Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=433&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>P3h3&lt;sup&gt;Tn(sb-T2/Bart3)2.310Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2304195</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="159332514" STOP_POS="159348428" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="157646242" STOP_POS="157662035" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="157359331" STOP_POS="157375186" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="224377005" STOP_POS="224392881" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="160964297" STOP_POS="160978321" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00433</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Leprel2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304214</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(CAG-ABO*B)2Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=526 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=526 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Hematology</RESEARCH_USE>
    <ALLELES>Abo3</ALLELES>
    <ALLELE_RGD_IDS>628609</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304214</CITATION_ID>
    <DESCRIPTION>This transgenic strain expresses the transferase B of the ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase ) driven by the CAG promoter established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304215</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(XPO1)1Hik</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=575&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=575&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer; Infectious</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304215</CITATION_ID>
    <DESCRIPTION>F344/DuCrj Tg rat inoculated with human crm1 genome (BAC)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304221</RGD_ID>
    <STRAIN_SYMBOL>WTC-&lt;i&gt;swh&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Kyoto University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=539&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2020-12-11)</AVAILABILITY>
    <RESEARCH_USE>Dermatology</RESEARCH_USE>
    <ALLELES>Edaradd&lt;sup&gt;&lt;i&gt;swhKyo&lt;/i&gt;&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14398765</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="92854776" STOP_POS="92854776" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="85870608" STOP_POS="85870608" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="90842152" STOP_POS="90842152" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="92462305" STOP_POS="92503399" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="67056373" STOP_POS="67143933" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304221</CITATION_ID>
    <DESCRIPTION>The rat showed abnormal hair texture and mammary gland hypoplasia which occurred in the WTC.ZI-&lt;i&gt;Atrn&lt;sup&gt;zi&lt;/sup&gt;&lt;/i&gt; colony at the National Cancer Center Research Institute in 1998. After elimination of &lt;i&gt;zi&lt;/i&gt; allele, this strain has been maintained by sib mating and transferred to Kyoto Univ. in April 2002.  In 2011, Kuramoto et al. (RGD:14398762) identified a missense mutation in the Edaradd gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304222</RGD_ID>
    <STRAIN_SYMBOL>WIAR/Iar</STRAIN_SYMBOL>
    <FULL_NAME>Inbred Wistar-Imamichi</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=536&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=536&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-04-21)</AVAILABILITY>
    <RESEARCH_USE>Metabolism; Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304222</CITATION_ID>
    <DESCRIPTION>Strain developed by the depositor. This strain was established by inbreeding of Wistar-Imamichi rats by sib-mating. Strain characteristic is same as that of Wistar-Imamichi. (Nov 6, 2009)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304241</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(CXCR4)1Hik</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=560&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=560&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Infectious</RESEARCH_USE>
    <ALLELES>CXCR4</ALLELES>
    <ALLELE_RGD_IDS>732176</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304241</CITATION_ID>
    <DESCRIPTION>Transgenic rat developed by microinjection of a human CXCR4: chemokine (C-X-C motif) receptor 4, containing BAC clone into F344/DuCrj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304242</RGD_ID>
    <STRAIN_SYMBOL>WTC-&lt;i&gt;Kcnq1&lt;sup&gt;dfk&lt;/sup&gt;&lt;/i&gt;Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=548&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=548&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-04-05)</AVAILABILITY>
    <RESEARCH_USE>Otorhinology; Internal Organ</RESEARCH_USE>
    <ALLELES>Kcnq1|Kcnq1&lt;sup&gt;dfk&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>621503|12802344</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="207721134" STOP_POS="208054073" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="198374486" STOP_POS="198376539" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="216377021" STOP_POS="216379067" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="223154713" STOP_POS="223490458" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="203383401" STOP_POS="203803687" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304242</CITATION_ID>
    <DESCRIPTION>Rats with abnormal behaviors such as head-tossing, drawing back, stepping back, and circling were discovered in the N12F10 generation of a WTC.ZI-&lt;i&gt;Atrn&lt;sup&gt;zi&lt;/sup&gt;&lt;/i&gt; congenic strain at the Institute of Laboratory Animals, Graduate School of Medicine, Kyoto University, in 1999. The WTC-&lt;i&gt;Kcnq1&lt;sup&gt;dfk&lt;/sup&gt;&lt;/i&gt;/Kyo rat is a mutant for circling behavior. although the Atrn&lt;sup&gt;zi&lt;/sup&gt; allele of WTC.ZI-&lt;i&gt;Atrn&lt;sup&gt;zi&lt;/sup&gt;&lt;/i&gt; congenic rats was eliminated, the circling behavior remained.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304277</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Rat36-D1Rat106&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=619&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=619&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="146593951" STOP_POS="146594089" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="127453884" STOP_POS="137184926" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="135022396" STOP_POS="145354344" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="136045631" STOP_POS="146282094" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="128874534" STOP_POS="139471673" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304277</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304278</RGD_ID>
    <STRAIN_SYMBOL>DA-Tg(Alb-HSVtk)5Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=651&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=651&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304278</CITATION_ID>
    <DESCRIPTION>This strain expresses HSVtk (herpes simplex virus thymidine kinase) liver-specific driven by mouse albumin enhancer/promoter established at Jichi Medical School. Administration of injection ganciclovir (GCV) in these transgenic rats causes hepatitis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304279</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(MT2A-Myc)1Ys</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=699&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=699&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Reproduction; Development</RESEARCH_USE>
    <ALLELES>Myc</ALLELES>
    <ALLELE_RGD_IDS>3130</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304279</CITATION_ID>
    <DESCRIPTION>This transgenic rat is expressing the rat c-myc gene under the control of the human metallothionein II A promoter, established at the YS Institute, Inc. (present: PhoenixBio Co., Ltd.).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304280</RGD_ID>
    <STRAIN_SYMBOL>SHR/Shi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=666&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=666&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304280</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304281</RGD_ID>
    <STRAIN_SYMBOL>SERC/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=657&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=657&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304281</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304282</RGD_ID>
    <STRAIN_SYMBOL>IEW/Ihr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=733&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=733&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Ophthalmology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304282</CITATION_ID>
    <DESCRIPTION>mutant of Ihara epileptic rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304283</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Mgh5-D1Wox18&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=614&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=614&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="103781063" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="94644553" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="100133395" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="101198506" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="94626661" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304283</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304284</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Mgh5-D1Rat116&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=609&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=609&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="87558729" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="212458660" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="232297227" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="239429964" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="218467340" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304284</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304285</RGD_ID>
    <STRAIN_SYMBOL>BDIX/NemOda</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=579&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=579&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304285</CITATION_ID>
    <DESCRIPTION>This strain was maintained in Germany and was transferred to Japan by Dr. Tanaka of Aichi Cancer Center. Thereafter, this strain was transferred to Research Institute of Environmental Medicine, Nagoya University in 1973 and to Department of Agricultural, Nagoya University in 1992.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304286</RGD_ID>
    <STRAIN_SYMBOL>DMYC/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=624&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=624&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304286</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304287</RGD_ID>
    <STRAIN_SYMBOL>ACI.F344-(&lt;i&gt;D16Rat17-D16Rat15&lt;/i&gt;)/Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=621&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=621&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304287</CITATION_ID>
    <DESCRIPTION>F344 rats are susceptible and ACI rats are resistant to PhIP(2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine)-induced ACF formation (Nagao, 1998). Targeting on susceptible gene for colon tumor on rat chromosome 16 (Nakagama, 1999), this congenic strain was established by backcrossing F344/Jcl, as a donor strain, and ACI/NJcl, as a recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304288</RGD_ID>
    <STRAIN_SYMBOL>ACI.BUF-(&lt;i&gt;D20Img2-D20Rat5&lt;/i&gt;)/Ncc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=595&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=595&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="17617832" STOP_POS="17617956" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="18872150" STOP_POS="18872273" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="21025611" STOP_POS="21025734" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="18411845" STOP_POS="18411969" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304288</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304289</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Mgh5-D1Rat349&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=617&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=617&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="138467015" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="78430678" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="136742994" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="137735636" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="130788777" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304289</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304290</RGD_ID>
    <STRAIN_SYMBOL>BUF.ACI-(&lt;i&gt;D20Img2-D20Rat5&lt;/i&gt;)/Ncc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=594&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=594&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="17617832" STOP_POS="17617956" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="18872150" STOP_POS="18872273" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="21025611" STOP_POS="21025734" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="18411845" STOP_POS="18411969" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304290</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304291</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(CAG-EGFP)1Ys</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=647&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=647&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304291</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein (EGFP) gene ubiquitously driven by CAG promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304292</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg((ROSA)26Sor-luc)21Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=650&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=650&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-08-08)</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304292</CITATION_ID>
    <DESCRIPTION>This strain expresses luciferase ubiquitously driven by the gene trap ROSA26 promoter established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304293</RGD_ID>
    <STRAIN_SYMBOL>F344.LEC-&lt;i&gt;xhs1&lt;/i&gt;/1Nrs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=592&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=592&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304293</CITATION_ID>
    <DESCRIPTION>LEC rats which had high X-ray susceptibility were backcrossed to F344. In every generation, highly X-ray susceptible rats were selected with the radiation susceptibility assay</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304294</RGD_ID>
    <STRAIN_SYMBOL>MPOD/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=622&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=622&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Cancer; Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304294</CITATION_ID>
    <DESCRIPTION>Myeloperoxidase deficient rat was detected in Std:Wistar rats which purchased Japan SLC, Inc. in 2001. The causative gene is inherited as an autosomal recessive trait.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304295</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;Igf1r-D1Rat36&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=616&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=616&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES>Igf1r</ALLELES>
    <ALLELE_RGD_IDS>2869</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="130959787" STOP_POS="131248664" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="121549831" STOP_POS="127454022" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="128924921" STOP_POS="135022531" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="129985761" STOP_POS="136045766" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="122704976" STOP_POS="128874670" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304295</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304296</RGD_ID>
    <STRAIN_SYMBOL>KB/Oda</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=581&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=581&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304296</CITATION_ID>
    <DESCRIPTION>Maintained by crossing heterozygotes of the albino locus (segregating inbred strain).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304297</RGD_ID>
    <STRAIN_SYMBOL>TM.KDP-&lt;i&gt;Cblb&lt;/i&gt;/Nyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=608&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=608&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Immunology</RESEARCH_USE>
    <ALLELES>Cblb</ALLELES>
    <ALLELE_RGD_IDS>620535</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="62058829" STOP_POS="62225904" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="48589878" STOP_POS="48756940" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="51037383" STOP_POS="51202761" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="54218260" STOP_POS="54383403" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="49690402" STOP_POS="49856762" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304297</CITATION_ID>
    <DESCRIPTION>Homozygous Cblb rats are usually infertile in both sexes and are therefore maintained by crossing heterozygous individuals (segregating inbred strain).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304298</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Tuba1a-EYFP)Okn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=603&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=603&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304298</CITATION_ID>
    <DESCRIPTION>This strain expresses the enhanced yellow fluorescent protein (YGFP) neuron-specific driven by the Tubulin, alpha 1A promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304299</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(Alb-GFP)6Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=652&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=652&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304299</CITATION_ID>
    <DESCRIPTION>This strain expresses the green fluorescent protein (GFP) liver-specific driven by the Albumin promoter established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304300</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(S100b-EGFP)Scell</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=673&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=673&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304300</CITATION_ID>
    <DESCRIPTION>Developed by microinjecting the transgene into Wistar rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304301</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;Slco3a1-D1Rat106&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=618&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=618&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES>Slco3a1</ALLELES>
    <ALLELE_RGD_IDS>620227</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="137516037" STOP_POS="146594089" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="128106232" STOP_POS="137184926" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="135790854" STOP_POS="145354344" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="136793300" STOP_POS="146282094" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="129580126" STOP_POS="139471673" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304301</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304302</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Rat44-D1Arb21&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=612&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=612&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="160283901" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="150872626" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="161493758" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="167707459" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="153754139" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304302</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304303</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(MT2A-Myc)2Ys</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=698&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=698&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Reproduction; Development</RESEARCH_USE>
    <ALLELES>Myc</ALLELES>
    <ALLELE_RGD_IDS>3130</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304303</CITATION_ID>
    <DESCRIPTION>This transgenic rat is expressing the rat c-myc gene under the control of the human metallothionein II A promoter, established at the YS Institute, Inc. (present: PhoenixBio Co., Ltd.).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304304</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Rat209-D1Arb21&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=613&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=613&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="144050731" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="134641522" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="142486986" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="206276946" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="187092235" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304304</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304305</RGD_ID>
    <STRAIN_SYMBOL>DOB/Oda</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=582&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=582&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304305</CITATION_ID>
    <DESCRIPTION>This strain was derived from wild specimens of the Rattus norvegicus trapped at goat shed in Sitara-cho, Kita-shitara-gun, Aichi, Japan, 2000.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304306</RGD_ID>
    <STRAIN_SYMBOL>BUF.ACI-(&lt;i&gt;D20Img2-Cdkn1a&lt;/i&gt;)/Ncc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=599&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=599&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES>Cdkn1a</ALLELES>
    <ALLELE_RGD_IDS>69328</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="7150820" STOP_POS="7161373" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="7149177" STOP_POS="7159727" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="6348422" STOP_POS="6358864" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="8592437" STOP_POS="8602879" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="7376325" STOP_POS="7386778" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304306</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304307</RGD_ID>
    <STRAIN_SYMBOL>ACI.BUF-(&lt;i&gt;D20Img2-Cdkn1a&lt;/i&gt;)/Ncc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=598&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=598&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES>Cdkn1a</ALLELES>
    <ALLELE_RGD_IDS>69328</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="7150820" STOP_POS="7161373" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="7149177" STOP_POS="7159727" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="6348422" STOP_POS="6358864" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="8592437" STOP_POS="8602879" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="7376325" STOP_POS="7386778" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304307</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304308</RGD_ID>
    <STRAIN_SYMBOL>ICR/Ihr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=731&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=731&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2019-08-05)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Ophthalmology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304308</CITATION_ID>
    <DESCRIPTION>A new rat strain has been developed, in which a spontaneous cataract occurs without exception at 3-4 months after birth and matures completely at 4-6 months of age, indicating that this strain possesses a maturity-onset cataract.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304309</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Mgh5-D1Rat106&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=611&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=611&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="146594089" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="137184926" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="145354344" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="146282094" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="139471673" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304309</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304310</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Nes/Hspa1b-EGFP)Okn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=602&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=602&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304310</CITATION_ID>
    <DESCRIPTION>This strain expresses green fluorescent protein (GFP) neural-specific driven by Nestin enhancer and Hspa1b promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304311</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg((ROSA)26Sor-lacZ)44JmskRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=648&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=298&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=648&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=298&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-08-08)</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00298</CITATION_ID>
    <DESCRIPTION>This strain expresses LacZ ubiquitously driven by the gene trap ROSA26 promoter established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304312</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Mgh5-D1Rat36&lt;/i&gt;)(&lt;i&gt;D1Rat44-D1Arb21&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=610&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=610&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304312</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304313</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Mgh5-D1Rat178&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=615&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=615&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="87558729" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="78430678" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="79689689" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="89601109" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="85128763" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304313</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304314</RGD_ID>
    <STRAIN_SYMBOL>BDIX.Cg-&lt;i&gt;Tal&lt;/i&gt;/NemOda</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=607&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=607&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Osteosis</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304314</CITATION_ID>
    <DESCRIPTION>Mating among heterozygoutes or between heterozygoute and normal individuals (segregating inbred strain).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304315</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;Calca-D1Arb21&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=620&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=620&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES>Calca</ALLELES>
    <ALLELE_RGD_IDS>2254</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="178312636" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="168878212" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="184184018" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="191158061" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="172686168" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304315</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304316</RGD_ID>
    <STRAIN_SYMBOL>F344.LEC-&lt;i&gt;xhs1&lt;/i&gt;/2Nrs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=593&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=593&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304316</CITATION_ID>
    <DESCRIPTION>LEC rats which had high X-ray susceptibility were backcrossed to F344. In every generation, highly X-ray susceptible rats were selected with the radiation susceptibility assay</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304329</RGD_ID>
    <STRAIN_SYMBOL>WKY/Ezo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=568&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=568&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304329</CITATION_ID>
    <DESCRIPTION>Deposited by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304330</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(HRAS)128Ncc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=668&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=668&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2021-04-30)</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304330</CITATION_ID>
    <DESCRIPTION>This strain is carrying three copies of the human c-Ha-ras proto-oncogene, including its own promoter region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304331</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(CCR5)1Hik</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=674&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=674&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Infectious</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304331</CITATION_ID>
    <DESCRIPTION>Deposited by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2304332</RGD_ID>
    <STRAIN_SYMBOL>HER/Wkmt</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=697&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=697&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2304332</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305934</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Spta1&lt;sup&gt;Tn(sb-T2/Bart3)2.315Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=439&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Spta1&lt;sup&gt;Tn(sb-T2/Bart3)2.315Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2305932</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="88735833" STOP_POS="88811697" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="86203504" STOP_POS="86279371" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="92264231" STOP_POS="92340091" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="96782387" STOP_POS="96860327" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="89951924" STOP_POS="90028592" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00439</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 48th intron of the Spta1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305935</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Rtn4&lt;sup&gt;Tn(sb-T2/Bart3)2.316Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=476&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rtn4&lt;sup&gt;Tn(sb-T2/Bart3)2.316Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2305933</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="107651001" STOP_POS="107698610" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="103450074" STOP_POS="103497687" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="114126931" STOP_POS="114174459" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="113792257" STOP_POS="113839936" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="110725089" STOP_POS="110772578" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00476</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Rtn4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305939</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D9Mit6-D9Rat83&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=690&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=690&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305939</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305940</RGD_ID>
    <STRAIN_SYMBOL>SHRSP-Chr 7&lt;sup&gt;WKY&lt;/sup&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=688&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=688&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305940</CITATION_ID>
    <DESCRIPTION>Chromosome 7 from WKY is introgressed into the genomic background of SHRSP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305941</RGD_ID>
    <STRAIN_SYMBOL>SHR-Chr 15&lt;sup&gt;WKY&lt;/sup&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=695&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=695&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305941</CITATION_ID>
    <DESCRIPTION>Chromosome 15 from WKY is introgressed into the genomic background of SHR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305942</RGD_ID>
    <STRAIN_SYMBOL>SHR-Chr 3&lt;sup&gt;WKY&lt;/sup&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=694&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=694&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305942</CITATION_ID>
    <DESCRIPTION>Chromosome 3 from WKY is introgressed into the genomic background of SHR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305943</RGD_ID>
    <STRAIN_SYMBOL>SHRSP-Chr 15&lt;sup&gt;WKY&lt;/sup&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=692&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=692&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305943</CITATION_ID>
    <DESCRIPTION>Chromosome 15 from WKY is introgressed into the genomic background of SHRSP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305944</RGD_ID>
    <STRAIN_SYMBOL>SHRSP-Chr 4&lt;sup&gt;WKY&lt;/sup&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=687&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=687&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305944</CITATION_ID>
    <DESCRIPTION>Chromosome 4 from WKY is introgressed into the genomic background of SHRSP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305945</RGD_ID>
    <STRAIN_SYMBOL>SHRSP-Chr 13&lt;sup&gt;WKY&lt;/sup&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=691&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=691&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305945</CITATION_ID>
    <DESCRIPTION>Chromosome 13 from WKY is introgressed into the genomic background of SHRSP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305946</RGD_ID>
    <STRAIN_SYMBOL>SHR-Chr 1&lt;sup&gt;WKY&lt;/sup&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=693&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=693&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305946</CITATION_ID>
    <DESCRIPTION>Chromosome 1 from WKY is introgressed into the genomic background of SHR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305947</RGD_ID>
    <STRAIN_SYMBOL>SHR-Chr 19&lt;sup&gt;WKY&lt;/sup&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=696&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=696&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305947</CITATION_ID>
    <DESCRIPTION>Chromosome 19 from WKY is introgressed into the genomic background of SHR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305948</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D8Rat77-D8Rat16&lt;/i&gt;)(&lt;i&gt;D8Tkyo10&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=689&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=689&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305948</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305949</RGD_ID>
    <STRAIN_SYMBOL>SHRSP-Chr 1&lt;sup&gt;WKY&lt;/sup&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=686&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=686&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305949</CITATION_ID>
    <DESCRIPTION>Chromosome 1 from WKY is introgressed into the genomic background of SHRSP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305966</RGD_ID>
    <STRAIN_SYMBOL>SHR.SHRSP-(&lt;i&gt;D1Rat93-D1Rat269&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=864&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=864&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="134387145" STOP_POS="134387335" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="65677942" STOP_POS="124977364" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="64252881" STOP_POS="132448306" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="63244295" STOP_POS="133485967" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="63990899" STOP_POS="126292805" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305966</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305967</RGD_ID>
    <STRAIN_SYMBOL>SHR.SHRSP-(&lt;i&gt;D18Rat73-D18Rat11&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=866&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=866&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="52198059" STOP_POS="70689286" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="49999958" STOP_POS="68414117" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="51609032" STOP_POS="70803264" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="50804228" STOP_POS="69942605" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="52290789" STOP_POS="71692408" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305967</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305968</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Wox18-D1Rat39&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=862&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=862&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="103780943" STOP_POS="103781063" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="94644435" STOP_POS="124668572" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="100133276" STOP_POS="132134441" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="101198387" STOP_POS="133172336" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="94626541" STOP_POS="125983558" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305968</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305969</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Mgh5-D1Rat178&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=861&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=861&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="87558729" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="78430678" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="79689689" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="89601109" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="85128763" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305969</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305970</RGD_ID>
    <STRAIN_SYMBOL>DA-Tg(Alb-TTR*V30M)7Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=703&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=703&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305970</CITATION_ID>
    <DESCRIPTION>This is the strain expresses human Amyloidogenic transthyretin (ATTR) V30M driven by the mouse albumin enhancer/promoter, established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305971</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D18Rat73-D18Rat11&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=865&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=865&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="52198059" STOP_POS="70689286" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="49999958" STOP_POS="68414117" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="51609032" STOP_POS="70803264" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="50804228" STOP_POS="69942605" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="52290789" STOP_POS="71692408" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305971</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305972</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;D1Wox29-D1Arb21&lt;/i&gt;)(&lt;i&gt;D9Mit6-D9Wox4&lt;/i&gt;)(&lt;i&gt;Bcl2-D13Mgh7&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=838&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=838&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305972</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305973</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D1Rat93-D1Rat269&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=863&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=863&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="134387145" STOP_POS="134387335" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="65677942" STOP_POS="124977364" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="64252881" STOP_POS="132448306" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="63244295" STOP_POS="133485967" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="63990899" STOP_POS="126292805" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305973</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305974</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;D1Wox29-D1Arb21&lt;/i&gt;)(&lt;i&gt;D9Mit6-D9Wox4&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=858&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=858&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305974</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305975</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Mgh5-D1Wox18&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=860&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=860&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="103781063" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="94644553" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="100133395" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="101198506" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="94626661" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305975</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305976</RGD_ID>
    <STRAIN_SYMBOL>DA-Tg(Alb-TTR*V30M)9Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=705&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=339&gt;Rat Resource &amp; Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=705&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=339&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00339</CITATION_ID>
    <DESCRIPTION>This is the strain expresses human Amyloidogenic transthyretin (ATTR) V30M driven by the mouse albumin enhancer/promoter, established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305977</RGD_ID>
    <STRAIN_SYMBOL>ACI.F344-(&lt;i&gt;D16Rat12-D16Mco2&lt;/i&gt;)/Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=702&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=702&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="387123" STOP_POS="387234" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="380245" STOP_POS="380356" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="1090054" STOP_POS="1090164" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="1084304" STOP_POS="67099528" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="350121" STOP_POS="67547357" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305977</CITATION_ID>
    <DESCRIPTION>F344 rats are susceptible and ACI rats are resistant to PhIP (2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine)-induced ACF (aberrant crypt foci) formation (Nagao, 1998). This congenic strain was established using 'speed congenic' method by backcrossing (F344/JclxACI/NJcl)F1 onto ACI/NJcl, followed by intercrossing in N8 generation. Thereafter this strain is maintained by crossing homozygous individuals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305978</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg((ROSA)26Sor-DsRed*)7Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=706&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=706&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-08-08)</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305978</CITATION_ID>
    <DESCRIPTION>This strain expresses DsRed monomer ubiquitously driven by the gene trap ROSA 26 promoter, established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305979</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;D1Wox29-D1Arb21&lt;/i&gt;)(&lt;i&gt;Bcl2-D13Mgh7&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=859&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=859&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305979</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305987</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Mgh16-D7Wox46&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=844&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=844&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="93145728" STOP_POS="93145964" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="91256311" STOP_POS="106845450" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="100004559" STOP_POS="116255796" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="100584458" STOP_POS="116158165" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="96491967" STOP_POS="113050225" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305987</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305988</RGD_ID>
    <STRAIN_SYMBOL>(F344.OLETF-(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;)(&lt;i&gt;D14Rat8-D14Rat26&lt;/i&gt;)/2Tj x F344.Cg-Lepr&lt;sup&gt;&lt;i&gt;fa&lt;/i&gt;&lt;/sup&gt;(&lt;i&gt;D7Mgh16-D7Mgh20&lt;/i&gt;))F1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=841&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=841&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305988</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305989</RGD_ID>
    <STRAIN_SYMBOL>(F344.OLETF-(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;)(&lt;i&gt;D14Rat8-D14Rat26&lt;/i&gt;)/2Tj x F344.Z-Lepr&lt;sup&gt;&lt;i&gt;fa&lt;/i&gt;&lt;/sup&gt;/Tj&lt;/i&gt;)F1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=842&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=842&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305989</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305990</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat23-D14Rat23&lt;/i&gt;)(&lt;i&gt;D14Rat8-D14Rat12&lt;/i&gt;)/2Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=836&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=836&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305990</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305991</RGD_ID>
    <STRAIN_SYMBOL>(F344.OLETF-(&lt;i&gt;D7Mgh16-D7Mgh20&lt;/i&gt;)/Tj X F344.OLETF-(&lt;i&gt;D8Rat54-D8Mgh17&lt;/i&gt;)/2Tj)F1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=839&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=839&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305991</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305992</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Mit16-D7Mgh20&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=820&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=820&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="115766234" STOP_POS="115766396" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="113886156" STOP_POS="113886318" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="123602837" STOP_POS="123602998" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="123587556" STOP_POS="123587717" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="120745845" STOP_POS="120746007" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305992</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305993</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat23&lt;/i&gt;)(&lt;i&gt;D14Rat12&lt;/i&gt;)/2Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=834&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=834&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305993</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305994</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat23-D14Rat23&lt;/i&gt;)(&lt;i&gt;D14Rat8-D14Rat12&lt;/i&gt;)/1Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=835&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=835&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305994</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305995</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Got130-D7Mgh20&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=837&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=837&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305995</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305996</RGD_ID>
    <STRAIN_SYMBOL>F344.Cg-Lepr&lt;sup&gt;&lt;i&gt;fa&lt;/i&gt;&lt;/sup&gt;(&lt;i&gt;D7Rat18-D7Mit2&lt;/i&gt;)(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=843&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=843&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305996</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305997</RGD_ID>
    <STRAIN_SYMBOL>(F344.OLETF-(&lt;i&gt;D7Mgh16-D7Mgh20&lt;/i&gt;)(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;)/2Tj x F344.OLETF-(&lt;i&gt;D8Rat54-D8Mgh17&lt;/i&gt;)/2Tj)F1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=840&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=840&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305997</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305998</RGD_ID>
    <STRAIN_SYMBOL>F344.Cg-Lepr&lt;sup&gt;&lt;i&gt;fa&lt;/i&gt;&lt;/sup&gt;(&lt;i&gt;D8Rat54-D8Mgh17&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=809&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=809&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="27588221" STOP_POS="27588390" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="69349194" STOP_POS="69349344" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="74917593" STOP_POS="80840067" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="21850030" STOP_POS="79245063" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="19796514" STOP_POS="73102155" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305998</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2305999</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Mgh16-D7Rat70&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=830&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=830&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="93145728" STOP_POS="112860286" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="91256311" STOP_POS="110979877" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="100004559" STOP_POS="120648531" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="100584458" STOP_POS="120641361" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="96491967" STOP_POS="117397170" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2305999</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306000</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Rat70-D7Mgh20&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=831&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=831&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="112860063" STOP_POS="112860286" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="110979654" STOP_POS="110979877" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="120648309" STOP_POS="120648531" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="120641139" STOP_POS="120641361" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="117396947" STOP_POS="117397170" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306000</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306001</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Rat176-D7Mgh20&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=832&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=832&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="107288231" STOP_POS="107288456" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="105399233" STOP_POS="105399458" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="114708083" STOP_POS="114708307" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="114641525" STOP_POS="114641749" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="111200727" STOP_POS="111200952" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306001</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306002</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat23&lt;/i&gt;)(&lt;i&gt;D14Rat12&lt;/i&gt;)/1Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=833&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=833&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306002</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306003</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Wox46-D7Mgh20&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=845&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=845&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="106845277" STOP_POS="106845450" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="116255624" STOP_POS="116255796" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="116157993" STOP_POS="116158165" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="113050053" STOP_POS="113050225" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306003</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306004</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Mgh16-D7Mit16&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=821&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=821&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="93145728" STOP_POS="115766396" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="91256311" STOP_POS="113886318" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="100004559" STOP_POS="123602998" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="100584458" STOP_POS="123587717" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="96491967" STOP_POS="120746007" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306004</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306013</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat8-D14Rat26&lt;/i&gt;)/2Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=853&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=853&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="30674469" STOP_POS="69239554" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="30320092" STOP_POS="65026991" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="32593926" STOP_POS="69517234" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="32389647" STOP_POS="69559504" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="32584630" STOP_POS="70077314" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306013</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306014</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D8Rat54-D8Mgh17&lt;/i&gt;)/2Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=848&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=848&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="27588221" STOP_POS="27588390" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="69349194" STOP_POS="69349344" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="74917593" STOP_POS="80840067" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="21850030" STOP_POS="79245063" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="19796514" STOP_POS="73102155" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306014</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306015</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D12Wox5-D12Rat21&lt;/i&gt;)/2Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=852&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=852&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="18749469" STOP_POS="48428269" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="13635523" STOP_POS="42767729" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="15714609" STOP_POS="48536609" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="17721341" STOP_POS="50319569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="43801711" STOP_POS="43801909" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306015</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306016</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D11Mgh4-D11Mgh1&lt;/i&gt;)/2Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=849&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=849&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="73308315" STOP_POS="96071021" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="59802622" STOP_POS="82566702" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="62653194" STOP_POS="86714631" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="65784365" STOP_POS="89808503" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="61504311" STOP_POS="84560241" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306016</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306017</RGD_ID>
    <STRAIN_SYMBOL>(F344.OLETF-(&lt;i&gt;D8Rat54-D8Mgh17&lt;/i&gt;)/2Tj x F344.Cg-Lepr&lt;sup&gt;&lt;i&gt;fa&lt;/i&gt;&lt;/sup&gt;(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;))F1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=856&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=856&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306017</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306018</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D9Mgh8-D9Mit2&lt;/i&gt;)/2Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=851&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=851&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="73930789" STOP_POS="73930979" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="36840385" STOP_POS="66437242" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="41139089" STOP_POS="71771476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="40808491" STOP_POS="70797404" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="33374546" STOP_POS="63705951" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306018</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306019</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D1Mit20-D1Mgh26&lt;/i&gt;)/2Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=850&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=850&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="172711200" STOP_POS="172711337" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="188051098" STOP_POS="188051234" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="100372156" STOP_POS="194998184" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="94356875" STOP_POS="176616212" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306019</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306020</RGD_ID>
    <STRAIN_SYMBOL>(F344.OLETF-(&lt;i&gt;D8Rat54-D8Mgh17&lt;/i&gt;)/2Tj x F344.Cg-Lepr&lt;sup&gt;&lt;i&gt;fa&lt;/i&gt;&lt;/sup&gt;(&lt;i&gt;D7Mgh16-D7Mgh20&lt;/i&gt;)(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;))F1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=857&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=857&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306020</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306021</RGD_ID>
    <STRAIN_SYMBOL>SHR-Chr 2&lt;sup&gt;WKY&lt;/sup&gt;/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=713&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=713&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306021</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306022</RGD_ID>
    <STRAIN_SYMBOL>KCI/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=630&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=630&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Pcdh15</ALLELES>
    <ALLELE_RGD_IDS>1590969</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306022</CITATION_ID>
    <DESCRIPTION>Rats showing abnormal behaviors characterized by constant circling movements were found in the F3 generation of Crl:CD(SD) rats purchased from Charles River Laboratory Japan in 2003.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306023</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(CCNT1)1Hik</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=712&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=712&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Infectious</RESEARCH_USE>
    <ALLELES>CCNT1</ALLELES>
    <ALLELE_RGD_IDS>1322457</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306023</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306024</RGD_ID>
    <STRAIN_SYMBOL>FOK/Ncu</STRAIN_SYMBOL>
    <FULL_NAME>Furuyama rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=759&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=759&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306024</CITATION_ID>
    <DESCRIPTION>These are resistant to hot environment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306025</RGD_ID>
    <STRAIN_SYMBOL>WMN/Nrs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=675&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=675&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cancer; Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306025</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306026</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D16Wox4-D16Rat13&lt;/i&gt;)/2Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=854&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=854&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="54876458" STOP_POS="54876610" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="48143982" STOP_POS="73187298" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="51339600" STOP_POS="78172206" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="51050772" STOP_POS="77759249" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="51452966" STOP_POS="77968799" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306026</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306027</RGD_ID>
    <STRAIN_SYMBOL>WM/Nrs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=676&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=676&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cancer; Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306027</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306028</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;)(&lt;i&gt;D14Rat8-D14Rat26&lt;/i&gt;)/2Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=847&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=847&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306028</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306029</RGD_ID>
    <STRAIN_SYMBOL>(F344.OLETF-(&lt;i&gt;D8Rat54-D8Mgh17&lt;/i&gt;)/2Tj x F344.Cg-Lepr&lt;sup&gt;&lt;i&gt;fa&lt;/i&gt;&lt;/sup&gt;(&lt;i&gt;D7Mgh16-D7Mgh20&lt;/i&gt;))F1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=855&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=855&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306029</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306030</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Mgh16-D7Mgh20&lt;/i&gt;)(&lt;i&gt;D14Rat8-D14Rat26&lt;/i&gt;)/2Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=846&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=846&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306030</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306033</RGD_ID>
    <STRAIN_SYMBOL>SHR.Cg-&lt;i&gt;Lepr&lt;sup&gt;cp&lt;/sup&gt;&lt;/i&gt;/NDmcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=734&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=734&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES>Lepr&lt;sup&gt;cp&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11570565</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306033</CITATION_ID>
    <DESCRIPTION>Nonsense mutation of leptin receptor gene in the obese spontaneously hypertensive Koletsky rat was transferred to SHR/N strain at NIH. This strain has been maintained at Disease Model Cooperative Research Association (DMCRA) scince 1999.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306034</RGD_ID>
    <STRAIN_SYMBOL>NER.F344-(&lt;i&gt;D1Mgh6-D1Rat132&lt;/i&gt;)(&lt;i&gt;D5Rat100-D5Rat234&lt;/i&gt;)/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=729&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=729&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306034</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306035</RGD_ID>
    <STRAIN_SYMBOL>F344.NER-(&lt;i&gt;D1Mgh6-D1Rat73&lt;/i&gt;)(&lt;i&gt;D5Mgh4-D5Rat36&lt;/i&gt;)/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=727&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=727&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306035</CITATION_ID>
    <DESCRIPTION>This double congenic strain was established by crossing F344.NER-(&lt;i&gt;D1Mgh6-D1Rat73&lt;/i&gt;)/Kyo and F344.NER-(&lt;i&gt;D5Mgh4-D5Rat36&lt;/i&gt;)/Kyo</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306036</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Apc&lt;sup&gt;m1&lt;/i&gt;Kyo&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=714&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=714&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-03-14)</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES>Apc|Apc&lt;sup&gt;m1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2123|12792252</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="26195060" STOP_POS="26195060" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="25920903" STOP_POS="25920903" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="27104372" STOP_POS="27104372" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="26725560" STOP_POS="26820837" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="26732147" STOP_POS="26790383" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306036</CITATION_ID>
    <DESCRIPTION>F344/NSlc rats that have an induced mutation in the Apc (S2523X) gene; Established by ENU mutagenesis (gene-driven).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306037</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(CD4)1Hik</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=700&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=700&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Infectious</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306037</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306041</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Scn1a&lt;sup&gt;m2Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=715&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=715&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Scn1a&lt;sup&gt;m2Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12792284</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="71360840" STOP_POS="71479870" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="50998498" STOP_POS="50998498" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="52437310" STOP_POS="52437310" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="59016641" STOP_POS="59135580" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="48238528" STOP_POS="48364143" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306041</CITATION_ID>
    <DESCRIPTION>Established by ENU mutagenesis. A point mutation in Scn1a gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306042</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Scn1a&lt;sup&gt;m1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=716&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=716&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-05-04)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Scn1a&lt;sup&gt;m1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12792283</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="71360840" STOP_POS="71479870" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="50969024" STOP_POS="50969024" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="52408707" STOP_POS="52408707" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="59016641" STOP_POS="59135580" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="48238528" STOP_POS="48364143" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306042</CITATION_ID>
    <DESCRIPTION>Established by ENU mutagenesis. A missense mutant N1417H (4246A&gt;G)was identified in the model.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306043</RGD_ID>
    <STRAIN_SYMBOL>SHR/4Dmcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=566&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=566&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES>Cd36</ALLELES>
    <ALLELE_RGD_IDS>2301</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306043</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR, this is one of the SHR substrains, CL line, which shows lower blood pressure</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306044</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/3Dmcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=567&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=567&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES>Cd36</ALLELES>
    <ALLELE_RGD_IDS>2301</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306044</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR, this is one of the SHRSP substrains, A4 line</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306045</RGD_ID>
    <STRAIN_SYMBOL>SHR/2Dmcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=564&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=564&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES>Cd36</ALLELES>
    <ALLELE_RGD_IDS>2301</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306045</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR, one of the SHR substrains from B2 line</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306046</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(CAG-EGFP)3Ys</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=741&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=741&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306046</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein (EGFP) gene ubiquitously driven by CAG promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306047</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Gnrh1-EGFP)Nphy</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=704&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=704&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gnrh1</ALLELES>
    <ALLELE_RGD_IDS>2720</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306047</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein (EGFP) gene driven by gonadotropin-releasing hormone 1 (Gnrh1) promoter. EGFP fluorescence is observed only in Gnrh1-immunoreactive neurons, approximately one third of which has strong EGFP fluorescence.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306048</RGD_ID>
    <STRAIN_SYMBOL>SHR/3Dmcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=565&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=565&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES>Cd36</ALLELES>
    <ALLELE_RGD_IDS>2301</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306048</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR, this is one of the SHR substrains, CH line, which shows high blood pressure</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306049</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/4Dmcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=736&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=736&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES>Cd36</ALLELES>
    <ALLELE_RGD_IDS>2301</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306049</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR, this is one of the SHRSP substrains, CT line, which shows cardiac thrombosis</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306050</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/5Dmcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=737&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=737&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES>Cd36</ALLELES>
    <ALLELE_RGD_IDS>2301</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306050</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR, This is one of the SHRSP substrains, ALR line, which is prone to arteiolipidosis</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306051</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/2Dmcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=563&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=563&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES>Cd36</ALLELES>
    <ALLELE_RGD_IDS>2301</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306051</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR, this is one of the SHRSP substrains, A1sb line</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306058</RGD_ID>
    <STRAIN_SYMBOL>LEC.W-Tg(CAG-Zfml)30Ncms/Ncms</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=782&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=782&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306058</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306059</RGD_ID>
    <STRAIN_SYMBOL>DA.Cg-&lt;i&gt;Foxn1&lt;sup&gt;rnu&lt;/sup&gt; Lyst&lt;sup&gt;bg&lt;/sup&gt;&lt;/i&gt;/Slc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=760&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=760&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Immunology; Hematology</RESEARCH_USE>
    <ALLELES>Foxn1|Lyst&lt;sup&gt;bg&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>3970|598099555</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306059</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306060</RGD_ID>
    <STRAIN_SYMBOL>LEC.W-Tg(CAG-Zfml)26Ncms/Ncms</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=781&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=781&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306060</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306061</RGD_ID>
    <STRAIN_SYMBOL>ACI.BUF-&lt;i&gt;Pur1, Thym2&lt;/i&gt;/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=739&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=739&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306061</CITATION_ID>
    <DESCRIPTION>The proteinuria-susceptible gene, Pur1 (on chr.13) and the thymus enlargement, Ten2 (Thym2) (on chr.13) loci of BUF/Mna were transferred to ACI by backcrossing from Matsuyama et al. Congenic rats are established in 2002.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306062</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Per1-luc)1Oa</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=740&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=273&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=740&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=273&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00273</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306063</RGD_ID>
    <STRAIN_SYMBOL>LEC.W-Tg(CAG-Zfml)21Ncms/Ncms</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=738&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=738&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306063</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306064</RGD_ID>
    <STRAIN_SYMBOL>MPR/Iar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=745&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=745&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Metabolism; Osteosis</RESEARCH_USE>
    <ALLELES>Arsb|Arsb&lt;sup&gt;MPR&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2158|12792967</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306064</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306070</RGD_ID>
    <STRAIN_SYMBOL>WIC-Tg(Wap-GH1)1Mni</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=789&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=789&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-04-21)</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306070</CITATION_ID>
    <DESCRIPTION>Ikeda developed transgenic rats carrying the human growth hormone (GH1) driven by murine Wap promoter, originated from Wistar-Imamichi (Ikeda, 1994). Two lines of this transgenic strain were established named Line 1: characterized by relatively high level of serum Gh1 (high line, NBRPNo.0490), and Line 2: relatively low level of serum Gh1 (low line, NBRPNo.0491).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306071</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(CAG-EGFP)Ncco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=576&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=576&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer; Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306071</CITATION_ID>
    <DESCRIPTION>Transgenic rat: CAG promoter, Enhanced Green Fluorescent Protein gene, microinjection method</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306072</RGD_ID>
    <STRAIN_SYMBOL>ACI.F344-(&lt;i&gt;D16Nkg74&lt;/i&gt;)/Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=768&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=768&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306072</CITATION_ID>
    <DESCRIPTION>A sub congenic strain of ACI/N.F344-(&lt;i&gt;D16Rat12-D16Mco2&lt;/i&gt;)/Nkg</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306073</RGD_ID>
    <STRAIN_SYMBOL>WIC-Tg(Wap-GH1)2Mni</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=788&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=788&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-04-21)</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306073</CITATION_ID>
    <DESCRIPTION>Ikeda developed transgenic rats carrying the human growth hormone (GH1) driven by murine Wap promoter, originated from Wistar-Imamichi (Ikeda, 1994). Two lines of this transgenic strain were established named Line 1: characterized by relatively high level of serum Gh1 (high line, NBRPNo.0490), and Line 2: relatively low level of serum Gh1 (low line, NBRPNo.0491).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306076</RGD_ID>
    <STRAIN_SYMBOL>ACI.F344-(&lt;i&gt;D16Nkg9-D16Nkg38&lt;/i&gt;)/Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=793&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=793&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306076</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by backcrossing ACI.F344-(&lt;i&gt;D16Rat12-D16Mco2&lt;/i&gt;)Nkg onto ACI/NJcl, followed by intercrossing in N8 generation, thereafter maintained by crossing homozygous individuals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306077</RGD_ID>
    <STRAIN_SYMBOL>ACI.F344-(&lt;i&gt;D16Rat64-D16Nkg105&lt;/i&gt;)/Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=791&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=791&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="62414464" STOP_POS="62414683" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="55711087" STOP_POS="55711306" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="59285775" STOP_POS="59285993" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="58966446" STOP_POS="58966664" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="59398206" STOP_POS="59398647" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306077</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by backcrossing ACI.F344-(&lt;i&gt;D16Rat12-D16Mco2&lt;/i&gt;)/Nkg onto ACI/NJcl, followed by intercrossing in N6 generation, thereafter maintained by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306078</RGD_ID>
    <STRAIN_SYMBOL>KFRS4A/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=801&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=801&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306078</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306079</RGD_ID>
    <STRAIN_SYMBOL>ACI.F344-(&lt;i&gt;D16Nkg87-D16Nkg105&lt;/i&gt;)/Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=792&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=792&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306079</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by backcrossing ACI.F344-(&lt;i&gt;D16Rat64-D16Nkg105&lt;/i&gt;)/Nkg onto ACI/NJcl, followed by intercrossing in N9 generation. maintained by crossing homozygous individuals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306085</RGD_ID>
    <STRAIN_SYMBOL>TCR/Ibu</STRAIN_SYMBOL>
    <FULL_NAME>Toyoda Circling Rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=800&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=800&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306085</CITATION_ID>
    <DESCRIPTION>A male rat shows circling behavior was found in the Wistar rats purchaced from Kiwa Laboratory Animals Co., Ltd. in 2007.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306089</RGD_ID>
    <STRAIN_SYMBOL>ACI.BUF-(&lt;i&gt;D7Wox16-D7Rat69&lt;/i&gt;)/Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=803&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=803&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="62345785" STOP_POS="62346019" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="60460452" STOP_POS="60460686" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="67801457" STOP_POS="67801690" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="67991394" STOP_POS="116151991" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="64611964" STOP_POS="113044228" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306089</CITATION_ID>
    <DESCRIPTION>The thymoma susceptible locus of rat-1, Tsr1 (on Chr.7) was transferred from BUF/Mna to ACI/NMs by repeated backcrossing.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306090</RGD_ID>
    <STRAIN_SYMBOL>ExHC/Ta</STRAIN_SYMBOL>
    <FULL_NAME>Exogenously hypercholesterolemic rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=804&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=804&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-04-19)</AVAILABILITY>
    <RESEARCH_USE>Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306090</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306098</RGD_ID>
    <STRAIN_SYMBOL>ACI.F344-(&lt;i&gt;D16Nkg30-D16Mgh6&lt;/i&gt;)/Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=828&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=828&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="45868397" STOP_POS="45868497" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="49051407" STOP_POS="49051506" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="48766016" STOP_POS="48766115" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="49150370" STOP_POS="49150515" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306098</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by backcrossing ACI.F344-(&lt;i&gt;D16Rat12-D16Mco2&lt;/i&gt;)/Nkg onto ACI/NJcl, followed by intercrossing in N9 generation, thereafter maintained by crossing homozygous individuals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306099</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D15Tkyo3-D15Rat68&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=807&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=807&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="62893434" STOP_POS="62893574" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="56484420" STOP_POS="56484560" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="63498932" STOP_POS="63499071" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="67139660" STOP_POS="67139799" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="62521452" STOP_POS="62521592" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306099</CITATION_ID>
    <DESCRIPTION>This congenic strain was established from WKY/Izm purchased from Japan SLC, Inc. and SHR/Izm at the Research Institute International Medical Center of Japan in 2001. The rats which have the heterozygous consomic segment were established in 2004, and were bred homozygous in 2005.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306100</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D3Tkyo7-D3Rat1&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=815&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=815&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="100769917" STOP_POS="168026850" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="105465332" STOP_POS="176418101" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="112038782" STOP_POS="180128021" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="99858951" STOP_POS="170016653" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306100</CITATION_ID>
    <DESCRIPTION>This congenic strain was established from WKY/Izm purchased from Japan SLC, Inc. and SHR/Izm at the Research Institute International Medical Center of Japan in 2001. The rats which have the heterozygous consomic segment were established in 2004, and were bred homozygous in 2005.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306101</RGD_ID>
    <STRAIN_SYMBOL>LEC.BN-(&lt;i&gt;D4Mgh16-D4Rat233&lt;/i&gt;)/Hkv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=875&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=875&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="63900458" STOP_POS="63900697" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="62933269" STOP_POS="107032773" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="61708103" STOP_POS="105384025" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="61427427" STOP_POS="170105737" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="61646674" STOP_POS="108329449" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306101</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306102</RGD_ID>
    <STRAIN_SYMBOL>BN.LEC-(&lt;i&gt;D4Rat128-D4Rat106&lt;/i&gt;)/Hkv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=879&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=879&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="81317600" STOP_POS="117737312" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="79986873" STOP_POS="116179656" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="80666353" STOP_POS="115372927" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="145335315" STOP_POS="179959894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="79189959" STOP_POS="117887968" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306102</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306103</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/Sums</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=873&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=873&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306103</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306104</RGD_ID>
    <STRAIN_SYMBOL>BN.LEC-(&lt;i&gt;D4Rat184-D4Rat238&lt;/i&gt;)/Hkv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=878&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=878&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="120485692" STOP_POS="141281683" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="118928273" STOP_POS="139725596" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="118283596" STOP_POS="138891201" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="182854846" STOP_POS="203361566" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="120665583" STOP_POS="142160377" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306104</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306105</RGD_ID>
    <STRAIN_SYMBOL>BN.LEC-(&lt;i&gt;D4Rat128-D4Rat238&lt;/i&gt;)/Hkv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=877&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=877&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="81317600" STOP_POS="141281683" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="79986873" STOP_POS="139725596" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="80666353" STOP_POS="138891201" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="145335315" STOP_POS="203361566" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="79189959" STOP_POS="142160377" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306105</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306106</RGD_ID>
    <STRAIN_SYMBOL>CLX/Ta</STRAIN_SYMBOL>
    <FULL_NAME>Circling behavior linked to the X-chromosome (CLX)</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=813&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=813&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306106</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306107</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Sp6)58Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=868&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=868&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-08-22)</AVAILABILITY>
    <RESEARCH_USE>Dentistry; Development</RESEARCH_USE>
    <ALLELES>Sp6</ALLELES>
    <ALLELE_RGD_IDS>1306768</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306107</CITATION_ID>
    <DESCRIPTION>The transgenic construct carrying rat Sp6 coding region was introduced to Slc:SD. Established at YS institute (PhoenixBio) in 2006 and introduced to the University of Tokushima.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306108</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D3Mit9-D3Wox16&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=814&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=814&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="50766145" STOP_POS="50766390" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="30356773" STOP_POS="90477342" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="34394121" STOP_POS="94028641" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="39535971" STOP_POS="100667805" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="26674018" STOP_POS="89245110" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306108</CITATION_ID>
    <DESCRIPTION>This congenic strain was established from WKY/Izm purchased from Japan SLC, Inc. and SHR/Izm at the Research Institute International Medical Center of Japan in 2001. The rats which have the heterozygous consomic segment were established in 2004, and were bred homozygous in 2005.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306109</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D3Mgh6-D3Rat1&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=817&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=817&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="73592512" STOP_POS="73592611" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="53184593" STOP_POS="168026850" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="54630948" STOP_POS="176418101" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="61249840" STOP_POS="180128021" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="50522618" STOP_POS="170016653" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306109</CITATION_ID>
    <DESCRIPTION>This congenic strain was established from WKY/Izm purchased from Japan SLC, Inc. and SHR/Izm at the Research Institute International Medical Center of Japan in 2001. The rats which have the heterozygous consomic segment were established in 2004, and were bred homozygous in 2005.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306110</RGD_ID>
    <STRAIN_SYMBOL>IER/Sums</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=870&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=870&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306110</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306111</RGD_ID>
    <STRAIN_SYMBOL>LEC.BN-(&lt;i&gt;D4Mgh16-D4Rat233&lt;/i&gt;)(&lt;i&gt;D4Rat271-D4Rat238&lt;/i&gt;)/Hkv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=876&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=876&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306111</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306112</RGD_ID>
    <STRAIN_SYMBOL>ZDF-&lt;i&gt;Lepr&lt;sup&gt;fa/fa&lt;/i&gt;/CrlCrlj&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=778&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=778&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2025-08-12)</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES>Lepr</ALLELES>
    <ALLELE_RGD_IDS>3001</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116294409" STOP_POS="116477904" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120503475" STOP_POS="120682281" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306112</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306113</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Sp6)6Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=867&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=867&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Dentistry; Development</RESEARCH_USE>
    <ALLELES>Sp6</ALLELES>
    <ALLELE_RGD_IDS>1306768</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306113</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306114</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D3Mgh16-D3Rat110&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=806&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=806&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="10778704" STOP_POS="10778823" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="6000748" STOP_POS="47155284" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="11361699" STOP_POS="53824856" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="6373335" STOP_POS="42729760" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306114</CITATION_ID>
    <DESCRIPTION>This congenic strain was established from WKY/Izm purchased from Japan SLC, Inc. and SHR/Izm at the Research Institute International Medical Center of Japan in 2001. The rats which have the heterozygous consomic segment were established in 2004, and were bred homozygous in 2005.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306115</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D3Mgh16-D3Rat166&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=816&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=816&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="122654702" STOP_POS="122654872" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="10778704" STOP_POS="102200699" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="6000748" STOP_POS="106900596" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="11361699" STOP_POS="113470358" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="6373335" STOP_POS="101359980" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306115</CITATION_ID>
    <DESCRIPTION>This congenic strain was established from WKY/Izm purchased from Japan SLC, Inc. and SHR/Izm at the Research Institute International Medical Center of Japan in 2001. The rats which have the heterozygous consomic segment were established in 2004, and were bred homozygous in 2005.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306116</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Sp6)5Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=819&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=819&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Dentistry; Development</RESEARCH_USE>
    <ALLELES>Sp6</ALLELES>
    <ALLELE_RGD_IDS>1306768</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306116</CITATION_ID>
    <DESCRIPTION>The transgenic construct carrying rat Sp6 cording region was introduced to Slc:SD. Established at YS institute (PhoenixBio) in 2006 and introduced to the University of Tokushima.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306117</RGD_ID>
    <STRAIN_SYMBOL>ACI.F344-(&lt;i&gt;D16Nkg9-D16Nkg27&lt;/i&gt;)/Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=827&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=827&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306117</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by backcrossing ACI.F344-(&lt;i&gt;D16Rat12-D16Mco2&lt;/i&gt;/Nkg onto ACI/NJcl, followed by intercrossing in N9 generation, thereafter maintained by crossing homozygous individuals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306118</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D15Rat95-D15Rat106&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=808&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=808&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="104694807" STOP_POS="104695021" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="63180675" STOP_POS="98288169" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="70559420" STOP_POS="106550657" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="74166614" STOP_POS="109944957" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="69469532" STOP_POS="106177917" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306118</CITATION_ID>
    <DESCRIPTION>This congenic strain was established from WKY/Izm purchased from Japan SLC, Inc. and SHR/Izm at the Research Institute International Medical Center of Japan in 2001. The rats which have the heterozygous consomic segment were established in 2004, and were bred homozygous in 2005.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306119</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(CD4,CCNT1)1Hik</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=805&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=805&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Infectious</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306119</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306120</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D4Wox27-D4Rat15&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=818&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=818&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="51085655" STOP_POS="51085803" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="5218294" STOP_POS="50119996" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="3044017" STOP_POS="48656399" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="3096322" STOP_POS="48448808" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="460493" STOP_POS="47890193" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306120</CITATION_ID>
    <DESCRIPTION>This congenic strain was established from WKY/Izm purchased from Japan SLC, Inc. and SHR/Izm at the Research Institute International Medical Center of Japan in 2001. The rats which have the heterozygous consomic segment were established in 2004, and were bred homozygous in 2005.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306276</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Exoc4&lt;sup&gt;Tn(sb-T2/Bart3)2.317Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=456&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Exoc4&lt;sup&gt;Tn(sb-T2/Bart3)2.317Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2306273</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="62774896" STOP_POS="63551541" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="61807706" STOP_POS="62584316" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="60549128" STOP_POS="61358305" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="60287465" STOP_POS="61081401" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="60406942" STOP_POS="61284294" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00456</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into  the 7th intron of the Exoc4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306277</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Gng12&lt;sup&gt;Tn(sb-T2/Bart3)2.320Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=454&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gng12&lt;sup&gt;Tn(sb-T2/Bart3)2.320Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2306274</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="97340830" STOP_POS="97464422" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="96011118" STOP_POS="96134767" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="97634925" STOP_POS="97763478" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="162420268" STOP_POS="162549350" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="96622363" STOP_POS="96624479" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00454</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into  the 1st intron of the Gng12 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306278</RGD_ID>
    <STRAIN_SYMBOL>F344-AW915325&lt;sup&gt;Tn(sb-T2/Bart3)2.319Mcwi&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=448&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-31)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>AW915325&lt;sup&gt;Tn(sb-T2/Bart3)2.319Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2306272</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00448</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the EST AW915325.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306279</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Diaph3&lt;sup&gt;Tn(sb-T2/Bart3)2.318Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=446&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Diaph3&lt;sup&gt;Tn(sb-T2/Bart3)2.318Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2306275</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="68951992" STOP_POS="69421623" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="62543375" STOP_POS="63013060" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="69928507" STOP_POS="70400077" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="73538942" STOP_POS="74007617" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="68905784" STOP_POS="69267707" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00446</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into  the 2nd intron of the Diaph3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306529</RGD_ID>
    <STRAIN_SYMBOL>BBDR.BBDP-(&lt;I&gt;D4Rhw11-D4Rhw10&lt;/I&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="76721312" STOP_POS="78654798" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="77380565" STOP_POS="79326833" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="142052025" STOP_POS="144005977" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="75808584" STOP_POS="77809321" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306529</CITATION_ID>
    <DESCRIPTION>Parental strain BBDR.BBDP-(&lt;I&gt;D4Rhw17-ss99306861&lt;/i&gt;)(&lt;I&gt;D4Rhw11-D4Rhw10&lt;/I&gt;)/Rhw were backcrossed to BBDR/Rhw, carefully DNA between D4Rhw17-ss99306861 was removed giving the desired congenic</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306532</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(&lt;i&gt;D4Rat27-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306532</CITATION_ID>
    <DESCRIPTION>Congenic substrains developed by crossing BBDR.F344-(&lt;i&gt;D4Rat153-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw to BBDR/Rhw producing animals which were intercrossed to produce F2 lymphonic rats that had reduced F344 DNA</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306533</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(&lt;i&gt;D4Rat102-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/2Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00469</CITATION_ID>
    <DESCRIPTION>Congenic substrains generated by intercrossing BBDR.F344-(&lt;i&gt;D4Rat253-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw and BBDR.F344-(&lt;i&gt;D4Got33-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306534</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(&lt;i&gt;D4Rat102-D4Rat27&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw11-D4Rhw10&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306534</CITATION_ID>
    <DESCRIPTION>Congenic substrains identified in F2 crosses of BBDR.F344-(&lt;i&gt;D4Rat153-D4Rat27&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw and BBDR/Rhw with BBDR.BBDP-(&lt;I&gt;D4Rhw11-D4Rhw10&lt;/I&gt;)/Rhw</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306535</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(&lt;i&gt;D4Rat253-D4Rat27&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw11-D4Rhw10&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306535</CITATION_ID>
    <DESCRIPTION>Congenic substrains identified in F2 crosses of BBDR.F344-(&lt;i&gt;D4Rat153-D4Rat27&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw and BBDR/Rhw with BBDR.BBDP-(&lt;I&gt;D4Rhw11-D4Rhw10&lt;/I&gt;)/Rhw</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306536</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(&lt;i&gt;D4Arb11-D4Rat27&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw11-D4Rhw10&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306536</CITATION_ID>
    <DESCRIPTION>Congenic substrains generated by intercrossing male BBDR.F344-(&lt;i&gt;D4Rat153-D4Rat27&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw11-D4Rhw10&lt;/i&gt;)/Rhw and female BBDR/Rhw</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306537</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(&lt;i&gt;D4Rat102-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/1Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306537</CITATION_ID>
    <DESCRIPTION>Congenic substrains generated by intercrossing BBDR.F344-(&lt;i&gt;D4Rat253-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw and BBDR.F344-(&lt;i&gt;D4Got33-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306538</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(&lt;i&gt;D4Rat153-D4Rat27&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw11-D4Rhw10&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306538</CITATION_ID>
    <DESCRIPTION>Congenic substrains generated by intercrossing BBDR.F344-(&lt;i&gt;D4Rat153-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw and BBDR.BBDP-(&lt;I&gt;D4Rhw11-D4Rhw10&lt;/I&gt;)/Rhw to reduce the proximal end of F344 DNA while retaining the Gimap5 mutation</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306539</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(&lt;i&gt;D4Rat102-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/3Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306539</CITATION_ID>
    <DESCRIPTION>Congenic substrains developed by crossing BBDR.F344-(&lt;i&gt;D4Rat153-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw to BBDR/Rhw producing animals which were intercrossed to produce F2 lymphonic rats that had reduced F344 DNA</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306540</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(&lt;i&gt;D4Got33-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306540</CITATION_ID>
    <DESCRIPTION>Congenic substrains developed by crossing BBDR.F344-(&lt;i&gt;D4Rat153-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw to BBDR/Rhw producing animals which were intercrossed to produce F2 lymphonic rats that had reduced F344 DNA</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306541</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(&lt;i&gt;D4Rat153-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=457&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00457</CITATION_ID>
    <DESCRIPTION>BBDR.BBDP-(&lt;I&gt;D4Mit6-D4Mit7&lt;/I&gt;)/Rhw were intercrossed with F344 giving a recombination proximal to Gimap1 fragment. Whole-genome scan, STS and SSLP analyses were done to determine the region introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306542</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(&lt;i&gt;D4Rat253-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306542</CITATION_ID>
    <DESCRIPTION>Congenic substrains developed by crossing BBDR.F344-(&lt;i&gt;D4Rat153-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw to BBDR/Rhw producing animals which were intercrossed to produce F2 lymphonic rats that had reduced F344 DNA</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306543</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(&lt;i&gt;D4Got59-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306543</CITATION_ID>
    <DESCRIPTION>BBDR.BBDP-(&lt;I&gt;D4Mit6-D4Mit7&lt;/I&gt;)/Rhw were intercrossed with F344 giving a recombination proximal to Gimap1 fragment. Whole-genome scan, STS and SSLP analyses were done to determine the region introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306544</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(&lt;i&gt;D4Rat26-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306544</CITATION_ID>
    <DESCRIPTION>Congenic substrains developed by crossing BBDR.F344-(&lt;i&gt;D4Rat153-D4Rhw8&lt;/i&gt;),BBDP-(&lt;i&gt;D4Rhw6-D4Rat62&lt;/i&gt;)/Rhw to BBDR/Rhw producing animals which were intercrossed to produce F2 lymphonic rats that had reduced F344 DNA</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306709</RGD_ID>
    <STRAIN_SYMBOL>BBDR.BBDP-(&lt;I&gt;D4Mit6-D4Mit7&lt;/I&gt;)/3Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="80216705" STOP_POS="80217004" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="76647384" STOP_POS="78886189" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="77307388" STOP_POS="79562753" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="141978848" STOP_POS="141979031" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="75732943" STOP_POS="75733127" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306709</CITATION_ID>
    <DESCRIPTION>This congenic strain was developed by cyclic cross-intercross breeding using diabetic prone and diabetic resistant BB rats. (DP x DR)F1 x DR cross intercross breeding was used to generate F2 lymphopenic rats. These were then genotyped for both the flanking markers of the Gimap5 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306710</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Lmln&lt;sup&gt;Tn(sb-T2/Bart3)2.322Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=447&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lmln&lt;sup&gt;Tn(sb-T2/Bart3)2.322Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2306701</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="81161330" STOP_POS="81230972" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="67656241" STOP_POS="67725889" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="70895141" STOP_POS="70963121" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="73980288" STOP_POS="74048100" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="69481117" STOP_POS="69547133" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00447</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 12th intron of the Lmln gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306711</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;FM117003&lt;sup&gt;Tn(sb-T2/Bart3)2.321McwiRrrc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=475&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>FM117003&lt;sup&gt;Tn(sb-T2/Bart3)2.321Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2306703</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00475</CITATION_ID>
    <DESCRIPTION>this Sleeping Beauty mutants were derived by crossing F344-Tg(T2/Bart3)2Ceb and F344-Tg(PGK2-SB11)Ceb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306712</RGD_ID>
    <STRAIN_SYMBOL>BBDR.BBDP-(&lt;I&gt;D4Mit6-D4Mit7&lt;/I&gt;)/2Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="80216705" STOP_POS="80217004" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="76647384" STOP_POS="78886189" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="77307388" STOP_POS="79562753" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="141978848" STOP_POS="141979031" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="75732943" STOP_POS="75733127" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306712</CITATION_ID>
    <DESCRIPTION>This congenic strain was developed by cyclic cross-intercross breeding using diabetic prone and diabetic resistant BB rats. (DP x DR)F1 x DR cross intercross breeding was used to generate F2 lymphopenic rats. These were then genotyped for both the flanking markers of the Gimap5 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306717</RGD_ID>
    <STRAIN_SYMBOL>BBDP/WorSunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine and Immunology, University of Toronto, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=787&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2018-11-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00787</CITATION_ID>
    <DESCRIPTION>These originated from the Worcester colony from the rats that were sent from Ottawa to Worcester in 1977. Now maintained at University of Toronto, Canada.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306784</RGD_ID>
    <STRAIN_SYMBOL>Kini:DA,PVG-G12</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>advanced_intercross_line</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306784</CITATION_ID>
    <DESCRIPTION>Two breeding pairs from inbred DA/Han and PVG/OlaHsd that share the RT1&lt;sup&gt;a&lt;/sup&gt; MHC haplotype were bred to create F&lt;sub&gt;1&lt;/sub&gt; generation, 7 couples of F&lt;sub&gt;1&lt;/sub&gt; with DA/Han and PVG/OlaHsd females founders generated F&lt;sub&gt;2&lt;/sub&gt;. F&lt;sub&gt;3&lt;/sub&gt; generation originated from breeding 50 random couples</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306815</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;D7Rat67-D7Mco7&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="107588339" STOP_POS="107588516" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="105699315" STOP_POS="105699492" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="115041287" STOP_POS="115041463" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="114961803" STOP_POS="116100169" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="111506104" STOP_POS="113014423" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306815</CITATION_ID>
    <DESCRIPTION>Congenic substrain developed by crossing SS.SR-(&lt;I&gt;D7Uia1-D7Mco7&lt;/I&gt;)/Jr to SS/Jr to produce F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed and genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306816</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;D7Mco19-D7Mco7&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="106571501" STOP_POS="106571759" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="115922628" STOP_POS="115922885" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="115828017" STOP_POS="116100169" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="112800232" STOP_POS="113014423" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306816</CITATION_ID>
    <DESCRIPTION>Congenic substrain developed by crossing SS.SR-(&lt;I&gt;D7Uia1-D7Mco7&lt;/I&gt;)/Jr to SS/Jr to produce F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed and genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306817</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;D7Uia1-D7Mco19&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="103146217" STOP_POS="106571759" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="112429186" STOP_POS="115922885" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="112367543" STOP_POS="115828274" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="108875615" STOP_POS="112800489" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306817</CITATION_ID>
    <DESCRIPTION>Congenic substrain developed by crossing SS.SR-(&lt;I&gt;D7Uia1-D7Mco7&lt;/I&gt;)/Jr to SS/Jr to produce F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed and genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306818</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;D7Rat131-D7Mco7&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="107963017" STOP_POS="107963207" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="106074002" STOP_POS="106074194" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="115421039" STOP_POS="115421228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="115334997" STOP_POS="116100169" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="111882387" STOP_POS="113014423" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306818</CITATION_ID>
    <DESCRIPTION>Congenic substrain developed by crossing SS.SR-(&lt;I&gt;D7Uia1-D7Mco7&lt;/I&gt;)/Jr to SS/Jr to produce F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed and genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306819</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;D7Uia1-D7Rat131&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="107963017" STOP_POS="107963207" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="103146217" STOP_POS="106074194" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="112429186" STOP_POS="115421228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="112367543" STOP_POS="115335186" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="108875615" STOP_POS="111882577" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306819</CITATION_ID>
    <DESCRIPTION>Congenic substrain developed by crossing SS.SR-(&lt;I&gt;D7Uia1-D7Mco7&lt;/I&gt;)/Jr to SS/Jr to produce F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed and genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306820</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D3Arb14-D3Mco36&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="168974481" STOP_POS="168974694" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="177366448" STOP_POS="177366660" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="181074759" STOP_POS="181074971" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="171009566" STOP_POS="171009778" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306820</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D3Mco19-D3Mco5&lt;/i&gt;)/Jr rats were crossed with SS to yield F1, these heterozygous rats were intercrossed to obtain F2 which were screened to identify the SR-rat derived region, these were then crossed with SS to duplicate the recombinant chromosome</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306823</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D3Arb14-D3Mco36&lt;/i&gt;)(&lt;i&gt;D7Mco19-D7Mco7&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306823</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D3Arb14-D3Mco36&lt;/i&gt;)/Mco were crossed with SS.SR-(&lt;i&gt;D7Mco19-D7Mco7&lt;/i&gt;)/Jr and then F&lt;sub&gt;1&lt;/sub&gt; rats were backcrossed with SS.SR-(&lt;i&gt;D3Arb14-D3Mco36&lt;/i&gt;)/Mco, animals heterozygous for chr 7 and homozygous for chr 3 were crossed and the resulting progeny homozygous for both segments were bred</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306840</RGD_ID>
    <STRAIN_SYMBOL>E3.DA-(&lt;i&gt;D4Wox22-D4Got132&lt;/i&gt;)(&lt;i&gt;D12Wox5-D12Rat26&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Lund University, Lund, Sweden.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306840</CITATION_ID>
    <DESCRIPTION>This congenic strain was obtained by the conventional backcross breeding to the parental strain with positive selection of microsatellite markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306841</RGD_ID>
    <STRAIN_SYMBOL>E3.DA-(&lt;i&gt;D12Wox5-D12Rat26&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Lund University, Lund, Sweden.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="18749469" STOP_POS="28329066" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="13635523" STOP_POS="22692658" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="15714609" STOP_POS="25711626" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="17721341" STOP_POS="27718984" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="23845554" STOP_POS="23845733" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306841</CITATION_ID>
    <DESCRIPTION>This congenic strain was obtained by the conventional backcross breeding to the parental strain with positive selection of microsatellite markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306842</RGD_ID>
    <STRAIN_SYMBOL>E3.DA-(&lt;i&gt;D20Rat45-D20Rat47&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Lund University, Lund, Sweden.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="1533083" STOP_POS="5306567" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="1527842" STOP_POS="5304690" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="2018654" STOP_POS="6567533" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="4059279" STOP_POS="8810333" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="133455626" STOP_POS="133455718" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="1616332" STOP_POS="5447494" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306842</CITATION_ID>
    <DESCRIPTION>This congenic strain was obtained by the conventional backcross breeding to the parental strain with positive selection of microsatellite markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306874</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Intu&lt;sup&gt;Tn(sb-T2/Bart3)2.324Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=441&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Intu&lt;sup&gt;Tn(sb-T2/Bart3)2.324Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2306873</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="125528965" STOP_POS="125613295" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="123600972" STOP_POS="123685331" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="127459089" STOP_POS="127521327" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="147063971" STOP_POS="147216092" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="127564813" STOP_POS="127639564" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00441</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 4th intron of the Intu gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306875</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Faslg&lt;sup&gt;Tn(sb-T2/Bart3)2.325Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Faslg&lt;sup&gt;Tn(sb-T2/Bart3)2.325Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2306872</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="76680885" STOP_POS="76706042" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="74151519" STOP_POS="74172760" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="79696811" STOP_POS="79717581" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="84590119" STOP_POS="84605900" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="77472950" STOP_POS="77480210" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306875</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Faslg gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306892</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D2Rat114-D2Rat123&lt;/i&gt;)/Jk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Heart Institute (InCor), University of Sao Paulo Medical School, Sao Paulo, Brazil.</ORIGINATION>
    <SOURCE>&lt;a href=http://genetica.incor.usp.br&gt;Genetica&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="38426449" STOP_POS="111295694" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="109366814" STOP_POS="109366971" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="36245223" STOP_POS="112175725" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="55361257" STOP_POS="131889716" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="36432989" STOP_POS="112326568" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306892</CITATION_ID>
    <DESCRIPTION>Backcross marker-assisted method was used to fix the BN fragment onto SHR genome, once selection was done using markers, male and female were crossed to get homozygous animals</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306893</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D16Rat87-D16Mgh1&lt;/i&gt;)/Jk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Heart Institute (InCor), University of Sao Paulo Medical School, Sao Paulo, Brazil.</ORIGINATION>
    <SOURCE>&lt;a href=http://genetica.incor.usp.br&gt;Genetica&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="3386790" STOP_POS="49757901" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="3380150" STOP_POS="43025077" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="4136355" STOP_POS="45905331" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="4082652" STOP_POS="45651269" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="3464719" STOP_POS="46137590" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306893</CITATION_ID>
    <DESCRIPTION>Backcross marker-assisted method was used to fix the BN fragment onto SHR genome, once selection was done using markers, male and female were crossed to get homozygous animals</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306894</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D4Rat33-D4Rat54&lt;/i&gt;)/Jk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Heart Institute (InCor), University of Sao Paulo Medical School, Sao Paulo, Brazil.</ORIGINATION>
    <SOURCE>&lt;a href=http://genetica.incor.usp.br&gt;Genetica&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="82336765" STOP_POS="82336920" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="81006124" STOP_POS="120102625" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="81874073" STOP_POS="119546974" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="146540904" STOP_POS="184799673" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="80205349" STOP_POS="121829076" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306894</CITATION_ID>
    <DESCRIPTION>Backcross marker-assisted method was used to fix the BN fragment onto SHR genome, once selection was done using markers, male and female were crossed to get homozygous animals</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306895</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D2Rat226-D2Rat294&lt;/i&gt;)/Jk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Heart Institute (InCor), University of Sao Paulo Medical School, Sao Paulo, Brazil. </ORIGINATION>
    <SOURCE>&lt;a href=http://genetica.incor.usp.br&gt;Genetica&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="166372086" STOP_POS="229820014" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="164073756" STOP_POS="227146641" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="177680772" STOP_POS="243901375" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="197020226" STOP_POS="262435073" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="170338294" STOP_POS="236153712" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306895</CITATION_ID>
    <DESCRIPTION>Backcross marker-assisted method was used to fix the BN fragment onto SHR genome, once selection was done using markers, male and female were crossed to get homozygous animals</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306961</RGD_ID>
    <STRAIN_SYMBOL>RLA/Verh</STRAIN_SYMBOL>
    <FULL_NAME>Roman low avoidance</FULL_NAME>
    <ORIGINATION>Laboratory for Experimental Medicine and Endocrinology, Catholic University of Leuven, Belgium</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306961</CITATION_ID>
    <DESCRIPTION>Bignami selected for low avoidance conditioning with light as a conditioned stimulus and electric shock as the unconditioned stimulus,these are now at Laboratory for Experimental Medicine and Endocrinology, Catholic University of Leuven, Belgium</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2306962</RGD_ID>
    <STRAIN_SYMBOL>RHA/Verh</STRAIN_SYMBOL>
    <FULL_NAME>Roman high avoidance</FULL_NAME>
    <ORIGINATION>Laboratory for Experimental Medicine and Endocrinology, Catholic University of Leuven, Belgium</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2306962</CITATION_ID>
    <DESCRIPTION>Bignami selected for high avoidance conditioning with light as a conditioned stimulus and electric shock as the unconditioned stimulus,these are now at Laboratory for Experimental Medicine and Endocrinology, Catholic University of Leuven, Belgium</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307077</RGD_ID>
    <STRAIN_SYMBOL>HXB4/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307077</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307078</RGD_ID>
    <STRAIN_SYMBOL>HXB27/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307078</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307079</RGD_ID>
    <STRAIN_SYMBOL>HXB3/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307079</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307080</RGD_ID>
    <STRAIN_SYMBOL>HXB20/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307080</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307081</RGD_ID>
    <STRAIN_SYMBOL>HXB31/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307081</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307082</RGD_ID>
    <STRAIN_SYMBOL>HXB18/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307082</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307083</RGD_ID>
    <STRAIN_SYMBOL>HXB10/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307083</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307084</RGD_ID>
    <STRAIN_SYMBOL>HXB24/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307084</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307085</RGD_ID>
    <STRAIN_SYMBOL>HXB17/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307085</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307086</RGD_ID>
    <STRAIN_SYMBOL>HXB7/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307086</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307087</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D18Rat32-D18Rat12&lt;/i&gt;)/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307087</CITATION_ID>
    <DESCRIPTION>A segment of chr 18 from BN was introgressed into the SHR background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307088</RGD_ID>
    <STRAIN_SYMBOL>HXB22/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307088</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307089</RGD_ID>
    <STRAIN_SYMBOL>HXB29/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307089</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307090</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN10/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307090</CITATION_ID>
    <DESCRIPTION>A segment of chr 10 from BN was introgressed into the SHR background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307091</RGD_ID>
    <STRAIN_SYMBOL>HXB13/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307091</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307092</RGD_ID>
    <STRAIN_SYMBOL>HXB14/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307092</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307093</RGD_ID>
    <STRAIN_SYMBOL>HXB23/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307093</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307094</RGD_ID>
    <STRAIN_SYMBOL>HXB1/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307094</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307095</RGD_ID>
    <STRAIN_SYMBOL>HXB15/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307095</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307096</RGD_ID>
    <STRAIN_SYMBOL>HXB2/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307096</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307097</RGD_ID>
    <STRAIN_SYMBOL>HXB21/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307097</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307098</RGD_ID>
    <STRAIN_SYMBOL>HXB25/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307098</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307099</RGD_ID>
    <STRAIN_SYMBOL>HXB5/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307099</CITATION_ID>
    <DESCRIPTION>Derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307115</RGD_ID>
    <STRAIN_SYMBOL>BXH5/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307115</CITATION_ID>
    <DESCRIPTION>Derived from founder strains BN-Lx/Cub and SHR/OlaIpcv</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307116</RGD_ID>
    <STRAIN_SYMBOL>PXO3-2/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307116</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307117</RGD_ID>
    <STRAIN_SYMBOL>PXO5-2/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307117</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307118</RGD_ID>
    <STRAIN_SYMBOL>PXO9/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307118</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307119</RGD_ID>
    <STRAIN_SYMBOL>PXO7-1/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307119</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307120</RGD_ID>
    <STRAIN_SYMBOL>PXO7-2/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307120</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307121</RGD_ID>
    <STRAIN_SYMBOL>BXH2/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307121</CITATION_ID>
    <DESCRIPTION>Derived from founder strains BN-Lx/Cub and SHR/OlaIpcv</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307122</RGD_ID>
    <STRAIN_SYMBOL>PXO8-1/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307122</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307123</RGD_ID>
    <STRAIN_SYMBOL>BXH13/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307123</CITATION_ID>
    <DESCRIPTION>Derived from founder strains BN-Lx/Cub and SHR/OlaIpcv</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307124</RGD_ID>
    <STRAIN_SYMBOL>BXH10/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307124</CITATION_ID>
    <DESCRIPTION>Derived from founder strains BN-Lx/Cub and SHR/OlaIpcv</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307125</RGD_ID>
    <STRAIN_SYMBOL>PXO6-2/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307125</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307126</RGD_ID>
    <STRAIN_SYMBOL>BXH8/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307126</CITATION_ID>
    <DESCRIPTION>Derived from founder strains BN-Lx/Cub and SHR/OlaIpcv</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307127</RGD_ID>
    <STRAIN_SYMBOL>BXH11/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307127</CITATION_ID>
    <DESCRIPTION>Derived from founder strains BN-Lx/Cub and SHR/OlaIpcv</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307128</RGD_ID>
    <STRAIN_SYMBOL>PXO5-1/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307128</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307129</RGD_ID>
    <STRAIN_SYMBOL>BXH9/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307129</CITATION_ID>
    <DESCRIPTION>Derived from founder strains BN-Lx/Cub and SHR/OlaIpcv</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307130</RGD_ID>
    <STRAIN_SYMBOL>PXO6-3/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307130</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307131</RGD_ID>
    <STRAIN_SYMBOL>PXO8-2/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307131</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307132</RGD_ID>
    <STRAIN_SYMBOL>PXO10/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307132</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307134</RGD_ID>
    <STRAIN_SYMBOL>BXH3/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307134</CITATION_ID>
    <DESCRIPTION>Derived from founder strains BN-Lx/Cub and SHR/OlaIpcv</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307135</RGD_ID>
    <STRAIN_SYMBOL>PXO4/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307135</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307136</RGD_ID>
    <STRAIN_SYMBOL>BXH6/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307136</CITATION_ID>
    <DESCRIPTION>Derived from founder strains BN-Lx/Cub and SHR/OlaIpcv</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307137</RGD_ID>
    <STRAIN_SYMBOL>PXO6-1/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307137</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307138</RGD_ID>
    <STRAIN_SYMBOL>PXO1/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307138</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307139</RGD_ID>
    <STRAIN_SYMBOL>BXH12/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307139</CITATION_ID>
    <DESCRIPTION>Derived from founder strains BN-Lx/Cub and SHR/OlaIpcv</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307155</RGD_ID>
    <STRAIN_SYMBOL>SHR/1NCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MRC Clinical Sciences Centre, College School of Medicine, London, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307155</CITATION_ID>
    <DESCRIPTION>To Charles River from NIH in 1973 at F32.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307156</RGD_ID>
    <STRAIN_SYMBOL>DA/ZtmKini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307156</CITATION_ID>
    <DESCRIPTION>Substrain of DA, to Hannover after 1965, now at Stockholm, Sweden.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307157</RGD_ID>
    <STRAIN_SYMBOL>PVG.1AV1/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307157</CITATION_ID>
    <DESCRIPTION>Originally derived by Dr. Hans J. Hendrich at Versuchstierzucht, Hannover, Germany, now at Stockholm, Sweden.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307159</RGD_ID>
    <STRAIN_SYMBOL>SHRSR.SHRSP-(&lt;i&gt;Klk1-Mt1-ps1&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mt1-ps1|Klk1c12</ALLELES>
    <ALLELE_RGD_IDS>3118|1303192</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="103514639" STOP_POS="190563849" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="94378103" STOP_POS="181133270" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="99298965" STOP_POS="197963072" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="100371040" STOP_POS="204941832" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="94355758" STOP_POS="185690396" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307159</CITATION_ID>
    <DESCRIPTION>SHRSP were crossed with SHRSR to give heterozygous F&lt;sub&gt;2&lt;/sub&gt; animals, these were backcrossed and heterozygotes with desired segment of interest selected and backcrossed to fix the allele of interest</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307160</RGD_ID>
    <STRAIN_SYMBOL>SHRSR.SHRSP-(&lt;i&gt;Klk1-D1Mit3&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Klk1c12</ALLELES>
    <ALLELE_RGD_IDS>1303192</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="103514639" STOP_POS="153680016" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="94378103" STOP_POS="144267916" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="99298965" STOP_POS="156446783" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="100371040" STOP_POS="162692800" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="94355758" STOP_POS="146971983" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307160</CITATION_ID>
    <DESCRIPTION>SHRSP were crossed with SHRSR to give heterozygous F&lt;sub&gt;2&lt;/sub&gt; animals, these were backcrossed and heterozygotes with desired segment of interest selected and backcrossed to fix the allele of interest</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307161</RGD_ID>
    <STRAIN_SYMBOL>SHRSR.SHRSP-(&lt;i&gt;D1Rat134-Mt1-ps1&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mt1-ps1</ALLELES>
    <ALLELE_RGD_IDS>3118</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="143044309" STOP_POS="190563849" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="133634986" STOP_POS="181133270" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="141429089" STOP_POS="197963072" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="142390027" STOP_POS="204941832" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="135467526" STOP_POS="185690396" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307161</CITATION_ID>
    <DESCRIPTION>SHRSP were crossed with SHRSR to give heterozygous F&lt;sub&gt;2&lt;/sub&gt; animals, these were backcrossed and heterozygotes with desired segment of interest selected and backcrossed to fix the allele of interest</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307166</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHRSR-(&lt;i&gt;Klk1-Mt1-ps1&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mt1-ps1|Klk1c12</ALLELES>
    <ALLELE_RGD_IDS>3118|1303192</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="103514639" STOP_POS="190563849" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="94378103" STOP_POS="181133270" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="99298965" STOP_POS="197963072" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="100371040" STOP_POS="204941832" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="94355758" STOP_POS="185690396" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307166</CITATION_ID>
    <DESCRIPTION>SHRSP were crossed with SHRSR to give heterozygous F&lt;sub&gt;2&lt;/sub&gt; animals, these were backcrossed and heterozygotes with desired segment of interest selected and backcrossed to fix the allele of interest</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307167</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHRSR-(&lt;i&gt;Klk1-D1Mit3&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Klk1c12</ALLELES>
    <ALLELE_RGD_IDS>1303192</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="103514639" STOP_POS="153680016" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="94378103" STOP_POS="144267916" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="99298965" STOP_POS="156446783" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="100371040" STOP_POS="162692800" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="94355758" STOP_POS="146971983" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307167</CITATION_ID>
    <DESCRIPTION>SHRSP were crossed with SHRSR to give heterozygous F&lt;sub&gt;2&lt;/sub&gt; animals, these were backcrossed and heterozygotes with desired segment of interest selected and backcrossed to fix the allele of interest</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307168</RGD_ID>
    <STRAIN_SYMBOL>SHRSR/Bbb</STRAIN_SYMBOL>
    <FULL_NAME>Spontaneously Hypertensive Rat, Stroke Resistant</FULL_NAME>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307168</CITATION_ID>
    <DESCRIPTION>This SHRSP colony as obtained from the original Japanese stock from Okamoto and Aoki in 1974 and is propagated by strict inbreeding. Now this colony is maintained at Max-Delbruck-Center for Molecular Medicine, Berlin, Germany.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307169</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHRSR-(&lt;i&gt;D1Rat134-Mt1-ps1&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mt1-ps1</ALLELES>
    <ALLELE_RGD_IDS>3118</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="143044309" STOP_POS="190563849" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="133634986" STOP_POS="181133270" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="141429089" STOP_POS="197963072" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="142390027" STOP_POS="204941832" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="135467526" STOP_POS="185690396" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307169</CITATION_ID>
    <DESCRIPTION>SHRSP were crossed with SHRSR to give heterozygous F&lt;sub&gt;2&lt;/sub&gt; animals, these were backcrossed and heterozygotes with desired segment of interest selected and backcrossed to fix the allele of interest</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307298</RGD_ID>
    <STRAIN_SYMBOL>BN/HanKini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307298</CITATION_ID>
    <DESCRIPTION>Substrain of BN derived from BN/Han (Dr. H.J. Hedrich, Hannover, Germany)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307299</RGD_ID>
    <STRAIN_SYMBOL>ACI/ZtmKini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307299</CITATION_ID>
    <DESCRIPTION>substrain of ACI derived from ACI/Ztm</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307300</RGD_ID>
    <STRAIN_SYMBOL>LEW.1AV1/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307300</CITATION_ID>
    <DESCRIPTION>Substrain of LEW.1AV1</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307301</RGD_ID>
    <STRAIN_SYMBOL>DA.LEW.RT1f-(&lt;i&gt;D20Wox15-D20Wox13&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Biomedical Center, Lund University, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="2646407" STOP_POS="6515143" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="3151827" STOP_POS="8034632" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="5249993" STOP_POS="10234922" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="2790524" STOP_POS="6695696" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307301</CITATION_ID>
    <DESCRIPTION>RT1f Haplotype on DA background, congenic strain was obtained by conventional backcross breeding to the parental DA/Ztm from LEW.1F/Ztm with positive selection of microsatellite markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307317</RGD_ID>
    <STRAIN_SYMBOL>MHS</STRAIN_SYMBOL>
    <FULL_NAME>Milan Hypertensive Strain</FULL_NAME>
    <ORIGINATION>Department of Sciences and Biomedical Technologies, University of Milan, Milan, Italy</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307317</CITATION_ID>
    <DESCRIPTION>Outbred Wistar rats with brother x sister mating and selection for high systolic blood pressure</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307318</RGD_ID>
    <STRAIN_SYMBOL>BDIX/Ifz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Duisburg-Essen University Medical School, Essen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307318</CITATION_ID>
    <DESCRIPTION>derived from Berlin-Druckrey strain BDIX</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307319</RGD_ID>
    <STRAIN_SYMBOL>MNS/N</STRAIN_SYMBOL>
    <FULL_NAME>Milan normotensive strain</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=171&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=171&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00171</CITATION_ID>
    <DESCRIPTION>Wistar rats with brother x sister mating and selection for low systolic blood pressure as a normotensive control for MHS.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307355</RGD_ID>
    <STRAIN_SYMBOL>PXO3-1/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307355</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307356</RGD_ID>
    <STRAIN_SYMBOL>PXO2/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Charles University, Department of Biology, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307356</CITATION_ID>
    <DESCRIPTION>Derived from polydactylous (P) SHR.&lt;i&gt;Lx&lt;/i&gt; congenic strain and oligodactylous (O) BXH2 recombinant inbred strain. These are homozygous in the &lt;i&gt;Lx&lt;/i&gt; allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307357</RGD_ID>
    <STRAIN_SYMBOL>BDV/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307357</CITATION_ID>
    <DESCRIPTION>Developed from a cross of a single BDI x BDII mating pair, with subsequent selection for coat colour alleles.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307358</RGD_ID>
    <STRAIN_SYMBOL>LUDW/OlaHsd</STRAIN_SYMBOL>
    <FULL_NAME>Ludwig</FULL_NAME>
    <ORIGINATION>&lt;a href =http://www.envigo.com/products-services/research-models-services/find-a-model/research-models/rats/inbred/ludw-inbred-rat/&gt; Envigo&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =http://www.envigo.com/products-services/research-models-services/find-a-model/research-models/rats/inbred/ludw-inbred-rat/&gt; Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307358</CITATION_ID>
    <DESCRIPTION>Wistar stock to Ludwig Institute, Sutton.From Ludwig Institute to Harlan in 1979.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307359</RGD_ID>
    <STRAIN_SYMBOL>BUF/SimRijHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan Sprague Dawley, Inc., Indianapolis, IN</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307359</CITATION_ID>
    <DESCRIPTION>Developed by Heston in 1946 from a Buffalo</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307360</RGD_ID>
    <STRAIN_SYMBOL>DA.BI.RT1i-(&lt;i&gt;D20Rat42-D20Rat31&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Lund University, Lund, Sweden.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="4461624" STOP_POS="10078622" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="4459698" STOP_POS="10078919" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="4186104" STOP_POS="10800530" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="6265460" STOP_POS="12972703" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="4582054" STOP_POS="10410227" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2307360</CITATION_ID>
    <DESCRIPTION>RT1i Haplotype on DA background, congenic strain originates from BI, formerly B3 (extinct strain) and was produced at Zentralinstitut for Versuchstierzucht, Hannover, Germany). It has been maintained by conventional backcross breeding to the parental DA/Han.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307441</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Cyyr1&lt;sup&gt;Tn(sb-T2/Bart3)2.328Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=452&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyyr1&lt;sup&gt;Tn(sb-T2/Bart3)2.328Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2307440</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="38044003" STOP_POS="38150391" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="24557620" STOP_POS="24664007" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="24967936" STOP_POS="25078740" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="28591553" STOP_POS="28702298" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="25036792" STOP_POS="25157304" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00452</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Cyyr1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2307442</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Robo1&lt;sup&gt;Tn(sb-T2/Bart3)2.327Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=451&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Robo1&lt;sup&gt;Tn(sb-T2/Bart3)2.327Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2307439</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="24067869" STOP_POS="25108694" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="10580863" STOP_POS="11621675" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="9079291" STOP_POS="10146302" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="13314508" STOP_POS="13808775" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="10784947" STOP_POS="11720646" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00451</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 2nd intron of the Robo1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2308816</RGD_ID>
    <STRAIN_SYMBOL>Crl:WI(Han)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.criver.com/products-services/find-model/wistar-han-igs-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/wistar-han-igs-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2308816</CITATION_ID>
    <DESCRIPTION>Rederived by GlaxoWellcome from Han Wistar stock supplied by BRL (under structural changed to RCC). Transferred to Charles River UK in 1996. Transferred to Charles River in 1997 and rederived into isolator maintained Foundation Colony. IGS refers to animals bred using the Charles River International Genetic Standard system.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2308851</RGD_ID>
    <STRAIN_SYMBOL>Crl:OP(CD)</STRAIN_SYMBOL>
    <FULL_NAME>Obese Prone Rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2308851</CITATION_ID>
    <DESCRIPTION>Developed from a line of Crl:CD(SD) rats. Two lines were developed from this outbred colony, the OP-CD(Obese Prone) and OR-CD (Obese Resistant). This model becomes obese when fed high-fat diets. Obesity develops despite having a fully functioning leptin receptor. The control for this model is the Crl:OR(CD).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2308852</RGD_ID>
    <STRAIN_SYMBOL>Crl:LE</STRAIN_SYMBOL>
    <FULL_NAME>Long-Evans Rats</FULL_NAME>
    <ORIGINATION>&lt;a href=https://www.criver.com/products-services/find-model/long-evans-rat?region=3611&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/long-evans-rat?region=3611&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2308852</CITATION_ID>
    <DESCRIPTION>Originated by Drs. Long and Evans in 1915 by crossing several Wistar white females with a wild gray male. To Charles River from Canadian Breeding Farm and Laboratories in 1978.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2308853</RGD_ID>
    <STRAIN_SYMBOL>Crl:OR(CD)</STRAIN_SYMBOL>
    <FULL_NAME>Obese Resistant Rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2308853</CITATION_ID>
    <DESCRIPTION>Developed from a line of Crl:CD(SD) rats. Two lines were developed from this outbred colony, the OP-CD (Obese Prone) and OR-CD (Obese Resistant). This model does not become obese when fed high-fat diets.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2308885</RGD_ID>
    <STRAIN_SYMBOL>GK/CskCrljCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2308885</CITATION_ID>
    <DESCRIPTION>The Goto-Kakizaki (GK) rat is a non-obese Wistar substrain which develops Type 2 diabetes mellitus early in life. The model was developed by Goto and Kakizaki at Tohoku University, Sendai, Japan in 1975. To Chugai Pharmaceutical Co. To Charles River Japan in 1995. To Charles River in 2006.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2308886</RGD_ID>
    <STRAIN_SYMBOL>SS/HsdMcwiCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.criver.com/products-services/find-model/dahlsalt-sensitive-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/dahlsalt-sensitive-rat?region=3611&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2308886</CITATION_ID>
    <DESCRIPTION>Inbred from a congenic control group of Dahl/SS rats (SS/JrHsd) obtained from Dr. Theodore Kurtz (UCSF, CA) which were originally derived from the Harlan SS/Jr colony. Maintained at the Medical College of Wisconsin since 1991, this strain has undergone considerable marker-selected breeding to eliminate residual heterozygosity and genetic contamination. To confirm homozygosity, the strain was tested with 200 microsatellite markers (genome-wide scan at 20cM) all of which were homozygous for all regions tested. (Cowley et al. 2000, Physiol. Genomics 2:107-115). To Charles River in 2001.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2311049</RGD_ID>
    <STRAIN_SYMBOL>SHROB/KolGmiCrl-&lt;i&gt;Lepr&lt;sup&gt;cp&lt;/i&gt;&lt;/sup&gt;/Crl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;cp&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11570565</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2311049</CITATION_ID>
    <DESCRIPTION>This mutation occurred in the laboratory of Dr. Simon Koletsky in 1969 at Case Western Reserve University School of Medicine. It was developed from a cross between a hypertensive female rat and a normotensive male Sprague Dawley rat. The colony was maintained as brother x sister matings in a closed colony at Case Western Reserve University School of Medicine since 1971. To Genetic Models, Inc. in 2000. To Charles River in 2001.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2311051</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/A3NCrl</STRAIN_SYMBOL>
    <FULL_NAME>Stroke Prone Rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2311051</CITATION_ID>
    <DESCRIPTION>The Spontaneously Hypertensive Stroke Prone Rat (SHRSP) was isolated from Wistar-Kyoto rats by Okamoto and Aoki in 1963. The A3 subline was transferred to the National Institutes of Health in 1975 from Yamori at generation F36. To Charles River in 2002.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2311070</RGD_ID>
    <STRAIN_SYMBOL>BUF/CrCrl</STRAIN_SYMBOL>
    <FULL_NAME>Buffalo Rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2311070</CITATION_ID>
    <DESCRIPTION>Heston in 1946 from Buffalo stock of H. Morris. To NIH in 1951 at F10. To Charles River in 1998 from the National Cancer Institute Animal Production Program (Cr).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2311071</RGD_ID>
    <STRAIN_SYMBOL>ZDF-&lt;i&gt;Lepr&lt;sup&gt;fa/fa&lt;/sup&gt;&lt;/i&gt;/Crl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.criver.com/products-services/find-model/zdf-rat-obese?region=3611&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/zdf-rat-obese?region=3611&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13432153</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116389200" STOP_POS="116389200" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120597857" STOP_POS="120597857" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2311071</CITATION_ID>
    <DESCRIPTION>A mutation occurred in a colony of outbred Zucker rats in the laboratory of Dr. Walter Shaw at Eli Lilly Research Laboratories in Indianapolis, IN in 1974???75. Part of this colony containing the mutation was moved to Indiana University Medical School (IUMS), to the laboratory of Dr. Julia Clark in 1977. Several groups of animals with diabetic lineage were identified and rederived in 1981. Inbreeding of selected pairs from this rederivation was done in the laboratory of Dr. Richard Peterson at IUMS. An inbred line of ZDF rat was established in 1985. To Genetic Models, Inc. in 1991. To Charles River in 2001. Control models for the ZDF Rat (Obese fa/fa) are the ZDF Rat (Lean fa/+) or ZDF Rat (Lean +/?).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2311072</RGD_ID>
    <STRAIN_SYMBOL>FHH/EurMcwiCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2311072</CITATION_ID>
    <DESCRIPTION>An outbred stock of fawn hooded rats was introduced into Europe by Tschopp in the early 1970s. Maintained as an outbred stock until the mid-1980s, when brother x sister mating was initiated by A.P. Provoost to produce two strains designated FHH (also known as FHR) and FHL, which differ in expression of hypertension and proteinuria. The colony was transferred to Erasmus University in Rotterdam, The Netherlands, then to the Medical College of Wisconsin in the 1990s. To Charles River in 2001.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2311073</RGD_ID>
    <STRAIN_SYMBOL>NBL/CrCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2311073</CITATION_ID>
    <DESCRIPTION>Bogden in the mid-1970s from Noble strain rats (brother x sister mated but not descended from a single pair, and therefore not necessarily isogenic). To National Cancer Institute Animal Production Program (Cr) in 1978. To Charles River in 1998.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2311074</RGD_ID>
    <STRAIN_SYMBOL>BDIX/CrCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2311074</CITATION_ID>
    <DESCRIPTION>Druckrey from a cross between BDI and BDVIII with subsequent selection of brother-sister pairs for agouti coat color and dark, pigmented eyes. To Charles River in 1998 from the National Cancer Institute Animal Production Program (Cr).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2311078</RGD_ID>
    <STRAIN_SYMBOL>Crl:CD-&lt;i&gt;Hr&lt;sup&gt;hr&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>CD hairless rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2311078</CITATION_ID>
    <DESCRIPTION>This spontaneous mutation model was isolated from a Crl:CD(SD) colony in Charles River, Wilmington, MA in the late 1980s. Rederived in 1993 and subsequently transferred to Charles River, Raleigh, NC for barrier room production. The model does not exhibit the typical characteristics of hair growth and loss found in other hairless models. Specific genetic analysis to identify the mutation has not been undertaken. Histopathology has determined the model is euthymic.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2311079</RGD_ID>
    <STRAIN_SYMBOL>WF/CrCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2311079</CITATION_ID>
    <DESCRIPTION>J. Furth in 1945 from a commercial Wistar stock in an attempt to develop a rat strain with a high incidence of leukemia. To Charles River in 1998 from the National Cancer Institute Animal Production Program (Cr).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2311082</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 13&lt;sup&gt;BN&lt;/sup&gt;/McwiCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2311082</CITATION_ID>
    <DESCRIPTION>Developed at the Medical College of Wisconsin. To Charles River in 2003.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2311692</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Myo1d&lt;sup&gt;Tn(sb-T2/Bart3)2.334Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=478&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Myo1d&lt;sup&gt;Tn(sb-T2/Bart3)2.334Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2311691</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="65986900" STOP_POS="66263538" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="65489153" STOP_POS="65765812" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="67866939" STOP_POS="68142864" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="67520649" STOP_POS="67811744" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="68720729" STOP_POS="68997721" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00478</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 18th intron of the Myo1d gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2311693</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Tmem22&lt;sup&gt;Tn(sb-T2/Bart3)2.332Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tmem22&lt;sup&gt;Tn(sb-T2/Bart3)2.332Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2311689</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="109964589" STOP_POS="109992347" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="101085579" STOP_POS="101113339" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="108854134" STOP_POS="108881519" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="108269643" STOP_POS="108297339" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="105416072" STOP_POS="105443969" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2311693</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Tmem22 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2311694</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Fam227a&lt;sup&gt;Tn(sb-T2/Bart3)2.333Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=484&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fam227a&lt;sup&gt;Tn(sb-T2/Bart3)2.333Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2311687</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="113054751" STOP_POS="113096898" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="111174362" STOP_POS="111216513" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="120846166" STOP_POS="120891738" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="120839737" STOP_POS="120881869" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="117441099" STOP_POS="117469873" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00484</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the Fam227a gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312352</RGD_ID>
    <STRAIN_SYMBOL>LEW.1N</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentralinstitut fur Versuchstierzucht, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312352</CITATION_ID>
    <DESCRIPTION>These congenic rats carry the RTl&lt;sup&gt;n&lt;/sup&gt; haplotype on the LEW strain genetic background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312447</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Pmp22)Kan</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max Planck Institute for Experimental Medicine, Gottingen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pmp22</ALLELES>
    <ALLELE_RGD_IDS>11125</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312447</CITATION_ID>
    <DESCRIPTION>This transgenic strain was derived by pronuclear microinjection of fertilized SD rats with a 43 kb fragment containing Pmp22 gene which was isolated from mouse SV129 cosmid library</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312466</RGD_ID>
    <STRAIN_SYMBOL>Crl:LIS</STRAIN_SYMBOL>
    <FULL_NAME>Lister Hooded Rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312466</CITATION_ID>
    <DESCRIPTION>These rats have taken their names from the Lister Institute, where the stocks first originated. From Glaxo to Charles River UK in 1990 and again in 1996. To Charles River Geramny in 2007. Noted for its docility and good breeding performance.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312471</RGD_ID>
    <STRAIN_SYMBOL>Crl:ZUC(Orl)-&lt;i&gt;Lepr&lt;/i&gt;&lt;sup&gt;fa&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13432153</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312471</CITATION_ID>
    <DESCRIPTION>The spontaneous mutation "obese" (Fatty) was found in the 13M rat stock of Sherman and Merck, by Doctor Lois Zucker, Harriet Bird Memorial Laboratory, Stow, Massachusetts 01775, USA, in 1961. The strain was introduced in Orleans at CSEAL, France in 1970; then transferred to Charles River France in 1991.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312472</RGD_ID>
    <STRAIN_SYMBOL>Crl:WI(WU)</STRAIN_SYMBOL>
    <FULL_NAME>Wistar Wu Rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312472</CITATION_ID>
    <DESCRIPTION>Selection by H.H. Donalson at the Wistar-Institute, USA, at the begining of 19th century. To Glaxo-lab. in 1927, continued as inbred. To Nederlands-Institute voor Volksfoending in 1993, to Unilever, Vlaardingen in 1941 and Institut Centraale Proefdierenbedrijf TNO in 1958. Caesarean rederived in 1963. As an outbred to SAVO, Kiblegg in 1975. Caesarean rederived at Charles River in 1987.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312473</RGD_ID>
    <STRAIN_SYMBOL>BDIX/OrlCrl</STRAIN_SYMBOL>
    <FULL_NAME>BDIX Rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312473</CITATION_ID>
    <DESCRIPTION>Rats selected in 1937 by H. Druckrey in Berlin from a strain of yellow coated, pink-eyed rats. It is part of a series of BD I to X strains produced at Max Planck Institute, Freiburg and was introduced to France in 1971 to the INSERM unit, Immunology Laboratory, Dijon where it was maintained in strict brother-sister inbreeding. Developed and studied by Dr. Ms. Martin, CNRS/CSEAL, Orleans who obtained it from Dijon in 1983. To Charles River France in 1991.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312474</RGD_ID>
    <STRAIN_SYMBOL>Crl:OFA(SD)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312474</CITATION_ID>
    <DESCRIPTION>The original strain was composed in 1925 by Robert Worthington Dawley. Carworth Farms obtained it in 1955 and renamed it CFE (Carworth Farms Elias). Transferred to Charles River France in 1967, it then became known as OFA (Oncins France Strain A), in 1968.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312498</RGD_ID>
    <STRAIN_SYMBOL>WAG/RijCrl</STRAIN_SYMBOL>
    <FULL_NAME>WAG Rats</FULL_NAME>
    <ORIGINATION>&lt;a href=https://www.criver.com/products-services/find-model/wag-rat?region=3611&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/wag-rat?region=3611&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312498</CITATION_ID>
    <DESCRIPTION>A.L. Bacharach, Glaxo Labs., U.K., 1924, from a Wistar stock. To Harrington in 1964 at F83. To MBL-TNO in 1953, after that to REP Institutes TNO, Rijswijk. To Charles River Germany from REP Institutes TNO in 1993.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312499</RGD_ID>
    <STRAIN_SYMBOL>Crl:NIH-&lt;i&gt;Foxn1&lt;/i&gt;&lt;sup&gt;rnu&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Nude Rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312499</CITATION_ID>
    <DESCRIPTION>The NIH nude rat was developed in 1979/80 through a series of matings involving 8 inbred rat strains. To Charles River USA from the NIH Animal Genetic Resources. Caesarian derived in 2001. This athymic model shows depleted cell populations in thymus-dependent areas of peripheral lymphoid organs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312504</RGD_ID>
    <STRAIN_SYMBOL>Crlj:WI</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312504</CITATION_ID>
    <DESCRIPTION>Wistar Institute to Scientific Products Farm, Ltd to CRLUS(1975) to CRLJ(1981)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312511</RGD_ID>
    <STRAIN_SYMBOL>WF/IcoCrl</STRAIN_SYMBOL>
    <FULL_NAME>Wistar Rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312511</CITATION_ID>
    <DESCRIPTION>Furth developed this strain at Roswell Park Memorial Institute, Buffalo, NY, USA in 1945 starting from a commercial colony of Wistar rats. Acquired by Charles River from the MIcrobiological Associates, Bethesda, Maryland, USA. Introduced to Charles River France in 1970.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312512</RGD_ID>
    <STRAIN_SYMBOL>ZSF1-&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt;, &lt;i&gt;Lepr&lt;sup&gt;cp&lt;/sup&gt;&lt;/i&gt;/Crl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Genetic Models International, Indianapolis.</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/zsf1-rat?region=3611&gt;Charles River Laboratories &lt;/a&gt;, &lt;a href=https://www.criver.com/products-services/find-model/zsf1-rat-lean?region=3611&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>hybrid</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312512</CITATION_ID>
    <DESCRIPTION>This F1 model was developed by crossing rat strains with two separate leptin receptor mutations (fa and cp), the lean female ZDF rat (+/fa) and the lean male SHHF rat (+/facp) ( RGD:401901201). Offspringcarring both mutations (fa:facp) are obese and develop insulin resistance, hyperglycaemia, and mild hypertension (ZSF1 obese). The heterozygous or wild type offspring (ZSF1 lean) are lean and exhibit no signs of obesity and diabetes. This model was developed at Genetic Models International, Indianapolis. To Charles River in 2001. The progeny that are heterozygous for leptin receptor or wild type are lean and are used as control for the obese counter part.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312513</RGD_ID>
    <STRAIN_SYMBOL>Crlj:DON</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312513</CITATION_ID>
    <DESCRIPTION>Dr. Sato(1952) to Nippon Rat to CRLJ(1990)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312514</RGD_ID>
    <STRAIN_SYMBOL>Crlj:LEC</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312514</CITATION_ID>
    <DESCRIPTION>Hokkaido Univ.(1975) to Otsuka Pharma. (1988) to CRLJ (1991).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312518</RGD_ID>
    <STRAIN_SYMBOL>Crlj:ZUC-&lt;i&gt;Lepr&lt;/i&gt;&lt;sup&gt;fa&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13432153</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312518</CITATION_ID>
    <DESCRIPTION>Zucker(1961) to Roche to CRLUS(1985) to CRLJ(2000)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312577</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D18Rat99-D18Rat82&lt;/i&gt;)/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="30809630" STOP_POS="72538878" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="30558524" STOP_POS="70263868" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="32487692" STOP_POS="73016546" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="32165265" STOP_POS="72695235" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="31654683" STOP_POS="73666623" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312577</CITATION_ID>
    <DESCRIPTION>F&lt;sub&gt;2&lt;/sub&gt; rats from SHR x SHR.BN-(&lt;i&gt;D18Rat113-D18Rat82&lt;/i&gt;)/Ipcv were genotyped and backcrossed with SHR/OlaIpcv and segment of interest fixed by intercrossing heterozygotes to get homozygosity</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312578</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D18Rat82&lt;/i&gt;)/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="72538710" STOP_POS="72538878" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="70263698" STOP_POS="70263868" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="73016379" STOP_POS="73016546" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="72695068" STOP_POS="72695235" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="73666205" STOP_POS="73666623" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312578</CITATION_ID>
    <DESCRIPTION>F&lt;sub&gt;2&lt;/sub&gt; rats from SHR x SHR.BN-(&lt;i&gt;D18Rat113-D18Rat82&lt;/i&gt;)/Ipcv were genotyped and backcrossed with SHR/OlaIpcv and segment of interest fixed by intercrossing heterozygotes to get homozygosity</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312579</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D18Rat40-D18Rat82&lt;/i&gt;)/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="61600384" STOP_POS="72538878" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="59330409" STOP_POS="70263868" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="61499531" STOP_POS="73016546" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="60695794" STOP_POS="72695235" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="62106066" STOP_POS="73666623" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312579</CITATION_ID>
    <DESCRIPTION>F&lt;sub&gt;2&lt;/sub&gt; rats from SHR x SHR.BN-(&lt;i&gt;D18Rat113-D18Rat82&lt;/i&gt;)/Ipcv were genotyped and backcrossed with SHR/OlaIpcv and segment of interest fixed by intercrossing heterozygotes to get homozygosity</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312580</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D18Rat113-D18Rat82&lt;/i&gt;)/Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="3811902" STOP_POS="72538878" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="70263698" STOP_POS="70263868" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="3719547" STOP_POS="73016546" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="72695068" STOP_POS="72695235" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="73666205" STOP_POS="73666623" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312580</CITATION_ID>
    <DESCRIPTION>SHR/OlaIpcv were crossed with BN/Crl, F&lt;sub&gt;1&lt;/sub&gt; animals were backcrossed with SHR/OlaIpcv and genotyped; heterozygotes with the region of interest were backcrossed with SHR/OlaIpcv and segment of interest fixed by intercrossing heterozygotes</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312609</RGD_ID>
    <STRAIN_SYMBOL>MWF-Chr 8&lt;sup&gt;SHR&lt;/sup&gt;/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Clinical Pharmacology and Toxicology, Charite-Universitatsmedizin Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312609</CITATION_ID>
    <DESCRIPTION>MWF/FubRkb male was crossed with female SHR/FubRkb to get F1 animals which in turn were backcrossed with female MWF/FubRkb and the desired consomic selected by marker assisted backcrossing</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312644</RGD_ID>
    <STRAIN_SYMBOL>DA.WOKW-(&lt;i&gt;D3Mit10-D3Rat189&lt;/i&gt;)/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Laboratory Animal Science, University of Greifswald, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="37796919" STOP_POS="59119581" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="38710365" STOP_POS="38710544" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="39773247" STOP_POS="39773425" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="44863125" STOP_POS="44863303" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="35797577" STOP_POS="35797756" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312644</CITATION_ID>
    <DESCRIPTION>A cross of DA/K and WOKW/K which resulted in a segment of chr 3 from WOKW/K introgressed in DA/K background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312645</RGD_ID>
    <STRAIN_SYMBOL>DA.WOKW-(&lt;i&gt;D16Rat88-D16Wox7&lt;/i&gt;)/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Laboratory Animal Science, University of Greifswald, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="839086" STOP_POS="66195506" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="832236" STOP_POS="59492508" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="1550187" STOP_POS="63210301" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="1534408" STOP_POS="62873174" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="819225" STOP_POS="63306215" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312645</CITATION_ID>
    <DESCRIPTION>A cross of DA/K and WOKW/K which resulted in a segment of chr 16 from WOKW/K introgressed in DA/K background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312646</RGD_ID>
    <STRAIN_SYMBOL>DA.WOKW-(&lt;i&gt;D5Mgh6-D5Mit5&lt;/i&gt;)/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Laboratory Animal Science, University of Greifswald, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="73779642" STOP_POS="73779782" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="68984307" STOP_POS="104251008" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="71154828" STOP_POS="108092802" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="75334610" STOP_POS="112058005" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="71814715" STOP_POS="109163425" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312646</CITATION_ID>
    <DESCRIPTION>A cross of DA/K and WOKW/K which resulted in a segment of chr 5 from WOKW/K introgressed in DA/K background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312647</RGD_ID>
    <STRAIN_SYMBOL>DA.WOKW-(&lt;i&gt;D3Mgh5-D3Rat1&lt;/i&gt;)/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Laboratory Animal Science, University of Greifswald, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="98535255" STOP_POS="168026850" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="103141814" STOP_POS="176418101" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="109733850" STOP_POS="180128021" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="97523869" STOP_POS="170016653" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312647</CITATION_ID>
    <DESCRIPTION>A cross of DA/K and WOKW/K which resulted in a segment of chr 3 from WOKW/K introgressed in DA/K background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312648</RGD_ID>
    <STRAIN_SYMBOL>DA.WOKW-(&lt;i&gt;D10Mgh2-D10Rat4&lt;/i&gt;)/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Laboratory Animal Science, University of Greifswald, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="102134116" STOP_POS="102134272" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="105875105" STOP_POS="105875260" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="105533457" STOP_POS="105533612" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="106422174" STOP_POS="107033716" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312648</CITATION_ID>
    <DESCRIPTION>A cross of DA/K and WOKW/K which resulted in a segment of chr 10 from WOKW/K introgressed in DA/K background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2312733</RGD_ID>
    <STRAIN_SYMBOL>BN-Chr 13&lt;sup&gt;SS&lt;/sup&gt; Chr 18&lt;sup&gt;SS&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2312733</CITATION_ID>
    <DESCRIPTION>A cross of BN and SS strains which results in a BN genomic background with a SS chromosomes 13 and 18 introgressed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313181</RGD_ID>
    <STRAIN_SYMBOL>LEW.1WR1/WorBrm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.biomere.com/type1diabetes.php&gt;Biomedical Research Models, Inc.&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.biomere.com/type1diabetes.php&gt;Biomedical Research Models, Inc.&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313181</CITATION_ID>
    <DESCRIPTION>Obtained from Hanover Institute, Hanover, Germany in 1989; then maintained in a closed colony by sibling mating at Universtiy of Massachusetts, Worcester, MA then moved to Biomedical Research Models, Inc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313209</RGD_ID>
    <STRAIN_SYMBOL>WF.ART2/Wor</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Universtiy of Massachusetts, Worcester, MA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313209</CITATION_ID>
    <DESCRIPTION>developed at the Universtiy of Massachusetts, Medical School</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313221</RGD_ID>
    <STRAIN_SYMBOL>SHHF-&lt;i&gt;Lepr&lt;sup&gt;cp&lt;/i&gt;&lt;/sup&gt;/Crl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;cp&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11570565</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313221</CITATION_ID>
    <DESCRIPTION>Developed by bx SHROB to SHR/N. 1983 from JE Miller, Searle, to McCune after 7th bx, she continued to inbreed to fix congestive heart failure trait. To GMI in 1994, to CR in 2001.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313222</RGD_ID>
    <STRAIN_SYMBOL>BN/HsdMcwiCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313222</CITATION_ID>
    <DESCRIPTION>BN/NHsdMcwi colony directly from Medical College of Wisconsin by brother-sister mating then to Charles River</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313231</RGD_ID>
    <STRAIN_SYMBOL>LEWBNF1/Crl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>hybrid</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313231</CITATION_ID>
    <DESCRIPTION>This hybrid rat is a cross between a LEW female and a BN male rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313232</RGD_ID>
    <STRAIN_SYMBOL>WFF344F1/Crl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>hybrid</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313232</CITATION_ID>
    <DESCRIPTION>This hybrid rat is a cross between a WF female and a F344 male rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313342</RGD_ID>
    <STRAIN_SYMBOL>BN-Chr 17&lt;sup&gt;LH&lt;/sup&gt;/Mav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratoire de Physiologie, Lyon Cedex , France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313342</CITATION_ID>
    <DESCRIPTION>Chr 17 from LH/Mav was introgressed onto the genetic background of BN/NHsdMcwi and then genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313343</RGD_ID>
    <STRAIN_SYMBOL>LH-Chr 13&lt;sup&gt;BN&lt;/sup&gt;/Mav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratoire de Physiologie, Lyon Cedex , France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313343</CITATION_ID>
    <DESCRIPTION>Chr 13 from BN/NHsdMcwi was introgressed onto the genetic background of LH/Mav and then genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313384</RGD_ID>
    <STRAIN_SYMBOL>Wild/Nov</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cytology and Genetics, Siberian Branch of the Academy of Sciences, Novosibirsk, Russia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>wild</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313384</CITATION_ID>
    <DESCRIPTION>These are wild-caught rats selected on the basis of level of tameness and defensive aggression at every generation since 1972 at Institute of Cytology and Genetics, Siberian Branch of the Academy of Sciences, Novosibirsk, Russia</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313463</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ppfia2&lt;sup&gt;Tn(sb-T2/Bart3)2.339Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=474&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ppfia2&lt;sup&gt;Tn(sb-T2/Bart3)2.339Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2313459</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="43652258" STOP_POS="44126555" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="41765716" STOP_POS="42240104" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="48548932" STOP_POS="49045852" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="48563521" STOP_POS="49058116" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="45140154" STOP_POS="45616620" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00474</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 5th intron of the Ppfia2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313464</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Large&lt;sup&gt;Tn(sb-T2/Bart3)2.336Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Large&lt;sup&gt;Tn(sb-T2/Bart3)2.336Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2313460</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="11609004" STOP_POS="12057174" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="11603129" STOP_POS="12048930" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="12481563" STOP_POS="12945320" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="23595328" STOP_POS="24054765" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="12043818" STOP_POS="12497663" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313464</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 6th intron of the Large gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313465</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Pld5&lt;sup&gt;Tn(sb-T2/Bart3)2.340Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=483&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pld5&lt;sup&gt;Tn(sb-T2/Bart3)2.340Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2313462</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="90426689" STOP_POS="90765072" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="87895694" STOP_POS="88232868" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="94025696" STOP_POS="94355219" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="98486317" STOP_POS="98812030" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="91715000" STOP_POS="92058036" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00483</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Pld5 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313466</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Agbl4&lt;sup&gt;Tn(sb-T2/Bart3)2.337Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=473&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Agbl4&lt;sup&gt;Tn(sb-T2/Bart3)2.337Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2313461</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="130483551" STOP_POS="131762906" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="125254963" STOP_POS="126534367" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="130742297" STOP_POS="131656581" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="134582789" STOP_POS="135484937" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00473</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 6th intron of the Agbl4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313588</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Ins2-IAPP)Soel</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Pfizer, Inc, Groton, Connecticut</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313588</CITATION_ID>
    <DESCRIPTION>Crl:SD rats were microinjected with cDNA encompassing the human IAPP was fused with rat insulin II promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313693</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(PEPCK-SREBF1)2Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>SREBF1</ALLELES>
    <ALLELE_RGD_IDS>69473</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313693</CITATION_ID>
    <DESCRIPTION>SHR/OlaIpcv zygotes were microinjected with a construct containing rat PEPCK promoter fused to truncated human cDNA encoding SREBF1 (SREBP-1a isoform) and human growth hormone poly-A signal</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313734</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(H1/tetO-RNAi:Insr)29Bdr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313734</CITATION_ID>
    <DESCRIPTION>Fertilized eggs of NTac:SD were microinjected with a construct containing shRNA cassette containing the insulin receptor under the control of H1 promoter with a tetO site and a cassette driving tetR from CAGGS promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313735</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(H1/tetO-RNAi:Insr)14Bdr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313735</CITATION_ID>
    <DESCRIPTION>Fertilized eggs of NTac:SD were microinjected with a construct containing shRNA cassette containing the insulin receptor under the control of H1 promoter with a tetO site and a cassette driving tetR from CAGGS promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313922</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(Cyp1a1-Ren2)10.LEW-(&lt;i&gt;D10Rat142-D10Rat15&lt;/i&gt;)/Jmul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Molecular Physiology Lab, CVS, QMRI, University of Edinburgh, Edinburgh, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="88207600" STOP_POS="92238497" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="91345679" STOP_POS="95508221" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="91113514" STOP_POS="95243104" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="92448353" STOP_POS="96667338" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313922</CITATION_ID>
    <DESCRIPTION>F344-Tg(Cyp1a1-Ren2)10Jmul (also named Ren2.F) males (carrying the transgene Ren2 on chr Y) and Lewis females were bred to produce F1 rats.F1 males were backcrossed to  F344 females to produce BC-F344. After 12 backcross nerations, males and females heterozygous for F344/Lew in the reduced MOD QTLregion were brother-sister mated to generate aimals that were homozygous Lew/Lew for the MOD QTL region but homozygous F344/F344 for the rest of the genome.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313923</RGD_ID>
    <STRAIN_SYMBOL>LEW-Chr YF344-Tg(Cyp1a1-Ren2)10.F344-(&lt;i&gt;D10Rat99-D10Rat11&lt;/i&gt;)/Jmul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Molecular Physiology Lab, CVS, QMRI, University of Edinburgh, Edinburgh, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="96620293" STOP_POS="96620484" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="85269536" STOP_POS="96121100" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="88250522" STOP_POS="99492409" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="88043769" STOP_POS="99184250" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="89278229" STOP_POS="100633982" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313923</CITATION_ID>
    <DESCRIPTION>F344-Tg(Cyp1a1-Ren2)10Jmul (also named Ren2.F) males (carrying the transgene Ren2 on chr Y) and Lewis females were bred to produce F1 rats.F1 males were backcrossed to  Lew females to produce BC-Lew. After 12 backcross generations, males and females heterozygous for F344/Lew in the  MOD QTLregion were brother-sister mated to generate aimals that were homozygous F344/F344 for the MOD QTL region but homozygous LEW/LEW for the rest of the genome.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2313924</RGD_ID>
    <STRAIN_SYMBOL>LEW-Chr YF344-Tg(Cyp1a1-Ren2)10/Jmul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Molecular Physiology Lab, CVS, QMRI, University of Edinburgh, Edinburgh, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2313924</CITATION_ID>
    <DESCRIPTION>F344-Tg(Cyp1a1-Ren2)10Jmul males (carrying the transgene Ren2 on chr Y) were backcrossed with LEW females to generate this consomic strain, confirmed by microsatellite markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314001</RGD_ID>
    <STRAIN_SYMBOL>N:HS</STRAIN_SYMBOL>
    <FULL_NAME>Heterogeneous stock</FULL_NAME>
    <ORIGINATION>Dept. of Psychiatry &amp; Forensic Medicine, School of Medicine, Autonomous University of Barcelona, Barcelona, Spain</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314001</CITATION_ID>
    <DESCRIPTION>Originated from a colony established in 1980 at NIH, animals were bred for 50 generations in a rotational outbreeding regime comprising of 8 inbred progenitors: BN/SsN, MR/N, BUF/N, M520/N, WN/N, ACI/N, WKY/N and F344/N; then to Dr. Eva Redei, Northwestern University (Chicago); 40 breeding pairs were sent from Northwestern University (Chicago) to Barcelona and 25 pairs to Dr. Solberg Woods, Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314009</RGD_ID>
    <STRAIN_SYMBOL>NMcwi:HS</STRAIN_SYMBOL>
    <FULL_NAME>Heterogeneous stock</FULL_NAME>
    <ORIGINATION>Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314009</CITATION_ID>
    <DESCRIPTION>25 breeding pairs were obtained from Dr. Eva Redei, Northwestern University (Chicago) at 55 breeding generations to  Dr. Solberg Woods, Medical College of Wisconsin ; these animals exhibit 30% genome-wide heterozygosity which is maintained by using a rotational breeding strategy were two parameters are used: The first is the number of cages used for breeding and the second is the spacing between each cage (containing a female for mating) and the cage to which it is mated (containing a male for mating). This spacing is called the rotational delay. A rotational delay of 1 is used, in which a female from cage 1 mates with a male from cage 2, a male from cage 2 mates with a female from cage 3, etc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314027</RGD_ID>
    <STRAIN_SYMBOL>SDT.Cg-&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt;/Jtt</STRAIN_SYMBOL>
    <FULL_NAME>SDT fatty</FULL_NAME>
    <ORIGINATION>Japan Tobacco Inc., Central Pharmaceutical Research Institute, Kanagawa, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314027</CITATION_ID>
    <DESCRIPTION>&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt; allele from ZDF was introgressed into SDT rats using the speed congenic method</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314161</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Kuru1&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Kuru1</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=720&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=720&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314161</CITATION_ID>
    <DESCRIPTION>A mutant rat showing circling phenotype was found in the G1 rats produced by ENU mutagenesis (phenotype-driven).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314162</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Oune&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Oune</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=718&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=718&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tbx6</ALLELES>
    <ALLELE_RGD_IDS>1307716</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314162</CITATION_ID>
    <DESCRIPTION>A mutant rat showing abnormal tail was found in the G1 rats produced by ENU mutagenesis (phenotype-driven).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314163</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Kcna1&lt;sup&gt;Adms&lt;/sup&gt;&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>ADMS (autosomal dominant myokymia and seizures) rat</FULL_NAME>
    <ORIGINATION>The University of Tokyo, The Institute of Medical Science</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=724&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-05-04)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcna1&lt;sup&gt;Adms&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12880383</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="161156316" STOP_POS="161156316" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="159470166" STOP_POS="159470166" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="159191568" STOP_POS="159191568" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="226188851" STOP_POS="226190596" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="163011777" STOP_POS="163013522" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314163</CITATION_ID>
    <DESCRIPTION>This strain was established by phenotype-driven ENU mutagenesis. A Kcna1 S309T mutation was identified in this model.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314164</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Kuru2&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Kuru2</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=721&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=721&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314164</CITATION_ID>
    <DESCRIPTION>A mutant rat showing circling phenotype was found in the G1 rats produced by ENU mutagenesis (phenotype-driven).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314165</RGD_ID>
    <STRAIN_SYMBOL>ACI-&lt;i&gt;Chib&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Chibi</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=717&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=717&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Dermatology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314165</CITATION_ID>
    <DESCRIPTION>This strain was established by phenotype-driven ENU mutagenesis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314166</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Tbr2&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Tsubura2</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=723&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=723&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314166</CITATION_ID>
    <DESCRIPTION>A mutant rat showing abnormal eyes was found in the G1 rats produced by ENU mutagenesis (phenotype-driven).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314167</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Kmch&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Komachi</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=719&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=719&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314167</CITATION_ID>
    <DESCRIPTION>This strain was established by phenotype-driven ENU mutagenesis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314168</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Tbr1&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Tsubura1</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=722&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=722&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314168</CITATION_ID>
    <DESCRIPTION>A mutant rat showing abnormal eyes was found in the G1 rats produced by ENU mutagenesis (phenotype-driven).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314169</RGD_ID>
    <STRAIN_SYMBOL>WTC.F344-&lt;i&gt;Scn1a&lt;sup&gt;m1Kyo&lt;/sup&gt;&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=754&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=754&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2024-04-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Scn1a&lt;sup&gt;m1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12792283</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314169</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by backcrossing F344-&lt;i&gt;Scn1a&lt;sup&gt;m1Kyo&lt;/sup&gt;&lt;/i&gt; onto WTC/Kyo.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314170</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Egr&lt;sup&gt;m1Kyo&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>EGR (Excessive Grooming Rat), Kaikai, Kyo1897</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=725&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=725&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314170</CITATION_ID>
    <DESCRIPTION>This strain was established by phenotype-driven ENU mutagenesis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314224</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D1Rat166-D1Rat90&lt;/i&gt;)/2Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=910&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=910&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="258334277" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="248393012" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="269279863" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="276721459" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="255026793" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314224</CITATION_ID>
    <DESCRIPTION>Congenic strain originated from backcrossing parental F344/Crlj and OLETF/Otk animals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314225</RGD_ID>
    <STRAIN_SYMBOL>F344-Chr 15&lt;sup&gt;OLETF&lt;/sup&gt;/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=914&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=914&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314225</CITATION_ID>
    <DESCRIPTION>Developed by the depositor</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314226</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(WSCD2)3Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=881&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=881&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>WSCD2</ALLELES>
    <ALLELE_RGD_IDS>1605710</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314226</CITATION_ID>
    <DESCRIPTION>A transgenic construct consisting of the human WSC domain containing 2 (WSCD2, also known as KIAA0789) within pEF6/Myc-HisA (downstream of the EF-1a promoter and upstream of the bovine growth hormone polyA signal) was injected into Wistar rat (Crlj:WI) embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314227</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(WSCD2)4Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=882&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=882&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>WSCD2</ALLELES>
    <ALLELE_RGD_IDS>1605710</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314227</CITATION_ID>
    <DESCRIPTION>A transgenic construct consisting of the human WSC domain containing 2 (WSCD2, also known as KIAA0789) within pEF6/Myc-HisA (downstream of the EF-1a promoter and upstream of the bovine growth hormone polyA signal) was injected into Wistar rat (Crlj:WI) embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314228</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(WSCD2)5Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=883&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=883&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>WSCD2</ALLELES>
    <ALLELE_RGD_IDS>1605710</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314228</CITATION_ID>
    <DESCRIPTION>A transgenic construct consisting of the human WSC domain containing 2 (WSCD2, also known as KIAA0789) within pEF6/Myc-HisA (downstream of the EF-1a promoter and upstream of the bovine growth hormone polyA signal) was injected into Wistar rat (Crlj:WI) embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314229</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D7Uwm22-D7Mgh20&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=916&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=916&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="118716298" STOP_POS="118716434" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="116836447" STOP_POS="116836583" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="126622888" STOP_POS="126623023" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="126334525" STOP_POS="126334660" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="123733466" STOP_POS="123733601" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314229</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314230</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Hr&lt;sup&gt;krh&lt;/i&gt;&lt;/sup&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Hairless Kyoto, Hanako</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=757&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=757&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Dermatology; Urology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314230</CITATION_ID>
    <DESCRIPTION>A mutant rat showing abnormal skin phenotype was found in the G1 rats produced by ENU mutagenesis (phenotype-driven).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314231</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D5Mgh5-D5Mgh23&lt;/i&gt;)/2Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=911&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=911&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="48523123" STOP_POS="115013661" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="43726656" STOP_POS="109897936" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="44404276" STOP_POS="114014945" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="49028773" STOP_POS="117961491" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="45499364" STOP_POS="115361927" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314231</CITATION_ID>
    <DESCRIPTION>Male OLETF was crossed with female F344. F1 were backcrossed to female F344 for 5 generations. Microsatellite-based genotyping was performed to select the best male that had the best OLETF donor genome. Once the region was fixed the resultant congenic strain was maintained by brother-sister mating.37.4 cM segment of the OLETF genome was transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314232</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(WSCD2)1Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=880&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=880&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>WSCD2</ALLELES>
    <ALLELE_RGD_IDS>1605710</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314232</CITATION_ID>
    <DESCRIPTION>A transgenic construct consisting of the human WSC domain containing 2 (WSCD2, also known as KIAA0789) within pEF6/Myc-HisA (downstream of the EF-1a promoter and upstream of the bovine growth hormone polyA signal) was injected into Wistar rat (Crlj:WI) embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314243</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D1Mgh2-D1Wox10&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=907&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=907&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="223964326" STOP_POS="223964440" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="22340647" STOP_POS="214537671" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="23406428" STOP_POS="236763528" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="24875821" STOP_POS="244066407" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="22842898" STOP_POS="220639653" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314243</CITATION_ID>
    <DESCRIPTION>Developed by the depositor</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314244</RGD_ID>
    <STRAIN_SYMBOL>BCR/Nn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=887&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=887&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314244</CITATION_ID>
    <DESCRIPTION>In the course of producing transgenic rats (DRPLA promoter + huntingtin exon1+EGFP on a Slc:SD background), a mutant rat showing involuntary movements (circling) and symptoms of dystonia was found in F6 progeny. Subsequent by the selection of the involuntary movement segregated the transgene from the phenotype. Thereafter this strain was maintained by only the phenotype (not the transgene).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314245</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(WSCD2)6Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=884&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=884&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>WSCD2</ALLELES>
    <ALLELE_RGD_IDS>1605710</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314245</CITATION_ID>
    <DESCRIPTION>A transgenic construct consisting of the human WSC domain containing 2 (WSCD2, also known as KIAA0789) within pEF6/Myc-HisA (downstream of the EF-1a promoter and upstream of the bovine growth hormone polyA signal) was injected into Wistar rat (Crlj:WI) embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314246</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Rat117-D1Rat90&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=906&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=906&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="269633753" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="213533809" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="233490105" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="240604381" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="219629755" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314246</CITATION_ID>
    <DESCRIPTION>Developed by the Depositor</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314247</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(Prl-EGFP)Yamp</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=904&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=904&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Metabolism; Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314247</CITATION_ID>
    <DESCRIPTION>A transgenic construct was designed with the rat prolactin promoter (-3221 - 3233) controlling EGFP. Transgenic rats originated from Crlj:WI (Wistar) rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314313</RGD_ID>
    <STRAIN_SYMBOL>NER.F344-(&lt;i&gt;D5Rat100-D5Rat234&lt;/i&gt;)/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=893&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=893&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="70969494" STOP_POS="127005370" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="66174080" STOP_POS="66174226" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="65696672" STOP_POS="65696815" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="70180341" STOP_POS="70180484" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="68843563" STOP_POS="68843964" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314313</CITATION_ID>
    <DESCRIPTION>The Ner3 region (D5Rat100-D5Rat234) was introgressed from F344/NSlc onto NER/Kyo by backcross breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314314</RGD_ID>
    <STRAIN_SYMBOL>NER.F344-(&lt;i&gt;D1Mgh6-D1Rat132&lt;/i&gt;)/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=892&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=892&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="96927100" STOP_POS="171890060" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="87790149" STOP_POS="162457491" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="91394009" STOP_POS="172789257" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="92524380" STOP_POS="179788206" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="87656636" STOP_POS="165996388" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314314</CITATION_ID>
    <DESCRIPTION>The Ner1 region (D1Mgh6-D1Rat132) was introgressed from F344/NSlc onto NER/Kyo by backcross breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314315</RGD_ID>
    <STRAIN_SYMBOL>F344.NER-(&lt;i&gt;D5Mgh4-D5Rat36&lt;/i&gt;)/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=891&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=891&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="38207390" STOP_POS="143398338" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="138113556" STOP_POS="138113774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="143846157" STOP_POS="143846372" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="147610023" STOP_POS="147610238" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="145186817" STOP_POS="145187034" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314315</CITATION_ID>
    <DESCRIPTION>The Ner3 region (D5Mgh4-D5Rat36) was introgressed from NER/Kyo onto F344/NSlc by backcross breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314316</RGD_ID>
    <STRAIN_SYMBOL>F344.NER-(&lt;i&gt;D1Mgh6-D1Rat73&lt;/i&gt;)/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=890&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=890&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="96927100" STOP_POS="228174736" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="87790149" STOP_POS="218748178" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="91394009" STOP_POS="238824901" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="92524380" STOP_POS="246113473" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="87656636" STOP_POS="224420760" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314316</CITATION_ID>
    <DESCRIPTION>The Ner1 region (D1Mgh6-D1Rat73) was introgressed from NER/Kyo onto F344/NSlc by backcross breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314317</RGD_ID>
    <STRAIN_SYMBOL>WTC.GRY-&lt;i&gt;Cacna1a&lt;sup&gt;gry&lt;/sup&gt;&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=894&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=894&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-05-04)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Cacna1a|Cacna1a&lt;sup&gt;gry&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2244|12880382</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314317</CITATION_ID>
    <DESCRIPTION>Developed by the depositor</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314339</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Patj&lt;sup&gt;Tn(sb-T2/Bart3)2.343Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=480&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Patj&lt;sup&gt;Tn(sb-T2/Bart3)2.343Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2314335</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="118177557" STOP_POS="118480301" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="113061985" STOP_POS="113364807" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="117038548" STOP_POS="117340308" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="120981525" STOP_POS="121281044" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="118806744" STOP_POS="119131114" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00480</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 15th intron of the Inadl gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314340</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Acoxl&lt;sup&gt;Tn(sb-T2/Bart3)2.342Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Acoxl&lt;sup&gt;Tn(sb-T2/Bart3)2.342Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2314337</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="135514340" STOP_POS="135820291" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="115061069" STOP_POS="115367032" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="120414311" STOP_POS="120724809" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="126606586" STOP_POS="126919666" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="115365279" STOP_POS="115687566" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314340</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 10th intron of the Acoxl gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314341</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Auts2&lt;sup&gt;Tn(sb-T2/Bart3)2.344Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Auts2&lt;sup&gt;Tn(sb-T2/Bart3)2.344Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2314338</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="24104187" STOP_POS="25194123" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="25518248" STOP_POS="25541023" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314341</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 14th intron of the Auts2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314342</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Palld&lt;sup&gt;Tn(sb-T2/Bart3)2.341Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Palld&lt;sup&gt;Tn(sb-T2/Bart3)2.341Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2314336</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="32985252" STOP_POS="33154619" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="27981315" STOP_POS="28143129" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="31349140" STOP_POS="31390340" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="31198863" STOP_POS="31240064" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="31144028" STOP_POS="31144544" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314342</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169). This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 19th intron of the Palld gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314360</RGD_ID>
    <STRAIN_SYMBOL>ACI.F344-(&lt;i&gt;D16Mit5-D16Nkg27&lt;/i&gt;)/Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=871&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=871&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="16278184" STOP_POS="16278352" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314360</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by backcrossing ACI.F344-(&lt;i&gt;D16Rat12-D16Mco2&lt;/i&gt;)Nkg onto ACI/NJcl, followed by intercrossing in N6 generation, thereafter maintained by crossing homozygous individuals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314361</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Slc32a1-YFP*)1Yyan</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=905&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=905&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314361</CITATION_ID>
    <DESCRIPTION>This transgenic rat was established at National Institute for Physiological Sciences in 2004, thereafter introduced to Gunma University in 2006.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314362</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Hrdk&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Hairless dominant Kyoto</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=899&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=899&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314362</CITATION_ID>
    <DESCRIPTION>Hairless mutation was found in the G1 rats that established by ENU mutagenesis (phenotype driven).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314363</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Slc32a1-YFP*)2Yyan</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=908&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=908&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314363</CITATION_ID>
    <DESCRIPTION>This transgenic rat was established at National Institute for Physiological Sciences in 2004, thereafter introduced to Gunma University in 2006.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314364</RGD_ID>
    <STRAIN_SYMBOL>ACI.F344-(&lt;i&gt;D16Nkg112-D16Nkg27&lt;/i&gt;)/Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=902&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=902&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314364</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by backcrossing ACI.F344-(&lt;i&gt;D16Nkg9-D16Nkg27&lt;/i&gt;)Nkg onto ACI/NJcl, followed by intercrossing in N3 generation, thereafter maintained by crossing homozygous individuals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314365</RGD_ID>
    <STRAIN_SYMBOL>KFRS2/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=901&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=901&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology; Dermatology</RESEARCH_USE>
    <ALLELES>Tyr|Tyr&lt;sup&gt;siaKyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>1589755|13207345</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150527687" STOP_POS="150622857" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="141115036" STOP_POS="141210207" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="151012598" STOP_POS="151106802" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157322968" STOP_POS="157416594" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143641257" STOP_POS="143746315" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314365</CITATION_ID>
    <DESCRIPTION>A male rat "SRR-Do Your Best" was introduced from American fancy rat colony (Spoiled Ratten Rattery: SRR, in Kansas City, Missouri) to Kyoto University on July 13, 2005. Inbreeding started from F1 progeny of male "SRR-Do Your Best" and a female PVG/Seac.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314368</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Kcnn2&lt;sup&gt;Trdk&lt;/sup&gt;&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Tremor dominant Kyoto</FULL_NAME>
    <ORIGINATION>The University of Tokyo, The Institute of Medical Science</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=898&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-07-15)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Kcnn2&lt;sup&gt;Trdk&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>149735330</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="40338434" STOP_POS="40338434" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="38151735" STOP_POS="38151735" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="39372884" STOP_POS="39372884" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="38822146" STOP_POS="38864110" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="39560962" STOP_POS="39705037" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314368</CITATION_ID>
    <DESCRIPTION>Tremor dominant Kyoto (Trdk) mutation is an autosomal dominant mutation that appeared in 2008 in a stock of F344/NSlc rats that had been mutagenized with N-ethyl-N-nitrosourea (ENU) (Mashimo et al., 2008). Rats heterozygous for Trdk (Trdk/+) exhibited tremor behavior that was evident around weaning. To remove latent ENU-induced mutations, the laboratory established an F344-Trdk/+ congenic strain by nine rounds of backcrossing. Using positional candidate approach,  Trdk mutation was identified as a missense substitution (c. 866 T &gt; A, p. I289N) in Kcnn2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314375</RGD_ID>
    <STRAIN_SYMBOL>LE.AR-&lt;i&gt;Ednrb&lt;sup&gt;sl&lt;/i&gt;&lt;/sup&gt;/Okkm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=823&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=823&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-03-28)</AVAILABILITY>
    <RESEARCH_USE>Internal Organ</RESEARCH_USE>
    <ALLELES>Ednrb|Ednrb&lt;sup&gt;sl&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2536|10755424</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="87055490" STOP_POS="87086765" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="80670748" STOP_POS="80671048" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="88034987" STOP_POS="88035287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="91500400" STOP_POS="91531979" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="87893141" STOP_POS="87898700" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314375</CITATION_ID>
    <DESCRIPTION>AR rats were found a by Ikadai et al. at Institute for Animal Reproduction in 1973. From 1997, backcross of AR rats onto Long Evans rats has started. After the 9th generation of backcrossing, it has been maintained by sib mating (F10 in May 2008).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314376</RGD_ID>
    <STRAIN_SYMBOL>KFRS4/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=919&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=919&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2021-10-05)</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology; Dermatology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314376</CITATION_ID>
    <DESCRIPTION>A male rat "TSR Louis" was introduced from American fancy rat colony (Spoiled Ratten Rattery: SRR, in Kansas City, Missouri) to Kyoto University on July 13, 2005. Inbreeding started from F1 progeny of male "TSR Louis" and a female PVG/Seac. This strain carries two mutations, head spot (hs) which causes white spotting on the head, and dumbo (dmbo) which causes abnormal ear morphology (Kuramoto, 2010, RGD:7800655). Ears are set lower on the head, and are larger and rounder. Genetic analyses mapped hs to Chr 15 and dmbo to Chr 14.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314377</RGD_ID>
    <STRAIN_SYMBOL>KFRS3B/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=918&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=918&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology; Dermatology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314377</CITATION_ID>
    <DESCRIPTION>A male rat "SRR-Rocket Science" was introduced from American fancy rat colony (Spoiled Ratten Rattery: SRR, in Kansas City, Missouri) to Kyoto University on July 13, 2005. Inbreeding started from F1 progeny of male "SRR-Rocket Science" and a female PVG/Seac. Homozygous rats for grey mutation were selected for inbreeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314378</RGD_ID>
    <STRAIN_SYMBOL>AR-&lt;i&gt;Ednrb&lt;sup&gt;sl&lt;/i&gt;&lt;/sup&gt;/Okkm</STRAIN_SYMBOL>
    <FULL_NAME>Aganglionosis rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=822&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=822&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2016-10-31)</AVAILABILITY>
    <RESEARCH_USE>Internal Organ</RESEARCH_USE>
    <ALLELES>Ednrb|Ednrb&lt;sup&gt;sl&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2536|10755424</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="87055490" STOP_POS="87086765" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="80670748" STOP_POS="80671048" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="88034987" STOP_POS="88035287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="91500400" STOP_POS="91531979" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="87893141" STOP_POS="87898700" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314378</CITATION_ID>
    <DESCRIPTION>Congenital megacolon rats were found in offspring of a female albino rat crossed with a wild male by Ikadai et al. at Institute for Animal Reproduction in 1973 and were named Aganglionosis Rat (AR)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314379</RGD_ID>
    <STRAIN_SYMBOL>KFRS6/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=921&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=921&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE>Dermatology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314379</CITATION_ID>
    <DESCRIPTION>A male rat "SRR Tustin" was introduced from American fancy rat colony (Spoiled Ratten Rattery: SRR, in Kansas City, Missouri) to Kyoto University on July 13, 2005. Inbreeding started from F1 progeny of male "SRR Tustin" and a female TM/Kyo.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314380</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-lacZ)541Htsu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=903&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=903&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314380</CITATION_ID>
    <DESCRIPTION>Developed by the depositor</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314381</RGD_ID>
    <STRAIN_SYMBOL>KFRS5A/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=920&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=920&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Dermatology</RESEARCH_USE>
    <ALLELES>Krt71&lt;sup&gt;Rex&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11570416</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="134758431" STOP_POS="134758437" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="132879723" STOP_POS="132879729" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="143351384" STOP_POS="143351390" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="141143396" STOP_POS="141166531" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314381</CITATION_ID>
    <DESCRIPTION>A male rat "SRR Coming Home" was introduced from American fancy rat colony (Spoiled Ratten Rattery: SRR, in Kansas City, Missouri) to Kyoto University on July 13, 2005. Inbreeding started from F1 progeny of male "SRR Coming Home" and a female TM/Kyo.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314382</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-HRAS*G12V)250Htsu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=790&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=790&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES>HRAS</ALLELES>
    <ALLELE_RGD_IDS>730881</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314382</CITATION_ID>
    <DESCRIPTION>This transgenic strain was established by CLEA Japan, Inc. The construct is as follows: CAG promoter, loxP sequence, neomycin resistance gene, loxP sequence and Ha-ras*G12V (HrasV12). It was injected into Jcl:SD embryos, the transgene is regulated by the Cre/loxP system. Human Ha-ras*G12V oncogene is driven by CAG promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314383</RGD_ID>
    <STRAIN_SYMBOL>KFRS3A/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=917&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=917&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology; Dermatology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314383</CITATION_ID>
    <DESCRIPTION>A male rat "SRR-Rocket Science" was introduced from American fancy rat colony (Spoiled Ratten Rattery: SRR, in Kansas City, Missouri) to Kyoto University on July 13, 2005. Inbreeding started from F1 progeny of male "SRR-Rocket Science" and a female PVG/Seac. Homozygous rats for mink were selected for inbreeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314396</RGD_ID>
    <STRAIN_SYMBOL>LCR/Mco</STRAIN_SYMBOL>
    <FULL_NAME>Low-capacity runners</FULL_NAME>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314396</CITATION_ID>
    <DESCRIPTION>Artificially selected for intrinsic aerobic running capacity from the heterogenous stock (N:HS); these were selected for low capacity based on distance run to exhaustion on a motorized treadmill.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314397</RGD_ID>
    <STRAIN_SYMBOL>HCR/Mco</STRAIN_SYMBOL>
    <FULL_NAME>High-capacity runners</FULL_NAME>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314397</CITATION_ID>
    <DESCRIPTION>Artificially selected for intrinsic aerobic running capacity from the heterogenous stock (N:HS); these were selected for high capacity based on distance run to exhaustion on a motorized treadmill.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314414</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(H1/tetO-RNAi:Insr)87Hrjb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Cellular and Molecular Immunology, University of Gottingen, Gottingen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Insr</ALLELES>
    <ALLELE_RGD_IDS>2917</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314414</CITATION_ID>
    <DESCRIPTION>LEW/Crl rat embryos were microinjected with an lentiviral single vector system comprising of Insr-specific shRNA construct under the control of H1t promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314415</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(H1/tetO-RNAi:Insr)4Hrjb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Cellular and Molecular Immunology, University of Gottingen, Gottingen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Insr</ALLELES>
    <ALLELE_RGD_IDS>2917</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314415</CITATION_ID>
    <DESCRIPTION>LEW/Crl rat embryos were microinjected with an lentiviral single vector system comprising of Insr-specific shRNA construct under the control of H1t promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314477</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;RT1&lt;sup&gt;DA&lt;/i&gt;&lt;/sup&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=391&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=391&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00391</CITATION_ID>
    <DESCRIPTION>Sprague-Dawley RT1&lt;sup&gt;u&lt;/sup&gt; haplotype backcrossed onto Lewis inbred strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314478</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;RT1.B&lt;sup&gt;m1Trg&lt;/i&gt;&lt;/sup&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME>RT1.B</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=392&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=392&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00392</CITATION_ID>
    <DESCRIPTION>ENU induced mutation in a Sprague Dawley rat resulting in a phenotypic change at the RT1.B MHC locus such that antibody binding to the RT1.B locus is no longer present. Animals carrying this mutation fail to have OX-6 antibody binding to the RT1.B locus. The exact nature of the mutation has not been genetically characterized. Mutation was backcrossed onto the Lewis strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314492</RGD_ID>
    <STRAIN_SYMBOL>SBN.SBH-(&lt;i&gt;D1Rat148-D1Rat89&lt;/i&gt;)/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Ben Gurion University Barzilai Medical Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="15760582" STOP_POS="257976495" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="16470664" STOP_POS="279986079" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="18951160" STOP_POS="287349830" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="16325337" STOP_POS="265343617" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314492</CITATION_ID>
    <DESCRIPTION>Segment of interest from chr 1 of SBH/Ygl was introgressed onto the genetic background of SBN/Ygl this was done by crossing male SBN/Ygl with female SBH/Ygl fixing the Y chr to SBN/Ygl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314493</RGD_ID>
    <STRAIN_SYMBOL>SBH.SBN-(&lt;i&gt;D1Mgh2-D1Rat74&lt;/i&gt;)/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Ben Gurion University Barzilai Medical Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="22340647" STOP_POS="221264292" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="23406428" STOP_POS="241482368" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="24875821" STOP_POS="248763894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="22842898" STOP_POS="227005733" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314493</CITATION_ID>
    <DESCRIPTION>Segment of interest from chr 1 of SBN/Ygl was introgressed onto the genetic background of SBH/Ygl this was done by crossing male SBH/Ygl with female SBN/Ygl fixing the Y chr to SBN/Ygl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314494</RGD_ID>
    <STRAIN_SYMBOL>SBH.SBN-(&lt;i&gt;D1Rat137-D1Rat123&lt;/i&gt;)/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Ben Gurion University Barzilai Medical Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="227535119" STOP_POS="227535316" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="90532338" STOP_POS="218108781" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="94225372" STOP_POS="238220385" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="95325941" STOP_POS="245519018" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="90306033" STOP_POS="223729371" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314494</CITATION_ID>
    <DESCRIPTION>Segment of interest from chr 1 of SBN/Ygl was introgressed onto the genetic background of SBH/Ygl this was done by crossing male SBH/Ygl with female SBN/Ygl fixing the Y chr to SBN/Ygl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314495</RGD_ID>
    <STRAIN_SYMBOL>SBN.SBH-(&lt;i&gt;D1Rat27-D1Mit7&lt;/i&gt;)/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Ben Gurion University Barzilai Medical Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="99645382" STOP_POS="99645535" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="90508614" STOP_POS="90508767" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="94201400" STOP_POS="94201552" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="95301716" STOP_POS="262617374" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="90282040" STOP_POS="240980321" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314495</CITATION_ID>
    <DESCRIPTION>Segment of interest from chr 1 of SBH/Ygl was introgressed onto the genetic background of SBN/Ygl this was done by crossing female SBN/Ygl with male SBH/Ygl fixing the Y chr to SBH/Ygl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314496</RGD_ID>
    <STRAIN_SYMBOL>SBH.SBN-(&lt;i&gt;D1Mgh2-D1Mgh11&lt;/i&gt;)/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Ben Gurion University Barzilai Medical Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="22340647" STOP_POS="22340797" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="23406428" STOP_POS="23406577" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="24875821" STOP_POS="24875970" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="22842898" STOP_POS="22843363" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314496</CITATION_ID>
    <DESCRIPTION>Segment of interest from chr 1 of SBN/Ygl was introgressed onto the genetic background of SBH/Ygl this was done by crossing female SBH/Ygl with male SBN/Ygl fixing the Y chr to SBN/Ygl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314497</RGD_ID>
    <STRAIN_SYMBOL>SBN.SBH-(&lt;i&gt;D1Rat101-D1Rat74&lt;/i&gt;)/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Ben Gurion University Barzilai Medical Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="97146283" STOP_POS="221264292" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102658741" STOP_POS="241482368" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103735751" STOP_POS="248763894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="97174943" STOP_POS="227005733" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314497</CITATION_ID>
    <DESCRIPTION>Segment of interest from chr 1 of SBH/Ygl was introgressed onto the genetic background of SBN/Ygl this was done by crossing male SBN/Ygl with female SBH/Ygl fixing the Y chr to SBN/Ygl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314498</RGD_ID>
    <STRAIN_SYMBOL>SBH.SBN-(&lt;i&gt;D1Rat137-D1Rat83&lt;/i&gt;)/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Ben Gurion University Barzilai Medical Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="90532338" STOP_POS="245701099" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="94225372" STOP_POS="266587220" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="95325941" STOP_POS="274017147" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="90306033" STOP_POS="252133935" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314498</CITATION_ID>
    <DESCRIPTION>Segment of interest from chr 1 of SBN/Ygl was introgressed onto the genetic background of SBH/Ygl this was done by crossing female SBH/Ygl with male SBN/Ygl fixing the Y chr to SBN/Ygl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314499</RGD_ID>
    <STRAIN_SYMBOL>SBN.SBH-(&lt;i&gt;D1Mgh17-D1Mgh14&lt;/i&gt;)/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Ben Gurion University Barzilai Medical Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="10426623" STOP_POS="266453731" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="8606496" STOP_POS="256448636" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="8387052" STOP_POS="278228889" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="10007292" STOP_POS="285604895" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="9082836" STOP_POS="263699089" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314499</CITATION_ID>
    <DESCRIPTION>Segment of interest from chr 1 of SBH/Ygl was introgressed onto the genetic background of SBN/Ygl this was done by crossing female SBN/Ygl with male SBH/Ygl fixing the Y chr to SBH/Ygl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314500</RGD_ID>
    <STRAIN_SYMBOL>SBH.SBN-(&lt;i&gt;D1Mgh2-D1Rat101&lt;/i&gt;)/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Ben Gurion University Barzilai Medical Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="22340647" STOP_POS="97146439" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="23406428" STOP_POS="102658898" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="24875821" STOP_POS="103735908" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="22842898" STOP_POS="97175101" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314500</CITATION_ID>
    <DESCRIPTION>Segment of interest from chr 1 of SBN/Ygl was introgressed onto the genetic background of SBH/Ygl this was done by crossing female SBH/Ygl with male SBN/Ygl fixing the Y chr to SBN/Ygl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314501</RGD_ID>
    <STRAIN_SYMBOL>SBH.SBN-(&lt;i&gt;D1Wox11-D1Rat137&lt;/i&gt;)/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Ben Gurion University Barzilai Medical Center, Ashkelon, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="65832929" STOP_POS="90532583" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="64407177" STOP_POS="94225616" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="63399232" STOP_POS="95326185" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="64145811" STOP_POS="90306478" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314501</CITATION_ID>
    <DESCRIPTION>Segment of interest from chr 1 of SBN/Ygl was introgressed onto the genetic background of SBH/Ygl this was done by crossing male SBH/Ygl with female SBN/Ygl fixing the Y chr to SBN/Ygl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314530</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D8Uia1-D8Rat90&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="119450421" STOP_POS="119450610" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="110572032" STOP_POS="110572221" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="118862625" STOP_POS="118862813" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="20954930" STOP_POS="118204000" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="19055857" STOP_POS="114974688" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314530</CITATION_ID>
    <DESCRIPTION>SS/Jr females were bred with SHR/NHsd males and their female F&lt;sub&gt;1&lt;/sub&gt; were backcrossed to SHR/NHsd males; this ensured that the mitochondrial genome came from SS/Jr; further selection was done using microsatellite markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314531</RGD_ID>
    <STRAIN_SYMBOL>SHR.SS-(&lt;i&gt;D13Rat1-D13Mgh6&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="21120177" STOP_POS="99745408" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="20605555" STOP_POS="97213863" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="24501968" STOP_POS="103613733" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="29679984" STOP_POS="108279142" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="10555730" STOP_POS="101704301" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314531</CITATION_ID>
    <DESCRIPTION>SS/Jr females were bred with SHR/NHsd males and their male F&lt;sub&gt;1&lt;/sub&gt; were backcrossed to SHR/NHsd females; this ensured that the mitochondrial genome came from SHR/NHsd; further selection was done using microsatellite markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314532</RGD_ID>
    <STRAIN_SYMBOL>SHR.SS-(&lt;i&gt;D8Uia1-D8Rat90&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="119450421" STOP_POS="119450610" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="110572032" STOP_POS="110572221" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="118862625" STOP_POS="118862813" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="20954930" STOP_POS="118204000" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="19055857" STOP_POS="114974688" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314532</CITATION_ID>
    <DESCRIPTION>SS/Jr females were bred with SHR/NHsd males and their male F&lt;sub&gt;1&lt;/sub&gt; were backcrossed to SHR/NHsd females; this ensured that the mitochondrial genome came from SHR/NHsd; further selection was done using microsatellite markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314655</RGD_ID>
    <STRAIN_SYMBOL>BRAT-&lt;i&gt;Avp&lt;sup&gt;di&lt;/i&gt;&lt;/sup&gt;/BluHsd</STRAIN_SYMBOL>
    <FULL_NAME>Brattleboro</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>Harlan</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2018-06-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Avp&lt;sup&gt;di&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13627261</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="138247039" STOP_POS="138247039" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="117793942" STOP_POS="117793942" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="123117977" STOP_POS="123117977" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="129615610" STOP_POS="129627147" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="118205007" STOP_POS="118206985" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314655</CITATION_ID>
    <DESCRIPTION>Hereditary hypothalamic diabetes insipidus was first described in offspring from a Long-Evans stock of rats by Dr. Schroeder, later named Brattleboro strain. In 1964 from Dr. Lewis Kinder, Harvard University, Boston to Blue Spruce Farms, Altamont, New York. to Harlan through acquisition in 1988.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314861</RGD_ID>
    <STRAIN_SYMBOL>WAG/RijYcb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://medfaculty.yale.edu/directory/public/profile.asp?pictID=58633&amp;nameSearch=&amp;department=&amp;keyword=booth&gt; Comparative Medicine, Yale University, Connecticut&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://medfaculty.yale.edu/directory/public/profile.asp?pictID=58633&amp;nameSearch=&amp;department=&amp;keyword=booth&gt; Comparative Medicine, Yale University, Connecticut&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314861</CITATION_ID>
    <DESCRIPTION>Substrain of WAG/Rij; from Netherlands to Yale University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314904</RGD_ID>
    <STRAIN_SYMBOL>WAG-&lt;i&gt;F8&lt;sup&gt;m1Ycb&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://medfaculty.yale.edu/directory/public/profile.asp?pictID=58633&amp;nameSearch=&amp;department=&amp;keyword=booth&gt; Comparative Medicine, Yale University, Connecticut&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://medfaculty.yale.edu/directory/public/profile.asp?pictID=58633&amp;nameSearch=&amp;department=&amp;keyword=booth&gt; Comparative Medicine, Yale University, Connecticut&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>F8&lt;i&gt;&lt;sup&gt;m1Ycb&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>2314903</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="155237" STOP_POS="187186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="145719" STOP_POS="145719" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="394478" STOP_POS="394478" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="413447" STOP_POS="444491" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="121134" STOP_POS="162008" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314904</CITATION_ID>
    <DESCRIPTION>This mutant strain carrying a naturally occurring missense mutation displays inherited coagulopathy was arising in an inbred colony of WAG/RijYcb (RGD:2314861). Mutation in the nucleotide 578 of the rat F8 gene changes amino acid 193 in the rat protein(amino acid 176 in human)from Leucine to Proline.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314928</RGD_ID>
    <STRAIN_SYMBOL>Slc:W</STRAIN_SYMBOL>
    <FULL_NAME>Slc: Wistar</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.labanimal.co.kr/product/slc03.html&gt; SLC, Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.labanimal.co.kr/product/slc03.html&gt; SLC, Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314928</CITATION_ID>
    <DESCRIPTION>Institute of Medical Science, University of Tokyo(1974). Hysterectomy and fostering are used for obtaining SPF animals of this strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314934</RGD_ID>
    <STRAIN_SYMBOL>WST.F344-&lt;i&gt;Ker&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Wistar/ST-Boo</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=755&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=755&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314934</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by backcrossing F344-&lt;i&gt;Ker&lt;/i&gt;/Kyo (NBRP No.0458) onto Slc:WST</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314935</RGD_ID>
    <STRAIN_SYMBOL>WST.F344-&lt;i&gt;Kmch&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>Wistar/ST-Komachi</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=756&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=756&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314935</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by backcrossing F344-&lt;i&gt;Kmch&lt;/i&gt;/Kyo (NBRP No.0458) onto Slc:WST.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314936</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(WSCD2)Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=874&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=874&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-08-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314936</CITATION_ID>
    <DESCRIPTION>A transgenic construct consisting of the human WSC domain containing 2 (WSCD2, also known as KIAA0789) within pEF6/Myc-HisA (downstream of the EF-1a promoter and upstream of the bovine growth hormone polyA signal) was injected into Wistar rat (Crlj:WI) embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2314937</RGD_ID>
    <STRAIN_SYMBOL>F344.OLETF-(&lt;i&gt;D5Mgh20-D5Mgh22&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=915&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=915&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="139201964" STOP_POS="156289444" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="133916727" STOP_POS="151006154" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="139267814" STOP_POS="157212422" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="143051962" STOP_POS="160953783" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="140925168" STOP_POS="157584492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2314937</CITATION_ID>
    <DESCRIPTION>Developed by the depositor</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2316631</RGD_ID>
    <STRAIN_SYMBOL>F344.GK-(&lt;i&gt;D1Swe8-D1Gpam-1&lt;/i&gt;)/Swe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adra2a|Pdcd4|Shoc2</ALLELES>
    <ALLELE_RGD_IDS>2056|620816|1308146</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="252645447" STOP_POS="252645657" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="274353782" STOP_POS="274353991" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="281763458" STOP_POS="281763667" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="259866528" STOP_POS="259866737" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2316631</CITATION_ID>
    <DESCRIPTION>This sub-congenic strain is generated from an F&lt;sub&gt;2&lt;/sub&gt;- intercross between F344/DuCrlSwe and F344.GK-(D1Arb42a-D1Rat90)/Swe</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2316632</RGD_ID>
    <STRAIN_SYMBOL>NEDH/KSim</STRAIN_SYMBOL>
    <FULL_NAME>New England Deaconess Hospital</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.simlab.com/&gt;Simonsen Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.simlab.com/&gt;Simonsen Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2316632</CITATION_ID>
    <DESCRIPTION>Inbred from Wistar rats by S. Warren then to Simonsen Laboratories in 1987 by B. Hoffman</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2316633</RGD_ID>
    <STRAIN_SYMBOL>F344.GK-(&lt;i&gt;D1Got251-D1Gpam-1&lt;/i&gt;)/Swe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="253439653" STOP_POS="253439819" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="275138749" STOP_POS="275138914" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="282550224" STOP_POS="282550389" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="260641680" STOP_POS="260641846" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2316633</CITATION_ID>
    <DESCRIPTION>This sub-congenic strain is generated from an F&lt;sub&gt;2&lt;/sub&gt;- intercross between F344/DuCrlSwe and F344.GK-(D1Arb42a-D1Rat90)/Swe</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2316653</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco102-D1Got46&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="32249735" STOP_POS="44011366" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="34888392" STOP_POS="44326906" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="36290530" STOP_POS="45656739" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="38394289" STOP_POS="38394434" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="2374083" STOP_POS="2374266" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2316653</CITATION_ID>
    <DESCRIPTION>A sub-congenic strain derived from SS.LEW-(&lt;i&gt;D1Uia8-D1Rat18&lt;i&gt;)/Mco contributing to the introgressed LEW allele</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2316654</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco102-D1Mco129&lt;/i&gt;)/1Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="32249735" STOP_POS="33038814" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="34888392" STOP_POS="35680732" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="36290530" STOP_POS="37078065" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="2374083" STOP_POS="3178843" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2316654</CITATION_ID>
    <DESCRIPTION>A sub-congenic strain derived from SS.LEW-(&lt;i&gt;D1Mco102-D1Got46&lt;/i&gt;)/Mco contributing to the introgressed LEW allele crossed to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2316655</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco102-D1Mco129&lt;/i&gt;)/2Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="32249735" STOP_POS="33038814" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="34888392" STOP_POS="35680732" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="36290530" STOP_POS="37078065" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="2374083" STOP_POS="3178843" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2316655</CITATION_ID>
    <DESCRIPTION>A sub-congenic strain derived from SS.LEW-(&lt;i&gt;D1Mco102-D1Got46&lt;/i&gt;)/Mco contributing to the introgressed LEW allele crossed to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2316925</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D3Rat159-D3Rat1&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="118950053" STOP_POS="168026850" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="124284647" STOP_POS="176418101" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="130776038" STOP_POS="180128021" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="119437175" STOP_POS="170016653" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2316925</CITATION_ID>
    <DESCRIPTION>50.6 Mb region of BN/SsNHsd is introgressed into the genomic background of SHR/NHsd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2316927</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D6Rat40-D6Rat170&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="22288360" STOP_POS="51275480" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="16536243" STOP_POS="45547114" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="1120393" STOP_POS="48179481" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="1111498" STOP_POS="56881356" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="1301952" STOP_POS="46792623" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2316927</CITATION_ID>
    <DESCRIPTION>45.5 Mb region of BN/SsNHsd is introgressed into the genomic background of SHR/NHsd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2316928</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D3Rat159-D3Rat1&lt;/i&gt;)(&lt;i&gt;D6Rat40-D6Rat170&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2316928</CITATION_ID>
    <DESCRIPTION>this double congenic strain is bred by crossing female SHR.BN-(D6Rat40-D6Rat170)/Mco with male SHR.BN-(D3Rat159-D3Rat1)/Mco and selecting heterozygous animals in the F1 progeny; these were then mated to fix the BN allele</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317196</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D8Rat146-D8Got145&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="69352596" STOP_POS="87043114" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="74920991" STOP_POS="93746162" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="76885501" STOP_POS="93261060" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="73105403" STOP_POS="91329867" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317196</CITATION_ID>
    <DESCRIPTION>Males with PVG.1AV1 allele were selected from the G8 advanced intercross line (AIL) and mated with DA females to tranfer a short well-defined (73.1-91.3 Mb) region that has the region of interest</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317197</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D8Rat41-D8Rat24&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="87018553" STOP_POS="87018707" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="47627235" STOP_POS="78138314" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="51633707" STOP_POS="84569318" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="50240107" STOP_POS="84140836" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="50354908" STOP_POS="82247243" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317197</CITATION_ID>
    <DESCRIPTION>Males with PVG.1AV1 allele were selected from the G8 advanced intercross line (AIL) and mated with DA females to tranfer a short well-defined (50.4-82.2 Mb) region that has the region of interest</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317201</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D8Rat24-D8Got145&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="87018553" STOP_POS="87018707" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="78138158" STOP_POS="87043114" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="84569165" STOP_POS="93746162" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="84140683" STOP_POS="93261060" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="82246890" STOP_POS="91329867" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317201</CITATION_ID>
    <DESCRIPTION>DA.PVG.1AV1-(&lt;i&gt;D8Rat146-D8Got145&lt;/i&gt;) was backcrossed to the recipient DA for 9 generations to create this congenic with less than 0.1% genome outside the desired locus</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317278</RGD_ID>
    <STRAIN_SYMBOL>Taiep/Dun</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept of Medical Sciences, University of Wisconsin-Madison, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317278</CITATION_ID>
    <DESCRIPTION>These mutants were found in Sprague-Dawley rats at University of Puebla in 1989</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317590</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat23-D4Rat108&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="61041057" STOP_POS="84174648" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="82844048" STOP_POS="82844186" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="83889402" STOP_POS="83889539" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="58518376" STOP_POS="148552304" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="58550170" STOP_POS="82090355" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317590</CITATION_ID>
    <DESCRIPTION>Congenic substrain established by intercrossing DA.PVG.1AV1-(&lt;i&gt;D4Rat155-Spr&lt;/i&gt;) with parental DA/Kini</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317595</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat23-D4Mit12&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="61041057" STOP_POS="61041206" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="103194805" STOP_POS="103194984" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="99066972" STOP_POS="99067150" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="58518376" STOP_POS="163844298" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="58550170" STOP_POS="104416171" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317595</CITATION_ID>
    <DESCRIPTION>Congenic substrain established by intercrossing DA.PVG.1AV1-(&lt;i&gt;D4Rat155-Spr&lt;/i&gt;) with parental DA/Kini</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317596</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat103-D4Mit12&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="83428419" STOP_POS="103194984" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="84475257" STOP_POS="99067150" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="149135946" STOP_POS="163844298" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="82700691" STOP_POS="104416171" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317596</CITATION_ID>
    <DESCRIPTION>Congenic substrain established by intercrossing DA.PVG.1AV1-(&lt;i&gt;D4Rat155-Spr&lt;/i&gt;) with parental DA/Kini</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317598</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat231-D4Mit12&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="89986808" STOP_POS="89987030" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="88656681" STOP_POS="103194984" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="89777552" STOP_POS="99067150" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="154593964" STOP_POS="163844298" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="88462327" STOP_POS="104416171" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317598</CITATION_ID>
    <DESCRIPTION>Congenic substrain established by intercrossing DA.PVG.1AV1-(&lt;i&gt;D4Rat155-Spr&lt;/i&gt;) with parental DA/Kini</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317599</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Got211-D4Mit12&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="81776043" STOP_POS="81776229" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="80445377" STOP_POS="103194984" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="81136696" STOP_POS="99067150" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="145804154" STOP_POS="163844298" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="79604076" STOP_POS="104416171" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317599</CITATION_ID>
    <DESCRIPTION>Congenic substrain established by intercrossing DA.PVG.1AV1-(&lt;i&gt;D4Rat155-Spr&lt;/i&gt;) with parental DA/Kini</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317791</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Got60-D4Kini1&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="82490359" STOP_POS="82490515" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="83531021" STOP_POS="83531176" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="147125280" STOP_POS="148194009" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="80704779" STOP_POS="81729771" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317791</CITATION_ID>
    <DESCRIPTION>Congenic substrain established by intercrossing DA.PVG.1AV1-(&lt;i&gt;D4Rat155-Spr&lt;/i&gt;) with parental DA/Kini</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317812</RGD_ID>
    <STRAIN_SYMBOL>AT.ANT-(&lt;i&gt;D1Uia12-D1Rat288&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Colorado Denver, Colorado</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=728&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="141624120" STOP_POS="196789885" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="132214399" STOP_POS="132214546" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="139972085" STOP_POS="139972231" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="140949643" STOP_POS="211567839" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="134007903" STOP_POS="192038535" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00728</CITATION_ID>
    <DESCRIPTION>F&lt;sub&gt;2&lt;/sub&gt; males with desired fragment of ANT were selected by genotyping and backcrossed to AT rats, this process was repeated for 6 generations and offsprings were tested</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317813</RGD_ID>
    <STRAIN_SYMBOL>AT.ANT-(&lt;i&gt;D1Rat234-D1Rat47&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Colorado Denver, Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="155422851" STOP_POS="155423009" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="166100317" STOP_POS="166100474" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="172296302" STOP_POS="172296459" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="41225047" STOP_POS="158511230" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317813</CITATION_ID>
    <DESCRIPTION>This sub-congenic was developed by crossing AT.ANT-(&lt;i&gt;D1Rat234-D1Rat228&lt;/i&gt;)/Rar with AT</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317814</RGD_ID>
    <STRAIN_SYMBOL>AT.ANT-(&lt;i&gt;D1Rat273-D1Rat158&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Colorado Denver, Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="147753973" STOP_POS="160111531" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="138344856" STOP_POS="150700247" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="146507930" STOP_POS="161321256" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="147436666" STOP_POS="167535765" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="140644473" STOP_POS="153578547" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317814</CITATION_ID>
    <DESCRIPTION>This sub-congenic was developed by crossing AT.ANT-(&lt;i&gt;D1Rat234-D1Rat228&lt;/i&gt;)/Rar with AT</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317815</RGD_ID>
    <STRAIN_SYMBOL>AT.ANT-(&lt;i&gt;D1Rat35-D1Rat47&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Colorado Denver, Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="132889797" STOP_POS="132889942" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="123479780" STOP_POS="155423009" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="130917121" STOP_POS="166100474" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="131958920" STOP_POS="172296459" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="124748920" STOP_POS="158511230" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317815</CITATION_ID>
    <DESCRIPTION>This sub-congenic was developed by crossing AT.ANT-(&lt;i&gt;D1Rat234-D1Rat228&lt;/i&gt;)/Rar with AT</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317816</RGD_ID>
    <STRAIN_SYMBOL>AT.ANT-(&lt;i&gt;D1Rat234-D1Rat158&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Colorado Denver, Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="160111426" STOP_POS="160111531" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="150700142" STOP_POS="150700247" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="161321152" STOP_POS="161321256" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="167535661" STOP_POS="167535765" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="41225047" STOP_POS="153578547" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317816</CITATION_ID>
    <DESCRIPTION>This sub-congenic was developed by crossing AT.ANT-(&lt;i&gt;D1Rat234-D1Rat228&lt;/i&gt;)/Rar with AT</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317817</RGD_ID>
    <STRAIN_SYMBOL>AT.ANT-(&lt;i&gt;D1Rat183-D1Rat288&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Colorado Denver, Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="138793931" STOP_POS="196789885" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="129384185" STOP_POS="129384427" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="137083889" STOP_POS="137084126" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="138077032" STOP_POS="211567839" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="131123181" STOP_POS="192038535" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317817</CITATION_ID>
    <DESCRIPTION>This sub-congenic was developed by crossing AT.ANT-(&lt;i&gt;D1Rat234-D1Rat288&lt;/i&gt;)/Rar with AT</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317818</RGD_ID>
    <STRAIN_SYMBOL>AT.ANT-(&lt;i&gt;D1Rat273-D1Rat288&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Colorado Denver, Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="147753973" STOP_POS="196789885" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="138344856" STOP_POS="138345017" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="146507930" STOP_POS="146508090" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="147436666" STOP_POS="211567839" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="140644473" STOP_POS="192038535" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317818</CITATION_ID>
    <DESCRIPTION>This sub-congenic was developed by crossing AT.ANT-(&lt;i&gt;D1Rat234-D1Rat288&lt;/i&gt;)/Rar with AT</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317819</RGD_ID>
    <STRAIN_SYMBOL>AT.ANT-(&lt;i&gt;D1Rat35-D1Rat288&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Colorado Denver, Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="132889797" STOP_POS="196789885" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="123479780" STOP_POS="123479925" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="130917121" STOP_POS="130917265" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="131958920" STOP_POS="211567839" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="124748920" STOP_POS="192038535" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317819</CITATION_ID>
    <DESCRIPTION>This sub-congenic was developed by crossing AT.ANT-(&lt;i&gt;D1Rat234-D1Rat288&lt;/i&gt;)/Rar with AT</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317820</RGD_ID>
    <STRAIN_SYMBOL>AT.ANT-(&lt;i&gt;D1Rat158-D1Rat288&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Colorado Denver, Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="160111426" STOP_POS="196789885" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="150700142" STOP_POS="150700247" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="161321152" STOP_POS="161321256" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="167535661" STOP_POS="211567839" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="153578442" STOP_POS="192038535" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317820</CITATION_ID>
    <DESCRIPTION>This sub-congenic was developed by crossing AT.ANT-(&lt;i&gt;D1Rat234-D1Rat288&lt;/i&gt;)/Rar with AT</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317822</RGD_ID>
    <STRAIN_SYMBOL>AT.ANT-(&lt;i&gt;D1Rat35-D1Rat38&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Colorado Denver, Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="132889797" STOP_POS="141173303" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="123479780" STOP_POS="131763614" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="130917121" STOP_POS="139524104" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="131958920" STOP_POS="140507239" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="124748920" STOP_POS="133567105" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317822</CITATION_ID>
    <DESCRIPTION>This sub-congenic was developed by crossing AT.ANT-(&lt;i&gt;D1Rat234-D1Rat228&lt;/i&gt;)/Rar with AT</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317825</RGD_ID>
    <STRAIN_SYMBOL>AT.ANT-(&lt;i&gt;D1Rat234-D1Rat35&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Colorado Denver, Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="132889797" STOP_POS="132889942" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="123479780" STOP_POS="123479925" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="130917121" STOP_POS="130917265" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="131958920" STOP_POS="131959064" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="41225047" STOP_POS="124749065" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317825</CITATION_ID>
    <DESCRIPTION>This sub-congenic was developed by crossing AT.ANT-(&lt;i&gt;D1Rat234-D1Rat228&lt;/i&gt;)/Rar with AT</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317827</RGD_ID>
    <STRAIN_SYMBOL>AT.ANT-(&lt;i&gt;D1Rat234-D1Rat38&lt;/i&gt;)/Rar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Colorado Denver, Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="141173126" STOP_POS="141173303" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="131763437" STOP_POS="131763614" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="139523928" STOP_POS="139524104" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="140507063" STOP_POS="140507239" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="41225047" STOP_POS="133567105" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317827</CITATION_ID>
    <DESCRIPTION>This sub-congenic was developed by crossing AT.ANT-(&lt;i&gt;D1Rat234-D1Rat228&lt;/i&gt;)/Rar with AT</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2317891</RGD_ID>
    <STRAIN_SYMBOL>SHR-Chr 6&lt;sup&gt;MWF&lt;/sup&gt;/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Clinical Pharmacology and Toxicology, Charite-Universitatsmedizin Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2317891</CITATION_ID>
    <DESCRIPTION>SHR/FubRkb male was crossed with female MWF/FubRkb to get F1 animals which in turn were backcrossed with female SHR/FubRkb, this was repeated for 7 generations, tested by sequential marker-assisted backcrossing</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2324631</RGD_ID>
    <STRAIN_SYMBOL>DA.E3-(&lt;i&gt;D4Wox49-D4Got136&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical Inflammation Research, Karolinska Institutet, Stockholm, Sweden.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Clec4a3</ALLELES>
    <ALLELE_RGD_IDS>1359528</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="155828194" STOP_POS="157232313" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="155414290" STOP_POS="156945571" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="222438489" STOP_POS="223964695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="159060677" STOP_POS="160528447" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2324631</CITATION_ID>
    <DESCRIPTION>This congenic strain was obtained by the conventional backcross breeding to the parental DA strain with the negative selection of all known Pia QTLs and positive selection of microsatellite markers.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325143</RGD_ID>
    <STRAIN_SYMBOL>SHR/NHsdMco</STRAIN_SYMBOL>
    <FULL_NAME>Spontaneously Hypertensive Rat</FULL_NAME>
    <ORIGINATION>University of Toledo, College of Medicine (Medical College of Ohio), Toledo, Ohio.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2325143</CITATION_ID>
    <DESCRIPTION>SHR strain obtained from Harlan Sprague-Dawley (Indianapolis, IN) and maintained at University of Toledo, College of Medicine (Medical College of Ohio), Toledo, Ohio.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325145</RGD_ID>
    <STRAIN_SYMBOL>LEW/CrlMco</STRAIN_SYMBOL>
    <FULL_NAME>Lewis</FULL_NAME>
    <ORIGINATION>University of Toledo, College of Medicine (Medical College of Ohio), Toledo, Ohio.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2325145</CITATION_ID>
    <DESCRIPTION>These were obtained from Charles River and maintained at University of Toledo, College of Medicine (Medical College of Ohio), Toledo, Ohio.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325146</RGD_ID>
    <STRAIN_SYMBOL>MNS/NMco</STRAIN_SYMBOL>
    <FULL_NAME>Milan normotensive strain</FULL_NAME>
    <ORIGINATION>University of Toledo, College of Medicine (Medical College of Ohio), Toledo, Ohio.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2325146</CITATION_ID>
    <DESCRIPTION>These were originally obtained from Veterinary Resource Branch, National Institutes of Health (Bethesda, MD) and maintained at University of Toledo, College of Medicine (Medical College of Ohio), Toledo, Ohio.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325202</RGD_ID>
    <STRAIN_SYMBOL>SS/JrSeac</STRAIN_SYMBOL>
    <FULL_NAME>Dahl Salt-Sensitive</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1041&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1041&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio- Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2325202</CITATION_ID>
    <DESCRIPTION>Substrain of Dahl SS, from a Sprague-Dawley outbred colony, selected for sensitivity to salt-induced hypertension developed at  Kyudo Co.,Ltd (http://www.kyudo.co.jp/) to Seac Yoshitomi, LTD Japan, now maintained at NBRP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325206</RGD_ID>
    <STRAIN_SYMBOL>LEW/Seac</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Seac Yoshitomi, LTD Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2325206</CITATION_ID>
    <DESCRIPTION>Substrain of LEW, from Dr Margaret Lewis from Wistar stock in early 1950s to Seac Yoshitomi, LTD Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325209</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/Hos</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Sankyo Lab Service, Japan.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2325209</CITATION_ID>
    <DESCRIPTION>Substrain of SHRSP purchased from Sankyo Lab Service, Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325724</RGD_ID>
    <STRAIN_SYMBOL>PVG.LEW-(&lt;i&gt;D1Rat270-D1Rat68&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="138003387" STOP_POS="197807511" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="128593600" STOP_POS="188377506" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="135611773" STOP_POS="205603226" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="136616460" STOP_POS="212591221" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="130290073" STOP_POS="193070197" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2325724</CITATION_ID>
    <DESCRIPTION>63-Mb fragment was selectively transferred from LEW.1AV1 to PVG.1AV1</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325754</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Pax6&lt;sup&gt;Sey&lt;/sup&gt;&lt;/i&gt;/Mce</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Ophthalmology, Okayama University Medical School, Okayama, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pax6|Pax6&lt;sup&gt;Sey&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>3258|737688</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="112590034" STOP_POS="112611771" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="92152512" STOP_POS="92152513" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="95724051" STOP_POS="95724052" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="102320059" STOP_POS="102348223" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="91127605" STOP_POS="91149178" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2325754</CITATION_ID>
    <DESCRIPTION>Autosomal dominant mutation that arose spontaneously in SD rats. Genomic DNA analysis from mutants revealed a single base(G) insertion in the exon generating a novel 5' donor splice site. This led to the internal a 602-bp deletion of Pax6 mRNA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325773</RGD_ID>
    <STRAIN_SYMBOL>WKY.LEW-(&lt;i&gt;D13Arb15-D13Rat58&lt;/i&gt;)/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Imperial College, London, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="70819836" STOP_POS="94968043" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="68269576" STOP_POS="92436175" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="73748382" STOP_POS="98985851" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="78673431" STOP_POS="103987907" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="71116479" STOP_POS="96441728" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2325773</CITATION_ID>
    <DESCRIPTION>Segment of interest from chr 13 of LEW/SsNHsd was introgressed into WKY/NCrl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325774</RGD_ID>
    <STRAIN_SYMBOL>WKY.LEW-(&lt;i&gt;D13Arb10-D13Arb15&lt;/i&gt;)(&lt;i&gt;D16Rat88-D16Rat40&lt;/i&gt;)/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Imperial College, London, UK</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=707&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00707</CITATION_ID>
    <DESCRIPTION>WKY.LEW-(&lt;i&gt;D13Arb10-D13Arb15&lt;/i&gt;) were crossed with WKY.LEW-(&lt;i&gt;D16Rat88-D16Rat40&lt;/i&gt;), the F&lt;sub&gt;1&lt;/sub&gt; were backcrossed to WKY.LEW-(&lt;i&gt;D13Arb10-D13Arb15&lt;/i&gt;) and then the offsprings were intercrossed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325796</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D3Rat52-D3Chm57&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="38708931" STOP_POS="38709087" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="18311454" STOP_POS="28441896" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="14090411" STOP_POS="29084626" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="19410399" STOP_POS="34290625" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="14051872" STOP_POS="24716931" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2325796</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D3Rat52-D3Rat130&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325798</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Got112-Igfbp4&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universiti de Montrial, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Igfbp4</ALLELES>
    <ALLELE_RGD_IDS>2875</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="76743133" STOP_POS="84503487" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="76246085" STOP_POS="84007272" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="78970279" STOP_POS="86962563" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="78816241" STOP_POS="86759484" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="79857808" STOP_POS="87834315" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2325798</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Rat27-Igfbp4&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325801</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D16Chm36-D16Mit2&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="4234212" STOP_POS="4234333" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="903314" STOP_POS="4227730" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="1619835" STOP_POS="5098704" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="1604056" STOP_POS="5038806" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="890512" STOP_POS="4304517" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2325801</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D16Rat12-D16Chm23&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>2325803</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D16Rat112-D16Chm60&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="117469" STOP_POS="117710" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="110590" STOP_POS="3080679" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="778415" STOP_POS="3525217" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="773329" STOP_POS="3491557" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="64718" STOP_POS="3165043" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_2325803</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D16Rat12-D16Chm23&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4107048</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;D7Rat16-D7Rat189&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="115406495" STOP_POS="115406693" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="102920123" STOP_POS="113526566" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="112204378" STOP_POS="123243402" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="112143411" STOP_POS="123228091" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="108647236" STOP_POS="120385575" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4107048</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived by crossing the congenic strain SS.SR-&lt;I&gt;Cyp11b1&lt;/I&gt;/Jr to SS/Jr to isolate which contains a smaller SR/Jr derived chromosome 7 segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4107052</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;D7Rat16-D7Mgh5&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="102920123" STOP_POS="109483487" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="112204378" STOP_POS="119131068" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="112143411" STOP_POS="119125830" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="108647236" STOP_POS="115820414" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4107052</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived by crossing the congenic strain SS.SR-&lt;I&gt;Cyp11b1&lt;/I&gt;/Jr to SS/Jr to isolate which contains a smaller SR/Jr derived chromosome 7 segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4107055</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;D7Rat16-D7Rat176&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="107288231" STOP_POS="107288456" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="102920123" STOP_POS="105399458" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="112204378" STOP_POS="114708307" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="112143411" STOP_POS="114641749" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="108647236" STOP_POS="111200952" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4107055</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived by crossing the congenic strain SS.SR-&lt;I&gt;Cyp11b1&lt;/I&gt;/Jr to SS/Jr to isolate which contains a smaller SR/Jr derived chromosome 7 segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4107057</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;I&gt;D7Mco7-D7Rat81&lt;/I&gt;)/Jr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="124100121" STOP_POS="124100394" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="122220558" STOP_POS="122220831" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="132252091" STOP_POS="132252361" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="116059683" STOP_POS="131926277" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="112979256" STOP_POS="129500555" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4107057</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived by crossing the congenic strain SS.SR-&lt;I&gt;Cyp11b1&lt;/I&gt;/Jr to SS/Jr to isolate which contains a smaller SR/Jr derived chromosome 7 segment</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4107063</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Uia8-D1Rat124&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4107063</CITATION_ID>
    <DESCRIPTION>A sub-congenic strain derived from SS.LEW-(&lt;i&gt;D1Rat268-D1Got35&lt;/i&gt;)/Jr contributing to the introgressed LEW allele</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4107065</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Uia8-D1Rat213&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology and Molecular Medicine, Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="90905258" STOP_POS="90905414" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="81777564" STOP_POS="81777720" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="83282659" STOP_POS="83282814" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="84537073" STOP_POS="84537228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="81548753" STOP_POS="81548909" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4107065</CITATION_ID>
    <DESCRIPTION>A sub-congenic strain derived from SS.LEW-(&lt;i&gt;D1Rat268-D1Got35&lt;/i&gt;)/Jr contributing to the introgressed LEW allele</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139872</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nckap5&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nckap5&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139862</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="39922576" STOP_POS="40835849" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="37369948" STOP_POS="38283257" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="42265875" STOP_POS="43049232" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="47369687" STOP_POS="48273649" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="38444115" STOP_POS="39275959" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139872</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ctctgaaccttcaactttcagatactgatgacaatgaa into SS/JrHsdMcwi rat embryos. The resulting mutation is a 4-bp frameshift deletion in exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139873</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rag1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rag1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139866</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108372087" STOP_POS="108383184" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87922895" STOP_POS="87922911" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91212228" STOP_POS="91212244" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97866048" STOP_POS="97877145" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86780782" STOP_POS="86791878" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139873</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence gtctactgcccaaggaatgtgaccgtggagtggca into SS/JrHsdMcwi rat embryos. The resulting mutation is a 17-bp frameshift deletion in exon1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139874</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ets1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ets1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139856</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="39303936" STOP_POS="39426022" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="31045909" STOP_POS="31168010" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="33851478" STOP_POS="33851485" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="33798598" STOP_POS="33921593" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="32481694" STOP_POS="32545237" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139874</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence aacccatgtccgggattgggtgatgtgggctgtgaatgag into SS/JrHsdMcwi rat embryos. The resulting mutation is a 8-bp frameshift deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139875</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Sorcs1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sorcs1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139864</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="259022007" STOP_POS="259535731" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="249207764" STOP_POS="249207777" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="269965824" STOP_POS="270473097" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="277404996" STOP_POS="277912261" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="255767411" STOP_POS="256279565" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139875</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ataaacctttcccaggatacattgacccggattct into FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;/Mcwi embryos. The resulting mutation is a 14-bp frameshift deletion mutation in exon 20.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139876</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mmp2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mmp2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139860</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="30327643" STOP_POS="30355856" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="14154657" STOP_POS="14182870" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="15542771" STOP_POS="15570589" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="26629728" STOP_POS="26658966" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="15246036" STOP_POS="15275061" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139876</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence aaccacaaccaactacgatgatgaccggaagtggggc into SS/JrHsdMcwi rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139877</RGD_ID>
    <STRAIN_SYMBOL>FHH.BN-(&lt;i&gt;D1Hmgc14-D1Hmgc15&lt;/i&gt;)/Mcwi-&lt;i&gt;Rab38&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rab38&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139867</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="151595153" STOP_POS="151675492" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="142182566" STOP_POS="142262923" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="152072716" STOP_POS="152153449" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="158385888" STOP_POS="158466621" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="144783919" STOP_POS="144864573" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139877</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CACCAAAACTTCTCCTCCCACTACCGGGCCACCATTGGT into FHH.BN-(&lt;i&gt;D1Hmgc14-D1Hmgc15&lt;/i&gt;)/Mcwi rat embryos. The resulting mutation is a 1-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139878</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mmp2&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mmp2&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139869</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="30327643" STOP_POS="30355856" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="14154657" STOP_POS="14182870" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="15542771" STOP_POS="15570589" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="26646695" STOP_POS="26646702" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="15246036" STOP_POS="15275061" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139878</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence aaccacaaccaactacgatgatgaccggaagtggggc into SS/JrHsdMcwi rat embryos. The resulting mutation is a 8-bp frameshift deletion in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139879</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nckap5&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nckap5&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139859</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="39922576" STOP_POS="40835849" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="37369948" STOP_POS="38283257" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="42265875" STOP_POS="43049232" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="47369687" STOP_POS="48273649" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="38444115" STOP_POS="39275959" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139879</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ctctgaaccttcaactttcagatactgatgacaatgaa into SS/JrHsdMcwi rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139880</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ren&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ren&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139863</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="47348312" STOP_POS="47359539" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="44803412" STOP_POS="44803421" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50502724" STOP_POS="50513953" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55555583" STOP_POS="55566812" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="46262936" STOP_POS="46275213" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139880</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence acccttcatgctggccaagtttgacggggttctgggcatg into SS/JrHsdMcwi rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139881</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nckap5&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nckap5&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139861</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="39922576" STOP_POS="40835849" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="37369948" STOP_POS="38283257" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="42265875" STOP_POS="43049232" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="47369687" STOP_POS="48273649" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="38444115" STOP_POS="39275959" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139881</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ctctgaaccttcaactttcagatactgatgacaatgaa into SS/JrHsdMcwi rat embryos. The resulting mutation is an 11-bp frameshift deletion in exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139882</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nppa&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nppa&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139857</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="163712184" STOP_POS="163713493" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="158429042" STOP_POS="158430351" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164808762" STOP_POS="164808783" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="168466309" STOP_POS="168467618" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="165074518" STOP_POS="165075827" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139882</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence gcctccgcaggccctgagcgagcagaccgatgaagcgggg into SS/JrHsdMcwi rat embryos. The resulting mutation is a 22-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139883</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nox4&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nox4&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139868</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150313736" STOP_POS="150491480" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="140900886" STOP_POS="141078844" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="150861996" STOP_POS="150862003" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157106652" STOP_POS="157285107" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143415816" STOP_POS="143603554" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139883</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ggttacagcttctacctatgcaataaggtaagggtc into SS/JrHsdMcwi rat embryos. The resulting mutation is an 8-bp frameshift deletion in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139884</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rag1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rag1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139865</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108372087" STOP_POS="108383184" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87922904" STOP_POS="87922916" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91212237" STOP_POS="91212249" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97866048" STOP_POS="97877145" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86780782" STOP_POS="86791878" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139884</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence gtctactgcccaaggaatgtgaccgtggagtggca into SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp frameshift deletion in exon1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139885</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sh2b3&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sh2b3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139858</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="40391755" STOP_POS="40414336" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="34750772" STOP_POS="34750777" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="40262913" STOP_POS="40262918" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="42132947" STOP_POS="42136714" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="35954679" STOP_POS="35958446" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139885</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ctcccccatcccacttgaatgtggagcagcctgtg into SS/JrHsdMcwi rat embryos. The resulting mutation is an in-frame 6-bp deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139889</RGD_ID>
    <STRAIN_SYMBOL>BHD/Dspe</STRAIN_SYMBOL>
    <FULL_NAME>Birt-Hogg-Dube rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=927&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=927&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2018-06-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Flcn</ALLELES>
    <ALLELE_RGD_IDS>735088</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139889</CITATION_ID>
    <DESCRIPTION>A rat showing hereditary renal cell carcinoma was found in a Jcl:SD rat colony  and named Nihon rat.  In this rat strain mutation was identified as an insertion of a cytosine (C) in a C tract within exon 3 of Flcn . This germline mutation results in a frameshift and produces a stop codon 26 amino-acids downstream. Thereafter they have been maintained at Dainippon Sumitomo Pharma Co., Ltd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139890</RGD_ID>
    <STRAIN_SYMBOL>TT/Sgn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=928&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=928&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fkbp6</ALLELES>
    <ALLELE_RGD_IDS>1308926</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="26947443" STOP_POS="27026913" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="21318251" STOP_POS="21390350" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="24365941" STOP_POS="24438088" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="26363264" STOP_POS="26435311" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="22474002" STOP_POS="22544784" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139890</CITATION_ID>
    <DESCRIPTION>Rats with bilateral small testes were found in a Wistar-Imamichi derived inbred strain in 1986 at the Institute for Animal Reproduction. TT was established from these mutant rats as known as aspermia rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139891</RGD_ID>
    <STRAIN_SYMBOL>F344-Chr 3&lt;sup&gt;SDT&lt;/sup&gt;/Nyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=896&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=896&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139891</CITATION_ID>
    <DESCRIPTION>This consomic strain carries Chromosome 3 of SDT/Jcl on F344/NSlc background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4139892</RGD_ID>
    <STRAIN_SYMBOL>ALD/Hyo</STRAIN_SYMBOL>
    <FULL_NAME>acid lipase deficiency rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=926&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=926&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Metabolism</RESEARCH_USE>
    <ALLELES>Lipa&lt;sup&gt;m1Hyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150519893</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4139892</CITATION_ID>
    <DESCRIPTION>In a colony of Donryu rats, Yoshida found a male rat showing hepatomegaly and splenomegaly in 1981. These mutant rats were transferred to Kagoshima University and maintained in heterozygous condition so far.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140402</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Gh1as)Nibs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=956&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=956&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140402</CITATION_ID>
    <DESCRIPTION>The construct which contains of rat growth hormone (&lt;i&gt;Gh1&lt;/i&gt;) promoter, 4 copies of thyroid hormone response element (TRE), and antisense sequences for rat &lt;i&gt;Gh1&lt;/i&gt; cDNA was injected into Jcl:Wistar embryo (Matsumoto, 1993). This transgenic rat was established at NT Science in 1992, and transferred to Japan Bio Science Laboratory Co., Ltd. in 2003. This strain has been maintained at Nagasaki University Graduate School of Biomedical Science.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140403</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Eno2-ATXN3*64Q)29Kakiz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=949&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=949&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140403</CITATION_ID>
    <DESCRIPTION>Background strain is Slc:SD.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140404</RGD_ID>
    <STRAIN_SYMBOL>ODS-&lt;i&gt;Gulo&lt;sup&gt;od/od&lt;/sup&gt;/ShiJcl</STRAIN_SYMBOL>
    <FULL_NAME>Osteogenic disorder Shionagi rat</FULL_NAME>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/en/products/other_disease/item_a0250&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/en/products/other_disease/item_a0250&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-04-29)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gulo&lt;sup&gt;od&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126848761</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140404</CITATION_ID>
    <DESCRIPTION>Dr. Susumu Makino and his colleagues found several animals that had gait abnormalities among Wistar rats maintained  at Shionogi Co. They named these animals osteogenic disorder (OD) rats because they exhibited prominent bone and joint abnormalities and systemic bleeding. Subsequent studies revealed that these symptoms were derived from an ascorbic acid (vitamin C) deficiency arising from defective gulonolactone oxidase (GLO) activity. This characteristic was confirmed to be the result of a mutation involving the autosomal single recessive gene od. Scurvy due to L-gulonolactone oxidase deficincy; phenotype normalizes if supplied with ascorbic acid 300mg/kg/d. od/od rats are more susceptible to dental caries as compared with +/+ rats, in only amoun parous females.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140405</RGD_ID>
    <STRAIN_SYMBOL>LEXF6A/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=960&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=960&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140405</CITATION_ID>
    <DESCRIPTION>The LEXF/FXLE RI strain set has been established by Shisa et al at Saitama Cancer Center Research Institute since 1985.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140406</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Wox29-D1Arb21&lt;/i&gt;)/IzmDmcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=964&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=964&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="132760429" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="123350408" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="130779148" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="131822204" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="124614679" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140406</CITATION_ID>
    <DESCRIPTION>To establish this congenic strain, the genetic region in which contains a QTL that is responsible for hypertension in SPRSP was introgressed from WKY/Izm to SHRSP/Izm by repeated backcrossing following sib-mating. This congenic strain was established to cover the QTL region between D1Wox29 and D1Arb21.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140407</RGD_ID>
    <STRAIN_SYMBOL>SDT.BN-&lt;i&gt;Gluco13&lt;/i&gt;/Nyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=958&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=958&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140407</CITATION_ID>
    <DESCRIPTION>The &lt;i&gt;Gluco13&lt;/i&gt; (&lt;i&gt;Gisdt1&lt;/i&gt;) region of BN/Seac was transferred onto the genetic background of SDT/Jcl strain. Established by speed congenic method since 2003 and afterwards maintained by sib mating (N9F6, May 2010) Please refer to STD.BN-&lt;i&gt;Gluco14&lt;/i&gt;/Nyo (NBRP No. 0602).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140408</RGD_ID>
    <STRAIN_SYMBOL>LEXF8C/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=959&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=959&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140408</CITATION_ID>
    <DESCRIPTION>The LEXF/FXLE RI strain set has been established by Shisa et al at Saitama Cancer Center Research Institute since 1985.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140409</RGD_ID>
    <STRAIN_SYMBOL>COP-Chr 16&lt;sup&gt;DA&lt;/sup&gt;/McoRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo College of Medicine, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140409</CITATION_ID>
    <DESCRIPTION>Transfer of the DA-rat chromosome 16 (RNO16) into the COP-rat background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140410</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Eno2-ATXN3*64Q)16Kakiz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=950&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=950&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140410</CITATION_ID>
    <DESCRIPTION>Background strain is Slc:SD.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140411</RGD_ID>
    <STRAIN_SYMBOL>SDT.BN-&lt;i&gt;Gluco14&lt;/i&gt;/Nyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=957&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=957&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140411</CITATION_ID>
    <DESCRIPTION>The &lt;i&gt;Gluco14&lt;/i&gt; (&lt;i&gt;Gisdt2&lt;/i&gt;) region of BN/Seac was transferred onto the genetic background of SDT/Jcl strain. Established by speed congenic method since 2003 and afterwards maintained by sib mating (N10F6, May 2010) Please refer to STD.BN-&lt;i&gt; Gluco13&lt;/i&gt;/Nyo (NBRP No. 0601).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140412</RGD_ID>
    <STRAIN_SYMBOL>LEXF1D/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=961&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=961&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140412</CITATION_ID>
    <DESCRIPTION>The LEXF/FXLE RI strain set has been established by Shisa et al at Saitama Cancer Center Research Institute since 1985.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140413</RGD_ID>
    <STRAIN_SYMBOL>LEXF1B/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=962&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=962&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140413</CITATION_ID>
    <DESCRIPTION>The LEXF/FXLE RI strain set has been established by Shisa et al at Saitama Cancer Center Research Institute since 1985.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140414</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;D1Wox29-D1Arb21&lt;/i&gt;)/IzmDmcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=965&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=965&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="132760429" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="123350408" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="130779148" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="131822204" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="124614679" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140414</CITATION_ID>
    <DESCRIPTION>To establish this congenic strain, the genetic region in which contains a QTL that is responsible for hypertension in SPRSP was introgressed from SHRSP/Izm to WKY/Izm by repeated backcrossing following sib-mating. This congenic strain was established to cover the QTL region between D1Wox29 and D1Arb21.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140415</RGD_ID>
    <STRAIN_SYMBOL>TRMRC/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=963&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=963&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140415</CITATION_ID>
    <DESCRIPTION>The coisogenic control strain for the TRMR strain (NBRP No.0016).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140416</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Eno2-Vcp)16Kakiz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=948&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=948&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140416</CITATION_ID>
    <DESCRIPTION>This transgenic strain was generated by microinjection into Slc:SD fertilized eggs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4140469</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Kmch&lt;/i&gt;/NSlc</STRAIN_SYMBOL>
    <FULL_NAME>Komachi</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=726&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=726&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4140469</CITATION_ID>
    <DESCRIPTION>from NBRP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4142540</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D4Rat10-D4Rat15&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=941&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=941&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="51085655" STOP_POS="51085803" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="29593287" STOP_POS="50119996" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="26753655" STOP_POS="48656399" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="26659360" STOP_POS="48448808" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="26280781" STOP_POS="47890193" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4142540</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by crossing between WKY/Izm and SHR/Izm in 2001. Heterozygous consomic rats were established in 2004, homozygous consomic rats were established in 2005, and homozygous congenic rats were established by crossing among consomic heterozygous rats in 2009.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4142541</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Tek-GFP)1Soh</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=943&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=943&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4142541</CITATION_ID>
    <DESCRIPTION>This transgenic strain was generated by microinjection into fertilized oocytes of Wistar rats. The vector containing the Tek/GFP plasmid (pSP14/15.t2hgfpPan5) was a gift from Dr. TN Sato of University of Texas Southwestern Medical Center at Dallas. The transgene was excised from the plasmid vector by Sal I digestion.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4142542</RGD_ID>
    <STRAIN_SYMBOL>BN.SDT-&lt;i&gt;Gluco14&lt;/i&gt;/Nyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=945&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=945&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4142542</CITATION_ID>
    <DESCRIPTION>The Gluco14 region, one of the significant QTL for glucose intolerance of SDT/Jcl was transferred onto the genetic background of BN/Seac strain. Established by speed congenic method since 2003 and afterwards maintained by sib mating (N6F10, July 2010) Please refer to STD.BN-Gluco14/Nyo.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4142543</RGD_ID>
    <STRAIN_SYMBOL>BN.SDT-&lt;i&gt;Gluco13&lt;/i&gt;/Nyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=944&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=944&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4142543</CITATION_ID>
    <DESCRIPTION>The Gluco13 region, one of the significant QTL for glucose intolerance of SDT/Jcl was transferred onto the genetic background of BN/Seac strain. Established by speed congenic method since 2003 and afterwards maintained by sib mating (N6F11, July 2010). Please refer to STD.BN-Gluco13/Nyo.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4142544</RGD_ID>
    <STRAIN_SYMBOL>WKY/Kiha</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=930&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=930&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4142544</CITATION_ID>
    <DESCRIPTION>A WKY rat showing higher serum adiponectin concentration was found in Department of Pathology, Kinki University School of Medicine. In 1974, this strain was transferred from Dr. Okamoto to Kyoto University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4142545</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D3Rat108-D3Rat166&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=937&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=937&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="82341288" STOP_POS="122654872" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="61934079" STOP_POS="102200699" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="63849481" STOP_POS="106900596" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="70419858" STOP_POS="113470358" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="59676608" STOP_POS="101359980" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4142545</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by crossing between WKY/Izm and SHR/Izm in 2001. Heterozygous consomic rats were established in 2004, homozygous consomic rats were established in 2005, and homozygous congenic rats were established by crossing among consomic heterozygous rats in 2009.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4142546</RGD_ID>
    <STRAIN_SYMBOL>AMI/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=929&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=929&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Dentistry</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4142546</CITATION_ID>
    <DESCRIPTION>Rats which showed a dental mutation such as morphological abnormalities of the teeth were found in the SHR-SP rats at Daiichi Seiyaku, Co., Ltd. in 1981. Transferred to Tokushima University in 2003.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4142547</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D4Wox27-D4Rat11&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=940&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=940&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="5218294" STOP_POS="36405277" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="3044017" STOP_POS="34379894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="3096322" STOP_POS="34240072" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="460493" STOP_POS="33407710" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4142547</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by crossing between WKY/Izm and SHR/Izm in 2001. Heterozygous consomic rats were established in 2004, homozygous consomic rats were established in 2005, and homozygous congenic rats were established by crossing among consomic heterozygous rats in 2009.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4142548</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D4Wox27-D4Rat10&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=939&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=939&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="5218294" STOP_POS="29593455" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="3044017" STOP_POS="26753822" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="3096322" STOP_POS="26659527" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="460493" STOP_POS="26280949" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4142548</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by crossing between WKY/Izm and SHR/Izm in 2001. Heterozygous consomic rats were established in 2004, homozygous consomic rats were established in 2005, and homozygous congenic rats were established by crossing among consomic heterozygous rats in 2009.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4142549</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D4Wox27-D4Rat4&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=938&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=938&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="8669431" STOP_POS="8669604" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="5218294" STOP_POS="7935781" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="3044017" STOP_POS="4364885" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="3096322" STOP_POS="4400584" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="460493" STOP_POS="3237361" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4142549</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by crossing between WKY/Izm and SHR/Izm in 2001. Heterozygous consomic rats were established in 2004, homozygous consomic rats were established in 2005, and homozygous congenic rats were established by crossing among consomic heterozygous rats in 2009.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4142550</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D4Rat101-D4Rat15&lt;/i&gt;)/IzmTkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=942&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=942&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="50097716" STOP_POS="51085803" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="49131906" STOP_POS="50119996" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="46898276" STOP_POS="48656399" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="46704280" STOP_POS="48448808" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="46605924" STOP_POS="47890193" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4142550</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by crossing between WKY/Izm and SHR/Izm in 2001. Heterozygous consomic rats were established in 2004, homozygous consomic rats were established in 2005, and homozygous congenic rats were established by crossing among consomic heterozygous rats in 2009.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4142799</RGD_ID>
    <STRAIN_SYMBOL>LEW.SS-(&lt;i&gt;D2Uia5-D2Rat143&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="105447770" STOP_POS="105448034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="15575840" STOP_POS="103519040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="13328947" STOP_POS="106156987" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="13186164" STOP_POS="125885146" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="13909383" STOP_POS="106236206" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4142799</CITATION_ID>
    <DESCRIPTION>LEW/Crlc and SS/Jr were backcrossed for 5 generations, then BC5 rat was mated with SS/Jr to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4142800</RGD_ID>
    <STRAIN_SYMBOL>LEW.SS-(&lt;i&gt;D18Chm31-D18Mit8&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="59796478" STOP_POS="59796643" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="2745212" STOP_POS="61985812" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="2761846" STOP_POS="61177004" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="2848113" STOP_POS="62229060" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4142800</CITATION_ID>
    <DESCRIPTION>LEW/Crlc and SS/Jr were backcrossed for 5 generations, then BC5 rat was mated with SS/Jr to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4143165</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Aqp5-GFP)ZboroRrrc</STRAIN_SYMBOL>
    <FULL_NAME>Aqp5EGFP</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=427&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=427&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Aqp5</ALLELES>
    <ALLELE_RGD_IDS>2144</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00427</CITATION_ID>
    <DESCRIPTION>This rat model was developed by perivitelline injection of one cell SD embryos with packaged lentiviral particles containing the pFUGW  vector containing the Aqp5 promoter and the EGFP gene.  Resulting transgenic founders with mated to wild-type SD rats and heterozygous offspring were obtained.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4143456</RGD_ID>
    <STRAIN_SYMBOL>BN.GK-(&lt;i&gt;D2Wox30-D2Wox68&lt;/i&gt;)/Ox</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="49858934" STOP_POS="221200097" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4143456</CITATION_ID>
    <DESCRIPTION>This congenic strain is derived from GK rats which were from a colony in Paris (CNRS) obtained in 1995. BN rats were initially obtained from Charles River Laboratories, Margate, UK.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4143457</RGD_ID>
    <STRAIN_SYMBOL>BN.GK-(&lt;i&gt;D2Rat40-D2Wox35&lt;/i&gt;)/Ox</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="159440760" STOP_POS="230628534" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="157142078" STOP_POS="157142209" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="169852670" STOP_POS="244719662" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="189197858" STOP_POS="189197988" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="163154227" STOP_POS="163154358" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4143457</CITATION_ID>
    <DESCRIPTION>This congenic strain is derived from GK rats which were from a colony in Paris (CNRS) obtained in 1995. BN rats were initially obtained from Charles River Laboratories, Margate, UK.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4143458</RGD_ID>
    <STRAIN_SYMBOL>BN.GK-(&lt;i&gt;D2Wox49-D2Rat70&lt;/i&gt;)/Ox</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="183756199" STOP_POS="245889826" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="198335799" STOP_POS="263179188" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="217822782" STOP_POS="281850471" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="191000085" STOP_POS="254933362" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4143458</CITATION_ID>
    <DESCRIPTION>This congenic strain is derived from GK rats which were from a colony in Paris (CNRS) obtained in 1995. BN rats were initially obtained from Charles River Laboratories, Margate, UK.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4143459</RGD_ID>
    <STRAIN_SYMBOL>BN.GK-(&lt;i&gt;D2Rat40-D2Got149&lt;/i&gt;)/Ox</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="159440760" STOP_POS="159440891" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="157142078" STOP_POS="213653017" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="169852670" STOP_POS="229036415" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="189197858" STOP_POS="248391122" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="163154227" STOP_POS="222343164" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4143459</CITATION_ID>
    <DESCRIPTION>This congenic strain is derived from GK rats which were from a colony in Paris (CNRS) obtained in 1995. BN rats were initially obtained from Charles River Laboratories, Margate, UK.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4145088</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D6Rat119-D6Arb3&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="112483610" STOP_POS="112483760" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="106752656" STOP_POS="132339866" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="111134524" STOP_POS="138065254" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="120420333" STOP_POS="147057860" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="111239053" STOP_POS="138260635" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4145088</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-6BN/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4145089</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D6Rat149-D6Rat18&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="10894415" STOP_POS="89763029" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="7009971" STOP_POS="93706327" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="6959479" STOP_POS="103168177" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="7161389" STOP_POS="93374504" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4145089</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-6BN/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4145090</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D6Rat149-D6Got171&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="10894415" STOP_POS="118863044" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="7009971" STOP_POS="123598338" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="6959479" STOP_POS="132827005" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="7161389" STOP_POS="123782965" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4145090</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-6BN/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4145091</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D6Rat149-D6Arb3&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="10894415" STOP_POS="132339866" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="7009971" STOP_POS="138065254" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="6959479" STOP_POS="147057860" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="7161389" STOP_POS="138260635" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4145091</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-6&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4145374</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Mit18-D1Rat90&lt;/i&gt;)(&lt;i&gt;D14Rat98-D14Hmgc18&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4145374</CITATION_ID>
    <DESCRIPTION>Congenic strain developed by crossing ACI.FHH-(&lt;i&gt;D1Rat74-D1Rat90&lt;/i&gt;)/Eur (Rf-1a) males to ACI.FHH-(&lt;i&gt;D1Mit18-D1Rat90&lt;/i&gt;)(&lt;i&gt;D14Mit11-D14Rat33&lt;/i&gt;)(&lt;i&gt;D14Rat65-D14Rat90&lt;/i&gt;)/EurMcwi (Rf-1a+4) double congenic females</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4889411</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Smu13-D1Wox33&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Functional Pathology, Shimane University School of Medicine, Izumo, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1079&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio- Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="156170341" STOP_POS="156170557" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="166884926" STOP_POS="166885141" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="224991853" STOP_POS="224991955" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="173074640" STOP_POS="174300801" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="160754901" STOP_POS="160755065" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="198300754" STOP_POS="198300855" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4889411</CITATION_ID>
    <DESCRIPTION>About 100 male pups were obtained by breeding SHRSP/Izm and SHRSP.WKY-(&lt;i&gt;D1Smu13-D1Arb21&lt;/i&gt;)/Izm; one pup that had the right recombination was found and  backcrossed to the parental strain to get the hetrozygotes, which were then mated brother-sister to get the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4889414</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;D1Rat171-D1Wox33&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Functional Pathology, Shimane University School of Medicine, Izumo, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1081&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="165278545" STOP_POS="165278781" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="155866514" STOP_POS="155866750" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="166577232" STOP_POS="166577467" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="172767534" STOP_POS="174300801" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="224991853" STOP_POS="224991955" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="158964262" STOP_POS="160755065" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="198300754" STOP_POS="198300855" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4889414</CITATION_ID>
    <DESCRIPTION>About 100 male pups were obtained by breeding SHRSP/Izm and WKY.SHRSP-(&lt;i&gt;D1Smu13-D1Smu11&lt;/i&gt;)/Izm; one pup that had the right recombination was found and  backcrossed to the parental strain to get the hetrozygotes, which were then mated brother-sister to get the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4889450</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D1Rat248-D1Rat10&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="7746121" STOP_POS="7746362" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="5925877" STOP_POS="24697545" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="5655772" STOP_POS="85706974" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="7306802" STOP_POS="86917075" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="6253932" STOP_POS="25271177" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4889450</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini females were mated with PVG.1AV1/Kini males that had PVG allele within the Eae29 region, one breeding pair from N7 generation was intercrossed to give homozygous congenic that had PVG allele from the begining of chr1 to D1Rat10 (approximately 25.4 Mb)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4889464</RGD_ID>
    <STRAIN_SYMBOL>GK/Ox</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4889464</CITATION_ID>
    <DESCRIPTION>Original breeders are from a colony in Paris (CNRS URA 307, Paris, France) which were obtained in 1995 and since then bred locally in Oxford, UK</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4889499</RGD_ID>
    <STRAIN_SYMBOL>CDS-Chr 4&lt;sup&gt;CDR&lt;/sup&gt;/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hebrew University Hospital and Hadassah-Hebrew Medical College, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4889499</CITATION_ID>
    <DESCRIPTION>Homozygous male CDS/Ygl were bred with CDR/Ygl females; F&lt;sub&gt;1&lt;/sub&gt; heterozygotes were mated with parental female CDS/Ygl and backcrossed again for 8 times till the allele was fixed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4889817</RGD_ID>
    <STRAIN_SYMBOL>SBN-Chr 1&lt;sup&gt;SBH&lt;/sup&gt;/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hebrew University Hospital and Hadassah-Hebrew Medical College, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4889817</CITATION_ID>
    <DESCRIPTION>Homozygous male SBN/Ygl were bred with SBH/Ygl females; F&lt;sub&gt;1&lt;/sub&gt; heterozygotes were mated with parental female SBN/Ygl and backcrossed again for 8 times till the allele was fixed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4889820</RGD_ID>
    <STRAIN_SYMBOL>SBH-Chr 1&lt;sup&gt;SBN&lt;/sup&gt;/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hebrew University Hospital and Hadassah-Hebrew Medical College, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4889820</CITATION_ID>
    <DESCRIPTION>Homozygous male SBH/Ygl were bred with SBN/Ygl females; F&lt;sub&gt;1&lt;/sub&gt; heterozygotes were mated with parental female SBH/Ygl and backcrossed again for 8 times till the allele was fixed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4889822</RGD_ID>
    <STRAIN_SYMBOL>SBN-Chr 17&lt;sup&gt;SBH&lt;/sup&gt;/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hebrew University Hospital and Hadassah-Hebrew Medical College, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4889822</CITATION_ID>
    <DESCRIPTION>Homozygous male SBN/Ygl were bred with SBH/Ygl females; F&lt;sub&gt;1&lt;/sub&gt; heterozygotes were mated with parental female SBN/Ygl and backcrossed again for 8 times till the allele was fixed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4889875</RGD_ID>
    <STRAIN_SYMBOL>SBH-Chr 2&lt;sup&gt;SBN&lt;/sup&gt;/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hebrew University Hospital and Hadassah-Hebrew Medical College, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4889875</CITATION_ID>
    <DESCRIPTION>Homozygous male SBH/Ygl were bred with SBN/Ygl females; F&lt;sub&gt;1&lt;/sub&gt; heterozygotes were mated with parental female SBH/Ygl and backcrossed again for 8 times till the allele was fixed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4889877</RGD_ID>
    <STRAIN_SYMBOL>SBH-Chr 20&lt;sup&gt;SBN&lt;/sup&gt;/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hebrew University Hospital and Hadassah-Hebrew Medical College, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4889877</CITATION_ID>
    <DESCRIPTION>Homozygous male SBH/Ygl were bred with SBN/Ygl females; F&lt;sub&gt;1&lt;/sub&gt; heterozygotes were mated with parental female SBH/Ygl and backcrossed again for 8 times till the allele was fixed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4889879</RGD_ID>
    <STRAIN_SYMBOL>SBH-Chr X&lt;sup&gt;SBN&lt;/sup&gt;/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hebrew University Hospital and Hadassah-Hebrew Medical College, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4889879</CITATION_ID>
    <DESCRIPTION>Homozygous male SBH/Ygl were bred with SBN/Ygl females; F&lt;sub&gt;1&lt;/sub&gt; heterozygotes were mated with parental female SBH/Ygl and backcrossed again for 8 times till the allele was fixed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4889882</RGD_ID>
    <STRAIN_SYMBOL>SBH-Chr 17&lt;sup&gt;SBN&lt;/sup&gt;/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hebrew University Hospital and Hadassah-Hebrew Medical College, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4889882</CITATION_ID>
    <DESCRIPTION>Homozygous male SBH/Ygl were bred with SBN/Ygl females; F&lt;sub&gt;1&lt;/sub&gt; heterozygotes were mated with parental female SBH/Ygl and backcrossed again for 8 times till the allele was fixed</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4889890</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D17Rat8-D17Rat37&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1096&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="69669116" STOP_POS="69669283" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="21782841" STOP_POS="64759263" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="23522321" STOP_POS="68114865" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="25486196" STOP_POS="69844594" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="27618789" STOP_POS="75802944" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4889890</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini females were mated with PVG.1AV1/Kini males and offsprings were selected for the PVG allele of interest, one breeding pair from N8 generation was intercrossed to give homozygous congenic that had PVG allele from D17Rat8 to D17Rat37</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891048</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D7Rat73-D7Rat128&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Avpr1a|Cyp11b1|Cyp11b2|Tac3|Trhr|Cox6c|Kcnv1|Kcns2|Nxph4|Cyp11b3</ALLELES>
    <ALLELE_RGD_IDS>2185|2453|2454|3809|3904|620616|621264|621525|628723|727886</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="55498584" STOP_POS="116408088" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="53612714" STOP_POS="114528048" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="61047589" STOP_POS="124246733" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="61044919" STOP_POS="124236725" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="57326196" STOP_POS="121524220" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891048</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891051</RGD_ID>
    <STRAIN_SYMBOL>LEW.SS-(&lt;i&gt;D7Rat73-D7Rat128&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Avpr1a|Cyp11b1|Cyp11b2|Tac3|Trhr|Cox6c|Kcnv1|Kcns2|Nxph4|Cyp11b3</ALLELES>
    <ALLELE_RGD_IDS>2185|2453|2454|3809|3904|620616|621264|621525|628723|727886</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="55498584" STOP_POS="116408088" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="53612714" STOP_POS="114528048" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="61047589" STOP_POS="124246733" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="61044919" STOP_POS="124236725" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="57326196" STOP_POS="121524220" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891051</CITATION_ID>
    <DESCRIPTION>LEW/Crlc and SS/Jr were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891103</RGD_ID>
    <STRAIN_SYMBOL>WMI/EerRrrc</STRAIN_SYMBOL>
    <FULL_NAME>WKY most immobile</FULL_NAME>
    <ORIGINATION>Dept. of Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, Chicago, Illinois</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=973&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00973</CITATION_ID>
    <DESCRIPTION>3 pairs of WKY males and females with highest immobility and lowest climbing scores in the forced swim test were mated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891107</RGD_ID>
    <STRAIN_SYMBOL>WLI/EerRrrc</STRAIN_SYMBOL>
    <FULL_NAME>WKY least immobile</FULL_NAME>
    <ORIGINATION>Dept. of Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, Chicago, Illinois</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=967&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00967</CITATION_ID>
    <DESCRIPTION>3 pairs of WKY males and females with lowest immobility and highest climbing scores in the forced swim test were mated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891165</RGD_ID>
    <STRAIN_SYMBOL>Wig/Ymas</STRAIN_SYMBOL>
    <FULL_NAME>wiggling</FULL_NAME>
    <ORIGINATION>Human Stress Signal Research Center, National Institute of Advanced Industrial Science and Technology, Tsukuba, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891165</CITATION_ID>
    <DESCRIPTION>These are congenic wiggling rats established by transferring the wiggling gene from Long-Evans Cinnamon (LEC) to Wistar King-Aptekman/Hokkaido (WKAH) strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891380</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mco95-D9Mco98&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="82931146" STOP_POS="82931342" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="75403227" STOP_POS="75482161" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="81100315" STOP_POS="81180041" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="80867159" STOP_POS="80946065" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891380</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D9Mco95-Resp18&lt;/i&gt;)/Mco was crossed with SS/Jr to generate F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed to generate F&lt;sub&gt;2&lt;/sub&gt;, these were genotyped using markers throughout 73140156-74554694 region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891383</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mco98-Resp18&lt;/i&gt;)/1Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Resp18</ALLELES>
    <ALLELE_RGD_IDS>3555</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="82931146" STOP_POS="84220186" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="75481963" STOP_POS="76771824" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="81179848" STOP_POS="82477136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="80945872" STOP_POS="82246695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="74551809" STOP_POS="74558151" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891383</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D9Mco95-Resp18&lt;/i&gt;)/Mco was crossed with SS/Jr to generate F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed to generate F&lt;sub&gt;2&lt;/sub&gt;, these were genotyped using markers throughout 73140156-74554694 region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891386</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mco98-Resp18&lt;/i&gt;)/2Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Resp18</ALLELES>
    <ALLELE_RGD_IDS>3555</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="82931146" STOP_POS="84220186" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="75481963" STOP_POS="76771824" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="81179848" STOP_POS="82477136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="80945872" STOP_POS="82246695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="74551809" STOP_POS="74558151" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891386</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D9Mco95-Resp18&lt;/i&gt;)/Mco was crossed with SS/Jr to generate F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed to generate F&lt;sub&gt;2&lt;/sub&gt;, these were genotyped using markers throughout 73140156-74554694 region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891388</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mco95-D9Mco100&lt;/i&gt;)/1Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="75403227" STOP_POS="75990271" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="81100315" STOP_POS="81688944" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="80867159" STOP_POS="81453493" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891388</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D9Mco95-Resp18&lt;/i&gt;)/Mco was crossed with SS/Jr to generate F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed to generate F&lt;sub&gt;2&lt;/sub&gt;, these were genotyped using markers throughout 73140156-74554694 region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891390</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mco95-D9Mco100&lt;/i&gt;)/2Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="75403227" STOP_POS="75990271" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="81100315" STOP_POS="81688944" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="80867159" STOP_POS="81453493" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891390</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D9Mco95-Resp18&lt;/i&gt;)/Mco was crossed with SS/Jr to generate F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed to generate F&lt;sub&gt;2&lt;/sub&gt;, these were genotyped using markers throughout 73140156-74554694 region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891392</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mco95-D9Mco102&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="75403227" STOP_POS="76175576" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="81100315" STOP_POS="81878831" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="80867159" STOP_POS="81641213" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891392</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D9Mco95-Resp18&lt;/i&gt;)/Mco was crossed with SS/Jr to generate F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed to generate F&lt;sub&gt;2&lt;/sub&gt;, these were genotyped using markers throughout 73140156-74554694 region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891394</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mco101-Resp18&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Resp18</ALLELES>
    <ALLELE_RGD_IDS>3555</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="84213844" STOP_POS="84220186" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="76145766" STOP_POS="76771824" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="81847677" STOP_POS="82477136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="81611825" STOP_POS="82246695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="74551809" STOP_POS="74558151" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891394</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D9Mco95-Resp18&lt;/i&gt;)/Mco was crossed with SS/Jr to generate F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed to generate F&lt;sub&gt;2&lt;/sub&gt;, these were genotyped using markers throughout 73140156-74554694 region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891396</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mco72-Resp18&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Resp18</ALLELES>
    <ALLELE_RGD_IDS>3555</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="84213844" STOP_POS="84220186" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="47902208" STOP_POS="76771824" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="52686874" STOP_POS="82477136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52352690" STOP_POS="82246695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="44842118" STOP_POS="74558151" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891396</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D9Mco95-Resp18&lt;/i&gt;)/Mco was crossed with SS/Jr to generate F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed to generate F&lt;sub&gt;2&lt;/sub&gt;, these were genotyped using markers throughout 73140156-74554694 region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891400</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mco14-Resp18&lt;/i&gt;)/1Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Resp18</ALLELES>
    <ALLELE_RGD_IDS>3555</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="84213844" STOP_POS="84220186" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="76650629" STOP_POS="76771824" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="82356030" STOP_POS="82477136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="82125291" STOP_POS="82246695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="74436883" STOP_POS="74558151" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891400</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D9Mco95-Resp18&lt;/i&gt;)/Mco was crossed with SS/Jr to generate F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed to generate F&lt;sub&gt;2&lt;/sub&gt;, these were genotyped using markers throughout 73140156-74554694 region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891402</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mco14-Resp18&lt;/i&gt;)/2Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Resp18</ALLELES>
    <ALLELE_RGD_IDS>3555</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="84213844" STOP_POS="84220186" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="76650629" STOP_POS="76771824" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="82356030" STOP_POS="82477136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="82125291" STOP_POS="82246695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="74436883" STOP_POS="74558151" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891402</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D9Mco95-Resp18&lt;/i&gt;)/Mco was crossed with SS/Jr to generate F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed to generate F&lt;sub&gt;2&lt;/sub&gt;, these were genotyped using markers throughout 73140156-74554694 region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4891404</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D9Mco14-Resp18&lt;/i&gt;)/3Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Resp18</ALLELES>
    <ALLELE_RGD_IDS>3555</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="84213844" STOP_POS="84220186" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="76650629" STOP_POS="76771824" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="82356030" STOP_POS="82477136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="82125291" STOP_POS="82246695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="74436883" STOP_POS="74558151" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4891404</CITATION_ID>
    <DESCRIPTION>SS.SR-(&lt;i&gt;D9Mco95-Resp18&lt;/i&gt;)/Mco was crossed with SS/Jr to generate F&lt;sub&gt;1&lt;/sub&gt; which were intercrossed to generate F&lt;sub&gt;2&lt;/sub&gt;, these were genotyped using markers throughout 73140156-74554694 region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>4892563</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Rat26-D5Uwm42&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="152279613" STOP_POS="152279821" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="113558156" STOP_POS="146996127" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="117554114" STOP_POS="153097789" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="121495621" STOP_POS="156871691" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="119332868" STOP_POS="153554465" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_4892563</CITATION_ID>
    <DESCRIPTION>WKY/NHsd rats were mated with WF/NHsd and the progeny was backcrossed to WF for 8-9 generations, selecting for Mcs5 region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5130721</RGD_ID>
    <STRAIN_SYMBOL>HXB1/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5130721</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131094</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Lx&lt;/i&gt;/CubPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131094</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131095</RGD_ID>
    <STRAIN_SYMBOL>BXH13/CubPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131095</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131097</RGD_ID>
    <STRAIN_SYMBOL>BXH12/CubPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131097</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131099</RGD_ID>
    <STRAIN_SYMBOL>BXH11/CubPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131099</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131101</RGD_ID>
    <STRAIN_SYMBOL>BXH10/CubPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131101</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131104</RGD_ID>
    <STRAIN_SYMBOL>BXH9/CubPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131104</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131106</RGD_ID>
    <STRAIN_SYMBOL>BXH8/CubPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131106</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131108</RGD_ID>
    <STRAIN_SYMBOL>BXH6/CubPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131108</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock BXH6/Cub provided by Dr. Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131110</RGD_ID>
    <STRAIN_SYMBOL>BXH5/CubPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131110</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131113</RGD_ID>
    <STRAIN_SYMBOL>HXB31/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131113</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131115</RGD_ID>
    <STRAIN_SYMBOL>HXB29/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131115</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131118</RGD_ID>
    <STRAIN_SYMBOL>HXB27/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131118</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131120</RGD_ID>
    <STRAIN_SYMBOL>HXB26/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131120</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131122</RGD_ID>
    <STRAIN_SYMBOL>HXB25/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131122</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131124</RGD_ID>
    <STRAIN_SYMBOL>HXB23/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131124</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131126</RGD_ID>
    <STRAIN_SYMBOL>HXB20/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131126</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131128</RGD_ID>
    <STRAIN_SYMBOL>HXB17/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131128</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131130</RGD_ID>
    <STRAIN_SYMBOL>HXB15/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131130</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131132</RGD_ID>
    <STRAIN_SYMBOL>HXB13/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131132</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131134</RGD_ID>
    <STRAIN_SYMBOL>HXB10/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131134</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained by Printz laboratory for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131136</RGD_ID>
    <STRAIN_SYMBOL>HXB7/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131136</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131138</RGD_ID>
    <STRAIN_SYMBOL>HXB4/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131138</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131140</RGD_ID>
    <STRAIN_SYMBOL>HXB3/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131140</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131142</RGD_ID>
    <STRAIN_SYMBOL>HXB2/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131142</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131144</RGD_ID>
    <STRAIN_SYMBOL>HXB18/IpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131144</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained for over 20 generations and verified by PLS phenotyping and microsatellite genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131910</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Acad10&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Acad10&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131905</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="40561900" STOP_POS="40604378" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="34901211" STOP_POS="34943973" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="40458754" STOP_POS="40458763" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="42285817" STOP_POS="42328189" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="36070275" STOP_POS="36075844" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131910</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GAAAGCTGCCCACCTCATGgatgtgGCCGGAAACAAGGTGGGA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131911</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Alms1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Alms1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131906</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="119683085" STOP_POS="119783471" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="118125581" STOP_POS="118226005" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="117371972" STOP_POS="117371988" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="181947469" STOP_POS="182048235" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="119846037" STOP_POS="119946085" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131911</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CCCGCCTCCGACTCCGCCtccgtcCTCCCGGCACCAGTA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 17-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131912</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Aldh2&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Aldh2&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131907</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="40610244" STOP_POS="40643220" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="34949549" STOP_POS="34982527" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="40486398" STOP_POS="40486404" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="42334057" STOP_POS="42366049" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="36081778" STOP_POS="36116445" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131912</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence AACGGCAAGCCTTATGtcatcTCCTACCTGGTGGAT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131920</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Apoe&lt;sup&gt;em8Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Apoe&lt;sup&gt;em8Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131915</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="88481889" STOP_POS="88485816" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="79353924" STOP_POS="79357852" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="80612894" STOP_POS="80616820" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="81878372" STOP_POS="81882298" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="79003634" STOP_POS="79006387" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131920</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CAGGCCCTGAACCGCttctggGATTACCTGCGCTGGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 24-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131921</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Apoe&lt;sup&gt;em7Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Apoe&lt;sup&gt;em7Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131918</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="88481889" STOP_POS="88485816" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="79353924" STOP_POS="79357852" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="80612894" STOP_POS="80616820" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="81878372" STOP_POS="81882298" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="79003634" STOP_POS="79006387" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131921</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CAGGCCCTGAACCGCttctggGATTACCTGCGCTGGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 15-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131922</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cdh13&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cdh13&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131919</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="63258251" STOP_POS="64296122" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="46349562" STOP_POS="47387462" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="50848896" STOP_POS="50848903" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="61621434" STOP_POS="62720155" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="48507173" STOP_POS="49575123" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131922</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTCACCCTGTGCGTCctgctgTCCCAGGTAGGGAATG into SS/JrHsdMcwi rat embryos. The resulting mutation is an 8-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131932</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp1a1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131928</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="66991940" STOP_POS="66998014" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="58096021" STOP_POS="58102130" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="62476212" STOP_POS="62476230" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="62249046" STOP_POS="62255081" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="61462207" STOP_POS="61468237" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131932</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGGTAACCAACCCTAGGatacagAGAAAGATCCAGGAGGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 19-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131933</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cyba&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyba&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131930</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="67396143" STOP_POS="67404214" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="50487598" STOP_POS="50495669" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="55257747" STOP_POS="55257782" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="65959818" STOP_POS="65967224" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="52713150" STOP_POS="52721609" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131933</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CGAGTGGGCCATgtgggCCAACGAACAGGCGC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 36-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131934</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp1a1&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131929</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="66991940" STOP_POS="66998014" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="58096021" STOP_POS="58102130" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="62472087" STOP_POS="62478122" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="62249046" STOP_POS="62255081" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="61462207" STOP_POS="61468237" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131934</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGGTAACCAACCCTAGGatacagAGAAAGATCCAGGAGGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is an 8-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131950</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Msra&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Msra&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131945</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="42514818" STOP_POS="42853278" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="38676395" STOP_POS="38676412" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="47488333" STOP_POS="47800662" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="51307920" STOP_POS="51550758" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="43509775" STOP_POS="43756283" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131950</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTCATCTTCGAAGGTCatcagcGCGGAGGAAGCT into SS/JrHsdMcwi rat embryos. The resulting mutation is an 18-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131951</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Prokr1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prokr1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131947</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="121579630" STOP_POS="121590695" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="120022301" STOP_POS="120033367" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="119375790" STOP_POS="119386551" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="183939201" STOP_POS="183949822" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="121750651" STOP_POS="121758116" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131951</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CGCCATGACCCTGTGCtatgcCAGGGTGTCCCGAGA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 126-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131952</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mas1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mas1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131946</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="50428064" STOP_POS="50459537" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="47910103" STOP_POS="47910112" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="48076761" STOP_POS="48108218" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="51644462" STOP_POS="51675365" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="42154786" STOP_POS="42185750" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131952</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CCTGGGGACTTCACACCCACccattcCCATAGTGCACTGGGT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131953</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Prokr1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prokr1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131948</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="121579630" STOP_POS="121590695" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="120022301" STOP_POS="120033367" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="119375790" STOP_POS="119386551" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="183939201" STOP_POS="183949822" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="121750651" STOP_POS="121758116" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131953</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CGCCATGACCCTGTGCtatgcCAGGGTGTCCCGAGA into SS/JrHsdMcwi rat embryos. The resulting mutation is an 11-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131954</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mstn&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mstn&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131949</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="55944513" STOP_POS="55950913" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="48452533" STOP_POS="48458933" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="53310977" STOP_POS="53315804" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52977371" STOP_POS="52982198" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="45426831" STOP_POS="45431658" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131954</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTTATTCCTTTGCAGCTGActttctAATGCAAGCGGATGGA into SS/JrHsdMcwi rat embryos. The resulting mutation is an 18-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131963</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nox4&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nox4&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131428</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150313736" STOP_POS="150491480" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="140900886" STOP_POS="141078844" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="150861998" STOP_POS="150862002" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157106652" STOP_POS="157285107" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143415816" STOP_POS="143603554" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131963</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ggttacagcttctacctatgcaataaggtaagggtc into SS/JrHsdMcwi rat embryos. The resulting mutation is a 5-bp frameshift deletion in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131964</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mstn&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mstn&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131962</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="55944513" STOP_POS="55950913" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="48456663" STOP_POS="48456670" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="53310977" STOP_POS="53315804" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52977371" STOP_POS="52982198" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="45426831" STOP_POS="45431658" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131964</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTTATTCCTTTGCAGCTGActttctAATGCAAGCGGATGGA into SS/JrHsdMcwi rat embryos. The resulting mutation is an 8-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131965</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mthfr&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mthfr&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131961</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="163748346" STOP_POS="163768141" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="158467728" STOP_POS="158467755" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164844642" STOP_POS="164864360" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="168502556" STOP_POS="168522350" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="165112850" STOP_POS="165126885" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131965</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CCCCAGCCCCCGATCtgaggGCAGCAGCAGTGGCA into SS/JrHsdMcwi rat embryos. The resulting mutation is an 28-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131966</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plod1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Plod1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131960</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="163623847" STOP_POS="163650737" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="158340674" STOP_POS="158367581" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164720629" STOP_POS="164747071" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="168379092" STOP_POS="168405534" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="164987252" STOP_POS="165012581" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131966</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CATCGCTGCCGAATCttccagAACCTGGATGGAGCCTTG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131974</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rasgrp3&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rasgrp3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131968</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="25647386" STOP_POS="25745952" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="19914449" STOP_POS="19914451" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="21072634" STOP_POS="21171619" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="30966364" STOP_POS="31065175" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="19808453" STOP_POS="19871923" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131974</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TTCCCCCACAACACCTAATaagcctGTGGTACCCCTGGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a net insertion of 5-bp frameshift deletion in exon 12.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131975</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ptpn11&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ptpn11&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131970</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="41026079" STOP_POS="41085577" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="35390381" STOP_POS="35390397" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="40895515" STOP_POS="40955999" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="42762630" STOP_POS="42822760" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="36501886" STOP_POS="36558055" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131975</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTCTCCGTCCGCACTggtgaTGACAAAGGGGAGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 17-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131976</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ptpn11&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ptpn11&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131969</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="41026079" STOP_POS="41085577" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="35365436" STOP_POS="35424925" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="40895515" STOP_POS="40955999" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="42762630" STOP_POS="42822760" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="36501886" STOP_POS="36558055" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131976</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTCTCCGTCCGCACTggtgaTGACAAAGGGGAGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is an 84-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131987</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tgfb1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tgfb1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131986</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="90324312" STOP_POS="90340627" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="81196532" STOP_POS="81212848" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="82480875" STOP_POS="82497196" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="83742151" STOP_POS="83758472" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="80894705" STOP_POS="80911020" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131987</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGCTCCCACTCCCGTGGcttctAGTGCTGACGCCCGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 12-bp frameshift deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131988</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Wdr72&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Wdr72&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131978</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="83718897" STOP_POS="83902128" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="74838338" STOP_POS="75020938" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="80965734" STOP_POS="81125710" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="80586841" STOP_POS="80744090" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="78891358" STOP_POS="79050751" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131988</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CCCTTCCTTACAGGCATActgccaTCTGCGTAAGTGCATGCC into SS/JrHsdMcwi rat embryos. The resulting mutation is a net 5-bp frameshift deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131989</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tgfb1&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tgfb1&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131980</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="90324312" STOP_POS="90340627" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="81196532" STOP_POS="81212848" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="82480875" STOP_POS="82497196" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="83742151" STOP_POS="83758472" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="80894705" STOP_POS="80911020" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131989</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGCTCCCACTCCCGTGGcttctAGTGCTGACGCCCGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 22-bp frameshift deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131990</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Slc30a8&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc30a8&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131981</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="85481864" STOP_POS="85517255" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="83603467" STOP_POS="83603483" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="91832988" STOP_POS="91869329" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="92476024" STOP_POS="92512365" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="88583770" STOP_POS="88617145" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131990</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TATCACTGCCACAACagcttcAAGGCCACAGGGAACAGGTC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 17-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5131991</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Slc30a8&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc30a8&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131979</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="85481864" STOP_POS="85517255" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="83603469" STOP_POS="83603485" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="91832988" STOP_POS="91869329" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="92476024" STOP_POS="92512365" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="88583770" STOP_POS="88617145" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5131991</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TATCACTGCCACAACagcttcAAGGCCACAGGGAACAGGTC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 17-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5134683</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D7Rat171-D7Rat128&lt;/i&gt;)/1Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison, Wisconsin, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="22126597" STOP_POS="116408088" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="20238970" STOP_POS="114528048" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="26359973" STOP_POS="124246733" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="26490428" STOP_POS="124236725" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="22382724" STOP_POS="121524220" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5134683</CITATION_ID>
    <DESCRIPTION>Chromosome 7 segment from WKY that had the Mcs6 QTL was introgressed into a WF genetic background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5134685</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D7Rat171-D7Rat128&lt;/i&gt;)/2Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison, Wisconsin, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="22126597" STOP_POS="116408088" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="20238970" STOP_POS="114528048" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="26359973" STOP_POS="124246733" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="26490428" STOP_POS="124236725" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="22382724" STOP_POS="121524220" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5134685</CITATION_ID>
    <DESCRIPTION>Chromosome 7 segment from WKY that had the Mcs6 QTL was introgressed into a WF genetic background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5134687</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D7Rat51-D7Rat128&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison, Wisconsin, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="49137999" STOP_POS="116408088" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="47251783" STOP_POS="114528048" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="54534996" STOP_POS="124246733" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="54558231" STOP_POS="124236725" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="50833677" STOP_POS="121524220" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5134687</CITATION_ID>
    <DESCRIPTION>Chromosome 7 segment from WKY that had the Mcs6 QTL was introgressed into a WF genetic background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5134689</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D7Uwm25-D7Rat128&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison, Wisconsin, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="116407851" STOP_POS="116408088" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="81134174" STOP_POS="114528048" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="89283487" STOP_POS="124246733" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="89318050" STOP_POS="124236725" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="121523977" STOP_POS="121524220" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5134689</CITATION_ID>
    <DESCRIPTION>Chromosome 7 segment from WKY that had the Mcs6 QTL was introgressed into a WF genetic background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5134692</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D7Rat171-D7Rat45&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison, Wisconsin, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="22126597" STOP_POS="65788017" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="20238970" STOP_POS="63902784" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="26359973" STOP_POS="71352127" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="26490428" STOP_POS="71522360" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="22382724" STOP_POS="68057251" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5134692</CITATION_ID>
    <DESCRIPTION>Chromosome 7 segment from WKY that had the Mcs6 QTL was introgressed into a WF genetic background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5134951</RGD_ID>
    <STRAIN_SYMBOL>WF.COP-(&lt;i&gt;D7Rat39-D7Uwm12&lt;/i&gt;)/1Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison, Wisconsin, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="83006128" STOP_POS="83006301" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="81116229" STOP_POS="81116402" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="89265543" STOP_POS="89265715" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="6276388" STOP_POS="89299904" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="4936703" STOP_POS="86007499" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5134951</CITATION_ID>
    <DESCRIPTION>Chromosome 7 segment from WKY that had the Mcs2 QTL was introgressed into a WF genetic background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5134953</RGD_ID>
    <STRAIN_SYMBOL>WF.COP-(&lt;i&gt;D7Rat39-D7Uwm12&lt;/i&gt;)/2Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison, Wisconsin, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="83006128" STOP_POS="83006301" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="81116229" STOP_POS="81116402" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="89265543" STOP_POS="89265715" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="6276388" STOP_POS="89299904" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="4936703" STOP_POS="86007499" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5134953</CITATION_ID>
    <DESCRIPTION>Chromosome 7 segment from WKY that had the Mcs2 QTL was introgressed into a WF genetic background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5135031</RGD_ID>
    <STRAIN_SYMBOL>BN.MES-&lt;i&gt;Cyba&lt;/i&gt;/Sna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Aging Biology, Institute on Aging and Adaptation, Shinshu University, Matsumoto, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyba&lt;sup&gt;mesSdi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13209000</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5135031</CITATION_ID>
    <DESCRIPTION>mutant Cyba gene from the MES/Slc strain is introduced into the background of BN/SsNSlc by standard procedures with seven backcrosses to BN/SsNSlc</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5135472</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;I&gt;D5Uwm70-D5Rat32&lt;/I&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="137971639" STOP_POS="137971798" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="132686313" STOP_POS="132686472" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="138123799" STOP_POS="138123957" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="141933225" STOP_POS="141933383" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="139659415" STOP_POS="139659574" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5135472</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 5 transferred to the ACI/SegHsd strain background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5135473</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;I&gt;D5Uwm70-D5Got42&lt;/I&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="124160767" STOP_POS="124160948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="129038716" STOP_POS="129038896" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="132878119" STOP_POS="132878299" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="130756424" STOP_POS="130756605" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5135473</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 5 transferred to the ACI/SegHsd strain background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5135475</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;I&gt;D5Rat60-D5Rat115&lt;/I&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="106513672" STOP_POS="117535258" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="101467719" STOP_POS="112419733" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="105304453" STOP_POS="116395137" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="109291409" STOP_POS="120337480" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="106262697" STOP_POS="118138413" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5135475</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 5 transferred to the ACI/SegHsd strain background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5135477</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;I&gt;D5Uwm70-D5Mgh15&lt;/I&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="161165494" STOP_POS="161165651" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="167739539" STOP_POS="167739697" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="171364494" STOP_POS="171364652" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="167844579" STOP_POS="167844737" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5135477</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 5 transferred to the ACI/SegHsd strain background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5135479</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;I&gt;D5Rat113-D5Rat36&lt;/I&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="143398122" STOP_POS="143398338" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="73483796" STOP_POS="138113774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="75809470" STOP_POS="143846372" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="79957402" STOP_POS="147610238" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="76707366" STOP_POS="145187034" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5135479</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 5 transferred to the ACI/SegHsd strain background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5135481</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;I&gt;D5Mgh17-D5Rat98&lt;/I&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="19327036" STOP_POS="100820403" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="14529225" STOP_POS="95774399" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="14408903" STOP_POS="99421638" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="19190627" STOP_POS="103451257" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="14730738" STOP_POS="100017265" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5135481</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 5 transferred to the ACI/SegHsd strain background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143940</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Rat74-D1Rat90&lt;/i&gt;)/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pediatric Surgery, Erasmus Medical Center, Rotterdam, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="269633753" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="221264111" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="241482188" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="248763714" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="227005311" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143940</CITATION_ID>
    <DESCRIPTION>Congenic substrain that originated from ACI.FHH-(&lt;i&gt;D1Rat298-D1Rat90&lt;/i&gt;)/Eur</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143941</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Mit18-D1Rat90&lt;/i&gt;)(&lt;i&gt;D14Mit11-D14Rat33&lt;/i&gt;)(&lt;i&gt;D14Rat65-D14Rat90&lt;/i&gt;)/EurMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143941</CITATION_ID>
    <DESCRIPTION>Triple congenic ACI.FHH-(&lt;i&gt;D1Mit18-D1Rat90&lt;/i&gt;)(&lt;i&gt;D14Mit11-D14Rat33&lt;/i&gt;)(&lt;i&gt;D14Rat65-D14Rat90&lt;/i&gt;)/Eur from Erasmus Medical Center, Rotterdam, Netherlands now bred and housed at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143942</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Mit18-D1Rat90&lt;/i&gt;)(&lt;i&gt;D14Mit11-D14Rat33&lt;/i&gt;)(&lt;i&gt;D14Rat65-D14Rat90&lt;/i&gt;)/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pediatric Surgery, Erasmus Medical Center, Rotterdam, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143942</CITATION_ID>
    <DESCRIPTION>Triple congenic strain which was generated using the speed congenic strategy by backcrossing ACI/Eur and FHH/Eur parental strains. Rf-1A QTL region of chr 1 and Rf4 QTL region of chr 14 are introgressed in this strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143943</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D14Mit11-D14Rat82&lt;/i&gt;)/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pediatric Surgery, Erasmus Medical Center, Rotterdam, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="4001839" STOP_POS="28557852" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="3857038" STOP_POS="28203397" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="4878162" STOP_POS="30412508" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="4874267" STOP_POS="30225437" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="4995006" STOP_POS="30258439" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143943</CITATION_ID>
    <DESCRIPTION>Congenic strain generated by using the speed congenic strategy by backcrossing ACI/Eur and FHH/Eur parental strains. Rf4 QTL region of chr 14 is introgressed in this strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143984</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plekha7&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Plekha7&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143978</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="179798856" STOP_POS="179982155" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="170364524" STOP_POS="170547843" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="185483638" STOP_POS="185483657" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="192397589" STOP_POS="192463974" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="174249022" STOP_POS="174316226" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143984</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CCTCTGCCCAGCTACgtcatcTCCCCGGTGGCCCCCGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 16-bp frameshift deletion in exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143985</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mstn&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mstn&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143964</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="55944513" STOP_POS="55950913" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="48456663" STOP_POS="48456680" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="53310977" STOP_POS="53315804" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52977371" STOP_POS="52982198" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="45426831" STOP_POS="45431658" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143985</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTTATTCCTTTGCAGCTGActttctAATGCAAGCGGATGGA into SS/JrHsdMcwi rat embryos. The resulting mutation deletes part of exon 2 and its splice acceptor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143986</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ulk3&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ulk3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143968</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="66888820" STOP_POS="66895380" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="57992396" STOP_POS="58000220" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="62368548" STOP_POS="62375229" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="62146130" STOP_POS="62152150" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="61343722" STOP_POS="61348824" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143986</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CGCTCTACATGGCTCCTGAgatggtGTGTCGGCGGCAGTA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143987</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Gpr183&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gpr183&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143961</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="105445129" STOP_POS="105457192" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="99037764" STOP_POS="99050550" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="108365659" STOP_POS="108365666" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="111751148" STOP_POS="111763869" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="107056367" STOP_POS="107067887" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143987</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGCCACTGCTCCtcaaaCCCATGTCTAAGCAGGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is an 8-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143988</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Gpr183&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gpr183&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143955</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="105445129" STOP_POS="105457192" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="99037764" STOP_POS="99050550" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="108365665" STOP_POS="108365668" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="111751148" STOP_POS="111763869" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="107056367" STOP_POS="107067887" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143988</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGCCACTGCTCCtcaaaCCCATGTCTAAGCAGGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 4-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143989</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Agtrap&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Agtrap&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143963</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="163795448" STOP_POS="163795531" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="158512310" STOP_POS="158512393" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164891661" STOP_POS="164891744" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164891661" STOP_POS="164891744" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="168546202" STOP_POS="168556520" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="165154252" STOP_POS="165164570" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143989</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ATCCTGGCCCTGGGTgtgtggGCTGTGGCCCAGCGG into SS/JrHsdMcwi rat embryos. The resulting mutation is an 84-bp mutation deleting part of exon 3 and the splice acceptor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143990</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ulk3&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ulk3&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143971</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="66888820" STOP_POS="66895380" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="57992396" STOP_POS="58000220" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="62368548" STOP_POS="62375229" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="62146130" STOP_POS="62152150" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="61343722" STOP_POS="61348824" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143990</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CGCTCTACATGGCTCCTGAgatggtGTGTCGGCGGCAGTA into SS/JrHsdMcwi rat embryos. The resulting mutation is an 88-bp frameshift deletion in exon 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143991</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Gpr183&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gpr183&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143957</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="105445129" STOP_POS="105457192" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="99037764" STOP_POS="99050550" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="108365661" STOP_POS="108365667" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="111751148" STOP_POS="111763869" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="107056367" STOP_POS="107067887" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143991</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGCCACTGCTCCtcaaaCCCATGTCTAAGCAGGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143992</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rasgrp3&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rasgrp3&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143946</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="25647386" STOP_POS="25745952" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="19914439" STOP_POS="19914458" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="21072634" STOP_POS="21171619" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="30966364" STOP_POS="31065175" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="19808453" STOP_POS="19871923" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143992</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TTCCCCCACAACACCTAATaagcctGTGGTACCCCTGGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 20-bp frameshift deletion in exon 12.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143993</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plcd3&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Plcd3&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143954</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="88547717" STOP_POS="88547877" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="88047635" STOP_POS="88047795" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="91185702" STOP_POS="91185862" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="90937117" STOP_POS="90958001" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="92275081" STOP_POS="92275241" METHOD="8"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143993</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GCCCGCGTCATCCGAtagcagCACCAAAAGGCCCGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 161-bp deletion in exon 1 including the splice donor</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143994</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plcd3&lt;sup&gt;em7Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Plcd3&lt;sup&gt;em7Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143976</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="88526802" STOP_POS="88548116" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="88026707" STOP_POS="88048080" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="91164801" STOP_POS="91186054" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="90937117" STOP_POS="90958001" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="92234651" STOP_POS="92275433" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143994</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GCCCGCGTCATCCGAtagcagCACCAAAAGGCCCGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 142-bp deletion, overlapping the start codon</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143995</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plekha7&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Plekha7&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143979</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="179798856" STOP_POS="179982155" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="170420191" STOP_POS="170420209" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="185483638" STOP_POS="185483656" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="192397589" STOP_POS="192463974" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="174249022" STOP_POS="174316226" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143995</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CCTCTGCCCAGCTACgtcatcTCCCCGGTGGCCCCCGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 19-bp frameshift deletion in exon 8.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5143996</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Agtrap&lt;sup&gt;em8Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Agtrap&lt;sup&gt;em8Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143970</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="163795365" STOP_POS="163795464" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="158512227" STOP_POS="158512326" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164891578" STOP_POS="164891677" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164891578" STOP_POS="164891677" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="168546202" STOP_POS="168556520" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="165154252" STOP_POS="165164570" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5143996</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ATCCTGGCCCTGGGTgtgtggGCTGTGGCCCAGCGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 100-bp mutation deleting part of exon 3 and the splice acceptor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5144101</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnq1&lt;sup&gt;em14Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnq1&lt;sup&gt;em14Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5144083</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="207721134" STOP_POS="208054073" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="198291711" STOP_POS="198624683" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="216293087" STOP_POS="216630339" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="223154713" STOP_POS="223490458" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="203383401" STOP_POS="203803687" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5144101</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GTCTGCAGGCTGCCGCagcaagTACGTGGGCATCTGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 17-bp frameshift deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5144102</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Mit18-D1Rat90&lt;/i&gt;)(&lt;i&gt;D14Mit11-D14Rat33&lt;/i&gt;)(&lt;i&gt;D14Rat65-D14Rat90&lt;/i&gt;)/EurMcwi-&lt;i&gt;Asip&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Asip&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5144099</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="163933768" STOP_POS="164021377" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="143473584" STOP_POS="143561170" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="150492010" STOP_POS="150579870" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="156860395" STOP_POS="156949277" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="145445175" STOP_POS="145536831" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5144102</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence agccacctggtatttgaggagacgcttggagatgac into ACI.FHH(D1Mit18-D1Rat90)(D14Mit11-D14Rat33)(D14Rat65-D14Rat90) embryos. The result is a 5-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5144103</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ldlr&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ldlr&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5144090</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="28546191" STOP_POS="28569075" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="20270020" STOP_POS="20292981" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="22750425" STOP_POS="22773305" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="22804325" STOP_POS="22827199" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="20824040" STOP_POS="20846920" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5144103</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TGCATCCCCAGCCTGTGGgcctgcGACGGGGACCGGGAC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5144104</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ncf2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ncf2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5144089</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="67505492" STOP_POS="67536015" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="64958217" STOP_POS="64958221" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="70229196" STOP_POS="70229200" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="67806516" STOP_POS="67834105" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5144104</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTCTACTACAGCATGgagaagTAAGTGGTGTCGGAGTGT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 5-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5144105</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Hexim2&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Hexim2&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5144095</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="88572102" STOP_POS="88584856" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="88077870" STOP_POS="88084776" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="91217079" STOP_POS="91222841" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="90988728" STOP_POS="90994491" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="92306494" STOP_POS="92312256" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5144105</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CAGCCCACTCGGCCCggcctcTCCCCGCGCCCGGAC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5144106</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnq1&lt;sup&gt;em9Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnq1&lt;sup&gt;em9Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5144076</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="207721134" STOP_POS="208054073" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="198291711" STOP_POS="198624683" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="216293087" STOP_POS="216630339" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="223154713" STOP_POS="223490458" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="203383401" STOP_POS="203803687" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5144106</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GTCTGCAGGCTGCCGCagcaagTACGTGGGCATCTGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp frameshift deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5144107</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Itga9&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Itga9&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5144077</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="127185244" STOP_POS="127493296" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="118383417" STOP_POS="118383503" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="127271029" STOP_POS="127576709" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="126493359" STOP_POS="126795566" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="123526904" STOP_POS="123838241" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5144107</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GTCGGAGCCTTCCTGTCCgacagcGTGGTTCTCCTCAGGT into SS/JrHsdMcwi rat embryos. The resulting mutation is an 87-bp deletion containing part of exon 13 and its splice acceptor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5144108</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ldlr&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ldlr&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5144075</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="28546191" STOP_POS="28569075" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="20270020" STOP_POS="20292981" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="22750425" STOP_POS="22773305" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="22804325" STOP_POS="22827199" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="20824040" STOP_POS="20846920" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5144108</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TGCATCCCCAGCCTGTGGgcctgcGACGGGGACCGGGAC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5144110</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D5Mgh17-D5Mgh15&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="19327036" STOP_POS="19327247" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="14529225" STOP_POS="161165651" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="14408903" STOP_POS="167739697" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="19190627" STOP_POS="171364652" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="14730738" STOP_POS="167844737" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5144110</CITATION_ID>
    <DESCRIPTION>This congenic strain is developed by further genotyping ACI.BN-(&lt;i&gt;D5Mgh17-D5Rat205&lt;/i&gt;)/Shul.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5147594</RGD_ID>
    <STRAIN_SYMBOL>FHH.PCK-(&lt;i&gt;D9Rat35-D9Rat70&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pkhd1&lt;sup&gt;pck&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11535943</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="24717838" STOP_POS="24717971" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="17220476" STOP_POS="25268236" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="19794101" STOP_POS="29075268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="18672124" STOP_POS="27914444" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="12916127" STOP_POS="21667256" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5147594</CITATION_ID>
    <DESCRIPTION>A FHH/EurMcwi male was crossed with a PCK/CrljCrl-&lt;i&gt;Pkhd1&lt;sup&gt;pck&lt;/i&gt;&lt;/sup&gt;/Crl female, and the male progeny were backcrossed to FHH/EurMcwi females for five generations by marker assisted breeding. In each generation, males were genotyped by fluorescent genotyping for three markers within the Pkhd1 gene, and 98 markers evenly spaced throughout the genome.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5490515</RGD_ID>
    <STRAIN_SYMBOL>FHH.BN(&lt;i&gt;D1Rat265-D1Rat76&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="90664883" STOP_POS="224569684" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="94364073" STOP_POS="244992610" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="95453405" STOP_POS="252243871" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="90448902" STOP_POS="230411453" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5490515</CITATION_ID>
    <DESCRIPTION>desired segments from BN were introgressed in FHH background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5490516</RGD_ID>
    <STRAIN_SYMBOL>FHH.BN(&lt;i&gt;D14Rat80-D14Hmgc4&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="12630840" STOP_POS="12630978" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="12326866" STOP_POS="19848266" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="13971208" STOP_POS="21555302" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="13914610" STOP_POS="21463742" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="13778105" STOP_POS="21435476" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5490516</CITATION_ID>
    <DESCRIPTION>desired segments from BN were introgressed in FHH background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5490517</RGD_ID>
    <STRAIN_SYMBOL>FHH.BN(&lt;i&gt;D14Rat78-D14Hmgc4&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="16279376" STOP_POS="16279486" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="15995099" STOP_POS="19848266" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="17499969" STOP_POS="21555302" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="17417347" STOP_POS="21463742" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="17564855" STOP_POS="21435476" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5490517</CITATION_ID>
    <DESCRIPTION>desired segments from BN were introgressed in FHH background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508304</RGD_ID>
    <STRAIN_SYMBOL>WUN-&lt;i&gt;Abcc2&lt;sup&gt;TR-&lt;/i&gt;&lt;/sup&gt;/HsdRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Unilever maintained at the Amsterdam Academic Medical Center (AMC).</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=442&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2019-08-02)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abcc2|Abcc2&lt;sup&gt;TR-&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2366|12792941</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="252613875" STOP_POS="252672459" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="242664657" STOP_POS="242723239" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="263554426" STOP_POS="263612556" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="270999832" STOP_POS="271057750" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00442</CITATION_ID>
    <DESCRIPTION>Spontaneous 1-bp deletion mutation occurred on a Wistar This mutation at amino acid 393 resulting a frameshift and premature stop at position 401.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508305</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Dpp4&lt;sup&gt;DPPIV-&lt;/i&gt;&lt;/sup&gt;/DchcHsdRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=443&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=443&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-03-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dpp4&lt;sup&gt;DPPIV&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12792942</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="67370794" STOP_POS="67452422" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="46962233" STOP_POS="47043870" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="48291055" STOP_POS="48372672" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="54957146" STOP_POS="55038628" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="44279255" STOP_POS="44360283" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00443</CITATION_ID>
    <DESCRIPTION>The DPP4 mutant rat was a spontaneous mutation in Fischer 344 rats, which caused a deficiency in DPPIV, was identified by Dr. Douglas C. Hixson at Rhode Island Hospital.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508356</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Gucy1a3&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gucy1a3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508351</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="169716684" STOP_POS="169780360" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="167418615" STOP_POS="167482293" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="181045694" STOP_POS="181103321" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="200453480" STOP_POS="200515219" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="173756824" STOP_POS="173818316" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508356</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CCCTGCTTCTCCCCGGTAtcattAAAGCGGCTGCT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 14-bp frameshift deletion in exon 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508357</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tfdp2&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tfdp2&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508332</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="105640018" STOP_POS="105781026" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="96760459" STOP_POS="96901466" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="104040795" STOP_POS="104181228" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="103489105" STOP_POS="103629520" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="101256112" STOP_POS="101392512" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508357</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GTCTGAGTTTACcaatgcGAGTAACCATCTGGCAGCT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp frameshift deletion in exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508358</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Wdr72&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Wdr72&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508327</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="83749190" STOP_POS="83749202" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="74868610" STOP_POS="74868622" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="80974477" STOP_POS="80974489" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="80586841" STOP_POS="80744090" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="78891358" STOP_POS="79050751" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508358</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CCCTTCCTTACAGGCATActgccaTCTGCGTAAGTGCATGCC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 14-bp deletion in exon 3 and intron 3</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508359</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Prune&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prune&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508348</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="185519569" STOP_POS="185548402" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="182859142" STOP_POS="182859271" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="196427714" STOP_POS="196457105" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="215924545" STOP_POS="215954221" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="190165356" STOP_POS="190192807" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508359</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ACCTCCGGCTTCACCATGgaggacTACTTGCAGGAC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 130-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508360</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Dguok&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dguok&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508323</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="117544784" STOP_POS="117572414" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="115987101" STOP_POS="116014733" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="115180433" STOP_POS="115208061" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="179770727" STOP_POS="179798683" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="117697251" STOP_POS="117725383" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508360</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GTCGGTTCCTTCTGCgtagacTCCGAGCGTCTTTCCG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 9-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508361</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Bcas3&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bcas3&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508329</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="70711084" STOP_POS="71170492" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="70213710" STOP_POS="70673080" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="72756587" STOP_POS="72756593" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="72660671" STOP_POS="73177317" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="73617547" STOP_POS="74078190" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508361</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TGGATCTGTACTCACttcgtACGGGGGAGATGGTCAAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp frameshift deletion in exon 9.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508362</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ncf2&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ncf2&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508342</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="67505492" STOP_POS="67536015" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="64958078" STOP_POS="64958221" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="70226441" STOP_POS="70259019" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75197561" STOP_POS="75229600" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="67806516" STOP_POS="67834105" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508362</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTCTACTACAGCATGgagaagTAAGTGGTGTCGGAGTGT into SS/JrHsdMcwi rat embryos. The resulting mutation is a net 139-bp deletion of part of intron 1 and exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508363</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sorcs2&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sorcs2&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508326</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="78592290" STOP_POS="78960582" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="74711199" STOP_POS="74711203" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="79538911" STOP_POS="79912333" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="79176694" STOP_POS="79547823" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="79968072" STOP_POS="80344330" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508363</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CACATCAGCTTCCGCTCTgactggGAGCTGGTCAAGGTGGAC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 5-bp frameshift deletion in exon 15.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508364</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Prune&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prune&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508341</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="185519569" STOP_POS="185548402" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="182858954" STOP_POS="182859151" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="196427714" STOP_POS="196457105" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="215924545" STOP_POS="215954221" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="190165356" STOP_POS="190192807" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508364</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ACCTCCGGCTTCACCATGgaggacTACTTGCAGGAC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 198-bp deletion in the 5 prime URT and exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508365</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Agtr1a&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Agtr1a&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508318</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="34383397" STOP_POS="34435523" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="34173446" STOP_POS="34226892" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="35908756" STOP_POS="35908774" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="37217810" STOP_POS="37270540" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="40629318" STOP_POS="40684982" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508365</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTTTGCCCCTGTGGGCAGtctatACCGCTATGGAGTACCGCT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 19-bp frameshift deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508366</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tfdp2&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tfdp2&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508334</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="105640018" STOP_POS="105781026" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="96760459" STOP_POS="96901466" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="104040795" STOP_POS="104181228" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="103489105" STOP_POS="103629520" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="101256112" STOP_POS="101392512" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508366</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GTCTGAGTTTACcaatgcGAGTAACCATCTGGCAGCT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 16-bp frameshift deletion in exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508367</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ulk4&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ulk4&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508340</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="129799048" STOP_POS="129799061" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="120921518" STOP_POS="120921531" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="129883120" STOP_POS="129883133" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="128829597" STOP_POS="129125286" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="125992455" STOP_POS="126284263" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508367</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTACCTTGTAGCTACccaggtGAGGCTGTCTGATGAA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 14-bp deletion in exon 15 and intron 15</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508368</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Trafd1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trafd1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508352</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="40826251" STOP_POS="40840169" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="35165606" STOP_POS="35179525" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="40695520" STOP_POS="40709438" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="42562635" STOP_POS="42576553" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="36301824" STOP_POS="36315741" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508368</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGTGGTGCCCGGACagagcTGTGTGGCAGCTGTG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp frameshift deletion in exon 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508369</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Myadml2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Myadml2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508317</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="106420856" STOP_POS="106425899" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="105922557" STOP_POS="105927867" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="109822170" STOP_POS="109827328" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="109418559" STOP_POS="109420196" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="110039330" STOP_POS="110040967" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508369</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGATGGGCAGCACCATGgaccccCCGGGGGGTGCA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508370</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nppb&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nppb&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508324</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="163700406" STOP_POS="163700505" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="158417264" STOP_POS="158417363" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164796627" STOP_POS="164796726" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164796229" STOP_POS="164797531" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="168454278" STOP_POS="168455640" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="165062348" STOP_POS="165063650" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508370</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TTCCCAATTCGTCACAgaagctGCTGGAGCTGATAAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 100-bp deletion of part of intron 1 and exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508371</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mylip&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mylip&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508336</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="19492826" STOP_POS="19514490" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="19286649" STOP_POS="19308295" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="19682040" STOP_POS="19703681" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="21703590" STOP_POS="21725205" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="25308147" STOP_POS="25329887" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508371</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GCCCCAGCCATGCTGTGCtatgtGACGAGGCCGGACGCGGTG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 51-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508380</RGD_ID>
    <STRAIN_SYMBOL>SS-TgTn(T2ONC)2Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508380</CITATION_ID>
    <DESCRIPTION>These rats were made by pronuclear injection of a linear plasmid fragment containing a Sleeping Beauty oncogenic transposon harboring the CAG (chicken beta-actin/rabbit beta-globin hybrid promoter), the mouse Foxf2 exon 1 splice donor, and two Adenovirus 2 splice acceptors on opposite DNA strands.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508381</RGD_ID>
    <STRAIN_SYMBOL>SS-TgTn(T2ONC)1Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508381</CITATION_ID>
    <DESCRIPTION>These rats were made by pronuclear injection of a linear plasmid fragment containing a Sleeping Beauty oncogenic transposon harboring the CAG (chicken beta-actin/rabbit beta-globin hybrid promoter), the mouse Foxf2 exon 1 splice donor, and two Adenovirus 2 splice acceptors on opposite DNA strands.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508392</RGD_ID>
    <STRAIN_SYMBOL>HsdHlr:ZUC-&lt;i&gt;Lepr&lt;/i&gt;&lt;sup&gt;fa&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.envigo.com/model/hsdhlr-zucker-leprfa/&gt;Envigo&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.envigo.com/model/hsdhlr-zucker-leprfa/&gt;Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13432153</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508392</CITATION_ID>
    <DESCRIPTION>Derived from a colony obtained in 1992 from Hoffmann-la-Roche, Nutley, New Jersey.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508393</RGD_ID>
    <STRAIN_SYMBOL>BN/RijHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =http://www.envigo.com/model/bn-rijhsd/&gt;Envigo&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =http://www.envigo.com/model/bn-rijhsd/&gt;Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508393</CITATION_ID>
    <DESCRIPTION>These were derived from a nucleus colony obtained directly from the TNO Institute, the Netherlands now available at Envigo.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508394</RGD_ID>
    <STRAIN_SYMBOL>F344BNF1/Hsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan</SOURCE>
    <STRAIN_TYPE>hybrid</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508394</CITATION_ID>
    <DESCRIPTION>Offspring of a cross between the F344/NHsd inbred female and  a BN male rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508395</RGD_ID>
    <STRAIN_SYMBOL>Hsd:RH-&lt;i&gt;Foxn1&lt;/i&gt;&lt;sup&gt;rnu&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Athymic Nude</FULL_NAME>
    <ORIGINATION>&lt;a href =https://www.envigo.com/model/hsd-rh-foxn1rnu/&gt;Envigo&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.envigo.com/model/hsd-rh-foxn1rnu/&gt;Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508395</CITATION_ID>
    <DESCRIPTION>Derived from animals obtained from the Rowett Research Institute, Aberdeen, Scotland.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508396</RGD_ID>
    <STRAIN_SYMBOL>HsdRccHan:WIST</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;https://www.envigo.com/model/rcchan-wist&gt;ENVIGO&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508396</CITATION_ID>
    <DESCRIPTION>Derived at Biological Research Laboratories Limited (BRL), formerly RCC, now Harlan Laboratories Ltd., Fullinsdorf, Switzerland from original colony at Zentralinstitute fur Versuchstierzucht, Hannover in 1989. Transferred to Harlan Sprague-Dawley, Inc. in 1993 (nomenclature HsdHan:WIST). Harlan became Envigo in 2015.
In 2004 Envigo acquired RCC Ltd. and new breeding stock was transferred in 2008 (nomenclature RccHan:WIST). Unlike competitive models, the RccHan:WIST rat has been maintained from the original nucleus of 156 breeding pairs in Hannover, Germany.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508397</RGD_ID>
    <STRAIN_SYMBOL>HotHsd:SD</STRAIN_SYMBOL>
    <FULL_NAME>Sprague Dawley</FULL_NAME>
    <ORIGINATION>&lt;a href =https://www.envigo.com/model/hsdhot-holtzman-sd-&gt; Envigo&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.envigo.com/model/hsdhot-holtzman-sd-&gt; Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508397</CITATION_ID>
    <DESCRIPTION>Originally developed by the Holtzman Company in Madison, Wisconsin, from Sprague Dawley stock in 1947; to Harlan through acquisition in 1986.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5508398</RGD_ID>
    <STRAIN_SYMBOL>BluHsd:LE</STRAIN_SYMBOL>
    <FULL_NAME>Long Evans (Blue Spruce)</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href =https://www.inotivco.com/model/hsdblu-le&gt;Harlan/Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5508398</CITATION_ID>
    <DESCRIPTION>From the University of Rochester, Rochester, New York; to Blue Spruce Farms, Altamont, New York, in 1964; to Harlan through acquisition in 1988. Harlan became Envigo in 2015.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5509086</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D5Rat72-D5Rat36&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="120088729" STOP_POS="143398338" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="114973303" STOP_POS="138113774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="119124918" STOP_POS="143846372" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="123027973" STOP_POS="147610238" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="120983238" STOP_POS="145187034" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5509086</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 5 transferred to the ACI/SegHsd strain background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5509087</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D5Rat113-D5Rat159&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="120737641" STOP_POS="120737780" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="73483796" STOP_POS="73483994" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="75809470" STOP_POS="75809667" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="79957402" STOP_POS="79957599" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="76707366" STOP_POS="76707563" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5509087</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 5 transferred to the ACI/SegHsd strain background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5509988</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nppb&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nppb&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509979</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="163700409" STOP_POS="163700546" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="158417267" STOP_POS="158417404" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164796630" STOP_POS="164796767" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164796229" STOP_POS="164797531" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="168454278" STOP_POS="168455640" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="165062348" STOP_POS="165063650" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5509988</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TTCCCAATTCGTCACAgaagctGCTGGAGCTGATAAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 138-bp deletion of part of intron 1 and exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5509989</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Msra&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Msra&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509977</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="42514818" STOP_POS="42853278" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="38676398" STOP_POS="38676402" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="47488333" STOP_POS="47800662" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="51307920" STOP_POS="51550758" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="43509775" STOP_POS="43756283" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5509989</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTCATCTTCGAAGGTCatcagcGCGGAGGAAGCT into SS/JrHsdMcwi rat embryos. The resulting mutation is a net 1-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5509990</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp1a1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509976</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="66996026" STOP_POS="66996213" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="58100139" STOP_POS="58100326" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="62476131" STOP_POS="62476318" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="62476131" STOP_POS="62476318" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="62249046" STOP_POS="62255081" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="61462207" STOP_POS="61468237" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5509990</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGGTAACCAACCCTAGGatacagAGAAAGATCCAGGAGGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 188-bp deletion encompassing exon 4</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5509991</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mylip&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mylip&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508333</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="19492826" STOP_POS="19514490" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="19308054" STOP_POS="19308102" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="19682040" STOP_POS="19703681" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="21703590" STOP_POS="21725205" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="25308147" STOP_POS="25329887" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5509991</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into SS/JrHsdMcwi rat embryos. The resulting mutation is a 49-bp deletion and one G insertion causing frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5509992</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ube2q2&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ube2q2&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509987</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="64414502" STOP_POS="64474425" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="55518402" STOP_POS="55578342" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="59709972" STOP_POS="59754102" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="58292660" STOP_POS="58349722" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="58688257" STOP_POS="58749088" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5509992</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TGCTAGATCAACcactaCCCACGGGTCAGGTA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp frameshift deletion in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5509993</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tcf7l2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tcf7l2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509981</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="264865827" STOP_POS="264865995" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="254860546" STOP_POS="254860714" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="276686911" STOP_POS="276730517" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="283387566" STOP_POS="284118928" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="262031823" STOP_POS="262226710" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5509993</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GGAAGCCTCCAGAGCagacaaGCCCTCAAGGATGCC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 169-bp deletion of exon5 and intron 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5509994</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sh2b3&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sh2b3&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509982</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="40391755" STOP_POS="40414336" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="34750773" STOP_POS="34750773" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="40261990" STOP_POS="40265757" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="42132947" STOP_POS="42136714" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="35954679" STOP_POS="35958446" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5509994</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNS targeting the sequence ctcccccatcccacttgaatgtggagcagcctgtg into SS/JrHsdMcwi rat embryos. The resulting mutation is a 1-bp deletion in exon 7 in SS/JrHsdMcwi.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5509995</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Adra2a&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adra2a&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509986</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="263066780" STOP_POS="263069580" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="253061480" STOP_POS="253064280" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="274766841" STOP_POS="274766847" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="282178475" STOP_POS="282181275" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5509995</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CAGGCATCCCAGGATATCctggtcACAATGGGATACCGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 47-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5509996</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Stk39&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Stk39&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509978</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="73321522" STOP_POS="73588397" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="52913583" STOP_POS="53179060" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="54359449" STOP_POS="54625702" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="60973443" STOP_POS="61244306" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="50249626" STOP_POS="50517085" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5509996</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence AACAGCCATTGAattagCAACGGGAGCAGCGC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 24-bp frameshift deletion in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5509997</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat20-D13Got22&lt;/i&gt;)/Mcwi-&lt;i&gt;Nckap5&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nckap5&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509975</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="39922576" STOP_POS="40835849" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="37369948" STOP_POS="38283257" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="42265875" STOP_POS="43049232" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="47369687" STOP_POS="48273649" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="38444115" STOP_POS="39275959" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5509997</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ctctgaaccttcaactttcagatactgatgacaatgaa into SS.BN-(&lt;i&gt;D13Rat20-D13Got22&lt;/i&gt;)/Mcwi rat embryos. The resulting mutation is an 11-bp frameshift deletion in exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5529230</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Hmgc16-D1Rat225&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="263946994" STOP_POS="263947135" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="246983819" STOP_POS="246984013" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="267871151" STOP_POS="271693968" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="275301183" STOP_POS="283061559" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="261180160" STOP_POS="261180301" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5529230</CITATION_ID>
    <DESCRIPTION>desired segments from FHH/EurMcwi were introgressed in ACI/Eur background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5529529</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Hmgc1-D1Hmgc19&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="243559115" STOP_POS="249583894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="264446896" STOP_POS="270462479" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="271889649" STOP_POS="277901651" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="249745626" STOP_POS="249745784" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5529529</CITATION_ID>
    <DESCRIPTION>desired segments from FHH/EurMcwi were introgressed in ACI/Eur background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5529731</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Hmgc20-D1Hmgc21&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="258079463" STOP_POS="258079658" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="246355367" STOP_POS="248138424" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="267241552" STOP_POS="269024803" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="274674350" STOP_POS="276466399" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5529731</CITATION_ID>
    <DESCRIPTION>desired segments from FHH/EurMcwi were introgressed in ACI/Eur background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5683886</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;.SS-(&lt;i&gt;D12Arb13-D12Mit2&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="11869368" STOP_POS="11869600" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="6833190" STOP_POS="19611091" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="8249608" STOP_POS="22650918" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="10334114" STOP_POS="24663199" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="7382721" STOP_POS="20932776" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5683886</CITATION_ID>
    <DESCRIPTION>These were generated by crossing SS/JrHsdMcwi with SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5683888</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;.SS-(&lt;i&gt;D12Hmgc3-D12Rat79&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="40749055" STOP_POS="40749280" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="13008296" STOP_POS="35088624" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="15085585" STOP_POS="40618007" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="17102817" STOP_POS="42485122" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="36223785" STOP_POS="36224090" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5683888</CITATION_ID>
    <DESCRIPTION>These were generated by crossing SS/JrHsdMcwi with SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5683890</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;.SS-(&lt;i&gt;D12Hmgc3-D12Hmgc6&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="24849518" STOP_POS="24849755" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="13008296" STOP_POS="19212979" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="15085585" STOP_POS="22283507" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="17102817" STOP_POS="24300160" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5683890</CITATION_ID>
    <DESCRIPTION>These were generated by crossing SS/JrHsdMcwi with SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5685369</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Agtr1a&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Agtr1a&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508331</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="34383397" STOP_POS="34435523" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="34173446" STOP_POS="34226892" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="35908769" STOP_POS="35908770" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="37217810" STOP_POS="37270540" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="40629318" STOP_POS="40684982" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5685369</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTTTGCCCCTGTGGGCAGtctatACCGCTATGGAGTACCGCT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 2-bp frameshift deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686300</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Adra2a&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Adra2a&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Adra2a&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-07-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adra2a&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509986</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="263066780" STOP_POS="263069580" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="253061480" STOP_POS="253064280" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="274766841" STOP_POS="274766847" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="282178475" STOP_POS="282181275" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686300</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686302</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Adra2a&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Adra2a&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Adra2a&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686302</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686304</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Agtrap&lt;sup&gt;em4Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Agtrap&lt;sup&gt;em4Mcwi-&lt;/sup&gt;/Agtrap&lt;sup&gt;em4Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686304</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686306</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Agtrap&lt;sup&gt;em4Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Agtrap&lt;sup&gt;em4Mcwi+&lt;/sup&gt;/Agtrap&lt;sup&gt;em4Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686306</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686308</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Hexim2&lt;sup&gt;em4Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Hexim2&lt;sup&gt;em4Mcwi-&lt;/sup&gt;/Hexim2&lt;sup&gt;em4Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686308</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686311</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Hexim2&lt;sup&gt;em4Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Hexim2&lt;sup&gt;em4Mcwi+&lt;/sup&gt;/Hexim2&lt;sup&gt;em4Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686311</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686314</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rasgrp3&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Rasgrp3&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Rasgrp3&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686314</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686316</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rasgrp3&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Rasgrp3&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Rasgrp3&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686316</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686318</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sh2b3&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Sh2b3&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Sh2b3&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sh2b3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139858</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="40391755" STOP_POS="40414336" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="34750772" STOP_POS="34750777" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="40262913" STOP_POS="40262918" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="42132947" STOP_POS="42136714" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="35954679" STOP_POS="35958446" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686318</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders. The resulting mutation is an in-frame 6-bp deletion in exon 2 .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686320</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sh2b3&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Sh2b3&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Sh2b3&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686320</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686322</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sh2b3&lt;sup&gt;em1Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Sh2b3&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Sh2b3&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sh2b3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139858</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="40391755" STOP_POS="40414336" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="34750772" STOP_POS="34750777" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="40262913" STOP_POS="40262918" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="42132947" STOP_POS="42136714" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="35954679" STOP_POS="35958446" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686322</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686326</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ulk3&lt;sup&gt;em4Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ulk3&lt;sup&gt;em4Mcwi-&lt;/sup&gt;/Ulk3&lt;sup&gt;em4Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686326</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686328</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ulk3&lt;sup&gt;em4Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ulk3&lt;sup&gt;em4Mcwi+&lt;/sup&gt;/Ulk3&lt;sup&gt;em4Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686328</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686330</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ulk3&lt;sup&gt;em4Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ulk3&lt;sup&gt;em4Mcwi-&lt;/sup&gt;/Ulk3&lt;sup&gt;em4Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686330</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686332</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Wdr72&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Wdr72&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Wdr72&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686332</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686335</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Wdr72&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Wdr72&lt;sup&gt;em2Mcwi+&lt;/sup&gt;/Wdr72&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686335</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686652</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Agtr1a&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Agtr1a&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Agtr1a&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686652</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686654</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Agtr1a&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Agtr1a&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Agtr1a&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686654</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686657</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Agtr1a&lt;sup&gt;em5Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Agtr1a&lt;sup&gt;em5Mcwi-&lt;/sup&gt;/Agtr1a&lt;sup&gt;em5Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686657</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686659</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Agtrap&lt;sup&gt;em8Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Agtrap&lt;sup&gt;em8Mcwi-&lt;/sup&gt;/Agtrap&lt;sup&gt;em8Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686659</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686662</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Agtrap&lt;sup&gt;em8Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Agtrap&lt;sup&gt;em8Mcwi+&lt;/sup&gt;/Agtrap&lt;sup&gt;em8Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686662</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686664</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Aldh2&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Aldh2&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Aldh2&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686664</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686666</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Aldh2&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Aldh2&lt;sup&gt;em2Mcwi+&lt;/sup&gt;/Aldh2&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686666</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686668</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cdh13&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Cdh13&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Cdh13&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686668</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686670</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cdh13&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Cdh13&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Cdh13&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686670</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686672</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Cyp1a1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-11-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686672</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686676</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Cyp1a1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686676</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686678</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Cyp1a1&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686678</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686680</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em2Mcwi+&lt;/sup&gt;/Cyp1a1&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686680</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686684</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em5Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em5Mcwi-&lt;/sup&gt;/Cyp1a1&lt;sup&gt;em5Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686684</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686687</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em5Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Cyp1a1&lt;sup&gt;em5Mcwi+&lt;/sup&gt;/Cyp1a1&lt;sup&gt;em5Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686687</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686689</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Prokr1&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Prokr1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Prokr1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686689</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686692</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Prokr1&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Prokr1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Prokr1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686692</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686695</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Prokr1&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Prokr1&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Prokr1&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686695</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686697</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Prokr1&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Prokr1&lt;sup&gt;em2Mcwi+&lt;/sup&gt;/Prokr1&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686697</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686700</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnq1&lt;sup&gt;em14Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Kcnq1&lt;sup&gt;em14Mcwi-&lt;/sup&gt;/Kcnq1&lt;sup&gt;em14Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686700</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686702</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnq1&lt;sup&gt;em14Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Kcnq1&lt;sup&gt;em14Mcwi+&lt;/sup&gt;/Kcnq1&lt;sup&gt;em14Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686702</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686704</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Msra&lt;sup&gt;em3Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Msra&lt;sup&gt;em3Mcwi-&lt;/sup&gt;/Msra&lt;sup&gt;em3Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686704</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686706</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Msra&lt;sup&gt;em3Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Msra&lt;sup&gt;em3Mcwi+&lt;/sup&gt;/Msra&lt;sup&gt;em3Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686706</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686708</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Msra&lt;sup&gt;em4Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Msra&lt;sup&gt;em4Mcwi-&lt;/sup&gt;/Msra&lt;sup&gt;em4Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686708</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686710</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Msra&lt;sup&gt;em4Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Msra&lt;sup&gt;em4Mcwi+&lt;/sup&gt;/Msra&lt;sup&gt;em4Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686710</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686713</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mstn&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Mstn&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Mstn&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-07-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mstn&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143964</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="55944513" STOP_POS="55950913" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="48456663" STOP_POS="48456680" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="53310977" STOP_POS="53315804" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52977371" STOP_POS="52982198" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="45426831" STOP_POS="45431658" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686713</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686715</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mstn&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Mstn&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Mstn&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686715</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686718</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mstn&lt;sup&gt;em3Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Mstn&lt;sup&gt;em3Mcwi-&lt;/sup&gt;/Mstn&lt;sup&gt;em3Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-07-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mstn&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131962</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="55944513" STOP_POS="55950913" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="48456663" STOP_POS="48456670" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="53310977" STOP_POS="53315804" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52977371" STOP_POS="52982198" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="45426831" STOP_POS="45431658" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686718</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686721</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mstn&lt;sup&gt;em3Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Mstn&lt;sup&gt;em3Mcwi+&lt;/sup&gt;/Mstn&lt;sup&gt;em3Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686721</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686723</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mstn&lt;sup&gt;em3Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Mstn&lt;sup&gt;em3Mcwi-&lt;/sup&gt;/Mstn&lt;sup&gt;em3Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686723</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686725</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nppa&lt;sup&gt;em4Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nppa&lt;sup&gt;em4Mcwi-&lt;/sup&gt;/Nppa&lt;sup&gt;em4Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686725</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686728</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nppa&lt;sup&gt;em4Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nppa&lt;sup&gt;em4Mcwi+&lt;/sup&gt;&lt;/i&gt;/&lt;i&gt;Nppa&lt;sup&gt;em4Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686728</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686730</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nppb&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nppb&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;/&lt;i&gt;Nppb&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nppb&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508324</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="163700406" STOP_POS="163700505" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="158417264" STOP_POS="158417363" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164796229" STOP_POS="164797531" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164796627" STOP_POS="164796726" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="168454278" STOP_POS="168455640" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="165062348" STOP_POS="165063650" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686730</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686732</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nppb&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nppb&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;/&lt;i&gt;Nppb&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686732</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686734</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nppb&lt;sup&gt;em4Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nppb&lt;sup&gt;em4Mcwi-&lt;/sup&gt;/Nppb&lt;sup&gt;em4Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686734</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686736</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nppb&lt;sup&gt;em4Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nppb&lt;sup&gt;em4Mcwi+&lt;/sup&gt;/Nppb&lt;sup&gt;em4Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686736</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686738</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plcd3&lt;sup&gt;em4Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Plcd3&lt;sup&gt;em4Mcwi-&lt;/sup&gt;/Plcd3&lt;sup&gt;em4Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686738</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686740</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plcd3&lt;sup&gt;em4Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Plcd3&lt;sup&gt;em4Mcwi+&lt;/sup&gt;/Plcd3&lt;sup&gt;em4Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686740</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686742</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plcd3&lt;sup&gt;em7Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Plcd3&lt;sup&gt;em7Mcwi-&lt;/sup&gt;/Plcd3&lt;sup&gt;em7Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686742</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686744</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plcd3&lt;sup&gt;em7Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Plcd3&lt;sup&gt;em7Mcwi+&lt;/sup&gt;/Plcd3&lt;sup&gt;em7Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686744</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686747</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plekha7&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Plekha7&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Plekha7&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686747</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686749</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plekha7&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Plekha7&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Plekha7&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686749</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686758</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plekha7&lt;sup&gt;em4Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Plekha7&lt;sup&gt;em4Mcwi-&lt;/sup&gt;/Plekha7&lt;sup&gt;em4Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Plekha7&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5143979</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="179798856" STOP_POS="179982155" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="170420191" STOP_POS="170420209" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="185483638" STOP_POS="185483656" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="192397589" STOP_POS="192463974" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="174249022" STOP_POS="174316226" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686758</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686760</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plekha7&lt;sup&gt;em4Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Plekha7&lt;sup&gt;em4Mcwi+&lt;/sup&gt;/Plekha7&lt;sup&gt;em4Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686760</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686762</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plod1&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Plod1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Plod1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686762</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686764</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Plod1&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Plod1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Plod1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686764</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686766</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sh2b3&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Sh2b3&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Sh2b3&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sh2b3&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509982</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="40391755" STOP_POS="40414336" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="34750773" STOP_POS="34750773" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="40261990" STOP_POS="40265757" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="42132947" STOP_POS="42136714" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="35954679" STOP_POS="35958446" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686766</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686768</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Slc30a8&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Slc30a8&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Slc30a8&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686768</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686770</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Slc30a8&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Slc30a8&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Slc30a8&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686770</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686772</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Slc30a8&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Slc30a8&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Slc30a8&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686772</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686776</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Slc30a8&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Slc30a8&lt;sup&gt;em2Mcwi+&lt;/sup&gt;/Slc30a8&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686776</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686778</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Stk39&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Stk39&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Stk39&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Stk39&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509978</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="73321522" STOP_POS="73588397" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="52913583" STOP_POS="53179060" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="54359449" STOP_POS="54625702" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="60973443" STOP_POS="61244306" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="50249626" STOP_POS="50517085" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686778</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686780</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Stk39&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Stk39&lt;sup&gt;em2Mcwi+&lt;/sup&gt;/Stk39&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686780</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686782</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Stk39&lt;sup&gt;em2Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Stk39&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Stk39&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Stk39&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509978</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="73321522" STOP_POS="73588397" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="52913583" STOP_POS="53179060" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="54359449" STOP_POS="54625702" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="60973443" STOP_POS="61244306" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="50249626" STOP_POS="50517085" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686782</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686784</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tcf7l2&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Tcf7l2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Tcf7l2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tcf7l2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509981</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="264865827" STOP_POS="264865995" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="254860546" STOP_POS="254860714" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="276686911" STOP_POS="276730517" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="283387566" STOP_POS="284118928" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="262031823" STOP_POS="262226710" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686784</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686786</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tcf7l2&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Tcf7l2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Tcf7l2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686786</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686788</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tcf7l2&lt;sup&gt;em1Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Tcf7l2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Tcf7l2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tcf7l2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5509981</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="264865827" STOP_POS="264865995" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="254860546" STOP_POS="254860714" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="276686911" STOP_POS="276730517" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="283387566" STOP_POS="284118928" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="262031823" STOP_POS="262226710" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686788</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686790</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ulk3&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ulk3&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Ulk3&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686790</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686792</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ulk3&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ulk3&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Ulk3&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686792</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686794</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ulk3&lt;sup&gt;em1Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ulk3&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Ulk3&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686794</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686797</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Wdr72&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Wdr72&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Wdr72&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686797</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686799</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Wdr72&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Wdr72&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Wdr72&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686799</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686826</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Mit18-D1Rat90&lt;/i&gt;)(&lt;i&gt;D3Rat84-D3Rat59&lt;/i&gt;)(&lt;i&gt;D14Mit11-D14Rat33&lt;/i&gt;)(&lt;i&gt;D14Rat65-D14Rat90&lt;/i&gt;)/Eur</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pediatric Surgery, Erasmus Medical Center, Rotterdam, Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686826</CITATION_ID>
    <DESCRIPTION>Triple congenic strain which was generated using the speed congenic strategy by backcrossing ACI/Eur and FHH/Eur parental strains. Rf-1A QTL region of chr 1, Rf-3 QTL region of chr 3, and Rf4 QTL region of chr 14 are introgressed in this strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686829</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Mit18-D1Rat90&lt;/i&gt;)(&lt;i&gt;D3Rat6-D3Got149&lt;/i&gt;)(&lt;i&gt;D14Mit11-D14Rat33&lt;/i&gt;)(&lt;i&gt;D14Rat65-D14Rat90&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686829</CITATION_ID>
    <DESCRIPTION>Triple congenic strain which was generated using the speed congenic strategy by backcrossing ACI.FHH-(&lt;i&gt;D1Mit18-D1Rat90&lt;/i&gt;)(&lt;i&gt;D3Rat84-D3Rat59&lt;/i&gt;)(&lt;i&gt;D14Mit11-D14Rat33&lt;/i&gt;)(&lt;i&gt;D14Rat65-D14Rat90&lt;/i&gt;)/Eur and ACI.FHH-(&lt;i&gt;D1Mit18-D1Rat90&lt;/i&gt;)(&lt;i&gt;D14Mit11-D14Rat33&lt;/i&gt;)(&lt;i&gt;D14Rat65-D14Rat90&lt;/i&gt;)/EurMcwi.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5686832</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(&lt;i&gt;D1Mit18-D1Rat90&lt;/i&gt;)(&lt;i&gt;D3Got102-D3Got149&lt;/i&gt;)(&lt;i&gt;D14Mit11-D14Rat33&lt;/i&gt;)(&lt;i&gt;D14Rat65-D14Rat90&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5686832</CITATION_ID>
    <DESCRIPTION>Multicongenic strain which was generated using the speed congenic strategy by backcrossing ACI.FHH-(&lt;i&gt;D1Mit18-D1Rat90&lt;/i&gt;)(&lt;i&gt;D3Rat84-D3Rat59&lt;/i&gt;)(&lt;i&gt;D14Mit11-D14Rat33&lt;/i&gt;)(&lt;i&gt;D14Rat65-D14Rat90&lt;/i&gt;)/Eur and ACI.FHH-(&lt;i&gt;D1Mit18-D1Rat90&lt;/i&gt;)(&lt;i&gt;D14Mit11-D14Rat33&lt;/i&gt;)(&lt;i&gt;D14Rat65-D14Rat90&lt;/i&gt;)/EurMcwi.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687688</RGD_ID>
    <STRAIN_SYMBOL>FHH-Tg(CAG-Rab38)1Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687688</CITATION_ID>
    <DESCRIPTION>A Sleeping Beauty transposon expressing the wild type (BN strain) Rab38 coding sequence under the control of the ubiquitous chicken-actin-globin (CAG) promoter was injected into FHH embryos with a mRNA source of transposase to produce (CAG-Rab38) transgenic on FHH background. This transgene insertion mapped to chromosome 14, roughly 13.2-Mbp, and was more than 100-kbp away from the nearest gene (downstream of Antrx2).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687689</RGD_ID>
    <STRAIN_SYMBOL>FHH-Tg(CAG-Rab38)2Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687689</CITATION_ID>
    <DESCRIPTION>A Sleeping Beauty transposon expressing the wild type (BN strain) Rab38 coding sequence under the control of the ubiquitous chicken-actin-globin (CAG) promoter was injected into FHH embryos with a mRNA source of transposase to produce (CAG-Rab38) transgenic on FHH background. This transgene insertion in line 2 was found to be within a long interspersed nuclear element (LINE) sequence and could not be unambiguously mapped to a specific chromosome location.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687969</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D2Rat251-D2Mgh3&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="64243590" STOP_POS="64243877" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="8634571" STOP_POS="62516896" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="6155132" STOP_POS="63538449" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="6118364" STOP_POS="81156651" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="6332896" STOP_POS="63001078" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687969</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 2 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687971</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D2Rat10-D2Rat202&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="37756937" STOP_POS="53462005" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="36023184" STOP_POS="51729300" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="34967269" STOP_POS="52507805" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="54092967" STOP_POS="70871600" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="35874553" STOP_POS="51821161" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687971</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 2 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687973</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D18Rat30-D18Rat89&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="62992208" STOP_POS="62992419" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="5584537" STOP_POS="60722497" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="5825946" STOP_POS="62905769" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="5795276" STOP_POS="62092559" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="5682011" STOP_POS="63697215" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687973</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 18 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687974</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 5&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Cyp4a2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp4a2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687724</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="134160356" STOP_POS="134170908" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="128922355" STOP_POS="128934188" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="134196910" STOP_POS="134207888" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="137989327" STOP_POS="138000302" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="135765673" STOP_POS="135773006" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687974</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGCTCTATGACCCTGACTatgtgAAGGTGGTTCTGGGAAGAT into SS-Chr 5&lt;sup&gt;BN&lt;/sup&gt;/Mcwi strain rat embryos. The resulting mutation is a 2-bp framesnift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687975</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Prex1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prex1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687719</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="175724939" STOP_POS="175875764" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="155306950" STOP_POS="155456688" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="163329580" STOP_POS="163477822" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="169494331" STOP_POS="169575981" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="157693897" STOP_POS="157863943" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687975</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CAGTACTTCCGCTTCcatgcgGACGAGGAGATGGAA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 14-bp frameshift deletion in exon 16.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687977</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Acad10&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Acad10&lt;sup&gt;em2Mcwi+&lt;/sup&gt;/Acad10&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687977</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687979</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Acad10&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Acad10&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Acad10&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-07-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Acad10&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131905</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="40561900" STOP_POS="40604378" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="34901211" STOP_POS="34943973" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="40458754" STOP_POS="40458763" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="42285817" STOP_POS="42328189" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="36070275" STOP_POS="36075844" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687979</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders. The homozygous mutant carries a 10-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687981</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Alms1&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Alms1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Alms1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Alms1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5131906</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="119683085" STOP_POS="119783471" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="118125581" STOP_POS="118226005" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="117371972" STOP_POS="117371988" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="181947469" STOP_POS="182048235" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="119846037" STOP_POS="119946085" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687981</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687983</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Alms1&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Alms1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Alms1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687983</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687985</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Apoe&lt;sup&gt;em7Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Apoe&lt;sup&gt;em7Mcwi+&lt;/sup&gt;/Apoe&lt;sup&gt;em7Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687985</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687987</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Apoe&lt;sup&gt;em7Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Apoe&lt;sup&gt;em7Mcwi-&lt;/sup&gt;/Apoe&lt;sup&gt;em7Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687987</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687989</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Apoe&lt;sup&gt;em8Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Apoe&lt;sup&gt;em8Mcwi-&lt;/sup&gt;/Apoe&lt;sup&gt;em8Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687989</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687992</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Apoe&lt;sup&gt;em8Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Apoe&lt;sup&gt;em8Mcwi+&lt;/sup&gt;/Apoe&lt;sup&gt;em8Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687992</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687994</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Bcas3&lt;sup&gt;em4Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Bcas3&lt;sup&gt;em4Mcwi+&lt;/sup&gt;/Bcas3&lt;sup&gt;em4Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687994</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687996</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Bcas3&lt;sup&gt;em4Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Bcas3&lt;sup&gt;em4Mcwi-&lt;/sup&gt;/Bcas3&lt;sup&gt;em4Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687996</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5687998</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cyba&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Cyba&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Cyba&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5687998</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688000</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cyba&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Cyba&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Cyba&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688000</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688002</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 5&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Cyp4a2&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-Chr 5&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Cyp4a2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Cyp4a2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688002</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688004</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 5&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Cyp4a2&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-Chr 5&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Cyp4a2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Cyp4a2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688004</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688006</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 5&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Cyp4a2&lt;sup&gt;em1Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-Chr 5&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Cyp4a2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Cyp4a2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688006</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688008</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ets1&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ets1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Ets1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688008</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688010</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ets1&lt;sup&gt;em1Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ets1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Ets1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ets1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139856</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="39303936" STOP_POS="39426022" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="31045909" STOP_POS="31168010" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="33851478" STOP_POS="33851485" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="33798598" STOP_POS="33921593" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="32481694" STOP_POS="32545237" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688010</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688012</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Gpr183&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Gpr183&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Gpr183&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688012</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688014</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Gpr183&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Gpr183&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Gpr183&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688014</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688016</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Gpr183&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Gpr183&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Gpr183&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688016</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688018</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Gpr183&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Gpr183&lt;sup&gt;em2Mcwi+&lt;/sup&gt;/Gpr183&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688018</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688020</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Gpr183&lt;sup&gt;em3Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Gpr183&lt;sup&gt;em3Mcwi-&lt;/sup&gt;/Gpr183&lt;sup&gt;em3Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688020</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688022</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Gpr183&lt;sup&gt;em3Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Gpr183&lt;sup&gt;em3Mcwi+&lt;/sup&gt;/Gpr183&lt;sup&gt;em3Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688022</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688024</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Itga9&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Itga9&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Itga9&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688024</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688026</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mas1&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Mas1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Mas1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688026</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688028</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mas1&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Mas1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Mas1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2017-07-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688028</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688030</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mmp2&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Mmp2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Mmp2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mmp2&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139869</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="30327643" STOP_POS="30355856" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="14154657" STOP_POS="14182870" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="15542771" STOP_POS="15570589" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="26646695" STOP_POS="26646702" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="15246036" STOP_POS="15275061" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688030</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offspring which were intercrossed and offspring maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688032</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mmp2&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Mmp2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Mmp2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688032</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688034</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mmp2&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Mmp2&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Mmp2&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-07-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688034</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688037</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mmp2&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Mmp2&lt;sup&gt;em2Mcwi+&lt;/sup&gt;/Mmp2&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688037</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688039</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mthfr&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Mthfr&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Mthfr&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688039</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688041</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mthfr&lt;sup&gt;em1Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Mthfr&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Mthfr&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688041</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688043</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nckap5&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nckap5&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Nckap5&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nckap5&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139859</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="39922576" STOP_POS="40835849" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="37369948" STOP_POS="38283257" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="42265875" STOP_POS="43049232" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="47369687" STOP_POS="48273649" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="38444115" STOP_POS="39275959" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688043</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688045</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nckap5&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nckap5&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Nckap5&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688045</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688047</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nckap5&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nckap5&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Nckap5&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nckap5&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139862</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="39922576" STOP_POS="40835849" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="37369948" STOP_POS="38283257" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="42265875" STOP_POS="43049232" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="47369687" STOP_POS="48273649" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="38444115" STOP_POS="39275959" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688047</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688049</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nckap5&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nckap5&lt;sup&gt;em2Mcwi+&lt;/sup&gt;/Nckap5&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688049</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688051</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nckap5&lt;sup&gt;em3Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nckap5&lt;sup&gt;em3Mcwi-&lt;/sup&gt;/Nckap5&lt;sup&gt;em3Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nckap5&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139861</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="39922576" STOP_POS="40835849" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="37369948" STOP_POS="38283257" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="42265875" STOP_POS="43049232" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="47369687" STOP_POS="48273649" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="38444115" STOP_POS="39275959" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688051</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688053</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nckap5&lt;sup&gt;em3Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nckap5&lt;sup&gt;em3Mcwi+&lt;/sup&gt;/Nckap5&lt;sup&gt;em3Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688053</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688059</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat20-D13Got22&lt;/i&gt;)/Mcwi-&lt;i&gt;Nckap5&lt;sup&gt;em4Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS.BN-(&lt;i&gt;D13Rat20-D13Got22&lt;/i&gt;)/Mcwi-&lt;i&gt;Nckap5&lt;sup&gt;em4Mcwi-&lt;/sup&gt;/Nckap5&lt;sup&gt;em4Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688059</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688061</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat20-D13Got22&lt;/i&gt;)/Mcwi-&lt;i&gt;Nckap5&lt;sup&gt;em4Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS.BN-(&lt;i&gt;D13Rat20-D13Got22&lt;/i&gt;)/Mcwi-&lt;i&gt;Nckap5&lt;sup&gt;em4Mcwi+&lt;/sup&gt;/Nckap5&lt;sup&gt;em4Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688061</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688063</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat20-D13Got22&lt;/i&gt;)/Mcwi-&lt;i&gt;Nckap5&lt;sup&gt;em4Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS.BN-(&lt;i&gt;D13Rat20-D13Got22&lt;/i&gt;)/Mcwi-&lt;i&gt;Nckap5&lt;sup&gt;em4Mcwi-&lt;/sup&gt;/Nckap5&lt;sup&gt;em4Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688063</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688066</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ncf2&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ncf2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Ncf2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ncf2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5144089</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="67505492" STOP_POS="67536015" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="64958217" STOP_POS="64958221" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="70229196" STOP_POS="70229200" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="67806516" STOP_POS="67834105" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688066</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688069</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ncf2&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ncf2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Ncf2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688069</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688074</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nox4&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nox4&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Nox4&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2019-01-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nox4&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139868</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150313736" STOP_POS="150491480" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="140900886" STOP_POS="141078844" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="150861996" STOP_POS="150862003" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157106652" STOP_POS="157285107" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143415816" STOP_POS="143603554" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688074</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders. This homozygous mutant carries an 8-bp frameshift deletion in exon 7 of rat Nox4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688077</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nox4&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nox4&lt;sup&gt;em2Mcwi+&lt;/sup&gt;/Nox4&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688077</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688080</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nox4&lt;sup&gt;em2Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Nox4&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Nox4&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2019-07-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nox4&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139868</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150313736" STOP_POS="150491480" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="140900886" STOP_POS="141078844" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="150861996" STOP_POS="150862003" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157106652" STOP_POS="157285107" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143415816" STOP_POS="143603554" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688080</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688083</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Prex1&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Prex1&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Prex1&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688083</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688087</RGD_ID>
    <STRAIN_SYMBOL>FHH.BN-(&lt;i&gt;D1Hmgc14-D1Hmgc15&lt;/i&gt;)/Mcwi-&lt;i&gt;Rab38&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>FHH.BN-(&lt;i&gt;D1Hmgc14-D1Hmgc15&lt;/i&gt;)/Mcwi-&lt;i&gt;Rab38&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Rab38&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rab38&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139867</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="151595153" STOP_POS="151675492" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="142182566" STOP_POS="142262923" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="152072716" STOP_POS="152153449" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="158385888" STOP_POS="158466621" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="144783919" STOP_POS="144864573" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688087</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with FHH.BN-(&lt;i&gt;D1Hmgc14-D1Hmgc15&lt;/i&gt;)/Mcwi to get heterozygous offspring which were intercrossed and offspring maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688090</RGD_ID>
    <STRAIN_SYMBOL>FHH.BN-(&lt;i&gt;D1Hmgc14-D1Hmgc15&lt;/i&gt;)/Mcwi-&lt;i&gt;Rab38&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>FHH.BN-(&lt;i&gt;D1Hmgc14-D1Hmgc15&lt;/i&gt;)/Mcwi-&lt;i&gt;Rab38&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Rab38&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rab38</ALLELES>
    <ALLELE_RGD_IDS>628752</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="151595153" STOP_POS="151675492" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="142182566" STOP_POS="142262923" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="152072716" STOP_POS="152153449" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="158385888" STOP_POS="158466621" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="144783919" STOP_POS="144864573" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688090</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with FHH.BN-(&lt;i&gt;D1Hmgc14-D1Hmgc15&lt;/i&gt;)/Mcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688092</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rag1&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Rag1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Rag1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688092</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688094</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rag1&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Rag1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Rag1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688094</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688096</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rag1&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Rag1&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Rag1&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688096</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688098</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rag1&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Rag1&lt;sup&gt;em2Mcwi+&lt;/sup&gt;/Rag1&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688098</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688100</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ren&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ren&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Ren&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688100</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688102</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ren&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ren&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Ren&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ren&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139863</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="47348312" STOP_POS="47359539" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="44803412" STOP_POS="44803421" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50502724" STOP_POS="50513953" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55555583" STOP_POS="55566812" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="46262936" STOP_POS="46275213" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688102</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688107</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Sorcs1&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Sorcs1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;/Sorcs1&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sorcs1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139864</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="259022007" STOP_POS="259535731" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="249207764" STOP_POS="249207777" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="269965824" STOP_POS="270473097" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="277404996" STOP_POS="277912261" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="255767411" STOP_POS="256279565" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688107</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;/Mcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders. The resulting mutation is a 14-bp frameshift deletion mutation in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688109</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Sorcs1&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Sorcs1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Sorcs1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688109</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;/Mcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688111</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tfdp2&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Tfdp2&lt;sup&gt;em2Mcwi-&lt;/sup&gt;/Tfdp2&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688111</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688113</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tfdp2&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Tfdp2&lt;sup&gt;em2Mcwi+&lt;/sup&gt;/Tfdp2&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688113</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688116</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tgfb1&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Tgfb1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Tgfb1&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688116</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offspring which were intercrossed and offspring maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688119</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tgfb1&lt;sup&gt;em3Mcwi+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Tgfb1&lt;sup&gt;em3Mcwi+&lt;/sup&gt;/Tgfb1&lt;sup&gt;em3Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-08-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688119</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688121</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ube2q2&lt;sup&gt;em3Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ube2q2&lt;sup&gt;em3Mcwi-&lt;/sup&gt;/Ube2q2&lt;sup&gt;em3Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688121</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688123</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ube2q2&lt;sup&gt;em3Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ube2q2&lt;sup&gt;em3Mcwi+&lt;/sup&gt;/Ube2q2&lt;sup&gt;em3Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688123</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688125</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ulk4&lt;sup&gt;em3Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ulk4&lt;sup&gt;em3Mcwi-&lt;/sup&gt;/Ulk4&lt;sup&gt;em3Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688125</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688396</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D3Rat80-D3Rat3&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="55937642" STOP_POS="180900654" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="35528428" STOP_POS="160482157" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="36599933" STOP_POS="169714239" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="41713824" STOP_POS="175796738" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="32056563" STOP_POS="162589029" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688396</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 3 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688400</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D4Rat5-D4Got131&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="15011050" STOP_POS="159947290" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="14118904" STOP_POS="158261065" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="10728623" STOP_POS="157981900" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="10720881" STOP_POS="224994372" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="9638281" STOP_POS="162284199" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688400</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 4 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688402</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D6Rat148-D6Rat109&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="145952555" STOP_POS="145952684" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="20894065" STOP_POS="139809723" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="22070168" STOP_POS="146778380" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="31958575" STOP_POS="155686896" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="20826657" STOP_POS="146162691" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688402</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 6 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688405</RGD_ID>
    <STRAIN_SYMBOL>ACI.COP-(&lt;i&gt;D5Rat12-D5Rat205&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="160071170" STOP_POS="160071397" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="67856776" STOP_POS="67856928" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="70038765" STOP_POS="70038916" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="74199071" STOP_POS="74199222" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="70669803" STOP_POS="70670361" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688405</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of COP/CrCrl chromosome 5 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688407</RGD_ID>
    <STRAIN_SYMBOL>ACI.COP-(&lt;i&gt;D5Rat28-D5Rat205&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="125969677" STOP_POS="160071397" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="120740824" STOP_POS="120740915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="125455818" STOP_POS="125455908" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="129313212" STOP_POS="129313302" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="126963761" STOP_POS="126963962" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688407</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of COP/CrCrl chromosome 5 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>5688409</RGD_ID>
    <STRAIN_SYMBOL>ACI.COP-(&lt;i&gt;D5Rat28-D5Rat36&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="125969677" STOP_POS="143398338" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="120740824" STOP_POS="138113774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="125455818" STOP_POS="143846372" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="129313212" STOP_POS="147610238" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="126963761" STOP_POS="145187034" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_5688409</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of COP/CrCrl chromosome 5 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6218997</RGD_ID>
    <STRAIN_SYMBOL>SHR/NCrlAnra</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Behavior Genetics Laboratory, Departamento de Biologia Celular, Embriologia e Genetica, Universidade Federal de Santa Catarina, Florianopolis, SC, Brazil</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6218997</CITATION_ID>
    <DESCRIPTION>These were originally from Harvard University, Boston MA, then at UNESP, Botucatu, SP, Brazil, now maintained at Behavior Genetics Laboratory, SC, Brazil</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6219002</RGD_ID>
    <STRAIN_SYMBOL>LEW/HsdUnibAnra</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Behavior Genetics Laboratory, Departamento de Biologia Celular, Embriologia e Genetica, Universidade Federal de Santa Catarina, Florianopolis, SC, Brazil</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6219002</CITATION_ID>
    <DESCRIPTION>LEW rats originally from Harlan Sprague Dawley, IN then bred at UNICAMP (Campinas, SP Brazil) now maintained at Behavior Genetics Laboratory, SC, Brazil</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6478788</RGD_ID>
    <STRAIN_SYMBOL>STOCK-&lt;i&gt;Tp53&lt;sup&gt;tm1(EGFP-Pac)Qly&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME>p53 knockout rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=485&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=485&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2024-04-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tp53|Tp53&lt;sup&gt;tm1(EGFP-Pac)Qly&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>3889|12792957</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="54798871" STOP_POS="54810300" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="54300070" STOP_POS="54311525" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="56186299" STOP_POS="56198449" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="55932658" STOP_POS="55944087" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="56399721" STOP_POS="56411150" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00485</CITATION_ID>
    <DESCRIPTION>This strain was made by electroporation of DAc8 embryonic stem cells with a targeting vector containing 6.7kb 5 prime and 1.6- kb 3 prime homology arms and a CAG-EGFP-IRES-Pac cassette. Chimeras were formed by microinjecting F344 blastocysts. Founder animals were mated with SD rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6478789</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(CAG-EGFP)YsRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=296&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=296&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2018-07-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00296</CITATION_ID>
    <DESCRIPTION>Transgene prepared from cDNA fragment of EGFP derived from pEGFP vector (No. 6077-1, Clontech Laboratories, Inc., Palo Alto, CA) and pCXN2 expression vector containing cytomegalovirus enhancer, chicken b-actin enhancer-promoter and rabbit b-globin poly(A) signal.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6478791</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(UBC-EGFP)F455Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=307&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=307&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00307</CITATION_ID>
    <DESCRIPTION>This transgenic strain was made by injecting the lentivirus vector containing the GFP construct (vector name FUGW) into Lewis rat embryos. Animals that exhibited fluorescence of tails were mated. Offspring were bred with Lewis wild-type mates to map transgene location. Animals were backcrossed 10 generations onto F344.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6480190</RGD_ID>
    <STRAIN_SYMBOL>NAft:HS</STRAIN_SYMBOL>
    <FULL_NAME>Heterogeneous stock</FULL_NAME>
    <ORIGINATION>Psychiatry and Forensic Medicine, Institute of Neurosciences, School of Medicine, Autonomous University of Barcelona, Barcelona, Spain</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6480190</CITATION_ID>
    <DESCRIPTION>From Dr. Eva Redei, Center for Comparative Medicine, Northwestern University to Dr. Alberto Fernandez-Teruel, Barcelona</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6480205</RGD_ID>
    <STRAIN_SYMBOL>MWF-Chr 6&lt;sup&gt;SHR&lt;/sup&gt; Chr 8&lt;sup&gt;SHR&lt;/sup&gt;/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Clinical Pharmacology and Toxicology, Charite-Universitatsmedizin Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6480205</CITATION_ID>
    <DESCRIPTION>Chr 8 and chr 6 were introgressed from albuminuria-resistant SHR/FubRkb into the sensitive isogenic background of MWF/FubRkb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6480210</RGD_ID>
    <STRAIN_SYMBOL>SHR-Chr 8&lt;sup&gt;MWF&lt;/sup&gt;/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Clinical Pharmacology and Toxicology, Charite-Universitatsmedizin Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6480210</CITATION_ID>
    <DESCRIPTION>SHR/FubRkb male was crossed with female MWF/FubRkb to get F1 animals which in turn were backcrossed with female SHR/FubRkb, this was repeated for 7 generations, tested by sequential marker-assisted backcrossing</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6480218</RGD_ID>
    <STRAIN_SYMBOL>AR-&lt;i&gt;Ednrb&lt;sup&gt;sl&lt;/i&gt;&lt;/sup&gt;/Hkv</STRAIN_SYMBOL>
    <FULL_NAME>Aganglionosis rat</FULL_NAME>
    <ORIGINATION>Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Hokkaido, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ednrb&lt;sup&gt;sl&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10755424</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="87055490" STOP_POS="87086765" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="80670748" STOP_POS="80671048" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="88034987" STOP_POS="88035287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="91500400" STOP_POS="91531979" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="87893141" STOP_POS="87898700" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6480218</CITATION_ID>
    <DESCRIPTION>Congenital megacolon rats were found in offspring of a female albino rat crossed with a wild male by Ikadai et al. at Institute for Animal Reproduction in 1973 and were named Aganglionosis Rat (AR), provided to Dr. Takashi Agui by Dr. Ozaki, National Institute for Physiological Sciences, Okazaki, Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6480220</RGD_ID>
    <STRAIN_SYMBOL>LEH/Hkv</STRAIN_SYMBOL>
    <FULL_NAME>Aganglionosis rat</FULL_NAME>
    <ORIGINATION>Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Hokkaido, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1210&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2016-11-15)</AVAILABILITY>
    <RESEARCH_USE>Internal Medicine</RESEARCH_USE>
    <ALLELES>Ednrb&lt;sup&gt;sl&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10755424</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="87055490" STOP_POS="87086765" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="80670748" STOP_POS="80671048" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="88034987" STOP_POS="88035287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="91500400" STOP_POS="91531979" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="87893141" STOP_POS="87898700" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6480220</CITATION_ID>
    <DESCRIPTION>This strain derived from AR (aganglionosis) rat found by Dr. Ikadai in 1973. AR-derived Ednrb&lt;sup&gt;sl&lt;/sup&gt; was introduced into Long-Evans by Dr. Ozaki (NBRP-Rat # 0557 LE.AR-EdnrbSl/Okkm),  and this rat was provided to Dr. Agui at Hokkaido University and inbred line was established by sib mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6480223</RGD_ID>
    <STRAIN_SYMBOL>F344.AR-&lt;i&gt;Ednrb&lt;sup&gt;sl&lt;/sup&gt;&lt;/i&gt;/Hkv</STRAIN_SYMBOL>
    <FULL_NAME>Aganglionosis rat</FULL_NAME>
    <ORIGINATION>Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Hokkaido, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1208&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2016-10-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ednrb&lt;sup&gt;sl&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10755424</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="87055490" STOP_POS="87086765" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="80670748" STOP_POS="80671048" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="88034987" STOP_POS="88035287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="91500400" STOP_POS="91531979" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="87893141" STOP_POS="87898700" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6480223</CITATION_ID>
    <DESCRIPTION>This strain derived from AR (aganglionosis) rat found by Dr. Ikadai in 1973. This congenic strain was established by backcrossing (over 10 generations) of AR rat to F344/NSlc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6480863</RGD_ID>
    <STRAIN_SYMBOL>BBDR/RhwRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=463&gt;Rat Resource &amp; Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=463&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00463</CITATION_ID>
    <DESCRIPTION>BBDR/Rhw from R. H. William Laboratory, University of Washington, Seattle, Washington to Rat Resource &amp; Research Center</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6480866</RGD_ID>
    <STRAIN_SYMBOL>BN-Chr 13&lt;sup&gt;LH&lt;/sup&gt;/MavRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratoire de Physiologie, Lyon Cedex , France</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=395&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00395</CITATION_ID>
    <DESCRIPTION>Chr 13 from LH/Mav was introgressed onto the genetic background of BN/NHsdMcwi and then genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6480868</RGD_ID>
    <STRAIN_SYMBOL>BN-Chr 2&lt;sup&gt;LH&lt;/sup&gt;/MavRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratoire de Physiologie, Lyon Cedex , France</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=396&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00396</CITATION_ID>
    <DESCRIPTION>Chr 2 from LH/Mav was introgressed onto the genetic background of BN/NHsdMcwi and then genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6480874</RGD_ID>
    <STRAIN_SYMBOL>COP.DA-(&lt;I&gt;D16Rat12-D16Rat90&lt;/I&gt;)/McoRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=444&gt;Rat Resource &amp; Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=444&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="387123" STOP_POS="387234" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="380245" STOP_POS="80345693" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="1090054" STOP_POS="86162972" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="1084304" STOP_POS="85597057" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="350121" STOP_POS="85734479" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00444</CITATION_ID>
    <DESCRIPTION>Male COP/OlaHsd were crossed with female DA/OlaHsd then the F1 males were backcrossed to COP females. Male progeny containing the fewest number of DA-alleles were backcrossed to female COP. These males were backcrossed to female COP. Transferred from Medical College of Toledo to Rat Resource &amp; Research Center</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482243</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Cit&lt;sup&gt;fhJjlo&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME>flathead rat</FULL_NAME>
    <ORIGINATION>Department of Physiology and Neurobiology, University of Connecticut</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=322&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2017-07-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cit&lt;sup&gt;fhJjlo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13204831</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="46263881" STOP_POS="46425642" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="40763699" STOP_POS="40763699" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="46493042" STOP_POS="46493042" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="48136329" STOP_POS="48295119" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="41858134" STOP_POS="42019601" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00322</CITATION_ID>
    <DESCRIPTION>Flathead rat was discovered at University of Connecticut in an inbred colony of Wistar rats. Spontaneous single G deletion in exon 1 of citron kinase (Cit) confers a premature stop codon and lack of citron kinase protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482244</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(APOA1)116OpazRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Massachusetts. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=282&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00282</CITATION_ID>
    <DESCRIPTION>SS/JrHsd embryos were microinjected with human APOA1 C3 promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482245</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(Atp1a1)24OpazRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Massachusetts. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=280&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2019-05-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00280</CITATION_ID>
    <DESCRIPTION>SS/JrHsd embryos were microinjected with rat alpha1 Na,K-ATPase promoter (-1288 5 flanking regulatory region isolated from Sprague Dawley genomic library);  transgene cDNA: Dahl R alpha1 Na,K-ATPase</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482247</RGD_ID>
    <STRAIN_SYMBOL>FDIO/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=60&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=60&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2022-10-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00060</CITATION_ID>
    <DESCRIPTION>Cross between F344 (lean phenotype) and SDDIO (diet-induced obese phenotype) then inbred for 6 generations with maintenance of obese phenotype.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482252</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(Pgk1-EGFP)/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=53&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=53&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00053</CITATION_ID>
    <DESCRIPTION>Multiple random integration of EGFP gene under the control of the PGK promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482254</RGD_ID>
    <STRAIN_SYMBOL>Gunn-&lt;i&gt;Ugt1a1&lt;sup&gt;j&lt;/i&gt;&lt;/sup&gt;/BluHsdRrrc</STRAIN_SYMBOL>
    <FULL_NAME>Gunn rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=341&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=341&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-09-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ugt1a1&lt;sup&gt;j&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13432064</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="96249143" STOP_POS="96256264" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="88805660" STOP_POS="88805660" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="95300017" STOP_POS="95300017" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="94982916" STOP_POS="94990037" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="87091241" STOP_POS="87098362" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00341</CITATION_ID>
    <DESCRIPTION>This mutation was first observed in normal Wistar albino rats in  a breeding colony at Cannaught Laboratories in 1934. Jaundice was evident at birth or shortly after and was persistant throughout life.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482256</RGD_ID>
    <STRAIN_SYMBOL>HS/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME>High Self-Administration</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=537&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=537&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2019-02-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00537</CITATION_ID>
    <DESCRIPTION>Developed from selective breeding of outbred Wistar rats. Selectively bred over six generations for increased intravenous drug self-administration with subsequent inbreeding within this strain over six generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482259</RGD_ID>
    <STRAIN_SYMBOL>LS/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME>Low Self-Administration</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=536&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=536&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2017-01-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00536</CITATION_ID>
    <DESCRIPTION>Developed from selective breeding of outbred Wistar rats. Selectively bred over six generations for increased intravenous drug self-administration with subsequent inbreeding within this strain over six generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482268</RGD_ID>
    <STRAIN_SYMBOL>BRAT-&lt;i&gt;Avp&lt;sup&gt;di&lt;/i&gt;&lt;/sup&gt;/BluHsdRrrc</STRAIN_SYMBOL>
    <FULL_NAME>Brattleboro</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=445&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2018-06-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Avp&lt;sup&gt;di&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13627261</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="138247039" STOP_POS="138247039" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="117793942" STOP_POS="117793942" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="123117977" STOP_POS="123117977" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="129615610" STOP_POS="129627147" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="118205007" STOP_POS="118206985" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00445</CITATION_ID>
    <DESCRIPTION>Hereditary hypothalamic diabetes insipidus was first described in offspring from a Long-Evans stock of rats by Dr. Schroeder, later named Brattleboro strain. In 1964 from Dr. Lewis Kinder, Harvard University, Boston to Blue Spruce Farms, Altamont, New York. to Harlan through acquisition in 1988. Brattleboro rats  transferred to the RRRC in 2009.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482271</RGD_ID>
    <STRAIN_SYMBOL>LEW.Cg-&lt;i&gt;Foxn1&lt;/i&gt;&lt;sup&gt;rnu&lt;/sup&gt;/NRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=363&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=363&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00363</CITATION_ID>
    <DESCRIPTION>The NIH nude rat was developed in 1979-1980 at the NIH through a series of matings involving the following inbred rat strains: BN/SsN, MR/N, BUF/N, WN/N, ACI/N, WKY/N, M520/N, and F344/N. Received from the National Institute of Health by NCI in 1983. The nude mutation was subsequently backcrossed 17 generations to the Lewis inbred strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482282</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(EGFP)463-5Rrrc</STRAIN_SYMBOL>
    <FULL_NAME>Lewis- GFP transgenic</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=83&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=83&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00083</CITATION_ID>
    <DESCRIPTION>insertion of EGFP transgene with Ubiquitin C promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482284</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(EGFP)456-9Rrrc</STRAIN_SYMBOL>
    <FULL_NAME>Lewis- GFP transgenic</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=84&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=84&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00084</CITATION_ID>
    <DESCRIPTION>insertion of EGFP transgene with Ubiquitin C promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482286</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(EGFP)458-7Rrrc</STRAIN_SYMBOL>
    <FULL_NAME>Lewis- GFP transgenic</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=86&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=86&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00086</CITATION_ID>
    <DESCRIPTION>insertion of EGFP transgene with Ubiquitin C promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482288</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(EGFP)463-1Rrrc</STRAIN_SYMBOL>
    <FULL_NAME>Lewis- GFP transgenic</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=85&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=85&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00085</CITATION_ID>
    <DESCRIPTION>insertion of EGFP transgene with Ubiquitin C promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482290</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(EGFP)455Rrrc</STRAIN_SYMBOL>
    <FULL_NAME>Lewis- GFP transgenic</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=62&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=62&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00062</CITATION_ID>
    <DESCRIPTION>This transgenic strain contains the enhanced green fluorescent protein gene under the control of the human ubiquitin-C promoter with a the woodchuck hepatitis virus posttranscriptional regulatory element (WRE). This transgenic strain was made by injecting the lentivirus vector containing the GFP construct (vector name FUGW) into Lewis rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482292</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg((ROSA)26Sor-lacZ)15Jmsk</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=297&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=297&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-08-08)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00297</CITATION_ID>
    <DESCRIPTION>This strain expresses LacZ ubiquitously driven by the  ROSA26 promoter established at Jichi Medical School.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482294</RGD_ID>
    <STRAIN_SYMBOL>LH-Chr 13&lt;sup&gt;BN&lt;/sup&gt;/MavRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=393&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=393&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00393</CITATION_ID>
    <DESCRIPTION>Chr 13 from BN/NHsdMcwi was introgressed onto the genetic background of LH/Mav and then genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482296</RGD_ID>
    <STRAIN_SYMBOL>LH-Chr 17&lt;sup&gt;BN&lt;/sup&gt;/MavRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=394&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=394&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00394</CITATION_ID>
    <DESCRIPTION>Chr 17 from BN/NHsdMcwi was introgressed onto the genetic background of LH/Mav and then genotyped</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482298</RGD_ID>
    <STRAIN_SYMBOL>MWF/ZtmRrrc</STRAIN_SYMBOL>
    <FULL_NAME>Munich Wistar Fromter</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=482&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=482&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2019-02-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00482</CITATION_ID>
    <DESCRIPTION>From outbred Wistar rats selected for large numbers of superficial glomeruli.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482643</RGD_ID>
    <STRAIN_SYMBOL>WIN/RhwRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=481&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=481&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00481</CITATION_ID>
    <DESCRIPTION>Submitted to Rat Resource &amp; Research Center</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482645</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Rho-S334X)3LavRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=643&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=643&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-08-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00643</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries a mouse rhodopsin gene that bears a termination codon at residue 334, which encodes a C-terminal truncated rhodopsin protein. Submitted to Rat Resource &amp; Research Center</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482654</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Rat36-D7Rat11&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="1248854" STOP_POS="113968036" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="664270" STOP_POS="112087821" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="2653138" STOP_POS="121762010" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="2632014" STOP_POS="121752141" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="1526177" STOP_POS="118826810" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6482654</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482674</RGD_ID>
    <STRAIN_SYMBOL>HIS/NdkRrrc</STRAIN_SYMBOL>
    <FULL_NAME>High-Saccharin-Consuming (HiS) Rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=366&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=366&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00366</CITATION_ID>
    <DESCRIPTION>The Occidental HiS (high-saccharin-consuming) rat strain was developed from a male Holtzman Sprague-Dawley rat that voluntarily consumed high levels of saccharin.This male was mated to several Holtzman Sprague-Dawley females and offspring displaying high saccharin consumption were selected. Selective breeding was continued in which offspring with high saccharin consumption were bred. To maintain the outbred status of this colony the donor backcrosses to Hsd:SD every 4-6 generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482676</RGD_ID>
    <STRAIN_SYMBOL>LOS/NdkRrrc</STRAIN_SYMBOL>
    <FULL_NAME>Low-Saccharin-Consuming (HiS) Rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=440&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=440&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00440</CITATION_ID>
    <DESCRIPTION>The Occidental LoS (low-saccharin-consuming) rat strain was developed from a male Holtzman Sprague-Dawley rat that did not voluntarily consume saccharin. This male was mated to several Holtzman Sprague-Dawley females and offspring displaying low saccharin consumption were selected. Selective breeding was continued in which offspring with low saccharin consumption (see phenotyping protocol) were bred. To maintain the outbred status of this colony the donor backcrosses to Hsd:SD every 4-6 generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6482680</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(MMTV-Erbb2)1UwmRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=365&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=365&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-04-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Erbb2</ALLELES>
    <ALLELE_RGD_IDS>2561</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00365</CITATION_ID>
    <DESCRIPTION>Hsd:SD background carrying a transgene which produces over-expression of the rat Erbb2 proto-oncogene under the control of the mouse mammary tumor virus (MMTV) long terminal repeat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6483453</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Dguok&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee WI</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dguok&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508354</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="117544784" STOP_POS="117572414" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="115987101" STOP_POS="116014733" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="115180433" STOP_POS="115208061" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="179770727" STOP_POS="179798683" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="117697251" STOP_POS="117725383" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6483453</CITATION_ID>
    <DESCRIPTION>This allele was made by ZFN mutagenesis. The resulting mutation is a 37-bp frameshift deletion in exon 1 (del 74-110)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6483454</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Dguok&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee WI</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dguok&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508345</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="117544784" STOP_POS="117572414" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="115987101" STOP_POS="116014733" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="115180433" STOP_POS="115208061" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="179770727" STOP_POS="179798683" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="117697251" STOP_POS="117725383" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6483454</CITATION_ID>
    <DESCRIPTION>This allele was made by ZFN mutagenesis. The resulting mutation is a 32-bp frameshift deletion in exon 1 (del 74-105)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6483455</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Dguok&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee WI</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dguok&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508325</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="117544784" STOP_POS="117572414" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="115987101" STOP_POS="116014733" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="115180433" STOP_POS="115208061" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="179770727" STOP_POS="179798683" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="117697251" STOP_POS="117725383" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6483455</CITATION_ID>
    <DESCRIPTION>This allele was made by ZFN mutagenesis. The resulting mutation is a net 57-bp frameshift deletion in exon 1 (del 3-102, ins. GCTTAGCAAGGCGGGCACTTCCGCCgagggcacttccgcctgc)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6483846</RGD_ID>
    <STRAIN_SYMBOL>HsdFcen:WI</STRAIN_SYMBOL>
    <FULL_NAME>Wistar</FULL_NAME>
    <ORIGINATION>Buenos Aires University, Ciudad Universitaria, Buenos Aires, Capital Federal, Argentina</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6483846</CITATION_ID>
    <DESCRIPTION>Descendants of rats from the Wistar Institute, Philadelphia, Pennsylvania then to Harlan and now maintained at School of Science, Buenos Aires University, Ciudad Universitaria, Buenos Aires, Capital Federal, Argentina</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484519</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;ROSA26&lt;sup&gt;em1(SB11)Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2017-08-08)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>ROSA26&lt;sup&gt;em1(SB11)Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6484518</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484519</CITATION_ID>
    <DESCRIPTION>This strain was produced by ZFN-stimulated knockin in the rat ROSA26 locus. ZFNs targeting the sequence CCTTCCCCCTTCTTCcctcgtGATCTGCAACTGGAGTCT were injected into SS/JrHsdMcwi rat embryos along with a plasmid template incorporating the Engrailed-2 mouse splice acceptor, a loxP site, the SB11 Sleeping Beauty transposase cDNA, and SV40 polyadenylation signal to integrate the transgene by homologous recombination. The resulting animal was confirmed by sequencing both junctions to harbor the SB11 gene knocked into the rat locus and expresses SB11 transposase in every cell by immunohistochemistry. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484559</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Slc34a1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc34a1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687699</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="9224010" STOP_POS="9238983" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="9232573" STOP_POS="9232584" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="9747766" STOP_POS="9762739" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="11856946" STOP_POS="11872100" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="15262929" STOP_POS="15277902" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484559</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CGTGCTCAGCTCTGCCTTccaactGGCCGGAGGTAGGGCCCG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 12-bp deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484560</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Pdc&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pdc&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687695</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="64847366" STOP_POS="64921865" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="62297281" STOP_POS="62371754" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="67545430" STOP_POS="67558600" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="72510251" STOP_POS="72523421" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="64622473" STOP_POS="64636031" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484560</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CACCACCATCGTGGTtaacaTTTACGAGGATGGTGTCAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 14-bp deletion in exon 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484561</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Comt&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Comt&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687725</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="96072371" STOP_POS="96091956" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="82568052" STOP_POS="82587642" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="86731828" STOP_POS="86731841" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="89809853" STOP_POS="89829568" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="84561591" STOP_POS="84581713" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484561</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGTTCCAGGTCACCATCctcaatGGGGCATCCCAGGATCTT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 14-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484562</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Fgf5&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fgf5&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687720</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="11627906" STOP_POS="11650243" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="11323827" STOP_POS="11346164" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="12995240" STOP_POS="12995246" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="12917742" STOP_POS="12938879" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="12713971" STOP_POS="12734634" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484562</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TGGATCCCACGAAGCcagtgtGTTAAGTAAGTTGCT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 5-bp deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484563</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cst3&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cst3&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687738</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="156790061" STOP_POS="156794116" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="136336923" STOP_POS="136340796" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="143223310" STOP_POS="143223311" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="149628692" STOP_POS="149632565" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="137650903" STOP_POS="137654776" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484563</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTTCGCCGTAAGCGAGTAcaacaaGGGCAGCAACGAT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 1-bp insertion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484564</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cd247&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd247&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687730</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="80576264" STOP_POS="80651422" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="78043302" STOP_POS="78118437" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="83996234" STOP_POS="83996246" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="88876046" STOP_POS="88951003" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="81515383" STOP_POS="81594699" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484564</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTCGCCTGCATCCTTCAAGtgcagtTCCCAGGAGCAGGTAAGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484565</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ldlr&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ldlr&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5144082</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="28546191" STOP_POS="28569075" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="20270020" STOP_POS="20292981" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="22750425" STOP_POS="22773305" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="22804325" STOP_POS="22827199" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="20824040" STOP_POS="20846920" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484565</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TGCATCCCCAGCCTGTGGgcctgcGACGGGGACCGGGAC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 12-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484566</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Slc6a12&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc6a12&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687736</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="156257518" STOP_POS="156275870" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="154586055" STOP_POS="154586107" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="153921199" STOP_POS="153941333" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="221009224" STOP_POS="221029242" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="157781178" STOP_POS="157800038" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484566</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GTCTCCCTCTCCAGTatggacAGAAAGGTTACAGTC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 53-bp deletion overlapping exon 2</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484567</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Sorcs3&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sorcs3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687731</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="257040442" STOP_POS="257675259" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="247570408" STOP_POS="247570435" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="267986305" STOP_POS="268620331" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="275416357" STOP_POS="276060204" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="254125935" STOP_POS="254345330" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484567</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TGCCCGCTCCATTGAcatcagtTCCCTGGTCGTCCAGGAT into FHH-Chr 1BN/Mcwi rat embryos. The resulting mutation is a 33-bp insertion in exon 7</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484568</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cd247&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd247&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687713</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="80576264" STOP_POS="80651422" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="78043302" STOP_POS="78118437" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="83996045" STOP_POS="84071408" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="88876046" STOP_POS="88951003" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="81515383" STOP_POS="81594699" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484568</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTCGCCTGCATCCTTCAAGtgcagtTCCCAGGAGCAGGTAAGG into SS/JrHsdMcwi rat embryos. The resulting mutation is an 8-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484569</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Adora2b&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adora2b&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687729</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="47439712" STOP_POS="47456092" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="46940394" STOP_POS="46956772" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="48569703" STOP_POS="48569816" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="48358068" STOP_POS="48374871" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="48421592" STOP_POS="48437967" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484569</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence AACTACTTTCTGGTGTccctgGCGACGGCGGACGTGGCT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 114-bp deletion in exon 1</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484570</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Stc1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Stc1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687722</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="50709439" STOP_POS="50720093" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="44299591" STOP_POS="44311695" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="50891137" STOP_POS="50901791" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="54622230" STOP_POS="54632884" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="49566885" STOP_POS="49577539" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484570</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CAGCTGCCCAATCACttctccAACAGGTATCCTGAGGGT into SS/JrHsdMcwi rat embryos. The resulting mutation is an 8-bp frameshift deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484571</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Myadml2&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Myadml2&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687726</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="106420856" STOP_POS="106425899" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="105922557" STOP_POS="105927867" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="109825513" STOP_POS="109827143" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="109418559" STOP_POS="109420196" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="110039330" STOP_POS="110040967" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484571</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGATGGGCAGCACCATGgaccccCCGGGGGGTGCA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 31-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484572</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Fgf5&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fgf5&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687727</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="11627906" STOP_POS="11650243" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="11323827" STOP_POS="11346164" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="12995243" STOP_POS="12995244" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="12917742" STOP_POS="12938879" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="12713971" STOP_POS="12734634" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484572</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TGGATCCCACGAAGCcagtgtGTTAAGTAAGTTGCT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 2-bp deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484573</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Clcn6&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Clcn6&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687740</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="163715593" STOP_POS="163748301" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="158434299" STOP_POS="158465174" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="164824701" STOP_POS="164824715" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="168469718" STOP_POS="168502323" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="165079773" STOP_POS="165110594" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484573</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GTCCCTGGTGACGACtgtggtGGTGTTTGTGGCCTCCATG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 15-bp frameshift deletion in exon 13.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484574</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Umod&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Umod&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687697</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="183247676" STOP_POS="183261665" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="173816341" STOP_POS="173829681" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="189186027" STOP_POS="189199939" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="196127939" STOP_POS="196141822" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="177729212" STOP_POS="177742552" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484574</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CACCACATGCTCCTGccaggCAGGCTTCACTGGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 104-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484575</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Resp18&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Resp18&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687714</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="84213844" STOP_POS="84220186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="76767473" STOP_POS="76767485" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="82470794" STOP_POS="82477136" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="82240055" STOP_POS="82246695" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="74551809" STOP_POS="74558151" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484575</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNS targeting the sequence CTCAGCAGACTCCATCCCCagtatcCATGCCGGAAGGAGGGGAA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp substitution in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484576</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Adipoq&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adipoq&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687709</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="91226524" STOP_POS="91240244" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="77721912" STOP_POS="77735644" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="81333964" STOP_POS="81334010" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="84363940" STOP_POS="84382663" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="79908291" STOP_POS="79911065" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484576</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CAGGCATCCCAGGATATCctggtcACAATGGGATACCGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 47-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484577</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Gnb3&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gnb3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687696</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="159328583" STOP_POS="159328693" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="157642311" STOP_POS="157642421" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="157355400" STOP_POS="157355510" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="157355400" STOP_POS="157355510" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="224370234" STOP_POS="224376918" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="160957524" STOP_POS="160963226" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484577</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GGCTCCCTCTCTCCTGGCagtccTTGTGGGACATTGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 111-bp deletion overlapping exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484578</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mylip&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mylip&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508347</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="19492826" STOP_POS="19514490" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="19286649" STOP_POS="19308295" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="19682040" STOP_POS="19703681" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="21703590" STOP_POS="21725205" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="25308147" STOP_POS="25329887" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484578</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGATGGGCAGCACCATGgaccccCCGGGGGGTGCA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 47-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484579</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 5&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Cyp4a3&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp4a3&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687737</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="134334396" STOP_POS="134352268" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="129097571" STOP_POS="129115488" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="134468666" STOP_POS="134484851" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="138258628" STOP_POS="138274813" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="135876140" STOP_POS="135893753" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484579</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGCTCTATGACCCTGACTatgtgAAGGTGGTTCTGGGAAGAT into SS-Chr 5&lt;sup&gt;BN&lt;/sup&gt;/Mcwi strain rat embryos. The resulting mutation is an 11-bp deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484580</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ldlr&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ldlr&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5144094</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="28546191" STOP_POS="28569075" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="20270020" STOP_POS="20292981" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="22750425" STOP_POS="22773305" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="22804325" STOP_POS="22827199" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="20824040" STOP_POS="20846920" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484580</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TGCATCCCCAGCCTGTGGgcctgcGACGGGGACCGGGAC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 123-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484581</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Resp18&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Resp18&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687705</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="84213844" STOP_POS="84220186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="76767473" STOP_POS="76767479" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="82470794" STOP_POS="82477136" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="82240055" STOP_POS="82246695" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="74551809" STOP_POS="74558151" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484581</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNS targeting the sequence CTCAGCAGACTCCATCCCCagtatcCATGCCGGAAGGAGGGGAA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484582</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cd247&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd247&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687703</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="80576264" STOP_POS="80651422" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="78043460" STOP_POS="78043470" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="83996233" STOP_POS="83996243" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="88876046" STOP_POS="88951003" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="81515383" STOP_POS="81594699" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484582</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTCGCCTGCATCCTTCAAGtgcagtTCCCAGGAGCAGGTAAGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 11-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484583</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nr2f2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nr2f2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687721</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="133419161" STOP_POS="133434290" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="124013926" STOP_POS="124013940" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="131452414" STOP_POS="131452428" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="132486697" STOP_POS="132499845" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="125280974" STOP_POS="125286929" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484583</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CCTTCTTCCCTGACCTGCagatcACGGACCAGGTGGCC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 15-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484584</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Adipoq&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adipoq&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687716</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="91226524" STOP_POS="91240244" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="77721912" STOP_POS="77735644" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="81333967" STOP_POS="81333970" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="84363940" STOP_POS="84382663" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="79908291" STOP_POS="79911065" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484584</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CAGGCATCCCAGGATATCctggtcACAATGGGATACCGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 4-bp frameshift deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484585</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Slc7a9&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc7a9&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687701</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="97246253" STOP_POS="97269546" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="88109517" STOP_POS="88132653" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="91709034" STOP_POS="91738492" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="92836837" STOP_POS="92865759" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="87976440" STOP_POS="87999102" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484585</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ATCGTCGCCATCATCATCatcagcGGACTGGTCCTCCTG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484711</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Atp2b1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Atp2b1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6484707</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="35622267" STOP_POS="35731904" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="33735595" STOP_POS="33845226" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="41196115" STOP_POS="41196231" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="41153926" STOP_POS="41262537" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="36493661" STOP_POS="36600280" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484711</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TACCTTCTGGGTTCAgaagagGCCGTGGCTTGCTGAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 117-bp deletion in intron 8 and exon 9.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484712</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Lpin1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lpin1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6484709</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="45039110" STOP_POS="45145845" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="39309198" STOP_POS="39417034" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="41799748" STOP_POS="41870046" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="51532422" STOP_POS="51638090" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="40253664" STOP_POS="40297195" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484712</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CCCATCCACTGGTTCtctgggGAAGAAGAGAAGGAAAAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 4-bp deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484713</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cubn&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cubn&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6484705</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="81293619" STOP_POS="81501694" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="76385046" STOP_POS="76593133" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="80783420" STOP_POS="80783432" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="82205509" STOP_POS="82425565" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="87545893" STOP_POS="87772079" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484713</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CGGGAGTACCTTCAGATTcatgatGGAGACTCCTCAGCG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp deletion in exon 14.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484714</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Lss&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lss&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6484706</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="12090641" STOP_POS="12118230" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="12118435" STOP_POS="12118448" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="12844522" STOP_POS="12870474" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="15000298" STOP_POS="15338473" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="12507575" STOP_POS="12534612" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484714</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CCCATCCACTGGTTCtctgggGAAGAAGAGAAGGAAAAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a net 12-bp deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484715</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Adora2b&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adora2b&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687698</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="47439712" STOP_POS="47456092" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="46940394" STOP_POS="46956772" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="48569563" STOP_POS="48586366" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="48358163" STOP_POS="48358324" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="48421592" STOP_POS="48437967" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484715</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence AACTACTTTCTGGTGTccctgGCGACGGCGGACGTGGCT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 162-bp deletion in exon 1</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484716</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Bcat1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bcat1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6484708</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="179695662" STOP_POS="179777973" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="177964834" STOP_POS="178046573" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="179289184" STOP_POS="179289198" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="243444839" STOP_POS="243491574" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="182641517" STOP_POS="182692917" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484716</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CAGTCTGTACATCCGCCCCacattCATCGGGATTGAGGTA into SS/JrHsdMcwi rat embryos. The resulting mutation is 15-bp deletion in exon 5</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484717</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cacna1h&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cacna1h&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6484703</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="14894630" STOP_POS="14952317" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="14390104" STOP_POS="14448204" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="14744474" STOP_POS="14744487" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="14547456" STOP_POS="14605627" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="14621372" STOP_POS="14679051" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484717</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CCGACCCACAGTGTCtgggagATCGTGGGGCAGGCAGAC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 14-bp deletion in exon 11.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484718</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ace&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-01-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ace&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6484704</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="91410129" STOP_POS="91430246" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="90910316" STOP_POS="90930437" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="94174778" STOP_POS="94174785" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="93922062" STOP_POS="93965127" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="95361338" STOP_POS="95381455" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484718</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GAAACCCAACCTCGATGTCaccagtACAATGGTACAGAAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 8-bp deletion in exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484719</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Lepr&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6484701</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116294409" STOP_POS="116477904" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120503475" STOP_POS="120682269" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484719</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence AGCATCGTACTGCCCacaatgGGACATGGTCACAAG into SS/JrHsdMcwi rat embryos. The resulting mutation was a 16-bp deletion in exon 11, predicted nonsense stop codon 30.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484720</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Lep&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lep&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6484700</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="58626529" STOP_POS="58640663" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="57661127" STOP_POS="57675262" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="56346978" STOP_POS="56351818" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="56085079" STOP_POS="56099209" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="55943837" STOP_POS="55945938" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484720</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTGTGCCTATCCacaaaGTCCAGGATGACACC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6484721</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ace&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-11-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ace&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6484702</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="91410129" STOP_POS="91430246" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="90910316" STOP_POS="90930437" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="94174776" STOP_POS="94174782" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="93922062" STOP_POS="93965127" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="95361338" STOP_POS="95381455" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6484721</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GAAACCCAACCTCGATGTCaccagtACAATGGTACAGAAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp deletion in exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6766770</RGD_ID>
    <STRAIN_SYMBOL>BBDR.BBDP-(&lt;I&gt;D4Mit6-D4Mit7&lt;/I&gt;)/RhwMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="80216705" STOP_POS="80217004" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="76647384" STOP_POS="78886189" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="77307388" STOP_POS="79562753" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="141978848" STOP_POS="141979031" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="75732943" STOP_POS="75733127" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6766770</CITATION_ID>
    <DESCRIPTION>This congenic strain was developed by cyclic cross-intercross breeding using diabetic prone and diabetic resistant BB rats. (DP x DR)F1 x DR cross intercross breeding was used to generate F2 lymphopenic rats. These were then genotyped for both the flanking markers of the Gimap5 gene; maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893382</RGD_ID>
    <STRAIN_SYMBOL>BBDR.BBDP-(&lt;I&gt;D4Mit6-D4Mit7&lt;/I&gt;)/RhwMcwi-&lt;i&gt;Il1r1&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il1r1&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893378</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="50000558" STOP_POS="50076579" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="42565971" STOP_POS="42565972" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="46962291" STOP_POS="47038139" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="46647422" STOP_POS="46723241" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="39434910" STOP_POS="39473552" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893382</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence AGCTTCATACAGCGGCtccatgTTGCAGGGGATGGAAGTC into BBDR.BBDP-(&lt;i&gt;D4Mit6-D4Mit7&lt;/i&gt;)/RhwMcwi rat embryos. The resulting mutation is a 1-bp insertion in exon 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893383</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Fyn&lt;sup&gt;em6Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fyn&lt;sup&gt;em6Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893380</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="44322635" STOP_POS="44514498" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="42767733" STOP_POS="42960903" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="44577477" STOP_POS="44577484" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="46160734" STOP_POS="46353456" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="43501853" STOP_POS="43695567" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893383</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TCCATCCCGAACTACAACaacttcCACGCAGCCGGGGGCCAG into SS/JrHsdMcwi rat embryos. The resulting mutation is an 8-bp deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893384</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnj11&lt;sup&gt;em9Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnj11&lt;sup&gt;em9Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893381</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="105727473" STOP_POS="105731167" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="96591048" STOP_POS="96594574" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102103094" STOP_POS="102106127" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103186859" STOP_POS="103190535" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="96614960" STOP_POS="96617993" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893384</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTACAGAGCCCAGGTAccgtacTCGGGAGAGGAGGGC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 5-bp deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893385</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnj11&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnj11&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893379</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="105727473" STOP_POS="105731167" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="96591048" STOP_POS="96594574" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102103094" STOP_POS="102106127" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103186859" STOP_POS="103190535" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="96614960" STOP_POS="96617993" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893385</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTACAGAGCCCAGGTAccgtacTCGGGAGAGGAGGGC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 8-bp deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893429</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nos3&lt;sup&gt;em8Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nos3&lt;sup&gt;em8Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893421</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="11686088" STOP_POS="11706604" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="10793834" STOP_POS="10814170" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="7322088" STOP_POS="7342400" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="7333272" STOP_POS="7353767" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="6158847" STOP_POS="6179441" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893429</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GACTTCATCAATCAGTACtataaCTCGATCAAAAGGTGGGT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 109-bp deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893430</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nat8&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nat8&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893413</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="119836986" STOP_POS="119837764" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="118279521" STOP_POS="118284671" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="117525963" STOP_POS="117527443" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="117525963" STOP_POS="117526741" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="120001277" STOP_POS="120002055" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893430</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CACATCCGCCAGTTCCAGgagaggGACTATGAACAGGTC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893431</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nos3&lt;sup&gt;em13Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nos3&lt;sup&gt;em13Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893422</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="11686088" STOP_POS="11706604" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="10811102" STOP_POS="10811266" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="7321908" STOP_POS="7342404" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="7333272" STOP_POS="7353767" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="6158847" STOP_POS="6179441" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893431</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GACTTCATCAATCAGTACtataaCTCGATCAAAAGGTGGGT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 165-bp deletion including part of exon 3, intron 3, and part of exon 4</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893432</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Hvcn1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Hvcn1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893410</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="40001205" STOP_POS="40030671" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="34341673" STOP_POS="34370010" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="39829785" STOP_POS="39829792" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="41702567" STOP_POS="41731349" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="35536954" STOP_POS="35556666" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893432</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CACACCCAGGCCATCCCTGgacttCAGGAGCCGGCTAAGGAA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 8-bp deletion in exon 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893433</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nos3&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nos3&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893418</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="11686088" STOP_POS="11706604" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="10793834" STOP_POS="10814170" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="7322088" STOP_POS="7342400" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="7333272" STOP_POS="7353767" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="6158847" STOP_POS="6179441" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893433</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GACTTCATCAATCAGTACtataaCTCGATCAAAAGGTGGGT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893434</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnj16&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnj16&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893423</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="96489329" STOP_POS="96520745" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="96018462" STOP_POS="96018479" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="99330894" STOP_POS="99391551" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="99027026" STOP_POS="99087674" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="100514180" STOP_POS="100515949" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893434</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence AGCTGCATCATAAACACCttcatcATTGGGGCAGCCTTGGCA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 18-bp deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893435</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tfdp2&lt;sup&gt;em6Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tfdp2&lt;sup&gt;em6Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893417</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="105640018" STOP_POS="105781026" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="96760459" STOP_POS="96901466" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="104040795" STOP_POS="104181228" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="103489105" STOP_POS="103629520" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="101256112" STOP_POS="101392512" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893435</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GTCTGAGTTTACcaatgcGAGTAACCATCTGGCAGCT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 14-bp deletion in exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893436</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnmb1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnmb1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893415</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="19062014" STOP_POS="19119005" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="18557510" STOP_POS="18614824" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="18911938" STOP_POS="18919640" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="18790595" STOP_POS="18800957" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="18904902" STOP_POS="18912604" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893436</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence AGCTGCATCATAAACACCttcatcATTGGGGCAGCCTTGGCA into SS/JrHsdMcwi rat embryos. The resulting allele is a net 4-bp deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893437</RGD_ID>
    <STRAIN_SYMBOL>BBDR.BBDP-(&lt;i&gt;D4Mit6-D4Mit7&lt;/i&gt;)/RhwMcwi-&lt;i&gt;Il1r1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il1r1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893425</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="50000558" STOP_POS="50076579" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="42504917" STOP_POS="42580958" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="46962291" STOP_POS="47038139" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="46647422" STOP_POS="46723241" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="39434910" STOP_POS="39473552" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893437</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence AGCTTCATACAGCGGCtccatgTTGCAGGGGATGGAAGTC into BBDR.BBDP-(&lt;i&gt;D4Mit6-D4Mit7&lt;/i&gt;)/RhwMcwi rat embryos. The resulting mutation is a 13-bp deletion in exon 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893438</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Fgf1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fgf1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893412</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="30937670" STOP_POS="31023786" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="30686555" STOP_POS="30772667" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="32351620" STOP_POS="32351629" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="31951411" STOP_POS="32037426" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="31785480" STOP_POS="31806452" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893438</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TTCCAGTTCAGCTGCAGCtcagtGCGGAAAGCGCGGGCGAA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 10-bp deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893439</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Hvcn1&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Hvcn1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893419</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="40001205" STOP_POS="40030671" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="34341673" STOP_POS="34370010" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="39829788" STOP_POS="39829795" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="41702567" STOP_POS="41731349" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="35536954" STOP_POS="35556666" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893439</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CACACCCAGGCCATCCCTGgacttCAGGAGCCGGCTAAGGAA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 8-bp deletion in exon 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893440</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Fyn&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fyn&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893411</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="44322635" STOP_POS="44514498" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="42767733" STOP_POS="42960903" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="44436354" STOP_POS="44630316" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="46160734" STOP_POS="46353456" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="43501853" STOP_POS="43695567" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893440</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TCCATCCCGAACTACAACaacttcCACGCAGCCGGGGGCCAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893441</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Grm7&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Grm7&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893416</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="145286714" STOP_POS="146169099" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="143730862" STOP_POS="144613230" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="142452616" STOP_POS="143367578" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="205768625" STOP_POS="206680107" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="146952340" STOP_POS="147270225" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893441</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ATCCGCCATGTTAACTTCaatggTAAGACTCCAATGTC into SS/JrHsdMcwi rat embryos. The resulting mutation is a 1-bp deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893442</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Pparg&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pparg&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893424</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="150095743" STOP_POS="150221104" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="148423102" STOP_POS="148548471" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="147274055" STOP_POS="147399383" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="210640676" STOP_POS="210640808" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="151492220" STOP_POS="151617331" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893442</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence TGCCATTCTGGCCCAccaactTCGGAATCAGCTCTG into SS/JrHsdMcwi rat embryos. The resulting mutation is a a 133-bp deletion of (RGSC 5.0/rn5): chr4:210,640,676-210,640,808, including part of intron 1 and exon 2 of isoform NM_013124.3</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893443</RGD_ID>
    <STRAIN_SYMBOL>BBDR.BBDP-(&lt;i&gt;D4Mit6-D4Mit7&lt;/i&gt;)/RhwMcwi-&lt;i&gt;Il1r1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il1r1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893414</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="50000558" STOP_POS="50076579" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="42504917" STOP_POS="42580958" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="46962291" STOP_POS="47038139" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="46647422" STOP_POS="46723241" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="39434910" STOP_POS="39473552" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893443</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence AGCTTCATACAGCGGCtccatgTTGCAGGGGATGGAAGTC into BBDR.BBDP-(&lt;i&gt;D4Mit6-D4Mit7&lt;/i&gt;)/RhwMcwi rat embryos. The resulting mutation is a 7-bp deletin in exon 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893444</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnmb1&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnmb1&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893420</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="19063869" STOP_POS="19063889" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="18559674" STOP_POS="18559694" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="18559674" STOP_POS="18559694" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="18913708" STOP_POS="18913728" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="18790595" STOP_POS="18800957" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="18904902" STOP_POS="18912604" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893444</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence AGCTGCATCATAAACACCttcatcATTGGGGCAGCCTTGGCA into SS/JrHsdMcwi rat embryos. The resulting allele is a 21-bp deletion in exon 2 and intron 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893530</RGD_ID>
    <STRAIN_SYMBOL>BBDR.LA-(&lt;i&gt;D5Rat98-D5Rat233&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>R. H. William Laboratory, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="100820198" STOP_POS="123943456" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="95774194" STOP_POS="118714492" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="99421434" STOP_POS="123480464" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="103451053" STOP_POS="127341295" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="100017060" STOP_POS="124932061" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893530</CITATION_ID>
    <DESCRIPTION>Koletsky rat leptin receptor mutant (lepr) from the LA/N-&lt;i&gt;cp&lt;/i&gt;  was introgressed into the BBDR/Rhw rats by marker-assisted breeding. This was initiated in 2001 by Dr. Hansen and completed in 2007 at the University of Washington, Seattle.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893535</RGD_ID>
    <STRAIN_SYMBOL>BBDR.LA-(&lt;i&gt;D5Rat98-D5Rat233&lt;/i&gt;), BBDP-(&lt;i&gt;D4Mit6-D4Mit7&lt;/i&gt;)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>R. H. William Laboratory, University of Washington, Seattle, Washington</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893535</CITATION_ID>
    <DESCRIPTION>Heterozygous BBDR.LA-(&lt;i&gt;D5Rat98-D5Rat233&lt;/i&gt;)/Rhw (DR.&lt;sup&gt;&lt;i&gt;lepr&lt;/sup&gt;&lt;/i&gt;) were crossed with homozygous BBDR.BBDP-(-(&lt;i&gt;D4Mit6-D4Mit7&lt;/i&gt;)/Rhw (DR.&lt;sup&gt;&lt;i&gt;Gimap5&lt;/sup&gt;&lt;/i&gt;), to generate double congenic rats that had mutations for Gimap5 and Lepr genes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893551</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D1Rat32-D1Rat51&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1097&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="156677124" STOP_POS="156677310" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="167394665" STOP_POS="195598217" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="173583273" STOP_POS="202649821" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="112148733" STOP_POS="159782631" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893551</CITATION_ID>
    <DESCRIPTION>DA/Kini females were bred to PVG.1AV1/Kini males and male offspring selected for PVG alleles within the fragment. To ensure that mitochondrial DNA was inherited from the DA/Kini strain, female rats were from the DA/Kini strain throughout the breeding program.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893554</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D1Rat193-D1Rat68&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1098&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="188241285" STOP_POS="197807511" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="178810256" STOP_POS="188377506" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="193968438" STOP_POS="205603226" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="201022827" STOP_POS="212591221" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="183163129" STOP_POS="193070197" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893554</CITATION_ID>
    <DESCRIPTION>DA/Kini females were bred to PVG.1AV1/Kini males and male offspring selected for PVG alleles within the fragment. To ensure that mitochondrial DNA was inherited from the DA/Kini strain, female rats were from the DA/Kini strain throughout the breeding program.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893599</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Pdc&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pdc&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687712</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="64847366" STOP_POS="64921865" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="62297281" STOP_POS="62371754" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="67545430" STOP_POS="67558600" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="72510251" STOP_POS="72523421" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="64622473" STOP_POS="64636031" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893599</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CACCACCATCGTGGTtaacaTTTACGAGGATGGTGTCAG into SS/JrHsdMcwi rat embryos. The resulting mutation is a net 47-bp deletion in exon 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6893600</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Abcb1b&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-07-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abcb1b&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>6893598</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="26197706" STOP_POS="26280156" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="25242761" STOP_POS="25325194" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="22303694" STOP_POS="22303791" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="22161597" STOP_POS="22244735" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="21829489" STOP_POS="21912239" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6893600</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GAAAGCTGCCCACCTCATGgatgtgGCCGGAAACAAGGTGGGA into SS/JrHsdMcwi rat embryos. The resulting mutation is a 98-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6902893</RGD_ID>
    <STRAIN_SYMBOL>BB.SHR-(&lt;i&gt;Acsm3-Igf2&lt;/i&gt;)/K</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Laboratory Animal Science, University of Greifswald, Karlsburg, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Igf2|Acsm3</ALLELES>
    <ALLELE_RGD_IDS>2870|62086</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="183564652" STOP_POS="207261263" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="174133260" STOP_POS="197831802" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="189514504" STOP_POS="215839081" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="196449042" STOP_POS="222733868" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="178054386" STOP_POS="202915231" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6902893</CITATION_ID>
    <DESCRIPTION>Congenics extablished as speed-congenics by cross of BB/OK and SHR/Mol rats and repeated backcrossing onto BB/OK rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903879</RGD_ID>
    <STRAIN_SYMBOL>SS/NEisSlc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903879</CITATION_ID>
    <DESCRIPTION>1962: Dr. L. K. Dahl found the mutant rat from SD at NIH; 1989: Moved to Eisai (Eisai Co., Ltd.); 1991: Moved to BMR Institute for breeding; 1994: Started selling by SLC, Shizuoka, Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903881</RGD_ID>
    <STRAIN_SYMBOL>SR/NEisSlc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903881</CITATION_ID>
    <DESCRIPTION>1962: Dr. L. K. Dahl found the mutant rat from SD at NIH; 1989: Moved to Eisai (Eisai Co., Ltd.); 1991: Moved to BMR Institute for breeding; 1994: Started selling by SLC, Shizuoka, Japan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903902</RGD_ID>
    <STRAIN_SYMBOL>WF.COP-(&lt;i&gt;D2Uwm14-D2Uwm13&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison, Wisconsin, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="15576151" STOP_POS="15576367" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="12654100" STOP_POS="13840758" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="10246312" STOP_POS="11522696" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="10116941" STOP_POS="11387756" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="10539188" STOP_POS="11957973" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903902</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 was transferred from COP into the WF background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903904</RGD_ID>
    <STRAIN_SYMBOL>WF.COP-(&lt;i&gt;D2Uwm17-D2Rat16&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison, Wisconsin, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="32373770" STOP_POS="43665178" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="31224612" STOP_POS="43643900" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="50381686" STOP_POS="62691053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="32051319" STOP_POS="43376636" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903904</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 was transferred from COP into the WF background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903912</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco72-D9Rat89&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="82150867" STOP_POS="82151090" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="47902208" STOP_POS="74701891" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="52686874" STOP_POS="80400631" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52352690" STOP_POS="80172715" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="44842118" STOP_POS="72258219" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903912</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Mco72-D9Mco93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903914</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco72-D9Rat55&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="79836951" STOP_POS="79837097" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="47902208" STOP_POS="47902417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="52686874" STOP_POS="77966876" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52352690" STOP_POS="77741892" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="44842118" STOP_POS="69875226" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903914</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Mco72-D9Mco93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903917</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco72-D9Mco109&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="47902208" STOP_POS="67020125" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="52686874" STOP_POS="72470724" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52352690" STOP_POS="52352896" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="44842118" STOP_POS="44842324" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903917</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Mco72-D9Mco93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903920</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco72-D9Uia4&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="47902208" STOP_POS="62072556" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="52686874" STOP_POS="67451944" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52352690" STOP_POS="67265755" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="44842118" STOP_POS="59247627" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903920</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Mco72-D9Mco93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903922</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco72-D9Mco106&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="47902208" STOP_POS="53185096" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="52686874" STOP_POS="58156770" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52352690" STOP_POS="52352896" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="44842118" STOP_POS="44842324" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903922</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Mco72-D9Mco93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903925</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco72-D9Mco105&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="47902208" STOP_POS="52283252" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="52686874" STOP_POS="57216771" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52352690" STOP_POS="52352896" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="44842118" STOP_POS="44842324" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903925</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Mco72-D9Mco93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903928</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Rat7-D9Got111&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="86722132" STOP_POS="86722302" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="90719946" STOP_POS="90720113" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="97276144" STOP_POS="97276310" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="83453664" STOP_POS="96967940" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="77172934" STOP_POS="89249893" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903928</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Rat7-D9Mco93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903932</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Rat7-D9Rat52&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="86722132" STOP_POS="90624686" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="83453664" STOP_POS="87395775" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="77172934" STOP_POS="81205197" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903932</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Rat7-D9Mco93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903934</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Rat7-D9Mco91&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="86722132" STOP_POS="86722302" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="80676321" STOP_POS="80676524" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="85112340" STOP_POS="85112539" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="83453664" STOP_POS="84866878" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="77172934" STOP_POS="78634594" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903934</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Rat7-D9Mco93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6903936</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Rat7-D9Rat84&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="86722132" STOP_POS="92642305" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="85193982" STOP_POS="85194188" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="91579562" STOP_POS="91579769" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="83453664" STOP_POS="91313982" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="77172934" STOP_POS="83316504" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6903936</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Rat7-D9Mco93&lt;/i&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907047</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm63-D5Uwm60&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="60360575" STOP_POS="60360793" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="55564549" STOP_POS="72943679" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="56733010" STOP_POS="75274687" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="61271852" STOP_POS="79426001" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="57848236" STOP_POS="76159022" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907047</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Wox7-D5Uwm37&lt;/i&gt;).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907054</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm67-D5Uwm98&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="76369776" STOP_POS="80145576" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="78777540" STOP_POS="82587133" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="82897463" STOP_POS="82897734" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="79919505" STOP_POS="79919776" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907054</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907057</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm76-D5Uwm61&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="80813116" STOP_POS="80813390" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="83268986" STOP_POS="83269259" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="87362775" STOP_POS="87363048" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="84434303" STOP_POS="84434576" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907057</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907059</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm76-D5Uwm98&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="80145359" STOP_POS="80145576" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="82586913" STOP_POS="82587133" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907059</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907061</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm67-D5Uwm78&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="76369776" STOP_POS="77541025" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="78777540" STOP_POS="79954846" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="82897463" STOP_POS="82897734" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="79919505" STOP_POS="79919776" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907061</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907063</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm76-D5Got18&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="79031392" STOP_POS="79031558" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="81457871" STOP_POS="81458036" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="85556660" STOP_POS="85556825" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="82406661" STOP_POS="82406827" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907063</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907076</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm78-D5Uwm98&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="77540762" STOP_POS="79031558" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="79954586" STOP_POS="81458036" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="85556660" STOP_POS="85556825" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="82406661" STOP_POS="82406827" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907076</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907078</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm95-D5Uwm98&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="78554205" STOP_POS="79031558" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="80975875" STOP_POS="81458036" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="85556660" STOP_POS="85556825" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="82406661" STOP_POS="82406827" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907078</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907080</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm67-D5Uwm81&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="76369776" STOP_POS="77714928" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="78777540" STOP_POS="80126657" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="82897463" STOP_POS="82897734" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="79919505" STOP_POS="79919776" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907080</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907084</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm76-D5Uwm92&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="78038840" STOP_POS="78039084" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="80451098" STOP_POS="80451339" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907084</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907087</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm78-D5Uwm84&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="77540762" STOP_POS="77791604" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="79954586" STOP_POS="80203685" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907087</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907090</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm78-D5Uwm93&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="77540762" STOP_POS="78102136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="79954586" STOP_POS="80518802" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907090</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907092</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm88-D5Uwm92&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="83004073" STOP_POS="83004331" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="77988604" STOP_POS="78039084" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="80401019" STOP_POS="80451339" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907092</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907094</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm87-D5Uwm92&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="77960535" STOP_POS="78039084" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="80372955" STOP_POS="80451339" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907094</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907096</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm85-D5Uwm92&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="77816155" STOP_POS="78039084" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="80229223" STOP_POS="80451339" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907096</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907098</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm82-D5Uwm92&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="77743239" STOP_POS="78039084" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="80154593" STOP_POS="80451339" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907098</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907100</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm82-D5Uwm91&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="77743239" STOP_POS="78018921" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="80154593" STOP_POS="80431178" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907100</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907104</RGD_ID>
    <STRAIN_SYMBOL>WF.WKY-(&lt;i&gt;D5Uwm77-D5Uwm91&lt;/i&gt;)/Uwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin School of Medicine, Madison, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="77521860" STOP_POS="78018921" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="79935684" STOP_POS="80431178" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907104</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain WF.WKY-(&lt;i&gt;D5Uwm68-D5Mit4&lt;/i&gt;)/Uwm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907436</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc41-D13Hmgc23&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="43830075" STOP_POS="43830298" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="49168131" STOP_POS="51182122" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="54236862" STOP_POS="56238470" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="45282442" STOP_POS="47299604" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907436</CITATION_ID>
    <DESCRIPTION>These were generated by crossing SS/JrHsdMcwi with SS-Chr 13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907438</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat77-D13Rat105&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="63483475" STOP_POS="63483695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="44139595" STOP_POS="60933518" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="49478067" STOP_POS="66075827" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="54552997" STOP_POS="71047437" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="45592985" STOP_POS="63175600" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907438</CITATION_ID>
    <DESCRIPTION>These were generated by crossing SS/JrHsdMcwi with SS-Chr 13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>6907445</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat124-D13Rat101&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="47780418" STOP_POS="50392939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45228358" STOP_POS="47841255" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50609228" STOP_POS="53264877" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55662705" STOP_POS="58314767" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="46721037" STOP_POS="49428577" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_6907445</CITATION_ID>
    <DESCRIPTION>These were generated by crossing SS/JrHsdMcwi with SS-Chr 13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7204133</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Rag1&lt;sup&gt;em1Ztm&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Zentrales Tierlaboratorium, Medizinische Hochschule Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rag1&lt;sup&gt;em1Ztm&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7204132</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108372087" STOP_POS="108383184" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87922910" STOP_POS="87922913" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91212243" STOP_POS="91212246" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97866048" STOP_POS="97877145" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86780782" STOP_POS="86791878" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7204133</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into LEW/Ztm rat embryos. The resulting mutation is a 4-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7204136</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Rag1&lt;sup&gt;em1Ang&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale (INSERM)</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rag1&lt;sup&gt;em1Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7204135</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108372087" STOP_POS="108383184" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87917061" STOP_POS="87928158" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91206394" STOP_POS="91217491" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97866048" STOP_POS="97877145" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86780782" STOP_POS="86791878" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7204136</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into Sprague-Dawley rat embryos. The resulting mutation is a 5-bp frameshift deletion in the Rag1 gene that predicts a protein with a normal sequence up to aa 245, followed by 5 aa from the insertions and mutations, followed by a stop codon in position 751.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7207880</RGD_ID>
    <STRAIN_SYMBOL>LEW.WKY-(&lt;i&gt;D13Arb15-D13Rat58&lt;/i&gt;)/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Imperial College, London, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="70819836" STOP_POS="94968043" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="68269576" STOP_POS="92436175" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="73748382" STOP_POS="98985851" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="78673431" STOP_POS="103987907" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="71116479" STOP_POS="96441728" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7207880</CITATION_ID>
    <DESCRIPTION>Segment of interest from chr 13 of WKY/NCrl was introgressed into LEW/SsNHsd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7240510</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat113-D4Kiru96&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, Rheumatology Unit, Karolinska Institutet, Karolinska University, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="157932452" STOP_POS="157932647" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="153826368" STOP_POS="156260744" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="153152949" STOP_POS="155869653" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="220242234" STOP_POS="220242357" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="157006984" STOP_POS="157007337" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7240510</CITATION_ID>
    <DESCRIPTION>congenic strain derived by marker-assisted transfer of the desired region from PVG.1AV1/Kini onto the genetic background of DA/ZtmKini</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7240512</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat113-D4Kiru80&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, Rheumatology Unit, Karolinska Institutet, Karolinska University, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="153826368" STOP_POS="156956242" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="153152949" STOP_POS="156629648" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="220242234" STOP_POS="220242357" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="157006984" STOP_POS="157007337" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7240512</CITATION_ID>
    <DESCRIPTION>congenic strain derived by marker-assisted transfer of the desired region from PVG.1AV1/Kini onto the genetic background of DA/ZtmKini</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7240513</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Kiru90-D4Kiru111&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, Rheumatology Unit, Karolinska Institutet, Karolinska University, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="156124880" STOP_POS="157432020" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="155730927" STOP_POS="157145363" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7240513</CITATION_ID>
    <DESCRIPTION>congenic strain derived by marker-assisted transfer of the desired region from PVG.1AV1/Kini onto the genetic background of DA/ZtmKini</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7240514</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Kiru12-D4Kiru55&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, Rheumatology Unit, Karolinska Institutet, Karolinska University, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="156207922" STOP_POS="156684523" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="155929794" STOP_POS="156347543" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7240514</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived by marker-assisted transfer of the desired region from DA.PVG.1AV1-(&lt;i&gt;D4Kiru90-D4Kiru111&lt;/i&gt;)/Kiru onto the genetic background of DA/ZtmKini</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7240521</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Kini3-D4Rat177&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Clinical Neuroscience, Neuroimmunology Unit, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="114036553" STOP_POS="114036742" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="112478605" STOP_POS="112478794" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="110635261" STOP_POS="110635449" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="175324865" STOP_POS="175325053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="114073976" STOP_POS="114074165" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7240521</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini females were mated with PVG.1AV1/Kini males; breeding pair from N5 generation were crossed for 2 generation to get the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7240522</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Kini3-D4Mgh14&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Clinical Neuroscience, Neuroimmunology Unit, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden, &lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1118&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Viral encephalitis (HSE)</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="40471453" STOP_POS="40471598" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="31021248" STOP_POS="39505420" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="28161938" STOP_POS="37685319" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="37534124" STOP_POS="37534268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="36592628" STOP_POS="36592773" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7240522</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini females were mated with PVG.1AV1/Kini males; breeding pair from N5 generation were crossed for 2 generation to get the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241047</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Lrrk1&lt;sup&gt;em1Sage&lt;/sup&gt;Lrrk2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/lrrk1-lrrk2-knockout-rat-tgrl6720&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/lrrk1-lrrk2-knockout-rat-tgrl6720&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-06-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrrk1&lt;sup&gt;em1Sage&lt;/sup&gt;|Lrrk2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241044|7241045</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="124706246" STOP_POS="124867234" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="129254815" STOP_POS="129390217" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="122826696" STOP_POS="122987711" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="119844360" STOP_POS="119972885" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="132857311" STOP_POS="133018549" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="127166866" STOP_POS="127301053" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="128248473" STOP_POS="128372456" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="132531591" STOP_POS="132694226" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="120695657" STOP_POS="120836324" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="130105902" STOP_POS="130267747" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241047</CITATION_ID>
    <DESCRIPTION>This strain was produced by crossing LE-Lrrk1&lt;sup&gt;em1Sage&lt;/sup&gt; with LE-Lrrk2&lt;sup&gt;em1Sage&lt;/sup&gt;</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241048</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Park7&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.sageresearchmodels.com/research-models/knockout-rats/park7-dj-1-knockout-rat&gt; Sigma Advanced Genetic Engineering Labs&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.sageresearchmodels.com/research-models/knockout-rats/park7-dj-1-knockout-rat&gt; Sigma Advanced Genetic Engineering Labs&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Park7&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241042</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="166636551" STOP_POS="166659825" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="161353718" STOP_POS="161376993" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="167982438" STOP_POS="168004724" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="171559202" STOP_POS="171582476" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="168050149" STOP_POS="168061616" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241048</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into Crl:LE rat embryos. The resulting mutation is a 9-bp deletion with 1-bp insertion in exon 5</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241049</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Pink1&lt;sup&gt;em1Sage-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Horizon Discovery</ORIGINATION>
    <SOURCE>&lt;a href=https://www.inotiv.com/model/hsdsage-le-pink1em1sage&gt; inotiv&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-11-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pink1&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241046</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="155813838" STOP_POS="155825950" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="150530523" STOP_POS="150542635" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="156677146" STOP_POS="156689258" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="160425715" STOP_POS="160437827" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="157091181" STOP_POS="157103293" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241049</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with Crl:LE to get heterozygous offspring which were intercrossed and offspring maintained as homozygous. This allele was made by ZFN mutagenesis. The resulting mutation is a 26-bp frameshift deletion in exon 4 (ACTACTACCCAGAAGGCCTGGGCCAC).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241050</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Lrrk2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/lrrk2-knockout-rat-tgrl4620&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/lrrk2-knockout-rat-tgrl4620&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-06-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrrk2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241045</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="124706246" STOP_POS="124867234" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="122826696" STOP_POS="122987711" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="132857311" STOP_POS="133018549" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="132531591" STOP_POS="132694226" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="130105902" STOP_POS="130267747" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241050</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into Crl:LE rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 30.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241051</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Lrrk1&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/lrrk1-knockout-rat-tgrl5880&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/lrrk1-knockout-rat-tgrl5880&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrrk1&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241044</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="129254815" STOP_POS="129390217" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="119844360" STOP_POS="119972885" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="127166866" STOP_POS="127301053" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="128248473" STOP_POS="128372456" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="120695657" STOP_POS="120836324" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241051</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into Crl:LE rat embryos. The resulting mutation is a 19-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241052</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Prkn&lt;sup&gt;em1Sage-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/park2-parkin-knockout-rat-tgrl4760&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/park2-parkin-knockout-rat-tgrl4760&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prkn&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241041</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="51236410" STOP_POS="52430242" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="48688651" STOP_POS="49882520" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="48880015" STOP_POS="50069998" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="49684308" STOP_POS="50875397" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="43151265" STOP_POS="44374470" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241052</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with Crl:LE to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous. The resulting mutation is a 5-bp frameshift deletion in exon 4 (TCAGT).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241053</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Lrrk1&lt;sup&gt;em1Sage-/-&lt;/sup&gt;Lrrk2&lt;sup&gt;em1Sage-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/lrrk1-lrrk2-knockout-rat-tgrl6720&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/lrrk1-lrrk2-knockout-rat-tgrl6720&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrrk1&lt;sup&gt;em1Sage&lt;/sup&gt;|Lrrk2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241044|7241045</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="124706246" STOP_POS="124867234" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="129254815" STOP_POS="129390217" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="122826696" STOP_POS="122987711" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="119844360" STOP_POS="119972885" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="132857311" STOP_POS="133018549" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="127166866" STOP_POS="127301053" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="128248473" STOP_POS="128372456" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="132531591" STOP_POS="132694226" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="120695657" STOP_POS="120836324" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="130105902" STOP_POS="130267747" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241053</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with Crl:LE to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241054</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Pink1&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.sageresearchmodels.com/research-models/knockout-rats/pink1-park6-knockout-rat&gt; Sigma Advanced Genetic Engineering Labs&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.sageresearchmodels.com/research-models/knockout-rats/pink1-park6-knockout-rat&gt; Sigma Advanced Genetic Engineering Labs&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pink1&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241046</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="155813838" STOP_POS="155825950" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="150530523" STOP_POS="150542635" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="156677146" STOP_POS="156689258" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="160425715" STOP_POS="160437827" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="157091181" STOP_POS="157103293" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241054</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into Crl:LE rat embryos. The resulting mutation is a 26-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241055</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Park7&lt;sup&gt;em1Sage-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/park7-dj-1-knockout-rat-tgrl4830&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/park7-dj-1-knockout-rat-tgrl4830&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-08)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Park7&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241042</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="166636551" STOP_POS="166659825" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="161353718" STOP_POS="161376993" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="167982438" STOP_POS="168004724" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="171559202" STOP_POS="171582476" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="168050149" STOP_POS="168061616" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241055</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with Crl:LE to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous. The resulting mutation is a 9-bp deletion with 1-bp insertion in exon 5 (TTGGTGAAGA).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241056</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Lrrk2&lt;sup&gt;em1Sage-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/lrrk2-knockout-rat-tgrl4620&gt; Sigma Advanced Genetic Engineering Labs&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/lrrk2-knockout-rat-tgrl4620&gt; Sigma Advanced Genetic Engineering Labs&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2018-08-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrrk2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241045</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="124706246" STOP_POS="124867234" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="122826696" STOP_POS="122987711" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="132857311" STOP_POS="133018549" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="132531591" STOP_POS="132694226" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="130105902" STOP_POS="130267747" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241056</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with Crl:LE to get heterozygous offspring which were intercrossed and offsprings maintained as homozygous</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241057</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Lrrk1&lt;sup&gt;em1Sage-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/lrrk1-knockout-rat-tgrl5880&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/lrrk1-knockout-rat-tgrl5880&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrrk1&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241044</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="129254815" STOP_POS="129390217" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="119844360" STOP_POS="119972885" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="127166866" STOP_POS="127301053" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="128248473" STOP_POS="128372456" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="120695657" STOP_POS="120836324" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241057</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders carrying a 19-bp frameshift deletion in exon 4 were backcrossed with Crl:LE to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241058</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Prkn&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.sageresearchmodels.com/research-models/knockout-rats/park2-knockout-rat&gt; Sigma Advanced Genetic Engineering Labs&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.sageresearchmodels.com/research-models/knockout-rats/park2-knockout-rat&gt; Sigma Advanced Genetic Engineering Labs&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prkn&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241041</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="51236410" STOP_POS="52430242" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="48688651" STOP_POS="49882520" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="48880015" STOP_POS="50069998" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="49684308" STOP_POS="50875397" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="43151265" STOP_POS="44374470" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241058</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into Crl:LE rat embryos. The resulting mutation is a 5-bp frameshift deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241239</RGD_ID>
    <STRAIN_SYMBOL>DA.BN-(&lt;i&gt;D9Wox18-D9Rat20&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="29567695" STOP_POS="57554279" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="22071200" STOP_POS="50062324" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="25692373" STOP_POS="54978814" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="24554204" STOP_POS="54685631" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="18347599" STOP_POS="47129300" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241239</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini females were mated with BN/Rj males, speed congenic strategy was used to generate these congenics; when the donor genome outside of the congenic segment was removed, two heterozygous animals were intercrossed to produce homozygous rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241240</RGD_ID>
    <STRAIN_SYMBOL>DA.BN-(&lt;i&gt;D9Mit6-D9Rat29&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="6714692" STOP_POS="6714888" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="25661188" STOP_POS="25661317" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="29466970" STOP_POS="29467098" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="28304251" STOP_POS="28304379" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="1526763" STOP_POS="22066432" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241240</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini females were mated with BN/Rj males, speed congenic strategy was used to generate these congenics; when the donor genome outside of the congenic segment was removed, two heterozygous animals were intercrossed to produce homozygous rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241241</RGD_ID>
    <STRAIN_SYMBOL>DA.BN-(&lt;i&gt;D9Mit6-D9Got15&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="6714692" STOP_POS="6714888" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="11735861" STOP_POS="11735976" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="13683965" STOP_POS="13684079" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="12615141" STOP_POS="12615255" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="1526763" STOP_POS="6948180" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241241</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini females were mated with BN/Rj males, speed congenic strategy was used to generate these congenics; when the donor genome outside of the congenic segment was removed, two heterozygous animals were intercrossed to produce homozygous rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241242</RGD_ID>
    <STRAIN_SYMBOL>DA.BN-(&lt;i&gt;D9Got8-D9Rat139&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="6096320" STOP_POS="6096447" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="4301731" STOP_POS="5859822" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="2657610" STOP_POS="3308009" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="2597055" STOP_POS="37252772" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="2174611" STOP_POS="3811711" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241242</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini females were mated with BN/Rj males, speed congenic strategy was used to generate these congenics; when the donor genome outside of the congenic segment was removed, two heterozygous animals were intercrossed to produce homozygous rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241243</RGD_ID>
    <STRAIN_SYMBOL>DA.BN-(&lt;i&gt;D9Wox24-D9Rat20&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1101&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="57554131" STOP_POS="57554279" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="1024537" STOP_POS="50062324" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="10869391" STOP_POS="54978814" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="9858502" STOP_POS="54685631" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="47129152" STOP_POS="47129300" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241243</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini females were mated with BN/Rj males, speed congenic strategy was used to generate these congenics; when the donor genome outside of the congenic segment was removed, two heterozygous animals were intercrossed to produce homozygous rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241244</RGD_ID>
    <STRAIN_SYMBOL>DA.BN-(&lt;i&gt;D9Wox24-D9Wox18&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="29567695" STOP_POS="29567893" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="1024537" STOP_POS="22071398" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="10869391" STOP_POS="25692570" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="9858502" STOP_POS="24554401" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="18347599" STOP_POS="18347796" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241244</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini females were mated with BN/Rj males, speed congenic strategy was used to generate these congenics; when the donor genome outside of the congenic segment was removed, two heterozygous animals were intercrossed to produce homozygous rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241245</RGD_ID>
    <STRAIN_SYMBOL>DA.BN-(&lt;i&gt;D9Wox24-D9Rat139&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="6096320" STOP_POS="6096447" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="1024537" STOP_POS="5859822" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="3307883" STOP_POS="10869489" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="9858502" STOP_POS="37252772" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="2174611" STOP_POS="2174738" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241245</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini females were mated with BN/Rj males, speed congenic strategy was used to generate these congenics; when the donor genome outside of the congenic segment was removed, two heterozygous animals were intercrossed to produce homozygous rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241246</RGD_ID>
    <STRAIN_SYMBOL>DA.BN-(&lt;i&gt;D9Wox24-D9Rat44&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="5346479" STOP_POS="5346648" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="1024537" STOP_POS="5109995" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="2880977" STOP_POS="10869489" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="2813697" STOP_POS="9858600" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="2948882" STOP_POS="2949051" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241246</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini females were mated with BN/Rj males, speed congenic strategy was used to generate these congenics; when the donor genome outside of the congenic segment was removed, two heterozygous animals were intercrossed to produce homozygous rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241247</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D9Got8-D9Got22&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="4301731" STOP_POS="16665381" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="2657610" STOP_POS="19076070" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="2597055" STOP_POS="17959093" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="3811425" STOP_POS="12324010" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241247</CITATION_ID>
    <DESCRIPTION>LEW/Rj females were mated with BN/Rj males, speed congenic strategy was used to generate these congenics; when the donor genome outside of the congenic segment was removed, two heterozygous animals were intercrossed to produce homozygous rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241248</RGD_ID>
    <STRAIN_SYMBOL>LEW.BN-(&lt;i&gt;D9Wox24-D9Got22&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="1024537" STOP_POS="16665381" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="10869391" STOP_POS="19076070" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="9858502" STOP_POS="17959093" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="12323882" STOP_POS="12324010" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241248</CITATION_ID>
    <DESCRIPTION>LEW/Rj females were mated with BN/Rj males, speed congenic strategy was used to generate these congenics; when the donor genome outside of the congenic segment was removed, two heterozygous animals were intercrossed to produce homozygous rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241265</RGD_ID>
    <STRAIN_SYMBOL>SHR-Chr Y&lt;sup&gt;WKY&lt;/sup&gt;/Akr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Universityof Akron breeding colonies, The University of Akron, Akron, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241265</CITATION_ID>
    <DESCRIPTION>WKY/NHsd males were crosssed with SHR/NHsd females to get F1 animals, the hybrid animals were backcrossed with female SHR/NHsd to transfer the Y chromosome</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241267</RGD_ID>
    <STRAIN_SYMBOL>WKY-Chr Y&lt;sup&gt;SHR&lt;/sup&gt;/Akr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Akron breeding colonies, The University of Akron, Akron, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241267</CITATION_ID>
    <DESCRIPTION>SHR/NHsd males were crosssed with WKY/NHsd females to get F1 animals, the hybrid animals were backcrossed with female WKY/NHsd to transfer the Y chromosome</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241271</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D10Mit4-D10Wox11&lt;/i&gt;)/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="35893263" STOP_POS="35893451" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="35392267" STOP_POS="51786432" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="36584373" STOP_POS="53637634" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="36354729" STOP_POS="53388667" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="36649906" STOP_POS="53793117" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241271</CITATION_ID>
    <DESCRIPTION>Segment of chromosome 10 from BN.&lt;i&gt;Lx&lt;/i&gt;/Cub was transferred to SHR/Ola after 9 backcrosses an intercross was done to obtain the desired congenic</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241594</RGD_ID>
    <STRAIN_SYMBOL>(SDxF344)F1-&lt;i&gt;Rbm20&lt;sup&gt;m1Mlgw&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-25)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rbm20&lt;i&gt;&lt;sup&gt;m1Mlgw&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241593</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="262671311" STOP_POS="262912551" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="252683760" STOP_POS="252907465" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="274391932" STOP_POS="274589816" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="281783646" STOP_POS="282003053" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="259905545" STOP_POS="260144190" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241594</CITATION_ID>
    <DESCRIPTION>This mutation, a deletion in chromosome 1 between bp 260,070,892 and 260,166,363, was originally found in the offspring of Hsd:SD x Hsd:SD. The phenotype was an altered titin isoform expression in the offspring. The parent carrier was identified by crossing both the male and the female Hsd:SD with F344/NHsd. This mutation is maintained on Hsd:SD X F344/NHsd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241595</RGD_ID>
    <STRAIN_SYMBOL>(SDxF344)F1xBN-&lt;i&gt;Rbm20&lt;sup&gt;m1Mlgw+/+&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rbm20&lt;i&gt;&lt;sup&gt;m1Mlgw&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241593</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="262671311" STOP_POS="262912551" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="252683760" STOP_POS="252907465" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="274391932" STOP_POS="274589816" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="281783646" STOP_POS="282003053" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="259905545" STOP_POS="260144190" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241595</CITATION_ID>
    <DESCRIPTION>Heterozygous offspring were intercrossed and maintained as wild type</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241596</RGD_ID>
    <STRAIN_SYMBOL>(SDxF344)F1-&lt;i&gt;Rbm20&lt;sup&gt;m1Mlgw+/+&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rbm20&lt;i&gt;&lt;sup&gt;m1Mlgw&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241593</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="262671311" STOP_POS="262912551" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="252683760" STOP_POS="252907465" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="274391932" STOP_POS="274589816" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="281783646" STOP_POS="282003053" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="259905545" STOP_POS="260144190" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241596</CITATION_ID>
    <DESCRIPTION>Heterozygous offsprings were intercrossed and maintained as wild type</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241597</RGD_ID>
    <STRAIN_SYMBOL>(SDxF344)F1xBN-&lt;i&gt;Rbm20&lt;sup&gt;m1Mlgw&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin, Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-25)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rbm20&lt;i&gt;&lt;sup&gt;m1Mlgw&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>7241593</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="262671311" STOP_POS="262912551" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="252683760" STOP_POS="252907465" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="274391932" STOP_POS="274589816" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="281783646" STOP_POS="282003053" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="259905545" STOP_POS="260144190" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241597</CITATION_ID>
    <DESCRIPTION>This mutation, a deletion in chromosome 1 between bp 260,070,892 and 260,166,363, was originally found in the offspring of Hsd:SD x Hsd:SD. The phenotype was an altered titin isoform expression in the offspring. The parent carrier was identified by crossing both the male and the female Hsd:SD with F344/NHsd. This mutation is maintained on Hsd:SD X F344/NHsd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241794</RGD_ID>
    <STRAIN_SYMBOL>SHR/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck Center for Molecular Medicine, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241794</CITATION_ID>
    <DESCRIPTION>This SHR colony is maintained at Max-Delbruck Center for Molecular Medicine, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7241811</RGD_ID>
    <STRAIN_SYMBOL>BBDP.WF-(&lt;i&gt;D8Rat73-D8Sunn1467&lt;/i&gt;)(&lt;i&gt;D13Rat124-D13Mgh5&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine and Immunology, University of Toronto, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7241811</CITATION_ID>
    <DESCRIPTION>a double congenic strain which has more than 38.74 Mb of chr 8 and more than 16.78 Mb of chr 13 of Wistar Furth introgressed into the gentic background of BBDP/WorSunn</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7243955</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;i&gt;D4Got44-D4Arb21&lt;/i&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="65117277" STOP_POS="103194936" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="63411811" STOP_POS="99067102" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="63125453" STOP_POS="163844250" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="63884916" STOP_POS="104416123" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7243955</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from backcrossing DA.F344-(&lt;i&gt;D4Got44-D4Arb4&lt;/i&gt;)/Arb (DA.F344(Cia3) with DA/BklArbN; after 10 backcrosses offsprings were intercrossed to ensure homozygosity</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7243960</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;i&gt;D4Got44-D4Rat128&lt;/i&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="81317600" STOP_POS="81317744" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="65117277" STOP_POS="79987019" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="63411811" STOP_POS="80666496" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="63125453" STOP_POS="145335458" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="63884916" STOP_POS="79190364" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7243960</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from backcrossing DA.F344-(&lt;i&gt;D4Got44-D4Arb4&lt;/i&gt;)/Arb (DA.F344(Cia3) with DA/BklArbN; after 10 backcrosses offsprings were intercrossed to ensure homozygosity</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7243963</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;i&gt;D4Uia2-D4Wox21&lt;/i&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="70331072" STOP_POS="80213769" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="69364375" STOP_POS="78882954" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="68379412" STOP_POS="79575667" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="133170446" STOP_POS="144249459" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="68131191" STOP_POS="78039646" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7243963</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from backcrossing DA.F344-(&lt;i&gt;D4Got44-D4Arb4&lt;/i&gt;)/Arb (DA.F344(Cia3) with DA/BklArbN; after 10 backcrosses offsprings were intercrossed to ensure homozygosity</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7243965</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;i&gt;D4Arb21-D4Arb4&lt;/i&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="103194656" STOP_POS="151805662" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="99066823" STOP_POS="150682594" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="163843971" STOP_POS="216606455" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="104415843" STOP_POS="154937227" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7243965</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from backcrossing DA.F344-(&lt;i&gt;D4Got44-D4Arb4&lt;/i&gt;)/Arb (DA.F344(Cia3) with DA/BklArbN; after 10 backcrosses offsprings were intercrossed to ensure homozygosity</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7243966</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;i&gt;D4Arb5-D4Arb4&lt;/i&gt;)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="118699819" STOP_POS="151805662" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="118044851" STOP_POS="150682594" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="182615641" STOP_POS="216606455" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="120436701" STOP_POS="154937227" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7243966</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from backcrossing DA.F344-(&lt;i&gt;D4Got44-D4Arb4&lt;/i&gt;)/Arb (DA.F344(Cia3) with DA/BklArbN; after 10 backcrosses offsprings were intercrossed to ensure homozygosity</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7244374</RGD_ID>
    <STRAIN_SYMBOL>FXLE/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Saitama Cancer Center Research Institute, 818 Komuro Saitama, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7244374</CITATION_ID>
    <DESCRIPTION>Recombinant inbred strain derived from Le/Stm (from Ben May, Laboratory for Cancer Research, University of Chicago, Chicago IL) and F344/DuCrlj (from Charles River Japan) and then maintained by brother-sister mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7244380</RGD_ID>
    <STRAIN_SYMBOL>DA.F344(Cia3c)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7244380</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from backcrossing DA.F344-(&lt;i&gt;D4Got44-D4Arb4&lt;/i&gt;)/Arb (DA.F344(Cia3) with DA/BklArbN; after 10 backcrosses offsprings were intercrossed to ensure homozygosity</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7244381</RGD_ID>
    <STRAIN_SYMBOL>DA.F344(Cia3e)/Arb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7244381</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from backcrossing DA.F344-(&lt;i&gt;D4Got44-D4Arb4&lt;/i&gt;)/Arb (DA.F344(Cia3) with DA/BklArbN; after 10 backcrosses offsprings were intercrossed to ensure homozygosity</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7245481</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(hsMt-LacZ)Reh</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=540&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=540&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2019-02-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00540</CITATION_ID>
    <DESCRIPTION>presses LacZ under the transcriptional control of the mouse metallothionein regulatory sequences. Transgene expression in germ cells is constitutive; expression of the transgene can be induced in liver by zinc or cadmium.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7245482</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg((ROSA)26-EGFP)RehRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=541&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=541&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2019-02-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00541</CITATION_ID>
    <DESCRIPTION>Strain carries a 1.8kb transgene consisting of the mouse ROSA26 regulatory sequences driving EGFP. FISH was used to localize the transgene insertion to Chromosome 11q11-q12, proximal to Grik1 and near Ncam2. The transgene is expressed exclusively in male and female germ cells throughtout development.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7245488</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Chat-tTA)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=632&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=632&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00632</CITATION_ID>
    <DESCRIPTION>Rats express a mouse tetracycline-controlled transactivator (tTA) driven by the mouse choline acetyltransferase (Chat) promotor. When mated to a second transgenic strain (RRRC:00633) that carries a target gene (TDP43) under the regulation of a tetracycline response element (TRE), the expression of TDP43 in Chat-expressing motor neurons in the double transgenic rats can be induced by withdrawal of doxycycline.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7245494</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(TRE-TARDBP-M337V)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=633&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=633&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>TARDBP</ALLELES>
    <ALLELE_RGD_IDS>1322081</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00633</CITATION_ID>
    <DESCRIPTION>Strain carries a transgene expressing human TDP43 with the M337V mutation under control of a tTA-dependent promoter (TRE). When mated to a second transgenic strain (RRRC:632) that carries a tetracycline-controlled transactivator driven by the mouse choline acetyltransferase (Chat) promoter, the expression of mutant TDP43 in Chat-expressing motor neurons in the double transgenic rats can be induced by withdrawal of doxycycline.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7245521</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Th-SNCA&lt;sup&gt;*&lt;/sup&gt;)3Ins</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=634&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=634&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00634</CITATION_ID>
    <DESCRIPTION>the transgene overexpressing double-mutated human alpha-synuclein (A53T and A30P) under the control of rat tyrosine hydroxylase (Th)promoter was microinjected into SD ovocytes to generate 3 transgenic rat lines. The MA3 line has pre-symptomatic olfactory deficits (beginning at 6 months of age) and motor deficits starting at a later age (19 months of age).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7245523</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Th-SNCA&lt;sup&gt;*&lt;/sup&gt;)4Ins</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=635&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=635&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00635</CITATION_ID>
    <DESCRIPTION>the transgene overexpressing duble-mutated human alpha-synuclein (A53T and A30P) under the control of rat tyrosine hydroxylase (Th)promoter was microinjected into SD ovocytes to generate 3 transgenic rat lines. This line, MA4, shows learning and memory deficits beginning at 9 months of age. It is a model for dementia with Lewy bodies.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7245527</RGD_ID>
    <STRAIN_SYMBOL>WKHA/Edh</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=663&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=663&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00663</CITATION_ID>
    <DESCRIPTION>derived from a cross between SHR/N and WKY/N starting in 1980; followed by selected brother/sister inbreedings from F2 generation forward, selecting WKHA for highest activity and lowest blood pressure</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7245556</RGD_ID>
    <STRAIN_SYMBOL>WKHT/Edh</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=664&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=664&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00664</CITATION_ID>
    <DESCRIPTION>WKHT rats are derived from a cross between SHR and WKY. Brother/sister inbreeding of the hybrids and successive generations was performed, selecting for the hypertension, but not the behavioral hyperactivity, of the SHR.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7246924</RGD_ID>
    <STRAIN_SYMBOL>HanTacFcfiq:WH</STRAIN_SYMBOL>
    <FULL_NAME>Wistar Hannover</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.usp.br/bioterio/Animais_Tipo_Linhagem.asp&gt;Universidade de Sao Paulo&lt;/a&gt;</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7246924</CITATION_ID>
    <DESCRIPTION>Received from Taconic in 2001; bred according to the Poiley rotation (1960) with permanent monogamous mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7246927</RGD_ID>
    <STRAIN_SYMBOL>NTacFcfiq:SD</STRAIN_SYMBOL>
    <FULL_NAME>Sprague Dawley</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.usp.br/bioterio/Animais_Tipo_Linhagem.asp&gt;Universidade de Sao Paulo&lt;/a&gt;</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7246927</CITATION_ID>
    <DESCRIPTION>Received from Taconic in 2001; bred according to the Poiley rotation (1960) with permanent monogamous mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7246928</RGD_ID>
    <STRAIN_SYMBOL>NTac:NIH-&lt;i&gt;Foxn1&lt;/i&gt;&lt;sup&gt;rnu&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>nude</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.taconic.com/wmspage.cfm?parm1=868&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7246928</CITATION_ID>
    <DESCRIPTION>The NIH nude Spontaneous mutant model was developed by NIH in 1979-1980 by intercrossing eight strains of rats. Taconic received stock from NIH Animal Genetic Resource in 1981. The rats were derived by hysterectomy in 1987 and again in 1998. Animals are randomly bred at Taconic without selection for coat color or pigmentation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7246929</RGD_ID>
    <STRAIN_SYMBOL>NTacFcfiq:NIH-&lt;i&gt;Foxn1&lt;/i&gt;&lt;sup&gt;rnu&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>nude</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.usp.br/bioterio/Animais_Tipo_Linhagem.asp&gt;Universidade de Sao Paulo&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.usp.br/bioterio/Animais_Tipo_Linhagem.asp&gt;Universidade de Sao Paulo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7246929</CITATION_ID>
    <DESCRIPTION>Received from Taconic in 2001; bred according to the Poiley rotation (1960) with permanent monogamous mating between homozygous male x heterozygous female.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7247278</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Camk2a-tTA)Xgx</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=655&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=655&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00655</CITATION_ID>
    <DESCRIPTION>Camk2a-tTA transgenic rats expressing tTA under regulatory control of the forebrain promotor Camk2a. Transgene expression can be blocked by administration of doxycycline to drinking water.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7247279</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(TRE-FUS-R521C)Xgx</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=656&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=656&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>FUS</ALLELES>
    <ALLELE_RGD_IDS>1318882</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00656</CITATION_ID>
    <DESCRIPTION>Overexpression of R521C mutant form of human FUS (Fused in Sarcoma) transgene is under regulatory control of tetracycline-responsive promoter element.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7247280</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(TRE-LacZ)Xgx</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=657&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=657&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00657</CITATION_ID>
    <DESCRIPTION>LacZ gene was assembled downstream of the TRE (tetracycline-responsive promoter elements) promoter, allowing inducible gene expression.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7247286</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(APP)21Besey</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=636&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=636&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>APP</ALLELES>
    <ALLELE_RGD_IDS>736021</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00636</CITATION_ID>
    <DESCRIPTION>F344/NHsd embryos were microinjected with a DNA construct containing human beta amyloid precursor protein (APP), Swedish (Swe) double mutation (K670N-M671L) and Indiana (Ind) single autosomal dominant mutation (V642F). The transgene is driven by an ubiquitin-C promoter. Homozygous transgenic rats exhibit approximately 2.9-fold more expression of APP mRNA than wild-type rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7247289</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(TETRA-EGFP)Besey</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=650&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=650&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00650</CITATION_ID>
    <DESCRIPTION>SD embryos were microinjected with a DNA construct containing the GFP gene downstream of a miniCMV promoter under the control of tetracycline response element (TRE). The pLV-Tet-GFP was generated by co-transfection of pLV-Tet-GFP, pÎ8.9 and pVSV-G  into a 293FT packaging cell line</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7247290</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Ubc-P2ry2)Besey</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=627&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=627&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-08-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>P2ry2</ALLELES>
    <ALLELE_RGD_IDS>62088</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00627</CITATION_ID>
    <DESCRIPTION>SD embryos were microinjected with a lentiviral construct containing the rat P2ry2 gene (G protein-coupled purinergic receptor P2Y2) under control of an ubiquitin-C promoter. Results in over-expression of P2ry2 mRNA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7247594</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;i&gt;D1Rat90-D1Mit18&lt;/i&gt;)/Iwai</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shiga University of Medical Science, Otsu, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="228180243" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="218753689" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="238830408" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="246118980" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="224426266" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7247594</CITATION_ID>
    <DESCRIPTION>Fragment of the chromosome 1 derived from SHR and repeated backcross to WKY</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248453</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D12Hmgc3-AU047911&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="13008296" STOP_POS="14942487" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="15085585" STOP_POS="17031347" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="17102817" STOP_POS="19021770" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="15420627" STOP_POS="15420833" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248453</CITATION_ID>
    <DESCRIPTION>Subcongenic strain generated by backcrossing SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;.SS-(&lt;i&gt;D12Hmgc3-D12Hmgc6&lt;/i&gt;)/Mcwi to SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, intercrossing the F&lt;sub&gt;1&lt;/sub&gt; generation, and genotyping for recombinations; recombinant strain was backcrossed to SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;/Mcwi and bred to homozygosity.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248454</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D12Hmgc7-D12Hmgc6&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="19801203" STOP_POS="24849755" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="19212614" STOP_POS="19212979" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="22283062" STOP_POS="22283507" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="24299715" STOP_POS="24300160" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248454</CITATION_ID>
    <DESCRIPTION>Subcongenic strain generated by backcrossing SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;.SS-(&lt;i&gt;D12Hmgc3-D12Hmgc6&lt;/i&gt;)/Mcwi to SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, intercrossing the F&lt;sub&gt;1&lt;/sub&gt; generation, and genotyping for recombinations; recombinant strain was backcrossed to SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;/Mcwi and bred to homozygosity.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248456</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D12Hmgc3-D12Got29&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="13008296" STOP_POS="13925040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="15085585" STOP_POS="16012213" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="17102817" STOP_POS="18009770" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="14395317" STOP_POS="14395596" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248456</CITATION_ID>
    <DESCRIPTION>Subcongenic strain generated by backcrossing SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;.SS-(&lt;i&gt;D12Hmgc3-D12Hmgc6&lt;/i&gt;)/Mcwi to SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, intercrossing the F&lt;sub&gt;1&lt;/sub&gt; generation, and genotyping for recombinations; recombinant strain was backcrossed to SS-Chr 12&lt;sup&gt;BN&lt;/sup&gt;/Mcwi and bred to homozygosity.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248716</RGD_ID>
    <STRAIN_SYMBOL>NAK/Nokh</STRAIN_SYMBOL>
    <FULL_NAME>Nodai aphakia</FULL_NAME>
    <ORIGINATION>Faculty of Bioindustry, Tokyo University of Agriculture in Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248716</CITATION_ID>
    <DESCRIPTION>This is an inbred anophthalmic rat strain derived from a Sprague-Dawley (SD) colony and designated it as Nodai aphakia (NAK) by Dr.Ryoichi Hashizume in Tokyo University of Agriculture. The NAK rats have decreased body size than wild-type rats and do not have both eyes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248725</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Rat164-D7Uwm27&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="65287247" STOP_POS="65287381" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="72752037" STOP_POS="72752170" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="72918736" STOP_POS="72918869" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="69506936" STOP_POS="69507070" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248725</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248727</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Rat164-D7Uwm30&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="65287247" STOP_POS="65287381" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="72752037" STOP_POS="72752170" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="72918736" STOP_POS="72918869" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="69506936" STOP_POS="69507070" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248727</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248729</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Rat206-D7Uwm30&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="72725037" STOP_POS="72725261" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="70840118" STOP_POS="70840342" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="78758303" STOP_POS="78758526" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="78786126" STOP_POS="78786349" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="75357125" STOP_POS="75357349" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248729</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248731</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Rat164-D7Uwm31&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="65287247" STOP_POS="65287381" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="72752037" STOP_POS="72752170" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="72918736" STOP_POS="72918869" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="69506936" STOP_POS="69507070" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248731</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248733</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Rat164-D7Uwm33&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="90922835" STOP_POS="90923079" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="65287247" STOP_POS="65287381" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="72752037" STOP_POS="72752170" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="72918736" STOP_POS="72918869" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="69506936" STOP_POS="69507070" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248733</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248736</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Uwm32-D7Uwm27&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248736</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248738</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Uwm36-D7Uwm27&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248738</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248740</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Uwm38-D7Uwm27&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248740</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248742</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Uwm33-D7Mit27&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="90922835" STOP_POS="95485241" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="93595631" STOP_POS="93595843" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="102588240" STOP_POS="102588450" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="103159379" STOP_POS="103159589" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="98955068" STOP_POS="98955278" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248742</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248744</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Uwm33-D7Uwm27&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="90922835" STOP_POS="90923079" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248744</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248746</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Uwm41-D7Mit16&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="93723715" STOP_POS="115766396" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="113886156" STOP_POS="113886318" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="123602837" STOP_POS="123602998" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="123587556" STOP_POS="123587717" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="120745845" STOP_POS="120746007" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248746</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7248748</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Uwm28-D7Mit16&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="115766234" STOP_POS="115766396" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="113886156" STOP_POS="113886318" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="123602837" STOP_POS="123602998" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="123587556" STOP_POS="123587717" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="120745845" STOP_POS="120746007" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7248748</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7257663</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Tlr4&lt;sup&gt;em1Geh&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Pittsburgh</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=694&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>alcohol action, immune system function, septic shock</RESEARCH_USE>
    <ALLELES>Tlr4&lt;sup&gt;em1Geh&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7257661</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="85161247" STOP_POS="85174882" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="80146180" STOP_POS="80146192" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="82587737" STOP_POS="82587749" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="86690670" STOP_POS="86704302" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="83564100" STOP_POS="83577735" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00694</CITATION_ID>
    <DESCRIPTION>This strain was produced by TALEN mediated 13 bp deletion in Exon 1 in the rat Tlr4 gene; background strain is Crl:WI</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7257722</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHR-(&lt;i&gt;D1Mgh14-D1Rat77&lt;/i&gt;)/Iwai</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shiga University of Medical Science, Otsu, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="266453608" STOP_POS="266453731" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="231688927" STOP_POS="256448636" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="252479838" STOP_POS="278228889" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="259703519" STOP_POS="285604895" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="238037373" STOP_POS="263699089" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7257722</CITATION_ID>
    <DESCRIPTION>Fragment of the chromosome 1 derived from SHR/NCrlj and repeated backcross to WKY/NCrlCrlj</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7349321</RGD_ID>
    <STRAIN_SYMBOL>LEXF2D/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Saitama Cancer Center Research Institute, Saitama, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7349321</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7349322</RGD_ID>
    <STRAIN_SYMBOL>LEXF8B/Stm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Saitama Cancer Center Research Institute, Saitama, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7349322</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7349357</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Got128-D4Got136&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="157757348" STOP_POS="157757491" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="156085418" STOP_POS="157232313" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="155691688" STOP_POS="156945571" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="222712454" STOP_POS="223964695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="159334251" STOP_POS="160528447" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7349357</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from marker assisted selection for PVG.1AV1 chromsome 4 alleles on the DA recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364879</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Apoe&lt;sup&gt;em9Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Apoe&lt;sup&gt;em9Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>7364878</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="88483107" STOP_POS="88483207" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="79355142" STOP_POS="79355242" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="80614112" STOP_POS="80614212" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="80614112" STOP_POS="80614212" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="81878372" STOP_POS="81882298" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="79003634" STOP_POS="79006387" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7364879</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CAGGCCCTGAACCGCttctggGATTACCTGCGCTGGG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 101-bp deletion in exon 2 and intron 3</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364880</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cst3&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cst3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687708</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="156790061" STOP_POS="156794116" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="136336923" STOP_POS="136340796" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="143223300" STOP_POS="143223317" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="149628692" STOP_POS="149632565" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="137650903" STOP_POS="137654776" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7364880</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CTTCGCCGTAAGCGAGTAcaacaaGGGCAGCAACGAT into SS/JrHsdMcwi rat embryos. The resulting mutation is a 18-bp deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364881</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Slc7a9&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc7a9&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5687700</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="97246253" STOP_POS="97269546" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="88109517" STOP_POS="88132653" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="91709034" STOP_POS="91738492" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="92836837" STOP_POS="92865759" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="87976440" STOP_POS="87999102" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7364881</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ATCGTCGCCATCATCATCatcagcGGACTGGTCCTCCTG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp frameshift deletion in exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364882</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sorcs2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sorcs2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5508343</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="78592290" STOP_POS="78960582" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="74711197" STOP_POS="74711230" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="79538911" STOP_POS="79912333" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="79176694" STOP_POS="79547823" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="79968072" STOP_POS="80344330" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7364882</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence ATCGTCGCCATCATCATCatcagcGGACTGGTCCTCCTG into SS/JrHsdMcwi rat embryos. The resulting mutation is a 34-bp frameshift deletion in exon 15.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364902</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 2&lt;sup&gt;BN&lt;/sup&gt;/1McwiAek</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=683&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=683&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2019-02-19)</AVAILABILITY>
    <RESEARCH_USE>Studies of ischemia reperfusion injury or hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00683</CITATION_ID>
    <DESCRIPTION>Compared to the current SS-Chr 2&lt;sup&gt;BN&lt;/sup&gt;/Mcwi colony at the Medical College of Wisconsin (where this strain originated) it is a more complete consomic strain (a smaller piece of distal Chromosome 2 is of the SS genotype compared to the SS-Chr 2&lt;sup&gt;BN&lt;/sup&gt;/Mcwi strain).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364919</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;rs64114288-rs107464428&lt;/i&gt;)/Aek</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=686&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=686&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-19)</AVAILABILITY>
    <RESEARCH_USE>cardiac ischemia</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="8528522" STOP_POS="220580657" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="6796723" STOP_POS="217906389" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="4124871" STOP_POS="233798506" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00686</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a fragment of chromosome 2 of the SS-Chr 2&lt;sup&gt;BN&lt;/sup&gt;/Mcwi from the top to ~227 Mb transferred to the SS/JrHsdMcwi strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364923</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;rs106982173-rs65057186&lt;/i&gt;)/Aek</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=685&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=685&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-19)</AVAILABILITY>
    <RESEARCH_USE>cardiac ischemia</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="95260959" STOP_POS="213148027" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="93353642" STOP_POS="210463377" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="95571004" STOP_POS="225944289" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00685</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a fragment of chromosome 2 of the SS-Chr 2&lt;sup&gt;BN&lt;/sup&gt;/Mcwi from ~95 to 219 Mb transferred to the SS/JrHsdMcwi strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364927</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;rs13453786-rs66377062&lt;/i&gt;)/Aek</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=684&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=684&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-19)</AVAILABILITY>
    <RESEARCH_USE>cardiac ischemia</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="218288393" STOP_POS="242222841" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="215613858" STOP_POS="239562817" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="231460803" STOP_POS="255813030" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00684</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a fragment of chromosome 2 of the SS-Chr 2&lt;sup&gt;BN&lt;/sup&gt;/Mcwi from ~95 to 219 Mb transferred to the SS/JrHsdMcwi strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364932</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Rat42-D7Uwm33&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="85043242" STOP_POS="92567115" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="83153392" STOP_POS="90677661" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="10173862" STOP_POS="108696915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="20168871" STOP_POS="116858395" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="88132195" STOP_POS="88132315" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7364932</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364934</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;rs199006987-D7Uwm27&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="94645200" STOP_POS="94645200" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="92755814" STOP_POS="92755814" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="101422284" STOP_POS="101422284" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7364934</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364936</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Arb15-D7Uwm27&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="91412389" STOP_POS="91412612" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="100160221" STOP_POS="100160441" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="100740218" STOP_POS="100740438" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="96648929" STOP_POS="96649150" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7364936</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364938</RGD_ID>
    <STRAIN_SYMBOL>(LE x RCS-&lt;i&gt;p&lt;/i&gt;&lt;sup&gt;+&lt;/sup&gt;/LavRrrc)F1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=662&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=662&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-18)</AVAILABILITY>
    <RESEARCH_USE>Retinal Research</RESEARCH_USE>
    <ALLELES>Mertk</ALLELES>
    <ALLELE_RGD_IDS>69283</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00662</CITATION_ID>
    <DESCRIPTION>RCS-&lt;i&gt;p&lt;/i&gt;&lt;sup&gt;+&lt;/sup&gt;/LavRrrc males were mated to LE females.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364940</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Tp53&lt;sup&gt;tm1(EGFP-Pac)Qly&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=661&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=661&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>tumorigenesis model</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00661</CITATION_ID>
    <DESCRIPTION>Backcrossed STOCK-&lt;i&gt;Tp53&lt;sup&gt;tm1(EGFP-Pac)Qly&lt;/sup&gt;&lt;/i&gt;Rrrc with F344 using speed congenic approach to move mutation onto F344 genetic background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364954</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D2Mit12-D2Got121&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Shore-Long Island Jewish Research Institute,350 Community Drive - Manhasset, NY 11030.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=668&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-18)</AVAILABILITY>
    <RESEARCH_USE>arthritis/autoimmunity studies</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="170656145" STOP_POS="170656389" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="168358098" STOP_POS="186483643" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="181990297" STOP_POS="201193787" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="201404917" STOP_POS="220662282" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="174730375" STOP_POS="193841840" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00668</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing DA/BklArbNsi and ACI/SegHsd 7 times then brother-sister mating to maintain in the homozygous state</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364956</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D2Wox20-D2Mit14&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Shore-Long Island Jewish Research Institute,350 Community Drive - Manhasset, NY 11030.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=669&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-18)</AVAILABILITY>
    <RESEARCH_USE>arthritis/autoimmunity studies</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="176839632" STOP_POS="192287892" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="174541858" STOP_POS="189599348" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="188448030" STOP_POS="204585731" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="207864396" STOP_POS="224018437" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="181213221" STOP_POS="197256313" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00669</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing DA/BklArbNsi and ACI/SegHsd 10 times then brother-sister mating to maintain in the homozygous state</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364959</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D2Uwm24-D2Rat54&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Shore-Long Island Jewish Research Institute,350 Community Drive - Manhasset, NY 11030.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=670&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-18)</AVAILABILITY>
    <RESEARCH_USE>arthritis/autoimmunity studies</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="204524174" STOP_POS="204524480" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="190460423" STOP_POS="201836059" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="205430606" STOP_POS="216878775" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="224860752" STOP_POS="234970326" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="198168347" STOP_POS="210012267" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00670</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing DA/BklArbNsi and ACI/SegHsd 8 times then brother-sister mating to maintain in the homozygous state</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364970</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D12Mit2-D12Got49&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Shore-Long Island Jewish Research Institute,350 Community Drive - Manhasset, NY 11030.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=671&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-18)</AVAILABILITY>
    <RESEARCH_USE>arthritis/autoimmunity studies</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="19610870" STOP_POS="23060532" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="22650702" STOP_POS="26079250" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="24662983" STOP_POS="28081151" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="20932559" STOP_POS="24257553" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00671</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing DA/BklArbNsi and ACI/SegHsd 12 times then brother-sister mating to maintain in the homozygous state</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364974</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;i&gt;D10Rat195-D10Rat92&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Shore-Long Island Jewish Research Institute,350 Community Drive - Manhasset, NY 11030.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=676&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-19)</AVAILABILITY>
    <RESEARCH_USE>arthritis/autoimmunity studies</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="63039991" STOP_POS="75083145" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="62541890" STOP_POS="74586024" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="65234285" STOP_POS="77269936" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="66394066" STOP_POS="77132664" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="63690620" STOP_POS="78170722" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00676</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing F344/NHsd into DA/BklArbNsi 8 times then brother-sister mating to maintain in the homozygous state</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364976</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;i&gt;D10Rat195-D10Arb27&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Shore-Long Island Jewish Research Institute,350 Community Drive - Manhasset, NY 11030.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=677&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-19)</AVAILABILITY>
    <RESEARCH_USE>arthritis/autoimmunity studies</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="63039991" STOP_POS="63040202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="62541890" STOP_POS="65927370" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="65234285" STOP_POS="68305173" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="66394066" STOP_POS="67971488" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="63690620" STOP_POS="69160517" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00677</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing F344 into DA/BklArbNsi 8 times then brother-sister mating to maintain in the homozygous state</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364978</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;i&gt;D10Arb27-D10Rat92&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Shore-Long Island Jewish Research Institute,350 Community Drive - Manhasset, NY 11030.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=678&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-19)</AVAILABILITY>
    <RESEARCH_USE>arthritis/autoimmunity studies</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="75082967" STOP_POS="75083145" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="65927233" STOP_POS="74586024" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="68305037" STOP_POS="77269936" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="67971352" STOP_POS="77132664" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="69160380" STOP_POS="78170722" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00678</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing F344 into DA/BklArbNsi 8 times then brother-sister mating to maintain in the homozygous state</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364981</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;i&gt;D7Rat22-D7Rat15&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=680&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-19)</AVAILABILITY>
    <RESEARCH_USE>arthritis/autoimmunity studies</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="101772987" STOP_POS="101773158" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="111043360" STOP_POS="111043530" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="110975825" STOP_POS="110975995" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="76615341" STOP_POS="107428439" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00680</CITATION_ID>
    <DESCRIPTION>Congenic strain created by backcrossing F344/NHsd into DA/BklArbNsi 11 times then brother-sister mating to maintain in the homozygous state</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7364991</RGD_ID>
    <STRAIN_SYMBOL>ACI/EurMcwi</STRAIN_SYMBOL>
    <FULL_NAME>ACI (August × Copenhagen Irish)</FULL_NAME>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;, contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;, contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-08-06)</AVAILABILITY>
    <RESEARCH_USE>Renal disease</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7364991</CITATION_ID>
    <DESCRIPTION>substrain of ACI derived from ACI/Eur</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7365040</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;rs65785750-rs13452155&lt;/i&gt;)/Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Massachusetts. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=612&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-05-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="106658272" STOP_POS="136728517" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="101612333" STOP_POS="131443083" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="105452223" STOP_POS="136738047" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7365040</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing SS/JrHsd and SR/JrHsd parental strains</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7365043</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;rs65785750-rs106808193&lt;/i&gt;)/Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Massachusetts. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=613&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="106658272" STOP_POS="140009902" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="101612333" STOP_POS="134724733" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="105452223" STOP_POS="140120264" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7365043</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing SS/JrHsd and SR/JrHsd parental strains</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7394698</RGD_ID>
    <STRAIN_SYMBOL>ZUC.BN-(&lt;i&gt;D1Rat42-D1Rat90&lt;/i&gt;)/Ste</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of California Davis, Davis, CA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="269633753" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="133587283" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="141381406" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="142342107" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="135418152" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7394698</CITATION_ID>
    <DESCRIPTION>homozygous lean wild-type ZUC-&lt;I&gt;Lepr&lt;/I&gt;&lt;sup&gt;+Ste&lt;/sup&gt; were crossed with BN/Crl to get F&lt;sub&gt;1&lt;/sub&gt;; these were backcrossed to lean ZUC males; congenics were selected by genotyping with markers</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7394818</RGD_ID>
    <STRAIN_SYMBOL>P.NP-(&lt;i&gt;D4Mgh16-D4Rat173&lt;/i&gt;)/Iusm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="63900458" STOP_POS="93819611" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="62933269" STOP_POS="92489678" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="61708103" STOP_POS="94143659" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="61427427" STOP_POS="158932336" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="61646674" STOP_POS="92716873" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7394818</CITATION_ID>
    <DESCRIPTION>P.NP-(&lt;i&gt;D4Rat119-D4Rat55&lt;/i&gt;)/Iusm and iP rats were crossed to get F1 animals which were further backcrossed to iP rats for 10 generations, this was followed by intercross to generate the congenic strains, these animals were selected by marker-assisted selection</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7394821</RGD_ID>
    <STRAIN_SYMBOL>P.NP-(&lt;i&gt;Snca-D4Rat35&lt;/i&gt;)/Iusm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Snca</ALLELES>
    <ALLELE_RGD_IDS>3729</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="91026474" STOP_POS="91127444" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="89696420" STOP_POS="91366774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="90782412" STOP_POS="92490285" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="155592411" STOP_POS="157297332" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="89613731" STOP_POS="91336908" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7394821</CITATION_ID>
    <DESCRIPTION>P.NP-(&lt;i&gt;D4Rat119-D4Rat55&lt;/i&gt;)/Iusm and iP rats were crossed to get F1 animals which were further backcrossed to P rats for 10 generations, this was followed by intercross to generate the congenic strains, these animals were selected by marker-assisted selection</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7401201</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D17Rat24-rs106534785&lt;/i&gt;)/Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Massachusetts. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=615&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="54263396" STOP_POS="65841305" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="49567911" STOP_POS="61149946" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="52424553" STOP_POS="63306062" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="50489557" STOP_POS="50489725" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="57724628" STOP_POS="57727194" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00615</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing SS/JrHsd and SR/JrHsd parental strains</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7401203</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;rs105019230-D17Rat44&lt;/i&gt;)/Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Massachusetts. </ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-05-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="59237618" STOP_POS="75066472" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="54542464" STOP_POS="70156904" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="57343133" STOP_POS="73981731" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="75653544" STOP_POS="75653670" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="81612361" STOP_POS="81612488" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00616</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing SS/JrHsd and SR/JrHsd parental strains. &lt;a href=http://www.rrrc.us/Strain/?x=616&gt;Rat Resource and Research Center&lt;/a&gt;</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7401261</RGD_ID>
    <STRAIN_SYMBOL>LOU/NimrOlaHsd</STRAIN_SYMBOL>
    <FULL_NAME>Louvain</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href =http://www.envigo.com/products-services/research-models-services/find-a-model/research-models/rats/inbred/lou-c-inbred-rat/&gt;Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2023-12-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7401261</CITATION_ID>
    <DESCRIPTION>LOU/C was selected for high immunocytoma incidence; to National Institute of Medical Research, Mill Hill; in 1985 from Nimr to Harlan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7411634</RGD_ID>
    <STRAIN_SYMBOL>WDB/Nips</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi, JAPAN</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7411634</CITATION_ID>
    <DESCRIPTION>Crlj:WI females were bred to DA/Slc males to generate F&lt;sub&gt;1&lt;/sub&gt; pups which were bred by brother-sister mating; only black (non-agouti) pups were picked for breeding. (The genotype of the pups was checked by backcrossing  to BN (for BB or Bb) and Hooded strains (for HH or Hh) genotype.) When the aaBBCCHH genotype of F2 was confirmed then the strain was maintained by brother-sister mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7411676</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D3Mgh16-D3Rat114&lt;/i&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Western Infirmary, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="167835447" STOP_POS="167835660" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="10778704" STOP_POS="147415807" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="6000748" STOP_POS="155263151" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="11361699" STOP_POS="160347840" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="6373335" STOP_POS="149496698" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7411676</CITATION_ID>
    <DESCRIPTION>Congenic strain created by speed congenic strategy where the desired region from Chromosome 3 of WKY/Gcrc was introgressed into the SHRSP/Gcrc background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7411679</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D2Rat13-D2Rat157&lt;/i&gt;)(&lt;i&gt;D3Mgh16-D3Rat114&lt;/i&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Glasgow, Western Infirmary, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7411679</CITATION_ID>
    <DESCRIPTION>F&lt;sub&gt;1&lt;/sub&gt; rats generated by crossing SHRSP.WKY-(&lt;i&gt;D3Mgh16-D3Rat114&lt;/i&gt;)/Gcrc and SHRSP.WKY-(&lt;i&gt;D2Rat13-D2Rat157&lt;/i&gt;)/Gcrc were backcrossed to SHRSP.WKY-(&lt;i&gt;D2Rat13-D2Rat157&lt;/i&gt;)/Gcrc; heterozygous animals for chr 3 fragment were crossed with homozygous animals for chr 2; animals that were homozygous for both fragments were intercrossed to get the desired bicongenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7411703</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D1Rat93-D1Rat269&lt;/i&gt;)(&lt;i&gt;D18Rat73-D18Rat11&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1083&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="134387145" STOP_POS="134387335" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="52198059" STOP_POS="70689286" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="49999958" STOP_POS="68414117" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="65677942" STOP_POS="124977364" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="51609032" STOP_POS="70803264" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="64252881" STOP_POS="132448306" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="50804228" STOP_POS="69942605" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="63244295" STOP_POS="133485967" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="63990899" STOP_POS="126292805" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="52290789" STOP_POS="71692408" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7411703</CITATION_ID>
    <DESCRIPTION>constructed by crossing and backcrossing the congenic strains for chr 1 and chr 18 segments</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7411705</RGD_ID>
    <STRAIN_SYMBOL>SHR.SHRSP-(&lt;i&gt;D1Rat93-D1Rat269&lt;/i&gt;)(&lt;i&gt;D18Rat73-D18Rat11&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1082&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="134387145" STOP_POS="134387335" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="52198059" STOP_POS="70689286" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="49999958" STOP_POS="68414117" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="65677942" STOP_POS="124977364" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="51609032" STOP_POS="70803264" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="64252881" STOP_POS="132448306" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="50804228" STOP_POS="69942605" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="63244295" STOP_POS="133485967" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="63990899" STOP_POS="126292805" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="52290789" STOP_POS="71692408" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7411705</CITATION_ID>
    <DESCRIPTION>constructed by crossing and backcrossing the congenic strains for chr 1 and chr 18 segments</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7411707</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D1Mgh5-D1Got87&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1084&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="87558729" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="86030749" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="91156803" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="92291485" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="85828306" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7411707</CITATION_ID>
    <DESCRIPTION>male SHRSP.SHR-(&lt;i&gt;D1Rat93-D1Rat269&lt;/i&gt;)/Izm were crossed with female SHRSP/Izm and the offsprings were intercrossed, animals were genotyped to get the desired recombinants which were then backcrossed to SHRSP/Izm</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7411709</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D1Mit30-D1Rat269&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1086&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="134387145" STOP_POS="134387335" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="94494440" STOP_POS="124977364" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="99983293" STOP_POS="132448306" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="101048742" STOP_POS="133485967" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="94473940" STOP_POS="126292805" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7411709</CITATION_ID>
    <DESCRIPTION>male SHRSP.SHR-(D1Rat93-D1Rat269)/Izm were crossed with female SHRSP/Izm and the offsprings were intercrossed, animals were genotyped to get the desired recombinants which were then backcrossed to SHRSP/Izm</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421599</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Chm64-D1Rat19&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="51940904" STOP_POS="51941022" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="49393172" STOP_POS="49393289" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="49578577" STOP_POS="49578693" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="50173150" STOP_POS="50173266" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="43872710" STOP_POS="43872827" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421599</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 1 was transferred from LEW/Crlc into the SS/Jr background, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421603</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Rat320-D1Mgh32&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="128019551" STOP_POS="128019780" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="118608292" STOP_POS="241799120" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="125875758" STOP_POS="262433692" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="126980427" STOP_POS="269885827" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="119536684" STOP_POS="247882384" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421603</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 1 was transferred from LEW/Crlc into the SS/Jr background, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421606</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Uia4-D1Rat320&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="128019551" STOP_POS="128019780" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="58114204" STOP_POS="58114246" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="17435338" STOP_POS="17435380" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="66023617" STOP_POS="118608521" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="146042096" STOP_POS="146042138" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="64588516" STOP_POS="125875986" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="63580258" STOP_POS="126980655" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="64343599" STOP_POS="119536913" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421606</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 1 was transferred from LEW/Crlc into the SS/Jr background, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421610</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mit5-D5M4Mit14&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="104250862" STOP_POS="104251008" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="108092659" STOP_POS="108092802" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="112057862" STOP_POS="112058005" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="109163281" STOP_POS="109163425" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421610</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 5 was transferred from LEW/Crlc into the SS/Jr background, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421612</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D16Chm48-D16Chm60&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="3080416" STOP_POS="3080679" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="3524957" STOP_POS="3525217" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="2471921" STOP_POS="3491557" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="2116303" STOP_POS="3165043" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421612</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 16 was transferred from LEW/Crlc into the SS/Jr background, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421617</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D17Chm14-D17Rat65&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="87387778" STOP_POS="87388164" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="68783937" STOP_POS="82479847" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="72580584" STOP_POS="86731080" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="74265283" STOP_POS="88435496" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="80181988" STOP_POS="93930006" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421617</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 17 was transferred from LEW/Crlc into the SS/Jr background, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421619</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D17Chm85-D17Chm71&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421619</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 17 was transferred from LEW/Crlc into the SS/Jr background, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421621</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D17Chm131-D17Chm93&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421621</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 17 was transferred from LEW/Crlc into the SS/Jr background, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421623</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D17Rat84-D17Chm17&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="23858926" STOP_POS="23859062" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="23653184" STOP_POS="23653323" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="21490950" STOP_POS="21491085" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="23473207" STOP_POS="23473342" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="29603712" STOP_POS="29604237" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421623</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 17 was transferred from LEW/Crlc into the SS/Jr background, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421634</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Got93-D2Rat222&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="137969690" STOP_POS="142404038" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="135818873" STOP_POS="140253961" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="140958240" STOP_POS="145514793" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="160649967" STOP_POS="164927046" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="140672373" STOP_POS="145318823" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421634</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 was transferred from MNS/N into the SS/Jr background, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421636</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm90-D2Rat38&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="151869660" STOP_POS="151869825" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="142323368" STOP_POS="149559726" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="148295267" STOP_POS="155965721" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="167706439" STOP_POS="175354471" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="147424195" STOP_POS="155102371" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421636</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 was transferred from MNS/N into the SS/Jr background, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421638</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm381-D2Chm225&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="150649899" STOP_POS="150650069" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="158268536" STOP_POS="158268703" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="177626917" STOP_POS="177627084" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="156267173" STOP_POS="156267340" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421638</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 2 was transferred from MNS/N into the SS/Jr background, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421640</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Rat155-D2Chm161&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="175279960" STOP_POS="175280164" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="172982062" STOP_POS="172982266" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="186889035" STOP_POS="186889238" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="206293779" STOP_POS="206293982" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="179581946" STOP_POS="179582150" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421640</CITATION_ID>
    <DESCRIPTION>Congenic substrain created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Chm25-D2Mit14&lt;/i&gt;)/Ayd strain into the parental Dahl Salt-sensitive (SS/Jr) strain, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421643</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm254-D2Chm161&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421643</CITATION_ID>
    <DESCRIPTION>Congenic substrain created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Chm25-D2Mit14&lt;/i&gt;)/Ayd strain into the parental Dahl Salt-sensitive (SS/Jr) strain, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421645</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Rat155-D2Chm419&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="175279960" STOP_POS="175280164" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="172982062" STOP_POS="172982266" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="186889035" STOP_POS="186889238" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="206293779" STOP_POS="206293982" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="179581946" STOP_POS="179582150" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421645</CITATION_ID>
    <DESCRIPTION>Congenic substrain created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Chm25-D2Mit14&lt;/i&gt;)/Ayd strain into the parental Dahl Salt-sensitive (SS/Jr) strain, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421647</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm161-D2Chm410&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421647</CITATION_ID>
    <DESCRIPTION>Congenic substrain created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Chm25-D2Mit14&lt;/i&gt;)/Ayd strain into the parental Dahl Salt-sensitive (SS/Jr) strain, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421649</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm153-D2Chm410&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421649</CITATION_ID>
    <DESCRIPTION>Congenic substrain created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Chm25-D2Mit14&lt;/i&gt;)/Ayd strain into the parental Dahl Salt-sensitive (SS/Jr) strain, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421651</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm442-D2Chm410&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421651</CITATION_ID>
    <DESCRIPTION>Congenic substrain created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Chm25-D2Mit14&lt;/i&gt;)/Ayd strain into the parental Dahl Salt-sensitive (SS/Jr) strain, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7421654</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm366-D2Rat52&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="195783205" STOP_POS="195783351" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="193094852" STOP_POS="193094998" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="208081050" STOP_POS="208081195" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="227502003" STOP_POS="227502148" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="200866667" STOP_POS="200866813" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7421654</CITATION_ID>
    <DESCRIPTION>Congenic substrain created by backcrossing congenic strain SS.MNS-(&lt;i&gt;D2Chm25-D2Mit14&lt;/i&gt;)/Ayd strain into the parental Dahl Salt-sensitive (SS/Jr) strain, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7771589</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D2Rat352-rs63922710&lt;/i&gt;)/Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Boston University School of Medicine, Boston, Massachusetts</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=610&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="169580635" STOP_POS="191378936" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="167282560" STOP_POS="188690312" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="180909971" STOP_POS="203646445" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="200318348" STOP_POS="200318555" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="173606885" STOP_POS="173607092" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00610</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing SS/JrHsd and SR/JrHsd parental strains</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7771600</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;rs106870553-rs63922710&lt;/i&gt;)/Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Boston University School of Medicine, Boston, Massachusetts</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=611&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="172499769" STOP_POS="191378936" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="170201741" STOP_POS="188690312" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="183864092" STOP_POS="203646445" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00611</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing SS/JrHsd and SR/JrHsd parental strains</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7771610</RGD_ID>
    <STRAIN_SYMBOL>SHRSP-Chr 1&lt;sup&gt;F344&lt;/sup&gt;/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Clinical Pharmacology and Toxicology, Charite-Universitatsmedizin Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7771610</CITATION_ID>
    <DESCRIPTION>SHRSP/Bbb male was crossed with female F344/Crl to get F1 animals which in turn were backcrossed with female SHRSP, this was repeated for 7 generations, tested by sequential marker-assisted backcrossing</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7777135</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mco39-D5Mco57&lt;/i&gt;)/1Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7777135</CITATION_ID>
    <DESCRIPTION>SS.LEW-(&lt;i&gt;D5Mco34-D5Rat108&lt;/i&gt;)/Jr was selectively backcrossed with the SS/Jr strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7777138</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mco41-D5Mco47&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="112175328" STOP_POS="117913688" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="116151523" STOP_POS="122679716" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7777138</CITATION_ID>
    <DESCRIPTION>SS.LEW-(&lt;i&gt;D5Mco34-D5Rat108&lt;/i&gt;)/Jr was selectively backcrossed with the SS/Jr strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7777140</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mco39-D5Mco57&lt;/i&gt;)(&lt;i&gt;D5Mco41-D5Mco47&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7777140</CITATION_ID>
    <DESCRIPTION>male and female pairs of the monocongenic SS.LEW-(&lt;i&gt;D5Mco39-D5Mco57&lt;/i&gt;)/1Mco and SS.LEW-(&lt;i&gt;D5Mco41-D5Mco47&lt;/i&gt;)/Mco were randomly selected and intercrossed to get F&lt;sub&gt;1&lt;/sub&gt;; the heterozygous animals for the desired region were intercrossed to get the bicongenics</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7777143</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mco39-D5Mco57&lt;/i&gt;)/2Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7777143</CITATION_ID>
    <DESCRIPTION>SS.LEW-(&lt;i&gt;D5Mco34-D5Rat108&lt;/i&gt;)/Jr was selectively backcrossed with the SS/Jr strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7777180</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mco42-D5Mco47&lt;/i&gt;)/1Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="112175328" STOP_POS="116047316" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="116151523" STOP_POS="120258299" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7777180</CITATION_ID>
    <DESCRIPTION>SS.LEW-(&lt;i&gt;D5Mco34-D5Rat108&lt;/i&gt;)/Jr was selectively backcrossed with the SS/Jr strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7794691</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mco39-D5Mco57&lt;/i&gt;)(&lt;i&gt;D5Mco42-D5Mco47&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7794691</CITATION_ID>
    <DESCRIPTION>male and female pairs of the monocongenic SS.LEW-(&lt;i&gt;D5Mco39-D5Mco57&lt;/i&gt;)/2Mco and SS.LEW-(&lt;i&gt;D5Mco42-D5Mco47&lt;/i&gt;)/1Mco were randomly selected and intercrossed to get F&lt;sub&gt;1&lt;/sub&gt;; the heterozygous animals for the desired region were intercrossed to get the bicongenics</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7794694</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mco39-D5Mco57&lt;/i&gt;)/3Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7794694</CITATION_ID>
    <DESCRIPTION>SS.LEW-(&lt;i&gt;D5Mco34-D5Rat108&lt;/i&gt;)/Jr was selectively backcrossed with the SS/Jr strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7794696</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mco43-D5Mco47&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="112175328" STOP_POS="112175546" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="116151523" STOP_POS="116151740" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7794696</CITATION_ID>
    <DESCRIPTION>SS.LEW-(&lt;i&gt;D5Mco34-D5Rat108&lt;/i&gt;)/Jr was selectively backcrossed with the SS/Jr strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7794698</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mco39-D5Mco57&lt;/i&gt;)(&lt;i&gt;D5Mco43-D5Mco47&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7794698</CITATION_ID>
    <DESCRIPTION>male and female pairs of the monocongenic SS.LEW-(&lt;i&gt;D5Mco39-D5Mco57&lt;/i&gt;)/3Mco and SS.LEW-(&lt;i&gt;D5Mco413-D5Mco47&lt;/i&gt;)/Mco were randomly selected and intercrossed to get F&lt;sub&gt;1&lt;/sub&gt;; the heterozygous animals for the desired region were intercrossed to get the bicongenics</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7794700</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mco39-D5Mco41&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="117913475" STOP_POS="117913688" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="122679504" STOP_POS="122679716" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7794700</CITATION_ID>
    <DESCRIPTION>SS.LEW-(&lt;i&gt;D5Mco34-D5Rat108&lt;/i&gt;)/Jr was selectively backcrossed with the SS/Jr strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7794704</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mco42-D5Mco47&lt;/i&gt;)/2Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="112175328" STOP_POS="116047316" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="116151523" STOP_POS="120258299" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7794704</CITATION_ID>
    <DESCRIPTION>SS.LEW-(&lt;i&gt;D5Mco34-D5Rat108&lt;/i&gt;)/Jr was selectively backcrossed with the SS/Jr strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7794706</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D5Mco39-D5Mco41&lt;/i&gt;)(&lt;i&gt;D5Mco42-D5Mco47&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7794706</CITATION_ID>
    <DESCRIPTION>male and female pairs of the monocongenic SS.LEW-(&lt;i&gt;D5Mco39-D5Mco41&lt;/i&gt;)/Mco and SS.LEW-(&lt;i&gt;D5Mco42-D5Mco47&lt;/i&gt;)/2Mco were randomly selected and intercrossed to get F&lt;sub&gt;1&lt;/sub&gt;; the heterozygous animals for the desired region were intercrossed to get the bicongenics</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7800659</RGD_ID>
    <STRAIN_SYMBOL>F344.Cg-&lt;i&gt;Du, Tyr&lt;sup&gt;C&lt;/sup&gt;&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME>downunder rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1057&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1057&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-10)</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7800659</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7800661</RGD_ID>
    <STRAIN_SYMBOL>F344.Cg-&lt;i&gt;Du, Tyr&lt;sup&gt;CKyo+/+&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>downunder rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1053&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1053&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7800661</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7800667</RGD_ID>
    <STRAIN_SYMBOL>F344.Cg-&lt;i&gt;Foxn1&lt;sup&gt;rnuKyo-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=152&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=152&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Immunology; Cancer</RESEARCH_USE>
    <ALLELES>Foxn1</ALLELES>
    <ALLELE_RGD_IDS>3970</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7800667</CITATION_ID>
    <DESCRIPTION>Jic N13 to Kyo (1988)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7800671</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Sv2a&lt;sup&gt;m1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Graduate School of Medicine, Kyoto University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1056&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sv2a|Sv2a&lt;sup&gt;m1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>619715|12792962</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="186430363" STOP_POS="186446161" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="183745872" STOP_POS="183745872" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="198325507" STOP_POS="198325507" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="217808165" STOP_POS="217823872" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="190989187" STOP_POS="191000859" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7800671</CITATION_ID>
    <DESCRIPTION>Established by ENU mutagenesis. A missense mutation (L174Q) mutation in Sv2a: synaptic vesicle glycoprotein 2a, was identified.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7800673</RGD_ID>
    <STRAIN_SYMBOL>KFRS2/Kyo&lt;sup&gt;-/+&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>KFRS2&lt;sup&gt;-/+&lt;/sup&gt;</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1002&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1002&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology; Dermatology</RESEARCH_USE>
    <ALLELES>Tyr|Tyr&lt;sup&gt;siaKyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>1589755|13207345</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150527687" STOP_POS="150622857" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="141115036" STOP_POS="141210207" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="151012598" STOP_POS="151106802" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157322968" STOP_POS="157416594" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143641257" STOP_POS="143746315" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7800673</CITATION_ID>
    <DESCRIPTION>A male rat "SRR-Do Your Best" was introduced from American fancy rat colony (Spoiled Ratten Rattery: SRR, in Kansas City, Missouri) to Kyoto University on July 13, 2005. Inbreeding started from F1 progeny of male "SRR-Do Your Best" and a female PVG/Seac.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7800676</RGD_ID>
    <STRAIN_SYMBOL>KFRS3A/Kyo&lt;sup&gt;+/+&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1059&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1059&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7800676</CITATION_ID>
    <DESCRIPTION>A male rat "SRR-Rocket Science" was introduced from American fancy rat colony (Spoiled Ratten Rattery: SRR, in Kansas City, Missouri) to Kyoto University on July 13, 2005. Inbreeding started from F1 progeny of male "SRR-Rocket Science" and a female PVG/Seac. Homozygous rats for mink were selected for inbreeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7800692</RGD_ID>
    <STRAIN_SYMBOL>MKO/Tami</STRAIN_SYMBOL>
    <FULL_NAME>Minko Rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=974&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=974&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7800692</CITATION_ID>
    <DESCRIPTION>MKO rat is derived from Wistar male rat which exhibited large-size and abnormal lipid metabolism.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7800694</RGD_ID>
    <STRAIN_SYMBOL>NER.F344-(&lt;i&gt;D1Rat132&lt;/i&gt;)(&lt;i&gt;D5Rat100&lt;/i&gt;)/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1051&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1051&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7800694</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7800702</RGD_ID>
    <STRAIN_SYMBOL>KHR/Kyo&lt;sup&gt;-/-&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>kaken hairless rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=678 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=678 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Dermatology</RESEARCH_USE>
    <ALLELES>Oca2</ALLELES>
    <ALLELE_RGD_IDS>2318412</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="116252026" STOP_POS="116581838" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="107116278" STOP_POS="107446093" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="114661970" STOP_POS="114987433" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="115683593" STOP_POS="115991040" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7800702</CITATION_ID>
    <DESCRIPTION>Kaken hairless rat were detected by Kimura from Gunn's rat at Kaken Pharmaceuticals in 1987. 2002 introduced to Kyoto University (F36).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>7800705</RGD_ID>
    <STRAIN_SYMBOL>KHR/Kyo&lt;sup&gt;-/+&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>kaken hairless rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=413 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=413 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Dermatology</RESEARCH_USE>
    <ALLELES>Oca2</ALLELES>
    <ALLELE_RGD_IDS>2318412</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="116252026" STOP_POS="116581838" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="107116278" STOP_POS="107446093" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="114661970" STOP_POS="114987433" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="115683593" STOP_POS="115991040" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_7800705</CITATION_ID>
    <DESCRIPTION>Kaken hairless rat were detected by Kimura from Gunn's rat at Kaken Pharmaceuticals in 1987. 2002 introduced to Kyoto University (F36).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8142383</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/BbbUtx</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Texas, Houston, TX</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8142383</CITATION_ID>
    <DESCRIPTION>Animals transferred from Harvard University/Brigham (Dr Klaus Lindpaintner) originating from SHRSP colony at University of Heidelberg</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8142385</RGD_ID>
    <STRAIN_SYMBOL>SHR/Utx</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Texas, Houston, TX</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8142385</CITATION_ID>
    <DESCRIPTION>Animals transferred from Professor T. Suzuki, Kinki University School of Medicine, Kinki, Japan in 2002, descended from the original SHR sub-strains reported by Okamoto, 1974</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8547938</RGD_ID>
    <STRAIN_SYMBOL>CrljJcl:SD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/en/products/outbred/item_a0350&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/en/products/outbred/item_a0350&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-04-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8547938</CITATION_ID>
    <DESCRIPTION>Sprague-Dawley from Charles River Laboratory Japan, to CLEA Japan, Inc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8548794</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(NC1-269B17)1Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=970 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=970 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Casp3</ALLELES>
    <ALLELE_RGD_IDS>2275</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8548794</CITATION_ID>
    <DESCRIPTION>BAC clone NC1-269B17 which containing about 120 kb of ACI/NJcl rat-derived &lt;i&gt;Casp3&lt;/i&gt; (caspase 3) was injected into F344/Jcl embryos. The founder rat was backcrossed into F344/Jcl rat to establish the transgenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8548809</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(NC1-269B17)2Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=971 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=971 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Casp3</ALLELES>
    <ALLELE_RGD_IDS>2275</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8548809</CITATION_ID>
    <DESCRIPTION>BAC clone NC1-269B17 which containing about 120 kb of ACI/NJcl rat-derived &lt;i&gt;Casp3&lt;/i&gt; (caspase 3) was injected into F344/Jcl embryos. The founder rat was backcrossed into F344/Jcl rat to establish the transgenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8548812</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(NC1-269B17)3Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=972 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=972 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Casp3</ALLELES>
    <ALLELE_RGD_IDS>2275</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8548812</CITATION_ID>
    <DESCRIPTION>BAC clone NC1-269B17 which containing about 120 kb of ACI/NJcl rat-derived &lt;i&gt;Casp3&lt;/i&gt; (caspase 3) was injected into F344/Jcl embryos. The founder rat was backcrossed into F344/Jcl rat to establish the transgenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8548815</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(NC1-269B17)4Nkg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=973 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=973 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Casp3</ALLELES>
    <ALLELE_RGD_IDS>2275</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8548815</CITATION_ID>
    <DESCRIPTION>BAC clone NC1-269B17 which containing about 120 kb of ACI/NJcl rat-derived &lt;i&gt;Casp3&lt;/i&gt; (caspase 3) was injected into F344/Jcl embryos. The founder rat was backcrossed into F344/Jcl rat to establish the transgenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8548817</RGD_ID>
    <STRAIN_SYMBOL>KDP.PVG-RT1&lt;sup&gt;a/u&lt;/sup&gt;/Nyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=993 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=993 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8548817</CITATION_ID>
    <DESCRIPTION>MHC haplotype (RT1.B&lt;i&gt;a&lt;/i&gt;D&lt;i&gt;a&lt;/i&gt;) of PVG.R23 was transferred onto the genetic background of KDP/Tky strain (RT1.B&lt;i&gt;u&lt;/i&gt;D&lt;i&gt;u&lt;/i&gt;). This allele has been maintained in heterozygous condition. Backcrossing has started since 2003 and afterwards maintained by sib mating</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8549599</RGD_ID>
    <STRAIN_SYMBOL>BN.LEW-(&lt;i&gt;D10Rat32-D10Rat133&lt;/i&gt;)/Ciml</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante et de la Recherche Medicale, Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="64939013" STOP_POS="64939207" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="51779662" STOP_POS="51779830" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="53630865" STOP_POS="53631032" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="53381898" STOP_POS="64823355" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="53786347" STOP_POS="65668639" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8549599</CITATION_ID>
    <DESCRIPTION>Congenic strain created from parental BN/Rj and LEW/Rj strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8549776</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Lep&lt;sup&gt;m1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>F344 OB rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=995&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=995&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-03-17)</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES>Lep|Lep&lt;sup&gt;m1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>3000|12792963</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="58626529" STOP_POS="58640663" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="57672294" STOP_POS="57672294" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="56348850" STOP_POS="56348850" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="56085079" STOP_POS="56099209" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="55943837" STOP_POS="55945938" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8549776</CITATION_ID>
    <DESCRIPTION>Established by ENU mutagenesis in F344/NSlc rats. This strain has Lep missense mutation (Q92X).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8549778</RGD_ID>
    <STRAIN_SYMBOL>PVG.KDP-&lt;i&gt;Cblb&lt;i&gt;/Nyo</STRAIN_SYMBOL>
    <FULL_NAME>PVG.KDP-Cblb congenic</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1010&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1010&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES>Cblb</ALLELES>
    <ALLELE_RGD_IDS>620535</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8549778</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8549779</RGD_ID>
    <STRAIN_SYMBOL>DRU/Uubc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=991&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=991&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8549779</CITATION_ID>
    <DESCRIPTION>The mutant rat showing microphthalmia was found in the colony of Donryu rats at Central Institute for Experimental Animals in 1974. A pair of F3 rats was transferred to The Third Department for Anatomy, School of Medicine, Chiba University in 1975 and maintained by sib mating. F50 rats were transferred to Faculty of Agriculture, Utsunomiya University by Dr. S Sugita in 1991</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8549782</RGD_ID>
    <STRAIN_SYMBOL>SD.Gunn-&lt;i&gt;Ugt1a1&lt;sup&gt;j&lt;/sup&gt;&lt;/i&gt;/Aon</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=975 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=975 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-09-15)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Metabolism</RESEARCH_USE>
    <ALLELES>Ugt1a1|Ugt1a1&lt;sup&gt;j&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>3935|13432064</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8549782</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8549785</RGD_ID>
    <STRAIN_SYMBOL>W.Gunn-&lt;i&gt;Ugt1a1&lt;sup&gt;j&lt;/i&gt;&lt;/sup&gt;/Aon</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=976 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=976 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Metabolism</RESEARCH_USE>
    <ALLELES>Ugt1a1|Ugt1a1&lt;sup&gt;j&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>3935|13432064</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8549785</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8549798</RGD_ID>
    <STRAIN_SYMBOL>WMS/SimNcp</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of cellular physiology, Institute of Nephrology, Niigata University, Niigata, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=997 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8549798</CITATION_ID>
    <DESCRIPTION>Munich, Germany from Wistar stock selectively bred for superficial glomeruli. To Simonsen Labs, CA via Veterans Administration Medical Center, San Francisco, California in 1979 at which time inbreeding was begun. Transferred at Nigata University from Simonsen Laboratory in 2005. at Niigata University</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551711</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551711</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551714</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)(&lt;i&gt;D10Chm246-D10Chm257&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551714</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Chm246-D10Chm257&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551716</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)(&lt;i&gt;D16Chm48-D16Chm60&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551716</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D16Chm48-D16Chm60&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551718</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)(&lt;i&gt;D16Chm48-D16Chm60&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551718</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D16Chm48-D16Chm60&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551721</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D8Rat58-D8Chm12&lt;/i&gt;)(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551721</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D8Rat58-D8Chm12&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551723</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D8Rat58-D8Chm12&lt;/i&gt;)(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551723</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D8Rat58-D8Chm12&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551725</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D8Chm12-D8Rat15&lt;/i&gt;)(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551725</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D8Chm12-D8Rat15&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551727</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D3Rat2-D3Chm79&lt;/i&gt;)(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551727</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D3Rat2-D3Chm79&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551730</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D3Rat2-D3Chm79&lt;/i&gt;)(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551730</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D3Rat2-D3Chm79&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551732</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D17Chm131-D17Chm93&lt;/i&gt;)(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551732</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D17Chm31-D17Chm93&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551734</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D17Chm131-D17Chm93&lt;/i&gt;)(&lt;i&gt;D17Rat84-D17Chm17&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551734</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D17Chm31-D17Chm93&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D17Rat84-D17Chm17&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551737</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D2Uia5-D2Mit6&lt;/i&gt;)(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551737</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D2Uia5-D2Mit6&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551739</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D2Uia5-D2Mit6&lt;/i&gt;)(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551739</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D2Uia5-D2Mit6&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551742</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D16Chm48-D16Chm60&lt;/i&gt;)(&lt;i&gt;D18Rat101-D18Rat92&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551742</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D16Chm48-D16Chm60&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D18Rat101-D18Rat92&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551748</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D3Rat17-D3Mco80&lt;/i&gt;)(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551748</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D3Rat17-D3Mco80&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551750</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Uia4-D1Rat320&lt;/i&gt;)(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551750</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D1Uia4-D1Rat320&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551752</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Rat320-D1Mgh32&lt;/i&gt;)(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551752</CITATION_ID>
    <DESCRIPTION>A triple congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D1Rat320-D1Mgh32&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551755</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Chm64-D1Rat19&lt;/i&gt;)(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551755</CITATION_ID>
    <DESCRIPTION>A triple congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D1Chm64-D1Rat19&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551757</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D7Uia3-D7Mgh1&lt;/i&gt;)(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551757</CITATION_ID>
    <DESCRIPTION>A triple congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D7Uia3-D7Mgh1&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551759</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm90-D2Rat38&lt;/i&gt;),LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551759</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.MNS-(&lt;i&gt;D2Chm90-D2Rat38&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551761</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm90-D2Rat38&lt;/i&gt;),LEW-(&lt;i&gt;D10Got112-Igfbp4&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551761</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.MNS-(&lt;i&gt;D2Chm90-D2Rat38&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Got112-Igfbp4&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551763</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Rat155-D2Chm419&lt;/i&gt;),LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551763</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.MNS-(&lt;i&gt;D2Rat155-D2Chm419&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551766</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Rat155-D2Chm419&lt;/i&gt;),LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551766</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.MNS-(&lt;i&gt;D2Rat155-D2Chm419&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551772</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm33-Tm2sf1&lt;/i&gt;),LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;),LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551772</CITATION_ID>
    <DESCRIPTION>A triple congenic strain derived from the progenitor strain SS.MNS-(&lt;i&gt;D2Chm33-Tm2sf1&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551774</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm33-Tm2sf1&lt;/i&gt;),LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551774</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.MNS-(&lt;i&gt;D2Chm33-Tm2sf1&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Chm10-D10Rat11&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551776</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm33-Tm2sf1&lt;/i&gt;),LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551776</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.MNS-(&lt;i&gt;D2Chm33-Tm2sf1&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551778</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm33-Tm2sf1&lt;/i&gt;),LEW-(&lt;i&gt;D3Rat2-D3Chm79&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551778</CITATION_ID>
    <DESCRIPTION>A double congenic strain derived from the progenitor strain SS.MNS-(&lt;i&gt;D2Chm33-Tm2sf1&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D3Rat2-D3Chm79&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551782</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D18Chm90-D18Chm4&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="12710576" STOP_POS="26538225" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="12441876" STOP_POS="27733166" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="12230011" STOP_POS="27443258" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="13071222" STOP_POS="27421017" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551782</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551785</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D18Wox7-D18Rat67&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="12219237" STOP_POS="12219384" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="11944273" STOP_POS="23012468" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="15539551" STOP_POS="24147513" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="15314151" STOP_POS="23867696" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="12406948" STOP_POS="23780206" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551785</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551787</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D18Rat55-D18Mgh2&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="61982204" STOP_POS="61982387" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="52539763" STOP_POS="59712417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="54108375" STOP_POS="61901354" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="53346348" STOP_POS="61092546" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="54856551" STOP_POS="62313296" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551787</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551789</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D18Chm59-D18Rat1&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="85487615" STOP_POS="85487725" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="65970331" STOP_POS="83213037" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="67627706" STOP_POS="87074531" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="66790645" STOP_POS="86108580" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="69138888" STOP_POS="86857890" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551789</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551864</RGD_ID>
    <STRAIN_SYMBOL>DA.LEW.1AV1-(&lt;i&gt;D4Mgh17-D4Mgh21&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="114921280" STOP_POS="114921417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="113100978" STOP_POS="179563872" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="177782842" STOP_POS="177926667" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="116611031" STOP_POS="116611168" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551864</CITATION_ID>
    <DESCRIPTION>LEW.1AV1/Kini allele is introgressed into the DA/ZtmKini rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551866</RGD_ID>
    <STRAIN_SYMBOL>LEW.1AV1.DA-(&lt;i&gt;D4Mgh17-D4Rat203&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="159798884" STOP_POS="159799026" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="114921280" STOP_POS="158112799" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="113100978" STOP_POS="157826751" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="177782842" STOP_POS="224843794" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="116611031" STOP_POS="161435775" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551866</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini allele is introgressed into the LEW.1AV1/kini rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551868</RGD_ID>
    <STRAIN_SYMBOL>PVG.1AV1.DA-(&lt;i&gt;D4Mgh17-D4Rat84&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="182430496" STOP_POS="182430611" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="114921280" STOP_POS="180699135" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="113100978" STOP_POS="182171018" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="177782842" STOP_POS="246313537" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="116611031" STOP_POS="185398530" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551868</CITATION_ID>
    <DESCRIPTION>DA/ZtmKini allele is introgressed into the PVG.1AV1/Kini rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551872</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat155-D4Rat113&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="50490466" STOP_POS="50490672" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="49524674" STOP_POS="153826492" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="48053950" STOP_POS="153153072" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="47848402" STOP_POS="220242357" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="157006984" STOP_POS="157007337" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551872</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from marker assisted selection for PVG.1AV1/Kini chromosome 4 alleles on the DA/ZtmKini recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551874</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat63-D4Rat84&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="154946424" STOP_POS="182430611" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="153274175" STOP_POS="180699135" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="152598827" STOP_POS="182171018" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="219683260" STOP_POS="246313537" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="156442644" STOP_POS="185398530" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551874</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from marker assisted selection for PVG.1AV1/Kini chromosome 4 alleles on the DA/ZtmKini recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551876</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat203-D4Got130&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="159798884" STOP_POS="159799026" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="158112655" STOP_POS="162281835" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="157826610" STOP_POS="162454686" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="224843653" STOP_POS="227653798" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="161435633" STOP_POS="166051402" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551876</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from marker assisted selection for PVG.1AV1/Kini chromosome 4 alleles on the DA/ZtmKini recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551880</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat63-D4Rat203&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="154946424" STOP_POS="159799026" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="153274175" STOP_POS="158112799" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="152598827" STOP_POS="157826751" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="219683260" STOP_POS="224843794" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="156442644" STOP_POS="161435775" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551880</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from marker assisted selection for PVG.1AV1/Kini chromosome 4 alleles on the DA/ZtmKini recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551882</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat203-D4Mit22&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="159798884" STOP_POS="159799026" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="158112655" STOP_POS="171728165" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="157826610" STOP_POS="172512411" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="224843653" STOP_POS="236764513" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="161435633" STOP_POS="175947418" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551882</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from marker assisted selection for PVG.1AV1/Kini chromosome 4 alleles on the DA/ZtmKini recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551885</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Mit22-D4Rat84&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="182430496" STOP_POS="182430611" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="171728017" STOP_POS="180699135" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="172512264" STOP_POS="182171018" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="236764366" STOP_POS="246313537" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="175947270" STOP_POS="185398530" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551885</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from marker assisted selection for PVG.1AV1/Kini chromosome 4 alleles on the DA/ZtmKini recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551887</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Got126-D4Rat203&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="159798884" STOP_POS="159799026" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="156050654" STOP_POS="158112799" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="155657051" STOP_POS="157826751" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="222677930" STOP_POS="224843794" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="159298584" STOP_POS="161435775" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551887</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from marker assisted selection for PVG.1AV1/Kini chromosome 4 alleles on the DA/ZtmKini recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551889</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat62-D4Got136&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="156389077" STOP_POS="156389245" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="154716992" STOP_POS="157232313" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="154054175" STOP_POS="156945571" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="221142142" STOP_POS="223964695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="157913800" STOP_POS="160528447" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551889</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from marker assisted selection for PVG.1AV1/Kini chromosome 4 alleles on the DA/ZtmKini recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8551892</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat113-D4Rat62&lt;/i&gt;)/Kiru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="156389077" STOP_POS="156389245" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="153826368" STOP_POS="154717160" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="153152949" STOP_POS="154054342" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="220242234" STOP_POS="221142309" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="157006984" STOP_POS="157913968" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8551892</CITATION_ID>
    <DESCRIPTION>Congenic substrain derived from marker assisted selection for PVG.1AV1/Kini chromosome 4 alleles on the DA/ZtmKini recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552235</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Pbsn-TAg)1Obs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=998 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=998 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-08-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pbsn</ALLELES>
    <ALLELE_RGD_IDS>708571</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552235</CITATION_ID>
    <DESCRIPTION>SV40 Large T Antigen along with Rat probasin promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552237</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(Nanog-GFP-PuroR)22Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1011 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1011 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552237</CITATION_ID>
    <DESCRIPTION>mouse Nanog-GFP IRES puromycin resistant BAC was injected into Crlj:WI rat embryos. 4 lines were established of which line 22 showed the best breeding performance</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552239</RGD_ID>
    <STRAIN_SYMBOL>F344.WI-Tg(Nanog-GFP-PuroR)Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1012 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1012 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552239</CITATION_ID>
    <DESCRIPTION>WI-Tg(Nanog-GFP-puro-R)/22Kyo rats were backcrossed to F344/Stm to transfer the transgene onto a different genetic background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552242</RGD_ID>
    <STRAIN_SYMBOL>ETR/Eis</STRAIN_SYMBOL>
    <FULL_NAME>Eisai Turning Rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1013 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1013 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552242</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552244</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Dsp-mCherry-DTR)Jfln</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1018 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1018 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552244</CITATION_ID>
    <DESCRIPTION>This rat carries a transgene consisting of the Dsp promoter followed by a STOP cassette flanked by FRT sites. The stop cassette consists of an mcherry gene encoding for a red fluorescent protein and a kanamycin resistant gene and three SV40polyA adenylation signals. The STOP cassette is followed by a gene encoding for the human diphtheria toxin receptor. Red fluorescence can be detected from the skin of the animals but not the brain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552247</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Neurod6-mCherry-DTR)Jfln</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1019 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1019 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-08-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552247</CITATION_ID>
    <DESCRIPTION>This rat carries a transgene consisting of the NeuroD6 promoter followed by a STOP cassette flanked by FRT sites. The stop cassette consists of an mcherry gene encoding for a red fluorescent protein and a kanamycin resistant gene and three SV40polyA adenylation signals. The STOP cassette is followed by a gene encoding for the human diphtheria toxin receptor. This model is yet to be validated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552249</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Camk2a-FLPo)Jfln</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1020 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1020 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-08-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552249</CITATION_ID>
    <DESCRIPTION>This transgene consists of approximately 6kb of the CamK2a promoter followed by a gene encoding FLP, optimised for mamalian exprssion (FLPo). This rat remains unvalidated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552252</RGD_ID>
    <STRAIN_SYMBOL>ACI.BUF-&lt;i&gt;Aftm1&lt;/i&gt;/2Mna</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=977&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=977&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552252</CITATION_ID>
    <DESCRIPTION>This congenic strain was established as a strain with the genetic background of ACI onto which a segment from the BUF/Mna has been transferred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552255</RGD_ID>
    <STRAIN_SYMBOL>LAP/Hshyo</STRAIN_SYMBOL>
    <FULL_NAME>low alcohol preference rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1009&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1009&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552255</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552257</RGD_ID>
    <STRAIN_SYMBOL>HAP/Hshyo</STRAIN_SYMBOL>
    <FULL_NAME>high alcohol preference rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1008&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1008&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552257</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552259</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ldlr&lt;sup&gt;m1Kyo&lt;/i&gt;&lt;/sup&gt;/Ta</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1030&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1030&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552259</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552261</RGD_ID>
    <STRAIN_SYMBOL>WIAR.MPR-&lt;i&gt;Arsb&lt;sup&gt;abd&lt;/i&gt;&lt;/sup&gt;/Ncchd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=992&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=992&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2023-03-07)</AVAILABILITY>
    <RESEARCH_USE>Osteology; Metabolism</RESEARCH_USE>
    <ALLELES>Arsb|Arsb&lt;sup&gt;MPR&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2158|12792967</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="26736395" STOP_POS="26895682" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="25020848" STOP_POS="25020849" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="23385154" STOP_POS="23543028" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="42559079" STOP_POS="42717753" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="24067560" STOP_POS="24223821" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552261</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR. This congenic strain was established by backcrossing MPR/Iar (RGD:2306064) (provided by Dr. Kunieda, Okayama University) to WIAR/Iar (RGD:2304222)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552267</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Rat116-D1Wox10&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1031&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1031&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="223964326" STOP_POS="223964440" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="212458494" STOP_POS="214537671" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="231729437" STOP_POS="236763528" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="238863547" STOP_POS="244066407" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="218466863" STOP_POS="220639653" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552267</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552269</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Tkyo58-D1Rat90&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1032&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1032&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="269633753" STOP_POS="269633915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="259647732" STOP_POS="259647894" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="281795624" STOP_POS="281795785" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="289137107" STOP_POS="289137268" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="267110921" STOP_POS="267111153" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552269</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552271</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Rat27-D1Wox18&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1033&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1033&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="99645382" STOP_POS="103781063" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="90508614" STOP_POS="94644553" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="94201400" STOP_POS="100133395" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="95301716" STOP_POS="101198506" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="90282040" STOP_POS="94626661" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552271</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552273</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Tkyo57-D1Wox18&lt;/i&gt;)/Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1034&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1034&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="103780943" STOP_POS="103781063" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="94644435" STOP_POS="94644553" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="100133276" STOP_POS="100133395" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="101198387" STOP_POS="101198506" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="94626541" STOP_POS="94626661" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552273</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552275</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Lgi1&lt;sup&gt;m1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The University of Tokyo, The Institute of Medical Science</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1036&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-03-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lgi1|Lgi1&lt;sup&gt;m1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>628742|12792970</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="245455691" STOP_POS="245497036" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="236083750" STOP_POS="236083750" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="256996315" STOP_POS="256996315" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="264436441" STOP_POS="264477332" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="242593236" STOP_POS="242634141" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552275</CITATION_ID>
    <DESCRIPTION>Developed by gene driven ENU mutagenesis in F344/NSlc rats. Lgi1-mutant rats carrying a missense mutation (c.1154 T &gt; G)(L385R).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552279</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(Per1-luc)Ylab</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1004&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1004&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552279</CITATION_ID>
    <DESCRIPTION>The original work using this transgenic rat was published in Science (Yamazaki et al. 2000). This transgenic rat was generated in the Wistar outbred strain (Charles River, Japan). We maintained the L1 line. The transgenic rat was generated using a DNA construct in which the mouse Period1 promoter drives firefly luciferase</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552285</RGD_ID>
    <STRAIN_SYMBOL>F344.WI-Tg(Per1-luc)Ylab</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1005&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1005&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552285</CITATION_ID>
    <DESCRIPTION>The original work using this transgenic rat was published in Science (Yamazaki et al. 2000). This transgenic rat was generated in the Wistar outbred strain (Charles River, Japan). We maintained the L1 line. The transgenic rat was generated using a DNA construct in which the mouse Period1 promoter drives firefly luciferase</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552287</RGD_ID>
    <STRAIN_SYMBOL>F344.WIC-Tg&lt;i&gt;&lt;sup&gt;rdw&lt;/i&gt;Kts&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1037&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1037&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-04-27)</AVAILABILITY>
    <RESEARCH_USE>Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552287</CITATION_ID>
    <DESCRIPTION>This is a F344 congenic carrying Tgrdw derived from WIC-Tgrdw/Kts.  WIC-Tgrdw/Kts was established from a closed colony of Wistar-Imamichi (WIC) rats as a spontaneous mutant exhibiting congenital dwarfism (rdw), is inherited as an autosomal recessive.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552289</RGD_ID>
    <STRAIN_SYMBOL>A5M/Khos</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1039&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1039&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552289</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552293</RGD_ID>
    <STRAIN_SYMBOL>SR/JrSeac</STRAIN_SYMBOL>
    <FULL_NAME>Dahl Salt-Resistant</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1042&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1042&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio- Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552293</CITATION_ID>
    <DESCRIPTION>Substrain of Dahl SR, from a Sprague-Dawley outbred colony, selected for resistance to salt-induced hypertension developed at  Kyudo Co.,Ltd (http://www.kyudo.co.jp/) to Seac Yoshitomi, LTD Japan, now maintained at NBRP</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552296</RGD_ID>
    <STRAIN_SYMBOL>UPL/CasTakeu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1040&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1040&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552296</CITATION_ID>
    <DESCRIPTION>Substrain of UPL</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552298</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Tyr&lt;sup&gt;em1Kyo&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1092&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1092&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-03-17)</AVAILABILITY>
    <RESEARCH_USE>Behavior; Dermatology</RESEARCH_USE>
    <ALLELES>Tyr|Tyr&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>1589755|12792972</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150527687" STOP_POS="150622857" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="141201016" STOP_POS="141201044" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="151097612" STOP_POS="151097640" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157322968" STOP_POS="157416594" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143641257" STOP_POS="143746315" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552298</CITATION_ID>
    <DESCRIPTION>The strain having a Endonuclease-induced 29-bp deletion mutation in Tyr gene was established by TALENs combined with Exonuclease 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552303</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Tyr&lt;sup&gt;em2Kyo&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1093&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1093&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Behavior; Dermatology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552303</CITATION_ID>
    <DESCRIPTION>Developed by the DEPOSITOR</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552309</RGD_ID>
    <STRAIN_SYMBOL>ODUS/Odu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1067&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1067&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552309</CITATION_ID>
    <DESCRIPTION>The mutant rat showing spontaneous gingivitis was found in the colony of WKY rats in 1972. The inbred strain was established in 1991.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552311</RGD_ID>
    <STRAIN_SYMBOL>ODUR/Odu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1066&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1066&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552311</CITATION_ID>
    <DESCRIPTION>This inbred strain was established from WKY rats as a control for ODUS/Odu.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552313</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D10Rat81-D10Rat238&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1100&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="48574589" STOP_POS="48574797" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="48075363" STOP_POS="60222446" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="49863561" STOP_POS="62214000" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="49641148" STOP_POS="61927099" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="49618846" STOP_POS="62685691" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552313</CITATION_ID>
    <DESCRIPTION>DA/Kini females were bred to PVG.1AV1/Kini males and male offspring selected for PVG alleles within the fragment. To ensure that mitochondrial DNA was inherited from the DA/Kini strain, female rats were from the DA/Kini strain throughout the breeding program.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552315</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Thy1-COP4/YFP*)4Jfhy</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1072&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1072&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology; Otorhinology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552315</CITATION_ID>
    <DESCRIPTION>The transgenic rats were established by injection of transgene consisting of ChR2 and Venus fused transgene driven by the Thy-1.2 promoter into Wistar rat fertile eggs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552317</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Thy1-COP4/YFP*)5Jfhy</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1077&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1077&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology; Otorhinology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552317</CITATION_ID>
    <DESCRIPTION>The transgenic rats were established by injection of transgene consisting of ChR2 and Venus fused transgene driven by the Thy-1.2 promoter into Wistar rat fertile eggs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552319</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Thy1-COP4/YFP*)6Jfhy</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1078&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1078&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology; Otorhinology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552319</CITATION_ID>
    <DESCRIPTION>The transgenic rats were established by injection of transgene consisting of ChR2 and Venus fused transgene driven by the Thy-1.2 promoter into Wistar rat fertile eggs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552321</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(APOC3-CETP)1Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1095&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1095&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552321</CITATION_ID>
    <DESCRIPTION>The transgenic rats were established by injection of transgene consisting of cholesterylester tansfer protein gene driven by the APOC3 promoter into SHR/Izm rat fertile eggs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552323</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(APOC3-CETP)2Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1114&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1114&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552323</CITATION_ID>
    <DESCRIPTION>The transgenic rats were established by injection of transgene consisting of cholesterylester tansfer protein gene driven by the APOC4 promoter into SHR/Izm rat fertile eggs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552325</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(APOC3-CETP)3Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1115&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1115&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552325</CITATION_ID>
    <DESCRIPTION>The transgenic rats were established by injection of transgene consisting of cholesterylester tansfer protein gene driven by the APOC5 promoter into SHR/Izm rat fertile eggs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552327</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(APOC3-CETP)4Tkyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1116&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1116&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552327</CITATION_ID>
    <DESCRIPTION>The transgenic rats were established by injection of transgene consisting of cholesterylester tansfer protein gene driven by the APOC4 promoter into SHR/Izm rat fertile eggs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552329</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Nqo1)Kop</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1107&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1107&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Oncology; Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552329</CITATION_ID>
    <DESCRIPTION>The transgenic rats were established by injection of transgene consisting of NAD(P)H quinone oxidoreductase 1 gene derived from a DA/Slc rat strain into Wistar rat fertile eggs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552331</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Il2rg&lt;sup&gt;em7Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1099&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1099&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Hematology; Immunology</RESEARCH_USE>
    <ALLELES>Il2rg&lt;sup&gt;em7Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13628732</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66395330" STOP_POS="66399026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552331</CITATION_ID>
    <DESCRIPTION>The strain having a Endonuclease-induced 7 bp deletion mutation in the 2nd exon of the rat Il2rg gene was established by TAL effector nuclease obtained from Dr. Yamamoto at Hiroshima University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552337</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D10Got406-D10Rat93&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1122&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="78707362" STOP_POS="78707585" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="65139038" STOP_POS="78210622" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="67495867" STOP_POS="80946110" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="67154600" STOP_POS="80788180" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="68361384" STOP_POS="81887390" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552337</CITATION_ID>
    <DESCRIPTION>Inbred Dark Agouti (DA) rats were originally obtained from Hannover, Germany and Piebald Virol Glaxo(PVG) rats from Harlan UK Limited (Blackthorn, UK). Animals for congenic breeding were selected from the 10th generation of an advanced intercross line (AIL) originating from the EAE-susceptible DA and EAE-resistant PVG.1AV1 rat strains. Selected males containing a PVG.1AV1 fragment in the Eae18b region (from OT24.18 to D10Rat93 marker, at 68.36 Mb and 81.9 Mb, respectively) were backcrossed with DA females for 8 generations, and offspring was genotyped using microsatellite markers in each generation. In the 8th generation, heterozygous males and females were crossed to obtain the experimental population of homozygous congenic rats and littermate controls.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552341</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D10Got6-D10Rat184&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1120&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="11813520" STOP_POS="11813673" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="3406320" STOP_POS="3406594" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="2847625" STOP_POS="11561989" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="1728277" STOP_POS="10319475" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="3219701" STOP_POS="11568211" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552341</CITATION_ID>
    <DESCRIPTION>Inbred Dark Agouti (DA) rats were originally obtained from Hannover, Germany and Piebald Virol Glaxo(PVG) rats from Harlan UK Limited (Blackthorn, UK). Congenic strain was established by transfer of the defined Vra4 segment selected from male donors of G8 generation of a DAxPVG1.AV1 andvanced intercross line. Subsequential backcrossing for 9 generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552346</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D4Rat107-D4Got132&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1121&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="154597593" STOP_POS="154597827" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="152925326" STOP_POS="158841762" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="152249616" STOP_POS="158564471" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="219336960" STOP_POS="225566369" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="156090003" STOP_POS="162362144" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552346</CITATION_ID>
    <DESCRIPTION>Inbred Dark Agouti (DA) rats were originally obtained from Hannover, Germany and Piebald Virol Glaxo(PVG) rats from Harlan UK Limited (Blackthorn, UK). Congenic strain was established by selective transferring of PVG alleles in the interval between D4Rat137 and D4Kiru157 onto DA background in minimum of 13 backcross generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552348</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D13Rat105-D13Rat131&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE> &lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1124&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="79846035" STOP_POS="79846190" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="44139595" STOP_POS="77313088" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="49478067" STOP_POS="83263907" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="54552997" STOP_POS="88144258" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="45592985" STOP_POS="80755583" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552348</CITATION_ID>
    <DESCRIPTION>Inbred Dark Agouti (DA) rats were originally obtained from Hannover, Germany and Piebald Virol Glaxo(PVG) rats from Harlan UK Limited (Blackthorn, UK). The congenic line was established from DA and MHC-identical PVG.A rats using a speed-congenic approach with marker assisted selection. DA females were mated with male offspring selected from F2 (DAxPVG.A) with heterozygote alleles within chromosome 13 and Eae34 QTL interval and with the lowest PVG.A background contamination using 96 microsatellite markers equally spaced throughout the genome (at 20 centimorgan cM intervals). A breeding pair selected from the N7 generation were crossed for two generations to produce homozygous DA.PVG-Eae34 congenic rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552351</RGD_ID>
    <STRAIN_SYMBOL>DA.PVG.1AV1-(&lt;i&gt;D9Wox24-D9Rat44&lt;/i&gt;)/Kini</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Molecular Medicine, Neuroimmunology Unit, Karolinska Institutet, Stockholm, Sweden</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1123&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="5346479" STOP_POS="5346648" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="1024537" STOP_POS="5109995" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="2880977" STOP_POS="10869489" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="2813697" STOP_POS="9858600" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="2948882" STOP_POS="2949051" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552351</CITATION_ID>
    <DESCRIPTION>Inbred Dark Agouti (DA) rats were originally obtained from Hannover, Germany and Piebald Virol Glaxo(PVG) rats from Harlan UK Limited (Blackthorn, UK).  Briefly, in each backcross generation, rats for further breeding were selected on the basis of genotyping of 8 microsatellite markers in the congenic region, from marker D9Wox24 to D9Rat20. The genetic background of rats was also screened with 100 markers. After the complete removal of the donor genome outside the congenic fragment, two heterozygous rats were intercrossed to produce the homozygous strains DA.BN-Eae4(N7F1). Subsequently, interval-specific recombinants were bred from an F2 breeding. R25 recombinant was established in 2003.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552364</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(L2-Venus)Nips</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi, JAPAN</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552364</CITATION_ID>
    <DESCRIPTION>The construct contains CAG--lox P--Neo-pA--lox P--Venus--pA (4.3 kb) which was injected into Crlj:WI embryos; now maintained as transgenic heterozygotes</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552366</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(CAG-cre)Nips</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi, JAPAN</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552366</CITATION_ID>
    <DESCRIPTION>The construct contains CAG--NLS-Cre--pA (3.3 kb)which was injected into Crlj:WI embryos; now maintained as transgenic heterozygotes</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552368</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(CAG-Venus)Nips</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi, JAPAN</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552368</CITATION_ID>
    <DESCRIPTION>The construct contains L2-Venus Ã¿ CAG-Cre (CAG--lox P--Venus--pA (3.1 kb)) which was injected into Crlj:WI embryos; now maintained as transgenic heterozygotes</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552371</RGD_ID>
    <STRAIN_SYMBOL>WDB-&lt;i&gt;ROSA26&lt;sup&gt;em1(RT2)Nips&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi, JAPAN</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552371</CITATION_ID>
    <DESCRIPTION>This strain was produced by knock-in in the rat ROSA26 locus using the construct 5' arm--tdTomato--IRES-Puro^r-pA--3' arm (11 kb) to the WDB/Nips strain. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8552996</RGD_ID>
    <STRAIN_SYMBOL>F344/Arc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.arc.wa.gov.au/?page_id=1517&gt; Animal Resources Centre, Australia&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.arc.wa.gov.au/?page_id=1517&gt; Animal Resources Centre, Australia&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8552996</CITATION_ID>
    <DESCRIPTION>substrain of F344 bred at Animal Resources Centre Australia</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8553001</RGD_ID>
    <STRAIN_SYMBOL>ArcCrl:CD(SD)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.arc.gov.au/?page_id=1469&gt; Animal Resources Centre, Australia&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.arc.gov.au/?page_id=1469&gt; Animal Resources Centre, Australia&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8553001</CITATION_ID>
    <DESCRIPTION>substrain derived from Crl:CD(SD); IGS refers to animals bred using the CRL International Genetic Standard system.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8553003</RGD_ID>
    <STRAIN_SYMBOL>ArcCrl:WI</STRAIN_SYMBOL>
    <FULL_NAME>Wistar rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.arc.wa.gov.au/?page_id=1473&gt; Animal Resources Centre, Australia&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.arc.wa.gov.au/?page_id=1473&gt; Animal Resources Centre, Australia&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8553003</CITATION_ID>
    <DESCRIPTION>From Charles River to Animal Resources Centre, Australia</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8553005</RGD_ID>
    <STRAIN_SYMBOL>BN/RijHsdArc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.arc.wa.gov.au/?page_id=1513&gt; Animal Resources Centre, Australia&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8553005</CITATION_ID>
    <DESCRIPTION>To Animal Resources Centre, Australia from Harlan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8553006</RGD_ID>
    <STRAIN_SYMBOL>DA/Arc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.arc.wa.gov.au/?page_id=1515&gt; Animal Resources Centre, Australia&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.arc.wa.gov.au/?page_id=1515&gt; Animal Resources Centre, Australia&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8553006</CITATION_ID>
    <DESCRIPTION>substrain of DA bred at Animal Resources Centre, Australia</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8553008</RGD_ID>
    <STRAIN_SYMBOL>LEW/CrlArc</STRAIN_SYMBOL>
    <FULL_NAME>Lewis</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.arc.wa.gov.au/?page_id=1519&gt; Animal Resources Centre, Australia&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.arc.wa.gov.au/?page_id=1519&gt; Animal Resources Centre, Australia&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8553008</CITATION_ID>
    <DESCRIPTION>Developed by Dr. Lewis from Wistar stock in the early 1950s. To Animal Resources Centre, Australia from Charles River</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8553010</RGD_ID>
    <STRAIN_SYMBOL>PVG/Arc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.arc.wa.gov.au/?page_id=1521&gt; Animal Resources Centre, Australia&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.arc.wa.gov.au/?page_id=1521&gt; Animal Resources Centre, Australia&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8553010</CITATION_ID>
    <DESCRIPTION>substrain of PVG maintained at Animal Resources Centre</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8553013</RGD_ID>
    <STRAIN_SYMBOL>SHR/NCrlArc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.arc.wa.gov.au/?page_id=1523&gt; Animal Resources Centre, Australia&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.arc.wa.gov.au/?page_id=1523&gt; Animal Resources Centre, Australia&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8553013</CITATION_ID>
    <DESCRIPTION>To Animal Resources Centre from Charles River</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8553015</RGD_ID>
    <STRAIN_SYMBOL>WKY/NCrlArc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.arc.wa.gov.au/?page_id=1511&gt; Animal Resources Centre, Australia&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.arc.wa.gov.au/?page_id=1511&gt; Animal Resources Centre, Australia&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8553015</CITATION_ID>
    <DESCRIPTION>To Animal Resources Centre from Charles River</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8553187</RGD_ID>
    <STRAIN_SYMBOL>FHH.BN(&lt;i&gt;D14Rat98-D14Hmgc4&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="13015311" STOP_POS="19848266" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="14673206" STOP_POS="21555302" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="14613528" STOP_POS="21463742" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="14535071" STOP_POS="21435476" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8553187</CITATION_ID>
    <DESCRIPTION>desired segments from BN were introgressed in FHH background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8655639</RGD_ID>
    <STRAIN_SYMBOL>WAG/Nov</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8655639</CITATION_ID>
    <DESCRIPTION>Substrain of WAG, now bred at the Institute of Cytology and Genetics, Russian Academy of Sciences (Novosibirsk)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8655660</RGD_ID>
    <STRAIN_SYMBOL>WAG.OXYS-(&lt;i&gt;D1Rat30-D1Rat219&lt;/i&gt;)/Nov</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cic|Arhgap33</ALLELES>
    <ALLELE_RGD_IDS>1310706|2318374</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="109493780" STOP_POS="193400781" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="100357752" STOP_POS="183970443" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="106002252" STOP_POS="202571904" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="107049754" STOP_POS="209588735" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="100539980" STOP_POS="188654926" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8655660</CITATION_ID>
    <DESCRIPTION>desired region was introgressed from OXYS/Nov into the genetic background of WAG/Nov by first intercrossing and then backcrossing to WAG/Nov</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8655663</RGD_ID>
    <STRAIN_SYMBOL>WAG.OXYS-(&lt;i&gt;D1Rat219-D1Rat81&lt;/i&gt;)/Nov</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Snurf|Ifit1|Zp2|Gtf3c1|Col17a1</ALLELES>
    <ALLELE_RGD_IDS>69269|620599|620605|621048|1311130</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="193400541" STOP_POS="193400781" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="183970203" STOP_POS="243914901" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="202571665" STOP_POS="264802994" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="209588496" STOP_POS="272245383" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="188654686" STOP_POS="250119874" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8655663</CITATION_ID>
    <DESCRIPTION>desired region was introgressed from OXYS/Nov into the genetic background of WAG/Nov by first intercrossing and then backcrossing to WAG/Nov</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8655977</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Lepr&lt;/i&gt;&lt;sup&gt;+/+&lt;/sup&gt;/Nin</STRAIN_SYMBOL>
    <FULL_NAME>Wistar NIN lean</FULL_NAME>
    <ORIGINATION>National Institute of Nutrition (NIN), Hyderabad, India</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8655977</CITATION_ID>
    <DESCRIPTION>The lean litter mates of WNIN-Ob (W-LeprfaNin, RGD:8655992). Both are derived from the inbred stock of Wistar rats (W/NIN) dating back to 1920 at National Institute of Nutrition (NIN), Hyderabad, India.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8655992</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Lepr&lt;/i&gt;&lt;sup&gt;faNin&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Institute of Nutrition (NIN), Hyderabad, India</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8655992</CITATION_ID>
    <DESCRIPTION>The spontaneously developed obese rat was derived from the colony of inbred W/Nin by selective breeding. Its lean litter mate ( W-Lepr+/+/Nin, RGD:8655977) was used as a control strain in obesity related study.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8657051</RGD_ID>
    <STRAIN_SYMBOL>F344/Nin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Institute of Nutrition (NIN), Hyderabad, India</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8657051</CITATION_ID>
    <DESCRIPTION>Substrain of F344 maintained at National Institute of Nutrition (NIN), Hyderabad, India.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8657079</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D18Chm124-D18Chm126&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre-CHUM, Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8657079</CITATION_ID>
    <DESCRIPTION>SS/Jr and LEW/Crlc were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8657135</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Chm280-D10Chm216&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universiti de Montrial, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="73073387" STOP_POS="73073589" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="75603400" STOP_POS="75603599" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="74503802" STOP_POS="74504001" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="76589831" STOP_POS="76590030" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8657135</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Chm224-D10Chm6&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8657348</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D17Chm131-D17Chm93&lt;/i&gt;),MNS-(&lt;i&gt;D2Rat155-D2Chm161&lt;/i&gt;),LEW-(&lt;i&gt;D18Chm41-D18Rat92&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8657348</CITATION_ID>
    <DESCRIPTION>A triple congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D17Chm31-D17Chm93&lt;/i&gt;)/Ayd, SS.MNS-(&lt;i&gt;D2Rat155-D2Chm161&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D18Chm41-D18Rat92&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8657351</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm366-D2Rat52&lt;/i&gt;),LEW-(&lt;i&gt;D18Rat61-D18Rat45&lt;/i&gt;),LEW-(&lt;i&gt;D10Chm128-D10Chm121&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8657351</CITATION_ID>
    <DESCRIPTION>A triple congenic strain derived from the progenitor strain SS.MNS-(&lt;i&gt;D2Chm366-D2Rat52&lt;/i&gt;)/Ayd, SS.LEW-(&lt;i&gt;D18Rat61-D18Rat45&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Chm128-D10Chm121&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8657361</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm254-D2Chm161&lt;/i&gt;),LEW-(&lt;i&gt;D10Chm246-D10Chm257&lt;/i&gt;),LEW-(&lt;i&gt;D16Chm48-D16Chm60&lt;/i&gt;),LEW-(&lt;i&gt;D18Rat55-D18Mgh2&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8657361</CITATION_ID>
    <DESCRIPTION>A congenic strain derived from the progenitor strain SS.MNS-(&lt;i&gt;D2Chm254-D2Chm161&lt;/i&gt;)/Ayd, SS.LEW-(&lt;i&gt;D10Chm246-D10Chm257&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D16Chm48-D16Chm60&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D18Rat55-D18Mgh2&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8657392</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10Rat155-D10Chm171&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="67476608" STOP_POS="67476781" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="66978955" STOP_POS="67750281" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="69385595" STOP_POS="70167191" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="69020437" STOP_POS="69797898" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="70229781" STOP_POS="71032765" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8657392</CITATION_ID>
    <DESCRIPTION>A sub congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D10Chm224-D10Chm6&lt;/i&gt;)/Ayd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8657399</RGD_ID>
    <STRAIN_SYMBOL>SS.MNS-(&lt;i&gt;D2Chm214-D2Chm302&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universite de Montreal (CRCHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8657399</CITATION_ID>
    <DESCRIPTION>Congenic substrain created by backcrossing congenic strain MNS/N strain with Dahl Salt-sensitive (SS/Jr) strain, the F&lt;sub&gt;2&lt;/sub&gt; rats were genotyped with markers that resided in the region of interest, heterozygous rat was then backcrossed to SS/Jr rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8657402</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D3Rat52-D3Chm57&lt;/i&gt;),MNS-(&lt;i&gt;D2Chm214-D2Chm302&lt;/i&gt;),LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Montreal (CHUM), Montreal, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8657402</CITATION_ID>
    <DESCRIPTION>A triple congenic strain derived from the progenitor strain SS.LEW-(&lt;i&gt;D3Rat52-D3Chm57&lt;/i&gt;)/Ayd, SS.MNS-(&lt;i&gt;D2Chm214-D2Chm302&lt;/i&gt;)/Ayd and SS.LEW-(&lt;i&gt;D10Rat194-D10Chm243&lt;/i&gt;)/Ayd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8661233</RGD_ID>
    <STRAIN_SYMBOL>SS-TgTn(T2GFP)53Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8661233</CITATION_ID>
    <DESCRIPTION>This strain was made by pronuclear microinjection of SS/JrHsdMcwi embryos with a Sleeping Beauty transposon vector harboring a ubiquitous CAG promoter driving enhanced green fluorescent protein along with mRNA encoding the SB100X transposase.  The transposon inserted into rat chromosome 15 near 35.6 Mb (rn4)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8661234</RGD_ID>
    <STRAIN_SYMBOL>SS-TgTn(T2ePet-eGFP)11Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8661234</CITATION_ID>
    <DESCRIPTION>This strain was made by pronuclear microinjection of SS/JrHsdMcwi embryos with a Sleeping Beauty transposon vector harboring a serotonergic neuron-specific ePet1 promoter driving enhanced green fluorescent protein along with mRNA encoding the SB100X transposase. The transposon inserted into rat chromosome 7 near 123.8Mb (rn4)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8661235</RGD_ID>
    <STRAIN_SYMBOL>FHH-TgTn(T2/Rab38)1Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rab38</ALLELES>
    <ALLELE_RGD_IDS>628752</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8661235</CITATION_ID>
    <DESCRIPTION>This strain was made by pronuclear microinjection of a Sleeping Beauty transposon vector harboring a ubiquitous CAG promoter driving the Brown Norway allele cDNA for Rab38 along with mRNA encoding the SB100X transposase.  The transposon inserted into rat chromosome 14 near 13.2 Mb (rn4)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8662449</RGD_ID>
    <STRAIN_SYMBOL>LOU/MBbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8662449</CITATION_ID>
    <DESCRIPTION>LOU/M strain maintained at Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8662861</RGD_ID>
    <STRAIN_SYMBOL>LOU.BN-(&lt;i&gt;D5Rat59-D5Rat133&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="7065535" STOP_POS="7065754" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="2282226" STOP_POS="47798053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="1666587" STOP_POS="48652920" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="1662934" STOP_POS="53233338" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="1368223" STOP_POS="49696253" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8662861</CITATION_ID>
    <DESCRIPTION>the desired chromosomal segment from BN/Rj was introgressed into the genetic background of LOU/MBbb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8662874</RGD_ID>
    <STRAIN_SYMBOL>LOU.BN-(&lt;i&gt;D5Rat59-D5Rat127&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="7065535" STOP_POS="31405251" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="2282226" STOP_POS="26607972" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="1666587" STOP_POS="26713119" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="1662934" STOP_POS="31408200" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="1368223" STOP_POS="27586431" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8662874</CITATION_ID>
    <DESCRIPTION>this congenic strain is produced by backcrossing LOU.BN-(&lt;i&gt;D5Rat59-D5Rat133&lt;/i&gt;)/Bbb to LOU/MBbb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8662878</RGD_ID>
    <STRAIN_SYMBOL>LOU.BN-(&lt;i&gt;D5Rat59-D5Rat125&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="7065535" STOP_POS="22195538" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="2282226" STOP_POS="17397969" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="1666587" STOP_POS="17263178" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="1662934" STOP_POS="22043910" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="1368223" STOP_POS="17703194" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8662878</CITATION_ID>
    <DESCRIPTION>this congenic strain is produced by backcrossing LOU.BN-(D5Rat59-D5Rat133)/Bbb to LOU/MBbb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8662925</RGD_ID>
    <STRAIN_SYMBOL>LOU.BN-(&lt;i&gt;D5Rat59-rs13448399&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="7065535" STOP_POS="10804074" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="2282226" STOP_POS="6020990" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="1666587" STOP_POS="5649731" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="1662934" STOP_POS="1663152" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="1368223" STOP_POS="1368442" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8662925</CITATION_ID>
    <DESCRIPTION>this congenic strain is produced by backcrossing LOU.BN-(D5Rat59-D5Rat133)/Bbb to LOU/MBbb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8662933</RGD_ID>
    <STRAIN_SYMBOL>LOU.BN-(&lt;i&gt;rs65016308-D5Rat133&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="15686915" STOP_POS="15686915" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="10898113" STOP_POS="47798053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="10652699" STOP_POS="48652920" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="53233142" STOP_POS="53233338" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="49696057" STOP_POS="49696253" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8662933</CITATION_ID>
    <DESCRIPTION>this congenic strain is produced by backcrossing LOU.BN-(D5Rat59-D5Rat133)/Bbb to LOU/MBbb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8662955</RGD_ID>
    <STRAIN_SYMBOL>LOU.BN-(&lt;i&gt;rs13448399-D5Rat133&lt;/i&gt;)/Bbb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="10804074" STOP_POS="10804074" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="6020990" STOP_POS="47798053" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="5649731" STOP_POS="48652920" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="53233142" STOP_POS="53233338" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="49696057" STOP_POS="49696253" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8662955</CITATION_ID>
    <DESCRIPTION>this congenic strain is produced by backcrossing LOU.BN-(D5Rat59-D5Rat133)/Bbb to LOU/MBbb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8662958</RGD_ID>
    <STRAIN_SYMBOL>LOU.BN-(&lt;i&gt;D5Rat59-rs13448399&lt;/i&gt;)/Bbb-/+</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbruck-Center for Molecular Medicine, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="7065535" STOP_POS="10804074" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="2282226" STOP_POS="6020990" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="1666587" STOP_POS="5649731" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="1662934" STOP_POS="1663152" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="1368223" STOP_POS="1368442" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8662958</CITATION_ID>
    <DESCRIPTION>this heterozygous congenic strain is produced by backcrossing LOU.BN-(D5Rat59-D5Rat133)/Bbb to LOU/MBbb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8663453</RGD_ID>
    <STRAIN_SYMBOL>BN.ACI-(&lt;i&gt;D14Uwm4-D14Rat39&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="76720835" STOP_POS="76721081" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="32471902" STOP_POS="72508789" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="34997325" STOP_POS="77240029" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="77221247" STOP_POS="77221492" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="77787938" STOP_POS="77788272" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8663453</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of ACI/SegHsd chromosome 14 transferred to the BN/SsNHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8663455</RGD_ID>
    <STRAIN_SYMBOL>BN.ACI-(&lt;i&gt;D14Uwm1-D14Uwm5&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="32061240" STOP_POS="33868895" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="31707011" STOP_POS="33514760" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="34228109" STOP_POS="36047474" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8663455</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of ACI/SegHsd chromosome 14 transferred to the BN/SsNHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8663458</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Rat164-D7Rat142&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="65287247" STOP_POS="71789091" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="72752037" STOP_POS="79629245" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="72918736" STOP_POS="79648829" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="69506936" STOP_POS="76323874" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8663458</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8663462</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Uwm32-D7Uwm43&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="95141405" STOP_POS="95141772" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8663462</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8663464</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;D7Uwm33-D7Uwm43&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="90922835" STOP_POS="95141772" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_8663464</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>8693598</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(DIO-mCherry)2OttcRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=687&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=687&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00687</CITATION_ID>
    <DESCRIPTION>The transgene contains Cre recombinase reporter rat expressing mCherry driven by the EF1 alpha promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9586448</RGD_ID>
    <STRAIN_SYMBOL>SHR/NCrlPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9586448</CITATION_ID>
    <DESCRIPTION>Substrain of SHR originally from Charles River now maintained at University of California</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9586450</RGD_ID>
    <STRAIN_SYMBOL>SHR/OlaIpcvPrin</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dept. of Pharmacology, University of California, San Diego, La Jolla, California</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9586450</CITATION_ID>
    <DESCRIPTION>These are substrains of SHR from Czech Academy of Sciences now maintained at University of California</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9587464</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(UBC-DsRedT3-emGFP)18Narl</STRAIN_SYMBOL>
    <FULL_NAME>SD-Tg(UBC-DsRedT3-emGFP)18</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.nlac.org.tw/rmrc/webc/html/data/show.aspx?ix=1&amp;page=1&amp;kw=23001&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.nlac.org.tw/rmrc/webc/html/data/show.aspx?ix=1&amp;page=1&amp;kw=23001&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>UBC</ALLELES>
    <ALLELE_RGD_IDS>1346853</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9587464</CITATION_ID>
    <DESCRIPTION>This strain was generated by microinjection of SD embyos with UBC-DsRed-emGFP transgene which is composed of DsRed flanked by loxP and followed by emerald GFP(emGFP).  The transgene is driven by human UBC promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9587466</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(UBC-cre/ERT2)7Narl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.nlac.org.tw/rmrc/webc/html/data/show.aspx?ix=1&amp;page=1&amp;kw=23002&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.nlac.org.tw/rmrc/webc/html/data/show.aspx?ix=1&amp;page=1&amp;kw=23002&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-05-31)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>UBC</ALLELES>
    <ALLELE_RGD_IDS>1346853</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9587466</CITATION_ID>
    <DESCRIPTION>This strain was generated by microinjection of SD embyos with UBC-Cre/ERT2 transgene which is composed of Cre/ERT2 recombinase gene driven by human UBC promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9587470</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(UBC-DsRedT3-emGFP)26Narl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.nlac.org.tw/rmrc/webc/html/data/show.aspx?ix=1&amp;page=1&amp;kw=23003&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.nlac.org.tw/rmrc/webc/html/data/show.aspx?ix=1&amp;page=1&amp;kw=23003&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>UBC</ALLELES>
    <ALLELE_RGD_IDS>1346853</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9587470</CITATION_ID>
    <DESCRIPTION>This strain was generated by microinjection of SD embyos with UBC-DsRed-emGFP transgene which is composed of DsRed flanked by loxP and followed by emerald GFP(emGFP). The transgene is driven by  human UBC promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9587473</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(UBC-emGFP)18Narl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.nlac.org.tw/rmrc/webc/html/data/show.aspx?ix=1&amp;page=1&amp;kw=23004&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.nlac.org.tw/rmrc/webc/html/data/show.aspx?ix=1&amp;page=1&amp;kw=23004&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>UBC</ALLELES>
    <ALLELE_RGD_IDS>1346853</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9587473</CITATION_ID>
    <DESCRIPTION>This strain was produced by microinjection of UBC-cre construct into embryos from SD-Tg(UBC-DsRedT3-emGFP)18Narl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9587475</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(UBC-DsRed-GFP)(Col1a(5A)-cre)Narl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Laboratory Animal Center, Taiwan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9587475</CITATION_ID>
    <DESCRIPTION>This strain was produced by microinjection of Col1a(5A)-Cre construct into embryos from SD-Tg(UBC-DsRedT3-emGFP)26Narl.  As loxP-flanked DsRed is removed by Col1a(5A) promoter-driven Cre recombinase</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9587825</RGD_ID>
    <STRAIN_SYMBOL>BN/SsNNarl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.nlac.org.tw/p3_animal2_detail.asp?cid=3&amp;nid=13&amp;ppage=0&amp;type=4&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.nlac.org.tw/p3_animal2_detail.asp?cid=3&amp;nid=13&amp;ppage=0&amp;type=4&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2018-03-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9587825</CITATION_ID>
    <DESCRIPTION>Imported from NIH, now maintained at National Laboratory Animal Center, Taiwan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9587827</RGD_ID>
    <STRAIN_SYMBOL>F344/NNarl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.nlac.org.tw/p3_animal2_detail.asp?cid=3&amp;nid=14&amp;ppage=0&amp;type=4&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.nlac.org.tw/p3_animal2_detail.asp?cid=3&amp;nid=14&amp;ppage=0&amp;type=4&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2018-03-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9587827</CITATION_ID>
    <DESCRIPTION>Imported from NIH, now maintained at National Laboratory Animal Center, Taiwan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9587829</RGD_ID>
    <STRAIN_SYMBOL>LEW/SsNNarl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.nlac.org.tw/p3_animal2_detail.asp?cid=3&amp;nid=15&amp;ppage=0&amp;type=4&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.nlac.org.tw/p3_animal2_detail.asp?cid=3&amp;nid=15&amp;ppage=0&amp;type=4&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2018-03-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9587829</CITATION_ID>
    <DESCRIPTION>Imported from NIH in 1995, now maintained at National Laboratory Animal Center, Taiwan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9587831</RGD_ID>
    <STRAIN_SYMBOL>SHR/NCrlNarl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.nlac.org.tw/p3_animal2_detail.asp?cid=3&amp;nid=16&amp;ppage=0&amp;type=4&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.nlac.org.tw/p3_animal2_detail.asp?cid=3&amp;nid=16&amp;ppage=0&amp;type=4&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2018-03-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9587831</CITATION_ID>
    <DESCRIPTION>Imported from NIH in 2000, now maintained at National Laboratory Animal Center, Taiwan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9587833</RGD_ID>
    <STRAIN_SYMBOL>WKY/NCrlNarl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.nlac.org.tw/p3_animal2_detail.asp?cid=3&amp;nid=19&amp;ppage=0&amp;type=4&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.nlac.org.tw/p3_animal2_detail.asp?cid=3&amp;nid=19&amp;ppage=0&amp;type=4&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2018-03-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9587833</CITATION_ID>
    <DESCRIPTION>Imported from NIH in 2000, now maintained at National Laboratory Animal Center, Taiwan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9587835</RGD_ID>
    <STRAIN_SYMBOL>CrlNarl:LE</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.nlac.org.tw/p3_animal2_detail.asp?cid=3&amp;nid=20&amp;ppage=0&amp;type=4&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.nlac.org.tw/p3_animal2_detail.asp?cid=3&amp;nid=20&amp;ppage=0&amp;type=4&gt; National Laboratory Animal Center, Taiwan &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2018-03-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9587835</CITATION_ID>
    <DESCRIPTION>Imported from Charles River in 1997, now maintained at National Laboratory Animal Center, Taiwan</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588294</RGD_ID>
    <STRAIN_SYMBOL>CrljKwl:SD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href="https://kwl-a.co.jp/rat/"&gt;Kiwa Laboratory Animals Co., Ltd. Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href="https://kwl-a.co.jp/rat/"&gt;Kiwa Laboratory Animals Co., Ltd. Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9588294</CITATION_ID>
    <DESCRIPTION>Sprague-Dawley from Charles River Laboratory Japan, to Kiwa Laboratory Animals Co.Ltd. Japan in 1985; these were turned into SPF by caesarean section</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588298</RGD_ID>
    <STRAIN_SYMBOL>Kwl:LE</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Kiwa Laboratory Animals Co.Ltd. Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9588298</CITATION_ID>
    <DESCRIPTION>Long Evans from Sasaki Institute, Japan, to Kiwa Laboratory Animals Co.Ltd. Japan in 1971; these were turned into SPF by caesarean section</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588544</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Ndufc2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ndufc2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>9588537</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="161122370" STOP_POS="161129413" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="151712157" STOP_POS="151712165" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="162369993" STOP_POS="162370001" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="168576274" STOP_POS="168582497" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="154635889" STOP_POS="154642112" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9588544</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GGCTTCCTGGGCTACTGCacgggcCTGATGGACAACATG into SHR/NCrl rat embryos. The resulting mutation is a 9-bp deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588546</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Ndufc2&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ndufc2&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>9588541</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="161122370" STOP_POS="161129413" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="151712052" STOP_POS="151712162" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="162369801" STOP_POS="162376024" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="168576274" STOP_POS="168582497" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="154635889" STOP_POS="154642112" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9588546</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence GGCTTCCTGGGCTACTGCacgggcCTGATGGACAACATG into SHR/NCrl rat embryos. The resulting mutation is a net 107-bp deltion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588552</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nfe2l2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nfe2l2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>9588549</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="81001529" STOP_POS="81031165" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="60621570" STOP_POS="60621610" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="62524893" STOP_POS="62524933" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="69041641" STOP_POS="69069190" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="58366693" STOP_POS="58394116" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9588552</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALENs targeting the sequence TAGTCCTGGCGGTGGCAATTCCAAGTCCATCATGCTGAGGGCGGACGCTGCGCTA into Crl:SD Sprague Dawley rat embryos. The resulting mutation is a 41-bp deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588559</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(DIO-iRFP)3Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=747&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=747&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00747</CITATION_ID>
    <DESCRIPTION>The transgene contains Cre recombinase reporter rat expressing the red fluorescent protein gene (iRFP) driven by the EF1 alpha promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588570</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(cFos-eGFP)2Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=766&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=766&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00766</CITATION_ID>
    <DESCRIPTION>The transgene contains reporter rat expressing eGFP in cFos expressing cells</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588572</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Slc6a3-icre)1Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=730&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=730&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>dopamine neurons in drug abuse or neurodegeneration</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00730</CITATION_ID>
    <DESCRIPTION>The transgene contains BAC transgenic using rat DAT promoter to express Cre recombinase in dopaminergic neurons</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588576</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Slc6a3-icre)5Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9588576</CITATION_ID>
    <DESCRIPTION>The transgene contains BAC transgenic using rat DAT promoter to express Cre recombinase in dopaminergic neurons</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588578</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Slc6a3-icre)6Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=758&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=758&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-31)</AVAILABILITY>
    <RESEARCH_USE>neurodegeneration</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00758</CITATION_ID>
    <DESCRIPTION>The transgene contains BAC transgenic using rat  dopamine transporterSlc6a3 (DAT) promoter to express Cre recombinase in dopaminergic neurons</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588581</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(cFos-LacZ)1Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=759&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=759&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00759</CITATION_ID>
    <DESCRIPTION>The transgene contains reporter rat expressing beta-galactosidase in cFos expressing cells</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588583</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(cFos-TetO-iCre)4Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=760&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=760&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00760</CITATION_ID>
    <DESCRIPTION>The transgene contains Cre recombinase expressed from cFos promoter and controllable by Tet activator/repressor</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588585</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(cFos-TetO-iCre)6Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=736&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=736&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00736</CITATION_ID>
    <DESCRIPTION>The transgene contains Cre recombinase expressed from cFos promoter and controllable by Tet activator/repressor</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588587</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(EEF1A1-TetR)1Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=761&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=761&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00761</CITATION_ID>
    <DESCRIPTION>The transgene expresses TetR using "ubiquitous" promoter; to be used in combination with TetO containing rats or viral vectors</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588589</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(EEF1A1-TetR)2Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=735&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=735&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00735</CITATION_ID>
    <DESCRIPTION>The transgene expresses TetR using "ubiquitous" promoter; to be used in combination with TetO containing rats or viral vectors</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588591</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Gad1-iCre)2Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2019-02-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9588591</CITATION_ID>
    <DESCRIPTION>The transgene expresses BAC transgenic using rat GAD1 promoter to express Cre recombinase in GABAergic neurons</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588593</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Gad1-icre)3Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=751&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=751&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2025-01-27)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00751</CITATION_ID>
    <DESCRIPTION>The transgene expresses BAC transgenic using rat GAD1 promoter to express Cre recombinase in GABAergic neurons</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9588595</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Slc6a5-icre)1Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=750&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=750&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00750</CITATION_ID>
    <DESCRIPTION>The transgene expresses BAC transgenic using rat GlyT2 (Slc6a5) promoter to express Cre recombinase in glycinergic neurons</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9589088</RGD_ID>
    <STRAIN_SYMBOL>ACI.COP-(&lt;i&gt;D3Rat130-D3Rat114&lt;/i&gt;)(&lt;i&gt;D6Rat80-D6Rat146&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=743&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2019-02-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00743</CITATION_ID>
    <DESCRIPTION>This congenic strain contains regions of COP/CrCrl chromosome 3 and COP/CrCrl chromosome 6 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9590284</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(ApoC3-CETP)25Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Massachusetts. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=637&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-02-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00637</CITATION_ID>
    <DESCRIPTION>SS/JrHsd embryos were microinjected with 1.57 kb human CETP cDNA construct into pSV-SPORT1 with human ApoC3 promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685623</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Pax6&lt;sup&gt;Sey2&lt;/sup&gt;&lt;/i&gt;/Mce</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Ophthalmology, Okayama University Medical School, Okayama, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1128&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-23)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pax6&lt;sup&gt;Sey2&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790970</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="112590034" STOP_POS="112611771" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="92128772" STOP_POS="92157022" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="95700241" STOP_POS="95728682" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="102320059" STOP_POS="102348223" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="91127605" STOP_POS="91149178" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685623</CITATION_ID>
    <DESCRIPTION>This rat (developed spontaneous microphthalmia) was found in a SD rat colony at Yamanouchi Pharma Inc. (Astellas Pharma Inc.)Genomic DNA analysis from mutants revealed a single base(c) insertion, resulting in a abnormal stop codon at 33-bp downstream from the insertion site due to frameshift.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685625</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Il2rg&lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=978&amp;s_References=&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=978&amp;s_References=&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-03-27)</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES>Il2rg&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12798560</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66395330" STOP_POS="66399026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685625</CITATION_ID>
    <DESCRIPTION>The strain having a zinc finger nuclease-induced 660-bp deletion mutation in Il2rg gene shows severe combined immunodeficiency and grows normally under SPF condition.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685748</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Il2rg&lt;sup&gt;em2Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=979&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=979&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-03-27)</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES>Il2rg&lt;sup&gt;em2Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12798561</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66395330" STOP_POS="66399026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685748</CITATION_ID>
    <DESCRIPTION>The severe combined immunodeficiency strain carries a zinc finger induced 1097-bp deletion mutation of Il2rg gene created in the F344/Stm embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685750</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Il2rg&lt;sup&gt;em3Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=980&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=980&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES>Il2rg&lt;sup&gt;em3Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13464340</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66395330" STOP_POS="66399026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685750</CITATION_ID>
    <DESCRIPTION>This strain shows severe combined immunodeficiency caused by a 332 bp deletion in Il2rg gene and grow normally under SPF condition.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685752</RGD_ID>
    <STRAIN_SYMBOL>TM-&lt;i&gt;Il2rg&lt;sup&gt;em4Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=981&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=981&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES>Il2rg&lt;sup&gt;em4Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13464339</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66395330" STOP_POS="66399026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685752</CITATION_ID>
    <DESCRIPTION>The severe combined immunodeficiency strain carries a zinc finger nuclease-induced 162-bp deletion mutation in rat  Il2rg gene. Grows normally under SPF condition.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685754</RGD_ID>
    <STRAIN_SYMBOL>TM-&lt;i&gt;Il2rg&lt;sup&gt;em5Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=982&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=982&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES>Il2rg&lt;sup&gt;em5Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910099</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66395330" STOP_POS="66399026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685754</CITATION_ID>
    <DESCRIPTION>This strain shows severe combined immunodeficiency caused by a zinc finger nuclease induced 653-bp deletion in Il2rg gene of TM/Kyo embryo. The rats grow normally under SPF condition.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685755</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(tetO-Pou5f1,-Klf4,-Sox2,Ubc-rtTA,-EGFP)T1-3Hina</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1103&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1103&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685755</CITATION_ID>
    <DESCRIPTION>Doxycycline induced mouse Oct3/4, Klf4, Sox2/ Ubc-promoter EGFP was introduced into embryonic fibroblast of Wistar rat (Slc:Wistar)by replication incompetent type lentivirus vector and iPS cells were induced. Chimeric rats (male) were generated from this iPS cells, and crossed with the wild-type Wistar rat (female).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685757</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Il2rg&lt;sup&gt;em1Hina&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1110&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1110&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-03-27)</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES>Il2rg&lt;sup&gt;em1Hina&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12798562</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66395330" STOP_POS="66399026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685757</CITATION_ID>
    <DESCRIPTION>This strain was generated by electroporation method: introduction of Il2rg gene-targeting vector (PKG promoter-HSV TK, loxp Tk2 promoter-Neor  loxp) into ES cells of Wistar rat(Crlj:Wistar)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685759</RGD_ID>
    <STRAIN_SYMBOL>LEW.WKY-(&lt;i&gt;D13Arb15-D13Rat77&lt;/i&gt;)(&lt;i&gt;D16Rat40-D16Rat88&lt;/i&gt;)/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Imperial College, London, UK</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1135&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=709&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="63483475" STOP_POS="94968043" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="839086" STOP_POS="63437135" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="832236" STOP_POS="56733837" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="60933298" STOP_POS="92436175" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="1550187" STOP_POS="60316851" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="66075608" STOP_POS="98985851" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="1534408" STOP_POS="59992088" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="71047218" STOP_POS="103987907" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="63175274" STOP_POS="96441728" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="819225" STOP_POS="60432230" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00709</CITATION_ID>
    <DESCRIPTION>Segment of interest from chr 13 and chr 16 of WKY/NCrl were introgressed into LEW/SsNHsd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685785</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco36-D1Mco54&lt;/i&gt;)/Bj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="131243790" STOP_POS="131244255" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="121833674" STOP_POS="127592440" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="129208943" STOP_POS="135158838" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="130267716" STOP_POS="136181734" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="122991895" STOP_POS="129013896" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685785</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing the progenitor strain SS.LEW-(&lt;I&gt;D1Mco36-D1Mco101&lt;/I&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685787</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco36-D1Rat200&lt;/i&gt;)/Bj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="131243790" STOP_POS="135021676" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="121833674" STOP_POS="125611741" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="129208943" STOP_POS="133164521" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="130267716" STOP_POS="134204042" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="122991895" STOP_POS="126939275" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685787</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing the progenitor strain SS.LEW-(&lt;I&gt;D1Mco36-D1Mco101&lt;/I&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685791</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco36-D1Mco61&lt;/i&gt;)/Bj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="131243790" STOP_POS="131244255" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="121833674" STOP_POS="123041501" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="129208943" STOP_POS="130446906" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="130267716" STOP_POS="131494744" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="122991895" STOP_POS="124296272" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685791</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing the progenitor strain SS.LEW-(&lt;I&gt;D1Mco36-D1Mco101&lt;/I&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685793</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Rat200-D1Mco136&lt;/i&gt;)/Bj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="135021436" STOP_POS="136574820" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="125611501" STOP_POS="125611741" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="133076978" STOP_POS="133164521" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="134116233" STOP_POS="134204042" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="126938969" STOP_POS="126939275" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685793</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing the progenitor strain SS.LEW-(&lt;I&gt;D1Mco36-D1Mco101&lt;/I&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685795</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco55-D1Wox6&lt;/i&gt;)/Bj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="139442053" STOP_POS="139442279" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="126540680" STOP_POS="126540917" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="134089429" STOP_POS="137787460" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="135124726" STOP_POS="138778112" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="127933558" STOP_POS="131956825" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685795</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing the progenitor strain SS.LEW-(&lt;I&gt;D1Mco36-D1Mco101&lt;/I&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9685797</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D1Mco134-D1Wox6&lt;/i&gt;)/Bj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Ohio, Toledo, Ohio, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="139442053" STOP_POS="139442279" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="137787261" STOP_POS="137787460" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="138777913" STOP_POS="138778112" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="131956599" STOP_POS="131956825" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9685797</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing the progenitor strain SS.LEW-(&lt;I&gt;D1Mco36-D1Mco101&lt;/I&gt;)/Mco to SS/Jr to get F2 which were again crossed with SS/Jr to duplicate the recombinant region</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9831158</RGD_ID>
    <STRAIN_SYMBOL>Y59/Zgd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Zagreb, Republic of Croatia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2020-10-05)</AVAILABILITY>
    <RESEARCH_USE>Immunology and transplantational research</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9831158</CITATION_ID>
    <DESCRIPTION>Strain developed by Prof. Borislav Nakic, Prof. Silobrcic and Prof. Andrija Kastelan from outbred Wistar rats during 1960s, maintained at Department of Animal Physiology,Faculty of Science, University of Zagreb, Republic of Croatia</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9835401</RGD_ID>
    <STRAIN_SYMBOL>ZDF-&lt;i&gt;Lepr&lt;sup&gt;m1Rll&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory of Human Behavior and Metabolism, Rockefeller University, New York</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;m1Rll&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>9835400</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116294409" STOP_POS="116477904" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120503475" STOP_POS="120682281" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9835401</CITATION_ID>
    <DESCRIPTION>The Zucker  rats from Charles River (ZDF-&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt;/Crl) carry the Lepr&lt;sup&gt;m1Rll&lt;/sup&gt; allele that has substitution of a nucleotide at 880 (A-C) results in Gln-Pro at position 269</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9835403</RGD_ID>
    <STRAIN_SYMBOL>WDF-&lt;i&gt;Lepr&lt;sup&gt;m1Rll&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory of Human Behavior and Metabolism, Rockefeller University, New York</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;m1Rll&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>9835400</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116294409" STOP_POS="116477904" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120503475" STOP_POS="120682281" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_9835403</CITATION_ID>
    <DESCRIPTION>The WDF colony at Vassar College (WDF/Vc) carry the Lepr&lt;sup&gt;m1Rll&lt;/sup&gt; allele that has substitution of a nucleotide at 880 (A-C) results in Gln-Pro at position 269</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9854707</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D4Rat143-D4Rat10&lt;/i&gt;)/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MRC Clinical Centre, London, UK</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=737&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Insulin Resistance</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="6542801" STOP_POS="6542917" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="5867662" STOP_POS="29593455" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="2380037" STOP_POS="26753822" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="2432766" STOP_POS="26659527" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="26280781" STOP_POS="26280949" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00737</CITATION_ID>
    <DESCRIPTION>This congenic strain was generated by introgressing the desired fragment from WKY/NCruk onto the genetic background of SHR/NCruk</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9854709</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D12Rat1-D12Mit3&lt;/i&gt;)/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MRC Clinical Centre, London, UK</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=738&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Insulin Resistance, Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="245071632" STOP_POS="245071725" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="6945260" STOP_POS="7384617" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="555108" STOP_POS="555654" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="223364189" STOP_POS="223364281" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00738</CITATION_ID>
    <DESCRIPTION>This congenic strain was generated by introgressing the desired fragment from WKY/NCruk onto the genetic background of SHR/NCruk</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9854711</RGD_ID>
    <STRAIN_SYMBOL>SHR.WKY-(&lt;i&gt;D16Rat88-D16Rat15&lt;/i&gt;)/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MRC Clinical Centre, London, UK</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=739&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Insulin Resistance</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="839086" STOP_POS="81928782" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="832236" STOP_POS="75226532" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="1550187" STOP_POS="80316424" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="1534408" STOP_POS="79886465" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="819225" STOP_POS="80047126" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00739</CITATION_ID>
    <DESCRIPTION>This congenic strain was generated by introgressing the desired fragment from WKY/NCruk onto the genetic background of SHR/NCruk</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9999141</RGD_ID>
    <STRAIN_SYMBOL>IRL/NCr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Cancer Institute, Animal Production Program</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=732&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Pulmonary hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00732</CITATION_ID>
    <DESCRIPTION>The IRL/NCr rat strain was received into the NIH Genetic Resources program in 1987, now maintained at NCI Animal production program</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9999143</RGD_ID>
    <STRAIN_SYMBOL>LOU/MNCr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Cancer Institute, Animal Production Program</ORIGINATION>
    <SOURCE>Delisted in December 2023, &lt;a href=http://www.rrrc.us/Strain/?x=733&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2023-12-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00733</CITATION_ID>
    <DESCRIPTION>The NCI Animal Production Program received this rat strain from NIH in 1987 for production and distribution of the LOU/MNCr rat strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>9999145</RGD_ID>
    <STRAIN_SYMBOL>F344/NCr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Cancer Institute, Animal Production Program</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=734&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Phenylketonuria</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00734</CITATION_ID>
    <DESCRIPTION>The F344/NCr rat strain was received into the NIH Genetic Resources program in 1987, now maintained at NCI Animal production program</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10002743</RGD_ID>
    <STRAIN_SYMBOL>DA.E3-(&lt;i&gt;D20Rat42-D20Rat49&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Lund University, Lund, Sweden.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="4461624" STOP_POS="8044044" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="4459698" STOP_POS="8042534" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="4186104" STOP_POS="8654464" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="6265460" STOP_POS="10844146" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="4582054" STOP_POS="8286657" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10002743</CITATION_ID>
    <DESCRIPTION>A fragment containing MHC region from E3/ZtmRhd was introduced in DA/ZtmRhd by marker-assisted breeding and verified as pure congenic line after six generations of backcross to DA/ZtmRhd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10002745</RGD_ID>
    <STRAIN_SYMBOL>DA.E3-(&lt;i&gt;D20Rat47-AA858870&lt;/i&gt;)/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Lund University, Lund, Sweden.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="1533083" STOP_POS="5769465" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="1527842" STOP_POS="5767669" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="2018654" STOP_POS="7289058" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="4059279" STOP_POS="9491404" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="1616332" STOP_POS="5924094" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10002745</CITATION_ID>
    <DESCRIPTION>A fragment containing MHC region from E3/ZtmRhd was introduced in DA/ZtmRhd by marker-assisted breeding and verified as pure congenic line after six generations of backcross to DA/ZtmRhd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10002782</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Sbf1&lt;sup&gt;m1Ipcv&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biology and Medical Genetics, Charles University, Prague</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sbf1&lt;i&gt;&lt;sup&gt;m1Ipcv&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>10002755</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="122237968" STOP_POS="122264591" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="120358338" STOP_POS="120385022" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="130261552" STOP_POS="130288566" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="129946572" STOP_POS="129973566" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="127583779" STOP_POS="127611043" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10002782</CITATION_ID>
    <DESCRIPTION>Spontaneous mutation in the colony of SHR/OlaIpcv in Prague.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10002787</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Krt71&lt;sup&gt;m1Yuyi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory Animal Center of Zhengzhou University, Henan Province, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Krt71&lt;i&gt;&lt;sup&gt;m1Yuyi&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>10002785</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="134752240" STOP_POS="134778765" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="132873532" STOP_POS="132898975" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="143345201" STOP_POS="143371346" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="141143396" STOP_POS="141166531" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10002787</CITATION_ID>
    <DESCRIPTION>Several rats curled arose spontaneously in a closed colony of SD rats maintained at Laboratory Animal Center of Zhengzhou University. a 3 bp deletion at position 420-422 of Krt71 which results in the deletion of aspartate was identified.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10002791</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Fah&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE>Availability contact: robcopenhaver@yecuris.com</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fah&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10002790</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="147957931" STOP_POS="147980708" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="138548830" STOP_POS="138571599" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="146713663" STOP_POS="146736339" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="147640316" STOP_POS="147662920" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="140851975" STOP_POS="140876187" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10002791</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALENs targeting the sequence CTCAGTGTTCCTACTCTgcccctcccagaggttcaATGCTTTGTGTTCAATGTCG into Crl:SD rat embryos. The resulting mutation is a 1-bp frameshift deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10002794</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Il2rg&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10002792</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66398582" STOP_POS="66398582" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10002794</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALENs targeting the sequence CTTAGACAACTCTCAATAGCTttatgggcctcggccAAGCGGCATGGAAGGAGGC into Crl:SD rat embryos. The resulting mutation is a 1-bp frameshift deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043120</RGD_ID>
    <STRAIN_SYMBOL>BBDP.ACI-(&lt;i&gt;D2Mit8-D2Rat69&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Sunnybrook Research Institute, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="145807215" STOP_POS="145807373" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="143657411" STOP_POS="143657569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="149614466" STOP_POS="254121739" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="169047256" STOP_POS="272813962" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="148790600" STOP_POS="247295816" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043120</CITATION_ID>
    <DESCRIPTION>104 Mb region from ACI.BBDP-(&lt;i&gt;RT1&lt;sup&gt;u&lt;/sup&gt;&lt;/i&gt;),(&lt;i&gt;Gimap5&lt;/i&gt;)/Sunn is introgressed into the BBDP/WorSunn background which includes Iddm26, Iddm33 QTL regions and a small fragment of Iddm32</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043122</RGD_ID>
    <STRAIN_SYMBOL>BBDP.ACI-(&lt;i&gt;D2Mit8-D2Arb16&lt;/i&gt;)(&lt;i&gt;D2Rat354-D2Rat69&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Sunnybrook Research Institute, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="145807215" STOP_POS="145807373" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="194675788" STOP_POS="194676010" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="191987426" STOP_POS="191987650" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="143657411" STOP_POS="190602963" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="206966406" STOP_POS="254121739" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="149614466" STOP_POS="205573168" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="226390296" STOP_POS="272813962" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="169047256" STOP_POS="225003755" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="148790600" STOP_POS="198312656" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="199719703" STOP_POS="247295816" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043122</CITATION_ID>
    <DESCRIPTION>104 Mb region from ACI.BBDP-(&lt;i&gt;RT1&lt;sup&gt;u&lt;/sup&gt;&lt;/i&gt;)(&lt;i&gt;Gimap5&lt;/i&gt;)/Sunn is introgressed into the BBDP/WorSunn background which includes Iddm26, Iddm33 QTL regions and a small fragment of Iddm32 the region from D2Rat99 and D2Rat354 is from the background ACI strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043124</RGD_ID>
    <STRAIN_SYMBOL>BBDP.ACI-(&lt;i&gt;D2Mit8-D2Arb16&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Sunnybrook Research Institute, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="145807215" STOP_POS="145807373" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="143657411" STOP_POS="190602963" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="149614466" STOP_POS="205573168" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="169047256" STOP_POS="225003755" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="148790600" STOP_POS="198312656" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043124</CITATION_ID>
    <DESCRIPTION>104 Mb region from ACI.BBDP-(&lt;i&gt;RT1&lt;sup&gt;u&lt;/sup&gt;&lt;/i&gt;),(&lt;i&gt;Gimap5&lt;/i&gt;)/Sunn is introgressed into the BBDP/WorSunn background which carries the centromeric region of Iddm26 and a small fragment of Iddm32</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043127</RGD_ID>
    <STRAIN_SYMBOL>BBDP.ACI-(&lt;i&gt;D2Mit8-D2Rat354&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Sunnybrook Research Institute, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="145807215" STOP_POS="194676010" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="143657411" STOP_POS="191987650" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="149614466" STOP_POS="206966627" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="169047256" STOP_POS="226390517" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="148790600" STOP_POS="199719925" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043127</CITATION_ID>
    <DESCRIPTION>104 Mb region from ACI.BBDP-(&lt;i&gt;RT1&lt;sup&gt;u&lt;/sup&gt;&lt;/i&gt;),(&lt;i&gt;Gimap5&lt;/i&gt;)/Sunn is introgressed into the BBDP/WorSunn background which carries the centromeric region of Iddm26 and a small fragment of Iddm32</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043129</RGD_ID>
    <STRAIN_SYMBOL>BBDP.ACI-(&lt;i&gt;D2Arb16-D2Rat63&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Sunnybrook Research Institute, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="225110556" STOP_POS="225110681" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="190602746" STOP_POS="222436696" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="205572952" STOP_POS="239166203" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="225003539" STOP_POS="257699856" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="198312439" STOP_POS="231465091" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043129</CITATION_ID>
    <DESCRIPTION>104 Mb region from ACI.BBDP-(&lt;i&gt;RT1&lt;sup&gt;u&lt;/sup&gt;&lt;/i&gt;),(&lt;i&gt;Gimap5&lt;/i&gt;)/Sunn is introgressed into the BBDP/WorSunn background which carries the centromeric region of Iddm33 and telomeric region of Iddm26</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043132</RGD_ID>
    <STRAIN_SYMBOL>BBDP.ACI-(&lt;i&gt;D2Rat50-D2Rat63&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Sunnybrook Research Institute, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="195313663" STOP_POS="225110681" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="192625307" STOP_POS="222436696" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="207612323" STOP_POS="239166203" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="227035223" STOP_POS="257699856" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="200390326" STOP_POS="231465091" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043132</CITATION_ID>
    <DESCRIPTION>104 Mb region from ACI.BBDP-(&lt;i&gt;RT1&lt;sup&gt;u&lt;/sup&gt;&lt;/i&gt;),(&lt;i&gt;Gimap5&lt;/i&gt;)/Sunn is introgressed into the BBDP/WorSunn background which carries the centromeric region of Iddm33 and telomeric region of Iddm26</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043368</RGD_ID>
    <STRAIN_SYMBOL>NER.F344-(&lt;i&gt;D3M2Mit327-D3Arb10&lt;/i&gt;)/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1065&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1065&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="110331010" STOP_POS="110331321" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="0" STOP_POS="93413837" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043368</CITATION_ID>
    <DESCRIPTION>The chromosome 3 region (D3M2Mit327-D3Arb10) was introgressed from F344/NSlc to NER/Kyo by backcrossing.&amp;#65288;Sep 12, 2012&amp;#65289;</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043382</RGD_ID>
    <STRAIN_SYMBOL>F344.NER-(&lt;i&gt;D1Mgh6-D1Rat73&lt;/i&gt;)(&lt;i&gt;D5Mgh4-D5Rat36&lt;/i&gt;)&lt;i&gt;Lgi1&lt;sup&gt;m1&lt;/sup&gt;&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Graduate School of Medicine, Kyoto University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1069&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-12-29)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Lgi1</ALLELES>
    <ALLELE_RGD_IDS>628742</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="96927100" STOP_POS="228174736" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="38207390" STOP_POS="143398338" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="138113556" STOP_POS="138113774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="87790149" STOP_POS="218748178" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="143846157" STOP_POS="143846372" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="91394009" STOP_POS="238824901" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="147610023" STOP_POS="147610238" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="92524380" STOP_POS="246113473" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="87656636" STOP_POS="224420760" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="145186817" STOP_POS="145187034" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043382</CITATION_ID>
    <DESCRIPTION>Triple congenic rat made by mating F344.NER-(&lt;i&gt;D1Mgh6-D1Rat132&lt;/i&gt;)(&lt;i&gt;D5Mgh4-D5Rat36&lt;/i&gt;)/Kyo and F344-Lgi1m1Kyo.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043385</RGD_ID>
    <STRAIN_SYMBOL>F344.NER-(&lt;i&gt;D1Mgh6-D1Rat73&lt;/i&gt;)(&lt;i&gt;D5Mgh4-D5Rat36&lt;/i&gt;)&lt;i&gt;Scn1a&lt;sup&gt;m1&lt;/sup&gt;&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1070&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1070&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Scn1a</ALLELES>
    <ALLELE_RGD_IDS>69364</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="38207390" STOP_POS="143398338" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="96927100" STOP_POS="228174736" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="71360840" STOP_POS="71479870" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="50952790" STOP_POS="51071804" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="138113556" STOP_POS="138113774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="87790149" STOP_POS="218748178" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="52388811" STOP_POS="52533365" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="143846157" STOP_POS="143846372" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="91394009" STOP_POS="238824901" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="147610023" STOP_POS="147610238" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="59016641" STOP_POS="59135580" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="92524380" STOP_POS="246113473" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="87656636" STOP_POS="224420760" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="145186817" STOP_POS="145187034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="48238528" STOP_POS="48364143" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043385</CITATION_ID>
    <DESCRIPTION>Triple congenic rat made by mating F344.NER-(&lt;i&gt;D1Mgh6-D1Rat132&lt;/i&gt;)(&lt;i&gt;D5Mgh4-D5Rat36&lt;/i&gt;)/Kyo and F344-LScn1am1Kyo.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043617</RGD_ID>
    <STRAIN_SYMBOL>SPRD-&lt;i&gt;Anks6&lt;sup&gt;PKD&lt;/sup&gt;&lt;/i&gt;/Fsn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1094&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1094&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-04-20)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Anks6&lt;sup&gt;PKD&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11534996</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="66112770" STOP_POS="66112770" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="61317180" STOP_POS="61317180" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="62650971" STOP_POS="62650971" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="67163440" STOP_POS="67204853" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="63633540" STOP_POS="63674953" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043617</CITATION_ID>
    <DESCRIPTION>This strain rats was provided to University of Kansas from Central Institute for Laboratory Animal Breeding (Hanover, Germany), and then was introduced to Fujita Health University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043620</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D1Smu13&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1080 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1080 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="156170341" STOP_POS="156170557" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="166884926" STOP_POS="166885141" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="173074640" STOP_POS="173074855" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043620</CITATION_ID>
    <DESCRIPTION>This congenic strain was made by introducing chromosome 1 region (D1Smu13) of WKY into SHRSP/Izm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043791</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D1Mgh5-D1Rat213&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1085&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="90905414" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="81777720" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="83282814" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="84537228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="81548909" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043791</CITATION_ID>
    <DESCRIPTION>male SHRSP.SHR-(&lt;i&gt;D1Rat93-D1Rat269&lt;/i&gt;)/Izm were crossed with female SHRSP/Izm and the offsprings were intercrossed, animals were genotyped to get the desired recombinants which were then backcrossed to SHRSP/Izm</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043794</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;D1Mgh5-D1Arb21&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1087&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1087&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043794</CITATION_ID>
    <DESCRIPTION>A congenic strain made by introducing a segments of chromosome 1 from SHRSP/Izm into WKY/Izm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043808</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;D1Mgh5-D1Arb21&lt;/i&gt;)(&lt;i&gt;D4Mgh7-D4Rat68&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1089&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1089&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="140059299" STOP_POS="169799698" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="138503169" STOP_POS="168069246" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="136351734" STOP_POS="168998263" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="200825021" STOP_POS="233267140" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="172169471" STOP_POS="172169650" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043808</CITATION_ID>
    <DESCRIPTION>A congenic strain made by introducing a segments of chromosome 1 from SHRSP/Izm into WKY/Izm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043811</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.MES-&lt;i&gt;Cyba&lt;sup&gt;MES&lt;/sup&gt;&lt;/i&gt;/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1108&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1108&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES>Cyba&lt;sup&gt;mesSdi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13209000</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043811</CITATION_ID>
    <DESCRIPTION>A congenic strain made by introducing a genetic locus of Cyba from Matsumoto Eosinophilic Shinshu (MES/Slc) rat into SHRSP/Izm rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043813</RGD_ID>
    <STRAIN_SYMBOL>SHR/HktIzm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1091&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1091&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043813</CITATION_ID>
    <DESCRIPTION>SHR/Kyushu rat (Kyushu University) was delivered to Shimane University in 2000 and maintained as inbred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043816</RGD_ID>
    <STRAIN_SYMBOL>LEA-Tg(Pou5f1-YFP*)3Ncco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1129&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1129&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Oncology, Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043816</CITATION_ID>
    <DESCRIPTION>Provided from Kyoto Bioresource center.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043826</RGD_ID>
    <STRAIN_SYMBOL>SHR/Kpo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1126 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1126 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043826</CITATION_ID>
    <DESCRIPTION>Spontaneously hypertensive rat (SHR) was segregated in Wistar-Kyoto rat in 1963.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10043828</RGD_ID>
    <STRAIN_SYMBOL>SHR/2Kpo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1125 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1125 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-09-24)</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10043828</CITATION_ID>
    <DESCRIPTION>Spontaneously hypertensive rat (SHR) was segregated in Wistar-Kyoto rat in 1963.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10044232</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/Kpo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1147 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1147 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10044232</CITATION_ID>
    <DESCRIPTION>Okamoto et al. found some rats that have cerebrovascular lesion in SHR rats (especially in line A). This strain was established in 1974 and named stroke-prone SHR (SHRSP) rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045545</RGD_ID>
    <STRAIN_SYMBOL>CDS/Sasz</STRAIN_SYMBOL>
    <FULL_NAME>Cohen diabetic-sensitive rat</FULL_NAME>
    <ORIGINATION>Hebrew University-Hadassah Medical School, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045545</CITATION_ID>
    <DESCRIPTION>Original breeders are from a colony at Hadassah University Hospital, Jerusalem, Israel: Professor Cohen AM et al. initiated the Cohen diabetic (CD) rat model at the Hadassah University Hospital in the 1950s to examine the role of constitutional (genetic) and environmental (dietary) factors in the development of type 2 diabetes mellitus. Since 1996, the original colony underwent a secondary inbreeding by Dr. Sarah Zangen designated by Prof. Cohen as responsible for the Cohen diabetic (CD) rat colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045548</RGD_ID>
    <STRAIN_SYMBOL>CDR/Sasz</STRAIN_SYMBOL>
    <FULL_NAME>Cohen diabetic-resistant rat</FULL_NAME>
    <ORIGINATION>Hebrew University-Hadassah Medical School, Jerusalem, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045548</CITATION_ID>
    <DESCRIPTION>Original breeders are from a colony at Hadassah University Hospital, Jerusalem, Israel: Professor Cohen AM et al. initiated the Cohen diabetic (CD) rat model at the Hadassah University Hospital in the 1950s to examine the role of constitutional (genetic) and environmental (dietary) factors in the development of type 2 diabetes mellitus. Since 1996, the original colony underwent a secondary inbreeding by Dr. Sarah Zangen designated by Prof. Cohen as responsible for the Cohen diabetic (CD) rat colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045576</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/2Kpo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1148 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1148 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045576</CITATION_ID>
    <DESCRIPTION>Okamoto et al. found some rats that have cerebrovascular lesion in SHR rats (especially in line A). This strain was established in 1974 and named stroke-prone SHR (SHRSP) rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045578</RGD_ID>
    <STRAIN_SYMBOL>MSHRSP/Kpo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1149 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1149 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Cardio-Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045578</CITATION_ID>
    <DESCRIPTION>Okamoto et al. found that a few rats developed higher blood pressure (over 230 mmHg) at 10 weeks old. They selected SHRSP rats that show severe hypertension from young age and M-SHRSP (malignant or precocious SHRSP) rat was established in 1985.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045580</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg((ROSA)26Sor-CAG-tdTomato)24Jfhy</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1139 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1139 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2016-11-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045580</CITATION_ID>
    <DESCRIPTION>Background strain: Long Evans | Transgene: CAG-loxP-flanked Neo/STOP cassette-tdTomato was inserted into mouse ROSA26 BAC (RP23 244D9).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045582</RGD_ID>
    <STRAIN_SYMBOL>ODURM/Odu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1162&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1162&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Dentistry</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045582</CITATION_ID>
    <DESCRIPTION>This strain shows malocclusion.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045584</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-HRAS*G12V)218Htsu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1146&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1146&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Oncology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045584</CITATION_ID>
    <DESCRIPTION>The transgene consisting of CAG promoter/loxP/neomycin resistant gene casette/lox/Ha-ras*G12V&amp;#65288;HrasV12&amp;#65289;was injected into embryos of SD rat (Jcl:SD). This strain was generated at CLEA Japan,Inc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045589</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-HRAS*G12V)246Htsu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1168&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1168&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Oncology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045589</CITATION_ID>
    <DESCRIPTION>The transgene consisting of CAG promoter/loxP/neomycin resistant gene casette/lox/Ha-ras*G12V&amp;#65288;HrasV12&amp;#65289;was injected into embryos of SD rat (Jcl:SD). This strain was generated at CLEA Japan,Inc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045590</RGD_ID>
    <STRAIN_SYMBOL>LEA.F344-(&lt;i&gt;D20Rat47-D20Mgh4&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1163 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1163 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="1533083" STOP_POS="6693431" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="1527842" STOP_POS="6691706" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="2018654" STOP_POS="5875448" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="4059279" STOP_POS="7910747" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="1616332" STOP_POS="6880472" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045590</CITATION_ID>
    <DESCRIPTION>Long-Evans Agouti (LEA), type 2 diabetes model, dies from lymphocytic insulitis induced by radiation (4 Gy). This LEA.F344-(D20Rat47-D20Mgh4) strain is a congenic strain made by introducing a segment of chromosome 20 (D20Rat47-D20Mgh4) from F344 strain into  LEA strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045591</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Cacna1a&lt;sup&gt;gry&lt;/sup&gt;&lt;/i&gt;&lt;i&gt;Scn1a&lt;sup&gt;m1Kyo&lt;/sup&gt;&lt;/i&gt;/Okym</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1144 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1144 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-05-05)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Cacna1a|Scn1a&lt;sup&gt;m1Kyo&lt;/sup&gt;|Cacna1a&lt;sup&gt;gry&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2244|12792283|12880382</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="40425560" STOP_POS="40724810" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="23520741" STOP_POS="23819971" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="25453236" STOP_POS="25749550" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="36502533" STOP_POS="36727039" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="25188170" STOP_POS="25424495" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045591</CITATION_ID>
    <DESCRIPTION>GRY/Idr (GRY/Idr has the M251K mutation in the Cacna1a gene) was backcrossed to F344/NSlc, and then crossed to HISS rat (HISS rat has the N1417H mutation in the Scn1a gene) to generate Scn1a/Cacna1a double mutant rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045593</RGD_ID>
    <STRAIN_SYMBOL>WIC-&lt;i&gt;Dmd&lt;sup&gt;em1Kykn&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1189 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1189 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-12-08)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Dmd&lt;sup&gt;em1Kykn&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10045592</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="51070098" STOP_POS="53437845" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="47272324" STOP_POS="49504219" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="51149358" STOP_POS="53519271" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="51475950" STOP_POS="53700033" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="71501362" STOP_POS="71671414" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045593</CITATION_ID>
    <DESCRIPTION>By CRISPR/Cas9 system, mutation was introduced in dystrophin (Dmd) gene of Wistar-Imamichi rat.  The resulting mutation is a 329-bp deletion around exon 3 and 2-bp substitution in exon16.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045597</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Nfe2l2&lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1185 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1185 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Diabetes Obesity</RESEARCH_USE>
    <ALLELES>Nfe2l2&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10045594</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="81001529" STOP_POS="81031165" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="60595852" STOP_POS="60595858" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="62499178" STOP_POS="62499184" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="69041641" STOP_POS="69069190" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="58366693" STOP_POS="58394116" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045597</CITATION_ID>
    <DESCRIPTION>Zinc-finger nucleases (ZFNs) method targeting exon 5 of Nfe2l2 (Nrf2) (ACCACTGTCCCCAGCCCAgaggccACACTGACAGAGATGGAC) was used; This strain has a 7-bp deletion in Nfe2l2 (Nrf2) gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045600</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Nfe2l2&lt;sup&gt;em2Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1191 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1191 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Diabetes Obesity</RESEARCH_USE>
    <ALLELES>Nfe2l2&lt;sup&gt;em2Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10045598</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="81001529" STOP_POS="81031165" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="60595852" STOP_POS="60595853" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="62499178" STOP_POS="62499179" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="69041641" STOP_POS="69069190" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="58366693" STOP_POS="58394116" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045600</CITATION_ID>
    <DESCRIPTION>Zinc-finger nucleases (ZFNs) method targeting exon 5 of Nfe2l2 (Nrf2) (ACCACTGTCCCCAGCCCAgaggccACACTGACAGAGATGGAC) was used; This strain has a 1 bp insertion in Nfe2l2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045602</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(CMV-Ddx54)19Tsuy</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1193 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1193 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045602</CITATION_ID>
    <DESCRIPTION>This transgenic rat was established by microinjection of transgene consisting of Ddx54 gene (NM_001191548.1) driven by CMV promoter (pCMV-Tag2B) derived from cytomegalovirus into Wistar rat (SLC) pronuclear fertile eggs at UNITECH Co., Ltd. in 2007.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10045606</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(CMV-Ddx54)37Tsuy</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1195 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1195 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10045606</CITATION_ID>
    <DESCRIPTION>This transgenic rat was established by microinjection of transgene consisting of Ddx54 gene (NM_001191548.1) driven by CMV promoter (pCMV-Tag2B) derived from cytomegalovirus into Wistar rat (SLC) pronuclear fertile eggs at UNITECH Co., Ltd. in 2007.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10046035</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D13Arb5-D13Arb8&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="48744711" STOP_POS="48744906" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="37902608" STOP_POS="46193066" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="42794724" STOP_POS="51577031" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="47898759" STOP_POS="56629737" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="38985717" STOP_POS="47698301" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10046035</CITATION_ID>
    <DESCRIPTION>A region of chromosome 13 containing the renin gene from the Dahl salt-resistant (Dahl R; SR/JrHsd) strain into the SS genetic background (SS/JrHsdMcwi)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10047085</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Fus&lt;sup&gt;em1Ionsz&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ion.ac.cn/index.asp&gt; Institute of Neuroscience, Chinese Academy of Sciences&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ion.ac.cn/index.asp&gt; Institute of Neuroscience, Chinese Academy of Sciences&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fus&lt;sup&gt;em1Ionsz&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10047084</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="192007011" STOP_POS="192020887" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="182576479" STOP_POS="182590417" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="199412805" STOP_POS="199426705" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="206435510" STOP_POS="206449423" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="187250871" STOP_POS="187264742" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10047085</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant; sgRNA+Cas9+Oligo was injected into zygote of SD rat. The mutation changed the 521th amino acid Arg (R) into Cys (C).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10047391</RGD_ID>
    <STRAIN_SYMBOL>LE/OrlBarth</STRAIN_SYMBOL>
    <FULL_NAME>Long-Evans/Cryptorchid</FULL_NAME>
    <ORIGINATION>A.I. duPont Hospital for Children Life Science Center, Wilmington, Delaware</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10047391</CITATION_ID>
    <DESCRIPTION>Obtained from Centre Nationale de la Researche Scientifique, Orleans, France; then bred at A.I. duPont Hospital for Children Life Science Center, Wilmington, Delaware</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10047393</RGD_ID>
    <STRAIN_SYMBOL>SDLEF7/Barth</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>A.I. duPont Hospital for Children Life Science Center, Wilmington, Delaware</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>hybrid</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10047393</CITATION_ID>
    <DESCRIPTION>This hybrid strain was created by interbreeding Crl:SD and Crl:LE for F7 generation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10053598</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Foxn1&lt;sup&gt;em1Nips&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi, JAPAN</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Foxn1&lt;sup&gt;em1Nips&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10053596</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="63749461" STOP_POS="63778468" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="63251400" STOP_POS="63273710" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="65621142" STOP_POS="65634666" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="66004940" STOP_POS="66030134" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="64243323" STOP_POS="64256847" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10053598</CITATION_ID>
    <DESCRIPTION>Foxn1 mutation was induced by injecting pX330 expressing Cas9 and sgRNA targeting the sequence GACTGGAGGGCGAACCCCAA into Crlj:WI rat embryos. The resulting mutation is a 44-bp frameshift deletion in exon 1 (del 54-97).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10053601</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Foxn1&lt;sup&gt;em2Nips&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi, JAPAN</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Foxn1&lt;sup&gt;em2Nips&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10053599</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="63749461" STOP_POS="63778468" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="63251400" STOP_POS="63273710" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="65621142" STOP_POS="65634666" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="66004940" STOP_POS="66030134" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="64243323" STOP_POS="64256847" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10053601</CITATION_ID>
    <DESCRIPTION>Foxn1 mutation was induced by injecting pX330 expressing Cas9 and sgRNA targeting the sequence GACTGGAGGGCGAACCCCAA into Crlj:WI rat embryos. The resulting mutation is a 60-bp frameshift deletion in exon 1 (del 46-105).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10053603</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Foxn1&lt;sup&gt;em1Nips&lt;/sup&gt;, &lt;i&gt;Foxn1&lt;sup&gt;em2Nips&lt;/sup&gt;&lt;/i&gt;F1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi, JAPAN</SOURCE>
    <STRAIN_TYPE>hybrid</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10053603</CITATION_ID>
    <DESCRIPTION>This strain is a hybrid of WI-Foxn1&lt;sup&gt;em1Nips&lt;/sup&gt; and WI-Foxn1&lt;sup&gt;em2Nips&lt;/sup&gt;</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054231</RGD_ID>
    <STRAIN_SYMBOL>HFJ/Hblac</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hebei Medical University, Shijiazhuang, Hebei, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054231</CITATION_ID>
    <DESCRIPTION>bred from Wistar rats that were from National Resource Center (NRLARC) for Rodent Laboratory Animal (Beijing, China)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054233</RGD_ID>
    <STRAIN_SYMBOL>MIJ/Hblac</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hebei Medical University, Shijiazhuang, Hebei, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054233</CITATION_ID>
    <DESCRIPTION>bred from Wistar rats that were from National Resource Center (NRLARC) for Rodent Laboratory Animal (Beijing, China)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054235</RGD_ID>
    <STRAIN_SYMBOL>MIJN/Hblac</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hebei Medical University, Shijiazhuang, Hebei, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054235</CITATION_ID>
    <DESCRIPTION>this strain is derived from MIJ/Hblac, they do not carry the infertile gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054239</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Abcd1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abcd1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054237</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="156579669" STOP_POS="156601448" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="151428334" STOP_POS="151450115" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="157094997" STOP_POS="157094998" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="152823436" STOP_POS="152844829" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="159614569" STOP_POS="159635963" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054239</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a  2-bp insertion mutation in the exon1 of the Abcd1 gene of DA/OlaHsd rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054242</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Abcd1&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abcd1&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054240</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="156579669" STOP_POS="156601448" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="151428334" STOP_POS="151450115" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="157094812" STOP_POS="157095014" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="152823436" STOP_POS="152844829" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="159614569" STOP_POS="159635963" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054242</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Abcd1 gene of DA/OlaHsd rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054245</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Adora1&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adora1&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054243</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="48210922" STOP_POS="48247826" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45658872" STOP_POS="45695821" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="51075440" STOP_POS="51075451" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="56097883" STOP_POS="56132155" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="47160292" STOP_POS="47192804" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054245</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Adora1 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp deletion in the Adora1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054276</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Vcp&lt;sup&gt;em1Ionsz&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ion.ac.cn/index.asp&gt; Institute of Neuroscience, Chinese Academy of Sciences&lt;/a&gt;</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Vcp&lt;sup&gt;em1Ionsz&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054274</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="62005984" STOP_POS="62025387" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="57210167" STOP_POS="57229571" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="58426548" STOP_POS="58445953" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="62951999" STOP_POS="62971402" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="59472100" STOP_POS="59491508" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054276</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant; sgRNA+Cas9+Oligo was injected into zygote of SD rat that  made the 155th amino acid Arg into His</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054279</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gfap&lt;sup&gt;em1(2A-Chr2-EYFP)Ionsz&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ion.ac.cn/index.asp&gt; Institute of Neuroscience, Chinese Academy of Sciences&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ion.ac.cn/index.asp&gt; Institute of Neuroscience, Chinese Academy of Sciences&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gfap&lt;sup&gt;em1Ionsz&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054277</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="88352987" STOP_POS="88361661" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="87852891" STOP_POS="87861631" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="90990762" STOP_POS="90999435" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="90763150" STOP_POS="90771823" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="92059881" STOP_POS="92068555" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054279</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant; sgRNA+Cas9+ plasmid was injected into zygote of SD rat that added a 2A ( the self-cleaving 2A peptide sequence from foot-and-mouth disease virus or other picornaviruses), blue light-gated cation channel channelrhodopsin-2 (ChR2)  and EYFP behind the last exon of Gfap.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054284</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Adora1&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adora1&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054282</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="48210922" STOP_POS="48247826" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45658872" STOP_POS="45695821" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="51075409" STOP_POS="51075445" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="56097883" STOP_POS="56132155" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="47160292" STOP_POS="47192804" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054284</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Adora1 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 34-bp deletion in the Adora1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054287</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Adora2a&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adora2a&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054285</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="13315270" STOP_POS="13332802" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="13315848" STOP_POS="13333386" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="14265251" STOP_POS="14282873" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="16457336" STOP_POS="16457433" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="13815719" STOP_POS="13834131" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054287</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Adora2a gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 98-bp deletion in the Adora2a gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054292</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Arhgef11&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Arhgef11&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054289</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="175372269" STOP_POS="175493852" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="173074383" STOP_POS="173195962" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="186979850" STOP_POS="187102523" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="206450722" STOP_POS="206450738" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="179676236" STOP_POS="179796785" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054292</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Arhgef11 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 17-bp deletion in the Arhgef11 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054296</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Arhgef11&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Arhgef11&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054293</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="175372269" STOP_POS="175493852" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="173074383" STOP_POS="173195962" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="186979850" STOP_POS="187102523" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="206384799" STOP_POS="206507431" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="179676236" STOP_POS="179796785" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054296</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Arhgef11 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 1-bp deletion in the Arhgef11 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054299</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat25-rs106935835&lt;/i&gt;)-&lt;i&gt;Btg2&lt;sup&gt;em11Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Btg2&lt;sup&gt;em11Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054297</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="48083931" STOP_POS="48087690" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45531881" STOP_POS="45535642" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50913185" STOP_POS="50916944" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55966299" STOP_POS="55970058" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="47026986" STOP_POS="47030745" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054299</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 16-bp deletion in the Btg2 gene of SS.BN-(&lt;i&gt;D13Rat25-rs106935835&lt;/i&gt;)/Mcwi rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054304</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat25-rs106935835&lt;/i&gt;)-&lt;i&gt;Btg2&lt;sup&gt;em13Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Btg2&lt;sup&gt;em13Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054302</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="48083931" STOP_POS="48087690" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45531881" STOP_POS="45535642" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50913185" STOP_POS="50916944" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55966299" STOP_POS="55970058" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="47026986" STOP_POS="47030745" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054304</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 2-bp deletion in the Btg2 gene of SS.BN-(&lt;i&gt;D13Rat25-rs106935835&lt;/i&gt;)/Mcwi rat embryos</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054307</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat25-rs106935835&lt;/i&gt;)-&lt;i&gt;Btg2&lt;sup&gt;em7Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Btg2&lt;sup&gt;em7Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054305</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="48083931" STOP_POS="48087690" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45535467" STOP_POS="45535510" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50913185" STOP_POS="50916944" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55966299" STOP_POS="55970058" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="47026986" STOP_POS="47030745" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054307</CITATION_ID>
    <DESCRIPTION>The Btg2 mutant rats were generated using transcription activator-like effector nuclease (TALEN) constructs specific for the rat Btg2 gene designed to target exon 1 using the target sequence  TAGGTTTCCTCACCAGTCtcctgaggactcggggcTGCGTGAGCGAGCAGAGA. The result was a 44-bp deletion mutation in exon 1 (RNO13:50,916,769-50,916,812;  aaaccttgagtctctgctcgctcacgcagccccgagtcctcagg) of  SS.BN-(&lt;i&gt;D13Rat25-rs106935835&lt;/i&gt;)/Mcwi rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054310</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Casr&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Casr&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054308</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="77738398" STOP_POS="77813639" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="64235251" STOP_POS="64304811" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="67188204" STOP_POS="67262261" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="70329456" STOP_POS="70329457" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="66084169" STOP_POS="66153292" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054310</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Casr gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 1-bp (T) insertion in the Casr gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054373</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Chrna3&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Chrna3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054371</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="64297755" STOP_POS="64311251" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="55401668" STOP_POS="55415165" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="59594007" STOP_POS="59607122" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="58186969" STOP_POS="58186970" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="58570223" STOP_POS="58583594" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054373</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Chrna3 gene of LEW/NCrl rat embryos.The resulting mutation is a 1-bp (G) insertion in the Chrna3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054376</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Chrna3&lt;sup&gt;em9Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-11-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Chrna3&lt;sup&gt;em9Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054374</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="64297755" STOP_POS="64311251" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="55412959" STOP_POS="55412975" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="59594007" STOP_POS="59607122" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="58176165" STOP_POS="58189008" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="58570223" STOP_POS="58583594" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054376</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Chrna3 gene of LEW/NCrl rat embryos. The resulting mutation is a 17-bp deletion in the Chrna3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054379</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Chrna4&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-11-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Chrna4&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054377</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="188506802" STOP_POS="188535558" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="168136246" STOP_POS="168157839" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="176533182" STOP_POS="176547965" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="180256391" STOP_POS="180256406" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="170171214" STOP_POS="170185998" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054379</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Chrna4 gene of LEW/NCrl rat embryos. The resulting mutation is a 5-bp deletion in the Chrna4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054383</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Chrna4&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-11-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Chrna4&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054380</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="188506802" STOP_POS="188535558" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="168136246" STOP_POS="168157839" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="176533182" STOP_POS="176547965" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="180256391" STOP_POS="180256406" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="170171214" STOP_POS="170185998" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054383</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Chrna4 gene of LEW/NCrl rat embryos. The resulting mutation is a 16-bp deletion in the Chrna4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054386</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Chrna5&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-11-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Chrna5&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054384</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="64265879" STOP_POS="64294233" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="55369794" STOP_POS="55398526" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="59561817" STOP_POS="59590172" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="58143974" STOP_POS="58172330" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="58538002" STOP_POS="58566388" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054386</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Chrna5 gene of LEW/NCrl rat embryos. The resulting mutation is a 1-bp insertion in the Chrna5 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054389</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Chrna5&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-11-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Chrna5&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054387</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="64265879" STOP_POS="64294233" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="55369794" STOP_POS="55398526" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="59561817" STOP_POS="59590172" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="58166756" STOP_POS="58166775" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="58538002" STOP_POS="58566388" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054389</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Chrna5 gene of LEW/NCrl rat embryos. The resulting mutation is a 20-bp deletion in the Chrna5 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054398</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Gla&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gla&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054395</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="102069216" STOP_POS="102069262" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="97775946" STOP_POS="97775992" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="105412632" STOP_POS="105412678" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="105301986" STOP_POS="105302032" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="122044703" STOP_POS="122056327" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054398</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Gla gene of DA/OlaHsd rat embryos. The resulting mutation is a 47-bp deletion in the Gla gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054401</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 3&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Helz2&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Helz2&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054399</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="188716370" STOP_POS="188730776" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="168338813" STOP_POS="168353219" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="176730024" STOP_POS="176744382" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="180439958" STOP_POS="180454321" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="170368815" STOP_POS="170382086" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054401</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Helz2 gene of FHH-Chr 3&lt;sup&gt;BN&lt;/sup&gt;/Mcwi rat embryos.The resulting mutation is a 11-bp deletion in the Helz2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054405</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 3&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Helz2&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Helz2&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054402</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="188716370" STOP_POS="188730776" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="168338813" STOP_POS="168353219" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="176730024" STOP_POS="176744382" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="180439958" STOP_POS="180454321" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="170368815" STOP_POS="170382086" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054405</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Helz2 gene of FHH-Chr 3&lt;sup&gt;BN&lt;/sup&gt;/Mcwi rat embryos.The resulting mutation is a 1-bp insertion in the Helz2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054408</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnj10&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnj10&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054406</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="87334510" STOP_POS="87367747" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="84802026" STOP_POS="84835383" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="90723077" STOP_POS="90752581" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="95245046" STOP_POS="95274535" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="88341102" STOP_POS="88370591" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054408</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Kcnj10 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 1-bp insertion in the Kcnj10 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054411</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnj10&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnj10&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054409</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="87334510" STOP_POS="87367747" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="84802026" STOP_POS="84835383" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="90723077" STOP_POS="90752581" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="95245046" STOP_POS="95274535" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="88341102" STOP_POS="88370591" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054411</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Kcnj10 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 3-bp deletion in the Kcnj10 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054414</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mmp9&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mmp9&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12743378</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="174103474" STOP_POS="174111434" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="153685624" STOP_POS="153685781" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="161413410" STOP_POS="161421473" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="167578904" STOP_POS="167605890" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="155985473" STOP_POS="155993433" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054414</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Mmp9 gene of SS/JrHsdMcwi rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054417</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mmp9&lt;sup&gt;em6Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mmp9&lt;sup&gt;em6Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054415</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="174103474" STOP_POS="174111434" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="153685771" STOP_POS="153685771" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="161413410" STOP_POS="161421473" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="167578904" STOP_POS="167605890" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="155985473" STOP_POS="155993433" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054417</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a delins  sequence alteration in the Mmp9 gene of SS/JrHsdMcwi rat embryos. The mutation is a 1-bp (t) deletion and a 5-bp (cgggta)  insertion in  in exon 4, which causes frameshift of the coded protein and premature stop codon in exon 8.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054420</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Mrpl28&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mrpl28&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054418</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="15653006" STOP_POS="15656062" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="15148698" STOP_POS="15151581" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="15495616" STOP_POS="15498527" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="15310467" STOP_POS="15310468" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="15394360" STOP_POS="15397270" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054420</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Mprl28 gene of LEW/NCrl rat embryos. The resulting mutation is a 7-bp insertion in the 2-bp deletion site in the Mrpl28 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054430</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Pkd1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pkd1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054428</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="14077733" STOP_POS="14125682" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="13573779" STOP_POS="13621138" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="13914057" STOP_POS="13962008" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="13769504" STOP_POS="13769511" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="13801445" STOP_POS="13848212" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054430</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Pkd1 gene of LEW/NCrl rat embryos. The resulting mutation is a 8-bp deletion in the Pkd1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054433</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Pkd1&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pkd1&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054431</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="14077733" STOP_POS="14125682" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="13573779" STOP_POS="13621138" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="13914057" STOP_POS="13962008" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="13769504" STOP_POS="13769511" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="13801445" STOP_POS="13848212" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054433</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Pkd1 gene of LEW/NCrl rat embryos. The resulting mutation is a 12-bp deletion in the Pkd1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054436</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Pkd1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pkd1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054434</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="14077733" STOP_POS="14125682" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="13573779" STOP_POS="13621138" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="13914057" STOP_POS="13962008" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="13731035" STOP_POS="13778993" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="13801445" STOP_POS="13848212" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054436</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Pkd1 gene of LEW/Crl rat embryos. The resulting mutation is a 16-bp deletion in the Pkd1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054439</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Pkd1&lt;sup&gt;em6Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pkd1&lt;sup&gt;em6Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054437</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="14077733" STOP_POS="14125682" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="13573779" STOP_POS="13621138" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="13914057" STOP_POS="13962008" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="13769504" STOP_POS="13769511" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="13801445" STOP_POS="13848212" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054439</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Pkd1 gene of LEW/NCrl rat embryos. The resulting mutation is a 8-bp deletion in the Pkd1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054444</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Rorc&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rorc&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054442</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="184698779" STOP_POS="184723942" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="182024120" STOP_POS="182024127" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="195612471" STOP_POS="195636797" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="189345134" STOP_POS="189369442" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054444</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Rorc gene of LEW/NCrl rat embryos. The resulting mutation is a 8-bp deletion in the Rorc gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054447</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Rorc&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rorc&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054445</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="184698779" STOP_POS="184723942" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="182024055" STOP_POS="182024123" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="195612471" STOP_POS="195636797" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="189345134" STOP_POS="189369442" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054447</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Rorc gene of LEW/NCrl rat embryos. The resulting mutation is a 59-bp deletion in the Rorc gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054450</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sirt3&lt;sup&gt;em25Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sirt3&lt;sup&gt;em25Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054448</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="205371703" STOP_POS="205394145" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="195955354" STOP_POS="195955366" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="213613502" STOP_POS="213636061" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="220539132" STOP_POS="220561380" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="201021391" STOP_POS="201043756" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054450</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Sirt3 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp deletion in the Sirt3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054453</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sirt3&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sirt3&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054451</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="205371703" STOP_POS="205394145" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="195955361" STOP_POS="195955367" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="213613502" STOP_POS="213636061" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="220539132" STOP_POS="220561380" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="201021391" STOP_POS="201043756" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054453</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Sirt3 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp deletion in the Sirt3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054456</RGD_ID>
    <STRAIN_SYMBOL>T2DN-&lt;i&gt;Sirt3&lt;sup&gt;em35Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sirt3&lt;sup&gt;em35Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054454</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="205371703" STOP_POS="205394145" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="195955280" STOP_POS="195955361" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="213613502" STOP_POS="213636061" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="220539132" STOP_POS="220561380" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="201021391" STOP_POS="201043756" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054456</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Sirt3 gene of T2DN/Mcwi rat embryos. The resulting mutation is a 82-bp deletion of exon 3 in the Sirt3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054459</RGD_ID>
    <STRAIN_SYMBOL>T2DN-&lt;i&gt;Sirt3&lt;sup&gt;em30Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sirt3&lt;sup&gt;em30Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054457</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="205371703" STOP_POS="205394145" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="195955335" STOP_POS="195955365" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="213613502" STOP_POS="213636061" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="220539132" STOP_POS="220561380" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="201021391" STOP_POS="201043756" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054459</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Sirt3 gene of T2DN/Mcwi rat embryos. The resulting mutation is a 31-bp deletion in the Sirt3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054462</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Stk39&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Stk39&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054460</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="73321522" STOP_POS="73588397" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="52913583" STOP_POS="53179060" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="54359449" STOP_POS="54625702" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="60973443" STOP_POS="61244306" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="50249626" STOP_POS="50517085" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054462</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Stk39 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 2-bp del in exon 5 in the Stk39 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054465</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Stk39&lt;sup&gt;em6Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Stk39&lt;sup&gt;em6Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10054463</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="73321522" STOP_POS="73588397" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="52913583" STOP_POS="53179060" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="54359449" STOP_POS="54625702" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="60973443" STOP_POS="61244306" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="50249626" STOP_POS="50517085" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054465</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Stk39 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 1-bp insertion in the Stk39 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10054473</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat124-D13Hmgc3694&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="47780418" STOP_POS="48086362" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45228358" STOP_POS="45228590" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50609228" STOP_POS="50609459" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55662705" STOP_POS="55662936" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="46721037" STOP_POS="46721269" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10054473</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10059570</RGD_ID>
    <STRAIN_SYMBOL>WI;WDB-&lt;i&gt;Kiss1&lt;sup&gt;tm1Nips&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Institute for Physiological Sciences, Okazaki Aichi, JAPAN, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kiss1&lt;sup&gt;tm1Nips&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>40902862</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="47327159" STOP_POS="47332759" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="44775106" STOP_POS="44780707" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50529506" STOP_POS="50537603" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55582365" STOP_POS="55590432" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="46244786" STOP_POS="46247288" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10059570</CITATION_ID>
    <DESCRIPTION>This strain was made by electroporation of WDB/Nips-ES1/Nips (RGD ID:10054010) embryonic stem cells with a targeting vector. Homologous recombination of the rKiss1 targeting construct (13.4kb) result in the deletion of 2.5 kb of the Kiss1 locus, consisting of 88 bp of the first coding exon, all of the 2.0-kb downstream intron, and 319 bp of the second coding exon, covering all of the coding region of this exon including the key active region of the processed peptide. Founder animals were backcrossed to Crlj:WI.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10059573</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Adora2a&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adora2a&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10059571</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="13315270" STOP_POS="13332802" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="13315848" STOP_POS="13333386" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="14274138" STOP_POS="14274144" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="16449385" STOP_POS="16466147" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="13815719" STOP_POS="13834131" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10059573</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Adora2a gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp deletion and 5-bp insertion in the Adora2a gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10059576</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Sik2&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sik2&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10059574</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="60121913" STOP_POS="60221707" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="51262005" STOP_POS="51262008" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="55309005" STOP_POS="55408608" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="53905730" STOP_POS="54005295" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="54240307" STOP_POS="54337976" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10059576</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Sik2 gene of WKY/NCrl rat embryos. The resulting mutation is a 4-bp deletion in exon 4 of the Sik2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10059635</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(GnRH-GFP)Mni</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Veterinary Physiology, Veterinary Medical Science, The University of Tokyo, Tokyo Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10059635</CITATION_ID>
    <DESCRIPTION>generated by Dr. Masugi Nishihara's group</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10395226</RGD_ID>
    <STRAIN_SYMBOL>Sim:LE</STRAIN_SYMBOL>
    <FULL_NAME>Long Evans</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.simlab.com/products.html&gt;Simonsen Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.simlab.com/products.html&gt;Simonsen Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10395226</CITATION_ID>
    <DESCRIPTION>Received from Dr. Evans, University of California, Berkeley - Experimental Institute of Biology in 1949. Caesarean rederived in 1997. Selection is based on the black-hooded phenotype.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10395228</RGD_ID>
    <STRAIN_SYMBOL>Sim:WI</STRAIN_SYMBOL>
    <FULL_NAME>Wistar</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.simlab.com/products.html&gt;Simonsen Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.simlab.com/products.html&gt;Simonsen Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10395228</CITATION_ID>
    <DESCRIPTION>Received from the Lobund Institute, University of Notre Dame in 1957. Caesarean rederived in 1997.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10395233</RGD_ID>
    <STRAIN_SYMBOL>Sim:SD</STRAIN_SYMBOL>
    <FULL_NAME>Sprague-Dawley Derived</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.simlab.com/products.html&gt;Simonsen Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.simlab.com/products.html&gt;Simonsen Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10395233</CITATION_ID>
    <DESCRIPTION>Received Sprague-Dawley derived breeding stock from Charles River Laboratory in 1958 and crossed with Sprague-Dawley rats received from ARS/Sprague-Dawley in 1975. Caesarean rederived in 1997.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10395235</RGD_ID>
    <STRAIN_SYMBOL>F344/NSim</STRAIN_SYMBOL>
    <FULL_NAME>FISCHER 344</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.simlab.com/products.html&gt;Simonsen Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.simlab.com/products.html&gt;Simonsen Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10395235</CITATION_ID>
    <DESCRIPTION>Gnotobiotic pedigreed breeders received from the NIH repository colony in 2005. Most widely used inbred rat strain, particularly for toxicology and teratology.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10395249</RGD_ID>
    <STRAIN_SYMBOL>FHH.FHH.3&lt;sup&gt;BN&lt;/sup&gt;-(&lt;i&gt;3p-D3Rat98&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="33703347" STOP_POS="33703538" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="33477354" STOP_POS="33477544" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="38636977" STOP_POS="38637167" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="30253942" STOP_POS="30254280" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10395249</CITATION_ID>
    <DESCRIPTION>(FHH X FHH-3&lt;sup&gt;BN&lt;/sup&gt;/Mcwi) F&lt;sub&gt;2&lt;/sub&gt; males were backcrossed with FHH-3&lt;sup&gt;BN&lt;/sup&gt;/Mcwi females to produce offsprings, these were intercrossed to generate this congenic line</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10395251</RGD_ID>
    <STRAIN_SYMBOL>FHH.FHH.3&lt;sup&gt;BN&lt;/sup&gt;-(&lt;i&gt;D3Hmgc24-3q&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10395251</CITATION_ID>
    <DESCRIPTION>(FHH X FHH-3&lt;sup&gt;BN&lt;/sup&gt;/Mcwi) F&lt;sub&gt;2&lt;/sub&gt; males were backcrossed with FHH-3&lt;sup&gt;BN&lt;/sup&gt;/Mcwi females to produce offsprings, these were intercrossed to generate this congenic line</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10395253</RGD_ID>
    <STRAIN_SYMBOL>FHH.FHH.3&lt;sup&gt;BN&lt;/sup&gt;-(&lt;i&gt;D3Hmgc24-3q&lt;/i&gt;)(&lt;i&gt;3p-D3Rat98&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="33703347" STOP_POS="33703538" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="33477354" STOP_POS="33477544" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="38636977" STOP_POS="38637167" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="30253942" STOP_POS="30254280" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10395253</CITATION_ID>
    <DESCRIPTION>(FHH X FHH-3&lt;sup&gt;BN&lt;/sup&gt;/Mcwi) F&lt;sub&gt;2&lt;/sub&gt; males were backcrossed with FHH-3&lt;sup&gt;BN&lt;/sup&gt;/Mcwi females to produce offsprings, these were intercrossed to generate this congenic line</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10395297</RGD_ID>
    <STRAIN_SYMBOL>GK/FarMcwi</STRAIN_SYMBOL>
    <FULL_NAME>Goto-Kakizaki</FULL_NAME>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin. &lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-08-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10395297</CITATION_ID>
    <DESCRIPTION>Generated by selective brother x sister breeding of 18 non-diabetic Jcl:Wistar rats which were glucose intolerant on oral glucose tolerant tests. This colony is from F36 generation of the Japanese colony provided by Drs. Suzuki and Toyota of Tokoku University , Sendai Japan. Now bred and maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401195</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG.LoxP.EGFP)Zi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=689&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=689&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm; Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00689</CITATION_ID>
    <DESCRIPTION>Random insertion of a Cre inducible expression cassette, controlled by the CAG promoter. LacZ is expressed constitutively, GFP only after Cre mediated recombination</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401201</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Th-cre)3.1Deis</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Stanford University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=659&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-05-31)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00659</CITATION_ID>
    <DESCRIPTION>Cre gene was introduced immediately before the ATG of the mouse tyrosine hydroxylase (Th) gene on BAC RP23-350E13</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401204</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(ChAT-cre)5.1DeisRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=658&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=658&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-05-31)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00658</CITATION_ID>
    <DESCRIPTION>Cre gene was introduced immediately before the ATG of the mouse choline acetyltransferase (Chat) gene in BAC RP23-246B12. This strain is estimated to carry 6 copies of the transgene at the integration site.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401208</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(Prp-APP,Prp-PS1)19/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=699&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=699&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2019-02-20)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00699</CITATION_ID>
    <DESCRIPTION>The strain was coinjected with two transgenes: one contains the human amyloid beta (A4) precursor protein (hAPP) gene with the Swedish mutation (K595N/M596L) driven by mouse prion promoter (Prp). The other contains the human presenilin 1 gene (PS1) with a deletion of exon 9, also driven by the mouse prion promoter (Prp). Based on segregation patterns, it is believed that the two transgenes have integrated at the same chromosomal site.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401212</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Thy1.2-NIPA1)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=700&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=700&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00700</CITATION_ID>
    <DESCRIPTION>Human NIPA1G106R mutation is made by site-directed mutagenesis and then inserted into Thy1.2-promotor cassette. Transgenic vector is injected into fertilized eggs to produce 2 independent lines (A, B)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401835</RGD_ID>
    <STRAIN_SYMBOL>WKY.F344-(&lt;i&gt;D17Got91-D17Rat51&lt;/i&gt;)/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MRC Clinical Centre, London, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="71003329" STOP_POS="85119583" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="74852634" STOP_POS="90012722" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="76512697" STOP_POS="91678127" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="82277434" STOP_POS="96587905" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10401835</CITATION_ID>
    <DESCRIPTION>A congenic strain made by introducing a 15 Mbp segment of chromosome 17 from F344/NHsd into WKY/Cruk, this region has the distal end of Cm15 QTL</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401837</RGD_ID>
    <STRAIN_SYMBOL>WKY.F344-(&lt;i&gt;D17Got91-D17Rat47&lt;/i&gt;)/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MRC Clinical Centre, London, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="71003329" STOP_POS="73951021" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="74852634" STOP_POS="77922655" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="76512697" STOP_POS="79573336" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="82277434" STOP_POS="85072478" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10401837</CITATION_ID>
    <DESCRIPTION>A congenic substrain derived from the progenitor strain WKY.F344-(&lt;i&gt;D17Got91-D17Rat51&lt;/i&gt;)/Tja</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401839</RGD_ID>
    <STRAIN_SYMBOL>WKY.F344-(&lt;i&gt;D17Rat47-D17Rat51&lt;/i&gt;)/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MRC Clinical Centre, London, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="73950871" STOP_POS="85119583" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="77922462" STOP_POS="90012722" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="79573143" STOP_POS="91678127" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="85072352" STOP_POS="96587905" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10401839</CITATION_ID>
    <DESCRIPTION>A congenic substrain derived from the progenitor strain WKY.F344-(&lt;i&gt;D17Got91-D17Rat51&lt;/i&gt;)/Tja</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401841</RGD_ID>
    <STRAIN_SYMBOL>WKY.F344-(&lt;i&gt;D17Rat131-D17Rat51&lt;/i&gt;)/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MRC Clinical Centre, London, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="81903264" STOP_POS="85119583" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="85994775" STOP_POS="90012722" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="87712049" STOP_POS="91678127" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="93347783" STOP_POS="96587905" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10401841</CITATION_ID>
    <DESCRIPTION>A congenic substrain derived from the progenitor strain WKY.F344-(&lt;i&gt;D17Got91-D17Rat51&lt;/i&gt;)/Tja</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401843</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Slc39a12&lt;sup&gt;em77Tja&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MRC Clinical Centre, London, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc39a12&lt;sup&gt;em77Tja&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10401842</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="82262303" STOP_POS="82348974" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="77353761" STOP_POS="77440384" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="81455731" STOP_POS="81541742" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="83202775" STOP_POS="83288616" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="88525527" STOP_POS="88605947" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10401843</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeted sequence into WKY/Cruk rat embryos. The resulting mutation 77 has a stop codon, 15 amino acids from the ZFN-binding site, that resulted in a 490 amino acids (54 kDa) truncated protein, 198 amino acids smaller than the WT protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401845</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Slc39a12&lt;sup&gt;em77Tja+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>WKY-&lt;i&gt;Slc39a12&lt;sup&gt;em77Tja+&lt;/sup&gt;&lt;/i&gt;/WKY-&lt;i&gt;Slc39a12&lt;sup&gt;em77Tja-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>MRC Clinical Centre, London, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc39a12&lt;sup&gt;em77Tja&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10401842</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="82262303" STOP_POS="82348974" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="77353761" STOP_POS="77440384" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="81455731" STOP_POS="81541742" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="83202775" STOP_POS="83288616" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="88525527" STOP_POS="88605947" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10401845</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with WKY/Cruk to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders. The resulting mutation 77 has a stop codon, 15 amino acids from the ZFN-binding site, that resulted in a 490 amino acids (54 kDa) truncated protein, 198 amino acids smaller than the WT protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401848</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Slc39a12&lt;sup&gt;em77Tja-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>WKY-&lt;i&gt;Slc39a12&lt;sup&gt;em77Tja-&lt;/sup&gt;&lt;/i&gt;/WKY-&lt;i&gt;Slc39a12&lt;sup&gt;em77Tja-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>MRC Clinical Centre, London, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc39a12&lt;sup&gt;em77Tja&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10401842</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="82262303" STOP_POS="82348974" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="77353761" STOP_POS="77440384" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="81455731" STOP_POS="81541742" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="83202775" STOP_POS="83288616" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="88525527" STOP_POS="88605947" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10401848</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with WKY/Cruk to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders. The resulting mutation 77 has a stop codon, 15 amino acids from the ZFN-binding site, that resulted in a 490 amino acids (54 kDa) truncated protein, 198 amino acids smaller than the WT protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401851</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lep&lt;sup&gt;em1Narl&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>National Laboratory Animal Center, Taiwan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lep</ALLELES>
    <ALLELE_RGD_IDS>3000</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="58626529" STOP_POS="58640663" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="57661127" STOP_POS="57675262" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="56337695" STOP_POS="56351818" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="56085079" STOP_POS="56099209" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="55943837" STOP_POS="55945938" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10401851</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant. This mutant strain has increased body weight, increased circulating cholesterol level and increased triglyceride level compared to its littermates</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10401918</RGD_ID>
    <STRAIN_SYMBOL>BDIX/HanHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.envigo.com/products-services/research-models-services/find-a-model/research-models/rats/inbred/bdix-inbred-rat/&gt;Envigo&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.envigo.com/products-services/research-models-services/find-a-model/research-models/rats/inbred/bdix-inbred-rat/&gt;Envigo&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10401918</CITATION_ID>
    <DESCRIPTION>BDIX/Han maintained at Envigo (Harlan)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402160</RGD_ID>
    <STRAIN_SYMBOL>HCR/1Tol</STRAIN_SYMBOL>
    <FULL_NAME>High-capacity runners; generation 5</FULL_NAME>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402160</CITATION_ID>
    <DESCRIPTION>HCR/Mco bred till the fifth generation</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402163</RGD_ID>
    <STRAIN_SYMBOL>HCR/2Tol</STRAIN_SYMBOL>
    <FULL_NAME>High-capacity runners; generation 26</FULL_NAME>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402163</CITATION_ID>
    <DESCRIPTION>HCR/Mco bred till the twenty-sixth generation</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402165</RGD_ID>
    <STRAIN_SYMBOL>LCR/1Tol</STRAIN_SYMBOL>
    <FULL_NAME>Low-capacity runners; generation 5</FULL_NAME>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402165</CITATION_ID>
    <DESCRIPTION>LCR/Mco bred till the fifth generation</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402167</RGD_ID>
    <STRAIN_SYMBOL>LCR/2Tol</STRAIN_SYMBOL>
    <FULL_NAME>Low-capacity runners; generation 26</FULL_NAME>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402167</CITATION_ID>
    <DESCRIPTION>LCR/Tol (LCR/Mco) bred till the twenty-sixth generation</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402390</RGD_ID>
    <STRAIN_SYMBOL>BNW/Jer</STRAIN_SYMBOL>
    <FULL_NAME>Brown Norway-wild</FULL_NAME>
    <ORIGINATION>Agricultural Omega Solutions LLC, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402390</CITATION_ID>
    <DESCRIPTION>This is a wild caught strain, characterized by Charles River Laboratories and has been bred brother x sister</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402393</RGD_ID>
    <STRAIN_SYMBOL>HPE/Jer</STRAIN_SYMBOL>
    <FULL_NAME>Hairless pink eye dilute</FULL_NAME>
    <ORIGINATION>Agricultural Omega Solutions LLC, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402393</CITATION_ID>
    <DESCRIPTION>This is a strain of unknown background, and has been bred brother x sister</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402395</RGD_ID>
    <STRAIN_SYMBOL>HBLS/Jer</STRAIN_SYMBOL>
    <FULL_NAME>Hairless black skin pigmented</FULL_NAME>
    <ORIGINATION>Agricultural Omega Solutions LLC, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402395</CITATION_ID>
    <DESCRIPTION>This is a result of a cross of the BNW and HPE, this spontaneous hairless black skin mutation was selected from the F2 offspring for the black hairless quality and subsequently bred brother x sister</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402819</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Tph2&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tph2&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10402817</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="52571909" STOP_POS="52676305" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="50685694" STOP_POS="50789424" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="58042279" STOP_POS="58149220" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="58053268" STOP_POS="58157949" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="54321033" STOP_POS="54430706" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402819</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CATGGCTCCGACCCCctctacACCCCGGAACCG into DA/OlaHsd rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402822</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Tph2&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tph2&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10402820</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="52571909" STOP_POS="52676305" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="50685694" STOP_POS="50789424" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="58112644" STOP_POS="58112654" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="58053268" STOP_POS="58157949" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="54321033" STOP_POS="54430706" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402822</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence CATGGCTCCGACCCCctctacACCCCGGAACCG into DA/OlaHsd rat embryos. The resulting mutation is a 11-bp frameshift deletion in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402834</RGD_ID>
    <STRAIN_SYMBOL>LEW.SS-(&lt;i&gt;D7Rat27-D7Mgh1&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="123682399" STOP_POS="123682549" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="29409683" STOP_POS="29409863" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="35867729" STOP_POS="35867908" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="35931747" STOP_POS="35931926" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="32004504" STOP_POS="32004684" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402834</CITATION_ID>
    <DESCRIPTION>LEW/Crlc and SS/Jr were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402836</RGD_ID>
    <STRAIN_SYMBOL>LEW.SS-(&lt;i&gt;D8Chm12-D8Rat15&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="107847991" STOP_POS="107848139" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="98968617" STOP_POS="98968765" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="106394231" STOP_POS="106394378" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="105836600" STOP_POS="105836747" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="103548728" STOP_POS="103548876" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402836</CITATION_ID>
    <DESCRIPTION>LEW/Crlc and SS/Jr were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402839</RGD_ID>
    <STRAIN_SYMBOL>LEW.SS-(&lt;i&gt;D10Mgh6-D10Mgh1&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="61843496" STOP_POS="61843633" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="61345276" STOP_POS="61345413" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="64648175" STOP_POS="64648311" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="63366082" STOP_POS="63366218" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="67677924" STOP_POS="67678060" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402839</CITATION_ID>
    <DESCRIPTION>LEW/Crlc and SS/Jr were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402842</RGD_ID>
    <STRAIN_SYMBOL>LEW.SS-(&lt;i&gt;D17Rat15-D17Rat51&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="31368391" STOP_POS="85119583" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="32055882" STOP_POS="90012722" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="33949701" STOP_POS="91678127" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="37727971" STOP_POS="96587905" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402842</CITATION_ID>
    <DESCRIPTION>LEW/Crlc and SS/Jr were backcrossed for 5 generations, then BC5 rat was mated with LEW/Crlc to produce the desired congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402850</RGD_ID>
    <STRAIN_SYMBOL>LEW.SS-(&lt;i&gt;D7Rat27-D7Mgh1&lt;/i&gt;)(&lt;i&gt;D17Rat15-D17Rat51&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="123682399" STOP_POS="123682549" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="31368391" STOP_POS="85119583" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="29409683" STOP_POS="29409863" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="32055882" STOP_POS="90012722" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="35867729" STOP_POS="35867908" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="33949701" STOP_POS="91678127" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="35931747" STOP_POS="35931926" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="37727971" STOP_POS="96587905" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="32004504" STOP_POS="32004684" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402850</CITATION_ID>
    <DESCRIPTION>double congenic strain was generated by combining the two separate congenic strains</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10402852</RGD_ID>
    <STRAIN_SYMBOL>LEW.SS-(&lt;i&gt;D7Rat27-D7Mgh1&lt;/i&gt;)(&lt;i&gt;D17Rat15-D17Rat51&lt;/i&gt;)(&lt;i&gt;D10Mgh6-D10Mgh1&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Research Centre, Centre Hospitalier de l'Universite de Monteal (CHUM), Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="123682399" STOP_POS="123682549" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="61843496" STOP_POS="61843633" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="61345276" STOP_POS="61345413" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="31368391" STOP_POS="85119583" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="29409683" STOP_POS="29409863" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="64648175" STOP_POS="64648311" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="35867729" STOP_POS="35867908" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="32055882" STOP_POS="90012722" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="63366082" STOP_POS="63366218" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="33949701" STOP_POS="91678127" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="35931747" STOP_POS="35931926" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="67677924" STOP_POS="67678060" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="32004504" STOP_POS="32004684" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="37727971" STOP_POS="96587905" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10402852</CITATION_ID>
    <DESCRIPTION>multiple congenic strain was generated by combining the three separate congenic strains</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10412325</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Drd1-icre)3Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=767&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=767&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2019-03-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Drd1</ALLELES>
    <ALLELE_RGD_IDS>2518</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="10545488" STOP_POS="10550029" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="10540440" STOP_POS="10544971" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="11099736" STOP_POS="11104352" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="13211031" STOP_POS="13215581" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="16655926" STOP_POS="16658161" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00767</CITATION_ID>
    <DESCRIPTION>The transgene expresses BAC transgenic using rat dopamine receptor 1 promoter to express Cre recombinase in D1R neurons</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10412327</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Drd2-iCre)1Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=768&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=768&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2019-03-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Drd1</ALLELES>
    <ALLELE_RGD_IDS>2518</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="10545488" STOP_POS="10550029" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="10540440" STOP_POS="10544971" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="11099736" STOP_POS="11104352" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="13211031" STOP_POS="13215581" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="16655926" STOP_POS="16658161" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00768</CITATION_ID>
    <DESCRIPTION>The transgene expresses BAC transgenic using rat dopamine receptor 2 promoter to express Cre recombinase in D2R neurons</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10412329</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Pvalb-icre)2Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=773&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=773&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2019-03-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pvalb</ALLELES>
    <ALLELE_RGD_IDS>3457</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00773</CITATION_ID>
    <DESCRIPTION>The transgene expresses BAC transgenic using rat parvalbumin promoter to express Cre recombinase in parvalbumin expressing neurons</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10413850</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abcc6&lt;sup&gt;em1Qlju-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Thomas Jefferson University, Philadelphia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abcc6&lt;sup&gt;em1Qlju&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10413843</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="105637772" STOP_POS="105637781" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="96501341" STOP_POS="96501350" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102013120" STOP_POS="102013129" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103042723" STOP_POS="103096453" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="96448588" STOP_POS="96524655" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10413850</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into SD embryos. ZFNs were designed to target exon 1 of rat Abcc6 gene at the binding site/cutting site 5-CACGCCTGGAGAGTCCTGcgcaggCCTGAGGGTGAGTCC-3 (c.24-c.62). The resulting mutation is a 10-bp deletion (CAGGCCTGAG)from the first coding exon of the rat Abcc6 gene. The mutation is predicted to cause out of frame translation and a premature stop codon. No protein in the homozygous mutant was detected by immunostaining.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10413852</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abcc6&lt;sup&gt;em2Qlju-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Thomas Jefferson University, Philadelphia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abcc6&lt;sup&gt;em2Qlju&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10413846</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="105637763" STOP_POS="105637785" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="96501332" STOP_POS="96501354" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102013111" STOP_POS="102013133" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103042723" STOP_POS="103096453" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="96448588" STOP_POS="96524655" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10413852</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into SD embryos. ZFNs were designed to target exon 1 of rat Abcc6 gene at the binding site/cutting site 5-CACGCCTGGAGAGTCCTGcgcaggCCTGAGGGTGAGTCC-3 (c.24-c.62). The resulting mutation is a 23 bp-deletion (TGCGCAGGCCTGAGGGTGAGTCC) from the first coding exon of the rat Abcc6 gene. The mutation is predicted to cause out of frame translation and a premature stop codon. No protein in the homozygous mutant was detected by immunostaining.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10413854</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abcc6&lt;sup&gt;em3Qlju-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Thomas Jefferson University, Philadelphia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abcc6&lt;sup&gt;em3Qlju&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10413847</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="105637774" STOP_POS="105637783" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="96501343" STOP_POS="96501352" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102013122" STOP_POS="102013131" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103042723" STOP_POS="103096453" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="96448588" STOP_POS="96524655" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10413854</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into SD embryos. ZFNs were designed to target exon 1 of rat Abcc6 gene at the binding site/cutting site 5-CACGCCTGGAGAGTCCTGcgcaggCCTGAGGGTGAGTCC-3 (c.24-c.62). The resulting mutation is a 10-bp deletion (CAGGCCTGAG)from the first coding exon of the rat Abcc6 gene. The mutation is predicted to cause out of frame translation and a premature stop codon. No protein in the homozygous mutant was detected by immunostaining.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10413856</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abcc6&lt;sup&gt;em4Qlju-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Thomas Jefferson University, Philadelphia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abcc6&lt;sup&gt;em4Qlju&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10413848</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="105637774" STOP_POS="105637793" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="96501343" STOP_POS="96501362" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102013122" STOP_POS="102013141" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103042723" STOP_POS="103096453" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="96448588" STOP_POS="96524655" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10413856</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into SD embryos. ZFNs were designed to target exon 1 of rat Abcc6 gene at the binding site/cutting site 5-CACGCCTGGAGAGTCCTGcgcaggCCTGAGGGTGAGTCC-3 (c.24-c.62). The resulting mutation is a 20-bp deletion from cDNA position 30-49 (GAGAGTCCTGCGCAGGCCTG). The mutation is predicted to cause out of frame translation and a premature stop codon. No protein in the homozygous mutant was detected by immunostaining.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10413858</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abcc6&lt;sup&gt;em5Qlju-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Thomas Jefferson University, Philadelphia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abcc6&lt;sup&gt;em5Qlju&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10413849</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="105637776" STOP_POS="105637786" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="96501345" STOP_POS="96501355" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102013124" STOP_POS="102013134" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103042723" STOP_POS="103096453" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="96448588" STOP_POS="96524655" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10413858</CITATION_ID>
    <DESCRIPTION>This strain was made by ZFN mutagenesis. ZFNs were designed to target exon 1 of rat Abcc6 gene at the binding site/cutting site 5-CACGCCTGGAGAGTCCTGcgcaggCCTGAGGGTGAGTCC-3 (c.24-c.62). The resulting mutation is a 11-bp deletion from cDNA position 39-49 (CTGCGCAGGCC). The mutation is predicted to cause out of frame translation and a premature stop codon. No protein in the homozygous mutant was detected by immunostaining.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10450489</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Bsn&lt;sup&gt;em1Ionsz&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ion.ac.cn/index.asp&gt; Institute of Neuroscience, Chinese Academy of Sciences&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ion.ac.cn/index.asp&gt; Institute of Neuroscience, Chinese Academy of Sciences&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bsn&lt;sup&gt;em1Ionsz&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10450488</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="117663447" STOP_POS="117754412" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="108784849" STOP_POS="108875819" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="116873721" STOP_POS="116965396" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="116227802" STOP_POS="116319071" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="113364208" STOP_POS="113455766" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10450489</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant; sgRNA+Cas9+ plasmid was injected into zygote of SD rat that added a 2a-NpHR-EYFP-2a-ChR2-mcherry-ires-WGA-cre behind the last exon of Bsn</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10755350</RGD_ID>
    <STRAIN_SYMBOL>F344.ZUC-(&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt;),OLETF-(&lt;i&gt;D14Rat23-D14Rat12&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=390&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=390&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES>Lepr</ALLELES>
    <ALLELE_RGD_IDS>3001</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="39507513" STOP_POS="39507682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116294409" STOP_POS="116477904" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="1217606" STOP_POS="39153750" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120503475" STOP_POS="120682281" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="2227825" STOP_POS="61783215" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="2222207" STOP_POS="61886417" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="1764386" STOP_POS="41707592" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10755350</CITATION_ID>
    <DESCRIPTION>The F344.ZUC,OLETF double congenic was produced by crossing F344.ZUC-&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt; with F344.OLETF-(&lt;i&gt; D14Rat23-D14Rat12&lt;/i&gt;) and then selecting Lepr&lt;sup&gt;fa&lt;/sup&gt; -Niddm20 (fa/fa-Nidd2/of)  homozygotes</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10755352</RGD_ID>
    <STRAIN_SYMBOL>LH/MavRrrcAek</STRAIN_SYMBOL>
    <FULL_NAME>Lyon Hypertensive</FULL_NAME>
    <ORIGINATION>Department of Pharmacology, University of Iowa, Iowa</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2023-10-25)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10755352</CITATION_ID>
    <DESCRIPTION>Lyon Hypertensive rats maintained at Department of Pharmacology, University of Iowa</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10755354</RGD_ID>
    <STRAIN_SYMBOL>LN/MavRrrcAek</STRAIN_SYMBOL>
    <FULL_NAME>lyon normotensive</FULL_NAME>
    <ORIGINATION>Department of Pharmacology, University of Iowa, Iowa</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-08-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10755354</CITATION_ID>
    <DESCRIPTION>Lyon normotensive rats maintained at Department of Pharmacology, University of Iowa</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>10759544</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gcdh&lt;sup&gt;em1Dba&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center of Molecular Diseases, CHUV, Switzerland</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gcdh&lt;sup&gt;em1Dba&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10758636</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="40168038" STOP_POS="40174536" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="23263215" STOP_POS="23269689" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="26000497" STOP_POS="26006970" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="36976120" STOP_POS="36982606" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="24919470" STOP_POS="24925943" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_10759544</CITATION_ID>
    <DESCRIPTION>this strain was produced by CRISPR/Cas9 system. The resulting knock-in mutation is R411W in exon 11 of the GCDH gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040455</RGD_ID>
    <STRAIN_SYMBOL>SHR.BN-(&lt;i&gt;D16Rat88-D16Rat9&lt;/i&gt;)/Cub</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="839086" STOP_POS="25639168" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="832236" STOP_POS="20872425" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="1550187" STOP_POS="22579213" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="1534408" STOP_POS="22473610" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="819225" STOP_POS="22577050" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040455</CITATION_ID>
    <DESCRIPTION>Segment of chromosome 16 from BN.&lt;i&gt;Lx&lt;/i&gt;/Cub was transferred to SHR/Ola after 9 backcrosses an intercross was done to obtain the desired congenic</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040519</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Ndufc2&lt;sup&gt;em1Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SHR-&lt;i&gt;Ndufc2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;/&lt;i&gt;Ndufc2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ndufc2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>9588537</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="161122370" STOP_POS="161129413" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="151712157" STOP_POS="151712165" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="162369993" STOP_POS="162370001" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="168576274" STOP_POS="168582497" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="154635889" STOP_POS="154642112" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040519</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SHR/NCrl to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040521</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Ndufc2&lt;sup&gt;em2Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SHR-&lt;i&gt;Ndufc2&lt;sup&gt;em2Mcwi-&lt;/sup&gt;&lt;/i&gt;/&lt;i&gt;Ndufc2&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040521</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SHR/NCrl to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040525</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Ndufc2&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SHR-&lt;i&gt;Ndufc2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;/&lt;i&gt;Ndufc2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040525</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SHR/NCrl to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040527</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Ndufc2&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SHR-&lt;i&gt;Ndufc2&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;/&lt;i&gt;Ndufc2&lt;sup&gt;em2Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040527</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SHR/NCrl to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040548</RGD_ID>
    <STRAIN_SYMBOL>CrlCembe:WI</STRAIN_SYMBOL>
    <FULL_NAME>Wistar rats</FULL_NAME>
    <ORIGINATION>Center for Biological Model Research (CeMBE), Pontifical Catholic University from Rio Grande do Sul (PUCRS), Brazil</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040548</CITATION_ID>
    <DESCRIPTION>CeMBE received breeding stock from Charles River (Crl:WI, strain code 003) in 2014, these are bred according to the Poiley rotation (1960) with permanent monogamous mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040561</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Htr7&lt;sup&gt;em1Geh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=745&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=745&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Htr7&lt;sup&gt;em1Geh&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14696714</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="243049064" STOP_POS="243173636" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="233636442" STOP_POS="233761063" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="254547964" STOP_POS="254671811" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="261759122" STOP_POS="261879914" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="240136279" STOP_POS="240260620" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00745</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant; this induced 89 base pair deletion in exon 1 of the Htr7 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040563</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Adra1a)Vccr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=756&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=756&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00756</CITATION_ID>
    <DESCRIPTION>Cardiac specific overexpression of the alpha 1A adrenergic receptor, 40 fold overexpression of the receptor</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040565</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(CAG-OFP)Pic</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=746&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=746&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00746</CITATION_ID>
    <DESCRIPTION>random insertion of a transgene carrying orange fluorescent protein (OFP) driven by the CAG promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040568</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(RNB1-116K03-EGFP-mRFP)3Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=931&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=931&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Atrn</ALLELES>
    <ALLELE_RGD_IDS>69063</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="138563271" STOP_POS="138697360" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="118110320" STOP_POS="118244326" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="123434409" STOP_POS="123567922" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="129934303" STOP_POS="130067267" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="118539268" STOP_POS="118701177" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040568</CITATION_ID>
    <DESCRIPTION>The transgene consists of the bacterial artificial chromosome (BAC) clone RNB1-116, which contains the attractin (Atrn) gene which is modified by in-frame insertion of the EGFP reporter gene upstream of the 29th exon and an in-frame insertion of the mRFP reporter gene between 24th exon and stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040570</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(RNB1-116K03-EGFP-mRFP)20Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=932&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=932&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Atrn</ALLELES>
    <ALLELE_RGD_IDS>69063</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="138563271" STOP_POS="138697360" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="118110320" STOP_POS="118244326" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="123434409" STOP_POS="123567922" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="129934303" STOP_POS="130067267" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="118539268" STOP_POS="118701177" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040570</CITATION_ID>
    <DESCRIPTION>The transgene consists of the bacterial artificial chromosome (BAC) clone RNB1-116, which contains the attractin (Atrn) gene which is modified by in-frame insertion of the EGFP reporter gene upstream of the 29th exon and an in-frame insertion of the mRFP reporter gene between 24th exon and stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040572</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(RNB1-116K03-EGFP-mRFP)21Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=933&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=933&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Atrn</ALLELES>
    <ALLELE_RGD_IDS>69063</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="138563271" STOP_POS="138697360" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="118110320" STOP_POS="118244326" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="123434409" STOP_POS="123567922" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="129934303" STOP_POS="130067267" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="118539268" STOP_POS="118701177" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040572</CITATION_ID>
    <DESCRIPTION>The transgene consists of the bacterial artificial chromosome (BAC) clone RNB1-116, which contains the attractin (Atrn) gene which is modified by in-frame insertion of the EGFP reporter gene upstream of the 29th exon and an in-frame insertion of the mRFP reporter gene between 24th exon and stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040574</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(RNB1-116K03-EGFP-mRFP)22Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=934&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=934&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Atrn</ALLELES>
    <ALLELE_RGD_IDS>69063</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="138563271" STOP_POS="138697360" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="118110320" STOP_POS="118244326" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="123434409" STOP_POS="123567922" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="129934303" STOP_POS="130067267" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="118539268" STOP_POS="118701177" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040574</CITATION_ID>
    <DESCRIPTION>The transgene consists of the bacterial artificial chromosome (BAC) clone RNB1-116, which contains the attractin (Atrn) gene which is modified by in-frame insertion of the EGFP reporter gene upstream of the 29th exon and an in-frame insertion of the mRFP reporter gene between 24th exon and stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040577</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(RNB1-116K03-EGFP-mRFP)41Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=935&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=935&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Atrn</ALLELES>
    <ALLELE_RGD_IDS>69063</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="138563271" STOP_POS="138697360" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="118110320" STOP_POS="118244326" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="123434409" STOP_POS="123567922" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="129934303" STOP_POS="130067267" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="118539268" STOP_POS="118701177" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040577</CITATION_ID>
    <DESCRIPTION>The transgene consists of the bacterial artificial chromosome (BAC) clone RNB1-116, which contains the attractin (Atrn) gene which is modified by in-frame insertion of the EGFP reporter gene upstream of the 29th exon and an in-frame insertion of the mRFP reporter gene between 24th exon and stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040579</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(RNB1-116K03-EGFP-mRFP)104Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=936&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=936&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Atrn</ALLELES>
    <ALLELE_RGD_IDS>69063</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="138563271" STOP_POS="138697360" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="118110320" STOP_POS="118244326" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="123434409" STOP_POS="123567922" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="129934303" STOP_POS="130067267" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="118539268" STOP_POS="118701177" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040579</CITATION_ID>
    <DESCRIPTION>The transgene consists of the bacterial artificial chromosome (BAC) clone RNB1-116, which contains the attractin (Atrn) gene which is modified by in-frame insertion of the EGFP reporter gene upstream of the 29th exon and an in-frame insertion of the mRFP reporter gene between 24th exon and stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040581</RGD_ID>
    <STRAIN_SYMBOL>TRM.W-Tg(RNB1-186G14)51Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1104&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1104&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040581</CITATION_ID>
    <DESCRIPTION>F344/Stm rat BAC clone RNB1-186G14 was microinjected into embryos of Wistar rats. The founder rats were backcrossed to TRM/Kyo rats. BAC vector:pKS145. RNB1-186G14 contains region between 60185236-60354841 of Rat Chr 10 and this region contains Spata22 gene expressed in testes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040675</RGD_ID>
    <STRAIN_SYMBOL>TRM.W-Tg(RNB1-186G14)33Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1102&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1102&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040675</CITATION_ID>
    <DESCRIPTION>F344/Stm rat BAC clone RNB1-186G14 was microinjected into embyos of Wistar rats. The founder rats were backcrossed to TRM/Kyo rats. BAC vector:pKS145. RNB1-186G14 contains region between 60185236-60354841 of Rat Chr 10 and this region contains Spata22 gene expressed in testes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040678</RGD_ID>
    <STRAIN_SYMBOL>TRMR.W-Tg(RNB1-186G14)51Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1106&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1106&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040678</CITATION_ID>
    <DESCRIPTION>F344/Stm rat BAC clone RNB1-186G14 was microinjected into embyos of Wistar rats. The founder rats were backcrossed to TRM/Kyo rats. BAC vector:pKS145. RNB1-186G14 contains region between 60185236-60354841 of Rat Chr 10 and this region contains Spata22 gene expressed in testes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040681</RGD_ID>
    <STRAIN_SYMBOL>TRMR.W-Tg(RNB1-186G14)33Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1105&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1105&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040681</CITATION_ID>
    <DESCRIPTION>F344/Stm rat BAC clone RNB1-186G14 was microinjected into embyos of Wistar rats. The founder rats were backcrossed to TRM/Kyo rats. BAC vector:pKS145. RNB1-186G14 contains region between 60185236-60354841 of Rat Chr 10 and this region contains Spata22 gene expressed in testes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040683</RGD_ID>
    <STRAIN_SYMBOL>SER.TRMR.W-Tg(RNB1-186G14)51Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1152&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1152&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040683</CITATION_ID>
    <DESCRIPTION>The sperms from N2 generation rat (ID#252) of TRMR.W-Tg(RNB1-186G14)51Kyo (NBRP-Rat#0677) were microinjected into SER embyos. The offspring with transgese was backcrossed with SER rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040916</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Zeb2&lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1169&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1169&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology; Development</RESEARCH_USE>
    <ALLELES>Zeb2</ALLELES>
    <ALLELE_RGD_IDS>1307272</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040916</CITATION_ID>
    <DESCRIPTION>Zinc-finger nucleases (ZFNs) method taregting exon 5 of Zeb2 gene (AGCCAAAGCTTGCCTCCA and GACTACTGACTCAAG) was used; This strain has a 5-bp deletion (cagag) and a 2-bp insertion (tc) in exon7 of Nrf2 gene, resulting in a deletion of Glutamine(Q)541. Background strain: F344/Stm</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040918</RGD_ID>
    <STRAIN_SYMBOL>WTC-&lt;i&gt;furue&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=550&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=550&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040918</CITATION_ID>
    <DESCRIPTION>WTC-furue rat was found in a colony of WTC.ZI-Atrn&lt;zi&gt; congenic strain at national cancer research center in 2000. The tremor phenotype is controlled by an autosomal recessive mutation ("furue")</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040920</RGD_ID>
    <STRAIN_SYMBOL>WTC.Cg-&lt;i&gt;dmy&lt;/i&gt;Tg(Mrs2-EGFP)39Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=909&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=909&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040920</CITATION_ID>
    <DESCRIPTION>CHORI230-9K13 recombinant BAC (Mrs2/EGFP) was introduced into Crlj:Wistar embyos. BAC Tg rats were backcrossed with WTC.DMY-dmy. dmy gene: homozygous, transgene: hemizygous. 4 lines: #15, #39, #92, #131</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040922</RGD_ID>
    <STRAIN_SYMBOL>WTC.Cg-&lt;i&gt;dmy&lt;/i&gt;Tg(Mrs2-EGFP)15Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=900&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=900&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040922</CITATION_ID>
    <DESCRIPTION>CHORI230-9K13 recombinant BAC (Mrs2-EGFP) was introduced into Crlj:Wistar embyos. BAC Tg rats were backcrossed with WTC.DMY-dmy. dmy gene: homozygous, transgene: hemizygous. 4 lines: #15, #39, #92, #131</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040934</RGD_ID>
    <STRAIN_SYMBOL>WTC.Cg-&lt;i&gt;dmy&lt;/i&gt;Tg(Mrs2-EGFP)92Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=912&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=912&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040934</CITATION_ID>
    <DESCRIPTION>CHORI230-9K13 recombinant BAC (Mrs2-EGFP) was introduced into Crlj:Wistar embyos. BAC Tg rats were backcrossed with WTC.DMY-dmy. dmy gene: homozygous, transgene: hemizygous. 4 lines: #15, #39, #92, #131</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040936</RGD_ID>
    <STRAIN_SYMBOL>WTC.Cg-&lt;i&gt;dmy&lt;/i&gt;Tg(Mrs2-EGFP)131Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=913&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=913&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040936</CITATION_ID>
    <DESCRIPTION>CHORI230-9K13 recombinant BAC (Mrs2/EGFP) was introduced into Crlj:Wistar embyos. BAC Tg rats were backcrossed with WTC.DMY-dmy. dmy gene: homozygous, transgene: hemizygous. 4 lines: #15, #39, #92, #131</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040939</RGD_ID>
    <STRAIN_SYMBOL>STOCK.&lt;i&gt;dmy&lt;/i&gt;Tg(CMV-Mrs2)Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=947&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=947&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mrs2</ALLELES>
    <ALLELE_RGD_IDS>708529</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040939</CITATION_ID>
    <DESCRIPTION>A transgene containing the CMV promoter and MRS2 gene was microinjected into the pronuclei of fertilized oocytes collected from Wistar rats. Transgenic offspring founder rats were backcrossed with WTC.DMy-dmy rats to obtain dmy/dmy homozygous and also hemizygous for the transgede (dmy/dmy, tg/+).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040941</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Gfap-Tk1)Jog</STRAIN_SYMBOL>
    <FULL_NAME>SD-Tg(Gfap-Tk1)</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1014&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2023-12-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gfap|Tk1</ALLELES>
    <ALLELE_RGD_IDS>2679|621014</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040941</CITATION_ID>
    <DESCRIPTION>The rats were originally generated by the University of Michigan Transgenic Animal Model Core, University of Michigan. They used a Crl:CD(SD) sub strain of Sprague-Dawley rats, obtained from Charles River Laboratory (Wilmington, MA, USA). The F1 rats have been bred in the UK with Hsd:Sprague Dawley (Harlan laboratories, UK), which are direct descendants of the original 1925 SD-company colony (Madison, Wisconsin, USA). The GFAP-TK rat was generated by pronuclear injection of a Gfap-Tk Bacterial Artificial Chromosome (BAC) construct, engineered using RedET-mediated homologous recombination methods.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040946</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Prkdc&lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1021&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1021&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-06-08)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prkdc|Prkdc&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>1308982|12910095</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="98544952" STOP_POS="98762499" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="85040790" STOP_POS="85258357" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="89293547" STOP_POS="89510948" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="92347175" STOP_POS="92565022" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="86951420" STOP_POS="87169229" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040946</CITATION_ID>
    <DESCRIPTION>This strain was established by Zinc-finger nucleases (ZFNs) method taregting exon1 of rat Prkdc gene, resulting a 46-deletion. Background strain: F344/Stm</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040948</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Prkdc&lt;sup&gt;em2Kyo&lt;/sup&gt;Il2rg&lt;sup&gt;em6Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1022&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1022&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-06-08)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg|Prkdc|Prkdc&lt;sup&gt;em2Kyo&lt;/sup&gt;|Il2rg&lt;sup&gt;em6Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>621466|1308982|12910096|12910097</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="98544952" STOP_POS="98762499" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="85040790" STOP_POS="85258357" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66395330" STOP_POS="66399026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="89293547" STOP_POS="89510948" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="92347175" STOP_POS="92565022" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="86951420" STOP_POS="87169229" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040948</CITATION_ID>
    <DESCRIPTION>This strain was established by Zinc-finger nucleases (ZFNs) method taregting rat Prkdc gene (227-bp deletion)  and Il2rg gene (332-bp deletion). Background strain: F344/Stm</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040950</RGD_ID>
    <STRAIN_SYMBOL>TM-&lt;i&gt;Prkdc&lt;sup&gt;em4Kyo&lt;/sup&gt;Il2rg&lt;sup&gt;em5Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1023&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1023&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-07-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg|Prkdc|Prkdc&lt;sup&gt;em4Kyo&lt;/sup&gt;|Il2rg&lt;sup&gt;em5Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>621466|1308982|12910098|12910099</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="98544952" STOP_POS="98762499" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="85040790" STOP_POS="85258357" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66395330" STOP_POS="66399026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="89293547" STOP_POS="89510948" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="92347175" STOP_POS="92565022" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="86951420" STOP_POS="87169229" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040950</CITATION_ID>
    <DESCRIPTION>This strain was established by Zinc-finger nucleases (ZFNs) method causing 20-bp deletion in the exon1 of Prkdc gene  and  a 653-bp deletion Il2rg gene. Background strain: TM/Kyo</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040952</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;D1Mgh5-D1Arb21&lt;/i&gt;)(&lt;i&gt;D3Mgh16-D3Rat144&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1088&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1088&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="10778704" STOP_POS="149313851" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="6000748" STOP_POS="156656443" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="11361699" STOP_POS="162886090" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="6373335" STOP_POS="151449116" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040952</CITATION_ID>
    <DESCRIPTION>A congenic strain made by introducing a segments of chromosome 1 and 3 from SHRSP/Izm into WKY/Izm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040954</RGD_ID>
    <STRAIN_SYMBOL>LEA-&lt;i&gt;Tp53&lt;sup&gt;tm1(AmCyan1)Ncco&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1130&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1130&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040954</CITATION_ID>
    <DESCRIPTION>LEA rats were provided from Kyoto Bioresource Center in 2006. Then LEA rat ES cells having Oct4-Venus gene and Oct4-Venus Tg rat strain (LEA-Tg(Pou5f1-YFP*)3Ncco) were established.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040957</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Tp53&lt;sup&gt;m1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1138&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1138&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tp53|Tp53&lt;sup&gt;m1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>3889|12792955</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="54798871" STOP_POS="54810300" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="54300070" STOP_POS="54311525" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="56186299" STOP_POS="56198449" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="55932658" STOP_POS="55944087" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="56399721" STOP_POS="56411150" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040957</CITATION_ID>
    <DESCRIPTION>This strain was established by ENU mutagenesis (gene-driven) using F344/NSlc and has a missense mutation&amp;#65288;R271C).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040959</RGD_ID>
    <STRAIN_SYMBOL>SER.TRMR.W-&lt;i&gt;tm&lt;sup&gt;TRM&lt;/sup&gt;Atrn&lt;sup&gt;zi&lt;/sup&gt;&lt;/i&gt;Tg(RNB1-186G14)/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1152&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1152&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040959</CITATION_ID>
    <DESCRIPTION>The sperms from N2 generation rat (NBRP Rat No:252) of TRMR.W-Tg(RNB1-186G14)51Kyo (NBRP Rat No:0677) were microinjected into SER embryos. The offspring with transgene was backcrossed with SER rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040962</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Bscl2&lt;sup&gt;m1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1178&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1178&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-01-09)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bscl2|Bscl2&lt;sup&gt;m1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>1308135|13838727</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="215160764" STOP_POS="215172540" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="205731828" STOP_POS="205743430" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="225035956" STOP_POS="225046137" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="231972073" STOP_POS="231983764" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="211509675" STOP_POS="211518963" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040962</CITATION_ID>
    <DESCRIPTION>T239A mutation was found by screening of 4608DNA sample from ENU mutagenesis library KURMA. This strain has a T239A (L80X) nonsense mutation in Bscl2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040969</RGD_ID>
    <STRAIN_SYMBOL>DWH/Iet</STRAIN_SYMBOL>
    <FULL_NAME>Dwarfism derived from Wistar Hannover GALAS rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1181&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1181&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo</AVAILABILITY>
    <RESEARCH_USE>Metabolism</RESEARCH_USE>
    <ALLELES>Tg</ALLELES>
    <ALLELE_RGD_IDS>3848</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="100307349" STOP_POS="100492246" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="98418293" STOP_POS="98603210" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="107467260" STOP_POS="107652897" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="107399165" STOP_POS="107602400" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="104035776" STOP_POS="104220754" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040969</CITATION_ID>
    <DESCRIPTION>derived from Wistar Hannover GALAS rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040971</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Tyr&lt;sup&gt;C&lt;/sup&gt;Kit&lt;sup&gt;H&lt;/sup&gt;/Kyo&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1183&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1183&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-07-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kit|Tyr</ALLELES>
    <ALLELE_RGD_IDS>620568|1589755</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="32901615" STOP_POS="32978895" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150527687" STOP_POS="150622857" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="32547459" STOP_POS="32624694" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="141115036" STOP_POS="141210207" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="35072131" STOP_POS="35149638" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="151012598" STOP_POS="151106802" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157322968" STOP_POS="157416594" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="34901860" STOP_POS="34979384" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143641257" STOP_POS="143746315" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="34906043" STOP_POS="34984819" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040971</CITATION_ID>
    <DESCRIPTION>1) point mutation in the exon 2 (896G&gt;A, p.R229H) of Tyrosinase (Tyr) gene (albino phenotype) and 2) retrotransposon insertion (7-bp) in kit gene (hooded phenotype) were targeted by CRISPR/Cas9 system using ssODN. The rat coat colour phenotype was changed from white to black. Background strain: F344/Stm</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040974</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Asip&lt;sup&gt;A&lt;/sup&gt;Tyr&lt;sup&gt;C&lt;/sup&gt;Kit&lt;sup&gt;H&lt;/sup&gt;/Kyo&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1184&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1184&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Asip|Kit|Tyr</ALLELES>
    <ALLELE_RGD_IDS>2003|620568|1589755</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="163933768" STOP_POS="164021377" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="32901615" STOP_POS="32978895" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150527687" STOP_POS="150622857" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="143473584" STOP_POS="143561170" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="141115036" STOP_POS="141210207" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="32547459" STOP_POS="32624694" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="150492010" STOP_POS="150579870" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="151012598" STOP_POS="151106802" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="35072131" STOP_POS="35149638" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="34901860" STOP_POS="34979384" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157322968" STOP_POS="157416594" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="156860395" STOP_POS="156949277" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143641257" STOP_POS="143746315" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="34906043" STOP_POS="34984819" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="145445175" STOP_POS="145536831" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040974</CITATION_ID>
    <DESCRIPTION>1) point mutation in the exon 2 of Tyrosinase (Tyr) gene (albino phenotype), 2) 19-bp deletion in Asip gene (Agouti phenotype), and 3) retrotransposon insertion (7-bp) in kit gene (hooded phenotype) were targeted by CRISPR/Cas9 system using ssODN. The rat coat colour phenotype was changed from white to Agouti. Background strain: F344/Stm</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040977</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;ROSA26&lt;sup&gt;em1(CAG-EGFP)Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1186&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1186&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-08-08)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040977</CITATION_ID>
    <DESCRIPTION>CAG-GFP vector was knock-in into the rat ROSA26 locus by CRISPR/Cas9 system. Background strain: Crlj:WI. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040980</RGD_ID>
    <STRAIN_SYMBOL>WIC-&lt;i&gt;Dmd&lt;sup&gt;em2Kykn&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1190&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1190&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-05-02)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dmd&lt;sup&gt;em2Kykn&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>630350394</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="51070098" STOP_POS="53437845" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="47272324" STOP_POS="49504219" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="51149358" STOP_POS="53519271" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="51475950" STOP_POS="53700033" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="71501362" STOP_POS="71671414" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040980</CITATION_ID>
    <DESCRIPTION>By CRISPR/Cas9 system, mutation was introduced in dystrophin (Dmd) gene of Wistar-Imamichi rat: deletion of exon3 to exon16</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040985</RGD_ID>
    <STRAIN_SYMBOL>WIC-&lt;i&gt;Dmd&lt;sup&gt;em3Kykn&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Keitaro Yamanouchi, The University of Tokyo</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1192&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-05-02)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dmd&lt;sup&gt;em3Kykn&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>630350395</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="51070098" STOP_POS="53437845" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="47272324" STOP_POS="49504219" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="51149358" STOP_POS="53519271" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="51475950" STOP_POS="53700033" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="71501362" STOP_POS="71671414" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040985</CITATION_ID>
    <DESCRIPTION>By CRISPR/Cas9 system, mutation was introduced in dystrophin (Dmd) gene of Wistar-Imamichi rat: Deletion of exon3 to exon16 (a part of intron 3 remain). This  strain died out in 2015.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11040987</RGD_ID>
    <STRAIN_SYMBOL>WIC-Tg(Nanog-YFP*)1Utr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1202&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1202&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-04-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nanog</ALLELES>
    <ALLELE_RGD_IDS>1303178</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11040987</CITATION_ID>
    <DESCRIPTION>BAC (containing rat Nanog gene) vector was injected into Iar:Wistar-Imamichi rats. The construct is as follows: Venus-IRES-puromycin resistance gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11041106</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Pvalb-tTA)15Hio</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1203&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1203&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11041106</CITATION_ID>
    <DESCRIPTION>background strain #65306; Long-Evans rat #65288; Iar:Long-Evans #65289; Transgene #65306; (1) Parvalbumin (PV) promoter #65306; mouse derived (MGI:97821). PV is calcium-binding protein. (2) tetracycline transactivator (tTA) #65306; Fusion protein of tetracycline repressor (Escherichia coli-derived) and VP16 (Herpes simplex virus-derived). In the absence of Doxycycline (Dox), tTA binds to tetracycline-responsive element (TRE) and expression of TRE-controlled genes can be induced. Vector #65306; pBlueScript (Stratagene), pBACe3.6 (CHORI)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11041108</RGD_ID>
    <STRAIN_SYMBOL>CV/Iet</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1222&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1222&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11041108</CITATION_ID>
    <DESCRIPTION>The Laboratory of Reproductive Toxicology at the Institute of Environmental Toxicology has been maintaining a Wistar derived PD strain of rats. In 1986, 1 female and 2 males exhibiting very short and sparse vibrissae were found in a litter of 7 parented by a pd/pd female and phenotypically normal pd/+ male. In 2008, a male Wistar rat and F56 female were crossed, and obtained heterozygous rats were sib-mated. After that, sib mating between homozygous rats was started.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11041128</RGD_ID>
    <STRAIN_SYMBOL>TM.KDP-&lt;i&gt;Cblb&lt;/i&gt;(&lt;i&gt;D9Rat13-D9Rat4&lt;/i&gt;)(&lt;i&gt;D12Rat5-D12Rat45&lt;/i&gt;)(&lt;i&gt;D18Mit9-D18Rat44&lt;/i&gt;)/Nyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1211&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1211&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES>Cblb</ALLELES>
    <ALLELE_RGD_IDS>620535</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11041128</CITATION_ID>
    <DESCRIPTION>The Cblb mutation, one of the causative gene in type 1 diabetes of KDP/Tky and KDP alleles in other modifier genes were transferred onto the genetic background of TM:Kyo strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11041139</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(Dct-lacZ)9Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1218&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1218&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES>Dct</ALLELES>
    <ALLELE_RGD_IDS>1564975</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11041139</CITATION_ID>
    <DESCRIPTION>The construct was made by connecting a 3,659 bp DNA fragment of rat Dct (dopachrome tautomerase) gene (5'-3237 to 422) with the upstream of lacZ gene. Dct gene was derived from F344/Stm. Background strain: F344/NSlc, plasmid: pLacZ-Basic (Clontech Laboratories)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11041143</RGD_ID>
    <STRAIN_SYMBOL>PL/Iet</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1223&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1223&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11041143</CITATION_ID>
    <DESCRIPTION>A new mutant gene that causes preaxial polydactyl in the hindlimbs was found in the Jcl:Wistar -derived strain of rats with fused pulmonary lobes (FRL) at the Laboratory of Reproductive Toxicology at the Institute of Environmental Toxicology . Genetic analysis has revealed that the new mutation is not closely linked with the fpl gene. This strain was established by sib mating (over 20 generations).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11049145</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Crh&lt;sup&gt;em1Ionsz&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ion.ac.cn/index.asp&gt; Institute of Neuroscience, Chinese Academy of Sciences&lt;/a&gt;</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Crh&lt;sup&gt;em1Ionsz&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11049142</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="104059184" STOP_POS="104061048" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="102143055" STOP_POS="102144919" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="104459999" STOP_POS="104461863" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="124182919" STOP_POS="124184783" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="104764023" STOP_POS="104765887" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11049145</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant; sgRNA+Cas9+ plasmid was injected into zygote of SD rat that added a GFP-Cre-2A behind the last exon of Crh.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11073612</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 13&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Mir29b&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mir29b1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11073608</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="60618334" STOP_POS="60618414" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="59650987" STOP_POS="59651067" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="58344310" STOP_POS="58344390" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="58100053" STOP_POS="58100133" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11073612</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALENs targeting the sequence TTTAAATAGTGATTGTCtagcaccatttgaaaTCAGTGTTCTTGGTGGA into SS-Chr 13BN/mcwi rat embryos. The resulting mutation is a 4-bp deletion in the mature rno-mir-29b-1-3p sequence</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11073719</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Drd1&lt;sup&gt;em1Ionsz&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.ion.ac.cn/index.asp&gt; Institute of Neuroscience, Chinese Academy of Sciences&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.ion.ac.cn/index.asp&gt; Institute of Neuroscience, Chinese Academy of Sciences&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Drd1&lt;sup&gt;em1Ionsz&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11073717</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="10545488" STOP_POS="10550029" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="10540440" STOP_POS="10544971" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="11099736" STOP_POS="11104352" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="13211031" STOP_POS="13215581" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="16655926" STOP_POS="16658161" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11073719</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant; sgRNA+Cas9+ plasmid was injected into zygote of SD rat that added a 2A-Chr2-EYFP behind the stop codon of Drd1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11081142</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Pgr&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Kansas Medical Center</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=741&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>reproduction, neurobiology, and cancer</RESEARCH_USE>
    <ALLELES>Pgr</ALLELES>
    <ALLELE_RGD_IDS>3317</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="14354398" STOP_POS="14413271" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="6072673" STOP_POS="6131552" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="7128656" STOP_POS="7187796" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="7113895" STOP_POS="7172761" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="5784717" STOP_POS="5845901" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00741</CITATION_ID>
    <DESCRIPTION>Crispr/Cas9 targeting of Exon 3 of rat Pgr gene resulting in a deletion of Exon3</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11081149</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Esr2&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=742&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=742&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>reproduction</RESEARCH_USE>
    <ALLELES>Esr2&lt;sup&gt;&lt;i&gt;em1Soar&lt;/i&gt;&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>40902840</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="100589553" STOP_POS="100645240" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="94858438" STOP_POS="94909630" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="99163953" STOP_POS="99214711" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="108576398" STOP_POS="108626196" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="98691167" STOP_POS="98775299" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00742</CITATION_ID>
    <DESCRIPTION>Zinc finger nuclease targeting of exon 4 of the rat estrogen receptor-2 gene resulting in the deletion of exon 4</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11081151</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Grm8&lt;sup&gt;em1Geh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=744&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=744&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>neurologic medications, neurologic diseases, normal brain functions</RESEARCH_USE>
    <ALLELES>Grm8</ALLELES>
    <ALLELE_RGD_IDS>619858</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="56771247" STOP_POS="57696951" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="55805762" STOP_POS="56731690" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="54474344" STOP_POS="55409526" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="54226315" STOP_POS="55151544" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="53976781" STOP_POS="54902331" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00744</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 induced 29 base pair deletion in exon 1</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11081153</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(DIO--iRFP)9Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=748&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=748&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2019-02-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00748</CITATION_ID>
    <DESCRIPTION>The transgene contains Cre recombinase reporter rat expressing the red fluorescent protein gene (iRFP) driven by the EF1 alpha promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11081177</RGD_ID>
    <STRAIN_SYMBOL>F344&lt;i&gt;&lt;sup&gt;tl&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>toothless (tl)</FULL_NAME>
    <ORIGINATION>University of Massachusetts Medical School.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=749&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>skeletal and osteoclast biology</RESEARCH_USE>
    <ALLELES>Csf1&lt;sup&gt;tl&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910954</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="198065400" STOP_POS="198084774" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="195396104" STOP_POS="195396105" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="210550359" STOP_POS="210550360" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="229989430" STOP_POS="230017945" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="203292765" STOP_POS="203307968" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00749</CITATION_ID>
    <DESCRIPTION>A spontaneous tooth less mutation was maintained in inbred Fisher colony maintained at the University of Massachusetts Medical School. The homozygous mutant is a 10-bp insertion near the beginning of the open reading of the Csf1 gene that yields a truncated, nonfunctional protein and an early stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11084925</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CD59-HBA1)Bryd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=754&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=754&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE>intravascular hemolysis and related sequelae of anemia, hemoglobinemia, and hemoglobinuria</RESEARCH_USE>
    <ALLELES>CD59</ALLELES>
    <ALLELE_RGD_IDS>736600</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00754</CITATION_ID>
    <DESCRIPTION>Transgene: human CD59 gene (cDNA) under control of alpha-globin regulatory elements (alpha-globin promoter and alpha hemoglobin locus control region). Upon administration of intermedilysin (ILY), cells expressing human CD59 will be selectively ablated</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11084928</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Jund&lt;sup&gt;em1Tja&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Genetics &amp; Molecular Medicine, University of Edinburgh</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=755&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE>leukemia, breast cancer</RESEARCH_USE>
    <ALLELES>Jund&lt;sup&gt;em1Tja&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11084926</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="18768093" STOP_POS="18769771" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="18734121" STOP_POS="18735799" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="20486368" STOP_POS="20486368" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="20342096" STOP_POS="20343775" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="19239694" STOP_POS="19241529" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00755</CITATION_ID>
    <DESCRIPTION>The mutation was generated using zinc finger nuclease technology. The mutation involves insertion of one extra C at position 16:20486368 in the intronless JunD gene (Rat (Rnor_6.0)Ensembl) resulting in a null mutation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11084931</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(RIP7-RLuc-YFP)Vpoit</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=757&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=757&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00757</CITATION_ID>
    <DESCRIPTION>Transgene: RIP7-RLuc-YFP. This transgene expresses a renilla luciferase-YFP fusion protein under control of the rat insulin 2 gene promoter (RIP7).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11087549</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(GFAP-TK)Hcam</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=764&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=764&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>neurogenesis</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00764</CITATION_ID>
    <DESCRIPTION>random insertion of human GFAP promoter driving herpes simples virus thymidine kinase</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11087551</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Il15&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Kansas Medical Center</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=769&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il15|Il15&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2887|12910491</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="42536160" STOP_POS="42611349" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="25696013" STOP_POS="25696019" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="23553406" STOP_POS="23553412" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="34532033" STOP_POS="34598725" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="27487268" STOP_POS="27498973" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00769</CITATION_ID>
    <DESCRIPTION>Zinc finger nuclease mediated 7bp deletion within exon 2 of the Il15 gene, resulting in a frameshift and premature stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11087553</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Mmp12&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=770&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=770&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2017-08-10)</AVAILABILITY>
    <RESEARCH_USE>allergy and lung responses and blood coagulation</RESEARCH_USE>
    <ALLELES>Mmp12|Mmp12&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>620195|12910500</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="12866652" STOP_POS="12876554" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="4582695" STOP_POS="4583358" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="5607502" STOP_POS="5608165" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="5610392" STOP_POS="5620294" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="4249938" STOP_POS="4259675" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00770</CITATION_ID>
    <DESCRIPTION>TALEN mediated 664 bp deletion that includes exon 2 of the Mmp12 gene, resulting in a frameshift and premature stop codon</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11354901</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco110-D9Mco124&lt;/i&gt;)/Bj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="88698037" STOP_POS="91114199" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="95162214" STOP_POS="97679852" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="94881322" STOP_POS="97361568" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="86987972" STOP_POS="89709209" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11354901</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Rat7-D9Rat84&lt;/i&gt;)/Mco to SS/Jr and the F1 were intercrossed to produce an F2 population,which was genotyped using microsatellite markers.  The selected recombinant rats were crossed to SS/Jr again to duplicate the recombinant region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11354903</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco110-D9Mco121&lt;/i&gt;)/Bj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="88698037" STOP_POS="90976105" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="95162214" STOP_POS="97532584" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="94881322" STOP_POS="97223353" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="86987972" STOP_POS="89541777" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11354903</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Rat7-D9Rat84&lt;/i&gt;)/Mco to SS/Jr and the F1 were intercrossed to produce an F2 population,which was genotyped using microsatellite markers.  The selected recombinant rats were crossed to SS/Jr again to duplicate the recombinant region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11354924</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco113-D9Mco124&lt;/i&gt;)/Bj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="91113977" STOP_POS="91114199" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="95430880" STOP_POS="97679852" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="95118069" STOP_POS="97361568" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="87225627" STOP_POS="89709209" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11354924</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Rat7-D9Rat84&lt;/i&gt;)/Mco to SS/Jr and the F1 were intercrossed to produce an F2 population,which was genotyped using microsatellite markers.  The selected recombinant rats were crossed to SS/Jr again to duplicate the recombinant region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11354926</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco110-D9Got111&lt;/i&gt;)/Bj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="88698037" STOP_POS="90720113" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="95162214" STOP_POS="97276310" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="94881322" STOP_POS="96967940" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="86987972" STOP_POS="89249893" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11354926</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Rat7-D9Rat84&lt;/i&gt;)/Mco to SS/Jr and the F1 were intercrossed to produce an F2 population,which was genotyped using microsatellite markers.  The selected recombinant rats were crossed to SS/Jr again to duplicate the recombinant region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11354928</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco110-D9Mco114&lt;/i&gt;)/Bj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="88698037" STOP_POS="88698287" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="95162214" STOP_POS="95162463" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="94881322" STOP_POS="95143906" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="86987972" STOP_POS="87252238" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11354928</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Rat7-D9Rat84&lt;/i&gt;)/Mco to SS/Jr and the F1 were intercrossed to produce an F2 population,which was genotyped using microsatellite markers.  The selected recombinant rats were crossed to SS/Jr again to duplicate the recombinant region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11354930</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D9Mco115-D9Mco124&lt;/i&gt;)/Bj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="89541728" STOP_POS="91114199" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="96024146" STOP_POS="97679852" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="95727999" STOP_POS="97361568" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="89708990" STOP_POS="89709209" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11354930</CITATION_ID>
    <DESCRIPTION>This is a congenic substrain developed by crossing SS.SHR-(&lt;i&gt;D9Rat7-D9Rat84&lt;/i&gt;)/Mco to SS/Jr and the F1 were intercrossed to produce an F2 population,which was genotyped using microsatellite markers.  The selected recombinant rats were crossed to SS/Jr again to duplicate the recombinant region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11528524</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Slc17a6-icre)3Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2019-02-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11528524</CITATION_ID>
    <DESCRIPTION>The BAC-based transgene contains Cre recombinase is expressed from rat Slc17a6 promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11528588</RGD_ID>
    <STRAIN_SYMBOL>SHR.LEW-(&lt;i&gt;D4Rat76-D4Mgh11&lt;/i&gt;)/Anra</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratorio de Genetica do Comportamento, Departamento de Biologia Celular, Embriologia e Genetica, Centro de Ciencias Biologicas, Universidade Federal de Santa Catarina, Florianopolis, Santa Catarina, Brazil</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="86583980" STOP_POS="168870974" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="85253748" STOP_POS="167139601" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="86312589" STOP_POS="168047091" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="150964994" STOP_POS="230565226" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="84886545" STOP_POS="171204531" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11528588</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a LEW chromosome 4 segment containing a QTL affecting anxiety-related response transferred to the SHR background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11530008</RGD_ID>
    <STRAIN_SYMBOL>CDS.CDR-(D4Rat9-D4Rat153)/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory for Molecular Medicine and
Israeli Rat Genome Center
Barzilai University Med Ctr Campus
2 Hahistadrut St
Ashkelon 78278, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="27862204" STOP_POS="27862366" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="26907285" STOP_POS="26907447" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="23991721" STOP_POS="23991882" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="23916923" STOP_POS="23917084" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="23537363" STOP_POS="23537525" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11530008</CITATION_ID>
    <DESCRIPTION>This CDS congenic containing genomic elements from CDR was created by crossing the consomic strain CDS-Chr 4CDR/Ygl(RGD:4889499) with CDS.  The congenic carries QTL affecting diabeties initation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11530011</RGD_ID>
    <STRAIN_SYMBOL>CDS.SBN-(D13Rat85-D13Mit4)/Ygl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory for Molecular Medicine and
Israeli Rat Genome Center
Barzilai University Med Ctr Campus
2 Hahistadrut St
Ashkelon 78278, Israel</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="71610804" STOP_POS="89333251" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="69060519" STOP_POS="86800898" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="74568378" STOP_POS="92916783" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="79488981" STOP_POS="97381801" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="72141292" STOP_POS="90551272" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11530011</CITATION_ID>
    <DESCRIPTION>This CDS congenic containing the genomic element from  SBN/Ygl was created by crossing the SBN/Ygl with CDS.  The congenic carries QTL affecting diabeties development.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11530028</RGD_ID>
    <STRAIN_SYMBOL>iNP-&lt;i&gt;Npy&lt;sup&gt;em6Sage&lt;/sup&gt;&lt;/i&gt;/Iusm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Gastroenterology, Indiana University School of Medicine, Indianapolis, IN 46202, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Npy&lt;sup&gt;em6Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11530022</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="80212111" STOP_POS="80219310" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="78881294" STOP_POS="78888495" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="79557856" STOP_POS="79565059" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="144233753" STOP_POS="144240956" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="78038013" STOP_POS="78045187" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11530028</CITATION_ID>
    <DESCRIPTION>These ZFN mutant rats were produced by injecting zinc finger nuclease targeting rat Npy into iNP/Iusm embryos. A 26-bp deletion, including 6 bp in intron 1 and 20 bp in exon 2  in rat Npy was created in the mutant founders.   These mutant founders were backcrossed with iNP/Iusm to produce heterozygous offspring, which were then intercrossed to produce homozygous and heterozygous offspring.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11531089</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;F8&lt;sup&gt;em1Sage+/-&lt;/sup&gt;&lt;/i&gt;/Novo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Novo Nordisk, Maaloev, Denmark</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>F8&lt;i&gt;&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>11531096</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="155237" STOP_POS="187186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="140848" STOP_POS="172330" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="367862" STOP_POS="399242" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="413447" STOP_POS="444491" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="121134" STOP_POS="162008" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11531089</CITATION_ID>
    <DESCRIPTION>The heterozygous ZFN mutant rats were produced by backcrossing mutant founders (SD/Novo-&lt;i&gt;F8&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;) with Sprague Dawley. Genotyping of the offspring was carried out by PCR amplification of the deletion fragment which caused a premature translation stop.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11531091</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;F8&lt;sup&gt;em1Sage-/-&lt;/sup&gt;&lt;/i&gt;/Novo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Novo Nordisk, Maaloev, Denmark</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>F8&lt;i&gt;&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>11531096</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="155237" STOP_POS="187186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="140848" STOP_POS="172330" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="367862" STOP_POS="399242" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="413447" STOP_POS="444491" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="121134" STOP_POS="162008" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11531091</CITATION_ID>
    <DESCRIPTION>The homozygous F8 mutant rats were produced by intercrossing the heterozygous ZFN mutants (SD-&lt;i&gt;F8&lt;sup&gt;em1Sage+/-&lt;/sup&gt;&lt;/i&gt;/Novo)   to produce homozygous and heterozygous offspring. Genotype of the homozygous  offspring was confirmed by PCR amplification of the deletion fragment which caused a premature translation stop.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11531094</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;F8&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;/Novo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Novo Nordisk, Maaloev, Denmark</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>F8&lt;i&gt;&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>11531096</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="155237" STOP_POS="187186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="140848" STOP_POS="172330" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="367862" STOP_POS="399242" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="413447" STOP_POS="444491" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="121134" STOP_POS="162008" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11531094</CITATION_ID>
    <DESCRIPTION>These ZFN mutant rats were produced by injecting zinc finger nuclease targeting rat F8 into Sprague Dawley embryos. A premature translation stop in rat F8 was created in the mutant founders carrying a 13-bp deletion in exon 16.   These mutant founders were backcrossed with Sprague Dawley to produce heterozygous offspring, which were then intercrossed to produce homozygous and heterozygous offspring.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11531104</RGD_ID>
    <STRAIN_SYMBOL>iNP-&lt;i&gt;Npy&lt;sup&gt;em6Sage+/-&lt;/sup&gt;&lt;/i&gt;/Iusm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Gastroenterology, Indiana University School of Medicine, Indianapolis, IN 46202, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Npy&lt;sup&gt;em6Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11530022</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="80212111" STOP_POS="80219310" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="78881294" STOP_POS="78888495" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="79557856" STOP_POS="79565059" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="144233753" STOP_POS="144240956" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="78038013" STOP_POS="78045187" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11531104</CITATION_ID>
    <DESCRIPTION>The heterozygous ZFN mutant rats were produced by backcrossing mutant founders  with iNP/Iusm. Genotyping of the offspring was carried out by PCR amplification of a 26-bp deleted fragment, including 6 bp in intron 1 and 20 bp in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11531106</RGD_ID>
    <STRAIN_SYMBOL>iNP-&lt;i&gt;Npy&lt;sup&gt;em6Sage-/-&lt;/sup&gt;&lt;/i&gt;/Iusm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Gastroenterology, Indiana University School of Medicine, Indianapolis, IN 46202, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Npy&lt;sup&gt;em6Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11530022</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="80212111" STOP_POS="80219310" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="78881294" STOP_POS="78888495" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="79557856" STOP_POS="79565059" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="144233753" STOP_POS="144240956" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="78038013" STOP_POS="78045187" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11531106</CITATION_ID>
    <DESCRIPTION>The homozygous Npy mutant rats were produced by intercrossing the heterozygous ZFN mutants (iNP-&lt;i&gt;Npy&lt;sup&gt;em6Sage+/- &lt;/sup&gt;&lt;/i&gt;/Iusm)   to produce homozygous and heterozygous offspring. Genotype of the homozygous offspring was confirmed by PCR amplification of a 26-bp deleted fragment, including
6 bp in intron 1 and 20 bp in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11532753</RGD_ID>
    <STRAIN_SYMBOL>F344.ZUC-(&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt;),OLETF-(&lt;i&gt;D5Rat166-D5Rat90&lt;/i&gt;)/Tj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=390&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=390&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11532753</CITATION_ID>
    <DESCRIPTION>The F344.ZUC,OLETF double congenic was produced by crossing F344.ZUC-&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt; with F344.OLETF-(&lt;i&gt; D5Rat166-D5Rat90&lt;/i&gt;) and then selecting Lepr&lt;sup&gt;fa&lt;/sup&gt; -Niddm24 (fa/fa-Nidd6/of)  homozygotes</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11535000</RGD_ID>
    <STRAIN_SYMBOL>PKD/Mhm</STRAIN_SYMBOL>
    <FULL_NAME>PKD</FULL_NAME>
    <ORIGINATION>Medical Research Centre, Klinikum Mannheim, University of Heidelberg, Mannheim, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2016-11-29)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Anks6&lt;sup&gt;PKD&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11534996</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11535000</CITATION_ID>
    <DESCRIPTION>The colony of inbred PKD/Mhm rats was established in the laboratory in Mannheim after 18 additional generations of inbreeding of the Han:SPRD (cy/+).The mutation was  a C to T transition that replaces an arginine by a tryptophan at amino acid 823 in the protein sequence.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11535031</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(hCMV-Anks6&lt;sup&gt;PKD&lt;/sup&gt;)Mhm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical Research Centre, Klinikum Mannheim, University of Heidelberg, Mannheim, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2016-11-29)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Anks6&lt;sup&gt;PKD&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11534996</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11535031</CITATION_ID>
    <DESCRIPTION>This transgenic strain was derived by pronuclear microinjection of fertilized Sprague Dawley oocytes with a 2.8-kb mutated Anks6&lt;sup&gt;PKD&lt;/sup&gt; cloned between a human cytomegalovirus promoter  upstream and an intron as well as a polyadenylation signal of SV40 downstream.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11535955</RGD_ID>
    <STRAIN_SYMBOL>Crlj:CD(SD)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11535955</CITATION_ID>
    <DESCRIPTION>A colony of outbred CD(SD) (RGD: 734476) maintained in the Charles River Laboratories Japan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553848</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Trpv4&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpv4&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553847</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="47599161" STOP_POS="47638143" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="41938533" STOP_POS="41977517" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="47698915" STOP_POS="47737902" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="49492064" STOP_POS="49529956" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="43226933" STOP_POS="43265889" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553848</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  Trpv4 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is a 5-bp deletion in Exon 4 of the Trpv4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553850</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Trpv4&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpv4&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553851</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="47599161" STOP_POS="47638143" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="41938533" STOP_POS="41977517" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="47698915" STOP_POS="47737902" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="49492064" STOP_POS="49529956" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="43226933" STOP_POS="43265889" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553850</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  Trpv4 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is a 4-bp deletion in Exon 4 of the Trpv4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553852</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Vnn1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Vnn1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553853</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="23356324" STOP_POS="23366629" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="21537084" STOP_POS="21547395" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="22614832" STOP_POS="22625134" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="24089365" STOP_POS="24099667" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="22087290" STOP_POS="22097592" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553852</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system and ssODN was used to introduce a N131S mutation in the Vnn1 gene of SS/HsdMcwiCrl rat embryos</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553855</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Vnn1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Vnn1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553856</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="23356324" STOP_POS="23366629" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="21537084" STOP_POS="21547395" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="22621640" STOP_POS="22621646" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="24089365" STOP_POS="24099667" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="22087290" STOP_POS="22097592" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553855</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 7-bp deletion mutation in the  Vnn1 gene of  SS/HsdMcwiCrl rat embryos</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553858</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rbm20&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rbm20&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553857</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="262671311" STOP_POS="262912551" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="252836316" STOP_POS="252836436" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="274391932" STOP_POS="274589816" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="281783646" STOP_POS="282003053" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="259905545" STOP_POS="260144190" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553858</CITATION_ID>
    <DESCRIPTION>ZFN system was used to introduce a mutation in the Rbm20 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 121-bp deletion in Exon 2 of the Rbm20 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553860</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Scn5a&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Scn5a&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553859</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="128098613" STOP_POS="128196515" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="119288929" STOP_POS="119289038" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="128169191" STOP_POS="128266681" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="127375781" STOP_POS="127471879" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="124446479" STOP_POS="124545301" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553860</CITATION_ID>
    <DESCRIPTION>ZFN system was used to introduce a mutation in the Scn5a gene of DA/MolTac rat embryos. The resulting mutation is a 110-bp deletion in Exon 4 of the Scn5a gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553862</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Shc1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Shc1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553854</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="177135649" STOP_POS="177147257" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="174837937" STOP_POS="174849538" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="188745503" STOP_POS="188757066" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="208159786" STOP_POS="208171348" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="181616581" STOP_POS="181628144" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553862</CITATION_ID>
    <DESCRIPTION>ZFN system was used to introduce a mutation in the Shc1 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 14-bp deletion in Exon 2 of the Shc1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553873</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Fmr1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Generated with support from the Simons Foundation Autism Research Initiative (&lt;a href=https://www.sfari.org/resource/rat-models/&gt;SFARI&lt;/a&gt;); MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/autism-rat-model-resource/ &gt; Autism Rat Model Resource&lt;/a&gt;,  Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE>Autism, ADHD, Developmental delay, Intellectual disability, Epilepsy (from &lt;a href=https://gene.sfari.org/database/human-gene/FMR1&gt;SFARI GENE&lt;/a&gt;)</RESEARCH_USE>
    <ALLELES>Fmr1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553872</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="152284857" STOP_POS="152322686" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="147240239" STOP_POS="147278057" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="154703634" STOP_POS="154703635" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="154756031" STOP_POS="154793782" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553873</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  Fmr1 gene of  Crl:LE rat embryos. The resulting mutation is a 2-bp insertion in exon 8 of the Fmr1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553875</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Fmr1&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fmr1&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553874</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="152284857" STOP_POS="152322686" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="147240239" STOP_POS="147278057" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="154703634" STOP_POS="154703635" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="154756031" STOP_POS="154793782" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553875</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  Fmr1 gene of  Crl:LE rat embryos. The resulting mutation is a 2-bp deletion in exon 8 of the Fmr1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553877</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;P2rx1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-07-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>P2rx1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553876</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="58117107" STOP_POS="58132167" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="57626708" STOP_POS="57626731" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="59566268" STOP_POS="59581328" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="59305737" STOP_POS="59320797" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="59889933" STOP_POS="59904985" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553877</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  P2rx1 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is a 24-bp deletion in Exon 1 of the P2rx1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553881</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rbm20&lt;sup&gt;em10Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rbm20&lt;sup&gt;em10Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553880</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="262671311" STOP_POS="262912551" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="252836430" STOP_POS="252836442" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="274391932" STOP_POS="274589816" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="281783646" STOP_POS="282003053" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="259905545" STOP_POS="260144190" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553881</CITATION_ID>
    <DESCRIPTION>ZFN system was used to introduce a mutation in the  Rbm20 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp deletion in Exon 2 of the Rbm20 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553883</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rbm20&lt;sup&gt;em8Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rbm20&lt;sup&gt;em8Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553882</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="262671311" STOP_POS="262912551" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="252836431" STOP_POS="252836488" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="274391932" STOP_POS="274589816" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="281783646" STOP_POS="282003053" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="259905545" STOP_POS="260144190" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553883</CITATION_ID>
    <DESCRIPTION>ZFN system was used to introduce a mutation in the  Rbm20 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is a 58-bp deletion in Exon 2 of the Rbm20 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553886</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Tp53&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tp53&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553885</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="54798871" STOP_POS="54810300" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="54300070" STOP_POS="54311525" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="56186299" STOP_POS="56198449" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="55932658" STOP_POS="55944087" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="56399721" STOP_POS="56411150" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553886</CITATION_ID>
    <DESCRIPTION>ZFN system was used to introduce a mutation in the  Trp53 gene of  Crl:SD rat embryos.The resulting mutation is a 84-bp deletion in Exon 3 of the Tp53 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553889</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Trpc3&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2018-10-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpc3&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553887</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="121409436" STOP_POS="121487095" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="119481313" STOP_POS="119619333" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="123329954" STOP_POS="123467574" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="142945309" STOP_POS="143022844" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="123117180" STOP_POS="123184016" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553889</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  Trpc3 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is a 25-bp deletion in Exon 2 of the Trpc3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553892</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Trpc3&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpc3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553891</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="121409436" STOP_POS="121487095" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="119481313" STOP_POS="119619333" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="123329954" STOP_POS="123467574" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="142945309" STOP_POS="143022844" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="123117180" STOP_POS="123184016" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553892</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  Trpc3 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is a 1-bp insertion in Exon 2 of the Trpc3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553894</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tpcn2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tpcn2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553893</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="209845827" STOP_POS="209875561" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="200416538" STOP_POS="200446252" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="218419182" STOP_POS="218448902" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="225286480" STOP_POS="225316685" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="205702971" STOP_POS="205732664" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553894</CITATION_ID>
    <DESCRIPTION>ZFN system was used to introduce a mutation in the Tpcn2 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 9-bp deletion in Exon 4 of theTpcn2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553896</RGD_ID>
    <STRAIN_SYMBOL>SHRSP-&lt;i&gt;Spp1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Spp1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553895</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="5613569" STOP_POS="5620695" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="5312021" STOP_POS="5312025" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="6673686" STOP_POS="6679965" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="6653086" STOP_POS="6658937" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553896</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Spp1 gene of SHRSP/A3NCrl rat embryos. The resulting mutation is a 5-bp deletion in Exon 3 of the Spp1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553899</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Trpv2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpv2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553898</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="47772223" STOP_POS="47797956" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="47265524" STOP_POS="47294263" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="48903540" STOP_POS="48925036" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="48686500" STOP_POS="48707996" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="48764894" STOP_POS="48786150" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553899</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  Trpv2 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is a 17-bp deletion in Exon 4 of the Trpv2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553902</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Trpc6&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpc6&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553901</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="14044216" STOP_POS="14148808" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="5759387" STOP_POS="5864000" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="6811543" STOP_POS="6917534" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="6799564" STOP_POS="6904623" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="5472515" STOP_POS="5577537" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553902</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  Trpc6 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is a 18-bp deletion in Exon 2 of the Trpc6 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553904</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Shc1&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Shc1&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553903</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="177135649" STOP_POS="177147257" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="174837937" STOP_POS="174849538" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="188745503" STOP_POS="188757066" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="208159786" STOP_POS="208171348" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="181616581" STOP_POS="181628144" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553904</CITATION_ID>
    <DESCRIPTION>ZFN system was used to introduce a mutation in the Shc1 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 27-bp deletion in Exon 1 of the Shc1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553908</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Trpc6&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpc6&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553907</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="14044216" STOP_POS="14148808" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="5759387" STOP_POS="5864000" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="6811543" STOP_POS="6917534" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="6799564" STOP_POS="6904623" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="5472515" STOP_POS="5577537" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553908</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  Trpc6 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is a 3-bp substitutions to generate P112Q in Exon 2 of the Trpc6 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553912</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Trpc6&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpc6&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553911</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="14044216" STOP_POS="14148808" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="5759387" STOP_POS="5864000" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="6811543" STOP_POS="6917534" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="6799564" STOP_POS="6904623" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="5472515" STOP_POS="5577537" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553912</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  Trpc6 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is a 2-bp insertion in Exon 2 of the Trpc6 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553914</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Shc1&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Shc1&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553913</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="177135649" STOP_POS="177147257" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="174837937" STOP_POS="174849538" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="188745503" STOP_POS="188757066" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="208159786" STOP_POS="208171348" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="181616581" STOP_POS="181628144" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553914</CITATION_ID>
    <DESCRIPTION>ZFN system was used to introduce a mutation in the Shc1 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 13-bp deletion in Exon 2 of theShc1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11553916</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Shc1&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-01-25)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Shc1&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11553915</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="177135649" STOP_POS="177147257" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="174837937" STOP_POS="174849538" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="188745503" STOP_POS="188757066" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="208159786" STOP_POS="208171348" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="181616581" STOP_POS="181628144" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11553916</CITATION_ID>
    <DESCRIPTION>ZFN system was used to introduce a T&gt;G transversion mutation in the Shc1 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a  substitution to generate S36A in Exon 2 of theShc1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11554327</RGD_ID>
    <STRAIN_SYMBOL>BDIX.BDIV-&lt;i&gt;D10Mit3-D10Mgh16&lt;/i&gt;/Zte</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cell Biology (Cancer Research) of Duisburg-Essen University Medical School, Essen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2016-10-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11554327</CITATION_ID>
    <DESCRIPTION>The BDIX.BDIV-&lt;i&gt;D10Mit3-D10Mgh16&lt;/i&gt;/Zte congenic strain was produced by crossing BDIX (tumor-susceptible) and BDIV (tumor resistant) and then selecting for strains carrying homozygous segments of the BDIV chromosome on a BDIX background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11554329</RGD_ID>
    <STRAIN_SYMBOL>BDIX.BDIV-&lt;i&gt;D10Got1-D10Rat45&lt;/i&gt;/Zte</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cell Biology (Cancer Research) of Duisburg-Essen University Medical School, Essen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2016-10-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="4765527" STOP_POS="19816042" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="4835638" STOP_POS="20170031" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="3662335" STOP_POS="20046466" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="4697541" STOP_POS="20233281" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11554329</CITATION_ID>
    <DESCRIPTION>The BDIX.BDIV-&lt;i&gt;D10Got1-D10Rat45&lt;/i&gt;/Zte congenic strain was produced by crossing BDIX (tumor-susceptible) and BDIV (tumor resistant) and then selecting for strains carrying homozygous segments of the BDIV chromosome on a BDIX background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11556280</RGD_ID>
    <STRAIN_SYMBOL>ACI.Cg-&lt;i&gt;Du&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1252&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1252&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-10)</AVAILABILITY>
    <RESEARCH_USE>Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11556280</CITATION_ID>
    <DESCRIPTION>Downunder (Du) mutation is introduced into ACI/Kyo strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11556282</RGD_ID>
    <STRAIN_SYMBOL>WKY-Tg(UBC-sb10)3Wmukf</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1170&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1170&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11556282</CITATION_ID>
    <DESCRIPTION>This strtain has transgene that express SleepingBeauty transposase under human Ubiquitin-C promoter. (insertion site of trans gene: unknown)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11561897</RGD_ID>
    <STRAIN_SYMBOL>Crl:WI-&lt;i&gt;Lrap&lt;sup&gt;em1Geh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Colorado</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>behavior, addiction</RESEARCH_USE>
    <ALLELES>Lrap&lt;sup&gt;em1Geh&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11561896</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="33562482" STOP_POS="33574339" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="39016258" STOP_POS="39017876" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="40910874" STOP_POS="40918231" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11561897</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 genome editing system was used to generate this knockout mutant rat strain. It created a 618-bp deletion in rat Lrap gene. The recipient zygotes were  the Wistar rats from Charles River.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11561902</RGD_ID>
    <STRAIN_SYMBOL>WKY-Tg(UBC-pb)5Wmukf</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1170&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1170&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11561902</CITATION_ID>
    <DESCRIPTION>This strtain has transgene that expresses piggyBac transposase under human Ubiquitin-C promoter. (insertion site of trans gene: unknown)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11561905</RGD_ID>
    <STRAIN_SYMBOL>WKY-Tg(Gabrb1&lt;sup&gt;Tn(pb-Bhr2)1Wmukf&lt;/sup&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1172&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1172&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gabrb1|Gabrb1&lt;sup&gt;Tn(pb-Bhr2)1Wmukf&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>2649|11561925</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="36434339" STOP_POS="36917920" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="36068725" STOP_POS="36548946" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="38631192" STOP_POS="39112598" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="38453142" STOP_POS="38924073" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="38530259" STOP_POS="39005615" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11561905</CITATION_ID>
    <DESCRIPTION>Transposed "Bhr2" was inserted into intron 4 of Gabrb1 gene by piggyBac (pb) transposon system.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11561909</RGD_ID>
    <STRAIN_SYMBOL>WKY-Tg(Samt4&lt;sup&gt;Tn(pb-Bhr7)1Wmukf&lt;/sup&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1170&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1170&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2016-11-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Samt4&lt;sup&gt;Tn(pb-Bhr7)1Wmukf&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11561928</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11561909</CITATION_ID>
    <DESCRIPTION>Transposed "Bhr7" was inserted into the first Met-coding exon region of rat Samt4 gene by  piggyBac (pb) transposon system.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11561970</RGD_ID>
    <STRAIN_SYMBOL>WKY-Tg(Zbtb20&lt;sup&gt;Tn(pb-Bhr7)1Wmukf&lt;/sup&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1170&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1170&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Zbtb20&lt;sup&gt;Tn(pb-Bhr7)1Wmukf&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11561972</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11561970</CITATION_ID>
    <DESCRIPTION>Transposed "Bhr7" was inserted into the Intron 3 of Zbtb20 gene by piggyBac (pb) transposon system.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11561976</RGD_ID>
    <STRAIN_SYMBOL>WKY-Tg(Plcb1&lt;sup&gt;Tn(pb-Bhr2)1Wmukf&lt;/sup&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1170&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1170&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Plcb1&lt;sup&gt;Tn(pb-Bhr2)1Wmukf&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11561974</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11561976</CITATION_ID>
    <DESCRIPTION>Transposed "Bhr2" was inserted into into Plcb1 gene by piggyBac (pb) transposon system.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11561979</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg((ROSA)26Sor-CAG-tdTomato)9Jfhy</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1139 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1139 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2016-11-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11561979</CITATION_ID>
    <DESCRIPTION>Background strain: Long-Evans (Institute for Animal Reproduction); pRSET-B tdTomato is provided by Dr. Roger Tsien(UCSD); Transgene: CAG promoter (CMV virus, chicken), tdTomato(Discosoma sp.); BAC clone: mouse ROSA26 BAC (RP23-244D9)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11564343</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg((ROSA)26Sor-CAG-tdTomato)14Jfhy</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1139 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1139 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2016-11-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11564343</CITATION_ID>
    <DESCRIPTION>Background strain: Long-Evans (Institute for Animal Reproduction); pRSET-B tdTomato is provided by Dr. Roger Tsien (UCSD); Transgene: CAG promoter (CMV virus, chicken), tdTomato (Discosoma sp.); BAC clone: mouse ROSA26 BAC (RP23-244D9)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11564346</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Aspa&lt;sup&gt;em31Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1099&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1099&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Aspa&lt;sup&gt;em31Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11564344</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="58390204" STOP_POS="58443790" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="57891704" STOP_POS="57945267" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="59839693" STOP_POS="59888244" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="59578788" STOP_POS="59627450" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="60178509" STOP_POS="60199207" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11564346</CITATION_ID>
    <DESCRIPTION>The TALEN genome editing system was used to generate this mutant rat strain.  The TALEN system caused a 14-bp deletion in the exon4 of Aspa gene, as a result created a premature stop codon in the gene. Decreased expression levels of Aspa gene and ASPA protein was observed. Histopatologically, this strain shows vacuole formation in the brain and spinal cord.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11564349</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Aspa&lt;sup&gt;em34Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1099&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1099&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Aspa&lt;sup&gt;em34Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11564348</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="58433303" STOP_POS="58433318" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="57934804" STOP_POS="57934819" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="59882494" STOP_POS="59882509" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="59578788" STOP_POS="59627450" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="60178509" STOP_POS="60199207" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11564349</CITATION_ID>
    <DESCRIPTION>The TALEN genome editing system was used to generate this mutant rat strain.  The TALEN system caused a 16-bp deletion in the exon4 of Aspa gene, as a result created a premature stop codon in the gene. Decreased expression levels of Aspa gene and ASPA protein was observed. Histopatologically, this strain shows vacuole formation in the brain and spinal cord.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11564350</RGD_ID>
    <STRAIN_SYMBOL>SCR/Sscr</STRAIN_SYMBOL>
    <FULL_NAME>Shumiya Cataract Rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2016-11-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fdft1|Lss</ALLELES>
    <ALLELE_RGD_IDS>61834|620955</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11564350</CITATION_ID>
    <DESCRIPTION>Genetic Cataract rat SCR&amp;#65288;Shumiya Cataract Rat&amp;#65289;was segrigated from a SHR-fa strain colony that developed nuclear cataract at adult stage. This strain is a double mutant caused by recessive gene (ctr1) and dominant lethal gene (Ctr2l) and established by Dr. Shumiya at Tokyo Metropolitan Institute of Gerontology. In 2003, this strain was introduced to Kyoritsu College of Pharmacy (keio University Faculty of Pharmacy). ctr1 is lanosterol synthase (Lss) and Ctr2 is farnesyl diphosphate farnesyl transferase 1 (Fdft1).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11565091</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ccdc85c&lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=27 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=27 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ccdc85c&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11565090</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="132877851" STOP_POS="132948744" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="127113440" STOP_POS="127184328" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="132113806" STOP_POS="132183434" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="141284186" STOP_POS="141353658" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="132572485" STOP_POS="132641431" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11565091</CITATION_ID>
    <DESCRIPTION>TALEN targeting the exon1 of rat Ccdc85c gene was designed and mRNA coding these TALEN was microinjected into F344/Stm embyo. Rats developed hydrocephalus and Subcortical heterotopia. Homozygous rats die within 1 month of hydrocephalus.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11565094</RGD_ID>
    <STRAIN_SYMBOL>F344.LEC-(&lt;i&gt;D4Nirs8-D4Nirs2&lt;/i&gt;)/Nrs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=592&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=592&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11565094</CITATION_ID>
    <DESCRIPTION>This strain was established by crossing F344.LEC-xhs1/1Nrs (NBR-rat #0293)(RGD:2304293) with F344/NSlc (RGD:1302627). The radiation sensitivity level of this strain is similar to F344.LEC-xhs1/1Nrs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11565097</RGD_ID>
    <STRAIN_SYMBOL>F344.LEC-(&lt;i&gt;D4Rat54-D4Got87&lt;/i&gt;)/Nrs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=592&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=592&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11565097</CITATION_ID>
    <DESCRIPTION>This strain was established by crossing F344.LEC-xhs1/1Nrs (NBRrat NO: 0293)(RGD:2304293) with F344/NSlc (RGD:1302627). The radiation sensitivity level of this strain is different from F344.LEC-xhs1/1Nrs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11565100</RGD_ID>
    <STRAIN_SYMBOL>NMC/Nrs</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=592&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=592&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11565100</CITATION_ID>
    <DESCRIPTION>This strain was found in a colony of F344.LEC-xhs1/1Nrs (NBRP Rat No: 0293). As to radiosensitivity gene, D4Nirs8-D4Rat45 region is LEC type. Affected females with dominant gene on Chr10 develop mammary gland cancer after pregnancy (histological type is undetermined). In many cases, this neoplastis lesion resolve spontaneously after delivery. No homozygous female is obtained at this time. Affected male rats don't show any phenotype.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11565116</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Chat-tdTomato)3Yyan</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1236 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1236 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11565116</CITATION_ID>
    <DESCRIPTION>Chat-tdToamto-polyA-FRT sequence was inserted into fertilized egg of Long Evans strain (Japan SLC). vector: BAC clone (RP23-246B12) from a C57BL/6J mouse genomic BAC library (BACPAC Resource Center, Oakland, CA, USA)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11565122</RGD_ID>
    <STRAIN_SYMBOL>SHR.Cg-&lt;i&gt;Lepr&lt;sup&gt;cp&lt;/sup&gt;&lt;/i&gt;-Tg(APOB)110/Dmcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1139 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1139 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2016-11-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;cp&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11570565</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11565122</CITATION_ID>
    <DESCRIPTION>A BAC clone (CTD-2257F14) containing whole human APOB gene was maicroinjected into fertilized eggs of Wistar rats (Takeda Pharmaceutical Company). Then this Tg rats were backcrossed 9 times with SHR/NDmcr-cp rats (NBRP No.0446, SHR.Cg-Leprcp/NDmcr)(RGD:  2306033)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11565125</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D18Rat87-D18Got66&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=865&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=865&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="65415948" STOP_POS="65416174" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="63140870" STOP_POS="77629361" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="65366908" STOP_POS="81115720" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="64552961" STOP_POS="80162163" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="66217583" STOP_POS="80805774" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11565125</CITATION_ID>
    <DESCRIPTION>A congenic strain made by introducing a segments of chromosome 18 from SHR/Izm into SHRSP/Izm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11565128</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D18Rat73-D18Rat52&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=865&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=865&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="52198059" STOP_POS="60806448" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="49999958" STOP_POS="58536311" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="51609032" STOP_POS="60532087" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="50804228" STOP_POS="59735418" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="52290789" STOP_POS="61290878" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11565128</CITATION_ID>
    <DESCRIPTION>A congenic strain made by introducing a segments of chromosome 18 from SHR/Izm into SHRSP/Izm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11565130</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D1Rat23-D1Rat213&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=863&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=863&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-21)</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="88098993" STOP_POS="90905414" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78970983" STOP_POS="81777720" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="80231217" STOP_POS="83282814" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="81497710" STOP_POS="84537228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78685103" STOP_POS="81548909" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11565130</CITATION_ID>
    <DESCRIPTION>A congenic strain made by introducing a segments of chromosome 1 from SHR/Izm into SHRSP/Izm</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11565132</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D1Rat95-D1Got87&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=863&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=863&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2016-11-21)</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="77152098" STOP_POS="77152283" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="68123229" STOP_POS="86030749" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="71706292" STOP_POS="91156803" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="73096563" STOP_POS="92291485" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="66832211" STOP_POS="85828306" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11565132</CITATION_ID>
    <DESCRIPTION>A congenic strain made by introducing a segments of chromosome 1 from SHR/Izm into SHRSP/Izm</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11565135</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;D1Rat25-St8sia2&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=863&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=863&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2016-11-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>St8sia2</ALLELES>
    <ALLELE_RGD_IDS>621843</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="81776081" STOP_POS="137247796" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="72703913" STOP_POS="127838017" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="66845268" STOP_POS="135406699" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="67633807" STOP_POS="136423629" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="72231246" STOP_POS="129191810" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11565135</CITATION_ID>
    <DESCRIPTION>A congenic strain established by introducing segments of chromosome 1 from SHRSP/Izm into WKY/Izm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11565826</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ttn&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>SAGE Laboratories</ORIGINATION>
    <SOURCE>Duke-National University of Singapore, Singapore</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2016-11-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ttn&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11565825</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="82059648" STOP_POS="82332130" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="61652432" STOP_POS="61924912" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="63565160" STOP_POS="63837815" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="70138896" STOP_POS="70408647" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="59404023" STOP_POS="59665308" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11565826</CITATION_ID>
    <DESCRIPTION>These ZFN mutant rats were produced by injecting zinc finger nuclease targeting rat Ttn into F344 embryos. The zinc-finger nuclease mediated genome editing system created a 12-bp deletion and a 2-bp insertion (TA) at 228,608-228,619 (Rnor_5.0) to introduce a stop codon in exon 303, corresponding to exon 327 in the human sequence.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11565829</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Ttn&lt;sup&gt;em2Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>SAGE laboratories</ORIGINATION>
    <SOURCE>Duke-National University of Singapore, Singapore</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2016-11-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ttn&lt;sup&gt;em2Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11565827</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="82059648" STOP_POS="82332130" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="61652432" STOP_POS="61924912" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="63565160" STOP_POS="63837815" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="70138896" STOP_POS="70408647" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="59404023" STOP_POS="59665308" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11565829</CITATION_ID>
    <DESCRIPTION>These ZFN mutant rats were produced by injecting zinc finger nuclease targeting rat Ttn into F344 embryos. The zinc-finger nuclease mediated genome editing system created a deletion of exons 2-6 (5,286-bp deletion, coordinates 2,323-7,608) to introduce a frameshift (Rnor_5.0).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11567272</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Mecp2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.horizondiscovery.com/mecp2-knockout-rat-tgra6090&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.horizondiscovery.com/mecp2-knockout-rat-tgra6090&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2016-12-13)</AVAILABILITY>
    <RESEARCH_USE>Autism, Rett syndrome, Cognition</RESEARCH_USE>
    <ALLELES>Mecp2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11568035</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="156932481" STOP_POS="156995981" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="151781177" STOP_POS="151844687" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="156650389" STOP_POS="156713813" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="152390961" STOP_POS="152461647" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="159980599" STOP_POS="160035260" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11567272</CITATION_ID>
    <DESCRIPTION>The ZFN mutant rat strain was produced by injecting zinc finger nuclease targeting rat Mecp2 into Sprague Dawley embryos. This mutant rat has a knockout of the methyl CpG binding protein 2 (Mecp2).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11568040</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Fmr1&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.horizondiscovery.com/fmr1-knockout-rat-tgrs5390&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.horizondiscovery.com/fmr1-knockout-rat-tgrs5390&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-09)</AVAILABILITY>
    <RESEARCH_USE>Autism, Fragile X syndrome</RESEARCH_USE>
    <ALLELES>Fmr1&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11568041</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="152284857" STOP_POS="152322686" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="147258833" STOP_POS="147258954" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="154703661" STOP_POS="154703782" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="154756031" STOP_POS="154793782" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11568040</CITATION_ID>
    <DESCRIPTION>The ZFN mutant rat strain was produced by injecting zinc finger nuclease targeting rat Fmr1 into Sprague Dawley embryos. The resulting mutation was a 122bp deletion of the intron 7/exon8 junction occurred at 18533bp-18654bp. This mutant rat has a knockout of Fmr1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11568058</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nrxn1&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.horizondiscovery.com/neurexin1-nrxn1-knockout-rat-tgra6160&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.horizondiscovery.com/neurexin1-nrxn1-knockout-rat-tgra6160&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2018-03-22)</AVAILABILITY>
    <RESEARCH_USE>Autism, Schizophrenia</RESEARCH_USE>
    <ALLELES>Nrxn1&lt;sup&gt;em1&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11568059</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="8931360" STOP_POS="10077381" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="3177788" STOP_POS="4323848" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="13886757" STOP_POS="15191660" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="23843153" STOP_POS="25145167" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="14050929" STOP_POS="15354069" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11568058</CITATION_ID>
    <DESCRIPTION>The ZFN mutant rat strain was produced by injecting zinc finger nuclease targeting rat Nrxn1 into Sprague Dawley embryos. This mutant rat has a 16-bp deletion in exon1 resulting in knockout of Nrxn1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11568062</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Pten&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.horizondiscovery.com/pten-knockout-rat-tgrs5810&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.horizondiscovery.com/pten-knockout-rat-tgrs5810&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2016-12-13)</AVAILABILITY>
    <RESEARCH_USE>Autism, cancer</RESEARCH_USE>
    <ALLELES>Pten&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11568063</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="240043707" STOP_POS="240110330" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="230630443" STOP_POS="230697070" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="251421814" STOP_POS="251487634" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="258651829" STOP_POS="258717009" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="236771027" STOP_POS="236837261" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11568062</CITATION_ID>
    <DESCRIPTION>The ZFN mutant rat strain was produced by injecting zinc finger nuclease targeting rat Pten into Sprague Dawley embryos. This mutant rat has a 7-bp deletion in exon7 resulting in knockout of Pten.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11568067</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Grm5&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.horizondiscovery.com/mglur5-knockout-rat-tgra6020&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.horizondiscovery.com/mglur5-knockout-rat-tgra6020&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2016-12-13)</AVAILABILITY>
    <RESEARCH_USE>Autism,  Fragile X syndrome,  Cognition, Schizophrenia,  Anxiety,  Pain</RESEARCH_USE>
    <ALLELES>Grm5&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11568068</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150722711" STOP_POS="151297585" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="141310069" STOP_POS="141884980" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="151207846" STOP_POS="151785038" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157517676" STOP_POS="158096869" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143857225" STOP_POS="144477419" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11568067</CITATION_ID>
    <DESCRIPTION>The ZFN mutant rat strain was produced by injecting zinc finger nuclease targeting rat Grm5 into Sprague Dawley embryos. The resulting mutation was a knockout of Grm5 demonstrated by western blot.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11568071</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Met&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.horizondiscovery.com/met-knockout-rat-tgrs8750&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.horizondiscovery.com/met-knockout-rat-tgrs8750&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2016-12-07)</AVAILABILITY>
    <RESEARCH_USE>Autism Spectrum Disorders, Synaptic Plasticity, Autoimmune disorders</RESEARCH_USE>
    <ALLELES>Met&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11568072</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="46756823" STOP_POS="46864041" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="45790456" STOP_POS="45898139" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="44747467" STOP_POS="44854628" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="45354290" STOP_POS="45461638" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="43134183" STOP_POS="43211355" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11568071</CITATION_ID>
    <DESCRIPTION>The ZFN mutant rat strain was produced by injecting zinc finger nuclease targeting rat Met into Sprague Dawley embryos. The resulting mutation was a  a-17 base pair deletion in exon 8 of Met.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11568646</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cntnap2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.horizondiscovery.com/cntnap2-knockout-rat-tgrs8820&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.horizondiscovery.com/cntnap2-knockout-rat-tgrs8820&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-05)</AVAILABILITY>
    <RESEARCH_USE>Autism Spectrum Disorders, Synaptic Plasticity, Language disorders</RESEARCH_USE>
    <ALLELES>Cntnap2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11568647</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="75109358" STOP_POS="77366258" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="74109455" STOP_POS="76366434" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="74700539" STOP_POS="77025463" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="140006078" STOP_POS="141697964" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="74277978" STOP_POS="75440178" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11568646</CITATION_ID>
    <DESCRIPTION>The ZFN mutant rat strain was produced by injecting zinc finger nuclease targeting rat Met into Sprague Dawley embryos. The resulting mutation was a  5-bp deletion in exon 6 of Cntnap2. Homozygous knockout rats exhibit complete loss of target protein as demonstrated by Western blot.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11568700</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nlgn3&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.horizondiscovery.com/neuroligin-3-nlgn3-knockout-rat-tgrs6650&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.horizondiscovery.com/neuroligin-3-nlgn3-knockout-rat-tgrs6650&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2016-12-13)</AVAILABILITY>
    <RESEARCH_USE>Autism, Asperger's syndrome, Synaptic plasticity</RESEARCH_USE>
    <ALLELES>Nlgn3&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11568701</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70469251" STOP_POS="70497380" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66439348" STOP_POS="66439405" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71209388" STOP_POS="71209445" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72051846" STOP_POS="72075119" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89376193" STOP_POS="89398665" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11568700</CITATION_ID>
    <DESCRIPTION>The ZFN mutant rat strain was produced by injecting zinc finger nuclease targeting rat Nlgn3 into Sprague Dawley embryos.  Homozygous knockout rats exhibit complete loss of target protein as demonstrated by Western blot.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11568703</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cacna1c&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.horizondiscovery.com/cacna1c-knockout-rat-tgra6930&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.horizondiscovery.com/cacna1c-knockout-rat-tgra6930&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2016-12-13)</AVAILABILITY>
    <RESEARCH_USE>Autism, Timothy syndrome, Long QT syndrome, Schizophrenia,Bipolar disorder</RESEARCH_USE>
    <ALLELES>Cacna1c&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11568704</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="153431169" STOP_POS="154051932" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="151764138" STOP_POS="152379454" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="150635808" STOP_POS="151270790" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="216562477" STOP_POS="217184927" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="154895691" STOP_POS="155517389" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_11568703</CITATION_ID>
    <DESCRIPTION>The ZFN mutant rat strain was produced by injecting zinc finger nuclease targeting rat Nlgn3 into Sprague Dawley embryos. This model contains 4-bp deletion at  460,649 to 460,652 bp in genomic sequence resulting in an early stop codon in exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11667072</RGD_ID>
    <STRAIN_SYMBOL>Sway/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=538&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=538&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00538</CITATION_ID>
    <DESCRIPTION>This phenotype arose spontaneously during the third generation of selective breeding for decreased intravenous drug self-administration in Wistar rats (see RGD:6482259). After 10 weeks of age no drug administration is needed to see phenotype in which animals exhibits motor abnormalities with degenerative changes in cerebellar Purkinje cells. It appears to be transmitted in an autosomal recessive pattern. Animals have an abnormal swaying gait, which is readily identified as a slow (2 to 3 cycles per second) tremor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11667077</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Esr2&lt;sup&gt;em2Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=719&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=719&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE>reproduction, neu7roscience, environmental healthg, cardiovascular</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00719</CITATION_ID>
    <DESCRIPTION>Zinc finger nuclease targeting of exon 3 of the rat estrogen receptor-2 gene resulting in the deletion of exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11667079</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Pgr&lt;sup&gt;em2Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=720&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=720&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE>Reproduction, neuroscience, environmental health, cardiovascular</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00720</CITATION_ID>
    <DESCRIPTION>zinc finger nucleases were used to generate a 136 bp deletion within the first exon of the progesterone receptor, resulting in a frameshift, premature stop codon, and a null.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11667081</RGD_ID>
    <STRAIN_SYMBOL>BDIV-&lt;i&gt;Myo5a&lt;/i&gt;/StcRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=784&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=784&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Myo5a&lt;sup&gt;m1Stc&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>42721971</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00784</CITATION_ID>
    <DESCRIPTION>Point mutation in Myo5a (Chromosome 8, end of exon 4)identified in In Berlin-Druckrey (BDIV) shaker rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11667084</RGD_ID>
    <STRAIN_SYMBOL>W&lt;sup&gt;Cat&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Wistar Cataract Rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=704&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=704&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00704</CITATION_ID>
    <DESCRIPTION>ENU induced total juvenile cataract in inbred Wistar.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11667088</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Esr1&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=701&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=701&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE>A range of experimentation examining the actions of estrogen in reproduction, cancer, cardiovascular, and neurobiology.</RESEARCH_USE>
    <ALLELES>Esr1&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910736</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="43511685" STOP_POS="43904454" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="41272347" STOP_POS="41272828" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="41358808" STOP_POS="41359289" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="42534049" STOP_POS="42935434" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="35523680" STOP_POS="35759891" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00701</CITATION_ID>
    <DESCRIPTION>zinc finger nucleases were used to generate a 482 bp deletion in Esr1 gene, resulting in a knock out.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11667094</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(CFH)Crl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=705&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=705&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00705</CITATION_ID>
    <DESCRIPTION>micro-injected with a ~6 kb transgenic cassette, which contained a CMV enhancer, chicken beta-actin promoter, the full-length cDNA encoding human complement factor H, and a rabbit beta-globin poly(A) sequence that had been isolated and purified from plasmid pCAGGS-human fH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>11667096</RGD_ID>
    <STRAIN_SYMBOL>WIST-&lt;i&gt;Tulane&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Tulane rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=721&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=721&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00721</CITATION_ID>
    <DESCRIPTION>Male Wistar rats with inbred congenital unilateral right hydronephrosis were bred from the colony described in 1979 by Friedman et al.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12437069</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat25-rs198199323&lt;/i&gt;)-&lt;i&gt;Btg2&lt;sup&gt;em21Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Btg2&lt;sup&gt;em21Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12798564</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="48083931" STOP_POS="48087690" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45535534" STOP_POS="45535535" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50913185" STOP_POS="50916944" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55966299" STOP_POS="55970058" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="47026986" STOP_POS="47030745" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12437069</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Btg2 gene of SS.BN-(&lt;i&gt;D13Rat25-rs198199323&lt;/i&gt;)/Mcwi rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12437071</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat25-rs198199323&lt;/i&gt;)-&lt;i&gt;Btg2&lt;sup&gt;em24Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Btg2&lt;sup&gt;em24Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12798565</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="48083931" STOP_POS="48087690" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45535534" STOP_POS="45535535" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50913185" STOP_POS="50916944" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55966299" STOP_POS="55970058" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="47026986" STOP_POS="47030745" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12437071</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 2-bp insertion in the exon 1  in the Btg2 gene of SS.BN-(&lt;i&gt;D13Rat25-rs198199323&lt;/i&gt;)/Mcwi rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12738212</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(LRRK2*R1441C)268Rwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=775&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=775&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-08-22)</AVAILABILITY>
    <RESEARCH_USE>Parkinson's Disease</RESEARCH_USE>
    <ALLELES>LRRK2</ALLELES>
    <ALLELE_RGD_IDS>1353141</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00775</CITATION_ID>
    <DESCRIPTION>These rats were created using BAC constructs consisting of the entire 144kb human LRRK2 locus containing the R1441C mutation and fused to a YPet reporter tag.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12738218</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;GEPR-9&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=304&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=304&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-01-30)</AVAILABILITY>
    <RESEARCH_USE>seizure</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00304</CITATION_ID>
    <DESCRIPTION>Genetically Epilepsy-Prone Rats (GEPR-9) have severe levels of seizure predisposition. This colony was bred to exhibit clonic convulsions (severe seizures with an ARS of 9) following a single wild running phase in response to sound. Seizures model human generalized tonic/clonic seizures.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12738365</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Rag2&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rag2&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12738366</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108357399" STOP_POS="108367186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87907941" STOP_POS="87907942" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91191837" STOP_POS="91200134" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97851318" STOP_POS="97859615" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86764810" STOP_POS="86773438" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12738365</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALENs targeting the sequence  into Crl:SD rat embryos. The resulting mutation is a 10-bp frameshift deletion,Atgttgagat, in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12738372</RGD_ID>
    <STRAIN_SYMBOL>BDIX.BDIV-&lt;i&gt;D6Mit1-D6Mgh2&lt;/i&gt;/Zte</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cell Biology (Cancer Research) of Duisburg-Essen University Medical School, Essen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12738372</CITATION_ID>
    <DESCRIPTION>The BDIX.BDIV-&lt;i&gt;D6Mit1-D6Mgh2&lt;/i&gt;/Zte congenic strain was produced by crossing BDIX (tumor-susceptible) and BDIV (tumor resistant) and then selecting for strains carrying homozygous segments of the BDIV chromosome on a BDIX background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12738388</RGD_ID>
    <STRAIN_SYMBOL>BDIX.BDIV-&lt;i&gt;D6Rat132-D6Mgh3&lt;/i&gt;/Zte</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cell Biology (Cancer Research) of Duisburg-Essen University Medical School, Essen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12738388</CITATION_ID>
    <DESCRIPTION>The BDIX.BDIV-&lt;i&gt;D6Rat132-D6Mgh3&lt;/i&gt;/Zte congenic strain was produced by crossing BDIX (tumor-susceptible) and BDIV (tumor resistant) and then selecting for strains carrying homozygous segments of the BDIV chromosome on a BDIX background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12738394</RGD_ID>
    <STRAIN_SYMBOL>BDIX.BDIV-&lt;i&gt;D6Mit8-D6Rat229&lt;/i&gt;/Zte</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cell Biology (Cancer Research) of Duisburg-Essen University Medical School, Essen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12738394</CITATION_ID>
    <DESCRIPTION>The BDIX.BDIV-&lt;i&gt;D6Mit8-D6Rat229&lt;/i&gt;/Zte congenic strain was produced by crossing BDIX (tumor-susceptible) and BDIV (tumor resistant) and then selecting for strains carrying homozygous segments of the BDIV chromosome on a BDIX background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12738452</RGD_ID>
    <STRAIN_SYMBOL>ACI.F344-&lt;i&gt;Apc&lt;sup&gt;Pirc&lt;/i&gt;Uwm&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin-Madison, Madison, Wisconsin</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=718&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Apc&lt;sup&gt;Pirc&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>1554322</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="26190901" STOP_POS="26190901" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="25916744" STOP_POS="25916744" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="27100213" STOP_POS="27100213" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="26725560" STOP_POS="26820837" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="26732147" STOP_POS="26790383" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00718</CITATION_ID>
    <DESCRIPTION>This strain develops twice the number of colonic tumors as the F344-ApcPircUwm rats (RGD:1641862).  Stop codon mutation at amino acid 1137 of the Apc gene. Nucleotide chr18:26,785,272 (Baylor 3.4/rn4) A to T transversion.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12738455</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;I&gt;D10Got155-D10Nsi55&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Feinstein Institute for Medical Research. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=674&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="102825374" STOP_POS="102825912" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="100299840" STOP_POS="100300011" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="103609431" STOP_POS="103609601" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="104692565" STOP_POS="104692735" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="105131088" STOP_POS="105131258" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00674</CITATION_ID>
    <DESCRIPTION>The Cia5a10 (D10Got155-D10Nsi55) interval was introgressed from F344 into DA/BklArb rats through 8 backcrosses into DA/BklArb rats followed by 7 additional backcrosses into DA/BklArbNsi rats. Heterozygous DA.F344(Cia5a10) rats were brother-sister mated, and the recombinant strain was maintained in the homozygous state thereafter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12738457</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;I&gt;D10Got152-D10Mcw1&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Feinstein Institute for Medical Research. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=675&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="97730563" STOP_POS="105813458" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="101211245" STOP_POS="109712946" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="100889652" STOP_POS="109306076" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="102307572" STOP_POS="109926395" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00675</CITATION_ID>
    <DESCRIPTION>DA/BklArb rats through 8 backcrosses into DA/BklArb rats followed by 7 additional backcrosses into DA/BklArbNsi rats. Heterozygous DA.F344(Cia5a5)(D10Got152-D10Mcw1) rats were brother-sister mated, and the recombinant strain was maintained in the homozygous state thereafter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12738460</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-(&lt;I&gt;D7Rat15-D7Mit2&lt;/I&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Feinstein Institute for Medical Research. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=681&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="101772987" STOP_POS="116294546" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="111043360" STOP_POS="126080454" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="110975825" STOP_POS="125794357" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="107428268" STOP_POS="123191874" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00681</CITATION_ID>
    <DESCRIPTION>The Cia4d (D7Rat15 -D7Mit2) interval was introgressed from F344 into DA/BklArb rats through 7 backcrosses into DA/BklArb rats followed by 3 additional backcrosses into DA/BklArbNsi rats. Heterozygous DA.F344(Cia4d) rats were brother-sister mated, and the recombinant strain was maintained in the homozygous state thereafter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12738466</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Asip&lt;sup&gt;m1&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=542&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=542&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-02-06)</AVAILABILITY>
    <RESEARCH_USE>This strain can be used to generate pigmented embryos for use with albino ES cell lines.</RESEARCH_USE>
    <ALLELES>Asip&lt;sup&gt;m1&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12738467</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="163933768" STOP_POS="164021377" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="143473584" STOP_POS="143561170" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="150492010" STOP_POS="150579870" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="156860395" STOP_POS="156949277" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="145445175" STOP_POS="145536831" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00542</CITATION_ID>
    <DESCRIPTION>Developed by Beth Bauer, University of Missouri. Spontaneous mutation of agouti gene with resultant black coat color from Sprague Dawley (SD) X Dark Agouti (DA).  Albino mutation and hooded mutation have been bred out of this line so that only the agouti mutation remains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12743611</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ren&lt;sup&gt;em1Mcwi+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Ren&lt;sup&gt;em1Mcwi+&lt;/sup&gt;/Ren&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ren&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139863</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="47348312" STOP_POS="47359539" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="44803412" STOP_POS="44803421" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50502724" STOP_POS="50513953" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55555583" STOP_POS="55566812" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="46262936" STOP_POS="46275213" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12743611</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12743623</RGD_ID>
    <STRAIN_SYMBOL>BN.F344-&lt;i&gt;Apc&lt;sup&gt;Pirc&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=783&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=783&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Apc&lt;sup&gt;Pirc&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>1554322</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="26190901" STOP_POS="26190901" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="25916744" STOP_POS="25916744" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="27100213" STOP_POS="27100213" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="26725560" STOP_POS="26820837" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="26732147" STOP_POS="26790383" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00783</CITATION_ID>
    <DESCRIPTION>The phenotype of the BN.F344-&lt;i&gt;Apc&lt;sup&gt;Pirc&lt;/i&gt;&lt;/sup&gt; congenic shows high resistance to cancer. The heterozygous animals get spontaneous intestinal lesions (small intestinal and colonic)starting at 60 days of age in males. BN animals are highly resistant to tumor development and can live over 2 years.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12743627</RGD_ID>
    <STRAIN_SYMBOL>cNLH-&lt;i&gt;Cat&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>congenital NLH Cataract Rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=702&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=702&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00702</CITATION_ID>
    <DESCRIPTION>inbreeding since 2003, juvenile total cataract developed in cNLH line. cNLH = congenital non-learned helpless. congenital non-learned helpless and congenital learned helpless (cLH)lines were developed from outbred Dpargue-Dawley from Charles River.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12743630</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Spib&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>spitzenborduere (spib)</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=703&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=703&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00703</CITATION_ID>
    <DESCRIPTION>Retinae display marked rosett formation in the outer nuclear layer; in the funduscopy irregular, dark pigment flecks are observed, which cannot be identified in the histology. Linkage analysis indicating at least two genes interacting.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12743640</RGD_ID>
    <STRAIN_SYMBOL>DA.E3-(&lt;i&gt;RT1-DMa-Ggnbp1&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=715&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=715&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>RT1-DMa|Ggnbp1</ALLELES>
    <ALLELE_RGD_IDS>735053|1359729</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="4708932" STOP_POS="5118034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="4707028" STOP_POS="5116185" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="3935512" STOP_POS="5625320" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="7302036" STOP_POS="7690734" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="4843458" STOP_POS="5271653" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00715</CITATION_ID>
    <DESCRIPTION>The Tcs1 QTL in DA.E3-(&lt;i&gt;RT1-DMa-Ggnbp1&lt;/i&gt;)(DA.1IR85) contains a ~0.5 Mb (min- max 0.43 - 0.63 Mb) insert from DA.1I (RGD:10002743, DA.E3-(D20Rat42-D20Rat49)/Rhd). The inserted fragment spans the MHC-I region but excludes most of the MHC-II region, inclduing the RT1-B and RT1-D genes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12743645</RGD_ID>
    <STRAIN_SYMBOL>DA.KHW-(&lt;i&gt;RT1-Db1-RT1-DMb&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=712&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=712&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>RT1-DMb|RT1-Db1</ALLELES>
    <ALLELE_RGD_IDS>735096|1593282</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="4550594" STOP_POS="4702560" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="4548664" STOP_POS="4700340" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="3945383" STOP_POS="4097190" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="6167759" STOP_POS="7295355" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="4671489" STOP_POS="4836772" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00712</CITATION_ID>
    <DESCRIPTION>The Tcs2 QTL in DA.KHW-(RT1-Db1-RT1-DMb)(DA.1HR10) contains a ~0.2 from DA.1H [DA.KHW-RT1h]. The insert spans 12 genes in the MHC-II region, including RT1-B and RT1-D. All genes in the insert have been sequenced and sequences are available at GenBank.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12743647</RGD_ID>
    <STRAIN_SYMBOL>DA.E3-(&lt;i&gt;Btnl2-RT1-DMb&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=713&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=713&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Btnl2|RT1-DMb</ALLELES>
    <ALLELE_RGD_IDS>620731|735096</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="4492100" STOP_POS="4702560" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="4490169" STOP_POS="4700340" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="3945383" STOP_POS="4156365" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="6221727" STOP_POS="7295355" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="4613726" STOP_POS="4836772" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00713</CITATION_ID>
    <DESCRIPTION>The Tcs2 QTL in DA.E3-(Btnl2-RT1-DMb)(DA.1UR10) contains a ~0.2 Mb fromDA.E3-(D20Rat47-AA858870)/Rhd (RGD:10002745). The insert spans 12 genes in the MHC-II region, including RT1-B and RT1-D. All genes in the insert have been sequenced and sequences are available from GenBank. The genomic sequences of DA/OlaHsd and E3 have been completed and will be available soon (Backdahl et al. BMC Genomics 2014)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12743650</RGD_ID>
    <STRAIN_SYMBOL>DA.AS2-(&lt;i&gt;Tesb-RT1-DMb&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=714&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=714&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>RT1-DMb|Tsbp1</ALLELES>
    <ALLELE_RGD_IDS>735096|1597063</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="4411926" STOP_POS="4702560" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="4410002" STOP_POS="4700340" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="3945383" STOP_POS="4235947" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="6258025" STOP_POS="7295355" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="4532358" STOP_POS="4836772" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12743650</CITATION_ID>
    <DESCRIPTION>DA.F-(Tesb-RT1-DMb) (DA.1FR61) contains a ~0.4 Mb (min- max 0.25 - 0.53 Mb) insert from DA.1F (RGD:2307301). The insert spans 12-19 genes in the MHC-II/MHC-III regions, including RT1-B and RT1-D. The 12 genes in the MHC-II region have been sequenced and sequences are available from GenBank.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12743652</RGD_ID>
    <STRAIN_SYMBOL>DA.KHW-(&lt;i&gt;RT1-DMa-Mln&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=716&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=716&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>RT1-DMa|Mln</ALLELES>
    <ALLELE_RGD_IDS>735053|1642907</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="4708932" STOP_POS="5310825" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="4707028" STOP_POS="5308948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="3935512" STOP_POS="6571791" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="7302036" STOP_POS="8814591" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="4843458" STOP_POS="5451752" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00716</CITATION_ID>
    <DESCRIPTION>The Tcs1 QTL in DA.KHW-(RT1-DMa-Mln)(DA.1HR83) contains a ~~0.85 Mb (min - max: 0.61 - 1.08 Mb) insert from DA.1H [DA.KHW-RT1h]. The inserted fragment spans the MHC-I region but excludes most of the MHC-II region, including the RT1-B and RT1-D genes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12743655</RGD_ID>
    <STRAIN_SYMBOL>DA.E3-(&lt;i&gt;RT1-DMa-Mln&lt;/i&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=717&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=717&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00717</CITATION_ID>
    <DESCRIPTION>The Tcs1 QTL in DA.E3-(RT1-DMa-Mln)(DA.1UR83) contains a ~0.85 Mb (min - max: 0.61 - 1.08 Mb) insert from DA.1U (RGD:10002745). The inserted fragment spans the MHC-I region but excludes most of the MHC-II region, including the RT1-B and RT1-D genes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790593</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;Gtf2ird1-D12Rat8&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Shore-Long Island Jewish Research Institute,350 Community Drive - Manhasset, NY 11030.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=672&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-16)</AVAILABILITY>
    <RESEARCH_USE>arthritis/autoimmunity studies</RESEARCH_USE>
    <ALLELES>Gtf2ird1</ALLELES>
    <ALLELE_RGD_IDS>620856</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="27890594" STOP_POS="28416002" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="22254113" STOP_POS="22779600" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="25264052" STOP_POS="25799259" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="27273535" STOP_POS="27805720" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="23319373" STOP_POS="23934871" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00672</CITATION_ID>
    <DESCRIPTION>The strain contains the Cia25 R11 recombinant interval  introgressed from ACI into DA/Hsd rats through 13 backcrosses. Heterozygous DA.ACI-(Chr12:27462118-Chr12:27611814) [also known as DA.ACI(Cia25) R11] rats were brother-sister mated, and the recombinant strain was maintained in the homozygous state thereafter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790595</RGD_ID>
    <STRAIN_SYMBOL>DA.ACI-(&lt;i&gt;D12Mit2-Gtf2i&lt;/i&gt;)/Nsi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Shore-Long Island Jewish Research Institute,350 Community Drive - Manhasset, NY 11030.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=673&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-16)</AVAILABILITY>
    <RESEARCH_USE>arthritis/autoimmunity studies</RESEARCH_USE>
    <ALLELES>Gtf2i</ALLELES>
    <ALLELE_RGD_IDS>727961</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="28037344" STOP_POS="28112677" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="19610870" STOP_POS="22476243" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="22650702" STOP_POS="25487970" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="24662983" STOP_POS="27497928" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="20932559" STOP_POS="23545621" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00673</CITATION_ID>
    <DESCRIPTION>The strain contains the Cia25 R12 recombinant interval  introgressed from ACI into DA/Hsd rats through 13 backcrosses. Heterozygous DA.ACI-(D12Got43-Chr12:27368751)/Nsi  [also known as DA.ACI(Cia25) R12] rats were brother-sister mated, and the recombinant strain was maintained in the homozygous state thereafter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790599</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Asic3&lt;sup&gt;em6Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Asic3&lt;sup&gt;em6Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790597</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="11652946" STOP_POS="11657415" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="10760509" STOP_POS="10764987" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="7292776" STOP_POS="7292836" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="7300219" STOP_POS="7304265" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="6125614" STOP_POS="6129660" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790599</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Asic3 gene of WKY/Ncrlrat embryos. The resulting mutation is a 61-bp deletion in the exon 1 of the Asic3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790602</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Axl&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Axl&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790600</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="90392864" STOP_POS="90424123" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="81265088" STOP_POS="81296278" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="82579723" STOP_POS="82579753" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="83812118" STOP_POS="83840542" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="80964751" STOP_POS="80994300" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790602</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Axl gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 31-bp deletion in the exon 2 of the Axl gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790604</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Axl&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Axl&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790605</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="90392864" STOP_POS="90424123" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="81265088" STOP_POS="81296278" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="82579711" STOP_POS="82579742" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="83812118" STOP_POS="83840542" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="80964751" STOP_POS="80994300" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790604</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Axl gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 32-bp deletion in the exon 2 of the Axl gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790608</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cd14&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd14&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790606</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="28609558" STOP_POS="28611409" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="28335522" STOP_POS="28337383" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="29561584" STOP_POS="29561585" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="29265328" STOP_POS="29267236" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="29374593" STOP_POS="29376190" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790608</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to introduce a 2-bp deletion in exon 2 of the Cd14 gene of SS/JrHsdMcwi rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790610</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cd14&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd14&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790611</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="28609558" STOP_POS="28611409" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="28335522" STOP_POS="28337383" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="29561568" STOP_POS="29561607" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="29265328" STOP_POS="29267236" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="29374593" STOP_POS="29376190" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790610</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Cd14 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a net 7-bp deletion of the Cd14 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790615</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Chrna4&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryorecovery (as of 2017-02-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Chrna4&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790616</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="188506802" STOP_POS="188535558" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="168136246" STOP_POS="168157839" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="176533182" STOP_POS="176547965" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="180256391" STOP_POS="180256406" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="170171214" STOP_POS="170185998" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790615</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Chrna4 gene of LEW/Crl rat embryos. The resulting mutation is a 4-bp deletion in the Chrna4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790621</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cybb&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cybb&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790620</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="16030596" STOP_POS="16065065" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="13358101" STOP_POS="13392570" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="14581655" STOP_POS="14581696" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="15359405" STOP_POS="15391317" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="25514572" STOP_POS="25547181" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790621</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Cybb gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 42-bp deletion in the exon 3 of the Cybb gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790623</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cybb&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cybb&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790624</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="16030596" STOP_POS="16065065" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="13358101" STOP_POS="13392570" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="14581662" STOP_POS="14581696" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="15359405" STOP_POS="15391317" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="25514572" STOP_POS="25547181" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790623</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Cybb gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 35-bp deletion in the exon 3 of the Cybb gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790627</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Igh-6&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Igh-6&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790625</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="147233687" STOP_POS="147233694" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="143205627" STOP_POS="143206076" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790627</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Igh-6 gene of LEW/NCrl rat embryos. The resulting mutation is a 8-bp deletion in the exon 2 of the Igh-6 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790629</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Igh-6&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Igh-6&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790630</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="147233691" STOP_POS="147233692" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="143205627" STOP_POS="143206076" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790629</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Igh-6 gene of LEW/Ncrl rat embryos. The resulting mutation is a 2-bp deletion in the exon 2 of the Igh-6 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790632</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790633</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66398567" STOP_POS="66398585" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790632</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALENs targeting the sequence of Il2rg gene  into the SS/JrHsdMcwi rat embryos. The resulting mutation is a 19-bp deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790659</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Il2rg&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-20)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790660</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66395330" STOP_POS="66399026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790659</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALENs targeting the Il2rg gene into Crl:SD rat embryos. The resulting mutation is a 2-bp deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790662</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Mb&lt;sup&gt;em6Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mb&lt;sup&gt;em6Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790663</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="110640511" STOP_POS="110647742" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="108762068" STOP_POS="108762092" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="118101633" STOP_POS="118108864" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="118094391" STOP_POS="118101622" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="115087558" STOP_POS="115094789" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790662</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Mb gene of WKY/NCrl rat embryos. The resulting mutation is a 25-bp deletion in the exon 2 of the Mb gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790676</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;P2rx1&lt;sup&gt;em6Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2017-02-20)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>P2rx1&lt;sup&gt;em6Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790677</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="58117107" STOP_POS="58132167" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="57626714" STOP_POS="57626715" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="59566268" STOP_POS="59581328" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="59305737" STOP_POS="59320797" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="59889933" STOP_POS="59904985" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790676</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  P2rx1 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is a 2-bp deletion in Exon 2 of the P2rx1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790679</RGD_ID>
    <STRAIN_SYMBOL>PCK-&lt;i&gt;P2rx7&lt;sup&gt;em8Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pkhd1&lt;sup&gt;pck&lt;/sup&gt;|P2rx7&lt;sup&gt;em8Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11535943|12790680</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="30040466" STOP_POS="30533834" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="39550531" STOP_POS="39594984" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="33917661" STOP_POS="33917662" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="26164969" STOP_POS="26736704" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="39353613" STOP_POS="39396042" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="41242368" STOP_POS="41808755" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="25025958" STOP_POS="25593163" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="18833903" STOP_POS="19338716" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="35074025" STOP_POS="35117152" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790679</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  P2rx7 gene of  PCK/CrljCrl-Pkhd1pck/Crl rat embryos. The resulting mutation is a 1-bp insertion in Exon 2 of the P2rx7 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790692</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Pon1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pon1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790693</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="34261312" STOP_POS="34292327" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="33294737" STOP_POS="33325759" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="30249749" STOP_POS="30276297" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="30174202" STOP_POS="30174203" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="29936314" STOP_POS="29964821" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790692</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Pon1 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp insertion of exon 4 in the Pon1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790695</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Pon1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2017-02-20)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pon1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790696</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="34261312" STOP_POS="34292327" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="33294737" STOP_POS="33325759" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="30249749" STOP_POS="30276297" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="30156712" STOP_POS="30183204" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="29936314" STOP_POS="29964821" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790695</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Pon1 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 8-bp deletion of exon 5 in the Pon1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790698</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Pon1&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pon1&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790699</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="34261312" STOP_POS="34292327" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="33294737" STOP_POS="33325759" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="30249749" STOP_POS="30276297" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="30156712" STOP_POS="30183204" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="29936314" STOP_POS="29964821" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790698</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Pon1 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 1-bp insertion of exon 5 in the Pon1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790702</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Pon3&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pon3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790703</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="34323546" STOP_POS="34350244" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="33356983" STOP_POS="33383681" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="30311981" STOP_POS="30338679" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="30218888" STOP_POS="30245586" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="30000505" STOP_POS="30027203" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790702</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Pon3 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 16-bp deletion of exon 4 in the Pon1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790710</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Rag2&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rag2&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790711</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108357399" STOP_POS="108367186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87907936" STOP_POS="87907945" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91191837" STOP_POS="91200134" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97851318" STOP_POS="97859615" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86764810" STOP_POS="86773438" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790710</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALENs targeting the sequence into Crl:SD rat embryos. The resulting mutation is a 10-bp deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790713</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rag2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rag2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790714</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108357399" STOP_POS="108367186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87907936" STOP_POS="87907943" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91191837" STOP_POS="91200134" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97851318" STOP_POS="97859615" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86764810" STOP_POS="86773438" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790713</CITATION_ID>
    <DESCRIPTION>This strain was produced by targeting the Rag2 sequence  in SS/JrHsdMcwi rat embryos. The resulting mutation is a 8-bp  deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790717</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rfwd2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rfwd2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790718</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="73954058" STOP_POS="74095283" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="71467164" STOP_POS="71561826" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="76942883" STOP_POS="77076015" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="81940125" STOP_POS="81940125" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="74552876" STOP_POS="74590608" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790717</CITATION_ID>
    <DESCRIPTION>This strain was produced by targeting the Rfwd2 sequence  in SS/JrHsdMcwi rat embryos. The resulting mutation is a 6-bp  insertion  ( 7-bp insertion in the 1-bp deletion site) in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790721</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat151-D13Rat197)-Serpinc1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Serpinc1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790722</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="75790558" STOP_POS="75804826" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="73257208" STOP_POS="73271476" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="78806107" STOP_POS="78820375" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="83700761" STOP_POS="83715029" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="76548456" STOP_POS="76562724" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790721</CITATION_ID>
    <DESCRIPTION>ZFN system was used to introduce a mutation in the Serpinc1 gene of SS.BN-(D13Rat151-D13Rat197)/Mcwi rat embryos. The resulting mutation is a 29-bp deletion in Exon 1 of the Serpinc1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790944</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Sik2&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sik2&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790945</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="60121913" STOP_POS="60221707" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="51262007" STOP_POS="51262012" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="55309005" STOP_POS="55408608" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="53905730" STOP_POS="54005295" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="54240307" STOP_POS="54337976" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790944</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Sik2 gene of WKY/NCrl rat embryos. The resulting mutation is a 5-bp deletion in exon 4 of the Sik2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790947</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sorcs2&lt;sup&gt;em7Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sorcs2&lt;sup&gt;em7Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790948</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="78592290" STOP_POS="78960582" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="74711190" STOP_POS="74711222" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="79538911" STOP_POS="79912333" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="79176694" STOP_POS="79547823" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="79968072" STOP_POS="80344330" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790947</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence of Sorcs2 into SS/JrHsdMcwi rat embryos. The resulting mutation is a 33-bp frameshift deletion in exon 15.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790950</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sorcs2&lt;sup&gt;em9Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sorcs2&lt;sup&gt;em9Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790952</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="78592290" STOP_POS="78960582" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="74371089" STOP_POS="74735943" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="79538911" STOP_POS="79912333" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="79176694" STOP_POS="79547823" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="79968072" STOP_POS="80344330" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790950</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence of Sorcs2 into SS/JrHsdMcwi rat embryos. The resulting mutation is a 1-bp frameshift deletion in exon 15.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790954</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Tert&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-02-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tert&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790955</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="31465766" STOP_POS="31488650" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="29637213" STOP_POS="29659561" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="32250876" STOP_POS="32275330" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="33675744" STOP_POS="33697542" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="30445180" STOP_POS="30465942" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12790954</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Tert gene of WKY/NCrl rat embryos. The resulting mutation is a 17-bp deletion in Tert gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790957</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;DXrat11-rs64754598&lt;/i&gt;)/Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Boston University School of Medicine, Boston, Massachusetts</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=651&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-02-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="44930883" STOP_POS="97072383" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="41052407" STOP_POS="92767050" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="44320616" STOP_POS="100046443" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="44619917" STOP_POS="44620040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="62691290" STOP_POS="62691414" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00651</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing SS/JrHsd and SR/JrHsd parental strains. The SR chromosome X region from DXRat11 to rs64754598 was introgressed on the genetic background of SS.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790959</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;D1Rat68-rs65309623&lt;/i&gt;)/Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Boston University School of Medicine, Boston, Massachusetts</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=608&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="197807365" STOP_POS="209814568" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="188377360" STOP_POS="200385273" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="205603081" STOP_POS="218387917" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="212591076" STOP_POS="212591221" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="193069836" STOP_POS="193070197" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00608</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing SS/JrHsd and SR/JrHsd parental strains. The SR  chromosome 1 region from D1Rat68 to rs65309623 was introgressed on the genetic background of SS.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790962</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;rs106908358-rs105920659&lt;/i&gt;)/Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Boston University School of Medicine, Boston, Massachusetts</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=609&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="142708560" STOP_POS="143351823" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="133299232" STOP_POS="133942528" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="141088073" STOP_POS="141088073" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00609</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing SS/JrHsd and SR/JrHsd parental strains. The SR  chromosome 1 region from rs106908358 to rs105920659 was introgressed on the genetic background of  SS.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12790964</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;rs66001705-D5Mgh16&lt;/i&gt;)/Opaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Boston University School of Medicine, Boston, Massachusetts</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=614&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-02-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="155093859" STOP_POS="166600247" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="149810483" STOP_POS="161317411" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="155945375" STOP_POS="167946134" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="171522628" STOP_POS="171522762" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="168005953" STOP_POS="168006088" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00614</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing SS/JrHsd and SR/JrHsd parental strains. The SR  chromosome 5 region from rs66001705 to D5Mgh16 was introgressed on the genetic background of  SS.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792211</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc1048-D13Hmgc664&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="73112455" STOP_POS="73112582" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="74144915" STOP_POS="74145142" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="79688409" STOP_POS="79688633" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792211</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Got45-D13Hmgc664)/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792212</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc1048-D13Hmgc1045&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="73112455" STOP_POS="74785810" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="82670970" STOP_POS="82671156" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="75435508" STOP_POS="75435694" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792212</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Got45-D13Hmgc664)/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792213</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc1048-D13Hmgc1050&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="73112455" STOP_POS="73825867" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792213</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Got45-D13Hmgc664)/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792214</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc1041-D13Hmgc664&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="73996529" STOP_POS="73996673" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="74144915" STOP_POS="74145142" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="79688409" STOP_POS="79688633" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="81886999" STOP_POS="81887143" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="74586260" STOP_POS="74586404" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792214</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Got45-D13Hmgc664)/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792216</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc885-D13Hmgc664&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="72402940" STOP_POS="74145142" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="77913594" STOP_POS="79688633" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792216</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Got45-D13Hmgc664)/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792217</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc1041-D13Hmgc885&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="73996529" STOP_POS="73996673" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="72402940" STOP_POS="72403109" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="77913594" STOP_POS="77913762" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="81886999" STOP_POS="81887143" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="74586260" STOP_POS="74586404" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792217</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Got45-D13Hmgc664)/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792226</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Got45-D13Hmgc664&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="66706825" STOP_POS="74145142" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="72031440" STOP_POS="79688633" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="76974692" STOP_POS="76974960" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="69494047" STOP_POS="69494326" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792226</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat151-D13Rat197)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792939</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Got42-D13Rat61&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="65960801" STOP_POS="67721227" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="63410813" STOP_POS="65170683" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="68686589" STOP_POS="70445080" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="73648968" STOP_POS="75412480" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="66200668" STOP_POS="68034927" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792939</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat151-D13Rat197)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792944</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Got42-D13Got45&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="65960801" STOP_POS="65960952" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="63410813" STOP_POS="66707096" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="68686589" STOP_POS="72031708" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="73648968" STOP_POS="76974960" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="66200668" STOP_POS="69494326" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792944</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat151-D13Rat197)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792945</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Got42-D13Rat130&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="65960801" STOP_POS="71713534" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="63410813" STOP_POS="69163391" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="68686589" STOP_POS="74672607" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="73648968" STOP_POS="79590001" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="66200668" STOP_POS="72283478" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792945</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat151-D13Rat197)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792946</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Got42-D13Hmgc354&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="65960801" STOP_POS="73133152" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="63410813" STOP_POS="70599672" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="68686589" STOP_POS="76116817" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="73648968" STOP_POS="73649118" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="66200668" STOP_POS="66200819" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792946</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat151-D13Rat197)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792947</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Got42-D13Hmgc497&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="65960801" STOP_POS="74171363" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="63410813" STOP_POS="71637916" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="68686589" STOP_POS="77151580" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="73648968" STOP_POS="73649118" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="66200668" STOP_POS="66200819" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792947</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat151-D13Rat197)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792948</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Got42-D13Hmgc885&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="65960801" STOP_POS="65960952" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="63410813" STOP_POS="72403109" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="68686589" STOP_POS="77913762" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="73648968" STOP_POS="73649118" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="66200668" STOP_POS="66200819" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792948</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat151-D13Rat197)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792949</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Got42-D13Hmgc664&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="65960801" STOP_POS="65960952" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="63410813" STOP_POS="74145142" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="68686589" STOP_POS="79688633" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="73648968" STOP_POS="73649118" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="66200668" STOP_POS="66200819" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792949</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat151-D13Rat197)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792950</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Mit5-D13Rat32&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="77275174" STOP_POS="77275418" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="74741916" STOP_POS="74862225" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="80285619" STOP_POS="80403666" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="85176659" STOP_POS="85295746" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="78070512" STOP_POS="78189379" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792950</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat151-D13Rat197)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792951</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc5885-D13Rat32&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="71870085" STOP_POS="74862225" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="77381168" STOP_POS="80403666" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="85295639" STOP_POS="85295746" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="78189125" STOP_POS="78189379" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792951</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat151-D13Rat197)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792952</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc354-D13Rat32&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="73132927" STOP_POS="73133152" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="70599447" STOP_POS="74862225" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="76116593" STOP_POS="80403666" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="85295639" STOP_POS="85295746" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="78189125" STOP_POS="78189379" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792952</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat151-D13Rat197)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792953</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat130-D13Rat32&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="71713331" STOP_POS="71713534" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="69163188" STOP_POS="74862225" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="74672405" STOP_POS="80403666" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="79589799" STOP_POS="85295746" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="72283275" STOP_POS="78189379" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792953</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat151-D13Rat197)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12792954</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Got45-D13Rat32&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="66706825" STOP_POS="74862225" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="72031440" STOP_POS="80403666" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="76974692" STOP_POS="85295746" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="69494047" STOP_POS="78189379" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12792954</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat151-D13Rat197)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12798529</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc37-D13Got22&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="30737550" STOP_POS="30737765" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="93541170" STOP_POS="93542503" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="35643050" STOP_POS="49720682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="96601805" STOP_POS="96603137" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="40757538" STOP_POS="54791605" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="100631702" STOP_POS="100633034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="32396527" STOP_POS="45828716" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="97701780" STOP_POS="97703112" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12798529</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat111-D13Got22)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12798530</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat115-D13Got22&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="34778619" STOP_POS="34778759" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="93541170" STOP_POS="93542503" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="39639775" STOP_POS="49720682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="96601805" STOP_POS="96603137" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="44763184" STOP_POS="54791605" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="100631702" STOP_POS="100633034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="35719010" STOP_POS="45828716" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="97701780" STOP_POS="97703112" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12798530</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat111-D13Got22)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12798531</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc86-D13Got22&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="35407990" STOP_POS="35408317" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="93541170" STOP_POS="93542503" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="40295163" STOP_POS="49720682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="96601805" STOP_POS="96603137" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="45412259" STOP_POS="54791605" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="100631702" STOP_POS="100633034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="36367611" STOP_POS="45828716" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="97701780" STOP_POS="97703112" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12798531</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat111-D13Got22)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12798532</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc40-D13Got22&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="38744968" STOP_POS="38745230" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="93541170" STOP_POS="93542503" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="43545977" STOP_POS="49720682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="96601805" STOP_POS="96603137" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="48645307" STOP_POS="54791605" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="100631702" STOP_POS="100633034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="45828608" STOP_POS="45828716" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="97701780" STOP_POS="97703112" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12798532</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat111-D13Got22)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12798533</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc85-D13Got22&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="93541170" STOP_POS="93542503" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="96601805" STOP_POS="96603137" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="44588357" STOP_POS="49720682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="54791498" STOP_POS="54791605" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="100631702" STOP_POS="100633034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="45828608" STOP_POS="45828716" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="97701780" STOP_POS="97703112" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12798533</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat111-D13Got22)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12798534</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat77-D13Got22&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="63483475" STOP_POS="63483695" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="93541170" STOP_POS="93542503" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="60933298" STOP_POS="60933518" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="49720575" STOP_POS="66075827" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="96601805" STOP_POS="96603137" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="100631702" STOP_POS="100633034" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="54791498" STOP_POS="71047437" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="97701780" STOP_POS="97703112" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="45828608" STOP_POS="63175600" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12798534</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat111-D13Got22)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12798535</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat111-D13Rat115&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="30395351" STOP_POS="34778759" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="35301263" STOP_POS="39639912" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="40421740" STOP_POS="44763321" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="32030139" STOP_POS="35719148" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12798535</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat111-D13Got22)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12798536</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat111-D13Hmgc86&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="30395351" STOP_POS="35408317" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="35301263" STOP_POS="40295487" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="40421740" STOP_POS="45412583" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="32030139" STOP_POS="36367935" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12798536</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat111-D13Got22)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12798537</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat111-D13Rat20&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="39814726" STOP_POS="39814866" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="30395351" STOP_POS="37262232" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="35301263" STOP_POS="42155682" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="40421740" STOP_POS="47267192" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="32030139" STOP_POS="38329229" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12798537</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat111-D13Got22)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12798538</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat111-D13Hmgc85&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="30395351" STOP_POS="30395471" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="35301263" STOP_POS="44588509" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="40421740" STOP_POS="40421859" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="32030139" STOP_POS="32030259" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12798538</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS.BN-(D13Rat111-D13Got22)/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12802362</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat25-RN34_13048990782&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="47601426" STOP_POS="47601601" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45049404" STOP_POS="45049579" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50260357" STOP_POS="50260531" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55314020" STOP_POS="55314194" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="46520126" STOP_POS="48990782" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12802362</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN(D13Rat123-D13Rat101)&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12802363</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat25-rs106935835&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="47601426" STOP_POS="48088755" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45049404" STOP_POS="45536711" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50260357" STOP_POS="50918009" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55314020" STOP_POS="55314194" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="46520126" STOP_POS="46520939" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12802363</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN(D13Rat123-D13Rat101)&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12802364</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Rat25-rs198199323&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="47601426" STOP_POS="48088755" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="45049404" STOP_POS="45536711" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50260357" STOP_POS="50918009" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55314020" STOP_POS="55314194" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="46520126" STOP_POS="46520939" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12802364</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN(D13Rat123-D13Rat101)&lt;/sup&gt;/Mcwi (RGD:2293145), rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12802365</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc64-D13Hmgc23&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="43763752" STOP_POS="43763948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="49102205" STOP_POS="51182122" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="54170894" STOP_POS="56238470" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="45215472" STOP_POS="47299604" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12802365</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN(D13Rat123-D13Rat101)&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12802366</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc64-4582&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="43763752" STOP_POS="43763948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="49102205" STOP_POS="49102400" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="54170894" STOP_POS="54171089" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="45215472" STOP_POS="46195314" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12802366</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN(D13Rat123-D13Rat101)&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12802367</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;2340-RN34_13048990782&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="48193952" STOP_POS="48194155" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="47139940" STOP_POS="48990782" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12802367</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-13&lt;sup&gt;BN(D13Rat123-D13Rat101)&lt;/sup&gt;/Mcwi, rats from F&lt;sub&gt;1&lt;/sub&gt; were intercrossed and genotyped to get the congenic strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12859278</RGD_ID>
    <STRAIN_SYMBOL>Slc:ZUC-&lt;I&gt;Lepr&lt;sup&gt;fa-/-&lt;/sup&gt;&lt;/I&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Zucker fatty rats</FULL_NAME>
    <ORIGINATION>Japan SLC, Inc. (Hamamatsu, Japan)</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr|Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>3001|13432153</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12859278</CITATION_ID>
    <DESCRIPTION>The spontaneous mutation "obese" (Fatty) was found in the 13M rat stock of Sherman and Merck, by Doctor Lois Zucker, Harriet Bird Memorial Laboratory, Stow, Massachusetts 01775, USA, in 1961.This strain was maintained at Japan SLC, Inc. (Hamamatsu, Japan.)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12859279</RGD_ID>
    <STRAIN_SYMBOL>Ho:ZFDM-&lt;I&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/I&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Zucker Fatty Diabetes Mellitus rats</FULL_NAME>
    <ORIGINATION>Hoshino Laboratory Animals, Inc. (Ibaraki, Japan)</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr|Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>3001|13432153</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12859279</CITATION_ID>
    <DESCRIPTION>In the Zucker fatty rat colony in Hoshino Laboratory Animals, Inc, they incidentally found fa/fa homozygous male rats having reproductive ability. The Selective breeding using the fa/fa male rats that exhibited relatively high blood glucose levels at 10 weeks of age, resulting in establishment of a diabetic strain. These fa/fa male rats developed diabetes as early as 10 weeks of age, reaching 100% incidence by 21 weeks of age, while none of the fa/+ male rats developed diabetes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12859287</RGD_ID>
    <STRAIN_SYMBOL>ZDF-&lt;i&gt;Lepr&lt;sup&gt;fa/fa&lt;/sup&gt;&lt;/i&gt;/Drt</STRAIN_SYMBOL>
    <FULL_NAME>Zucker Diabetic Fatty Rat</FULL_NAME>
    <ORIGINATION>Indiana University School of Medicine, Indianapolis.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr</ALLELES>
    <ALLELE_RGD_IDS>3001</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12859287</CITATION_ID>
    <DESCRIPTION>"Zucker" fatty rats of undefined outbred background, inbred with selection for non-insulin-dependent diabetes mellitus by mating diabetic homozygous fatty males to heterozygous sisters.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12879386</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Ghsr&lt;sup&gt;em1Ottc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=827&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;, &lt;a href=http://www.rrrc.us/Strain/?x=827&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2018-12-04)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ghsr&lt;sup&gt;em1Ottc&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12880435</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="112196158" STOP_POS="112201666" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="110268489" STOP_POS="110271865" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="113065953" STOP_POS="113071265" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="132784207" STOP_POS="132789319" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="113269623" STOP_POS="113272999" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00827</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 genome editing system was used to generate this knock out rat strain with 846- bp deletion in the rat Ghsr gene. The rat strain had Ghsr exon1 deletion in the genome and did not express detectable Ghsr mRNA in brain regions.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12879394</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Atm&lt;sup&gt;m1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Atm missense rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=994&amp;s_Immunology=1&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=994&amp;s_Immunology=1&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-04-18)</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES>Atm&lt;sup&gt;m1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12879395</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="62724939" STOP_POS="62829040" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="53854010" STOP_POS="53854010" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="58041203" STOP_POS="58041203" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="56598503" STOP_POS="56703115" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="56894746" STOP_POS="56996565" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12879394</CITATION_ID>
    <DESCRIPTION>This strain is an Atm missense mutant (amino acid change of leucine (L) to proline (P) at position 2262 (L2262P))rat and was established by ENU mutagenesis using F344/NSlc strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12879400</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Atm&lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>ZFN-Atm  rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1024&amp;s_Neurobiology=1&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1024&amp;s_Neurobiology=1&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2017-04-18)</AVAILABILITY>
    <RESEARCH_USE>neurobiology</RESEARCH_USE>
    <ALLELES>Atm&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12879401</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="62724939" STOP_POS="62829040" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="53828741" STOP_POS="53932773" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="58015938" STOP_POS="58119973" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="56598503" STOP_POS="56703115" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="56894746" STOP_POS="56996565" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12879400</CITATION_ID>
    <DESCRIPTION>This rat strain was established by ZFN method targeting rat Atm gene (resulting in a 8-bp deletion of exon13). Background strain: F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12879423</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(HCRT-cre-EGFP)B5Ahky</STRAIN_SYMBOL>
    <FULL_NAME>orexin-Cre rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1175&amp;StrainsDir=Asc&amp;StrainsPageSize=100&amp;s_Pharmacology=1 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1175&amp;StrainsDir=Asc&amp;StrainsPageSize=100&amp;s_Pharmacology=1 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12879423</CITATION_ID>
    <DESCRIPTION>This transgenic rat strain was established by Dr. Yamanaka (Nagoya University) in 2012. Background strain: Wistar rat (CLEA Japan). plasmid backbone: pCR2.1. Transgene: human HCRT gene promoter, cre recombinase, EGFP gene, 2A gene. EGFP and cre recombinase are specifically expressed in orexin neurons.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12879424</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;ROSA26&lt;sup&gt;em1(CAG-COP4*/EGFP)Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1253&amp;s_Behavior=1&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1253&amp;s_Behavior=1&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2017-04-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12879424</CITATION_ID>
    <DESCRIPTION>This strain was established  at Kyoto University. ChR90/EGFP fusion gene  sequence  under CAG promoter is knock-in at the ROSA26 locus. Background strain: Long-Evans strain (charles river).  COP4*: Stigeoclonium helveticum-derived channelrhodopsin (Chronos, ChR90). ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12879426</RGD_ID>
    <STRAIN_SYMBOL>ExHC.BN-(&lt;i&gt;D14Got74-D14Rat132&lt;/i&gt;)/Kyu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1255&amp;s_Metabolism=1&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1255&amp;s_Metabolism=1&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-04-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="104348403" STOP_POS="104348525" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="96644199" STOP_POS="100147478" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="107428559" STOP_POS="110402569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="107489676" STOP_POS="110102984" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="103289672" STOP_POS="107101727" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12879426</CITATION_ID>
    <DESCRIPTION>This congenic strain was established by introducing a segment of chromosome14 (D14Got74-D14Rat132 including Smek2 gene) from Brown Norway(BN)/seac strain into ExHC/Seac strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12879428</RGD_ID>
    <STRAIN_SYMBOL>WKY.SHRSP-(&lt;i&gt;D1Mgh5-D1Arb21&lt;/i&gt;)(&lt;i&gt;D3Rat36-D3Rat144&lt;/i&gt;)(&lt;i&gt;D4Mgh7-D4Rat68&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1258&amp;StrainsOrder=Sorter_NBRRATNo&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1258&amp;StrainsOrder=Sorter_NBRRATNo&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-04-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="191848948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="100822652" STOP_POS="100822830" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="140059299" STOP_POS="169799698" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="80367329" STOP_POS="149313851" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="138503169" STOP_POS="168069246" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="182418476" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="136351734" STOP_POS="168998263" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="199254774" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="83300114" STOP_POS="156656443" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="200825021" STOP_POS="233267140" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="206277202" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="89999731" STOP_POS="162886090" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="78808731" STOP_POS="151449116" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="187092492" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="172169471" STOP_POS="172169650" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12879428</CITATION_ID>
    <DESCRIPTION>A double congenic strain bade by introducing segments of chromosome 1, 3, and 4 from SHRSP/Izm into WKY/Izm. This strain was established by mating between WKY.SHRSP-(D1Mgh5-D1Arb21)(D3Mgh16-D3Rat144)/Izm(NBRP Rat No:0713)and WKY.SHRSP-(D1Mgh5-D1Arb21) (D4Mgh7-D4Rat68)/IzmCNBRP Rat No:0714). This strain was established and is maintained in Shimane University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12879431</RGD_ID>
    <STRAIN_SYMBOL>Jcl:WI</STRAIN_SYMBOL>
    <FULL_NAME>Wistar rats</FULL_NAME>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/en/products/outbred/item_a0360&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/en/products/outbred/item_a0360&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-04-22)</AVAILABILITY>
    <RESEARCH_USE>behavioral pharmacology, toxicity, pharmacology, drug efficacy, and safety testing.</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12879431</CITATION_ID>
    <DESCRIPTION>This strain is a rat strain originating from the Wistar Institute in Philadelphia (USA). The Wistar Institute was named as a memorial to the famous anatomist Professor Casper Wistar at the University of Pennsylvania. CLEA Japan, Inc. started the production and supply of this strain after it was introduced from Carworth (UK).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12879432</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Ift140&lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Institute of Environmental Toxicology</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1262&amp;StrainsOrder=Sorter_NBRRATNo&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-04-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ift140&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12879433</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="14537134" STOP_POS="14624926" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="14032665" STOP_POS="14121682" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="14373668" STOP_POS="14461509" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="14189328" STOP_POS="14276940" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="14258556" STOP_POS="14348468" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12879432</CITATION_ID>
    <DESCRIPTION>This strain was established by CRISPR/Cas9 system at Kyoto University and introduced to the Institute of Environmental Toxicology. Background strain: Jcl:Wistar. This line 1 (em1) has 2-bp insertion (c.23_24insGG) in the exon 1 of Ift140 (intraflagellar transport 140) gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12879434</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Ift140&lt;sup&gt;em2Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Institute of Environmental Toxicology</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1263&amp;StrainsOrder=Sorter_NBRRATNo&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-04-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ift140&lt;sup&gt;em2Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12879435</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12879434</CITATION_ID>
    <DESCRIPTION>This strain was established by CRISPR/Cas9 system at Kyoto University and introduced to the Institute of Environmental Toxicology. Background strain: Jcl:Wistar. This line 2 (em2) has 2-bp deletion (c.23_24del) in the exon 1 of Ift140 (intraflagellar transport 140) gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12879437</RGD_ID>
    <STRAIN_SYMBOL>SHC/Ta</STRAIN_SYMBOL>
    <FULL_NAME>spontaneously hypercholesterolemic rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1264&amp;StrainsOrder=Sorter_NBRRATNo&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1264&amp;StrainsOrder=Sorter_NBRRATNo&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-04-19)</AVAILABILITY>
    <RESEARCH_USE>Metabolism</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12879437</CITATION_ID>
    <DESCRIPTION>This strain (Nephropathy model) was segrigated from SD strain (CLEA Japan,Inc.) by selective mating on the basis of total cholesterol level in blood.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12879438</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(CAG-EGFP,Acr-EGFP)2Osb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1265&amp;s_Development=1&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1265&amp;s_Development=1&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-04-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12879438</CITATION_ID>
    <DESCRIPTION>This double transgenic strain was established by co-injection of CAG-EGFP and mouse Acr-EGFP into F344/NSlc at Osaka University (over 5 generations, Dec 2016). There are two lines; GBGS&amp;#65288;green body, green sperm&amp;#65289;#2 and GBGS #6, but copy numbers and insertion site are not identified. Both lines show enough intensity of GFP fluorescence (no quantitative data).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12879439</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(CAG-EGFP,Acr-EGFP)6Osb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1266&amp;s_Development=1&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1266&amp;s_Development=1&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-04-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12879439</CITATION_ID>
    <DESCRIPTION>This double transgenic strain was established by co-injection of CAG-EGFP and mouse Acr-EGFP into F344/NSlc at Osaka University (over 5 generations, Dec 2016). There are two lines; GBGS(green body, green sperm)#2 and GBGS #6, but copy numbers and insertion site are not identified. Both lines show enough intensity of GFP fluorescence (no quantitative data).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12880021</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Apoe&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/apoe-knockout-rat-tgra3710&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/apoe-knockout-rat-tgra3710&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-01)</AVAILABILITY>
    <RESEARCH_USE>Alzheimer's disease, Neurodegenerative diseases</RESEARCH_USE>
    <ALLELES>Apoe&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12880022</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="88481889" STOP_POS="88485816" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="79353924" STOP_POS="79357852" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="80612894" STOP_POS="80616820" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="81878372" STOP_POS="81882298" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="79003634" STOP_POS="79006387" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12880021</CITATION_ID>
    <DESCRIPTION>The  mutant rat strain was produced by injecting zinc endonuclease targeting the exon 3 of rat Apoe into Sprague Dawley embryos. This mutant rat has a 16-bp deletion in the gene and resulted in complete loss of   Apoe protein in homozygotes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12880026</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;App&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/app-knockout-rat-tgrs5460&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/app-knockout-rat-tgrs5460&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-05-01)</AVAILABILITY>
    <RESEARCH_USE>Alzheimer's disease, Neurodegenerative diseases</RESEARCH_USE>
    <ALLELES>App&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12880027</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="37506207" STOP_POS="37724351" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="24019774" STOP_POS="24236584" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="24425013" STOP_POS="24641872" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="28048897" STOP_POS="28265250" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="24457855" STOP_POS="24693851" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12880026</CITATION_ID>
    <DESCRIPTION>This rat model carries a bi-allelic deletion of the amyloid precursor protein (APP) gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12880037</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Dmd&lt;sup&gt;em1Ang&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dmd&lt;sup&gt;em1Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12880032</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="51070098" STOP_POS="53437845" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="48090661" STOP_POS="48090671" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="52104979" STOP_POS="52104989" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="51475950" STOP_POS="53700033" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="71501362" STOP_POS="71671414" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12880037</CITATION_ID>
    <DESCRIPTION>This mutant strain was generated by injecting  TALEN targeting exon23 of rat Dmd into Crl:SD embryo. The resulting mutant is a 11 bp-deletion in exon 23 leading to a +1 grame shift and premature stop codon 81 bp after the mutation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12902614</RGD_ID>
    <STRAIN_SYMBOL>SS.LEW-(&lt;i&gt;D10M11Mit119-D10Rat27&lt;/i&gt;)/Ayd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre Hospitalier de Universiti de Montrial, Quebec, Canada</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="73950209" STOP_POS="73950353" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="73452992" STOP_POS="73453136" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="75983662" STOP_POS="75983805" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="74127825" STOP_POS="74127968" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="77091834" STOP_POS="77092169" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12902614</CITATION_ID>
    <DESCRIPTION>A segment of chromosome 10 was transferred from LEW into the SS background. Two congenic strains, designated S.L4 and S.L5, that were previously shown to have trapped 2 BP QTLs, were used to derive congenic substrains. The F2 rats were genotyped for markers that resided in a region of interest. Each rat was then backcrossed to an SS rat to duplicate the fragment.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12902616</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Apoe&lt;sup&gt;tm1(APOE*)Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/hapoe4-knock-in-rat-tgra8960&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/hapoe4-knock-in-rat-tgra8960&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-09)</AVAILABILITY>
    <RESEARCH_USE>Alzheimer's disease,  Neurodegenerative diseases</RESEARCH_USE>
    <ALLELES>APOE</ALLELES>
    <ALLELE_RGD_IDS>736378</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12902616</CITATION_ID>
    <DESCRIPTION>These rats were created using CrISPR/Cas9 system to replace the Rat ApoE gene with the Human  4 allele  APOE gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12902621</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Bdnf&lt;sup&gt;em1Sage+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/bdnf-knockout-rat-tgrs3850&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/bdnf-knockout-rat-tgrs3850&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-06-20)</AVAILABILITY>
    <RESEARCH_USE>Schizophrenia and Alzheimer's Disease</RESEARCH_USE>
    <ALLELES>Bdnf&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12902622</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="116619633" STOP_POS="116670212" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="96165042" STOP_POS="96215621" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="100768637" STOP_POS="100819216" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="107371329" STOP_POS="107421908" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12902621</CITATION_ID>
    <DESCRIPTION>This ZFN model contains a monoallelic deletion of the Bdnf gene, encoding for the nerve growth factor protein BDNF. Homozygous animals carrying the Bdnf deletion are postnatal lethal. Reductions of BDNF have been observed in patients with Alzheimer's disease (AD), and this model may be useful for understanding the role of BDNF in AD.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12902625</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nr1i2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/pxr-knockout-rat-tgrs4130&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/pxr-knockout-rat-tgrs4130&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-09)</AVAILABILITY>
    <RESEARCH_USE>Xenobiotic Sensors</RESEARCH_USE>
    <ALLELES>Nr1i2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12902626</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="75965717" STOP_POS="76006733" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="62460213" STOP_POS="62496665" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="65022100" STOP_POS="65058546" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="67024185" STOP_POS="67060494" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="64239918" STOP_POS="64276702" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12902625</CITATION_ID>
    <DESCRIPTION>This ZFN  model contains a 20-bp deletion within the Nr1i2 gene. No induction of Cyp3a1 in the model.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12903250</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ahr&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/ahr-knockout-rat-tgrs8890&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/ahr-knockout-rat-tgrs8890&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-10)</AVAILABILITY>
    <RESEARCH_USE>Xenobiotic Sensors</RESEARCH_USE>
    <ALLELES>Ahr&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12903271</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="57961423" STOP_POS="57998901" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="52234089" STOP_POS="52271568" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="54963990" STOP_POS="55001806" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="64589066" STOP_POS="64624078" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="54205104" STOP_POS="54240268" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12903250</CITATION_ID>
    <DESCRIPTION>This ZFN model contains a 760-bp deletion in the rat Ahr gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12903251</RGD_ID>
    <STRAIN_SYMBOL>LH-Chr 17&lt;sup&gt;LN&lt;/sup&gt;/Aek</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>consomic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12903251</CITATION_ID>
    <DESCRIPTION>Chr 17 from LN was introgressed onto the genetic background of LH by crossing LH/MRrrcAek male to LN/MRrrcAek female rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12903257</RGD_ID>
    <STRAIN_SYMBOL>LH.LH-Chr 17&lt;sup&gt;LN&lt;/sup&gt;-(&lt;i&gt;rs199194111-rs105876746&lt;/i&gt;)/Aek</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=822&gt;Rat Resource &amp; Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=822&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="77633666" STOP_POS="84432719" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="72724339" STOP_POS="79524188" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="76673662" STOP_POS="83549032" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00822</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a fragment of chromosome 17 from the LH-Chr 17&lt;sup&gt;LN&lt;/sup&gt;/Aek from rs199194111 through rs1056876746 transferred to the LH/MRrrcAek  background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12903267</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nr1i3&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/car-knockout-rat-tgrs8190&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/car-knockout-rat-tgrs8190&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-10)</AVAILABILITY>
    <RESEARCH_USE>Xenobiotic Sensors</RESEARCH_USE>
    <ALLELES>Nr1i3&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12903268</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="86165327" STOP_POS="86170362" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="83632940" STOP_POS="83638193" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="89585072" STOP_POS="89591278" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="94211961" STOP_POS="94218143" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="87104241" STOP_POS="87108563" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12903267</CITATION_ID>
    <DESCRIPTION>This model contains a ZFN-induced 10-bp deletion within rat Nr1i3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12903270</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nr1i2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;Nr1i3&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/pxr-car-knockout-rat-tgrs9100&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/pxr-car-knockout-rat-tgrs9100&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-10)</AVAILABILITY>
    <RESEARCH_USE>Xenobiotic Sensors</RESEARCH_USE>
    <ALLELES>Nr1i2&lt;sup&gt;em1Sage&lt;/sup&gt;|Nr1i3&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12902626|12903268</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="86165327" STOP_POS="86170362" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="75965717" STOP_POS="76006733" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="83632940" STOP_POS="83638193" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="62460213" STOP_POS="62496665" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="89585072" STOP_POS="89591278" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="65022100" STOP_POS="65058546" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="67024185" STOP_POS="67060494" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="94211961" STOP_POS="94218143" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="64239918" STOP_POS="64276702" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="87104241" STOP_POS="87108563" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12903270</CITATION_ID>
    <DESCRIPTION>This model contains two knockout genes, the  20-bp deletion within rat Nr1i2 and the  ZFN-induced 10-bp deletion within rat Nr1i3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12903272</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nr1i2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;Nr1i3&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;Ahr&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/pxr-car-ahr-knockout-rat-tgrs9030&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/pxr-car-ahr-knockout-rat-tgrs9030&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-05-10)</AVAILABILITY>
    <RESEARCH_USE>Xenobiotic Sensors</RESEARCH_USE>
    <ALLELES>Nr1i2&lt;sup&gt;em1Sage&lt;/sup&gt;|Nr1i3&lt;sup&gt;em1Sage&lt;/sup&gt;|Ahr&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12902626|12903268|12903271</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="75965717" STOP_POS="76006733" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="86165327" STOP_POS="86170362" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="57961423" STOP_POS="57998901" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="62460213" STOP_POS="62496665" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="52234089" STOP_POS="52271568" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="83632940" STOP_POS="83638193" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="65022100" STOP_POS="65058546" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="54963990" STOP_POS="55001806" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="89585072" STOP_POS="89591278" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="94211961" STOP_POS="94218143" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="64589066" STOP_POS="64624078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="67024185" STOP_POS="67060494" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="54205104" STOP_POS="54240268" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="87104241" STOP_POS="87108563" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="64239918" STOP_POS="64276702" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12903272</CITATION_ID>
    <DESCRIPTION>This model contains three knockout genes, the  20-bp deletion within rat Nr1i2, the  ZFN-induced 10-bp deletion within rat Nr1i3 gene and the 760-bp deletion in the rat Ahr gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904057</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abcb1a&lt;sup&gt;em1Sage -/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SD-&lt;i&gt;Abcb1a&lt;sup&gt;em1&lt;/sup&gt;-&lt;/sup&gt;/Abcb1a&lt;sup&gt;em1&lt;/sup&gt;-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/mdr1a-knockout-rat-tgrs3570&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/mdr1a-knockout-rat-tgrs3570&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-16)</AVAILABILITY>
    <RESEARCH_USE>Efflux Transporter</RESEARCH_USE>
    <ALLELES>Abcb1a&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904058</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="26312403" STOP_POS="26488456" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="25357467" STOP_POS="25529941" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="22339829" STOP_POS="22517642" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="22276390" STOP_POS="22448913" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="21709855" STOP_POS="21796628" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904057</CITATION_ID>
    <DESCRIPTION>This ZFN  model contains  biallelic 20 bp deletion within Abcba1 gene. Animals exhibit increased oral bioavailability of P-gp-specific substrates. The homozygous knockout rats display total loss of protein via Western blot.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904059</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;(Abcb1a- Abcb1b)&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/mdr1a-1b-knockout-rat-tgrs7070&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/mdr1a-1b-knockout-rat-tgrs7070&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-16)</AVAILABILITY>
    <RESEARCH_USE>Efflux Transporter</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904059</CITATION_ID>
    <DESCRIPTION>This model carries knockout of Abcb1a and Abcb1b.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904063</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abcg2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/bcrp-knockout-rat-tgrs4200&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/bcrp-knockout-rat-tgrs4200&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-16)</AVAILABILITY>
    <RESEARCH_USE>Efflux Transporter</RESEARCH_USE>
    <ALLELES>Abcg2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904064</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="89006056" STOP_POS="89132915" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="87676241" STOP_POS="87802757" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="88765441" STOP_POS="88890268" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="153587206" STOP_POS="153712481" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="87502584" STOP_POS="87560017" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904063</CITATION_ID>
    <DESCRIPTION>This  ZFN model carries  a 588-bp deletion within Abcg2 gene. Homozygous knockouts display total loss of protein via Western blot</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904679</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Cyp2j4&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;/Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp2j4&lt;i&gt;&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904681</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="116295691" STOP_POS="116323219" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="111179981" STOP_POS="111207490" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="119546458" STOP_POS="119564843" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="119130644" STOP_POS="123455814" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="116702370" STOP_POS="116729722" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904679</CITATION_ID>
    <DESCRIPTION>ZFN system was used to introduce a 25-bp deletion mutation in the exon 4 of Cyp2j4 gene of WKY/NCrl rat embryos. This deletion results in premature stop of protein translation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904684</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abcb1a&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;Abcg2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/mdr1a-bcrp-knockout-rat-tgrs7490&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/mdr1a-bcrp-knockout-rat-tgrs7490&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-17)</AVAILABILITY>
    <RESEARCH_USE>Efflux Transporter</RESEARCH_USE>
    <ALLELES>Abcb1a&lt;sup&gt;em1Sage&lt;/sup&gt;|Abcg2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904058|12904064</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="26312403" STOP_POS="26488456" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="89006056" STOP_POS="89132915" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="25357467" STOP_POS="25529941" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="87676241" STOP_POS="87802757" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="22339829" STOP_POS="22517642" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="88765441" STOP_POS="88890268" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="153587206" STOP_POS="153712481" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="22276390" STOP_POS="22448913" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="87502584" STOP_POS="87560017" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="21709855" STOP_POS="21796628" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904684</CITATION_ID>
    <DESCRIPTION>This model contains two knockout genes, the  20-bp deletion within rat Abcba1 and the  588-bp deletion within rat Abcg2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904685</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abcc2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/mrp2-knockout-rat-tgrs4340&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/mrp2-knockout-rat-tgrs4340&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-17)</AVAILABILITY>
    <RESEARCH_USE>Efflux Transporter</RESEARCH_USE>
    <ALLELES>Abcc2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904687</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="252613875" STOP_POS="252672459" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="242664657" STOP_POS="242723239" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="263554426" STOP_POS="263612556" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="270999832" STOP_POS="271057750" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904685</CITATION_ID>
    <DESCRIPTION>This ZFN model contains a biallelic 726 bp deletion within the Abcc2 gene. Animals exhibit decreased transport of endogenous glutathione and hyperbilirubinemia. The homozygous knockout rats display total loss of protein via Western blot.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904730</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abcb11&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/bsep-knockout-rat-tgrs8050&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/bsep-knockout-rat-tgrs8050&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-19)</AVAILABILITY>
    <RESEARCH_USE>Efflux Transporter</RESEARCH_USE>
    <ALLELES>Abcb11&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904731</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="74424620" STOP_POS="74520646" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="54016854" STOP_POS="54112797" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="55480024" STOP_POS="55587946" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="62091490" STOP_POS="62195528" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904730</CITATION_ID>
    <DESCRIPTION>This ZFN induced knockout model contains  biallelic 8-bp deletion within Abcb11 gene.  The homozygous knockout rats display total loss of protein via Western blot.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904733</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Slc22a1&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/oct1-knockout-rat-tgrs5600&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/oct1-knockout-rat-tgrs5600&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-05-19)</AVAILABILITY>
    <RESEARCH_USE>Uptake Transporters</RESEARCH_USE>
    <ALLELES>Slc22a1&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904734</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="50624339" STOP_POS="50651437" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="48076657" STOP_POS="48103679" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="48273639" STOP_POS="48300645" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="51452604" STOP_POS="51479610" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="42351239" STOP_POS="42378295" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904733</CITATION_ID>
    <DESCRIPTION>This ZFN induced knockout model contains  11 bp bi-allelic deletion within exon 1 of the Slc22a1. The homozygous knockout rats display total loss of protein via Western blot.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904891</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Slc22a2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/oct2-knockout-rat-tgrs6580&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/oct2-knockout-rat-tgrs6580&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-24)</AVAILABILITY>
    <RESEARCH_USE>Uptake Transporters</RESEARCH_USE>
    <ALLELES>Slc22a2</ALLELES>
    <ALLELE_RGD_IDS>61936</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="50668817" STOP_POS="50711019" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="48121061" STOP_POS="48163268" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="48318025" STOP_POS="48360219" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="51394014" STOP_POS="51435104" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="42395676" STOP_POS="42442847" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904891</CITATION_ID>
    <DESCRIPTION>This ZFN model carries the knockout of the rat Slc22a2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904892</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Slc22a6&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/oat1-knockout-rat-tgrs6440&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/oat1-knockout-rat-tgrs6440&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-05-24)</AVAILABILITY>
    <RESEARCH_USE>Uptake Transporters</RESEARCH_USE>
    <ALLELES>Slc22a6</ALLELES>
    <ALLELE_RGD_IDS>69338</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="214951493" STOP_POS="214960317" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="205522579" STOP_POS="205531179" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="224824809" STOP_POS="224833284" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="231761600" STOP_POS="231772550" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="211294178" STOP_POS="211302398" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904892</CITATION_ID>
    <DESCRIPTION>This ZFN model carries the knockout of the rat Slc22a6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904893</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Slc22a8&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/oat3-knockout-rat-tgrs6510&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/oat3-knockout-rat-tgrs6510&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-05-24)</AVAILABILITY>
    <RESEARCH_USE>Uptake Transporters</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904893</CITATION_ID>
    <DESCRIPTION>This ZFN model carries the knockout of the rat Slc22a8.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904897</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Tp53&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Horizon Discovery</ORIGINATION>
    <SOURCE>Horizon Discovery</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2024-04-16)</AVAILABILITY>
    <RESEARCH_USE>carcinogenicity</RESEARCH_USE>
    <ALLELES>Tp53&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904898</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="54798871" STOP_POS="54810300" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="54307287" STOP_POS="54307297" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="56194211" STOP_POS="56194221" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="55932658" STOP_POS="55944087" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="56399721" STOP_POS="56411150" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904897</CITATION_ID>
    <DESCRIPTION>This ZFN model carries the monoallelic 11 base pair deletion in Tp53 gene. Animals exhibit broad tumor spectrum with high degree of tumor malignancy.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904900</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Rag1&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/rag1-knockout-rat-sprague-dawley-tgrs3920&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/rag1-knockout-rat-sprague-dawley-tgrs3920&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-05-24)</AVAILABILITY>
    <RESEARCH_USE>immunology/Inflamation and Immunodeficient</RESEARCH_USE>
    <ALLELES>Rag1&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904901</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108372087" STOP_POS="108383184" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87917061" STOP_POS="87928158" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91206394" STOP_POS="91217491" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97866048" STOP_POS="97877145" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86780782" STOP_POS="86791878" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904900</CITATION_ID>
    <DESCRIPTION>This ZFN model carries a 29 bp deletion within exon 2 of the Rag1 gene on chromosome 3. Homozygous animals display loss of Rag1 protein and loss of B and T cells by FACS analysis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904902</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Rag1&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/rag1-knockout-rat-fischer-344-tgrf7980&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/rag1-knockout-rat-fischer-344-tgrf7980&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-05-24)</AVAILABILITY>
    <RESEARCH_USE>immunology/Inflamation and Immunodeficient</RESEARCH_USE>
    <ALLELES>Rag1&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904901</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108372087" STOP_POS="108383184" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87917061" STOP_POS="87928158" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91206394" STOP_POS="91217491" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97866048" STOP_POS="97877145" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86780782" STOP_POS="86791878" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904902</CITATION_ID>
    <DESCRIPTION>This ZFN model carries a 29 bp deletion within exon 2 of the Rag1 gene on chromosome 3. Rag1 knockout rats lack mature B and T lymphocytes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904903</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Rag2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/rag2-knockout-rat-sprague-dawley-tgrs4410&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/rag2-knockout-rat-sprague-dawley-tgrs4410&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-24)</AVAILABILITY>
    <RESEARCH_USE>immunology/Inflamation and Immunodeficient</RESEARCH_USE>
    <ALLELES>Rag2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904904</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108357399" STOP_POS="108367186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87902373" STOP_POS="87910227" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91191837" STOP_POS="91200134" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97851318" STOP_POS="97859615" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86764810" STOP_POS="86773438" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904903</CITATION_ID>
    <DESCRIPTION>This ZFN model carries a 2 bp deletion within exon 3 of the Rag2 gene on chromosome 3. Homozygous Rag2 knockout rats display loss of RAG2 protein via Western blot. Homozygous Rag2 knockout rats show loss of B and T cells by FACS analysis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904905</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Rag2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/rag2-knockout-rat-fischer-344-tgrf7840&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/rag2-knockout-rat-fischer-344-tgrf7840&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-05-24)</AVAILABILITY>
    <RESEARCH_USE>immunology/Inflamation and Immunodeficient</RESEARCH_USE>
    <ALLELES>Rag2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904904</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108357399" STOP_POS="108367186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87902373" STOP_POS="87910227" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91191837" STOP_POS="91200134" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97851318" STOP_POS="97859615" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86764810" STOP_POS="86773438" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904905</CITATION_ID>
    <DESCRIPTION>This ZFN model carries a 2 bp deletion within exon 3 of the Rag2 gene.on chromosome 3 Rag2 knockout rats completely lack B and T cells.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904907</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Prkdc&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/prkdc-knockout-rat-tgrs4550&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/prkdc-knockout-rat-tgrs4550&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-24)</AVAILABILITY>
    <RESEARCH_USE>immunology/Inflamation and Immunodeficient</RESEARCH_USE>
    <ALLELES>Prkdc&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>151232284</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="98544952" STOP_POS="98762499" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="85040790" STOP_POS="85258357" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="89293547" STOP_POS="89510948" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="92347175" STOP_POS="92565022" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="86951420" STOP_POS="87169229" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904907</CITATION_ID>
    <DESCRIPTION>This ZFN induced knockout rats carrying a shorter truncated gene, 872 by PCR vs 1627 in wild type,  have severe combined immunodeficiency (SCID) and lack of both B and T cells</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904908</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ldlr&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/ldlr-knockout-rat-tgrs4060&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/ldlr-knockout-rat-tgrs4060&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ldlr&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904909</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="28546191" STOP_POS="28569075" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="20270020" STOP_POS="20292981" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="22750425" STOP_POS="22773305" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="22804325" STOP_POS="22827199" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="20824040" STOP_POS="20846920" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904908</CITATION_ID>
    <DESCRIPTION>In this ZFN induced model, a total of 337 bp were deleted at the junction of intron 3 and exon 4 (on chromosome 8), and 4 bp ccgt were inserted rat Ldlr gene on chromosome 8. Homozygous knockout rats display loss of LDLR protein via Western blot. Homozygous knockout rats have increased body weight as compared to wild type. Homozygous knockout rats show significantly elevated serum cholesterol levels.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12904912</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lep&lt;sup&gt;em1Sage-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.inotivco.com/model/hsdsage-sd-lepem1sage&gt;Inotiv&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.inotivco.com/model/hsdsage-sd-lepem1sage&gt;Inotiv&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2017-05-24)</AVAILABILITY>
    <RESEARCH_USE>Cardiovascular</RESEARCH_USE>
    <ALLELES>Lep&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904927</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="58626529" STOP_POS="58640663" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="57670525" STOP_POS="57670675" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="56347081" STOP_POS="56347231" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="56085079" STOP_POS="56099209" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="55943837" STOP_POS="55945938" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12904912</CITATION_ID>
    <DESCRIPTION>This ZFN model possesses a 151 bp deletion spanning exon 1/intron 1 junction of Leptin gene. Homozygous knockout rats display loss of Leptin protein via Western blot.  Homozygous knockout rats demonstrate significant weight gain compared to wild type littermates. Homozygous knockout rats show significantly elevated serum cholesterol levels</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12905029</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Th&lt;sup&gt;tm1(cre)Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/th-cre-rat-tyrosine-hydroxylase-tgra8400&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/th-cre-rat-tyrosine-hydroxylase-tgra8400&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-31)</AVAILABILITY>
    <RESEARCH_USE>Optogenetics Rats</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12905029</CITATION_ID>
    <DESCRIPTION>This ZFN knock in model expresses cre-recombinase under the control of the endogenous tyrosine hydroxylase promoter enabling specific expression in dopaminergic neurons. This model possesses a targeted insertion of (IRES)-cre immediately after the translational stop in the open reading frame of Th. The TH-Cre rat is useful for applications requiring tissue specific expression, including optogenetics and breeding with transgenic floxed lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12905031</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Slc6a3&lt;sup&gt;tm1(cre)Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/dopamine-transporter-dat-cre-rat-tgra8330&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/dopamine-transporter-dat-cre-rat-tgra8330&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-31)</AVAILABILITY>
    <RESEARCH_USE>Optogenetics Rats</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12905031</CITATION_ID>
    <DESCRIPTION>This model expresses cre-recombinase under the control of the endogenous dopamine transporter promoter enabling specific expression in dopaminergic neurons. This model possesses a targeted insertion of (IRES)-cre immediately after the translational stop in the open reading frame of DAT. The DAT-Cre rat is useful for applications requiring tissue specific expression, including optogenetics and breeding with transgenic floxed lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12905032</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Camk2a&lt;sup&gt;tm1(cre)Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/camkiia-cre-rat-tgrl9170&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/camkiia-cre-rat-tgrl9170&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-31)</AVAILABILITY>
    <RESEARCH_USE>Optogenetics Rats</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12905032</CITATION_ID>
    <DESCRIPTION>This model expresses cre-recombinase under the control of the endogenous camkIIa promoter enabling specific expression in excititory neurons. This model possesses a targeted insertion of (IRES)-cre immediately after the translational stop in the open reading frame of CamkIIa. The CamkIIa-Cre rat is useful for applications requiring tissue specific expression, including optogenetics and breeding with transgenic floxed lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12905033</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Slc32a1&lt;sup&gt;tm1(cre)Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/vgat-cre-rat-tgrl9310&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/vgat-cre-rat-tgrl9310&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-31)</AVAILABILITY>
    <RESEARCH_USE>Optogenetics Rats</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12905033</CITATION_ID>
    <DESCRIPTION>This model expresses cre-recombinase under the control of the endogenous solute carrier family 32 member 1 (Vgat) promoter enabling specific expression in Vgat positive GABAergic neurons. This model possesses a targeted insertion of (IRES)-cre immediately after the translational stop in the open reading frame of the Vgat gene. The Vgat-Cre rat is useful for applications requiring tissue specific expression, including optogenetics and breeding with transgenic floxed lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12905034</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Vip&lt;sup&gt;tm1(cre)Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/vip-cre-rat-tgrl9450&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/vip-cre-rat-tgrl9450&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2017-05-31)</AVAILABILITY>
    <RESEARCH_USE>Optogenetics Rats</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12905034</CITATION_ID>
    <DESCRIPTION>This model expresses cre-recombinase under the control of the endogenous vasoactive intestinal peptide (VIP) promoter enabling specific expression in VIP positive GABAergic interneurons. This model possesses a targeted insertion of (T2A)-cre immediately before the translational stop in the open reading frame of the VIP gene. The VIP-Cre rat is useful for applications requiring tissue specific expression, including optogenetics and breeding with transgenic floxed lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12905035</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Tph2&lt;sup&gt;tm1(cre)Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/tph2-cre-rat-tgrl9590&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/tph2-cre-rat-tgrl9590&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-31)</AVAILABILITY>
    <RESEARCH_USE>Optogenetics Rats</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12905035</CITATION_ID>
    <DESCRIPTION>This model expresses cre-recombinase under the control of the endogenous Tryptophan Hydroxylase 2 (Tph2) promoter enabling specific expression in Tph2 positive serotonergic neurons. This model possesses a targeted insertion of (T2A)-cre immediately before the translational stop in the open reading frame of the Tph2 gene. The Tph2-Cre rat is useful for applications requiring tissue specific expression, including optogenetics and breeding with transgenic floxed lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12905036</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Htr3a&lt;sup&gt;tm1(cre)Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/5ht3a-cre-rat-tgrl9380&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/5ht3a-cre-rat-tgrl9380&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-31)</AVAILABILITY>
    <RESEARCH_USE>Optogenetics Rats</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12905036</CITATION_ID>
    <DESCRIPTION>This model expresses cre-recombinase under the control of the endogenous 5 prime-hydroxytryptamine receptor 3A (5Ht3a) promoter enabling specific expression in 5Ht3a positive serotonergic neurons. This model possesses a targeted insertion of (T2A)-cre immediately before the translational stop in the open reading frame of the 5Ht3a gene. The 5Ht3a-Cre rat is useful for applications requiring tissue specific expression, including optogenetics and breeding with transgenic floxed lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12905037</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;ROSA26&lt;sup&gt;em1(CAG-tdTomato)1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/tdtomato-reporter-rat-tgrl9660&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/tdtomato-reporter-rat-tgrl9660&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-31)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12905037</CITATION_ID>
    <DESCRIPTION>This CRISPR knock in model possesses the fluorophore tdTomato, sitting behind a floxed stop codon in the ROSA26 locus under control of the CAG promoter. By introducing Cre-recombinase through viral transduction or crossing with one of our Cre-driver rats, tdTomato fluorescence will be observed anywhere Cre- is expressed. The tdTomato Reporter rat is useful for applications requiring tissue specific expression, including optogenetics and breeding with Cre-driver lines. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12905038</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;ROSA26&lt;sup&gt;em1(CAG-tdTomato-NpHR)1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/halorhodopsin-rat-tgrl9730&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/halorhodopsin-rat-tgrl9730&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-05-31)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12905038</CITATION_ID>
    <DESCRIPTION>This CRISPR knock in model possesses the Halorhodopsin fused to TdTomato, sitting behind a floxed stop codon in the ROSA26 locus under the control of the CAG promoter. By introducing Cre-recombinase by crossing with one of our Cre-driver rats, neuronal subtype-specific expression of halorhodopsin and TdTomato will be observed anywhere Cre- is expressed. The Halorhodopsin rat is useful for applications requiring tissue specific expression, including optogenetics and breeding with Cre-driver lines. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12907568</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Abcb1a&lt;sup&gt;em2Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abcb1a&lt;sup&gt;em2Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12907569</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="26312403" STOP_POS="26488456" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="25413964" STOP_POS="25413982" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="22396614" STOP_POS="22396632" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="22276390" STOP_POS="22448913" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="21709855" STOP_POS="21796628" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12907568</CITATION_ID>
    <DESCRIPTION>This model contains  biallelic 19- bp deletion in exon 7 of Abcba1 gene.  The homozygous knockout rats display total loss of protein via Western blot.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12907570</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Abcb1a&lt;sup&gt;em3Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abcb1a&lt;sup&gt;em3Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12907571</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="26312403" STOP_POS="26488456" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="25357467" STOP_POS="25529941" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="22339829" STOP_POS="22517642" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="22276390" STOP_POS="22448913" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="21709855" STOP_POS="21796628" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12907570</CITATION_ID>
    <DESCRIPTION>This model contains  one 19- bp deletion and one 428-bp deletion within Abcba1 gene.  The homozygous knockout rats display total loss of protein via Western blot.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12910101</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ldlr&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ldlr&lt;sup&gt;em1&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910102</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="28546191" STOP_POS="28569075" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="20283596" STOP_POS="20283614" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="22763920" STOP_POS="22763938" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="22804325" STOP_POS="22827199" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="20824040" STOP_POS="20846920" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12910101</CITATION_ID>
    <DESCRIPTION>This model possesses a 19-bp deletion in the seventh exon of the ldlr gene by ZFN method.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12910127</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Th-Ghsros)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ghsr</ALLELES>
    <ALLELE_RGD_IDS>621397</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12910127</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries a synthetic 108-nucleotide DNA fragment spanning the 5 prime extracellular region of GHS-R was cloned in the antisense orientation driven by tyrosine hydroxylase (Th) promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12910483</RGD_ID>
    <STRAIN_SYMBOL>Slc:SD</STRAIN_SYMBOL>
    <FULL_NAME>Sprague-Dawley Derived</FULL_NAME>
    <ORIGINATION>&lt;a href =http://www.jslc.co.jp/english/animals/rat.php#rat-cat-01/&gt; Japan SLC, Inc.&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =http://www.jslc.co.jp/english/animals/rat.php#rat-cat-01/&gt; Japan SLC, Inc.&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12910483</CITATION_ID>
    <DESCRIPTION>Derived from Charles River Laboratory Inc. USA in 1968.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12910493</RGD_ID>
    <STRAIN_SYMBOL>LEW.1WR1-&lt;i&gt;Ifnar1&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Massachusetts Medical School, Worcester, MA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ifnar1&lt;sup&gt;em1&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910495</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="44211769" STOP_POS="44238206" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="30738535" STOP_POS="30738615" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="31653152" STOP_POS="31653232" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="35248575" STOP_POS="35272235" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="31454789" STOP_POS="31478449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12910493</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 genome editing system was used to generate this mutant rat strain. The resulting strains carrying a 81-bp deletion in exon 4 of Ifnar1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12910494</RGD_ID>
    <STRAIN_SYMBOL>LEW.1WR1-&lt;i&gt;Ifnar1&lt;sup&gt;em2&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine, University of Massachusetts Medical School, Worcester, MA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ifnar1&lt;sup&gt;em2&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910496</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="11" START_POS="44211769" STOP_POS="44238206" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="11" START_POS="30725774" STOP_POS="30752227" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="11" START_POS="31640407" STOP_POS="31666839" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="11" START_POS="35248575" STOP_POS="35272235" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="11" START_POS="31454789" STOP_POS="31478449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12910494</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 genome editing system was used to generate this mutant rat strain. The resulting strains carrying a 81-bp deletion and 4-bp insertion in exon 4 of Ifnar1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12910505</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Mmp12&lt;sup&gt;em2Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mmp12&lt;sup&gt;em2Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910506</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="12866652" STOP_POS="12876554" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="4582897" STOP_POS="4583503" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="5607704" STOP_POS="5608310" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="5610392" STOP_POS="5620294" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="4249938" STOP_POS="4259675" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12910505</CITATION_ID>
    <DESCRIPTION>TALEN mediated 607 bp deletion that includes exon 2 of the Mmp12 gene, resulting in a frameshift and premature stop codon</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12910514</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lepr&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>East  China  Normal  University, Shanghai, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;em1&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910515</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116294409" STOP_POS="116477904" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120503475" STOP_POS="120682281" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12910514</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALEN targeting the sequence of rat Lepr into SD embryos. The resulting mutation is a 57-bp deletion.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12910517</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lepr&lt;sup&gt;em2&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>East  China  Normal  University, Shanghai, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;em2&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910518</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116372431" STOP_POS="116372431" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120581486" STOP_POS="120581486" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12910517</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALEN targeting the sequence of rat Lepr into SD embryos. The resulting mutation is a 1-bp deletion.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12910519</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lepr&lt;sup&gt;em3&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>East  China  Normal  University, Shanghai, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;em3&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910546</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116294409" STOP_POS="116477904" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120503475" STOP_POS="120682281" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12910519</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALEN targeting the sequence of rat Lepr into SD embryos. The resulting mutation is a 18-bp insertion.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12910762</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Kit&lt;sup&gt;Ws&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kit&lt;sup&gt;Ws&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910763</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="32901615" STOP_POS="32978895" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="32554595" STOP_POS="32554606" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="35079269" STOP_POS="35079280" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="34901860" STOP_POS="34979384" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="34906043" STOP_POS="34984819" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12910762</CITATION_ID>
    <DESCRIPTION>A spontaneous mutant male with a large white spot and coat color dilution was identified in the BN/fMai colony in Yagi Memorial Park (kani-gun, Japan).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>12910940</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cdkn1b&lt;sup&gt;we&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cdkn1b&lt;sup&gt;we&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910941</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="169491273" STOP_POS="169496500" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="167760067" STOP_POS="167765177" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="168689043" STOP_POS="168694159" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="232962218" STOP_POS="232967323" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="171841705" STOP_POS="171846506" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_12910940</CITATION_ID>
    <DESCRIPTION>The multiple endocrine neoplasia (MEN)-like phenotype was initially identified in a Sprague Dawley rat-breeding colony and subsequently maintained by matings between affected and nonaffected littermates. Because cataracts are the first visible sign of the phenotype it was provisionally designated as "Sprague Dawley white eye." The abbreviation SDwe is used to denote animals expressing the mutant phenotype.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13204704</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Myo7a&lt;sup&gt;tnd&lt;/sup&gt;&lt;/i&gt;/Hubr</STRAIN_SYMBOL>
    <FULL_NAME>Wistar tornado rat</FULL_NAME>
    <ORIGINATION>Hubrecht Laboratory, Centre for Biomedical Genetics, 3584 CT Utrecht, The Netherlands.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Myo7a&lt;sup&gt;tnd&lt;/sup&gt;/Hubr</ALLELES>
    <ALLELE_RGD_IDS>13204705</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="161755110" STOP_POS="161825397" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="152392431" STOP_POS="152392431" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="163049850" STOP_POS="163049850" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="169206150" STOP_POS="169276706" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="155292620" STOP_POS="155362698" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13204704</CITATION_ID>
    <DESCRIPTION>Male Wistar founder rats  were mutagenized using ENU and mated with untreated female to establish F1 population. Selected F1 progeny were mated to produce F2 and then to breed induced mutation to homozygosity.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13204756</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(D13Hmgc1048-D13Hmgc1050)-&lt;i&gt;Pappa2&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pappa2&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13204758</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="73407385" STOP_POS="73683699" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="71117638" STOP_POS="71117642" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="76389150" STOP_POS="76660248" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="81303663" STOP_POS="81574402" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="74286881" STOP_POS="74379736" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13204756</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 5-bp deletion in exon 2 of the rat Pappa2 gene of SS.BN-(D13Hmgc1048-D13Hmgc1050)/Mcwi rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13204788</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(D13Hmgc1048-D13Hmgc1050)-&lt;i&gt;Pappa2&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pappa2&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13204789</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="73407385" STOP_POS="73683699" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="71117585" STOP_POS="71117644" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="76389150" STOP_POS="76660248" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="81303663" STOP_POS="81574402" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="74286881" STOP_POS="74379736" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13204788</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 60-bp deletion in exon 2 of the rat Pappa2 gene of SS.BN-(D13Hmgc1048-D13Hmgc1050)/Mcwi rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207339</RGD_ID>
    <STRAIN_SYMBOL>LH.LH-Chr 17&lt;sup&gt;LN&lt;/sup&gt;-(&lt;i&gt;Fancc&lt;sup&gt;rgdv551196202-C&lt;/sup&gt;-rs106387478&lt;/i&gt;)/Aek</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=824&gt;Rat Resource &amp; Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=824&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="50412360" STOP_POS="50412360" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="45716725" STOP_POS="45716725" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="946321" STOP_POS="47839901" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="939418" STOP_POS="939418" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="7228496" STOP_POS="7228496" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00824</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a fragment of chromosome 17 from the LH-Chr 17&lt;sup&gt;LN&lt;/sup&gt;/Aek from Fancc&lt;sup&gt;rgdv551196202-C&lt;/sup&gt; through rs106387478 transferred to the LH/MRrrcAek  background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207341</RGD_ID>
    <STRAIN_SYMBOL>LH.LH-Chr 17&lt;sup&gt;LN&lt;/sup&gt;-(&lt;i&gt;Fancc&lt;sup&gt;rgdv551196202-C&lt;/sup&gt;-rs107291522&lt;/i&gt;)/Aek</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=825&gt;Rat Resource &amp; Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=825&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="24136127" STOP_POS="24136127" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="23930421" STOP_POS="23930421" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="946321" STOP_POS="24556663" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="939418" STOP_POS="939418" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="7228496" STOP_POS="7228496" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00825</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a fragment of chromosome 17 from the LH-Chr 17&lt;sup&gt;LN&lt;/sup&gt;/Aek from Fancc&lt;sup&gt;rgdv551196202-C&lt;/sup&gt; through  rs107291522 transferred to the LH/MRrrcAek  background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207416</RGD_ID>
    <STRAIN_SYMBOL>LH.LH-Chr 17&lt;sup&gt;LN&lt;/sup&gt;-(&lt;i&gt;rgdv421102132&lt;sup&gt;T&lt;/sup&gt;-rgdv413679765&lt;sup&gt;T&lt;/sup&gt;&lt;/i&gt;)/Aek</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=826&gt;Rat Resource &amp; Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=826&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="30894361" STOP_POS="74169166" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00826</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a fragment of chromosome 17 from the LH-Chr 17&lt;sup&gt;LN&lt;/sup&gt;/Aek from Fancc&lt;sup&gt;rgdv551196202-C&lt;/sup&gt; through rs106387478 transferred to the LH/MRrrcAek  background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207488</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Chrnb4&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Chrnb4&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13207489</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="64312644" STOP_POS="64333319" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="55417583" STOP_POS="55437027" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="59610489" STOP_POS="59629073" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="58198875" STOP_POS="58198878" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="58586961" STOP_POS="58605545" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207488</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Chrnb4 gene of LEW/NCrl rat embryos. The resulting mutation is a 4-bp deletion of exon 4 in the Chrnb4 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207491</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Col3a1-loxP-eGFP-loxP-TurboRFP)Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-02-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207491</CITATION_ID>
    <DESCRIPTION>Bacterial artificial chromosome (BAC) Transgenic rats containing a Cre-inducible reporter switch from eGFP to TurboRFP under the control of the promoter of Col3a1 (BAC: CH230-401H12 )</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207492</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cd55&lt;sup&gt;em6Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-08-02)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd55&lt;sup&gt;em6Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13207493</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="44409574" STOP_POS="44438913" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="41884980" STOP_POS="41884984" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="47125156" STOP_POS="47153557" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="52177543" STOP_POS="52206137" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="43322246" STOP_POS="43348334" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207492</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a  4-bp deletion of exon 2 in the rat Cd55 gene of Crl:SD embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207494</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cd55&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd55&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13207495</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="44409574" STOP_POS="44438913" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="41857242" STOP_POS="41885966" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="47152655" STOP_POS="47152684" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="52177543" STOP_POS="52206137" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="43322246" STOP_POS="43348334" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207494</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a  22-bp deletion of exon 2 in the rat Cd55 gene of Crl:SD embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207497</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnj13&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnj13&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13207498</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="95509228" STOP_POS="95528400" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="88066091" STOP_POS="88066092" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="94486719" STOP_POS="94495333" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="94208941" STOP_POS="94224828" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="86206927" STOP_POS="86216659" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207497</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Kcnj13 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 1-bp insertion of exon 2 in the Kcnj13 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207501</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nlrp10&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nlrp10&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13207502</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="172357648" STOP_POS="172365205" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="162924483" STOP_POS="162924493" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="173521412" STOP_POS="173528969" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="180511615" STOP_POS="180519172" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="166411647" STOP_POS="166419204" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207501</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Nlrp10 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 11-bp deletion of exon 2 in the Nlrp10 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207503</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nlrp10&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nlrp10&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13207504</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="172357648" STOP_POS="172365205" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="162924489" STOP_POS="162924498" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="173521412" STOP_POS="173528969" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="180511615" STOP_POS="180519172" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="166411647" STOP_POS="166419204" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207503</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Nlrp10 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 10-bp deletion of exon 2 in the Nlrp10 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207507</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nlrp12&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nlrp12&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13207508</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="74848020" STOP_POS="74885945" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="65941549" STOP_POS="65941550" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="64506750" STOP_POS="64543908" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="63493575" STOP_POS="63521356" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="64242875" STOP_POS="64271212" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207507</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Nlrp12 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 2-bp deletion of exon 3 in the Nlrp12 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207509</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;P2rx1&lt;sup&gt;em7Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>P2rx1&lt;sup&gt;em7Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13207510</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="58117107" STOP_POS="58132167" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="57626713" STOP_POS="57626719" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="59566268" STOP_POS="59581328" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="59305737" STOP_POS="59320797" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="59889933" STOP_POS="59904985" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207509</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  P2rx1 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp deletion in Exon 2 of the P2rx1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207511</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(D13Rat151-D13Rat197)-Tg(Slc12a1-Ncf2-2A-Luc)26Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2017-08-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ncf2</ALLELES>
    <ALLELE_RGD_IDS>1309424</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207511</CITATION_ID>
    <DESCRIPTION>A transgenic rat created by Sleeping Beauty transposon system with proximal tubule-specific overexpression of Ncf2 and Luciferase via a self cleaving 2A peptide, under control of the Slc12a1 (also known as Nkcc2) promoter produced in the line 26 strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207513</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(Slc12a1-Ncf2-2A-Luc)-Ncf2&lt;sup&gt;em1&lt;/sup&gt;Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2017-08-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ncf2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>5144089</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="67505492" STOP_POS="67536015" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="64958217" STOP_POS="64958221" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="70229196" STOP_POS="70229200" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="67806516" STOP_POS="67834105" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207513</CITATION_ID>
    <DESCRIPTION>This is compound transgenic/mutant rat strain derived from the breeding of SS-Tg(Slc12a1-Ncf2-2A-Luc) and  SS-Ncf2em1Mcwi.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207514</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;ROSA26&lt;sup&gt;em1(Epac-SH187)Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-08-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207514</CITATION_ID>
    <DESCRIPTION>CRISPR/SpCas9 was used to knock in the Epac-SH187, Epac-based FRET sensor into the Rosa26 locus under the control of the endogenous promoter using an Ad2 splice acceptor.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207516</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Rag2&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;&lt;i&gt;Il2rg&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em2Mcwi&lt;/sup&gt;|Rag2&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10002792|12790711</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108357399" STOP_POS="108367186" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87907936" STOP_POS="87907945" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66398582" STOP_POS="66398582" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91191837" STOP_POS="91200134" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97851318" STOP_POS="97859615" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86764810" STOP_POS="86773438" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207516</CITATION_ID>
    <DESCRIPTION>This strain was produced by crossing of SD-Rag2em3Mcwi and SD-Il2rgem2Mcwi.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207518</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Hspa1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2018-05-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Hspa1b|Hspa1a|Hspa1l</ALLELES>
    <ALLELE_RGD_IDS>2840|1593284|1595925</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="3875411" STOP_POS="3877866" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="3859756" STOP_POS="3863800" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="3853496" STOP_POS="3860223" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="3855104" STOP_POS="3859148" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="3848843" STOP_POS="3855571" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="3870765" STOP_POS="3873221" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="2699707" STOP_POS="2701856" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="4877638" STOP_POS="4880112" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="4879998" STOP_POS="4965191" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="7032557" STOP_POS="7038454" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="6956234" STOP_POS="6962151" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="4802576" STOP_POS="7033025" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="3945716" STOP_POS="3959552" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="3955274" STOP_POS="3957748" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207518</CITATION_ID>
    <DESCRIPTION>CRISPR/SpCas9 was used to create indel mutations in Hspa1a, Hspa1b, Hspa1L in SHR/NCrl embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207525</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Spp1&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>spp1&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13207528</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="5613569" STOP_POS="5620695" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="5308885" STOP_POS="5315120" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="5312020" STOP_POS="5312025" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="6653086" STOP_POS="6658937" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207525</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Spp1 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 4-bp deletion in Exon 3 of the Spp1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207529</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Spp1&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Spp1&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13207530</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="5613569" STOP_POS="5620695" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="5308885" STOP_POS="5315120" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="6673686" STOP_POS="6679965" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="6653086" STOP_POS="6658937" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207529</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Spp1 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 5-bp deletion in Exon 3 of the Spp1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207537</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Cdh5-cre)2Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-08-04)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207537</CITATION_ID>
    <DESCRIPTION>Transgenic rat overexpressing Cre under the control of the Cdh5 (VECadherin) promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207551</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(Nphs2-cre/ERT2)4Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-08-04)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207551</CITATION_ID>
    <DESCRIPTION>Transgenic rat overexpressing tamoxifen inducible Cre/ERT2 under the control of the Nphs2 (Podocin) promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207560</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(Aqp2-cre/ERT2)4Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-08-04)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207560</CITATION_ID>
    <DESCRIPTION>Transgenic overexpressing tamoxifen inducible cre/ERT2 under the control of the Aquaporin 2 promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207563</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(Mylpf-cre/ERT2)22Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-08-04)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207563</CITATION_ID>
    <DESCRIPTION>Transgenic overexpressing tamoxifen inducible CreERT2 under the control of the Mylpf (also known ad Mlc2) promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13207595</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Tph1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tph1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13208230</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="106293695" STOP_POS="106314628" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="97157375" STOP_POS="97178415" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102669868" STOP_POS="102699442" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103746878" STOP_POS="103774100" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="97186071" STOP_POS="97207551" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13207595</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Tph1 gene of WKY/NCrl rat embryos. The resulting mutation is a 1-bp deletion in the exon 4 of the Tph1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208223</RGD_ID>
    <STRAIN_SYMBOL>LE-ROSA26&lt;sup&gt;em1(LTR-nLuc)Ottc&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=924&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=924&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00924</CITATION_ID>
    <DESCRIPTION>The CRISPR/Case9 knock-in rats have cre recombinase-dependent expression of  nanoluciferase under the control of HIV LTR promoter inserted to the rat ROSA26 locus. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208224</RGD_ID>
    <STRAIN_SYMBOL>LE-ROSA26 &lt;sup&gt;em1(CAG-Cas9)Ottc&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=833&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=833&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2025-08-29)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00833</CITATION_ID>
    <DESCRIPTION>The CRISPR/Case9 knock-in rats have cre recombinase-dependent expression of  Cas9 under the control of CAG promoter inserted to the rat ROSA26 locus. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208231</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Tph1&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tph1&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13208232</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="106293695" STOP_POS="106314628" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="97157375" STOP_POS="97178415" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102669868" STOP_POS="102699442" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103746878" STOP_POS="103774100" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="97186071" STOP_POS="97207551" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13208231</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Tph1 gene of WKY/NCrl rat embryos. The resulting mutation is a 1-bp insertion in the exon 4 of the Tph1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208517</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nfe2l2&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SD-&lt;i&gt;Nfe2l2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;/Nfe2l2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-08-09)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13208517</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALENs targeting the sequence TAGTCCTGGCGGTGGCAATTCCAAGTCCATCATGCTGAGGGCGGACGCTGCGCTA into Crl:SD Sprague Dawley rat embryos. The resulting mutation is a 41-bp deletion in exon 1.Founders were backcrossed with Crl:SD to get heterozygous offspring which were intercrossed and offspring maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208518</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nfe2l2&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SD-&lt;i&gt;Nfe2l2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;/Nfe2l2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-08-09)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nfe2l2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>9588549</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="81001529" STOP_POS="81031165" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="60621570" STOP_POS="60621610" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="62524893" STOP_POS="62524933" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="69041641" STOP_POS="69069190" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="58366693" STOP_POS="58394116" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13208518</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALENs targeting the sequence TAGTCCTGGCGGTGGCAATTCCAAGTCCATCATGCTGAGGGCGGACGCTGCGCTA into Crl:SD Sprague Dawley rat embryos. The resulting mutation is a 41-bp deletion in exon 1.Founders were backcrossed with Crl:SD to get heterozygous offspring which were intercrossed and offspring maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208519</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nfe2l2&lt;sup&gt;em1Mcwi+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SD-&lt;i&gt;Nfe2l2&lt;sup&gt;em1Mcwi+&lt;/sup&gt;&lt;/i&gt;/Nfe2l2&lt;sup&gt;em1Mcwi-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-08-09)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13208519</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALENs targeting the sequence TAGTCCTGGCGGTGGCAATTCCAAGTCCATCATGCTGAGGGCGGACGCTGCGCTA into Crl:SD Sprague Dawley rat embryos. The resulting mutation is a 41-bp deletion in exon 1.Founders were backcrossed with Crl:SD to get heterozygous offspring which were intercrossed and offspring maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208537</RGD_ID>
    <STRAIN_SYMBOL>HsdFfyb:WI</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Bioterio Central- Facultad de Farmacia y BioquÃ¿Â¿mica de la Universidad de Buenos Aires. Contact: Junin 956 8 piso Ciudad AutÃ¿Â¿noma de Buenos Aires, Argentina Tel/Fax: +54 11 5287 4811 Mail: bioterio@ffyb.uba.ar</ORIGINATION>
    <SOURCE>Bioterio Central - FFyB - Universidad de Bs As</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-08-11)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13208537</CITATION_ID>
    <DESCRIPTION>Descendants of rats from the Wistar Institute, Philadelphia, Pennsylvania then to Harlan (Indianapolis).Since 1995 maintained at Bioterio Central- Facultad de Farmacia y BioquÃ¿Â¿mica de la Universidad de Buenos Aires. Contact: Junin 956 8 piso Ciudad AutÃ¿Â¿noma de Buenos Aires, Argentina Tel/Fax: +54 11 5287 4811 Mail: bioterio@ffyb.uba.ar</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208540</RGD_ID>
    <STRAIN_SYMBOL>CrlFfyb:SD</STRAIN_SYMBOL>
    <FULL_NAME>Sprague Dawley</FULL_NAME>
    <ORIGINATION>Descendants of rats from the Charles River Laboratories (USA),then to Fvet at Buenos Aires University and since 2014 maintained at Bioterio Central of Facultad de Farmacia y Bioquimica de la Universidad de Buenos Aires. Junin 956 Ciudad Autonoma de Buenos Aires, Argentina</ORIGINATION>
    <SOURCE>Bioterio Central of Facultad de Farmacia y Bioquimica de la Universidad de Buenos Aires. Junin 956 Ciudad Autonoma de Buenos Aires, Argentina</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2024-09-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13208540</CITATION_ID>
    <DESCRIPTION>Descendants of rats from the Charles River Laboratories (USA),then to Fvet at Buenos Aires University and since 2014 maintained at Bioterio Central of Facultad de Farmacia y Bioquimica de la Universidad de Buenos Aires. Junin 956 Ciudad Autonoma de Buenos Aires, Argentina</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208571</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(Cyp11b2-cre/ERT2)2Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2019-04-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13208571</CITATION_ID>
    <DESCRIPTION>Transgenic overexpressing tamoxifen inducible cre/ERT2 under the control of the Cyp11b2 promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208576</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(Slc5a2-cre/ERT2)2Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-08-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13208576</CITATION_ID>
    <DESCRIPTION>Transgenic overexpressing tamoxifen inducible cre/ERT2 under the control of the Slc12a1 (Sglt2) promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208583</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(Ubc-Wisp2)2Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-08-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13208583</CITATION_ID>
    <DESCRIPTION>Transgenic overexpressing Wisp2 under the control of the Ubiqutin C promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208584</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(Ubc-Wisp2)3Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2017-08-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13208584</CITATION_ID>
    <DESCRIPTION>Transgenic overexpressing Wisp2 under the control of the Ubiqutin C promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208842</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ptgs2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ptgs2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13208843</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="64714063" STOP_POS="64722320" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="62165923" STOP_POS="62165975" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="67351230" STOP_POS="67356920" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="72315959" STOP_POS="72324483" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="64427288" STOP_POS="64432978" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13208842</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Ptgs2 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 53-bp deletion of exon 4 in the Ptgs2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13208844</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ptgs2&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ptgs2&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13208845</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="64714063" STOP_POS="64722320" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="62165974" STOP_POS="62165981" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="67351230" STOP_POS="67356920" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="72315959" STOP_POS="72324483" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="64427288" STOP_POS="64432978" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13208844</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Ptgs2 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 7-bp deletion of exon 4 in the Ptgs2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13210578</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lep&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lep&lt;sup&gt;em1&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13210580</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="58626529" STOP_POS="58640663" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="57661127" STOP_POS="57675262" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="56337695" STOP_POS="56351818" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="56085079" STOP_POS="56099209" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="55943837" STOP_POS="55945938" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13210578</CITATION_ID>
    <DESCRIPTION>This CRISPR/Cas9 model possesses a 3 bp(ATC) deletion resulting in the deletion of isoleucine at position 14.  The Lep mutant rats exhibited similar mutant phenotypes to Lep and Lepr null rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13210773</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;Fer1l6&lt;sup&gt;rgdv775925951-C&lt;/sup&gt;-D7Uwm27&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2017-09-07)</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="92058260" STOP_POS="92058524" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="98507649" STOP_POS="98507649" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13210773</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13210774</RGD_ID>
    <STRAIN_SYMBOL>ACI.BN-(&lt;i&gt;Fer1l6&lt;sup&gt;rgdv775925951-C&lt;/sup&gt;-D7Uwm28&lt;/i&gt;)/Shul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>mammary cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="92058260" STOP_POS="92058524" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="98507649" STOP_POS="98507649" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13210774</CITATION_ID>
    <DESCRIPTION>This congenic strain contains a region of BN/SsNHsd chromosome 7 transferred to the ACI/SegHsd strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13432148</RGD_ID>
    <STRAIN_SYMBOL>SS.ZUC-&lt;i&gt;Lepr&lt;sup&gt;fa-/-&lt;/sup&gt;&lt;/i&gt;/Slc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES>Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13432153</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13432148</CITATION_ID>
    <DESCRIPTION>SS.ZUC-Leprfa/Slc rats were generated as the result of an initial mating of a male Zucker rat (Japan SLC) heterozygous for the fa allele of Lepr with a female DahlS/JrSeac rat (Seac, Japan), followed by multiple rounds of backcrossing of the resulting progeny to the SS strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13432150</RGD_ID>
    <STRAIN_SYMBOL>SS.ZUC-&lt;i&gt;Lepr&lt;sup&gt;fa-/+&lt;/sup&gt;&lt;/i&gt;/Slc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES>Lepr|Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>3001|13432153</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13432150</CITATION_ID>
    <DESCRIPTION>SS.ZUC-Leprfa/Slc rats were generated as the result of an initial mating of a male Zucker rat (Japan SLC) heterozygous for the fa allele of Lepr with a female DahlS/JrSeac rat (Seac, Japan), followed by multiple rounds of backcrossing of the resulting progeny to the SS strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13432151</RGD_ID>
    <STRAIN_SYMBOL>SS.ZUC-&lt;i&gt;Lepr&lt;sup&gt;fa+/+&lt;/sup&gt;&lt;/i&gt;/Slc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity</RESEARCH_USE>
    <ALLELES>Lepr</ALLELES>
    <ALLELE_RGD_IDS>3001</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13432151</CITATION_ID>
    <DESCRIPTION>SS.ZUC-Leprfa/Slc rats were generated as the result of an initial mating of a male Zucker rat (Japan SLC) heterozygous for the fa allele of Lepr with a female DahlS/JrSeac rat (Seac, Japan), followed by multiple rounds of backcrossing of the resulting progeny to the SS strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13432199</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D3Wox20-D3Rat114&lt;/i&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cardiovascular &amp; Medical Sciences, BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13432199</CITATION_ID>
    <DESCRIPTION>Congenic sub-strains were generated by backcrossing male SHRSP.WKY-(D3Mgh16-D3Rat114)/Gcrc rats to SHRSP females. Progeny generated from this backcross were heterozygous throughout the original congenic interval. Brother X sister mating was carried out to generate sub-strains containing smaller congenic intervals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13432200</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D3Mgh16-D3Rat80&lt;/i&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cardiovascular &amp; Medical Sciences, BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13432200</CITATION_ID>
    <DESCRIPTION>Congenic sub-strains were generated by backcrossing male SHRSP.WKY-(D3Mgh16-D3Rat114)/Gcrc rats to SHRSP females. Progeny generated from this backcross were heterozygous throughout the original congenic interval. Brother X sister mating was carried out to generate sub-strains containing smaller congenic intervals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13432201</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D3Mgh16-D3Wox3&lt;/i&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cardiovascular &amp; Medical Sciences, BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13432201</CITATION_ID>
    <DESCRIPTION>Congenic sub-strains were generated by backcrossing male SHRSP.WKY-(D3Mgh16-D3Rat114)/Gcrc rats to SHRSP females. Progeny generated from this backcross were heterozygous throughout the original congenic interval. Brother X sister mating was carried out to generate sub-strains containing smaller congenic intervals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13432202</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D3Mgh16-rs65433898&lt;/i&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cardiovascular &amp; Medical Sciences, BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13432202</CITATION_ID>
    <DESCRIPTION>Congenic sub-strains were generated by backcrossing male SHRSP.WKY-(D3Mgh16-D3Rat114)/Gcrc rats to SHRSP females. Progeny generated from this backcross were heterozygous throughout the original congenic interval. Brother X sister mating was carried out to generate sub-strains containing smaller congenic intervals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13432203</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D3Mgh16-rs197649383&lt;/i&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cardiovascular &amp; Medical Sciences, BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13432203</CITATION_ID>
    <DESCRIPTION>Congenic sub-strains were generated by backcrossing male SHRSP.WKY-(D3Mgh16-D3Rat114)/Gcrc rats to SHRSP females. Progeny generated from this backcross were heterozygous throughout the original congenic interval. Brother X sister mating was carried out to generate sub-strains containing smaller congenic intervals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13432204</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.WKY-(&lt;i&gt;D3Mgh16-D3Mit10&lt;/i&gt;)/Gcrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cardiovascular &amp; Medical Sciences, BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13432204</CITATION_ID>
    <DESCRIPTION>Congenic sub-strains were generated by backcrossing male SHRSP.WKY-(D3Mgh16-D3Rat114)/Gcrc rats to SHRSP females. Progeny generated from this backcross were heterozygous throughout the original congenic interval. Brother X sister mating was carried out to generate sub-strains containing smaller congenic intervals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13437612</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Adamts16&lt;sup&gt;em1Bj&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adamts16&lt;sup&gt;em1Bj&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13437613</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="34258899" STOP_POS="34388952" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="32430681" STOP_POS="32430697" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="35067513" STOP_POS="35067529" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="36468949" STOP_POS="36599799" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="2559771" STOP_POS="2690663" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13437612</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs target sequence CCGCGGTTGCTTTGCGCTCTGGGTGCTGTTGCTGGCGCA into  Dahl S rat eggs as . The resulting mutation is a 17-bp  deletion of the sequence gctctgggtgctgttgc in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13441557</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Cx3cr1-cre/ERT2)3Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=858&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=858&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00858</CITATION_ID>
    <DESCRIPTION>This strain was generated by microinjection of LE embyos with a BAC DNA containing the Cx3cr1-cre/ERT2 transgene which is composed of cre/ERT2 recombinase gene driven by the rat genomic Cx3cr1promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13441560</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Galt&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Galt&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13441563</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13441560</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 2-base pair insertion mutation into  exon 6 in the rat Galt gene of Crl:SD embryos</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13446407</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Camk2a-cre/ERT2)/ZiRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=688&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=688&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2017-11-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00688</CITATION_ID>
    <DESCRIPTION>The hemizygous rats have random insertion of calcium/calmodulin-dependent protein kinase II alpha (Camk2a)- cre/ERT2 (tamoxifen inducible Cre recombinase) transgene in the genome. This transgenic  exhibits expression of cre/ERT2 fusion protein in neural populations where the mouse Camk2a promoter region found in the transgene is active.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13450922</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;GEPR-3&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=798&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=798&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>seizure</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00798</CITATION_ID>
    <DESCRIPTION>Genetically Epilepsy-Prone Rats (GEPR-3) have moderate levels of seizure predisposition. This colony,initially referred to as an AGS (audiogenic response score) colony, was bred to exhibit clonic convulsions (moderate seizures with an ARS of 3) following a single wild running phase in response to sound. Siezures model human generalized tonic/clonic seizures.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13451132</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Crb1&lt;sup&gt;m1&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Crb1&lt;sup&gt;m1&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13451133</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="53352932" STOP_POS="53540019" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="50801484" STOP_POS="50989261" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="56270519" STOP_POS="56462893" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="61292273" STOP_POS="61480872" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="52558317" STOP_POS="52725099" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13451132</CITATION_ID>
    <DESCRIPTION>This Brown Norway from Janvier rat strain spontaneously develops progressive focal retinal layer disorganization, loss of photoreceptors, cystic cavitation, and RMG abnormalities associated with early retinal vascular telangiectasia and late stage subretinal neovascularization. This phenotype bears reminiscent of human Macular telangiectasia 2. A deletion insertion mutation in exon 6 of the rat crb1 was identified to be responsible for this retinal phenotype.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13451538</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Dusp5&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dusp5&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13451539</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="262543774" STOP_POS="262557201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="252538408" STOP_POS="252555320" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="274245184" STOP_POS="274258595" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="281658075" STOP_POS="281671486" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="259754234" STOP_POS="259767645" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13451538</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the following sequence CAGGGCAGCCGC-CACtggcaGAAGCTGCGGGAGGA in exon 1 of the rat Dusp5 gene into FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;/Mcwi embryos. The resulting mutation is a 14 bp deletion and a 3 bp insertion between nucleotides 449 and 464 in Dusp5 mRNA that creates a frame shift mutation which is predicted to introduce a premature stop codon at amino acid 121.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13452382</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Htt&lt;sup&gt;*&lt;/sup&gt;)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>HTT</ALLELES>
    <ALLELE_RGD_IDS>68472</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13452382</CITATION_ID>
    <DESCRIPTION>This rat model was developed by  injection of SD embryos with  construct containing rat huntingtin cDNA fragment with 51 CAG repeats (from HD  patient) under control of the native rat huntingtin promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13452406</RGD_ID>
    <STRAIN_SYMBOL>SHR/NHsdAkr</STRAIN_SYMBOL>
    <FULL_NAME>Spontaneously Hypertensive Rat</FULL_NAME>
    <ORIGINATION>University of Akron breeding colonies, Akron, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13452406</CITATION_ID>
    <DESCRIPTION>SHR strain obtained from Harlan Sprague-Dawley (Indianapolis, IN) and maintained at the  University of Akron breeding colonies, Akron, Ohio</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13452407</RGD_ID>
    <STRAIN_SYMBOL>WKY/NHsdAkr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Akron breeding colonies, Akron, Ohio.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13452407</CITATION_ID>
    <DESCRIPTION>These animals were bought from Harlan Indianapolis, Indiana U.S.A. and maintained at the University of Akron breeding colonies, Akron, Ohio.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13462044</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Thy1-GCaMP6f)9Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Janelia Research Campus and Princeton University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=829&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00829</CITATION_ID>
    <DESCRIPTION>Pronuclear injection was used to introduce an expression cassette containing the Thy-1 enhancer and GCaMP6f protein coding sequence. GCaMP6f is a genetically encoded calcium indicator.  It is a synthetic fusion of green fluorescent protein, calmodulin, and M13, a peptide sequence from myosin light-chain kinase.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13462045</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Thy1-GCaMP6f)7Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Janelia Research Campus and Princeton University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=830&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-01-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00830</CITATION_ID>
    <DESCRIPTION>Pronuclear injection was used to introduce an expression cassette containing the Thy-1 enhancer and GCaMP6f protein coding sequence. GCaMP6f is a genetically encoded calcium indicator.  It is a synthetic fusion of green fluorescent protein, calmodulin, and M13, a peptide sequence from myosin light-chain kinase.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13464263</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Il2rg&lt;sup&gt;em1Iexas&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1295&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1295&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2018-01-02)</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES>Il2rg&lt;sup&gt;em1Iexas&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13464264</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66395330" STOP_POS="66399026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13464263</CITATION_ID>
    <DESCRIPTION>This strain was established by CRISPR/Cas9 targeting rat Il2rg gene using electroporation. background strain: F344/Jcl. This strain shows severe combined immunodeficiency (SCID) caused by 5-bp deletion of Il2rg gene. This strain grows normally under SPF condition.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13464268</RGD_ID>
    <STRAIN_SYMBOL>GH/Htru</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1293&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1293&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2018-01-02)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13464268</CITATION_ID>
    <DESCRIPTION>University of Otago Medical School from rats of Wistar origin imported from England in 1930. Selection for high blood pressure started by Smirk in 1955. A number of sublines have been developed. Closely related to strain AS (Heslop and Phelan 1973). Characteristics Develops hypertension, cardiac hypertrophy and vascular disease (Phelan 1968, Simpson and Phelan 1984, Simpson et al, 1994).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13464270</RGD_ID>
    <STRAIN_SYMBOL>Seac:LIS</STRAIN_SYMBOL>
    <FULL_NAME>Lister  Rat, Sea:Lister Hooded</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1272&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2018-01-02)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13464270</CITATION_ID>
    <DESCRIPTION>In 1990, this strain was introduced from Harlan Olac (UK) to Seiwa Institute of Experimental Animals. Then this strain was introduced to KYUDO Company in 2004.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13464272</RGD_ID>
    <STRAIN_SYMBOL>CrljJclKud:SD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1271&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1271&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2018-01-02)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13464272</CITATION_ID>
    <DESCRIPTION>In 2004, this strain was introduced from CLEA Japan,Inc to KYUDO company. This strain was maintained and supplied as the SPF animal until April 2016.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13464273</RGD_ID>
    <STRAIN_SYMBOL>JclKud:WI</STRAIN_SYMBOL>
    <FULL_NAME>Wistar rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1270&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1270&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2018-01-02)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13464273</CITATION_ID>
    <DESCRIPTION>In 1977, this strain was introduced from CLEA Japan,Inc to KYUDO company. This strain was maintained and supplied as the SPF animal until April 2016.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13464320</RGD_ID>
    <STRAIN_SYMBOL>STOCK &lt;i&gt;Aspa&lt;sup&gt;em34Kyo&lt;/sup&gt;  Hcn1&lt;sup&gt;A354V&lt;/sup&gt;&lt;/i&gt;/Kyo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1273&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1273&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Aspa&lt;sup&gt;em34Kyo&lt;/sup&gt;|Hcn1&lt;sup&gt;A354V&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11564348|13464319</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13464320</CITATION_ID>
    <DESCRIPTION>This double mutant strain was established by crossing WTC/Kyo (NBRP Rat No. 0020) and F344-&lt;i&gt;Aspa&lt;sup&gt;em34Kyo&lt;/sup&gt;&lt;/i&gt; (NBRP Rat No. 0806). WTC/Kyo has a missense mutation (Hcn1A354V) in Hcn1 (Hyperpolarization-activated cyclic nucleotide-gated channel 1) gene and F344-&lt;i&gt;Aspa&lt;sup&gt;em34Kyo&lt;/sup&gt;&lt;/i&gt; has a 16-bp deletion in the exon4 of Aspa (Aspartoacylase) gene (c.622_637del).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13464326</RGD_ID>
    <STRAIN_SYMBOL>LE.W-Tg(Slc32a1-YFP*)1Yyan/Vip</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1281&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1281&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2018-01-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13464326</CITATION_ID>
    <DESCRIPTION>The original strain, W-Tg(Slc32a1-YFP*)1Yyan (NBRP No.0554 rat), was established at National Institute for Physiological Sciences in 2004, thereafter introduced to Gunma University in 2006 &amp;#65288;Uematsu et al. Cerebral Cortex (2008). This original strain rats were was crossed with Long-Evans rat (Iar:Long-Evans) for 10 generations to establish the congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13464327</RGD_ID>
    <STRAIN_SYMBOL>WKY.Cg-&lt;i&gt;clest&lt;/i&gt;/Iet</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1269&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1269&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-01-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13464327</CITATION_ID>
    <DESCRIPTION>When the depositor (The Institute of Environmental Toxicology ) conducted mating experiment using male Crl:CD(SD) rats,  the offsprings of backcrossed-generation showed multiple malformations such as ectrodactylism, cleft palate or lip in 2013. These phenotype might be inherited in an autosomal recessive pattern. Therefore the congenic strain was established using WKY strain as the recipient strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13464329</RGD_ID>
    <STRAIN_SYMBOL>FPL/Iet</STRAIN_SYMBOL>
    <FULL_NAME>Fused pulmonary lobes, FPL</FULL_NAME>
    <ORIGINATION>The Institute of Environmental Toxicology</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1268&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2023-09-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Frem2&lt;sup&gt;fpl&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13464330</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="139753055" STOP_POS="139891046" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="137637371" STOP_POS="137637371" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="142782178" STOP_POS="142782178" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="162430795" STOP_POS="162568910" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="142464169" STOP_POS="142604059" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13464329</CITATION_ID>
    <DESCRIPTION>This spontaneous mutant strain wa found in a colony of Jcl:Wistar strain at the Institute of Environmental Toxicology in 1978: 3 rats out of 13 rats showed fused right pulmonary lobes with reduction deformity of middle pulmonary lobes. These rats also had  the syndactylism or paten tof the eyelid. It was difficult to maintain this strain in homozygous condition, mating system has been changed to sib mating between heterozygous rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13503336</RGD_ID>
    <STRAIN_SYMBOL>W;Cg-&lt;i&gt;Acr&lt;sup&gt;tm1Osb&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Acr KO, Acr {tm1 Osb}</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1294&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1294&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-01-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13503336</CITATION_ID>
    <DESCRIPTION>After homologous recombination using ES cells derived from hybrid (mix) breed of Slc:Wistar (female) and F344/NSlc (male), Acr KO strain was established by GLT at Osaka University. The genomic region including exon 1 to exon 3 is replaced by Neo resistance gene. After mating with Slc:Wistar, this strain is maintained by sib mating or with Slc:Wistar rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13506176</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nox4&lt;sup&gt;em2&lt;/sup&gt;Ncf2&lt;sup&gt;em1&lt;/sup&gt;Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2018-11-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nox4&lt;sup&gt;em2Mcwi&lt;/sup&gt;|Ncf2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>4139868|5144089</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150313736" STOP_POS="150491480" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="67505492" STOP_POS="67536015" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="64958217" STOP_POS="64958221" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="70229196" STOP_POS="70229200" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="150861996" STOP_POS="150862003" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="75200283" STOP_POS="75200287" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="67806516" STOP_POS="67834105" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143415816" STOP_POS="143603554" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13506176</CITATION_ID>
    <DESCRIPTION>Breeding together of SS-Nox4em2Mcwi (RGDID: 4139883) and SS-Ncf2em1Mcwi (RGDID: 5144104), both models  were generated by ZFN mutagenesis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13506177</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sdha&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2018-01-31)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sdha&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13506178</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="30764553" STOP_POS="30789523" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="28941814" STOP_POS="28941824" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="31545631" STOP_POS="31570601" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="32971779" STOP_POS="32996749" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="29739359" STOP_POS="29764329" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13506177</CITATION_ID>
    <DESCRIPTION>CRISPR/SpCas9  targeting was used to introduce an 11-bp putative frame-shift deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13506737</RGD_ID>
    <STRAIN_SYMBOL>GK</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13506737</CITATION_ID>
    <DESCRIPTION>The Goto-Kakizaki (GK) rat is a non-obese Wistar substrain which develops Type 2 diabetes mellitus early in life. The model was developed by Goto and Kakizaki at Tohoku University, Sendai, Japan in 1975. The GK line was established by repeated inbreeding from Wistar rats selected at the upper limit of normal distribution for glucose tolerance. Repeated selection of rats with tendency to lowest glucose tolerance resulted in clear-cut glucose intolerance after five generations.Until the end of 1980s, GK rats were initiated with breeding pairs in several places and also commercially available  from Japanese breeders Charles River Japan, Yokohama, Oriental Yeast, Tokyo, Clea Japan Inc., Osaka (GK/Clea), Japan SLC, Shizuoka (GK/SLC), Takeda Lab Ltd., Osaka (GK/Taked), and from Taconic, USA (GK/Mol/Tac).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13506738</RGD_ID>
    <STRAIN_SYMBOL>GK/Par</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13506738</CITATION_ID>
    <DESCRIPTION>The Goto-Kakizaki (GK) rat is a non-obese Wistar substrain which develops Type 2 diabetes mellitus early in life. The model was developed by Goto and Kakizaki at Tohoku University, Sendai, Japan in 1975. The GK line was established by repeated inbreeding from Wistar rats selected at the upper limit of normal distribution for glucose tolerance. Repeated selection of rats with tendency to lowest glucose tolerance resulted in clear-cut glucose intolerance after five generation.In 1988, GK/Par substrain was established in Paris, France by initiating breeding pairs F35 from Japanese colonies .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13506739</RGD_ID>
    <STRAIN_SYMBOL>GK/Jcl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/en/products/diabetes/item_a0130&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/en/products/diabetes/item_a0130&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13506739</CITATION_ID>
    <DESCRIPTION>The Goto-Kakizaki (GK) rat is a non-obese Wistar substrain which develops Type 2 diabetes mellitus early in life. The model was developed by Goto and Kakizaki at Tohoku University, Sendai, Japan in 1975. The GK line was established by repeated inbreeding from Wistar rats selected at the upper limit of normal distribution for glucose tolerance. Repeated selection of rats with tendency to lowest glucose tolerance resulted in clear-cut glucose intolerance after five generations.This strain was introduced from Tohoku University, and CLEA Japan Inc started its production and supply as GK/Jcl.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13506831</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;P2rx7&lt;sup&gt;em10Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-02-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>P2rx7&lt;sup&gt;em10Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13792805</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="39550531" STOP_POS="39594984" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="33917656" STOP_POS="33917666" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="39353613" STOP_POS="39396042" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="41242368" STOP_POS="41808755" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="35074025" STOP_POS="35117152" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13506831</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  P2rx7 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is an  11-bp putative frame-shift deletion in exon 2</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13506832</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;P2rx7&lt;sup&gt;em13Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>P2rx7&lt;sup&gt;em13Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13792806</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="39550531" STOP_POS="39594984" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="33917654" STOP_POS="33917663" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="39353613" STOP_POS="39396042" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="41242368" STOP_POS="41808755" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="35074025" STOP_POS="35117152" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13506832</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  P2rx7 gene of  SS/JrHsdMcwi rat embryos. The resulting mutation is an  10-bp putative frame-shift deletion in exon 2</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13506918</RGD_ID>
    <STRAIN_SYMBOL>F344/N</STRAIN_SYMBOL>
    <FULL_NAME>Fischer</FULL_NAME>
    <ORIGINATION>NIH Autoimmune Rat Model Repository and Development Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13506918</CITATION_ID>
    <DESCRIPTION>Curtiss and Dunning 1920 at Columbia University Institute for Cancer Research, To National Institutes of Health in 1951 (Hansen et al 1982). Subsequent sublines from  NIH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13506919</RGD_ID>
    <STRAIN_SYMBOL>F344/Nctr</STRAIN_SYMBOL>
    <FULL_NAME>Fischer</FULL_NAME>
    <ORIGINATION>National Center for Toxicological Research, FDA.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13506919</CITATION_ID>
    <DESCRIPTION>Curtiss and Dunning 1920 at Columbia University Institute for Cancer Research, To National Center for Toxicological Research, FDA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13508588</RGD_ID>
    <STRAIN_SYMBOL>WI</STRAIN_SYMBOL>
    <FULL_NAME>Wistar rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13508588</CITATION_ID>
    <DESCRIPTION>The Wistar rat is an outbred albino rat. This breed was developed at the Wistar Institute in 1906 for use in biological and medical research, and is notably the first rat developed to serve as a model organism.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13513909</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Ren2)27&lt;sup&gt;-/-&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Genome Research, University of Edinburgh, UK</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13513909</CITATION_ID>
    <DESCRIPTION>This is a littermate wild type control strain for SD-Tg(Ren2)27 (RGD:629501), which was generated by the mouse Ren2 renin gene along with its 5' and 3' flanking sequences being microinjected into fertilized eggs from a Hannover Sprague-Dawley (SD) background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13524863</RGD_ID>
    <STRAIN_SYMBOL>LEC/Crlj</STRAIN_SYMBOL>
    <FULL_NAME>Long Evans Cinnamon</FULL_NAME>
    <ORIGINATION>Japan Charles River Inc. (Yokohama, Japan)</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13524863</CITATION_ID>
    <DESCRIPTION>The LEC/Crlj is available at Japan Charles River Inc. (Yokohama, Japan) since 1991 from  the Center for Experimental Plants and Animals, Hokkaido University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13524998</RGD_ID>
    <STRAIN_SYMBOL>UPL</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13524998</CITATION_ID>
    <DESCRIPTION>In 1989, a femal sprague-Dawley rat with spontaneous cataracts was observed in the Upjohn Pharmaceuticals Limited Tsukuba Research Laboratory colony. The cataract was demonstrated to be hereditary and it was determined that there are two cataract types with different onset ages.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13525002</RGD_ID>
    <STRAIN_SYMBOL>Gunn rats</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>segregating_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13525002</CITATION_ID>
    <DESCRIPTION>This mutation was   observed for the first time in the breeding stock of the rat colony of the Connaught Laboratories in 1934. It is of Wistar origin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13592602</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(LRRK2*G2019S)418Rwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=776&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=776&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2018-05-14)</AVAILABILITY>
    <RESEARCH_USE>Parkinson's Disease</RESEARCH_USE>
    <ALLELES>LRRK2</ALLELES>
    <ALLELE_RGD_IDS>1353141</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00776</CITATION_ID>
    <DESCRIPTION>These rats were created using BAC constructs consisting of the entire 144kb human LRRK2 locus containing the G2019S mutation and fused to a YPet reporter tag.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13592603</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(LRRK2)302Rwn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=778&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=778&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2018-05-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>LRRK2</ALLELES>
    <ALLELE_RGD_IDS>1353141</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00778</CITATION_ID>
    <DESCRIPTION>These rats were created using BAC constructs consisting of the entire 144kb human wild type LRRK2 locus fused to a YPet reporter tag.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13592604</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(LRRK2*G2019S)416Rwm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=785&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=785&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2018-05-14)</AVAILABILITY>
    <RESEARCH_USE>Parkinson's Disease</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00785</CITATION_ID>
    <DESCRIPTION>These rats were created using BAC constructs consisting of the entire 144kb human LRRK2 locus containing the G2019S mutation and fused to a YPet reporter tag.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13592605</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(CAG-loxP-STOP-loxP-ZsGreen)561Bryd</STRAIN_SYMBOL>
    <FULL_NAME>F344-Tg(CAG-loxP-STOP-loxP-ZsGreen)561</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=797&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=797&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2019-03-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00797</CITATION_ID>
    <DESCRIPTION>The transgene consists of a SpeI fragment from plasmid pCAG-loxPSTOPloxP-ZsGreen (Addgene plasmid #51269, donated by Pawel Pelczar). Hemizygous animals contain approximately 4 copies of the transgene integrated at a site on Chromosome 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13602097</RGD_ID>
    <STRAIN_SYMBOL>LE.Cg-(ROSA26) &lt;sup&gt;em1(CAG-Cas9*D10A)Ottc&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=834&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=834&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00834</CITATION_ID>
    <DESCRIPTION>This mutant strain was created using highly efficient CRISPR-Cas9-mediated homology-directed repair (HDR) in rat spermatogonial stem cell cultures. The CRISPR/Case9 knock-in rats have cre recombinase-dependent expression of CRISPR associated protein 9 (Cas9) catalytic mutant protein D10A under the control of CAG promoter inserted to the rat ROSA26 locus. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.The resulting mutant rats in Prague-Dawley background was backcrossed with WT LE for three or four generations for studies.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13628730</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Il2rg&lt;sup&gt;em1Ang&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre de Recherche en Transplantation et Immunologie UMR1064, INSERM, University de Nantes, Nantes, France.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em1Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13628731</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66398441" STOP_POS="66398520" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71168483" STOP_POS="71168562" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13628730</CITATION_ID>
    <DESCRIPTION>TALEN targeting the 2nd exon of rat Il2rg gene was designed and mRNA coding these TALEN was microinjected into Crl:SD embyo.This strain carrying an 80 bp deletion generated a premature stop codon in the 3rd exon. No Il2rg protein was detected by western blot.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13673907</RGD_ID>
    <STRAIN_SYMBOL>NMcwiWfsm:HS</STRAIN_SYMBOL>
    <FULL_NAME>Heterogeneous stock</FULL_NAME>
    <ORIGINATION>Department of Internal Medicine, Molecular Medicine
Wake Forest Baptist Medical Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13673907</CITATION_ID>
    <DESCRIPTION>These HS rats were derived from NMcwi:HS, used to be maintained by  Dr. Solberg Woods at Medical College of Wisconsin and now are maintained at Wake Forest Baptist Medical Center by Dr. Solberg Woods's Laboratory starting in 2017.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13702080</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ahr&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Kansas Medical Center</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=831&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2019-01-21)</AVAILABILITY>
    <RESEARCH_USE>Toxicology, reproduction, cancer</RESEARCH_USE>
    <ALLELES>Ahr&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13702081</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="57961423" STOP_POS="57998901" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="52234089" STOP_POS="52271568" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="54963990" STOP_POS="55001806" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="64589066" STOP_POS="64624078" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="54205104" STOP_POS="54240268" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00831</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 targeted deletion of the Ahr basic helix loop helix DNA binding domain of the rat Ahr was injected into the embyos of outbred HsdHot:SD. The gRNA was targeted to Exon 2 of the Ahr gene, which encodes the bHLH DNA binding domain (target sequence: CTTCTAAACGACACAGAGACCGG; corresponding to NM_001308254). The established Ahr null strain lacks responsiveness to Ahr ligands.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13702084</RGD_ID>
    <STRAIN_SYMBOL>BBDP.BBDR-&lt;i&gt;Gimap5&lt;/i&gt;/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Philippe Poussier,Sunnybrook Research Institute/University of Toronto</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gimap5</ALLELES>
    <ALLELE_RGD_IDS>628871</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13702084</CITATION_ID>
    <DESCRIPTION>To generated Gimap5 congenic BBDP/WorSunn rats, the laboratory introgressed the wild-type Gimap5 locus derived from BBDR (BBDR/Wor) rats (Biomedical Research Models) into BBDP/WorSunn rats. Briefly, BBDP/WorSunn and BBDR/Wor rats were crossed, and the resulting F1 animals were backcrossed to BBDP/WorSunn rats. This step was followed by 10 more, marker- assisted backcrosses of Gimap5 heterozygous progeny to BBDP/WorSunn rats. After the eleventh backcross, nonlymphopenic rats were intercrossed, and their progeny homozygous for wild-type Gimap5 were selected for establishing the congenic non-lymphopenic BBDP/WorSunn line (also called BBDP/WorSunn.BBDR-Iddm2).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13702085</RGD_ID>
    <STRAIN_SYMBOL>BBDP.BBDR-Gimap5, WF-(&lt;i&gt;D13Rat124-D13Mgh5&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Medicine and Immunology, University of Toronto, Toronto, Ontario, Canada</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=791&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2019-03-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ptprc|Gimap5</ALLELES>
    <ALLELE_RGD_IDS>3451|628871</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00791</CITATION_ID>
    <DESCRIPTION>The Gimap5 congenic BBDP/WorSunn rats (BBDP.BBDR-Gimap5/Sunn) were corssed with the BBDP/WorSunn.WF-CD45 inbred line (BBDP.WF-(D13Rat124-D13Mgh5)/Sunn)  to develop an inbred BBDP/WorSunn strain that would be congenic for both wild type Gimap5, hence non T lymphopenic (and consequently diabetes resistant), and for the WF-derived CD45.2 (RT7) allele (the original BBDP/WorSunn strain carries the CD45.1 allele).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13703119</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lamp2&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>State Key Laboratory of Cancer Biology, National Clinical Research Centre for Digestive Diseases and Xijing Hospital of Digestive Diseases, Fourth Military Medical University, Xi'an, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lamp2&lt;sup&gt;em1&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13703121</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="122038734" STOP_POS="122087745" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="117173097" STOP_POS="117222090" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="124722628" STOP_POS="124766079" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="124809053" STOP_POS="124852509" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="6908285" STOP_POS="6951772" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13703119</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALEN targeting exon 2 of rat Lamp2  into SD embryos. The resulting mutation is a 2-bp deletion and results in knockout of Lamp2 protein in Lamp2 y/- male.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13781890</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Rnaset2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rnaset2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13781891</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="55133532" STOP_POS="55150701" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="52576344" STOP_POS="52603151" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="53174879" STOP_POS="53192048" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="54425133" STOP_POS="54442302" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="47227491" STOP_POS="47244660" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13781890</CITATION_ID>
    <DESCRIPTION>Two pairs of CRISPR guide RNAs were designed to cleave together to delete all 9 exons of RNaseT2. The CRISPR guide RNA and Cas9 mRNA mixtures were microinjected into the pronuclei of fertilized embryos of Sprague-Dawley rats and transferred to pseudopregnant female rats. WT, heterozygous and homozygous (KO) rats were born in the expected Mendelian ratio, and homozygous RNaseT2 KO rats were viable and fertile.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13782128</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Pde4b&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/pde4b-knockout-rat-tgra7210&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/pde4b-knockout-rat-tgra7210&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2018-08-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pde4b&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13782129</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="122028956" STOP_POS="122598267" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116799819" STOP_POS="117369155" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="121759236" STOP_POS="122136814" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="125623815" STOP_POS="126001128" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="123158156" STOP_POS="123533877" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13782128</CITATION_ID>
    <DESCRIPTION>These ZFN mutant rats were produced by injecting zinc finger nuclease targeting exon 1 of rat Pde4b into Sprague Dawley embryos. The 16-bp frameshift deletion (AGCGGCGTCGCTTCAC) in exon 1  in rat was created in the mutant founders.   These mutant founders were backcrossed with Sprague Dawley to produce heterozygous offspring, which were then intercrossed to produce homozygous and heterozygous offspring.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13782146</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Bace1&lt;sup&gt;em1Sage-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SD-&lt;i&gt;Bace1&lt;sup&gt;em1Sage-&lt;/sup&gt;&lt;/i&gt;/&lt;i&gt;Bace1&lt;sup&gt;em1Sage-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bace1&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13782148</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="55039152" STOP_POS="55039289" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="46142434" STOP_POS="46142571" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="50140402" STOP_POS="50140539" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="48766315" STOP_POS="48766452" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="48817824" STOP_POS="48839681" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13782146</CITATION_ID>
    <DESCRIPTION>Bace1 (-/-) rats were generated by SAGE Labs using zinc-finger nuclease (ZFN) technology to create a 137-base pair deletion spanning the translation initiation start site in exon 1 of the rat Bace1 gene, corresponding to chr8:48,766,315-48,766,452 (RGSC 5.0/rn5 assembly)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13782163</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Snca&lt;sup&gt;tm1(SNCA*)Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/in-vivo-models/knockout-rats/all-products/alpha-synuclein-a53t-knock-in-rat&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/in-vivo-models/knockout-rats/all-products/alpha-synuclein-a53t-knock-in-rat&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2018-08-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13782163</CITATION_ID>
    <DESCRIPTION>This model contains a knockin of the A53T-mutated SNCA gene deeming the rat SNCA gene non-functional. The knockin contains humanized amino acids for the region spanning amino acids 53-122. The resulting model expresses a humanized A53T alpha-synuclein protein without endogenous rat alpha-synuclein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13782164</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Snca&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/alpha-synuclein-knockout-rat&gt; Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/alpha-synuclein-knockout-rat&gt; Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2018-08-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13782164</CITATION_ID>
    <DESCRIPTION>This model contains a deletion of the endogenous rat SNCA gene, encoding the alpha-synuclein protein. This model was generated using the CRISPR/Cas9 genome targeting strategy.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13782280</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnj1&lt;sup&gt;em1Kasu+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Departments  of Cardiovascular Diseases,  Merck   Research Laboratories,  Merck&amp;Co.,Inc</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13782280</CITATION_ID>
    <DESCRIPTION>Zinc Finger Nuclease (ZFN) was utilized to knockout rat Kcnj1 function. ZFN constructs targeting the gene were designed and purchased from Sigma Aldrich (St. Louis, MO, USA). The targeting site sequence is CTCAAGTGACCATAGGTTACGgattcaGGTTTGTGAC (lower case represents the ZFN cleavage site). Kcnj1 knockout founders were generated by microinjection of ZFN mRNAs into single-cell SS (from Harlan) rat embryos. The resulting mutation is 209 bp deletion from G225 to G433, leading to frameshift and premature termination of Kcnj1 protein. This strain is the wild type littermate from heterozygous cross.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13782351</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnj1&lt;sup&gt;em1Kasu+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Departments  of Cardiovascular Diseases,  Merck   Research Laboratories,  Merck&amp;Co.,Inc</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnj1&lt;sup&gt;em1Kasu&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13782352</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="39014822" STOP_POS="39066716" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="30779883" STOP_POS="30808607" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="33490280" STOP_POS="33519127" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="33453597" STOP_POS="33454750" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="32158243" STOP_POS="32162370" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13782351</CITATION_ID>
    <DESCRIPTION>Zinc Finger Nuclease (ZFN) was utilized to knockout rat Kcnj1 function. ZFN constructs targeting the gene were designed and purchased from Sigma Aldrich (St. Louis, MO, USA). The targeting site sequence is TCAAGTGACCATAGGTTACGgattcaGGTTTGTGAC (lower case represents the ZFN cleavage site). Kcnj1 knockout founders were generated by microinjection of ZFN mRNAs into single -cell SS (from Harlan) rat embryos. The resulting mutation is 209 bp deletion from G225 to G433, leading to frameshift and premature termination of Kcnj1 protein in homozygotes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13782353</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnj1&lt;sup&gt;em1Kasu-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Departments  of Cardiovascular Diseases,  Merck   Research Laboratories,  Merck&amp;Co.,Inc</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnj1&lt;sup&gt;em1Kasu&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13782352</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="39014822" STOP_POS="39066716" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="30779883" STOP_POS="30808607" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="33490280" STOP_POS="33519127" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="33453597" STOP_POS="33454750" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="32158243" STOP_POS="32162370" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13782353</CITATION_ID>
    <DESCRIPTION>Zinc Finger Nuclease (ZFN) was utilized to knockout rat Kcnj1 function. ZFN constructs targeting the gene were designed and purchased from Sigma Aldrich (St. Louis, MO, USA). The targeting site sequence is CTCAAGTGACCATAGGTTACGgattcaGGTTTGTGAC (lower case represents the ZFN cleavage site). Kcnj1 knockout founders were generated by microinjection of ZFN mRNAs into single-cell SS (from Harlan) rat embryos. The resulting mutation is 209 bp deletion from G225 to G433, leading to frameshift and premature termination of Kcnj1 protein in homozygotes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13782371</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cacna1f &lt;sup&gt;csnb&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>congenital stationary night blindness rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cacna1f &lt;sup&gt;csnb&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13782372</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="17539992" STOP_POS="17568308" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="14868096" STOP_POS="14896413" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="15712709" STOP_POS="15741135" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="16504174" STOP_POS="16532670" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="26908850" STOP_POS="26937165" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13782371</CITATION_ID>
    <DESCRIPTION>A naturally-occurring mutation in  Cacna1f was identified in a male Sprague Dawley rat with the phenotype of congenital stationary night blindness.Sequence analysis revealed a point mutation of C to T at position 2941, which changes codon 981 from arginine (CGA) to a stop codon (TGA). This R981Stop point mutation was predicted to lead to a version of protein shortened by a total of 999 amino acids, and missing the C-terminal and, in particular, part of the third and all of the fourth ion transport domains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792570</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Oprl1&lt;sup&gt;m1Hubr+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hubrecht Laboratory, Utrecht, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Oprl1&lt;sup&gt;m1Hubr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13792571</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="189209495" STOP_POS="189225406" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="168831934" STOP_POS="168839920" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="177223779" STOP_POS="177231663" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="180932344" STOP_POS="180943574" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="170869862" STOP_POS="170873417" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792570</CITATION_ID>
    <DESCRIPTION>The original mutants were created by target-selected ENU-induced mutagenesis in a Brown Norway background. The animals were outcrossed for two generations on a Brown Norway background.  they were subsequently backcrossed on a Wistar (Crl:WI) background for four generations. Backcrossings were performed to eliminate possible additional mutations induced by ENU-mutagenesis. Heterozygous oprl1+/- rats were crossed to generate the experimental animals. A  C to G transversion at position 3657 in the oprl1 gene (ENSRNOG00000016768), resulting into a premature stop codon (TAC&gt;TAG) in the third exon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792572</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Oprl1&lt;sup&gt;m1Hubr-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>NOPr knockout rat</FULL_NAME>
    <ORIGINATION>Hubrecht Laboratory, Utrecht, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Oprl1&lt;sup&gt;m1Hubr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13792571</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="189209495" STOP_POS="189225406" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="168831934" STOP_POS="168839920" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="177223779" STOP_POS="177231663" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="180932344" STOP_POS="180943574" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="170869862" STOP_POS="170873417" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792572</CITATION_ID>
    <DESCRIPTION>The original mutants were created by target-selected ENU-induced mutagenesis in a Brown Norway background. The animals were outcrossed for two generations on a Brown Norway background.  they were subsequently backcrossed on a Wistar (Crl:WI) background for four generations. Backcrossings were performed to eliminate possible additional mutations induced by ENU-mutagenesis. Heterozygous oprl1+/- rats were crossed to generate the experimental animals. A  C to G transversion at position 3657 in the oprl1 gene (ENSRNOG00000016768), resulting into a premature stop codon (TAC&gt;TAG) in the third exon.NOPr is completely absent in homozygous mutants.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792573</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lep&lt;sup&gt;em1Sage+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com/leptin-knockout-rat-8212-kilorat-8482-tgra3780&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com/leptin-knockout-rat-8212-kilorat-8482-tgra3780&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2018-09-13)</AVAILABILITY>
    <RESEARCH_USE>Cardiovascular</RESEARCH_USE>
    <ALLELES>Lep&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12904927</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="58626529" STOP_POS="58640663" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="57670525" STOP_POS="57670675" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="56347081" STOP_POS="56347231" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="56085079" STOP_POS="56099209" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="55943837" STOP_POS="55945938" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792573</CITATION_ID>
    <DESCRIPTION>This ZFN model possesses a 151 bp deletion spanning exon 1/intron 1 junction of Leptin gene. Homozygous knockout rats display loss of Leptin protein via Western blot.  Homozygous knockout rats demonstrate significant weight gain compared to wild type littermates. Homozygous knockout rats show significantly elevated serum cholesterol levels</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792575</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lep&lt;sup&gt;em1Sage+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2018-09-13)</AVAILABILITY>
    <RESEARCH_USE>Cardiovascular</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792575</CITATION_ID>
    <DESCRIPTION>These wild type rats are littermates of homozygous knockout rats from heterozygote matings. The Lepr knockout model possesses a 151 bp deletion spanning the exon 1/intron 1 junction of the Leptin gene. Homozygous knockout rats display loss of Leptin protein via Western blot.  Homozygous knockout rats demonstrate significant weight gain compared to wild type littermates. Homozygous knockout rats show significantly elevated serum cholesterol levels</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792606</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cd59&lt;sup&gt;em1Ask&lt;/sup&gt;-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SD-&lt;i&gt;Cd59&lt;sup&gt;em1&lt;/sup&gt;-/&lt;/sup&gt;&lt;/i&gt;&lt;i&gt;Cd59&lt;sup&gt;em1&lt;/sup&gt;-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>Cardiovascular Research Institute,University of California San Francisco, CA 94143-0521
USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd59&lt;sup&gt;em1Ask&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13792720</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="110914008" STOP_POS="110932489" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="90459085" STOP_POS="90477571" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="94010481" STOP_POS="94028660" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="100650411" STOP_POS="100668036" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="89243600" STOP_POS="89245129" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792606</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 genome editing system was used to generate Cd59 mutation in the Sprague Dawley embryos. The CRISPR/Cas9 targeting exon 3 of the rat Cd59 created a 11 bp-deletion (TGCAAAACAAA) in exon 3. No protein expression was detected in the blood smear of homozygous mutants.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792607</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cd59&lt;sup&gt;em1Ask+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Cardiovascular Research Institute,University of California San Francisco, CA 94143-0521
USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792607</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 genome editing system was used to generate Cd59 mutation in the Sprague Dawley embryos. The CRISPR/Cas9 targeting exon 3 of the rat Cd59 created a 11 bp-deletion in exon 3. No protein expression was detected in the blood smear of homozygous mutants. Breeding of CD59 +/- rats was done to generate wildtype (CD59+/+)and homozygous mutant (CD59-/-) rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792682</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abcc6&lt;sup&gt;em2Qlju+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Thomas Jefferson University, Philadelphia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abcc6&lt;sup&gt;em2Qlju&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10413846</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="105637763" STOP_POS="105637785" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="96501332" STOP_POS="96501354" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102013111" STOP_POS="102013133" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103042723" STOP_POS="103096453" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="96448588" STOP_POS="96524655" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792682</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into SD embryos. ZFNs were designed to target exon 1 of rat Abcc6 gene at the binding site/cutting site 5-CACGCCTGGAGAGTCCTGcgcaggCCTGAGGGTGAGTCC-3 (c.24-c.62). The resulting mutation is a 23 bp-deletion (TGCGCAGGCCTGAGGGTGAGTCC) from the first coding exon of the rat Abcc6 gene. The mutation is predicted to cause out of frame translation and a premature stop codon. No protein in the homozygous mutant was detected by immunostaining.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792683</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abcc6&lt;sup&gt;em2Qlju+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Thomas Jefferson University, Philadelphia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792683</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs into SD embryos. ZFNs were designed to target exon 1 of rat Abcc6 gene at the binding site/cutting site 5-CACGCCTGGAGAGTCCTGcgcaggCCTGAGGGTGAGTCC-3 (c.24-c.62). The resulting mutation is a 23 bp-deletion (TGCGCAGGCCTGAGGGTGAGTCC) from the first coding exon of the rat Abcc6 gene. This wild type mutant is the wild type offspring from the cross of heterozygous mutants.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792701</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Trpv1&lt;sup&gt;em1Sage-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.horizondiscovery.com//trpv1-knockout-rat-tgrs5530&gt;Horizon Discovery&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.horizondiscovery.com//trpv1-knockout-rat-tgrs5530&gt;Horizon Discovery&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2018-09-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpv1&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13792702</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="58349936" STOP_POS="58375021" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="57851428" STOP_POS="57876513" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="59799123" STOP_POS="59824208" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="59538296" STOP_POS="59563441" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="60109656" STOP_POS="60134939" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792701</CITATION_ID>
    <DESCRIPTION>These ZFN mutant rats were produced by injecting zinc finger nuclease targeting exon 13 of rat Trpv1 into Sprague Dawley embryos. A 2-bp (CA) frameshift deletion  in exon 13  was created. Homozygous knockout rats exhibit complete loss of Trpv1 protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792705</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Trpv1&lt;sup&gt;em1Sage+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792705</CITATION_ID>
    <DESCRIPTION>These ZFN mutant rats were produced by injecting zinc finger nuclease targeting exon 13 of rat Trpv1 into Sprague Dawley embryos. A 2-bp (CA) frameshift deletion in exon 13 was created ( SD-Trpv1em1Sage-/-). This wild type mutant is the wild type offspring from the cross of heterozygous mutants.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792727</RGD_ID>
    <STRAIN_SYMBOL>HanRj:WI</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.janvier-labs.com/rodent-research-models-services/research-models/per-species/outbred-rats/product/wistar.html&gt; Janvier Labs&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.janvier-labs.com/rodent-research-models-services/research-models/per-species/outbred-rats/product/wistar.html&gt; Janvier Labs&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792727</CITATION_ID>
    <DESCRIPTION>Zentralinstitut fur Versuchstierzucht (Hannover) 1982 (from Allington Farm - UK 1964). This strain was selected by DONALDSON in 1906 at the Wistar Institute (USA), from a batch belonging to Chicago University (RUSSEL-LINDSAY, 1979).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792794</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Fh&lt;sup&gt;em1+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fh&lt;sup&gt;em1&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13792797</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="90056565" STOP_POS="90082450" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="87524331" STOP_POS="87550215" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="93651486" STOP_POS="93677371" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="98116496" STOP_POS="98142636" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="91329837" STOP_POS="91355722" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792794</CITATION_ID>
    <DESCRIPTION>A pair of TALENs targeting exon 1 of the Fh gene was injected into SD embryos to create Fh knock out mutants. The resulting mutation was an 11-bp deletion (acacctttggt) on exon 1 that caused premature stop of FH protein. No homozygous -/- mutant was revealed in litters.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792795</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Fh&lt;sup&gt;em1+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792795</CITATION_ID>
    <DESCRIPTION>A pair of TALENs targeting exon 1 of the Fh gene was injected into SD embryos to create Fh knock out mutants. The resulting mutation was an 11-bp deletion (acacctttggt) on exon 1 that caused premature stop of FH protein. Breeding of Fh +/- rats was done to generate wildtype (Fh+/+)and Fh (+/-). No  homozygous mutant were observed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792801</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nlrp3&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-09-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nlrp3&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13792799</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="44826299" STOP_POS="44853373" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="44326770" STOP_POS="44353814" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="45893673" STOP_POS="45893686" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="45648191" STOP_POS="45674617" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="45850224" STOP_POS="45874533" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792801</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Nlrp3 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 14-bp deletion of exon 1 in the Nlrp3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792803</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;P2rx7&lt;sup&gt;em12Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-06-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>P2rx7&lt;sup&gt;em12Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13792802</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="39550531" STOP_POS="39594984" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="33917654" STOP_POS="33917663" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="39353613" STOP_POS="39396042" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="41242368" STOP_POS="41808755" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="35074025" STOP_POS="35117152" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792803</CITATION_ID>
    <DESCRIPTION>This allele was made by CRISPR/Cas9 system. The resulting mutation is a 10-bp deletion in Exon 2 of the P2rx7 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792808</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ptk2b&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ptk2b&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13792810</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="44536275" STOP_POS="44656754" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="40414764" STOP_POS="40414771" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="42827306" STOP_POS="42947796" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="48646476" STOP_POS="48766708" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="45589222" STOP_POS="45717866" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792808</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Ptk2b gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 8-bp deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792811</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ptk2b&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ptk2b&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13792812</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="40414760" STOP_POS="40414771" METHOD="8"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792811</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Ptk2b gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a7-bp deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792813</RGD_ID>
    <STRAIN_SYMBOL>SHRSP-&lt;i&gt;Spp1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Spp1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13792814</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="5613569" STOP_POS="5620695" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="5312019" STOP_POS="5312029" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="6673686" STOP_POS="6679965" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="6653086" STOP_POS="6658937" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792813</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Spp1 gene of SHRSP/A3NCrl rat embryos. The resulting mutation is a 11-bp deletion in Exon 3 of the Spp1 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792821</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-loxP-stop-loxP-Drp1-GFP)1Mcwi</STRAIN_SYMBOL>
    <FULL_NAME>SD-Tg(CAG-loxP-stop-loxP-Drp1-GFP)1</FULL_NAME>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792821</CITATION_ID>
    <DESCRIPTION>The Sleeping Beauty transposon system was used to introduce a Drp1-GFP fusion driven by a ubiquitous promoter, interupted by a floxed stop cassette.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792822</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-loxP-stop-loxP-Drp1-GFP)2Mcwi</STRAIN_SYMBOL>
    <FULL_NAME>SD-Tg(CAG-loxP-stop-loxP-Drp1-GFP)2</FULL_NAME>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792822</CITATION_ID>
    <DESCRIPTION>The Sleeping Beauty transposon system was used to introduce a Drp1-GFP fusion driven by a ubiquitous promoter, interupted by a floxed stop cassette.This is line B.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792823</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-loxP-stop-loxP-Drp1-GFP)3Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792823</CITATION_ID>
    <DESCRIPTION>The Sleeping Beauty transposon system was used to introduce a Drp1-GFP fusion driven by a ubiquitous promoter, interupted by a floxed stop cassette.This is line C.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792825</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-loxP-stop-loxP-Mfn1-GFP)1Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792825</CITATION_ID>
    <DESCRIPTION>The Sleeping Beauty transposon system was used to introduce a Mfn1-GFP fusion driven by a ubiquitous promoter, interupted by a floxed stop cassette. This is line A.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792827</RGD_ID>
    <STRAIN_SYMBOL>WKY-Tg(Ubc-cre/ERT2)4Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-02)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792827</CITATION_ID>
    <DESCRIPTION>The Sleeping Beauty transposon system was used to introduce a cre-ERT2 fusion, driven by the UbC promoter. This is line D.Cre activity is detected even without tamoxifen induction.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13792828</RGD_ID>
    <STRAIN_SYMBOL>WKY-Tg(Ubc-cre/ERT2)5Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-02)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13792828</CITATION_ID>
    <DESCRIPTION>The Sleeping Beauty transposon system was used to introduce a cre-ERT2 fusion, driven by the UbC promoter. This is line E.Cre activity is detected even without tamoxifen induction.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13793372</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tlr4&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tlr4&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13793373</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="85161247" STOP_POS="85174882" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="80145867" STOP_POS="80159501" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="82587424" STOP_POS="82601056" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="86690670" STOP_POS="86704302" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="83564100" STOP_POS="83577735" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13793372</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Tlr4 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 1-bp deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13793374</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Tph1&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tph1&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13793375</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="106293695" STOP_POS="106314628" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="97157375" STOP_POS="97178415" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102694238" STOP_POS="102694238" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103746878" STOP_POS="103774100" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="97186071" STOP_POS="97207551" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13793374</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Tph1 gene of DA/MolTac rat embryos. The resulting mutation is a 1-bp deletion in exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13793376</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Avpr2&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2018-10-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Avpr2&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13793377</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="156785009" STOP_POS="156787477" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="151633501" STOP_POS="151636155" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="156890489" STOP_POS="156890518" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="152637074" STOP_POS="152640726" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="159821860" STOP_POS="159823488" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13793376</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Avpr2 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is  a 30-bp deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13793378</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Avpr2&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Avpr2&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13793379</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="156785009" STOP_POS="156787477" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="151633501" STOP_POS="151636155" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="156890484" STOP_POS="156890492" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="152637074" STOP_POS="152640726" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="159821860" STOP_POS="159823488" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13793378</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Avpr2 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is  a 9-bp deletion in exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13799346</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cgnl1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cgnl1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13799347</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="81154169" STOP_POS="81305598" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="72273401" STOP_POS="72424842" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="78232373" STOP_POS="78232452" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="74800532" STOP_POS="74950938" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="76088865" STOP_POS="76241145" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13799346</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 80-bp deletion on exon 2  of Cgnl1 gene in SS/JrHsdMcwi embryos</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13799348</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cgnl1&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cgnl1&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13799349</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="81154169" STOP_POS="81305598" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="72273401" STOP_POS="72424842" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="78232367" STOP_POS="78232454" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="74800532" STOP_POS="74950938" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="76088865" STOP_POS="76241145" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13799348</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 88-bp deletion on exon 2  of Cgnl1 gene in SS/JrHsdMcwi embryos</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13799350</RGD_ID>
    <STRAIN_SYMBOL>T2DN-&lt;i&gt;F2r&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>F2r&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13799351</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="28604066" STOP_POS="28620579" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="26872357" STOP_POS="26872358" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="26118760" STOP_POS="26135340" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="45254489" STOP_POS="45257761" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="25985800" STOP_POS="25989072" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13799350</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 2-bp deletion in exon 1 of F2r gene in the T2DN/Mcwi embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800555</RGD_ID>
    <STRAIN_SYMBOL>F344/IcoCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.criver.com/products-services/find-model/fischer-344-rat?region=3611#&gt; Charles River</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/fischer-344-rat?region=3611#&gt; Charles River</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800555</CITATION_ID>
    <DESCRIPTION>From mating #344 of rats purchased from a local breeder (Fischer). The colony was originated by M. R. Curtis, Columbia University in 1920. To the Germ-Free Animal Laboratory at CNRS, Gif-sur-Yvette, France from the Lobund Institute, University of Notre-Dame, South Bend, Indiana, U.S.A. Subsequently introduced to Charles River France in 1970 as an axenic colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800556</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Hsd11b2&lt;sup&gt;em1Jmul-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>F344-&lt;i&gt;Hsd11b2&lt;sup&gt;em1Jmul-&lt;/sup&gt;/Hsd11b2&lt;sup&gt;em1Jmul-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Hsd11b2&lt;sup&gt;em1Jmul&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13800560</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="50307569" STOP_POS="50312812" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="33397656" STOP_POS="33402899" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="37476083" STOP_POS="37481326" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="48341841" STOP_POS="48347084" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="35336342" STOP_POS="35341585" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800556</CITATION_ID>
    <DESCRIPTION>The ZFN system targeting exon 2 of Hsd11b2 gene was injected into the F344/IcoCrl embryos to induce a 123-bp deletion removing the 3' end of exon 2 and the first 16-bp of intron B and create a premature stop coden TAG.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800557</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Hsd11b2&lt;sup&gt;em1Jmul+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>F344-&lt;i&gt;Hsd11b2&lt;sup&gt;em1Jmul+&lt;/sup&gt;/Hsd11b2&lt;sup&gt;em1Jmul+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800557</CITATION_ID>
    <DESCRIPTION>This is the wild-type litter mates of the Hsd11b2 F344 mutants created by  ZFN system targeting exon 2 of Hsd11b2 gene was injected into the F344/IcoCrl embryos to induce a 123-bp deletion removing the 3' end of exon 2 and the first 16-bp of intron B and create a premature stop coden TAG.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800746</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;F8&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>F8&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13800747</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="155237" STOP_POS="187186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="140848" STOP_POS="172330" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="367862" STOP_POS="399242" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="413447" STOP_POS="444491" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="121134" STOP_POS="162008" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800746</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to delete the entire F8 gene in the SS/JrHsdMcwi embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800749</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Glp1r&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Glp1r&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13800750</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="8979403" STOP_POS="8979486" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="8978014" STOP_POS="8978097" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="9592085" STOP_POS="9592168" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="11768479" STOP_POS="11808416" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="9225881" STOP_POS="9264184" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800749</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 84-bp deletion and skipping of exon 5 of the Glp1r gene in Lew/NCrl embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800810</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnq1&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2018-10-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnq1&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13800813</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="207721134" STOP_POS="208054073" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="198291711" STOP_POS="198624683" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="216293087" STOP_POS="216630339" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="223154713" STOP_POS="223490458" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="203383401" STOP_POS="203803687" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800810</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system and the single-stranded oligodeoxynucleotide (ssODN ) were combined to  introduce  the R231H mutation in the Kcnq1 gene of SS/JrHsdMcwi rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800825</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Muc1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-10-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Muc1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13800827</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="176933312" STOP_POS="176938497" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="174635989" STOP_POS="174640738" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="188543137" STOP_POS="188547874" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="207957206" STOP_POS="207962396" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="181399482" STOP_POS="181403640" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800825</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 2-bp deletion in exon 2 of rat Muc1 gene in the FHH/EurMcwi embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800838</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Mybphl&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mybphl&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13800841</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="198692857" STOP_POS="198706953" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="196005516" STOP_POS="196005517" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="211158902" STOP_POS="211173036" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="230628901" STOP_POS="230643002" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="203934530" STOP_POS="203948031" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800838</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 2-bp deletion in exon 1 of rat Mybphl gene in the FHH/EurMcwi embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800845</RGD_ID>
    <STRAIN_SYMBOL>FHH-&lt;i&gt;Mybphl&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-06-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mybphl&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13800846</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="198692857" STOP_POS="198706953" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="196005534" STOP_POS="196005535" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="211158902" STOP_POS="211173036" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="230628901" STOP_POS="230643002" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="203934530" STOP_POS="203948031" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800845</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a  2-bp deletion in exon 1 of rat Mybphl gene in the FHH/EurMcwi embryos. embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800848</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Nlrp3&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nlrp3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13800850</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="44826299" STOP_POS="44853373" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="44329222" STOP_POS="44329231" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="45884324" STOP_POS="45918290" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="45648191" STOP_POS="45674617" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="45850224" STOP_POS="45874533" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800848</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Nlrp3 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 10-bp deletion of exon 1 in the Nlrp3 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800869</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;P2ry2&lt;sup&gt;em6Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>P2ry2&lt;sup&gt;em6Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13800870</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="164764119" STOP_POS="164779578" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="155354365" STOP_POS="155354496" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="166031228" STOP_POS="166045423" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="172227726" STOP_POS="172241921" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="158440018" STOP_POS="158454213" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800869</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the P2ry2 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 132-bp deletion in exon 3 in the P2ry2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800871</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;P2ry2&lt;sup&gt;em7Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>P2ry2&lt;sup&gt;em7Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13800873</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="164764119" STOP_POS="164779578" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="155354367" STOP_POS="155354481" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="166031228" STOP_POS="166045423" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="172227726" STOP_POS="172241921" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="158440018" STOP_POS="158454213" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800871</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the P2ry2 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 115-bp deletion in exon 3 in the P2ry2 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800875</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Prl&lt;sup&gt;tm1(PRL)Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>PRL</ALLELES>
    <ALLELE_RGD_IDS>736187</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800875</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 and plasmid donor containing floxed human prolactin  cDNA were used to insert the human  cDNA into the start coden of rat prolactin gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13800877</RGD_ID>
    <STRAIN_SYMBOL>LH-Chr 17&lt;sup&gt;LN&lt;/sup&gt;-&lt;i&gt;C17h6orf52&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2026-01-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>C17h6orf52&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13800878</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="23959124" STOP_POS="23981978" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="23767016" STOP_POS="23767016" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="21600326" STOP_POS="21615888" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="23581681" STOP_POS="23595498" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="29733271" STOP_POS="29746771" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13800877</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a net 10-bp insertion in exon 2 of rat C17h6orf52.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13825143</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Gja5&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gja5&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13825144</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="187291227" STOP_POS="187310770" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="184602407" STOP_POS="184621952" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="199181973" STOP_POS="199181973" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="218648368" STOP_POS="218669354" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="191824118" STOP_POS="191843867" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13825143</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce  a 1-bp substitution and premature stop codon in exon 2 of rat Gja5 gene of WKY/NCrl rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13825147</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Per1&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Per1&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13825148</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="54299002" STOP_POS="54313804" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="53800126" STOP_POS="53814963" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="55687124" STOP_POS="55696020" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="55424863" STOP_POS="55439853" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="55859851" STOP_POS="55868747" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13825147</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 1-bp deletion in exon 1 of Per1 gene in  SS/JrHsdMcwi rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13825196</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Sh2b3&lt;sup&gt;tm1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2018-11-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sh2b3&lt;sup&gt;tm1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14394610</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13825196</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 and two ssODNs (single-stranded oligodeoxynucleotide) were used to insert loxP sites flanking multiple exons</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13825199</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Mc4r&lt;sup&gt;m1Hubr&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hubrecht Laboratory, Centre for Biomedical Genetics, 3584 CT Utrecht, The Netherlands. Hera Biolabs, Taconic.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mc4r&lt;sup&gt;m1Hubr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13825200</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="62689798" STOP_POS="62691685" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="60419832" STOP_POS="60421719" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="62612838" STOP_POS="62614725" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="61799166" STOP_POS="61801053" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="63390922" STOP_POS="63392809" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13825199</CITATION_ID>
    <DESCRIPTION>The Mc4r mutant rat line was generated by target-selected ENU-driven mutagenesis, and high-throughput resequencing of genomic target sequences in progeny from mutagenized rats (Wistar/Crl background) revealed an ENU-induced premature stop codon in helix 8 (K314X) of Mc4r. The heterozygous mutant rat was backcrossed to wild-type Wistar background for six generations to eliminate confounding effects from background mutations induced by ENU.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>13838845</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ahr&lt;sup&gt;em2Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ahr&lt;sup&gt;em2Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126790510</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="57990798" STOP_POS="57990826" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="52263464" STOP_POS="52263492" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="54993362" STOP_POS="54993390" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="64589066" STOP_POS="64624078" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="54205104" STOP_POS="54240268" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_13838845</CITATION_ID>
    <DESCRIPTION>ZFN constructs were designed to target exon 2 which contains the DNA binding bHLH motif of the AHR gene.This ZFN model contains a 29-bp deletion in the rat Ahr gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14390067</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Slc6a4&lt;sup&gt;m1Hubr-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hubrecht Laboratory, Utrecht, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc6a4&lt;sup&gt;m1Hubr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14390068</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="62322688" STOP_POS="62357060" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="61824208" STOP_POS="61858924" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="63153656" STOP_POS="63188377" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="62851326" STOP_POS="62872481" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="67134790" STOP_POS="67155891" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14390067</CITATION_ID>
    <DESCRIPTION>The Slc6a4 knockout rat  was generated by target-selected ENU-induced mutagenesis. An ENU-induced premature stop codon in exon 3 of the Slc6a4 gene in a female rat (Wistar from Crl) was identified.The homozygoous mutant rats were generated by incrossed between heterozygous Slc6a4 knock out rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14390069</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Slc6a4&lt;sup&gt;m1Hubr+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hubrecht Laboratory, Utrecht, The Netherlands</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc6a4&lt;sup&gt;m1Hubr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14390068</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="62322688" STOP_POS="62357060" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="61824208" STOP_POS="61858924" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="63153656" STOP_POS="63188377" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="62851326" STOP_POS="62872481" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="67134790" STOP_POS="67155891" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14390069</CITATION_ID>
    <DESCRIPTION>The Slc6a4 knockout rat  was generated by target-selected ENU-induced mutagenesis. An ENU-induced premature stop codon in exon 3 of the Slc6a4 gene in a female rat (Wistar from Crl) was identified.The heterozygoous mutant rats were used to  generate homozygous Slc6a4 knock out rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14390082</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Fos-LacZ)Bhope</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=865&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=865&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00865</CITATION_ID>
    <DESCRIPTION>The lacZ gene was inserted between NcoI and SalI sites in exon 4 of the murine Fos gene . The linearized DNA was then microinjected into fertilized rat oocytes and line 1-8 was chosen for continuation. Rats were rederived from frozen embryos in 2002 and bred onto SD background for &gt;35 generations at NIDA IRP (Bruce Hope lab)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14390083</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(Fos-LacZ)Bhope</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14390083</CITATION_ID>
    <DESCRIPTION>The lacZ gene was inserted between NcoI and SalI sites in exon 4 of the murine Fos gene . The linearized DNA was then microinjected into fertilized rat oocytes and line 1-8 was chosen for continuation.  Initial SD rats were then bred onto Wistar background for &gt;10 generations at NIDA IRP (Bruce Hope lab)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14392784</RGD_ID>
    <STRAIN_SYMBOL>ACI.SD-&lt;i&gt;Esr1&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=849&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=849&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2019-02-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Esr1&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910736</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="43511685" STOP_POS="43904454" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="41272347" STOP_POS="41272828" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="41358808" STOP_POS="41359289" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="42534049" STOP_POS="42935434" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="35523680" STOP_POS="35759891" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00849</CITATION_ID>
    <DESCRIPTION>This strain was produced by backcrossing the ZFN induced 482 deletion allele (Esr1em1Soar) in HsdHot:SD to the ACI/SegHsd background for 12 generations. ACI strain is particularly sensitive to Estrogen-induced tumorigenesis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14392813</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cftr&lt;sup&gt;em1Sage+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.inotivco.com/model/hsdsage-sd-cftrem1sage&gt;inotiv&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.inotivco.com/model/hsdsage-sd-cftrem1sage&gt;inotiv&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryorecovery (as of 2023-06-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cftr&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14392814</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="47571723" STOP_POS="47571738" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="46605832" STOP_POS="46605847" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="42737752" STOP_POS="42737767" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="42281040" STOP_POS="42448571" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="43874852" STOP_POS="44041870" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14392813</CITATION_ID>
    <DESCRIPTION>Cftr ZFN knockout rats possess a 16 bp deletion in exon 3 of the Cystic Fibrosis transmembrane conductance regulator (Cftr), resulting in loss of protein expression.  This Cftr heterozygous rats exhibited similar bioelectric and other characteristics to wild-type.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14392815</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cftr&lt;sup&gt;em1Sage-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.inotivco.com/model/hsdsage-sd-cftrem1sage&gt;inotiv&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.inotivco.com/model/hsdsage-sd-cftrem1sage&gt;inotiv&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2019-03-04)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cftr&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14392814</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="47571723" STOP_POS="47571738" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="46605832" STOP_POS="46605847" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="42737752" STOP_POS="42737767" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="42281040" STOP_POS="42448571" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="43874852" STOP_POS="44041870" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14392815</CITATION_ID>
    <DESCRIPTION>CFTR ZFN knockout rats possess a 16 bp deletion in exon 3 of the Cystic Fibrosis transmembrane conductance regulator (Cftr), resulting in loss of protein expression.  The homozygous mutant rats are produced by crossing the Cftr heterozygous rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14392817</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cftr&lt;sup&gt;em1Sage+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14392817</CITATION_ID>
    <DESCRIPTION>CFTR ZFN knockout rats possess a 16 bp deletion in exon 3 of the Cystic Fibrosis transmembrane conductance regulator (Cftr), resulting in loss of protein expression.  The homozygous mutant rats and wild-type rats are produced by crossing the Cftr heterozygous rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394485</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Bace1&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bace1&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13782148</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="55039152" STOP_POS="55039289" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="46142434" STOP_POS="46142571" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="50140402" STOP_POS="50140539" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="48766315" STOP_POS="48766452" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="48817824" STOP_POS="48839681" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394485</CITATION_ID>
    <DESCRIPTION>The mutant rats were generated by SAGE Labs using zinc-finger nuclease (ZFN) technology to create a 137-base pair deletion spanning the translation initiation start site in exon 1 of the rat Bace1 gene, corresponding to chr8:48,766,315-48,766,452 (RGSC 5.0/rn5 assembly)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394486</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Bace1&lt;sup&gt;em1Sage+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SD-&lt;i&gt;Bace1&lt;sup&gt;em1Sage+&lt;/sup&gt;/Bace1&lt;sup&gt;em1Sage-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bace1&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13782148</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="55039152" STOP_POS="55039289" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="46142434" STOP_POS="46142571" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="50140402" STOP_POS="50140539" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="48766315" STOP_POS="48766452" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="48817824" STOP_POS="48839681" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394486</CITATION_ID>
    <DESCRIPTION>The Bace1 (+/-) rats were generated by SAGE Labs using zinc-finger nuclease (ZFN) technology to create a 137-base pair deletion spanning the translation initiation start site in exon 1 of the rat Bace1 gene, corresponding to chr8:48,766,315-48,766,452 (RGSC 5.0/rn5 assembly)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394487</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Bace1&lt;sup&gt;em1Sage+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SD-&lt;i&gt;Bace1&lt;sup&gt;em1Sage+&lt;/sup&gt;/Bace1&lt;sup&gt;em1Sage+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394487</CITATION_ID>
    <DESCRIPTION>The Bace1 (+/+) rats were generated by crossing SD-Bace1em1Sage. The mutant rats were generated by SAGE Labs using zinc-finger nuclease (ZFN) technology to create a 137-base pair deletion spanning the translation initiation start site in exon 1 of the rat Bace1 gene, corresponding to chr8:48,766,315-48,766,452 (RGSC 5.0/rn5 assembly)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394488</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Glp1r&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2026-02-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Glp1r&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14394489</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="8979479" STOP_POS="8979488" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="8978090" STOP_POS="8978099" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="9592161" STOP_POS="9592170" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="11768479" STOP_POS="11808416" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="9225881" STOP_POS="9264184" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394488</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 10-bp deletion in exon 2 of the Glp1r gene in Lew/NCrl embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394491</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Glp1r&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2026-02-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Glp1r&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14394492</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="8979480" STOP_POS="8979483" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="8978091" STOP_POS="8978094" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="9592162" STOP_POS="9592165" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="11768479" STOP_POS="11808416" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="9225881" STOP_POS="9264184" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394491</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 4-bp deletion in exon 2 of the Glp1r gene in Lew/NCrl embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394494</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnj2&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-03-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnj2&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14394495</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="96560225" STOP_POS="96570788" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="96066338" STOP_POS="96066365" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="99429337" STOP_POS="99442520" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="99125234" STOP_POS="99134077" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="100574985" STOP_POS="100576268" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394494</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 28-bp deletion mutation in exon 1 of the Kcnj2 gene of SS/JrHsdMcwi rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394496</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Kcnj2&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnj2&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14394497</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="96560225" STOP_POS="96570788" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="96066345" STOP_POS="96066346" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="99429337" STOP_POS="99442520" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="99125234" STOP_POS="99134077" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="100574985" STOP_POS="100576268" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394496</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 2-bp deletion mutation in exon 1 of the Kcnj2 gene of SS/JrHsdMcwi rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394501</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Klrb1a&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-03-25)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Klrb1a&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14394503</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="163576672" STOP_POS="163590201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="161901789" STOP_POS="161901793" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="161950270" STOP_POS="161966582" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="227150602" STOP_POS="227167004" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="165637478" STOP_POS="165654188" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394501</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 5-bp deletion in exon 2 in SHR/NCrl embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394504</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Klrb1a&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2019-03-25)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Klrb1a&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14394505</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="163576672" STOP_POS="163590201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="161901790" STOP_POS="161901891" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="161950270" STOP_POS="161966582" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="227150602" STOP_POS="227167004" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="165637478" STOP_POS="165654188" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394504</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 102-bp deletion in exon 2 in SHR/NCrl embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394506</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;P2ry2&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-03-25)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>P2ry2&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14394507</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="155354461" STOP_POS="155354487" METHOD="8"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394506</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to induce a mutation in the P2ry2 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 27-bp deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394508</RGD_ID>
    <STRAIN_SYMBOL>BBDR.BBDP-(D4Mit6-D4Mit7)-&lt;i&gt;Tlr4&lt;sup&gt;em5Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-03-25)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tlr4&lt;sup&gt;em5Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14394509</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="85161247" STOP_POS="85174882" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="80145867" STOP_POS="80159501" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="82587424" STOP_POS="82601056" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="86690670" STOP_POS="86704302" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="83564100" STOP_POS="83577735" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394508</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 5-bp deletion in exon2 in the Tlr4 gene of BBDR.BBDP-(D4Mit6-D4Mit7)/RhwMcwi embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394515</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Grin2b&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Generated with support from the Simons Foundation Autism Research Initiative (&lt;a href=https://www.sfari.org/resource/rat-models/&gt;SFARI&lt;/a&gt;); MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/autism-rat-model-resource/ &gt; Autism Rat Model Resource&lt;/a&gt;, Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2025-02-20)</AVAILABILITY>
    <RESEARCH_USE>Autism, Developmental delay, Intellectual disability, Epilepsy (from &lt;a href=https://gene.sfari.org/database/human-gene/GRIN2B&gt;SFARI GENE&lt;/a&gt;)</RESEARCH_USE>
    <ALLELES>Grin2b&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14394517</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="170297811" STOP_POS="170775420" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="168580824" STOP_POS="169044110" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="169751704" STOP_POS="169752731" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="233806406" STOP_POS="234260360" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="172721895" STOP_POS="173183187" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394515</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  Grin2b gene of  Crl:LE rat embryos. The resulting mutation is deletion of exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394518</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Arid1b&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Generated with support from the Simons Foundation Autism Research Initiative (&lt;a href=https://www.sfari.org/resource/rat-models/&gt;SFARI&lt;/a&gt;); MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/autism-rat-model-resource/ &gt; Autism Rat Model Resource&lt;/a&gt;,  Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2025-02-20)</AVAILABILITY>
    <RESEARCH_USE>Autism, ADHD, Developmental delay, Intellectual disability, Epilepsy  (from &lt;a href=https://gene.sfari.org/database/human-gene/ARID1B&gt;SFARI GENE&lt;/a&gt;)</RESEARCH_USE>
    <ALLELES>Arid1b&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14394519</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="47973199" STOP_POS="48328793" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="45567991" STOP_POS="45923644" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="46130110" STOP_POS="46131244" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="47197399" STOP_POS="47550032" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="40012872" STOP_POS="40324266" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394518</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Arid1b gene of  Crl:LE rat embryos. The resulting mutation is deletion of exon 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394520</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(CAG-loxP-stop-loxP-Rpl10a-GFP)1Mcwi</STRAIN_SYMBOL>
    <FULL_NAME>SS-Tg(CAG-loxP-stop-loxP-Rpl10a-GFP)1</FULL_NAME>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394520</CITATION_ID>
    <DESCRIPTION>The Sleeping Beauty transposon system was used to introduce a Rpl10a-GFP fusion driven by a ubiquitous promoter, interupted by a floxed stop cassette</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394616</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Tph2&lt;sup&gt;em3Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tph2&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10402820</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="52571909" STOP_POS="52676305" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="50685694" STOP_POS="50789424" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="58112644" STOP_POS="58112654" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="58053268" STOP_POS="58157949" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="54321033" STOP_POS="54430706" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394616</CITATION_ID>
    <DESCRIPTION>This wild type strain was produced by crossing Tph2em3Mcwi heterozygous rats and confirmed by sequencing. The Tph2em3Mcwi heterozygous mutant was created by injecting ZFNs targeting the sequence CATGGCTCCGACCCCctctacACCCCGGAACCG into DA/OlaHsd rat embryos. The resulting mutation is a 11-bp frameshift deletion in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394617</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Tph2&lt;sup&gt;em3Mcwi+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tph2&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10402820</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="52571909" STOP_POS="52676305" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="50685694" STOP_POS="50789424" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="58112644" STOP_POS="58112654" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="58053268" STOP_POS="58157949" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="54321033" STOP_POS="54430706" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394617</CITATION_ID>
    <DESCRIPTION>The Tph2em3Mcwi heterozygous mutant was created by injecting ZFNs targeting the sequence CATGGCTCCGACCCCctctacACCCCGGAACCG into DA/OlaHsd rat embryos. The resulting mutation is a 11-bp frameshift deletion in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394618</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Tph2&lt;sup&gt;em3Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tph2&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10402820</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="52571909" STOP_POS="52676305" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="50685694" STOP_POS="50789424" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="58112644" STOP_POS="58112654" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="58053268" STOP_POS="58157949" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="54321033" STOP_POS="54430706" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394618</CITATION_ID>
    <DESCRIPTION>This homozygous mutant strain was produced by crossing Tph2em3Mcwi heterozygous rats and confirmed by sequencing. The Tph2em3Mcwi heterozygous mutant was created by injecting ZFNs targeting the sequence CATGGCTCCGACCCCctctacACCCCGGAACCG into DA/OlaHsd rat embryos. The resulting mutation is a 11-bp frameshift deletion in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394619</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Tph2&lt;sup&gt;em2Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394619</CITATION_ID>
    <DESCRIPTION>This wild type strain was produced by crossing Tph2em2Mcwi heterozygous rats and confirmed by sequencing. The Tph2em2Mcwi was produced by injecting ZFNs targeting the sequence CATGGCTCCGACCCCctctacACCCCGGAACCG into DA/OlaHsd rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394620</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Tph2&lt;sup&gt;em2Mcwi+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tph2&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10402817</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="52571909" STOP_POS="52676305" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="50685694" STOP_POS="50789424" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="58042279" STOP_POS="58149220" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="58053268" STOP_POS="58157949" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="54321033" STOP_POS="54430706" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394620</CITATION_ID>
    <DESCRIPTION>The Tph2em2Mcwi was produced by injecting ZFNs targeting the sequence CATGGCTCCGACCCCctctacACCCCGGAACCG into DA/OlaHsd rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14394621</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Tph2&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tph2&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10402817</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="52571909" STOP_POS="52676305" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="50685694" STOP_POS="50789424" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="58042279" STOP_POS="58149220" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="58053268" STOP_POS="58157949" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="54321033" STOP_POS="54430706" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14394621</CITATION_ID>
    <DESCRIPTION>The Tph2em2Mcwi was produced by injecting ZFNs targeting the sequence CATGGCTCCGACCCCctctacACCCCGGAACCG into DA/OlaHsd rat embryos. The resulting mutation is a 10-bp frameshift deletion in exon 7. This homozygous mutant strain was produced by crossing Tph2em3Mcwi heterozygous rats and confirmed by sequencing.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14398460</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Cd40&lt;sup&gt;em1Uthal-/-&lt;/sup&gt;&lt;/I&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=840&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cd40&lt;sup&gt;em1Uthal&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14398461</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="174209113" STOP_POS="174224592" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="153790372" STOP_POS="153805279" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="161519789" STOP_POS="161534943" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="167711248" STOP_POS="167711258" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="156092602" STOP_POS="156107427" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00840</CITATION_ID>
    <DESCRIPTION>Zinc Finger Nuclease (ZFN) was utilized to knockout rat CD40 function in the embryos of SS/JrHsd rats.  The  target sequence (CAGCACCGACACTGCgaactcAGTGCGTGGGGCTGCCGGG) introduced an 11 bp-deletion (CTGCGAACTCA) in the third exon of the Cd40 gene, resulted in a trucated protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14398463</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Prr5&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-04-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prr5&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>40818256</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="117675308" STOP_POS="117717833" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="115795351" STOP_POS="115837880" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="125569791" STOP_POS="125609340" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="125317939" STOP_POS="125338782" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="122693577" STOP_POS="122714377" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14398463</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Prr5 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 19-bp deletion in the exon 1 of the gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14398465</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Prr5&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-04-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prr5&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>40818255</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="117675308" STOP_POS="117717833" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="115795351" STOP_POS="115837880" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="125569791" STOP_POS="125609340" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="125317939" STOP_POS="125338782" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="122693577" STOP_POS="122714377" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14398465</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Prr5 gene of SS/JrHsdMcwi rat embryos. The resulting mutation is a 5-bp deletion in the exon 1 of the gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14398479</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Xdh&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2024-05-29)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Xdh&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14398480</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="27282319" STOP_POS="27344022" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="21530463" STOP_POS="21592172" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="25149570" STOP_POS="25211273" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="34996983" STOP_POS="35059195" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="21417685" STOP_POS="21590015" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14398479</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 7-bp deletion in exon 4 of rat Xdh gene in the SS/JrHsdMcwi embryos. There was no Xdh protein detected in the kidney cortex tissue of 6-week old homozygous mutants.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14398481</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Xdh&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Xdh&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14398482</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="27282319" STOP_POS="27344022" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="21530463" STOP_POS="21592172" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="25149570" STOP_POS="25211273" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="34996983" STOP_POS="35059195" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="21417685" STOP_POS="21590015" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14398481</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 12-bp deletion in exon 4 of rat Xdh gene in the SS/JrHsdMcwi embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14398499</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Drd1&lt;sup&gt;em1(iCre)Berke&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=856&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=856&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-02-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Drd1&lt;sup&gt;em1(iCre)Berke&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14398500</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="10545488" STOP_POS="10550029" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="10540440" STOP_POS="10544971" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="11099736" STOP_POS="11104352" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="13211031" STOP_POS="13215581" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="16655926" STOP_POS="16658161" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00856</CITATION_ID>
    <DESCRIPTION>The CRISPR system was used to created target insertion of iCre recombinase to the Drd1 (Drd1a) locus of the embryos of  BluHsd:LE.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14398734</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Adora2a&lt;sup&gt;em1(iCre)Berke&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=857&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=857&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-02-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adora2a&lt;sup&gt;em1(iCre)Berke&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14398735</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00857</CITATION_ID>
    <DESCRIPTION>The CRISPR system was used to created target insertion of iCre recombinase immediately after  Adora2a gene, with P2A linker, of  the embryos of  BluHsd:LE.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14398825</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Fah&lt;sup&gt;em15Dlli-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>East China Normal University, Shanghai, China.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fah&lt;sup&gt;em15Dlli-/-&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14398826</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="147957931" STOP_POS="147980708" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="138548830" STOP_POS="138571599" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="146713663" STOP_POS="146736339" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="147640316" STOP_POS="147662920" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="140851975" STOP_POS="140876187" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14398825</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting Sprague Dawley embryo with CRISPR/Cas9 system targeting the exon 2 of rat Fah gene. The resulting mutation is line 15 with a frameshift deletion causing Fah null in homozygotes. None of the Fah-/- newborns survived longer than three days after birth in the absence of NTBC. Upon NTBC addition to the drinking water, the Fah-/- rats underwent normal growth and were indistinguishable from their WT littermates.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14398828</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Fah&lt;sup&gt;em10Dlli-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>East China Normal University, Shanghai,
China.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fah&lt;sup&gt;em10Dlli-/-&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14398829</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="147957931" STOP_POS="147980708" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="138548830" STOP_POS="138571599" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="146713663" STOP_POS="146736339" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="147640316" STOP_POS="147662920" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="140851975" STOP_POS="140876187" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14398828</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting Sprague Dawley embryo with CRISP/Case9 system targeting the exon 2 of rat Fah gene. The resulting mutation is a 10-bp deletion in exon 2 caused premature stop in the Fah protein. None of the Fah-/- newborns survived longer than three days after birth in the absence of NTBC. Upon NTBC addition to the drinking water, the Fah-/- rats underwent normal growth and were indistinguishable from their WT littermates</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14402419</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Chrna5&lt;sup&gt;em18Pas&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Strains were produced at Institut Pasteur (France), Departement de Neuroscience, Benoit Forget. The lines will be maintained at Charles River Laboratory France (CRLF).</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Chrna5&lt;sup&gt;em18Pas&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14402420</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="64265879" STOP_POS="64294233" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="55369794" STOP_POS="55398526" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="59561817" STOP_POS="59590172" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="58143974" STOP_POS="58172330" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="58538002" STOP_POS="58566388" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14402419</CITATION_ID>
    <DESCRIPTION>The Zinc Finger Nuclease system was used to create184-bp deletion at the beginning of exon 5 thus created the premature stop coden. The embryos were from breeding of Long Evans from Janvier Labs (RjOrl:LE) and reimplanted to foster mother Dark Agouti (Janvier). Heterozygous rats are currently bred to generate heterozygous and homozygous.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14402421</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Chrna5&lt;sup&gt;em20(D398N)Pas&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Strains were produced at Institut Pasteur (France), Departement de Neuroscience, Benoit Forget. The lines will be maintained at Charles River Laboratory France (CRLF).</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Chrna5&lt;sup&gt;em20(D398N)Pas&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14402422</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="64265879" STOP_POS="64294233" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="55369794" STOP_POS="55398526" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="59561817" STOP_POS="59590172" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="58143974" STOP_POS="58172330" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="58538002" STOP_POS="58566388" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14402421</CITATION_ID>
    <DESCRIPTION>The Zinc Finger Nuclease system was used to knock-in SNP rs16969968 in exon 5 (D398N) thus created a missense mutation. The embryos were from breeding of Long Evans from Janvier Labs (RjOrl:LE) and reimplanted to foster mother Dark Agouti (Janvier). Heterozygous rats are currently bred to generate heterozygous and homozygous.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14694847</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Pvalb&lt;sup&gt;em1(flpo)Berke&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=859&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=859&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pvalb&lt;sup&gt;em1(flpo)Berke&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14694849</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="111653820" STOP_POS="111668469" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="109772939" STOP_POS="109787954" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="119428657" STOP_POS="119443674" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="119420581" STOP_POS="119435235" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="116115034" STOP_POS="116127508" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00859</CITATION_ID>
    <DESCRIPTION>A double-stranded DNA plasmid donor was synthesized  to introduce self-cleaving peptide 2A (P2A),followed by Flpo recombinase,and the V5 peptide tag (GKPIPNPLLGLDST) before the termination codon in exon 5 of rat Parvalbumin. The  CRISPR/Cas9 system was used to knock in the plasmid into the targeted gene in the Crl:LE embryo. (ref:bioRxiv preprint first posted online Aug. 7, 2018; doi: http://dx.doi.org/10.1101/386474. )</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14694998</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Sdhb&lt;sup&gt;em1Ast&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=853&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=853&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00853</CITATION_ID>
    <DESCRIPTION>This mutant strain was generated by injecting  TALEN targeting rat Sdhb into NTac:SD embryo. The resulting mutant is a 4 bp-deletion in Sdhb.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14694999</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Sdhb&lt;sup&gt;em2Ast&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=854&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=854&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00854</CITATION_ID>
    <DESCRIPTION>This mutant strain was generated by injecting  TALEN targeting rat Sdhb into NTac:SD embryo. The resulting mutant is a 6 bp-deletion in Sdhb.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695000</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Sdhb&lt;sup&gt;em3Ast&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=855&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=855&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00855</CITATION_ID>
    <DESCRIPTION>This mutant strain was generated by injecting  TALEN targeting rat Sdhb into NTac:SD embryo. The resulting mutant is a 15 bp-deletion in Sdhb.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695002</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;L1cam&lt;sup&gt;em1Jgn&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=850&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=850&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>L1cam&lt;sup&gt;em1Jgn&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599015</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="156748597" STOP_POS="156775116" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="151597270" STOP_POS="151623776" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="156901244" STOP_POS="156928064" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="152649353" STOP_POS="152676124" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="159784792" STOP_POS="159801553" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00850</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 genome editing system was used to generate L1cam mutation in the Sprague Dawley embryos. The CRISPR/Cas9 targeting exon 4 of the rat L1cam created a 1bp-insertion (206_207insT) in exon 4. No protein expression was detected in the brain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695003</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;L1cam&lt;sup&gt;em2Jgn&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=851&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=851&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>L1cam&lt;sup&gt;em2Jgn&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14696788</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="156748597" STOP_POS="156775116" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="151597270" STOP_POS="151623776" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="156901244" STOP_POS="156928064" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="152649353" STOP_POS="152676124" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="159784792" STOP_POS="159801553" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00851</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 genome editing system was used to generate L1cam mutation in the Sprague Dawley embryos. The CRISPR/Cas9 targeting exon 4 of the rat L1cam created a 300 bp-deletion(c.205_505del) in exon 4. No protein expression was detected in the brain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695004</RGD_ID>
    <STRAIN_SYMBOL>BBDR.F344-(D4Mgh24-D4Rhw6),BBDP-(D4Rhw6-D4Rhw10)/Rhw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=458&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=458&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2019-06-27)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00458</CITATION_ID>
    <DESCRIPTION>3 Mb of F344 DNA introgressed on Chr.4 between D4Mgh24 (73.75 Mb) and D4Rhw6 (76.83 Mb), and BB diabetes prone (DP) DNA introgressed from D4Rhw6 to D4Rhw10 (the most distal marker the end of the chromosome)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695026</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Crh-cre)Msg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=852&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=852&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-02-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00852</CITATION_ID>
    <DESCRIPTION>Cre recombinase has been inserted into the genome under the control of the Crh promoter. Generated on Wistar and backcrossed to Wistar every generation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695028</RGD_ID>
    <STRAIN_SYMBOL>SD.DA-&lt;i&gt;Kcnh2&lt;sup&gt;tm(EGFP-Pac)1Qly &lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=847&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=847&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00847</CITATION_ID>
    <DESCRIPTION>This strain was made by electroporation of DAc8 embryonic stem cells with a targeting vector containing 6.3kb 5' and 2.1kb 3' homology arm. The Kcnh2 gene 7th and 8th exons are replaced with a CAG-EGFP-IRES-Pac cassette. Chimeras were formed by microinjecting into F344 blastocysts. Founder animals were mated with SD rats to produce this strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695029</RGD_ID>
    <STRAIN_SYMBOL>SD.DA-&lt;i&gt;Kcnh2&lt;sup&gt;tm(CAG-EGFP)1Qly &lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=848&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=848&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00848</CITATION_ID>
    <DESCRIPTION>This strain was made by electroporation of DAc8 embryonic stem cells with a targeting vector containing 7.5kb 5' and 1.6kb 3' homology arm. A FRT-CAG-EGFP-IRES-Pac-FRT cassette is inserted into the intron between 8th and 9th exons of Kcnh2 gene. Chimeras were formed by microinjecting into F344 blastocysts. Founder animals were mated with SD rats to produce this strain</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695030</RGD_ID>
    <STRAIN_SYMBOL>SD.DA-&lt;i&gt;Pex1&lt;sup&gt;tm(G843D-FRT-CAG-Pac-FRT)1Qly&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=846&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=846&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00846</CITATION_ID>
    <DESCRIPTION>This strain was made by electroporation of DAc8 embryonic stem cells with a targeting vector containing 5.8kb 5' and 1.7kb 3' homology arms. A G843D point mutation is introduced into the Pex1 gene. The 12th and 13th exons are flanked with two loxP sites. A FRT-CAG-Pac-FRT cassette is inserted into the intron between Pex1 13th and 14th exon. This strain mimics the Peroxisomal Disorders. Heterozygote does not show any abnormalities.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695031</RGD_ID>
    <STRAIN_SYMBOL>SD.DA-&lt;i&gt;Il2rg&lt;sup&gt;Tm(G843D-FRT-CAG-Pac-FRT)1Qly&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=845&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=845&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00845</CITATION_ID>
    <DESCRIPTION>This strain was made by electroporation of DAc8 embryonic stem cells with a targeting vector containing 6.0kb 5' and 1.8kb 3' homology arms and a FRT-CAG-Pac-FRT cassette. The FRT-CAG-Pac-FRT cassette is inserted into the intron between Il2rg 4th and 5th exon. No genomic sequence is deleted. Chimeras were formed by microinjecting into F344 blastocysts. Founder animals were mated with SD rats to produce this strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695032</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-loxP-mCherry-loxP-EGFP)1Qly</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=844&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=844&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00844</CITATION_ID>
    <DESCRIPTION>A CAG-loxP-mCherry-loxP-EGFP cassette was injected into SD zygote to generate this line. The integration site is not determined. This transgenic line could be mated to other rat lines that express Cre/CreER for lineage tracing.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695033</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-Flpe)Qly</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=843&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=843&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00843</CITATION_ID>
    <DESCRIPTION>A CAG-Flpe cassette was injected into SD zygote to generate this line. The integration site is not determined.This transgenic line could be used to mate with other rat models that contains FRT sites to remove the cassette that is flanked by those FRT sites.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695034</RGD_ID>
    <STRAIN_SYMBOL>ZUC-&lt;I&gt;Lepr&lt;/I&gt;&lt;sup&gt;fa&lt;/sup&gt;.BN-(D1Rat183-D1Rat90)/Ste</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=837&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=837&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00837</CITATION_ID>
    <DESCRIPTION>Congenic for distal half of Chromosome 1 from D1Rat183 to D1Rat90 from Brown Norway (BN) on the UC Davis ZUC Lepr faSte/+ strain background. The genetic backgound of the ZUC strain carries a defective leptin receptor on Chromosome 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695052</RGD_ID>
    <STRAIN_SYMBOL>ACI-Tg(ROSA26-ALPP)Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=817&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=817&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2019-07-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>ALPP</ALLELES>
    <ALLELE_RGD_IDS>1314395</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00817</CITATION_ID>
    <DESCRIPTION>F344-Tg(ROSA26-ALPP)EpsRrrc (RGD:1566458) received in 1999 from Dr. Eric Sandgren, Univ. Wisconsin-Madison. Since 1999 bred on ACI background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695053</RGD_ID>
    <STRAIN_SYMBOL>ZDF-&lt;i&gt;Cnr1&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME>ZDF-&lt;i&gt;Cnr1&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=800&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=800&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00800</CITATION_ID>
    <DESCRIPTION>11bp deletion from genomic DNAfor the cannabinoid-1 receptor (Cnr1)using Zinc-Fingers Nucleases. Animals are resistant to the development of type-2 diabetes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695054</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(CAG-loxP-STOP-loxP-ZsGreen)551Bryd</STRAIN_SYMBOL>
    <FULL_NAME>F344-Tg(CAG-loxP-STOP-loxP-ZsGreen)551</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=795&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=795&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2019-07-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00795</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>14695055</RGD_ID>
    <STRAIN_SYMBOL>MHS/Roman</STRAIN_SYMBOL>
    <FULL_NAME>Milan Hypertensive Strain</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=794&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=794&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00794</CITATION_ID>
    <DESCRIPTION>Inbred hypertension model linked to a mutation in Add1 gene that has been validated as one of the genes linked to hypertension in numerous human genetic studies. Inbred strain originally developed by Dr. Bianchi in Milan in 1979.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695058</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Add3&lt;sup&gt;em1Roman&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=792&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=792&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00792</CITATION_ID>
    <DESCRIPTION>frame shift deletion in an exon 12 of Add3 gene causing a stop codon and loss of function. SD outbred background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695059</RGD_ID>
    <STRAIN_SYMBOL>BBDP/WorSunn.WAG-rnu/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=789&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=789&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00789</CITATION_ID>
    <DESCRIPTION>To develop BBDP rats congenic for the rnu mutation (nude BBDP), researchers introgressed the rnu mutation from inbred rnu/rnu WAG rats (obtained from Biomedical Research Models) using marker assisted genotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695060</RGD_ID>
    <STRAIN_SYMBOL>WKY-Tg(Eef1a1-GFP)Tja</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=780&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=780&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00780</CITATION_ID>
    <DESCRIPTION>Transgenic strain using Sleeping Beauty transposon germline transgenesis, ubiquitously expressing green fluorescent protein (GFP) under the rat eukaryotic translation elongation factor 1 alpha (Eef1a1) promoter. Two integration sites located on chromosome 8:28170658 and chromosome 1:276465837, both located in intronic gene areas, Jam3 (RGD:1303248) intron 1 and Vti1a (RGD:621490) intron 6, respectively. The Jam3 intron 1 is 51bp long, and the transgene resides at 37kb from exon 1 and 13kb from exon 2. In Vti1a intron 6, 102 bp long, the transgene is located at 81.4 kb from exon 5 and 21 kb from exon 6.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695061</RGD_ID>
    <STRAIN_SYMBOL>LobRrrc:WI</STRAIN_SYMBOL>
    <FULL_NAME>Lobund-Wistar</FULL_NAME>
    <ORIGINATION>Freimann Life Science Center, University of Notre Dame, Indiana</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=962&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00962</CITATION_ID>
    <DESCRIPTION>Male L-W develop spontaneous tumors in the anterior and ventral prostate and the seminal vesicle @ an average of 20 months. Tumors can be induced with N-methylnitrosourea and testosterone propinate in an average of 10 months. A cell line of a prostate adenocarcinoma was also created from the strain (PAIII) and can be administer SC in L-W rats with palpable tumor in 7-14 days and metastasis to the lymph nodes and lungs in 28-30 days.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695063</RGD_ID>
    <STRAIN_SYMBOL>BN.LEW-(&lt;i&gt;D10Rat258 and D10Rat51&lt;/i&gt;)/Ssn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Massachusetts Medical School</ORIGINATION>
    <SOURCE>Deposited at &lt;a href=http://www.rrrc.us/Strain/?x=752&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2024-01-11)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="13650386" STOP_POS="13650598" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="11072115" STOP_POS="13146036" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="11278340" STOP_POS="13486971" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="10039921" STOP_POS="13302032" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="11212678" STOP_POS="13365903" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00752</CITATION_ID>
    <DESCRIPTION>Severe osteopetrosis with numerous non-functioning osteoclasts. Locus on chromosome 10. Homozygotes not fertile, need to test breed to ID heterozygotes. Homozygotes have no teeth, require ground food. One of only 4 osteopetrotic mutations in rat. Genetic lesion is not yet known but mutation is inherited in an autosomal recessive manner. The candidate gene region has been localized to Chr 10 between D10Rat258 and D10Rat51. original background strain is LEW/Ssn.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695083</RGD_ID>
    <STRAIN_SYMBOL>W/LnneRrrc</STRAIN_SYMBOL>
    <FULL_NAME>Audiogenic Wistar rat</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=697&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=697&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00697</CITATION_ID>
    <DESCRIPTION>Wistar rats maintained at the  animal  facility  of  the  Ribeirao  Preto  School  of Medicine at the University of Sao Paulo, Brazil, were tested for audiogenic seizures, using as criteria an SI and the L1 (ref. RGD:14695082). The WAR colony foundation stock was produced  by  mating  animals  displaying  at  least procursive behaviors in three consecutive  tests,  one  every  4  days  (two  males  and four females). Each couple produced two or three lit-ters,  from  which  selected  individuals  displaying  the highest SI and shortest L1 were mated, at adult age,with their fathers and mothers. From the second generation on, brother  and sister matings were done, in a ratio of one male to two females, selected accordingto the criteria above.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695085</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Trim63&lt;sup&gt;em1(hiLuc)&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=731&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=731&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trim63&lt;sup&gt;em1(hiLuc)&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14696789</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="151817209" STOP_POS="151831026" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="146533492" STOP_POS="146547332" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="152533362" STOP_POS="152547138" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="156292566" STOP_POS="156306092" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="153059573" STOP_POS="153073907" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00731</CITATION_ID>
    <DESCRIPTION>The use of zinc finger nuclease technology (ZFN) to knockin a luciferase reporter directly downstream of MuRF1 (Trim63) coding sequences in rats,leaving endogenous MuRF1 gene expression intact and bicistro-nically linking it to the inserted reporter through a hepatitis CIRES (HCV-IRES). The resulting knockin rat line, MuRF1-hiLUCs, has reporter characteristics that are fully reflective ofendogenous MuRF1 gene expression, can be used as a universalbiomarker  of  skeletal  muscle  atrophyin   vivo,  and  has  abioluminescent readout compatible with whole animal imagingmodalities.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695086</RGD_ID>
    <STRAIN_SYMBOL>Zuc/VcJw</STRAIN_SYMBOL>
    <FULL_NAME>Zucker fatty</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=740&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=740&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00740</CITATION_ID>
    <DESCRIPTION>The original background strain derived from Sherman and Merck stock M rats (13 M strain). Obese animals produced by crossing homozygous obese males to heterozygous lean females.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695088</RGD_ID>
    <STRAIN_SYMBOL>WMS/SimfBR</STRAIN_SYMBOL>
    <FULL_NAME>Munich Wistar</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=832&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=832&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2019-07-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00832</CITATION_ID>
    <DESCRIPTION>Received from Munich, Germany via the V.A. San Francisco as line bred stock. Caesarean rederived when pedigreed brother x sister matings began. Selected for surface glomeruli and prominent elongated nephrons at the 6th, 12th and 18th .This strain also possess elongated nephrons. Unlike other Wistar strains with surface glomeruli, these animals do not become proteinuric as they age, which allows for the study of long term, chronic models. Age related proteinuria and spontaneous renal disease could interfere with experimentally-induced conditions.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695547</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(HLA-B*2705,B2M)33-3Trg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=624&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=624&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2019-07-08)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>B2M|HLA-B</ALLELES>
    <ALLELE_RGD_IDS>735892|1352836</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00624</CITATION_ID>
    <DESCRIPTION>This strain was made by pronuclear injection into LEW/Crl embryos. The embryos were co-injected with DNA fragments containing the HLA-B*2705 human gene  and the human beta-2-microglobulin gene.   The strain carries 55 copies of HLA-B*2705 and 29 copies of human beta-2-microglobulin gene. The transgenic strain  was transferred from Dr. Joel Taurog, University of Texas Southwestern Medical School in Dallas to the Rat Resource and Research Center .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14695548</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(HLA-B*2705,B2M)21-4HTrg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=622&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=622&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2019-07-08)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>B2M|HLA-B</ALLELES>
    <ALLELE_RGD_IDS>735892|1352836</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00622</CITATION_ID>
    <DESCRIPTION>This strain was made by pronuclear injection into LEW/Crl embryos. The embryos were co-injected with DNA fragments containing the HLA-B*2705 human gene  and the human beta-2-microglobulin gene.   The strain carries 150 copies of HLA-B*2705 and 90 copies of human beta-2-microglobulin gene. The transgenic strain  was transferred from Dr. Joel Taurog, University of Texas Southwestern Medical School in Dallas to the Rat Resource and Research Center .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14696715</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Htr7&lt;sup&gt;em1Msu&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Transgenic and Genome Editing Facility, and Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, Michigan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Htr7&lt;sup&gt;em1Msu&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14696716</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="243049064" STOP_POS="243173636" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="233636442" STOP_POS="233761063" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="254547964" STOP_POS="254671811" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="261759122" STOP_POS="261879914" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="240136279" STOP_POS="240260620" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14696715</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant; this induced an 11 bp deletion in exon 1 and a 4 bp deletion in exon 2 of the Htr7 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14696719</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Trpc4&lt;sup&gt;Tn(sb-T2/Bart3)2.192Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=344&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00344</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Trpc4 gene. The heterozygotes were intercrossed to produce the wild type mutant.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14696720</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Trpc4&lt;sup&gt;Tn(sb-T2/Bart3)2.192Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=344&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00344</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Trpc4 gene. The heterozygotes were intercrossed to produce the homozygous mutant.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14696721</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Trpc4&lt;sup&gt;Tn(sb-T2/Bart3)2.192Mcwi-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>PhysGen, Transposagen</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=344&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00344</CITATION_ID>
    <DESCRIPTION>These Sleeping Beauty mutants were derived by crossing F344-TgTn(T2/Bart3)2Ceb (RGD:2290163) and F344-Tg(PGK2-sb11)Ceb (RGD:2290169).  This mutation consists of an insertion of a Sleeping Beauty transposable element gene trap construct into the 1st intron of the Trpc4 gene. The heterozygotes were intercrossed to produce the heterozygous mutant.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14696722</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cyp3a23/3a1&lt;sup&gt;em1Myliu&lt;/sup&gt;&lt;/i&gt;,&lt;i&gt;Cyp3a2&lt;sup&gt;em1Myliu&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>East China Normal University and Shanghai Changzheng Hospital Joint Research Center for Orthopedic Oncology, Shanghai Key Laboratory of Regulatory Biology
Institute of Biomedical Sciences and School of Life Sciences. Shanghai, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp3a23-3a1&lt;sup&gt;em1Myliu&lt;/sup&gt;|Cyp3a2&lt;sup&gt;em1Myliu&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14696724|14696725</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="14321771" STOP_POS="14343886" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="14369950" STOP_POS="14398803" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="9207978" STOP_POS="9230064" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="9256159" STOP_POS="9285020" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="11641500" STOP_POS="11677818" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="11053888" STOP_POS="11082742" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="13145742" STOP_POS="13174596" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="13719927" STOP_POS="13740743" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="9567120" STOP_POS="9595974" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="9517016" STOP_POS="9541000" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14696722</CITATION_ID>
    <DESCRIPTION>This rat strain is a double knock out for Cyp3a23/3a1 and Cyp3a2 created by using CRISPR/Cas9 targeting  exons of Cyp3a23/3a1 and Cyp3a2. This strain carries a 22-bp deletion of Cyp3a23/3a1 and a 10-bp deletion of Cyp3a2 on Sprague Dawley background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14700890</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Cx3cr1-cre/ERT2)3Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=862&amp;log=yes&gt;Rat Resource &amp; Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=862&amp;log=yes&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-02-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00862</CITATION_ID>
    <DESCRIPTION>This strain was generated by microinjection of Sprague-Dawley embyos with a BAC DNA containing the Cx3cr1-cre/ERT2 transgene which is composed of cre/ERT2 recombinase gene driven by the rat genomic Cx3cr1promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14975242</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(rs105487995-rs105373896)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14975242</CITATION_ID>
    <DESCRIPTION>This congenic line was produced by backcrossing ACI.FHH-[D1Rat74-D1Rat90] (also named Rf-1A, RGD:5143940) congenic rats to ACI rats to initiate the generation of Rf-1 congenic sublines. Offspring that had inherited a desirable recombination within the Rf-1 region were selected. These selected offspring were backcrossed and intercrossed to produce homozygous congenic sublines used for phenotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14975243</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(rs105487995-rs106411696)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14975243</CITATION_ID>
    <DESCRIPTION>This congenic line was produced by backcrossing ACI.FHH-[D1Rat74-D1Rat90] (also named Rf-1A, RGD:5143940) congenic rats to ACI rats to initiate the generation of Rf-1 congenic sublines. Offspring that had inherited a desirable recombination within the Rf-1 region were selected. These selected offspring were backcrossed and intercrossed to produce homozygous congenic sublines used for phenotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14975244</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(rgdv393055223-rs107095981)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14975244</CITATION_ID>
    <DESCRIPTION>This congenic line was produced by backcrossing ACI.FHH-[D1Rat74-D1Rat90] ((also named Rf-1A, RGD:5143940) congenic rats to ACI rats to initiate the generation of Rf-1 congenic sublines. Offspring that had inherited a desirable recombination within the Rf-1 region were selected. These selected offspring were backcrossed and intercrossed to produce homozygous congenic sublines used for phenotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14975245</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(rgdv393055223-rs198922144)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14975245</CITATION_ID>
    <DESCRIPTION>This congenic line was produced by backcrossing ACI.FHH-[D1Rat74-D1Rat90] (also named Rf-1A, RGD:5143940) congenic rats to ACI rats to initiate the generation of Rf-1 congenic sublines. Offspring that had inherited a desirable recombination within the Rf-1 region were selected. These selected offspring were backcrossed and intercrossed to produce homozygous congenic sublines used for phenotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14975246</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(rgdv393055223-rs198076037)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14975246</CITATION_ID>
    <DESCRIPTION>This congenic line was produced by backcrossing ACI.FHH-[D1Rat74-D1Rat90] (also named Rf-1A, RGD:5143940) congenic rats to ACI rats to initiate the generation of Rf-1 congenic sublines. Offspring that had inherited a desirable recombination within the Rf-1 region were selected. These selected offspring were backcrossed and intercrossed to produce homozygous congenic sublines used for phenotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14975247</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(rs105373896-rgdv253272372)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14975247</CITATION_ID>
    <DESCRIPTION>This congenic line was produced by backcrossing ACI.FHH-[D1Rat74-D1Rat90] (also named Rf-1A, RGD:5143940) congenic rats to ACI rats to initiate the generation of Rf-1 congenic sublines. Offspring that had inherited a desirable recombination within the Rf-1 region were selected. These selected offspring were backcrossed and intercrossed to produce homozygous congenic sublines used for phenotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14975248</RGD_ID>
    <STRAIN_SYMBOL>ACI.FHH-(rs198076037-rs105278863)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14975248</CITATION_ID>
    <DESCRIPTION>This congenic line was produced by backcrossing ACI.FHH-[D1Rat74-D1Rat90] (also named Rf-1A, RGD:5143940) congenic rats to ACI rats to initiate the generation of Rf-1 congenic sublines. Offspring that had inherited a desirable recombination within the Rf-1 region were selected. These selected offspring were backcrossed and intercrossed to produce homozygous congenic sublines used for phenotyping.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14975305</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Bmpr2&lt;sup&gt;em1Sage+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>VA Palo Alto Health Care System, Stanford University School of Medicine</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bmpr2&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14981587</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="68685942" STOP_POS="68801353" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="61192718" STOP_POS="61307280" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="66568074" STOP_POS="66683019" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="66371542" STOP_POS="66486121" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="58327587" STOP_POS="58436057" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14975305</CITATION_ID>
    <DESCRIPTION>These ZFN mutant rats were produced by injecting zinc finger nuclease targeting rat Bmpr2 into F344 embryos. The zinc-finger nuclease mediated genome editing system created a deletion of  527 bp across intron and exon1 boundary. The strains of both sexes were confirmed  Bmpr2 haplodeficiency.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14981588</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Bmpr2&lt;sup&gt;em2Sage+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>VA Palo Alto Health Care System, Stanford University School of Medicine</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bmpr2&lt;sup&gt;em2Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14981589</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="68685942" STOP_POS="68801353" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="61192718" STOP_POS="61307280" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="66568074" STOP_POS="66683019" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="66371542" STOP_POS="66486121" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="58327587" STOP_POS="58436057" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14981588</CITATION_ID>
    <DESCRIPTION>These ZFN mutant rats were produced by injecting zinc finger nuclease targeting rat Bmpr2 into F344 embryos. The zinc-finger nuclease mediated genome editing system created a deletion of  16 bp in exon1. The strains of both sexes were confirmed  Bmpr2 haplodeficiency.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14981597</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(SOD1*G93A)26DwcTac</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href= https://www.taconic.com/rat-model/sod1-rat&gt;TACONIC&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>SOD1</ALLELES>
    <ALLELE_RGD_IDS>730855</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14981597</CITATION_ID>
    <DESCRIPTION>SD rats were microinjected with a linear 12 kb EcoRI-BamH1 fragment containing the coding sequence and promoter region of human SOD1 gene with G93A mutation. Originally created by John Kulik at Wyeth. Transgenic Model of SOD1 mediated Amyotrophic Lateral Sclerosis (ALS, Lou Gehrig's Disease). Came to Taconic in April 2002 for David Howland at Wyeth for distribution as an Emerging Model. Joint collaboration between Wyeth and The ALS Association.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14985210</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Cyfip1&lt;sup&gt;em1Sage+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyfip1&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14985211</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="115842754" STOP_POS="115935163" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="106710924" STOP_POS="106799393" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="114258773" STOP_POS="114347138" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="115265128" STOP_POS="115353515" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="107245993" STOP_POS="107334337" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14985210</CITATION_ID>
    <DESCRIPTION>The bioinformatics software (Horizon Discovery, St. Louis, USA) was used to design a short guide RNA (sgRNA) targeting a Protospacer Adjacent Motif (PAM) sequence within exon 7 of the rat Cyfip1gene (GGCAGATCCACAATCCATCCagg) on chromosome 1 (first 21 of 32 exons, Refseq: NC_005100.4, NM_001107517.1).sgRNA-Cas9 was performed by nucleofecting the sgRNA-Cas9 into rat C6 glial cells. Genomic DNA (gDNA) PCR products were subsequently generated from nucleofected C6 cells using primers flanking the sgRNA site (FOR: GCCAAAGCTTCCCCTAAAGT; REV: TGGGCGTCAAGTACATTCTG; 497bp amplicon). Embryos were collected from donor female Long Evans rats and injected with the  validated  sgRNA-Cas9.   Then implanted into synchronized pseudopregnant Long Evans recipient female This mutant carries 4bp out of frame heterozygous deletion in exon 7 of the Cyfip1, resulting bioinformatics prediction of an early stop codon in exon 8.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>14995941</RGD_ID>
    <STRAIN_SYMBOL>Wpk</STRAIN_SYMBOL>
    <FULL_NAME>Wistar polycystic kidney  rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tmem67&lt;sup&gt;wpk&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14995943</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="30333793" STOP_POS="30386702" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="25567678" STOP_POS="25567678" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="25666138" STOP_POS="25721056" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="30371964" STOP_POS="30424943" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="26324625" STOP_POS="26377531" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_14995941</CITATION_ID>
    <DESCRIPTION>The wpk mutation was first recognized in 1994 in a colony of outbred Wistar rats at Utrecht University (Utrecht, The Netherlands).  In 1996, a breeding pair of test-proven heterozygotes were transferred to the University of Rotterdam (Rotterdam, The Netherlands), and a new subcolony was initiated. This colony has been maintained by brother-sister matings for more than five generations. Individuals heterozygous for the mutant allele were identified in each generation by test-crossing phenotypically normal offspring from known heterozygotes. A single C to T substitution in exon 12 was identified as the mutated allele in the Wpk rat. This mutation converts a proline to a leucine in the protein products(P394L). This mutation was not present in the parental Wistar strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>15017093</RGD_ID>
    <STRAIN_SYMBOL>Wpk &lt;sup&gt;+/-&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Wpk heterozygous rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tmem67&lt;sup&gt;wpk&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14995943</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="30333793" STOP_POS="30386702" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="25567678" STOP_POS="25567678" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="25666138" STOP_POS="25721056" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="30371964" STOP_POS="30424943" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="26324625" STOP_POS="26377531" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_15017093</CITATION_ID>
    <DESCRIPTION>The wpk mutation was first recognized in 1994 in a colony of outbred Wistar rats at Utrecht University (Utrecht, The Netherlands).  In 1996, a breeding pair of test-proven heterozygotes were transferred to the University of Rotterdam (Rotterdam, The Netherlands), and a new subcolony was initiated. This colony has been maintained by brother-sister matings for more than five generations. Individuals heterozygous for the mutant allele were identified in each generation by test-crossing phenotypically normal offspring from known heterozygotes. A single C to T substitution in exon 12 was identified as the mutated allele in the Wpk rat. This mutation converts a proline to a leucine in the protein products(P394L).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>15017094</RGD_ID>
    <STRAIN_SYMBOL>Wpk &lt;sup&gt;-/-&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Wpk homozygous rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tmem67&lt;sup&gt;wpk&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14995943</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="30333793" STOP_POS="30386702" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="25567678" STOP_POS="25567678" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="25666138" STOP_POS="25721056" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="30371964" STOP_POS="30424943" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="26324625" STOP_POS="26377531" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_15017094</CITATION_ID>
    <DESCRIPTION>The wpk mutation was first recognized in 1994 in a colony of outbred Wistar rats at Utrecht University (Utrecht, The Netherlands).  In 1996, a breeding pair of test-proven heterozygotes were transferred to the University of Rotterdam (Rotterdam, The Netherlands), and a new subcolony was initiated. This colony has been maintained by brother-sister matings for more than five generations. Individuals heterozygous for the mutant allele were identified in each generation by test-crossing phenotypically normal offspring from known heterozygotes. A single C to T substitution in exon 12 was identified as the mutated allele in the Wpk rat. This mutation converts a proline to a leucine in the protein products(P394L).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>15036806</RGD_ID>
    <STRAIN_SYMBOL>WKAH/Tj</STRAIN_SYMBOL>
    <FULL_NAME>Wistar-King A, WKA</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2019-11-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_15036806</CITATION_ID>
    <DESCRIPTION>WKAH/Tj inbred rats were bred in the Institute for Animal Experimentation, the University of Tokushima School of Medicine, under specific pathogen free conditions.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>15045605</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Prnp-LacZ/EGFP)12084</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_15045605</CITATION_ID>
    <DESCRIPTION>This transgenic strain line 12084 carries the dual-reporter LacZ/EGFP (enhanced green fluorescent protein) cloned into the  rat  Prnp vector (raPrnp) and the expression of transgenes were  driven by rat Prnp promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>15045606</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Prnp-LacZ/EGFP)12085</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_15045606</CITATION_ID>
    <DESCRIPTION>This transgenic strain line Tg12085 carries the dual-reporter LacZ/EGFP (enhanced green fluorescent protein) cloned into the  rat  Prnp vector (raPrnp) and the expression of transgenes were  driven by rat Prnp promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>15045607</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Prnp-Prnp)2919</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_15045607</CITATION_ID>
    <DESCRIPTION>This transgenic strain line Tg2919 carries the open reading frame of rat Prnp (prion protein) cloned into the  rat  Prnp vector (raPrnp) and the expression of transgene were  driven by rat Prnp promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>15045608</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Prnp-Prnp)2922</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_15045608</CITATION_ID>
    <DESCRIPTION>This transgenic strain line Tg2922 carries the open reading frame of rat Prnp (prion protein) cloned into the  rat  Prnp vector (raPrnp) and the expression of transgene were  driven by rat Prnp promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>15090817</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Ahr&lt;sup&gt;em1Hyama+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ahr&lt;sup&gt;em1Hyama&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>15090818</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_15090817</CITATION_ID>
    <DESCRIPTION>Heterozygous rats carrying a defective exon 2 in rat Ahr gene was created by injecting TALEN mRNA containing 5'-TTCTAAACGACACAGAGACCGGCTGAACACAGAGTTAGACCGCCTGGCTA-3' to embryos of JclKud:WI.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>15090819</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Ahr&lt;sup&gt;em1Hyama-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ahr&lt;sup&gt;em1Hyama&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>15090818</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_15090819</CITATION_ID>
    <DESCRIPTION>The homozygous rats carrying 2 defective Ahr genes. The deletion of part of  exon 2 in rat Ahr gene was created by injecting TALEN mRNA containing 5'-TTCTAAACGACACAGAGACCGGCTGAACACAGAGTTAGACCGCCTGGCTA-3' to embryos of JclKud:WI.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>18182944</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Vwf&lt;sup&gt;em2Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center, through Versiti Blood Research Institute</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2020-01-14)</AVAILABILITY>
    <RESEARCH_USE>Bleeding Disorders</RESEARCH_USE>
    <ALLELES>Vwf&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>18182945</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="160042900" STOP_POS="160177757" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="158360152" STOP_POS="158491539" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="158085059" STOP_POS="158219525" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="225098521" STOP_POS="225229257" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="161723415" STOP_POS="161854766" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_18182944</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 mediated gene editing was used to delete a 130,954bp region of the VWF gene in DahlSS/Mcw (SS/JrHsdMcwi ) rat embryos</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>18182946</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Vwf&lt;sup&gt;em3Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center, through Versiti Blood Research Institute</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-01-14)</AVAILABILITY>
    <RESEARCH_USE>Bleeding Disorders</RESEARCH_USE>
    <ALLELES>Vwf&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>18182947</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="160042900" STOP_POS="160177757" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="158360152" STOP_POS="158491539" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="158085059" STOP_POS="158219525" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="225098521" STOP_POS="225229257" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="161723415" STOP_POS="161854766" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_18182946</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 mediated gene editing was used to delete a 130,921bp region of the VWF gene in DahlSS/Mcw (SS/JrHsdMcwi ) rat embryos</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>18337282</RGD_ID>
    <STRAIN_SYMBOL>Iar: LE</STRAIN_SYMBOL>
    <FULL_NAME>Long-Evans Rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.iar.or.jp/english/index_la.html&gt;Institute for Animal Reproduction&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.iar.or.jp/english/index_la.html&gt;Institute for Animal Reproduction&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Ophthalmology, Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_18337282</CITATION_ID>
    <DESCRIPTION>This strain was established by Dr. Long and Dr. Evans in 1915. This traces its roots to Monash University to Tohoku University in 1984; to Institute for Animal Reproduction through acquisition in 1996.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>19165133</RGD_ID>
    <STRAIN_SYMBOL>F344;SD-&lt;i&gt;C3&lt;sup&gt;em1Linf&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The animal facility of Lerner Research Institute, Cleveland Clinic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>C3&lt;sup&gt;em1Linf&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>19165134</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="2174412" STOP_POS="2201339" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="2087437" STOP_POS="2114366" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="9721137" STOP_POS="9747084" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="8728465" STOP_POS="8754412" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_19165133</CITATION_ID>
    <DESCRIPTION>This mutant strain was created by CRISPR/Cas9 genome editing system. The mutant carried insertion of a premature termination codon in exon 2 and was predicted to result in loss of protein expression due to non-sense mediated decay of mRNA. The heterozygous knock out rats (F344/Sprague Dawley mixed background) were bred to each other, and the pups were genotyped to identify the WT and C3 homozygous knock out littermates.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>19165362</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Krtcap3&lt;sup&gt;em3Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Krtcap3&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>19165363</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="30840906" STOP_POS="30842500" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="25120938" STOP_POS="25122522" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="26486391" STOP_POS="26486394" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="36304329" STOP_POS="36305898" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_19165362</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Krtcap3  gene of WKY/Ncrlrat embryos. The resulting mutation is a net 2-bp deletion in the exon 2 of the targeted gene, which led to a frameshift mutation and early termination of the KRTCAP3 protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>19165364</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Adcy3&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact Dr. Solberg-Woods  at Wake Forest University School of Medicine, Email: lsolberg@wakehealth.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-03-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adcy3&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>19165365</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="32845554" STOP_POS="32845556" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="27126062" STOP_POS="27126064" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="28572367" STOP_POS="28572369" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="38378060" STOP_POS="38454926" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="27118325" STOP_POS="27202275" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_19165364</CITATION_ID>
    <DESCRIPTION>Cas9 protein and sgRNA targeting the sequence CCTTTTTGCAGAGCACGAAA within exon 2 of Adcy3 were injected into embryos of the WKY/NCrl strain.  A 3-bp deletion resulted (rn7: chr6:27,126,062-27,126,064).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>19165366</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Adcy3&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact Dr. Solberg-Woods  at Wake Forest University School of Medicine, Email: lsolberg@wakehealth.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-03-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adcy3&lt;sup&gt;em3Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>616390062</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_19165366</CITATION_ID>
    <DESCRIPTION>Cas9 protein and sgRNA targeting the sequence CCTTTTTGCAGAGCACGAAA within exon 2 of Adcy3 were injected into embryos of the WKY/NCrl strain.  A 1-bp deletion resulted (rn7: chr6:27,126,062).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>19259464</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Camk2n1&lt;sup&gt;em1Tja-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SHR-&lt;i&gt;Camk2n1&lt;sup&gt;em1Tja-&lt;/sup&gt;/Camk2n1&lt;sup&gt;em1Tja-&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Camk2n1&lt;sup&gt;em1Tja&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>19259465</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="155958116" STOP_POS="155959897" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="150674819" STOP_POS="150676600" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="156876706" STOP_POS="156878486" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="160625616" STOP_POS="160627396" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="157235534" STOP_POS="157237314" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_19259464</CITATION_ID>
    <DESCRIPTION>SHR-Camk2n1-/- knockout rats were generated on an SHR/NCrl background by microinjecting zinc-finger nuclease (ZFN) mRNA (Sigma), targeted to exon 1 of Camk2n1, into one-cell stage SHR/NCrl embryos that were implanted into pseudopregnant rats. Heterozygous progeny, from a founder harboring a 38bp deletion in Camk2n1, were intercrossed to generate homozygous knockout rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>21079475</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lepr&lt;sup&gt;em4Lizh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Chinese Academy of Medical Sciences &amp; Comparative Medical Center, Peking Union Medical College, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_21079475</CITATION_ID>
    <DESCRIPTION>The Lepr knockout rats were generated by CRISPR/Cas9.  Two pairs of synthesized oligonucleotides for gRNA targeting on the exon 4 of Lepr, TAGGCAAATCATCTATAACTTC and AAACGAAGTTATAGATGATTTG; TAGGCTGAAAGCTGTCTTTCAG and AAACCTGAAAGACAGCTTTCAG were microinjected into Sprague Dawley (originally from Charles River) zygotes. The rat was genotyped by PCR with the primers, 5-prime-CTTGTGTCCAGAGCCTTCCTATAAC and 5-prime-ATTCCCCATGTTGTCTAGTAGTGATC. For genotyping, a 662-bp fragment of WT and a 368-bp fragment of the Lepr knockout gene were amplified with PCR. Founder 2 was chosen to establish a colony (designated as Lepr-/-), which carried a 298-bp deletion from No. 90043 bp to 90341 bp in the Lepr genome DNA sequence (NC_005104.4) and a 4-bp insertion and resulted in a termination codon TGA, deleting 997 amino acid of LEPR. Western blot analysis of total protein from liver tissue of the Lepr-/- rats confirmed the absence of LEPR.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>21083604</RGD_ID>
    <STRAIN_SYMBOL>SD-ROSA26 &lt;sup&gt;em1(LTR-nLuc)Ottc&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_21083604</CITATION_ID>
    <DESCRIPTION>The CRISPR/Case9 knock-in rats have cre recombinase-dependent expression of  nanoluciferase under the control of HIV LTR promoter inserted to the rat ROSA26 locus. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>21409748</RGD_ID>
    <STRAIN_SYMBOL>DA/Mmab</STRAIN_SYMBOL>
    <FULL_NAME>Dark Agouti</FULL_NAME>
    <ORIGINATION>Military Medical Academy, Serbia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_21409748</CITATION_ID>
    <DESCRIPTION>Dark Agouti rats which were bred and housed at the Military Medical Academy in Belgrade, Serbia</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>21409752</RGD_ID>
    <STRAIN_SYMBOL>DA/Ibiss</STRAIN_SYMBOL>
    <FULL_NAME>Dark Agouti</FULL_NAME>
    <ORIGINATION>Dark agouti rats were bred and housed  at Institute for biological research Sinisa Stankovic, Belgrade, Serbia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_21409752</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>25314294</RGD_ID>
    <STRAIN_SYMBOL>MWF/Ztm</STRAIN_SYMBOL>
    <FULL_NAME>Munich Wistar Fromter</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_25314294</CITATION_ID>
    <DESCRIPTION>Fromter selected from outbred Munich-Wistar rats for large numbers of superficial glomeruli.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>25330087</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Cntnap2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Generated with support from the Simons Foundation Autism Research Initiative (&lt;a href=https://www.sfari.org/resource/rat-models/&gt;SFARI&lt;/a&gt;); MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/autism-rat-model-resource/ &gt; Autism Rat Model Resource&lt;/a&gt;. Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Autism, ADHD, Developmental delay, Intellectual disability, Epilepsy, Bipolar disorder  (from &lt;a href=https://gene.sfari.org/database/human-gene/CNTNAP2&gt;SFARI GENE&lt;/a&gt;)</RESEARCH_USE>
    <ALLELES>Cntnap2&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>25330101</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="75691075" STOP_POS="75691075" METHOD="8"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_25330087</CITATION_ID>
    <DESCRIPTION>The rat strain was produced by injecting CRISPR/Cas9 targeting rat  Cntnap2 into Crl:LE embryos. The result is a 1-bp deletion in exon 6 of the gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>25330088</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Chd8&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Generated with support from the Simons Foundation Autism Research Initiative (&lt;a href=https://www.sfari.org/resource/rat-models/&gt;SFARI&lt;/a&gt;); MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/autism-rat-model-resource/ &gt; Autism Rat Model Resource&lt;/a&gt;, Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2025-02-20)</AVAILABILITY>
    <RESEARCH_USE>Autism, ADHD, Developmental delay, Intellectual disability, Epilepsy, Schizophrenia  (from &lt;a href=https://gene.sfari.org/database/human-gene/CHD8&gt;SFARI GENE&lt;/a&gt;)</RESEARCH_USE>
    <ALLELES>Chd8&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>25330100</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="27379285" STOP_POS="27438959" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="24905789" STOP_POS="24965461" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="28646442" STOP_POS="28646446" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="32423198" STOP_POS="32482762" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="27642767" STOP_POS="27704443" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_25330088</CITATION_ID>
    <DESCRIPTION>The rat strain was produced by injecting the CRISPR/Cas9  system targeting rat  Chd8 gene of Crl:LE embryos. The result is  a 5-bp deletion in exon 3 of rat Chd8 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>25330089</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Nrxn1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Generated with support from the Simons Foundation Autism Research Initiative (&lt;a href=https://www.sfari.org/resource/rat-models/&gt;SFARI&lt;/a&gt;); MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/autism-rat-model-resource/ &gt; Autism Rat Model Resource&lt;/a&gt;.  Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Autism, ADHD, Developmental delay, Intellectual disability, Epilepsy, Schizophrenia, Bipolar disorder  (from &lt;a href=https://gene.sfari.org/database/human-gene/NRXN1&gt;SFARI GENE&lt;/a&gt;)</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_25330089</CITATION_ID>
    <DESCRIPTION>The rat strain was produced by injecting  CRISPR/Cas9  targeting rat Nrxn1 into Crl:LE embryos. The result is a 4-bp deletion in exon 1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>25330091</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rictor&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rictor&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>40818254</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="57539279" STOP_POS="57631291" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="55811877" STOP_POS="55903893" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="56013898" STOP_POS="56105818" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="75754848" STOP_POS="75846705" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="55982784" STOP_POS="56071528" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_25330091</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 11-bp deletion in exon 19 of rat Rictor gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>25330093</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Mir146b&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mir146b&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>152600899</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="255144860" STOP_POS="255144947" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="245203438" STOP_POS="245203525" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="266089488" STOP_POS="266089575" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="273520429" STOP_POS="273520516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="251558047" STOP_POS="251558134" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_25330093</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  Crl:SD rat embryos. The resulting mutation is a 7-bp deletion  in Mir146b.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>25394526</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Dyrk1a&lt;sup&gt;em3Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Generated with support from the Simons Foundation Autism Research Initiative (&lt;a href=https://www.sfari.org/resource/rat-models/&gt;SFARI&lt;/a&gt;); MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/autism-rat-model-resource/ &gt; Autism Rat Model Resource&lt;/a&gt;. Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Developmental delay, Intellectual disability, Epilepsy (from &lt;a href=https://gene.sfari.org/database/human-gene/DYRK1A&gt;SFARI GENE&lt;/a&gt;)</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_25394526</CITATION_ID>
    <DESCRIPTION>The rat strain was produced by injecting  CRISPR/Cas9  targeting rat Dyrk1a into Crl:LE embryos. The result is a 5-bp deletion in exon 3 of the gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>25394528</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ephx2&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ephx2&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>25394529</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="44492065" STOP_POS="44492087" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="40316520" STOP_POS="40316542" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="42783099" STOP_POS="42783121" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="48799823" STOP_POS="48836848" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="45497660" STOP_POS="45556101" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_25394528</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the  Crl:SD rat embryos. The resulting mutation is a a 23-bp deletion in exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>25394530</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Scn2a&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/autism-rat-model-resource/ &gt; Autism Rat Model Resource&lt;/a&gt;. Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-02-20)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Scn2a&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>25394531</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="70710862" STOP_POS="70845569" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="50302781" STOP_POS="50437504" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="51749425" STOP_POS="51749430" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="58322640" STOP_POS="58456658" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="47588413" STOP_POS="47722800" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_25394530</CITATION_ID>
    <DESCRIPTION>The rat strain was produced by injecting  CRISPR/Cas9  targeting rat  Scn2a into Crl:LE embryos. The mutant allele was produced by injecting CRISPR/Cas9 targeting rat Scn2a into Crl:LE embryos. The resulting mutation is net 4-bp deletion in exon 5 comprising a 10-bp deletion (shown in lower case: CTACGGGATccctggaattGGTTGGATTTCACAGTCATT ) and a 6-bp insertion (TTCACT).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>25394532</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Scn2a&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Scn2a&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>25394533</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="70710862" STOP_POS="70845569" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="50302781" STOP_POS="50437504" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="51749425" STOP_POS="51749430" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="58322640" STOP_POS="58456658" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="47588413" STOP_POS="47722800" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_25394532</CITATION_ID>
    <DESCRIPTION>The rat strain was produced by injecting  CRISPR/Cas9  targeting rat  Scn2a into Crl:LE embryos. The result is a 6-bp deletion in exon 5 of the gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>25394534</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;ROSA26&lt;sup&gt;em1(CAG-tdTomato)1Sage&lt;/sup&gt;&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_25394534</CITATION_ID>
    <DESCRIPTION>LE-ROSA26em1(CAG-tdTomato)1Sage (RGDID: 12905037) was backcrossed to SS/JrHsdMcwi for more than 8 generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>25824850</RGD_ID>
    <STRAIN_SYMBOL>NHla:SD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Hilltop Lab Animals, Inc. (http://www.hilltoplabs.com/public/sd.html) &lt;a href=http://www.hilltoplabs.com/public/sd.html&gt;Hilltop Lab Animals, Inc.&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_25824850</CITATION_ID>
    <DESCRIPTION>The colony history began with a colony of rats established by Robert Dawley around 1925. SD rats are often referred to as "Sprague-Dawley" Mr. Dawley used both his name and the maiden name, "Sprague", of his wife to create the name of the stock. The colony then went to Sprague Dawley, Inc. in 1945. NIH began a closed colony with animals obtained from Sprague Dawley, Inc. Hilltop Lab Animals, Inc. received animals from NIH in 1984. Through cesarean rederivation, the animals were fostered onto gnotobiotic rats in isolation. Descendants of these animals then became the colonies currently available. All colony histories contain some possibility of inaccuracy. This information is provided to the best of Hilltop's knowledge.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>27095885</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc41-D13Rat101&lt;/i&gt;)-&lt;i&gt;Ren&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ren&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>27095886</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_27095885</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the sequence acccttcatgctggccaagtttgacggggttctgggcatg into SS.BN(D13Hmgc41-D13Rat101)/Mcwi rat embryos. The resulting mutation is a net 4-bp frameshift deletion in exon 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>30309956</RGD_ID>
    <STRAIN_SYMBOL>SS.BN-(&lt;i&gt;D13Hmgc41-D13Rat101&lt;/i&gt;)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="50392759" STOP_POS="50392939" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="43830075" STOP_POS="47841255" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="49168131" STOP_POS="53264877" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="54236862" STOP_POS="58314767" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="45282442" STOP_POS="49428577" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_30309956</CITATION_ID>
    <DESCRIPTION>These were generated by crossing SS/JrHsdMcwi with SS-Chr 13&lt;sup&gt;BN&lt;/sup&gt;/Mcwi, rats from F1 were intercrossed and genotyped to get the congenic strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>32716420</RGD_ID>
    <STRAIN_SYMBOL>BDIX.BDIV-&lt;i&gt;D6Rat132-D6Rat229&lt;/i&gt;/Zte</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cell Biology (Cancer Research) of Duisburg-Essen University Medical School, Essen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="56545837" STOP_POS="101593851" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="50818445" STOP_POS="50818672" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="53553892" STOP_POS="53554118" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="63175341" STOP_POS="63175567" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="52753065" STOP_POS="99750142" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_32716420</CITATION_ID>
    <DESCRIPTION>The BDIX.BDIV-&lt;i&gt;D6Rat132-D6Rat229&lt;/i&gt;/Zte congenic strain was produced by crossing BDIX (tumor-susceptible) and BDIV (tumor resistant) and then selecting for strains carrying homozygous segments of the BDIV chromosome on a BDIX background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>35668858</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(HLA-B*2705m1,B2M)133-1Trg&lt;sup&gt;Tg/0&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_35668858</CITATION_ID>
    <DESCRIPTION>This strain was made by pronuclear injection into Lewis embryos. The embryos were co-injected with DNA fragments containing the HLA-B*2705 human gene (human HLA-B27 gene  with Serine replacing Cys67)  and the human beta-2-microglobulin gene. The strain carries 12 copies of HLA-B*2705 and 4 copies of the human beta-2-microglobulin gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>35668859</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Gnrh1&lt;sup&gt;tm1(cre)Aeh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>(1.) Allan Herbison at Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.; (2.) Vincent Prevot in INSERM, Lille, France.</ORIGINATION>
    <SOURCE>(1.) Allan Herbison at Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.; (2.) Vincent Prevot in INSERM, Lille, France.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2020-07-09)</AVAILABILITY>
    <RESEARCH_USE>Neuroendocrinology, Neurobiology, Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_35668859</CITATION_ID>
    <DESCRIPTION>This model was generated using zinc finger nuclease (ZFN) method. Cre recombinase was expressed under the control of the endogenous Gnrh1 gene by inserting an internal ribosomal entry site (IRES)-Cre cassette 30bp downstream from the translational stop site of the Gnrh1 open reading frame.  This was achieved by pronuclear co-injection of zinc finger nucleases (ATCCACAACATCCGAGTGtgacattGACGCTGAGATCCATGAC; cleavage site in lower case) along with a donor plasmid containing two 800bp homologous arms (HA) flanking IRES-Cre into a one-cell stage rat embryo.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>35668861</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(HLA-B*2705,B2M)&lt;sup&gt;Tg/0&lt;/sup&gt;21-3Reh</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_35668861</CITATION_ID>
    <DESCRIPTION>This strain was made by pronuclear injection into LEW/Crl embryos. The embryos were co-injected with DNA fragments containing the HLA-B*2705 human gene  and the human beta-2-microglobulin gene.   The strain carries 20 copies of HLA-B*2705 and 15 copies of the human beta-2-microglobulin gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>35668863</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(HLA-B*2705,B2M)21-3Reh&lt;sup&gt;Tg/Tg&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_35668863</CITATION_ID>
    <DESCRIPTION>This strain was made by pronuclear injection into LEW/Crl embryos. The embryos were co-injected with DNA fragments containing the HLA-B*2705 human gene  and the human beta-2-microglobulin gene.   The strain carries 40 copies of HLA-B*2705 and 30 copies of human beta-2-microglobulin gene. Founder 21-3 was selected and carrier animals from this founder were mated and bred to homozygosity.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>36174030</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Hamp&lt;sup&gt; em1Jfcol +/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Rat Resource &amp; Research Center (RRRC)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-07-28)</AVAILABILITY>
    <RESEARCH_USE>This rat models hereditary hemochromatosis (Type 2B) in humans. Iron overload research.</RESEARCH_USE>
    <ALLELES>Hamp&lt;sup&gt; em1Jfcol &lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38455987</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="95298332" STOP_POS="95300271" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="86170926" STOP_POS="86172865" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="89368021" STOP_POS="89369960" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="90523506" STOP_POS="90525473" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="85978120" STOP_POS="85980059" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_36174030</CITATION_ID>
    <DESCRIPTION>Hamp KO, Sprague-Dawley rats were generated by Transposagen Biopharmaceuticals (Lexington, KY). Four different genetically engineered rat lines, each with different sized Hamp deletions (with or without concurrent insertions), were created using TALEN technology. SD-Hamp em1Jfcol +/- (RGD: 36174030) is heterozygous carrying  a 169-bp deletion between exons 2 &amp; 3 of rat Hamp gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>36174220</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Hamp&lt;sup&gt; em1Jfcol -/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Rat Resource &amp; Research Center (RRRC)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-07-29)</AVAILABILITY>
    <RESEARCH_USE>This rat models hereditary hemochromatosis (Type 2B) in humans. Iron overload research.</RESEARCH_USE>
    <ALLELES>Hamp&lt;sup&gt; em1Jfcol &lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38455987</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="95298332" STOP_POS="95300271" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="86170926" STOP_POS="86172865" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="89368021" STOP_POS="89369960" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="90523506" STOP_POS="90525473" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="85978120" STOP_POS="85980059" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00907</CITATION_ID>
    <DESCRIPTION>Hamp KO, Sprague-Dawley rats were generated by Transposagen Biopharmaceuticals (Lexington, KY). Four different genetically engineered rat lines, each with different sized Hamp deletions (with or without concurrent insertions), were created using TALEN technology. SD-Hamp em1Jfcol -/- (RGD:36174220) is homozygous carrying  the 169-bp deletion between exons 2 &amp; 3 of  both rat Hamp alleles.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>36174221</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Hamp&lt;sup&gt; em2Jfcol +/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Rat Resource &amp; Research Center (RRRC)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-07-29)</AVAILABILITY>
    <RESEARCH_USE>This rat models hereditary hemochromatosis (Type 2B) in humans. Iron overload research.</RESEARCH_USE>
    <ALLELES>Hamp&lt;sup&gt; em2Jfcol &lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38455989</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="95298332" STOP_POS="95300271" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="86170926" STOP_POS="86172865" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="89368021" STOP_POS="89369960" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="90523506" STOP_POS="90525473" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="85978120" STOP_POS="85980059" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_36174221</CITATION_ID>
    <DESCRIPTION>Hamp KO, Sprague-Dawley rats were generated by Transposagen Biopharmaceuticals (Lexington, KY). Four different genetically engineered rat lines, each with different sized Hamp deletions (with or without concurrent insertions), were created using TALEN technology. SD-Hamp em2Jfcol +/- (RGD:36174221)  is heterozygous carrying a 230-bp deletion and a 1-bp insertion between exons 2 &amp; 3 of the rat Hamp gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>36174222</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Hamp&lt;sup&gt; em2Jfcol -/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Rat Resource &amp; Research Center (RRRC)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-07-29)</AVAILABILITY>
    <RESEARCH_USE>This rat models hereditary hemochromatosis (Type 2B) in humans. Iron overload research.</RESEARCH_USE>
    <ALLELES>Hamp&lt;sup&gt; em2Jfcol &lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38455989</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="95298332" STOP_POS="95300271" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="86170926" STOP_POS="86172865" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="89368021" STOP_POS="89369960" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="90523506" STOP_POS="90525473" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="85978120" STOP_POS="85980059" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00909</CITATION_ID>
    <DESCRIPTION>Hamp KO, Sprague-Dawley rats were generated by Transposagen Biopharmaceuticals (Lexington, KY). Four different genetically engineered rat lines, each with different sized Hamp deletions (with or without concurrent insertions), were created using TALEN technology. SD-Hamp em2Jfcol -/- (RGD:36174222) is homozygous carrying a 230-bp deletion and a 1-bp insertion between exons 2 &amp; 3 of both rat Hamp alleles.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>36174223</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Hamp&lt;sup&gt; em3Jfcol +/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Rat Resource &amp; Research Center (RRRC)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-07-29)</AVAILABILITY>
    <RESEARCH_USE>This rat models hereditary hemochromatosis (Type 2B) in humans. Iron overload research.</RESEARCH_USE>
    <ALLELES>Hamp&lt;sup&gt; em3Jfcol &lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38455990</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="95298332" STOP_POS="95300271" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="86170926" STOP_POS="86172865" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="89368021" STOP_POS="89369960" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="90523506" STOP_POS="90525473" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="85978120" STOP_POS="85980059" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_36174223</CITATION_ID>
    <DESCRIPTION>Hamp KO, Sprague-Dawley rats were generated by Transposagen Biopharmaceuticals (Lexington, KY). Four different genetically engineered rat lines, each with different sized Hamp deletions (with or without concurrent insertions), were created using TALEN technology. SD-Hamp em3Jfcol +/- (RGD:36174223)  is heterozygous carrying a 20-bp deletion and a 3-bp insertion in exon 2 of the rat Hamp gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>36174224</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Hamp&lt;sup&gt; em3Jfcol -/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Rat Resource &amp; Research Center (RRRC)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-07-29)</AVAILABILITY>
    <RESEARCH_USE>This rat models hereditary hemochromatosis (Type 2B) in humans. Iron overload research.</RESEARCH_USE>
    <ALLELES>Hamp&lt;sup&gt; em3Jfcol &lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38455990</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="95298332" STOP_POS="95300271" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="86170926" STOP_POS="86172865" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="89368021" STOP_POS="89369960" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="90523506" STOP_POS="90525473" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="85978120" STOP_POS="85980059" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00911</CITATION_ID>
    <DESCRIPTION>Hamp KO, Sprague-Dawley rats were generated by Transposagen Biopharmaceuticals (Lexington, KY). Four different genetically engineered rat lines, each with different sized Hamp deletions (with or without concurrent insertions), were created using TALEN technology. SD-Hamp em3Jfcol -/- (RGD:36174224)  is homozygous carrying a 20-bp deletion and a 3-bp insertion in exon 2 of both rat Hamp alleles.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>36174225</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Hamp&lt;sup&gt; em4Jfcol +/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Rat Resource &amp; Research Center (RRRC)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-07-29)</AVAILABILITY>
    <RESEARCH_USE>This rat models hereditary hemochromatosis (Type 2B) in humans. Iron overload research.</RESEARCH_USE>
    <ALLELES>Hamp&lt;sup&gt; em4Jfcol &lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38455991</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="95298332" STOP_POS="95300271" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="86170926" STOP_POS="86172865" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="89368021" STOP_POS="89369960" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="90523506" STOP_POS="90525473" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="85978120" STOP_POS="85980059" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_36174225</CITATION_ID>
    <DESCRIPTION>Hamp KO, Sprague-Dawley rats were generated by Transposagen Biopharmaceuticals (Lexington, KY). Four different genetically engineered rat lines, each with different sized Hamp deletions (with or without concurrent insertions), were created using TALEN technology. SD-Hamp em4Jfcol +/- (RGD:36174225)  is heterozygous carrying a 15-bp deletion in exon 2 of the rat Hamp gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>36174226</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Hamp&lt;sup&gt; em4Jfcol -/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Rat Resource &amp; Research Center (RRRC)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-07-29)</AVAILABILITY>
    <RESEARCH_USE>This rat models hereditary hemochromatosis (Type 2B) in humans. Iron overload research.</RESEARCH_USE>
    <ALLELES>Hamp&lt;sup&gt; em4Jfcol &lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38455991</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="95298332" STOP_POS="95300271" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="86170926" STOP_POS="86172865" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="89368021" STOP_POS="89369960" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="90523506" STOP_POS="90525473" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="85978120" STOP_POS="85980059" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00913</CITATION_ID>
    <DESCRIPTION>Hamp KO, Sprague-Dawley rats were generated by Transposagen Biopharmaceuticals (Lexington, KY). Four different genetically engineered rat lines, each with different sized Hamp deletions (with or without concurrent insertions), were created using TALEN technology. SD-Hamp em4Jfcol -/- (RGD:36174226)  is homozygous carrying a 15-bp deletion in exon 2 of both  rat Hamp alleles</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38456008</RGD_ID>
    <STRAIN_SYMBOL>LOU/C</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institut National de la Sante' et de la Recherche Medicale, Bichat-Claude Bernard, Paris, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38456008</CITATION_ID>
    <DESCRIPTION>Bazin and Beckers from rats of presumed Wistar origin kept at the Universite Catholique de Louvain. LOU/C was selected among 28 parallel sublines for its high incidence of immunocytomas, and LOU/M for its low incidence. The two are histocomaptible (Bazin 1977, Bazin and Beckers 1978).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38500209</RGD_ID>
    <STRAIN_SYMBOL>NISAG</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38500209</CITATION_ID>
    <DESCRIPTION>NISAG  were   stress-sensitive hypertensive  rats that exhibited normal systolic pressure during the first weeks after birth. The development of hypertension in these rats is accompanied by increased sensitivity of the hypothalamic-pituitary-adrenocortical and sympathoadrenal systems to stress.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38501059</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cp&lt;sup&gt;em1Ang+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38501059</CITATION_ID>
    <DESCRIPTION>The wild type rats were littermates of cross of heterozygotes Cp mutant rats. The mutations created by CRISPR/Cas9 contained  a 54- bp  deletion and a 2-bp insertion in exon1 of Cp, resulted a premature stop coden in exon 2. The sgRNAcr377 (TacGene, Paris, France) used targeted the exon 1 of Cp and had the following sequence: 59-GGAAT-TACTGAAGCAGTTT-39.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38501060</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cp&lt;sup&gt;em1Ang+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cp&lt;sup&gt;em1Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38501062</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="104368336" STOP_POS="104427119" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="102439433" STOP_POS="102498075" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="104744249" STOP_POS="104803034" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="124467383" STOP_POS="124524140" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="105086278" STOP_POS="105135367" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38501060</CITATION_ID>
    <DESCRIPTION>The heterozygous Cp mutant rats were  created by CRISPR/Cas9. They  contained  a 54- bp  deletion and a 2-bp insertion in exon1 of Cp, resulted a premature stop coden in exon 2. The sgRNAcr377 (TacGene, Paris, France) used targeted the exon 1 of Cp and had the following sequence: 59-GGAAT-TACTGAAGCAGTTT-39.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38501061</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cp&lt;sup&gt;em1Ang-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cp&lt;sup&gt;em1Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38501062</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="104368336" STOP_POS="104427119" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="102439433" STOP_POS="102498075" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="104744249" STOP_POS="104803034" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="124467383" STOP_POS="124524140" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="105086278" STOP_POS="105135367" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38501061</CITATION_ID>
    <DESCRIPTION>The homozygous Cp mutant rats are littermates of cross of heterozygotes Cp mutant rats . The mutations created by CRISPR/Cas9 contained  a 54- bp  deletion and a 2-bp insertion in exon1 of Cp, resulted a premature stop codon in exon 2. The sgRNAcr377 (TacGene, Paris, France) used targeted the exon 1 of Cp and had the following sequence: 59-GGAAT-TACTGAAGCAGTTT-39.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38501086</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Bmpr2&lt;sup&gt;em1Ang+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bmpr2&lt;sup&gt;em1Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38501087</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="68685942" STOP_POS="68801353" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="61192718" STOP_POS="61307280" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="66568074" STOP_POS="66683019" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="66371542" STOP_POS="66486121" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="58327587" STOP_POS="58436057" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38501086</CITATION_ID>
    <DESCRIPTION>BMPR2-deficient rats were generated by using zinc-finger nucleases (Sigma, St. Louis, MO). The mRNA encoding mRNA at 5 ng/&amp;#956;L encoding a pair of zinc-finger nucleases recognizing rat BMPR2 sequences was injected to the cytoplasm of Sprague-Dawley zygotes.  A rat line with a heterozygous 140 base pairs deletion in the first exon (BMPR2&amp;#916;140Ex1/+ rats) was chosen for this study becauseit displayed an intense pulmonary vascular remodeling at 3 months of life that was absent in the wild-type littermates.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38508891</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(Cx3cr1-cre/ERT2)3Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38508891</CITATION_ID>
    <DESCRIPTION>The transgene of LE-Tg(Cx3cr1-cre)3Ottc (RGD: 13441557) was crossed onto  Fischer344 background by backcrossing  the hybrid to Fischer344 and select for the presence of transgene. The donor LE transgenic  was generated by microinjection of LE embyos with a BAC DNA containing the Cx3cr1-cre/ERT2 transgene which is composed of cre/ERT2 recombinase gene driven by the rat genomic Cx3cr1promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38508893</RGD_ID>
    <STRAIN_SYMBOL>F344.LE-ROSA26 &lt;sup&gt;em1(LTR-nLuc)Ottc&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38508893</CITATION_ID>
    <DESCRIPTION>The mutated ROSA26 locus  of  LE-(ROSA)26 em1(LTR-nLuc)Ottc (RGD:13208223) was crossed onto  Fischer344 background by backcrossing  the hybrid to Fischer344 and select for the presence of mutated locus. The LE donor is CRISPR/Case9 knock-in strain that  has cre recombinase-dependent expression of nanoluciferase under the control of HIV LTR promoter inserted to the rat ROSA26 locus.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38543943</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Rag2&lt;sup&gt;em1Hera&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38543943</CITATION_ID>
    <DESCRIPTION>The Rag2 gene in rat spermatogonia stem cells (SSC, SD-WT2) was targeted by TALENs and resulted in a 27-bp in-frame deletion. The genome modified SSC was transplanted to Busulfan-treated, Dazl-deficient male Sprague Dawley rats and mated with wild type female Sprague Dawley rats 70 to 81 later. The allele was then bred to homozygosity to generate the Sprague-Dawley Rag2 (SDR)-knockout rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38548914</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Rag1/Rag2&lt;sup&gt;em1Mlit&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The animal facility at Tongji University (Shanghai, China).</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38548914</CITATION_ID>
    <DESCRIPTION>The Rag1, Rag2 double-knock rats were obtained by injecting the mixture of Rag1- and Rag2-targeting sgRNA into 1-cell embryo. The resulted mutations were a 1564-bp deletion in Rag1 and 85-bp deletion in Rag2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38548915</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Il2rg&lt;sup&gt;em1-/y&lt;/sup&gt;&lt;/i&gt;/Mlit</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The animal facility at Tongji University (Shanghai, China).</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38548915</CITATION_ID>
    <DESCRIPTION>The Il2rg knock-out rats were obtained by  injecting Il2rg-targeting sgRNA into 1-cell  embryos. The resulted mutation is  1-bp insertion (A) at 71169012 position. No protein was detected in the spleen of  this Il2rg knock out.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38548916</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Rag1/Rag2&lt;sup&gt;em1Mlit&lt;/sup&gt;Il2rg&lt;sup&gt;em1Mlit-/y&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The animal facility at Tongji University (Shanghai, China).</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38548916</CITATION_ID>
    <DESCRIPTION>The Rag1, Rag2, and Il2rg triple-knockout rats were obtained by intercrossing Rag1 and Rag2 double-knockout rat (RGD:38548914) with Il2rg knockout rat (RGD:38548915).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38548927</RGD_ID>
    <STRAIN_SYMBOL>HsdCpb:WU</STRAIN_SYMBOL>
    <FULL_NAME>Wistar Wu Rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.envigo.com/model/hsdcpb-wu/&gt;ENVIGO &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38548927</CITATION_ID>
    <DESCRIPTION>The Wistar rat is selected at the Wistar Institute, Philadelphia, USA, prior to 1910. In 1932, from Wistar Institute to Glaxo Laboratory, UK. In 1933, from Glaxo to the Dutch Institution for Nutrition, Amsterdam. In 1941, the Unilever Company, Vlaardingen, the Netherlands, obtained a breeding stock from Dutch Institution for Nutrition. Thereafter, the Unilever stock was referred as the Wistar Unilever or WU rat. In 1958, transferred from Unilever to TNO Central Institute for the Breeding of Laboratory Animals. To Harlan Laboratories through acquisition in 1986. Harlan became Envigo in 2015.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38549341</RGD_ID>
    <STRAIN_SYMBOL>RP/AEurRijHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38549341</CITATION_ID>
    <DESCRIPTION>Muhlbock, Amsterdam, 1947, from Wistar stock. To University of Leiden in 1958. To Erasmus University, Rotterdam in 1968. To Rijswick in 1982 (Greenhouse et al 1991). To Harlan (?).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38549343</RGD_ID>
    <STRAIN_SYMBOL>WKY/NIcoCrlf</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Charles River, France</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38549343</CITATION_ID>
    <DESCRIPTION>A substrain of WKY   from Charles River France and bred at Institut Francois Magendie, Bordeaux Cedax, France.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38549351</RGD_ID>
    <STRAIN_SYMBOL>HXB10/IpcvMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38549351</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, and maintain by Medical College of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38549352</RGD_ID>
    <STRAIN_SYMBOL>SHR/OlaIpcvMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2024-08-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38549352</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of SHR substrain (SHR/OlaIpcv, RGD:9586450)  from Czech Academy of Sciences now maintained at Medical College of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38549353</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Defb23&lt;sup&gt;em1Mlit&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>School of Life Science and Technology, Tong Ji University, Shanghai, China.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Defb23&lt;sup&gt;em1Mlit&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599011</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="161383615" STOP_POS="161390685" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="140923474" STOP_POS="140927715" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="147928201" STOP_POS="147932413" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="154275191" STOP_POS="154279834" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="142780126" STOP_POS="142784338" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38549353</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant; sgRNA targeting exon2 of Defb23 was injected into the cytoplasm of fertilized embryos of Slc:SD. The resulting mutation is a 171-bp deletion in exon2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38549354</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Defb26&lt;sup&gt;em1Mlit&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>School of Life Science and Technology, Tong Ji University, Shanghai, China.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Defb26&lt;sup&gt;em1Mlit&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599012</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="161437500" STOP_POS="161441234" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="140977214" STOP_POS="140980949" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="147982213" STOP_POS="147985616" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="154391632" STOP_POS="154395035" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="142834066" STOP_POS="142837469" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38549354</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant; sgRNA targeting exon2 of Defb26 was injected into the cytoplasm of fertilized embryos of Slc:SD. The resulting mutations is a 246-bp deletion  in exon2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38549355</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Defb42&lt;sup&gt;em1Mlit&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>School of Life Science and Technology, Tong Ji University, Shanghai, China.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Defb42&lt;sup&gt;em1Mlit&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599013</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="41410651" STOP_POS="41417610" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="37234662" STOP_POS="37241621" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="46159511" STOP_POS="46166335" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="49925455" STOP_POS="49932279" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="42247668" STOP_POS="42254485" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38549355</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant; sgRNA targeting exon2 of Defb42 was injected into the cytoplasm of fertilized embryos of Slc:SD. The resulting mutation is a 85 -bp deletion in exon2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38549356</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Defb23&lt;sup&gt;em2Mlit&lt;/sup&gt;Defb26&lt;sup&gt;em2Mlit&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>School of Life Science and Technology, Tong Ji University, Shanghai, China.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Defb23&lt;sup&gt;em2Mlit&lt;/sup&gt;Defb26&lt;sup&gt;em2Mlit&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599014</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38549356</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this double-gene knockout. The Slc:SD zygotes were injected with sgRNAs that containing 4 sgRNAs (5 ng/ml each) targeting 2 adjacent sites (target sites 1 and 2) of each of the 2 genes.  The resulting mutations are 317 bp (Defb23) and 380 bp (Defb26) fragments which were deleted in the Defb23/Defb26 double-mutant strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38549357</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Defb23&lt;sup&gt;em2Mlit&lt;/sup&gt;Defb26&lt;sup&gt;em2Mlit&lt;/sup&gt;Defb42&lt;sup&gt;em1Mlit&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>School of Life Science and Technology, Tong Ji University, Shanghai, China.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Defb42&lt;sup&gt;em1Mlit&lt;/sup&gt;|Defb23&lt;sup&gt;em2Mlit&lt;/sup&gt;Defb26&lt;sup&gt;em2Mlit&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599013|38599014</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="41410651" STOP_POS="41417610" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="37234662" STOP_POS="37241621" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="46159511" STOP_POS="46166335" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="49925455" STOP_POS="49932279" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="42247668" STOP_POS="42254485" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38549357</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate the Defb23, Defb26 double-gene knockout (RGD:38549356) and Defb42 (RGD:38549355). The triple-KO rats were generated by crossing the heterozygous Defb23/26 mutation rats with the heterozygous Defb42 mutation rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38549372</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Eif2ak4&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Eif2ak4&lt;sup&gt;em1&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599016</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="125810207" STOP_POS="125895574" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="105356261" STOP_POS="105441630" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="110159624" STOP_POS="110245382" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="116705333" STOP_POS="116791037" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="104870871" STOP_POS="104875529" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38549372</CITATION_ID>
    <DESCRIPTION>The  sgRNA  targeted  the following  sequence:  GGACTTCCAGGATCTGCGGC  CGG on the rat  Eif2ak4  was injected to the one-cell stage embryos collected from female rats (Crl:SD). The  strain carrying the biallelic deletion of 152 bp in the first exon of Eif2ak4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38596327</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Tbc1d4&lt;sup&gt;em1Gdcz&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Unit for Laboratory Animal Medicine, University of Michigan.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tbc1d4&lt;sup&gt;em1&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38596330</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="84670756" STOP_POS="84848876" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="78256030" STOP_POS="78434168" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="85927978" STOP_POS="86105829" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="89695614" STOP_POS="89871879" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="85359159" STOP_POS="85561229" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38596327</CITATION_ID>
    <DESCRIPTION>The mutant rats were created with CRISPR/Cas9 system. A single guide RNA (sgRNA) and protospacer adjacent motif was designed targeting coding strand: 5' GCGACAAGCGCTTCCGGCTA TGG 3' with a predicted cut site 111 bp downstream of the initiation codon. Fertilized eggs, produced by mating superovulated Wistar female rats (Envigo Hsd:WI, Strain Code 001) with Wistar males, were microinjected with sgRNA and implanted to pseudopregnant rats. A founder line carrying a 20-bp substitution deletion (TGGCGACAAGCGTTCCGGC) was selected and backcrossed with wild type Wistar outbred rats (Charles River Laboratory; Wilmington, VA) to establish heterozygous (+/-) colony. No protein product was detected from knock out T homozygous mutant (-/-) .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38596339</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Rarres2&lt;sup&gt;em1Msu&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, USA.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rarres2&lt;sup&gt;em1Msu&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38596341</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="78853450" STOP_POS="78856652" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="77522549" STOP_POS="77525733" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="78205809" STOP_POS="78208956" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="142869493" STOP_POS="142872619" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="76659507" STOP_POS="76662465" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38596339</CITATION_ID>
    <DESCRIPTION>Rat zygotes, produced by mating superovulated Sprague-Dawley females with males of the same strain [Crl:CD(SD), were microinjected with CRISPR/Cas9 reagents targeting arres2 exon2. The resulting allele lacked the splice site and the first 13 aa of exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599146</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Aire&lt;sup&gt;em1Ang-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre de Recherche en Transplantation et Immunologie UMR 1064, ITUN, 30 Boulevard Jean Monnet, 44093 Nantes Cedex 01, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Aire&lt;sup&gt;em1Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599148</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="10636775" STOP_POS="10636791" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="10637123" STOP_POS="10637139" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="11366697" STOP_POS="11366713" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="13535776" STOP_POS="13550486" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="10980031" STOP_POS="10996102" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599146</CITATION_ID>
    <DESCRIPTION>The homozygous Aire mutant rats are littermates of cross of heterozygotes Aire mutant rats . The mutations created by ZFN reagents targeting to a DNA sequence 59-TGCCACCCAGACCCCCCACAAAGAGAAGAGCCCTGGAAGAG-
39 in exon 3 of the Aire gene. This mutant carries a 17-bp deletion in the nuclear
localization signal sequence, causing a premature stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599147</RGD_ID>
    <STRAIN_SYMBOL>SD.BN-&lt;i&gt;Aire&lt;sup&gt;em1Ang-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre de Recherche en Transplantation et Immunologie UMR 1064, ITUN, 30 Boulevard Jean Monnet, 44093 Nantes Cedex 01, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Aire&lt;sup&gt;em1Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599148</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="10636775" STOP_POS="10636791" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="10637123" STOP_POS="10637139" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="11366697" STOP_POS="11366713" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="13535776" STOP_POS="13550486" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="10980031" STOP_POS="10996102" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599147</CITATION_ID>
    <DESCRIPTION>The BN homozygous Aire mutant rats were derived from founder rats that were backcrossed in a Sprague Dawley (SD; outbred strain) background for six generations to obtain AIRE-deficient SD rats. The original founder were from  BN mutants carrying the mutations created by ZFN reagents targeting to a DNA sequence 59-TGCCACCCAGACCCCCCACAAAGAGAAGAGCCCTGGAAGAG-
39 in exon 3 of the Aire gene. This mutant carriesa 17-bp deletion in the nuclear
localization signal  sequence, causing a premature stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599152</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Lpin1&lt;sup&gt;m1Hubr&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>From the Hubrecht Institute-KNAW and University Medical Center Utrecht, 3584 CT Utrecht, The Netherlands,</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lpin1&lt;sup&gt;m1Hubr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599153</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="45039110" STOP_POS="45145845" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="39309198" STOP_POS="39417034" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="41796214" STOP_POS="41905149" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="51532422" STOP_POS="51638090" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="40253664" STOP_POS="40297195" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599152</CITATION_ID>
    <DESCRIPTION>The mutant rats were created using N-ethyl-N-nitrosourea (ENU) mutagenesis. A point mutation in the 5'-end splice site of intron 18 resulting in mis-splicing, a reading frameshift, and a premature stop codon was identified.  As this mutation does not induce nonsense-mediated decay, it allows the production of a truncated Lipin 1 protein lacking phosphatidate phosphatase 1 activity.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599155</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Themis&lt;sup&gt;m1Adej&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>UMR Inserm, U1043, Toulouse, France, UMR CNRS, U5282, Toulouse, France, Universit de Toulouse, UPS, Centre de Physiopathologie de Toulouse Purpan (CPTP), Toulouse, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Themis&lt;sup&gt;m1Adej&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599156</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="18251136" STOP_POS="18483851" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="16433906" STOP_POS="16623889" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="17152973" STOP_POS="17378225" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="18308043" STOP_POS="18532366" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="17032677" STOP_POS="17226924" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599155</CITATION_ID>
    <DESCRIPTION>This autosomal recessive mutation occurred spontaneously in a Brown-Norway  rat colony and was identified as causing marked T cell lymphopenia.  The mutation was identified as a frameshift mutation caused by a four-nucleotide insertion in the Themis gene, leading to its disruption.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599157</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Depdc5&lt;sup&gt;em1Kyo+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>National Bio Resource Project Rat in Japan</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Depdc5&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599194</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="81956777" STOP_POS="82087392" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="77732297" STOP_POS="77862924" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="83089000" STOP_POS="83219576" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="83775510" STOP_POS="83906381" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="83484354" STOP_POS="83614818" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599157</CITATION_ID>
    <DESCRIPTION>TALEN mRNAs targeting exon 2 of rat Depdc5 were microinjected into fertilized eggs of Fisher 344 (F344) rats to yield two founder mutant rats named Depdc5em1kyo (c.40_44delins17/p.Gly15*) and Depdc5em2kyo (c.39_55delinsT/p.Lys13fs*8). The genome edited fragment was identified by PCR.   A 267 bp band was detected for wildtype, a 279 bp band for Depdc5em1kyo mutant and a 251 bp band for Depdc5em2kyo mutant. Depdc5 mutant homozygous pups were never observed at birth. Deletion of both alleles resulted in in utero lethality started around E14.5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599158</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Depdc5&lt;sup&gt;em2Kyo+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1154&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1154&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Depdc5&lt;sup&gt;em2Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599195</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="81956777" STOP_POS="82087392" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="77732297" STOP_POS="77862924" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="83089000" STOP_POS="83219576" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="83775510" STOP_POS="83906381" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="83484354" STOP_POS="83614818" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599158</CITATION_ID>
    <DESCRIPTION>TALEN mRNAs targeting exon 2 of rat Depdc5 were microinjected into fertilized eggs of Fisher 344 (F344) rats to yield two founder mutant rats named Depdc5em1kyo (c.40_44delins17/p.Gly15*) and Depdc5em2kyo (c.39_55delinsT/p.Lys13fs*8). The genome edited fragment was identified by PCR.   A 267 bp band was detected for wildtype, a 279 bp band for Depdc5em1kyo mutant and a 251 bp band for Depdc5em2kyo mutant. Depdc5 mutant homozygous pups were never observed at birth. Deletion of both alleles resulted in in utero lethality started around E14.5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599187</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D1Mgh5-D1Got87&lt;/i&gt;)(&lt;i&gt;D18Rat73-D18Rat11&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1296&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1296&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-14)</AVAILABILITY>
    <RESEARCH_USE>Hypertension and cerebral apoplexy</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="87558587" STOP_POS="87558729" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="52198059" STOP_POS="70689286" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78430536" STOP_POS="86030749" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="49999958" STOP_POS="68414117" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="79689548" STOP_POS="91156803" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="51609032" STOP_POS="70803264" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="50804228" STOP_POS="69942605" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="80946174" STOP_POS="92291485" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="52290789" STOP_POS="71692408" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78134304" STOP_POS="85828306" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599187</CITATION_ID>
    <DESCRIPTION>A double congenic strain made by introducing a segments of chromosome 1 and 18 from SHR/Izm into SHRSP/Izm. Developed by Dr. Tohru Nabika  from Shimane University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599188</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D1Rat23-D1Rat213&lt;/i&gt;)(&lt;i&gt;D18Rat73-D18Rat11&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1297&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1297&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-14)</AVAILABILITY>
    <RESEARCH_USE>Hypertension and cerebral apoplexy</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="88098993" STOP_POS="90905414" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="52198059" STOP_POS="70689286" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78970983" STOP_POS="81777720" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="49999958" STOP_POS="68414117" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="80231217" STOP_POS="83282814" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="51609032" STOP_POS="70803264" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="50804228" STOP_POS="69942605" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="81497710" STOP_POS="84537228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="52290789" STOP_POS="71692408" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78685103" STOP_POS="81548909" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599188</CITATION_ID>
    <DESCRIPTION>A double congenic strain made by introducing a segments of chromosome 1 and 18 from SHR/Izm into SHRSP/Izm. Developed by Dr. Tohru Nabika  from Shimane University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599189</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Rag2&lt;sup&gt;em1Iexas&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1299&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1299&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2020-09-14)</AVAILABILITY>
    <RESEARCH_USE>immunology/Inflamation and Immunodeficient</RESEARCH_USE>
    <ALLELES>Rag2&lt;sup&gt;em1Iexas&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38599191</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108357399" STOP_POS="108367186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87902373" STOP_POS="87910227" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91191837" STOP_POS="91200134" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97851318" STOP_POS="97859615" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86764810" STOP_POS="86773438" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599189</CITATION_ID>
    <DESCRIPTION>This strain was established by targeting Rag2 gene in F344/Jcl using CRISPR/Cas9 system. gRNA to Rag2: AACATAGCCTTAATTCAACCAGG (PAM: last AGG); Cas 9 mRNA transcribed from T7-NLS hCas9-pA (RDB13130) was used for the system. Gene transfer was performed by electroporation. This strain shows severe combined immunodeficiency (SCID) caused by 1-bp insertion in Rag2 gene on chromosome 3. This strain grows normally under SPF condition.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599190</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Il2rg&lt;sup&gt;em1Iexas&lt;/sup&gt;Rag2&lt;sup&gt;em1Iexas&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1300&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1300&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2020-09-14)</AVAILABILITY>
    <RESEARCH_USE>severe combined immunodeficiency</RESEARCH_USE>
    <ALLELES>Il2rg&lt;sup&gt;em1Iexas&lt;/sup&gt;|Rag2&lt;sup&gt;em1Iexas&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13464264|38599191</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108357399" STOP_POS="108367186" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="87902373" STOP_POS="87910227" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66395330" STOP_POS="66399026" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91191837" STOP_POS="91200134" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97851318" STOP_POS="97859615" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86764810" STOP_POS="86773438" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599190</CITATION_ID>
    <DESCRIPTION>This strain was established by targeting Il2rg gene and Rag2 gene in F344/Jcl using CRISPR/Cas9 system. gRNA seq to Il2rg: CCAACCTCACTATGCACTATAGG (PAM: first CCA); gRNA to Rag2: AACATAGCCTTAATTCAACCAGG (PAM: last AGG); Cas 9 mRNA transcribed from T7-NLS hCas9-pA (RDB13130) was used for the system. Gene transfer was performed by electroporation.This strain shows severe combined immunodeficiency (SCID) caused by 5-bp deletion in Il2rg gene on X chromosome and 1-bp insertion in Rag2 gene on chromosome 3. This strain grows normally under SPF condition. The sexual maturation is a bit late.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599197</RGD_ID>
    <STRAIN_SYMBOL>W.F344-&lt;i&gt;Lep&lt;sup&gt;m1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=996&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=996&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2020-09-14)</AVAILABILITY>
    <RESEARCH_USE>Obesity</RESEARCH_USE>
    <ALLELES>Lep&lt;sup&gt;m1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12792963</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="58626529" STOP_POS="58640663" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="57672294" STOP_POS="57672294" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="56348850" STOP_POS="56348850" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="56085079" STOP_POS="56099209" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="55943837" STOP_POS="55945938" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599197</CITATION_ID>
    <DESCRIPTION>This cocngenic strain was made by backcrossing F344-Lepm1Kyo(RGD: 8549776, F344/NSlc rats having an induced mutation in the Lep gene by ENU mutagenesis) to W/Kyo (RGD:1302672).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599201</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D18Rat73-D18Rat8&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1243&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1243&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-15)</AVAILABILITY>
    <RESEARCH_USE>Hypertension and cerebral apoplexy</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="52198059" STOP_POS="71415821" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="49999958" STOP_POS="69140759" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="51609032" STOP_POS="71692768" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="50804228" STOP_POS="70825941" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="52290789" STOP_POS="72450442" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599201</CITATION_ID>
    <DESCRIPTION>A congenic strain made by introducing a segments of chromosome 18 from SHR/Izm into SHRSP/Izm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599202</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D1Rat23-D1Rat213&lt;/i&gt;)(&lt;i&gt;D18Rat73-D18Rat52&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1240&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1240&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;, Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-15)</AVAILABILITY>
    <RESEARCH_USE>Hypertension and cerebral apoplexy</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="88098993" STOP_POS="90905414" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="52198059" STOP_POS="60806448" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="78970983" STOP_POS="81777720" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="49999958" STOP_POS="58536311" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="80231217" STOP_POS="83282814" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="51609032" STOP_POS="60532087" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="50804228" STOP_POS="59735418" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="81497710" STOP_POS="84537228" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="52290789" STOP_POS="61290878" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="78685103" STOP_POS="81548909" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599202</CITATION_ID>
    <DESCRIPTION>A double congenic strain made by introducing a segments of chromosome 1 and 18 from SHR/Izm into SHRSP/Izm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599203</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Gt(ROSA)26Sor-CAG-COP4*C167A/YFP*)2Jfhy</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1238 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1238 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599203</CITATION_ID>
    <DESCRIPTION>The transgenic LE line 2(Back ground strain: Iar:Long-Evans (RGD:18337282) (Kumagai-shigeyasu Co.,Ltd)) carrying  Transgene: ROSA26 (mouse ROSA26 BAC: RP23 244D9),  and Channel rhodopsin fast receiver (ChRFR)(COP4*C167A) (Chlamydomonas reinhardtii) fused with YFP* (Venus). Copy number: 3, In this strain, COP4*C167A, modified photosensitivity cation channel, is expressed ubiquitously in the presence of exogenous Cre protein. The ChRFR(COP4*C167A), one of the channel rhodopsin (step-function opsin, SFO), opens under blue light and is closed under yellow light. The Venus (YFP*) is tagged with channel rhodopsin. There is no differences between line 1 and 2 except for copy number.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599204</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Gt(ROSA)26Sor-CAG-COP4*C167A/YFP*)1Jfhy</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1237 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1237 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599204</CITATION_ID>
    <DESCRIPTION>The transgenic LE line 2(Back ground strain: Iar:Long-Evans (RGD:18337282) (Kumagai-shigeyasu Co.,Ltd)) carrying  Transgene: ROSA26 (mouse ROSA26 BAC: RP23 244D9),  and Channel rhodopsin fast receiver (ChRFR)(COP4*C167A) (Chlamydomonas reinhardtii) fused with YFP* (Venus). Copy number: 1, In this strain, COP4*C167A, modified photosensitivity cation channel, is expressed ubiquitously in the presence of exogenous Cre protein. The ChRFR(COP4*C167A), one of the channel rhodopsin (step-function opsin, SFO), opens under blue light and is closed under yellow light. The Venus (YFP*) is tagged with channel rhodopsin. There is no differences between line 1 and 2 except for copy number.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599206</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Prdx2&lt;sup&gt;em2Izm&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1217&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1217&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599206</CITATION_ID>
    <DESCRIPTION>This strain is established at Kyoto University: By CRISPR/Cas9 system, mutation was introduced in Peroxiredoxin-2 (Prdx2) gene of SHR/Izm rat. This KO rat strain has 6-bp deletion (5'-CTCCGG-3', c.6_12del6) in the exon2 of Prdx2 gene.
Target sequence is 5?-CCTCCGGCAACGCGCACATCGGA-3?(PAM sequence:CCT).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599208</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Prdx2&lt;sup&gt;em1Izm&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1216&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1216&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599208</CITATION_ID>
    <DESCRIPTION>This strain is established at Kyoto University: By CRISPR/Cas9 system, mutation was introduced in Peroxiredoxin-2 (Prdx2) gene of SHR/Izm rat. This KO rat strain has 7-bp deletion (5'-CTCCGGC-3', c.6_13del7) in the exon2 of Prdx2 gene. Target sequence is 5?-CCTCCGGCAACGCGCACATCGGA-3?(PAM sequence:CCT).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599241</RGD_ID>
    <STRAIN_SYMBOL>SD;DA-Tg(Thy1-APP*)1Dspb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1301&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1301&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-16)</AVAILABILITY>
    <RESEARCH_USE>dementia</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599241</CITATION_ID>
    <DESCRIPTION>Mutant human amyloid beta (APP*) combined Thy1 promoter which is specifically expressed in neurons, was induced to ES cells from DA strain rats, and chimera rats obtained from the ES cells.  The F1 rats were backcrossed with Crl:CD (SD) strain rats and F3 rats was deposited to NBRP.  The expression levels of mutant human APP mRNA are different among Lines  (12&gt;1&gt;14&gt;6).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599242</RGD_ID>
    <STRAIN_SYMBOL>SD;DA-Tg(Thy1-APP*)6Dspb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1302&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1302&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-16)</AVAILABILITY>
    <RESEARCH_USE>dementia</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599242</CITATION_ID>
    <DESCRIPTION>Mutant human amyloid beta (APP*) combined Thy1 promoter which is specifically expressed in neurons, was induced to ES cells from DA strain rats, and chimera rats obtained from the ES cells.  The F1 rats were backcrossed with Crl:CD (SD) strain rats and F3 rats was deposited to NBRP.  The expression levels of mutant human APP mRNA are difficult among Lines (12&gt;1&gt;14&gt;6).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599243</RGD_ID>
    <STRAIN_SYMBOL>SD;DA-Tg(Thy1-APP*)12Dspb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1303&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1303&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-16)</AVAILABILITY>
    <RESEARCH_USE>dementia</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599243</CITATION_ID>
    <DESCRIPTION>Mutant human amyloid beta (APP*) combined Thy1 promoter which is specifically expressed in neurons, was induced to ES cells from DA strain rats, and chimera rats obtained from the ES cells.  The F1 rats were backcrossed with Crl:CD (SD) strain rats and F3 rats was deposited to NBRP.  The expression levels of mutant human APP mRNA are difficult among Lines (12&gt;1&gt;14&gt;6).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599244</RGD_ID>
    <STRAIN_SYMBOL>SD;DA-Tg(Thy1-APP*)14Dspb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1304&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1304&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-16)</AVAILABILITY>
    <RESEARCH_USE>dementia</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599244</CITATION_ID>
    <DESCRIPTION>Mutant human amyloid beta (APP*) combined Thy1 promoter which is specifically expressed in neurons, was induced to ES cells from DA strain rats, and chimera rats obtained from the ES cells.  The F1 rats were backcrossed with Crl:CD (SD) strain rats and F3 rats was deposited to NBRP.  The expression levels of mutant human APP mRNA are difficult among Lines (12&gt;1&gt;14&gt;6).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599245</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Tac1-cre)6-7Koba</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1305&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1305&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599245</CITATION_ID>
    <DESCRIPTION>Background strain: Long-Evans rat (Iar:Long-Evans, RGD:18337282). This strain was established by injection of modified BAC (cre gene was inserted into the exon 2 of rat Tac1 gene) into Long-Evans rat's fertile eggs. This transgenic strain expresses Cre recombinase under the control of Tac1 promoter. The expression levels of Cre recombinase in LE-Tg(Tac1-cre)6-7Koba are lower than in LE-Tg(Tac1-cre)4-1Koba (RGD:38599247)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38599247</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Tac1-cre)4-1Koba</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1314&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1314&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38599247</CITATION_ID>
    <DESCRIPTION>Background strain: Long-Evans rat (Iar:Long-Evans, RGD:18337282). This strain was established by injection of modified BAC (cre gene was inserted into the exon 2 of rat Tac1 gene) into Long-Evans rat's fertile eggs.This transgenic strain expresses Cre recombinase under the control of Tac1 promoter. The expression levels of Cre recombinase in LE-Tg(Tac1-cre)4-1Koba are higher than in LE-Tg(Tac1-cre)6-7Koba (RGD:38599245).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676250</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Hcn1&lt;sup&gt;em3Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1306&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1306&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676250</CITATION_ID>
    <DESCRIPTION>TALEN (Left:ttcag&amp;#65313;&amp;#65313;&amp;#65332;&amp;#65319;&amp;#65313;&amp;#65332;&amp;#65332;&amp;#65315;&amp;#65313;&amp;#65332;&amp;#65319;&amp;#65319;&amp;#65319;, Right:&amp;#65313;&amp;#65315;&amp;#65319;&amp;#65315;&amp;#65313;&amp;#65315;&amp;#65332;&amp;#65315;&amp;#65332;&amp;#65332;&amp;#65315;&amp;#65313;&amp;#65313;&amp;#65313;&amp;#65319;&amp;#65315;&amp;#65332;&amp;#65313;&amp;#65289;targeting the exon4 of hyperpolarization-activated cyclic nucleotide-gated 1 channel (Hcn1) gene was designed and mRNA coding these TALEN was microinjected into F344/NSlc embyo. A 13-bp deletion in the exon4 of Hcn1 gene: as a result of frameshift mutation, stop codon is produced. Decreased expression levels of Hcn1 gene and HCN1 protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676251</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Hcn1&lt;sup&gt;em2Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1307&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1307&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676251</CITATION_ID>
    <DESCRIPTION>TALEN (Left: ttcagAATGATTCATGGG, Right : ACGCACTCTTCAAAGCTA) targeting the exon4 of hyperpolarization-activated cyclic nucleotide-gated 1 channel (Hcn1) gene was designed and mRNA coding these TALEN was microinjected into F344/NSlc embyo. A 24-bp deletion in the exon4 of Hcn1 gene. It is predicted that 8 amino-acid deleted HCN1 protein is expressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676253</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Hcn1&lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1308&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1308&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Hcn1&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150429632</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="51531189" STOP_POS="51531195" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="49798369" STOP_POS="49798375" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="50399472" STOP_POS="50399478" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="68473431" STOP_POS="68874494" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="49525949" STOP_POS="49939066" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676253</CITATION_ID>
    <DESCRIPTION>TALEN (Left: ttcagAATGATTCATGGG, Right : ACGCACTCTTCAAAGCTA) targeting the exon4 of hyperpolarization-activated cyclic nucleotide-gated 1 channel (Hcn1) gene was designed and mRNA coding these TALEN was microinjected into F344/NSlc embyo. A 7-bp deletion in the exon4 of Hcn1 gene: as a result of frameshift mutation, stop codon is produced. Decreased expression levels of Hcn1 gene and HCN1 protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676254</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Pparg&lt;sup&gt;m1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1182&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1182&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pparg&lt;sup&gt;m1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127285617</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="150095743" STOP_POS="150221104" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="148423102" STOP_POS="148548471" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="147274055" STOP_POS="147399383" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="210562928" STOP_POS="210688585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="151492220" STOP_POS="151617331" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676254</CITATION_ID>
    <DESCRIPTION>By using ENU mutagenesis followed by MuT-POWER screening of the KURMA (Kyoto University Rat Mutant Archive) samples, the depositors generated a heterozygous PPARg mutant (Ppargmkyo/+) rat with a missense mutation (G488T p.C163F in Pparg1 or G578T  p.C193F  for Pparg2) in Pparg. The PpargG488T homozygous rats are embryonic lethal. Heterozygous Ppargmkyo/+ rats showed reduced fat mass with adipocyte hypertrophy and insulin resistance, which were highly predictable from known actions of Pparg agonists and phenotypes of patients with the PPARG mutation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676255</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Hcn1&lt;sup&gt;em4Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1309&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1309&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676255</CITATION_ID>
    <DESCRIPTION>TALEN (Left: ttcagAATGATTCATGGG, Right : ACGCACTCTTCAAAGCTA) targeting the exon4 of hyperpolarization-activated cyclic nucleotide-gated 1 channel (Hcn1) gene was designed and mRNA coding these TALEN was microinjected into F344/NSlc embyo.  A 18-bp deletion in the exon4 of Hcn1 gene. It is predicted that 6 amino-acid deleted HCN1 protein is expressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676310</RGD_ID>
    <STRAIN_SYMBOL>RjHan:SD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Janvier Labs, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2020-09-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676310</CITATION_ID>
    <DESCRIPTION>The outbred strain [Sprague-Dawley] was created by R. W. Dawley in 1925, from a hooded male hybrid of unknown origin and an albino female (probably Wistar), and was crossed with the female's progeny for 7 generations. Janvier Labs received from  Zentralinstitut fur Versuchstierzucht (Hannover) in1982.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676445</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Slc32a1-cre)1_4Fusa</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1310&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1310&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676445</CITATION_ID>
    <DESCRIPTION>This strain was established by Bac transgenic method (construct: Kazuhiro Yamakawa, phD) supported by C.B.S.Nresource (Dr. Kazuto Kobayashi, Dr. Yuchio Yanagawa) in 2014 and maintained at Jikei University School of Medicine. Background: Crlj:WI. Transgene: VGAT (Slc32a1: mouse, Kanamycin registance gene (E. coli), Cre (P1 phage), polyA signal (SV40 virus. Mouse BAC clone: RP23-392-P11). Cre recombinase is expressed under the control of mouse Slc32a1 (VGAT) promoter. This strain is used for GABAergic neuron-specific Cre-Lox site-specific recombination system.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676446</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Slc32a1-cre)2_5Fusa</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1311&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1311&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676446</CITATION_ID>
    <DESCRIPTION>This strain was established by Bac transgenic method (construct: Kazuhiro Yamakawa, phD) supported by C.B.S.Nresource (Dr. Kazuto Kobayashi, Dr. Yuchio Yanagawa) in 2014 and maintained at Jikei University School of Medicine. Background: Crlj:WI. Transgene: VGAT (Slc32a1: mouse, Kanamycin registance gene (E. coli), Cre (P1 phage), polyA signal (SV40 virus. Mouse BAC clone: RP23-392-P11). Cre recombinase is expressed under the control of mouse Slc32a1 (VGAT) promoter. This strain is used for GABAergic neuron-specific Cre-Lox site-specific recombination system.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676447</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Slc32a1-cre)5_9Fusa</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1312&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1312&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676447</CITATION_ID>
    <DESCRIPTION>This strain was established by Bac transgenic method (construct: Kazuhiro Yamakawa, phD) supported by C.B.S.Nresource (Dr. Kazuto Kobayashi, Dr. Yuchio Yanagawa) in 2014 and maintained at Jikei University School of Medicine. Background: Crlj:WI. Transgene: VGAT (Slc32a1: mouse, Kanamycin registance gene (E. coli), Cre (P1 phage), polyA signal (SV40 virus. Mouse BAC clone: RP23-392-P11). Cre recombinase is expressed under the control of mouse Slc32a1 (VGAT) promoter. This strain is used for GABAergic neuron-specific Cre-Lox site-specific recombination system.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676448</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Trpa1&lt;sup&gt;em1Kcrd&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1313&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1313&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2020-09-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpa1&lt;sup&gt;em1Kcrd&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38676449</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="9163060" STOP_POS="9217325" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="4379862" STOP_POS="4434133" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="3783247" STOP_POS="3836485" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="3764339" STOP_POS="3818781" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="3531163" STOP_POS="3584401" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676448</CITATION_ID>
    <DESCRIPTION>This Trpa1-deleted Wistar (background: Crl:WI) strain was generated by using Zinc Finger Nuclease at Kirin Company, Limited in 2013. Exon 22-24, which form ion channel pore required for the activation in Trpa1 gene, was deleted.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676450</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Phf24&lt;sup&gt;em2Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1316&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1316&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2021-07-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676450</CITATION_ID>
    <DESCRIPTION>In 2013, F344/Stm female rat deleted 392b (delta392) of KIAA1045 (Phf24) was generated by Platinum TALEN methods.  Although spontaneous GTCS is not observed, seizure susceptibility is increased and kindling induced by PTZ is promoted. In addition, locomotor activity is increased, disturbed behavior and spacial memory are decreased, and emotional behavior is increased due to unpleasant stimulation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676451</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Phf24&lt;sup&gt;em11Iexas&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1317&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1317&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676451</CITATION_ID>
    <DESCRIPTION>This strain was establishe by CRISPR-Cas9 system at Osaka University. Target sequence is CCATGGGGGTGTTGATGTCCAAG (CCA is PAM sequence). Back ground strain is Crlj:Wistar (WI). This strain is line No. 11 and has a 128-bp deletion in Phf24 gene. Off-target effects (214 candidate region) have not yet been examined.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676452</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Phf24&lt;sup&gt;em24Iexas&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1318&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1318&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676452</CITATION_ID>
    <DESCRIPTION>This strain was establishe by CRISPR-Cas9 system at Osaka University. Target sequence is CCATGGGGGTGTTGATGTCCAAG (CCA is PAM sequence). Back ground strain is Crlj:Wistar (WI). This strain is line No. 24 and has a 141-bp deletion in Phf24 gene. Off-target effects (214 candidate region) have not yet been examined.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676453</RGD_ID>
    <STRAIN_SYMBOL>F344;  W-&lt;i&gt;Phf24&lt;sup&gt;em6(EGFP)Iexas&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1319&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1319&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-17)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676453</CITATION_ID>
    <DESCRIPTION>This strain (line No. 6) was establishe by CRISPR-Cas9 system at Osaka University and EGFP sequence was knock-in in Phf24 gene. Back ground strain is Crlj:Wistar (WI). Founder rats were crossed with F344/NSlc, and this strain was maintained by crossing with F344/NSlc (F2 or F3 generation, November 2017). At the point of sperm cryopreservation, this strain is not "congenic" strain (backcross generation was &lt;5 generations), but background is mix of Crlj:Wistar and F344/NSlc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676459</RGD_ID>
    <STRAIN_SYMBOL>HHR/Hat</STRAIN_SYMBOL>
    <FULL_NAME>Hirosaki hairless rat</FULL_NAME>
    <ORIGINATION>Depart of Biochemistry and Genome Biology, Hirosaki Univer-sity School of Medicine</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676459</CITATION_ID>
    <DESCRIPTION>Hirosaki hairless rat (HHR) is a mutant strain spontaneously derived from Sprague-Dawley rats, and its inheritance is autosomal recessive. .  These mutations are autosomal recessive and are suggested to be due to deletion of the keratin gene cluster.  HHR attain sexualmaturity at approximately 10 weeks of age and give birth to young but are not able to nurse them.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676461</RGD_ID>
    <STRAIN_SYMBOL>HiSER/Hat</STRAIN_SYMBOL>
    <FULL_NAME>Hirosaki small-eye rat</FULL_NAME>
    <ORIGINATION>Depart of Biochemistry and Genome Biology, Hirosaki Univer-sity School of Medicine</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676461</CITATION_ID>
    <DESCRIPTION>HiSER was established in 2013 as a spontaneous mutant of Sprague-Dawley rat.  This mutant strain has retinal detachment and the disease is progressively exacerbated. The muation is autosomal recessive and is suggested to be due to deletion of the crystallin gene Cryba1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676463</RGD_ID>
    <STRAIN_SYMBOL>HHSE/Hat</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1320&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;
;Depart of Biochemistry and Genome Biology, Hirosaki Univer-sity School of Medicine</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1320&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;
;Depart of Biochemistry and Genome Biology, Hirosaki Univer-sity School of Medicine</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2020-09-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cryba1&lt;sup&gt;Hiser&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>38676462</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="63106465" STOP_POS="63113020" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="62608373" STOP_POS="62614726" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="65160777" STOP_POS="65167504" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="66458061" STOP_POS="66480390" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="63758929" STOP_POS="63765451" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676463</CITATION_ID>
    <DESCRIPTION>HHSE/Hat was derived from Hirosaki hairless rat (HHR) and Hirosaki small-eye rat (HiSER), which are Sprague-Dawley rat (SDR)mutant lines. HHR was established in 1984 as a spontaneous mutant of SDR that has been inbred in Department of Biochemistry and Genome Biology Hirosaki University Graduate School of Medicine. Whole body shows hypotrichosis, abnormal differentiation of thymus, and regressed mammary gland in females. These mutations are autosomal recessive and are suggested to be due to deletion of the keratin gene cluster and the lectin-like receptor gene Ly49s3. HiSER was established in 2013 as a spontaneous mutant of Sprague-Dawley rat maintained in our course in the same way as HHR/Hat. This mutant strain has retinal detachment and the disease is progressively exacerbated. The muation is autosomal recessive and is suggested to be due to deletion of the crystallin gene Cryba1. The mutations in HHR and HiSER are on different chromosomes and do not affect each other. The mutations in HHR and HiSER are on different chromosomes and do not affect each other.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676464</RGD_ID>
    <STRAIN_SYMBOL>WIC-&lt;i&gt;Cspg4&lt;sup&gt;em1Kyst&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1321&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1321&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676464</CITATION_ID>
    <DESCRIPTION>By CRISPR/Cas9 system, mutation was introduced in &lt;i&gt;Cspg4&lt;/i&gt; gene of Wistar-Imamichi rat. 7 bp deletion on Exon1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>38676495</RGD_ID>
    <STRAIN_SYMBOL>BN-&lt;i&gt;Lx&lt;/i&gt;/CubMcwi</STRAIN_SYMBOL>
    <FULL_NAME>Brown Norway with polydactyly-luxate</FULL_NAME>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2024-08-06)</AVAILABILITY>
    <RESEARCH_USE>The Hybrid Rat Diversity Panel</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_38676495</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of  BN-Lx/Cub now maintained at Medical College of Wisconsin. The parent strain was derived by introgressing mutant Lx gene of the polydactylous (PD/Cub) rat onto the BN background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39128162</RGD_ID>
    <STRAIN_SYMBOL>WIC-&lt;i&gt;Cspg4&lt;sup&gt;em2Kyst&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1322&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1322&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-23)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39128162</CITATION_ID>
    <DESCRIPTION>By CRISPR/Cas9 system, mutation was introduced in &lt;i&gt;Cspg4&lt;/i&gt; gene of Wistar-Imamichi rat. 7 bp deletion on Exon1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39128163</RGD_ID>
    <STRAIN_SYMBOL>WIC-&lt;i&gt;Cspg4&lt;sup&gt;em3Kyst&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1323&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1323&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-23)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39128163</CITATION_ID>
    <DESCRIPTION>By CRISPR/Cas9 system, mutation was introduced in &lt;i&gt;Cspg4&lt;/i&gt; gene of Wistar-Imamichi rat. 2 bp insertion on Exon1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39128166</RGD_ID>
    <STRAIN_SYMBOL>WIC-&lt;i&gt;Sparc&lt;sup&gt;em1Kykn&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1324&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1324&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-23)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39128166</CITATION_ID>
    <DESCRIPTION>By CRISPR/Cas9 system, mutation was introduced in Sparc  gene of Wistar-Imamichi rat. 7 bp deletion around Exon7.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39128167</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Grp-YFP*)14Hskmt</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1325&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1325&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2020-09-23)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39128167</CITATION_ID>
    <DESCRIPTION>This strain was generated by microinjecting YFP* (Venus): yellow fluorescent protein variant, which is inserted at downstream of Grp-promoter (4 kb) to Wistar rat zygotes. The number of inserted gene is approximately 100 copy.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39128170</RGD_ID>
    <STRAIN_SYMBOL>SHRSP-&lt;i&gt;Stim1&lt;sup&gt;em1Izm&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1326&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1326&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-23)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39128170</CITATION_ID>
    <DESCRIPTION>"This strain was generated by co-introducing fertilized eggs of SHRSP/Izm with the guide RNA/Cas9 nuclease expression plasmid and ssODN, which targets the Stim1 gene, at the Institute of Laboratory Animals, Graduate School of Medicine, Kyoto University. SHRSP/Izm strain has a nonsense mutation (c.1918C&gt;T, p.Arg640X) in the Stim1 gene, but homologous recombination with the introduced ssODN replaces this mutation with a normal sequence.
The sequence of the guide RNA target site is as follows,
Stim1: 5'-GCAGGGTAGCTGAAACACAC-3'
The sequence of the ssODN for homologous recombination is as follows,
5'-ATAGCCTTCTTGCCAGCCAAGTGGGGAATTCGTGTGTTTCGGCTACCCTGCAGGGCTCGGCTGTCCCCAACTGGAGATGGCCATCTCCAGTTGGGGACAGCCGAGCCCTGCAGGGTAGCCGAAACACACGAATTCCCCACTTGGCTGGCAAGAAGGCTAT-3'"</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39128171</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Pvalb-cre)2-28Koba</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1261&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1261&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2020-09-23)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39128171</CITATION_ID>
    <DESCRIPTION>This strain is established by injection of modified BAC (cre gene was inserted into the exon 2 of mouse Pvalb gene) into Long-Evans rat's fertile eggs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39128172</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Slc32a1-cre)3_5Fusa</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1248&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1248&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-09-23)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39128172</CITATION_ID>
    <DESCRIPTION>This strain was established by Bac transgenic method (construct: Kazuhiro Yamakawa, phD) in 2014 and maintained at Jikei University School of Medicine. Background: Crlj:WI. Transgene: VGAT&amp;#65288;Slc32a1: mouse, Kanamycin resistance gene&amp;#65288;E. coli&amp;#65289;, Cre&amp;#65288;P1 phage), polyA signal&amp;#65288;SV40 virus). Mouse BAC clone: RP23-392-P11</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39128239</RGD_ID>
    <STRAIN_SYMBOL>GK/CskCrlj</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Charles River Laboratories Japan</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39128239</CITATION_ID>
    <DESCRIPTION>The Goto-Kakizaki (GK) rat is a non-obese Wistar substrain which develops Type 2 diabetes mellitus early in life. The model was developed by Goto and Kakizaki at Tohoku University, Sendai, Japan in 1975. To Chugai Pharmaceutical Co. To Charles River Japan in 1995.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39128242</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Vwf&lt;sup&gt;em1Mcwi-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center, through Versiti Blood Research Institute</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2020-10-09)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Vwf&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>39457948</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="160042900" STOP_POS="160177757" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="158360152" STOP_POS="158491539" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="158085059" STOP_POS="158219525" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="225098521" STOP_POS="225229257" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="161723415" STOP_POS="161854766" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39128242</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 mediated gene editing  resulted   a 130,938-bp deletion between 32-bp in front of the 5' end of Exon 1 and 122bp after the stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39131285</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(DIO-mCherry)2Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39131285</CITATION_ID>
    <DESCRIPTION>This Cre recombinase reporter rat expressing mCherry was generated by backcrossing Sprague-Dawley to LE-Tg(DIO-mCherry)2Ottc (RGD:8693598). 
The transgene contains Cre recombinase reporter rat expressing mCherry driven by the EF1 alpha promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39456105</RGD_ID>
    <STRAIN_SYMBOL>F344/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity  program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39456105</CITATION_ID>
    <DESCRIPTION>F344/StmMcwi was redelivered from F344/Stm which was derived from F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39456107</RGD_ID>
    <STRAIN_SYMBOL>LE/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39456107</CITATION_ID>
    <DESCRIPTION>The LE/StmMcwi was rederived  from LE/Stm and maintained at Medical College of Wisconsin. The LE/Stm rats were introduced into Saitama Cancer Center Research Institute in 1969 from a closed colony of Long Evans rats maintained in the Ben May Laboratory for Cancer Research, University of Chicago. A mutant with red-eyed dilution was found in 1970 in the Long-Evans colony, and the mutation was fixed by selective mating. Thereafter, they were maintained by sister-brother mating more than F50.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39456108</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Trpv4&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpv4&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>39456109</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="47599161" STOP_POS="47638143" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="41938533" STOP_POS="41977517" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="47698915" STOP_POS="47737902" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="49492064" STOP_POS="49529956" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="43226933" STOP_POS="43265889" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39456108</CITATION_ID>
    <DESCRIPTION>TRPV4 gene?specific zinc finger constructs directed against exon 13, containing the coding sequence for part of TM5, the pore region, and TM6, were injected in zygotes from Sprague-Dawley rats. An animal with an 899 bp deletion in the TRPV4 gene was selected as a founder for further breeding. This deletion completely removes exon 13, plus parts of intron 12-13 and intron 13-14 .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39457682</RGD_ID>
    <STRAIN_SYMBOL>LCR-mt&lt;sup&gt;HCR&lt;/sup&gt;/Tol</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>conplastic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39457682</CITATION_ID>
    <DESCRIPTION>Mitochodrial genome of LCR/ was selectively replaced by HCR  to create this conplastic strain; these have the mitochondrial genome of HCRl on LCR nuclear genetic background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39457683</RGD_ID>
    <STRAIN_SYMBOL>HCR-mt&lt;sup&gt;LCR&lt;/sup&gt;/Tol</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo College of Medicine
and Life Sciences, Toledo, OH 43614</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>conplastic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39457683</CITATION_ID>
    <DESCRIPTION>Mitochodrial genome of HCR/ was selectively replaced by LCR  to create this conplastic strain; these have the mitochondrial genome of LCRl on HCR nuclear genetic background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39457699</RGD_ID>
    <STRAIN_SYMBOL>LCR/Tol</STRAIN_SYMBOL>
    <FULL_NAME>Low-capacity runners</FULL_NAME>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39457699</CITATION_ID>
    <DESCRIPTION>Artificially selected for  aerobic running capacity from the genetic heterogenous rats; these were selected for low capacity based on distance run to exhaustion on a motorized treadmill.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39457701</RGD_ID>
    <STRAIN_SYMBOL>HCR/Tol</STRAIN_SYMBOL>
    <FULL_NAME>High-capacity runners</FULL_NAME>
    <ORIGINATION>University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39457701</CITATION_ID>
    <DESCRIPTION>Artificially selected for  aerobic running capacity from the genetic heterogenous rats; these were selected for high capacity based on distance run to exhaustion on a motorized treadmill.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39457945</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt; Lpar1&lt;sup&gt;m1Hubr&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hubrecht Laboratory, Centre for Biomedical Genetics, 3584 CT Utrecht, The Netherlands. Hera Biolabs, Taconic.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lpar1&lt;sup&gt;m1Hubr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126848739</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="78024139" STOP_POS="78147071" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="73229047" STOP_POS="73347874" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="75557038" STOP_POS="75678067" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="79707131" STOP_POS="79825313" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="76449470" STOP_POS="76571458" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39457945</CITATION_ID>
    <DESCRIPTION>The  Lpar1 mutant rat line was generated by target-selected ENU-driven mutagenesis of male MSH6 knockout rats, and high-throughput resequencing of genomic target sequences in progeny from mutagenized rats  revealed an ENU-induced missense mutation in Lpar1 that resulted in the change of a methionine into an arginine (p.M318R) in the 8th helix and that was predicted to be deleterious for protein function. The founder animal was mated with wild type Msh6 females. The Msh6 mutated allele was eliminated by systematic selection of F2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39457947</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Bckdk&lt;sup&gt;m1Dbsa&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Spring Valley Laboratories, Inc (Woodbine,MD)</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39457947</CITATION_ID>
    <DESCRIPTION>The frogleg phenotype arose in a breeding colony of Sprague-Dawley rats which had originated with animals purchased from Taconic Farms (Hamilton, NY). The frogleg rats, which require no special husbandry, were bred and maintained at Spring Valley Laboratories, Inc (Woodbine,MD). The complex phenotype seen in the frogleg rat arises from a missense mutation (p.G369E) in the gene Bckdk.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>39457950</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ngly1&lt;sup&gt;em1Ta-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1164&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1164&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-07-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ngly1&lt;sup&gt;em1Ta&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>149735565</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="11584475" STOP_POS="11640977" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="9153738" STOP_POS="9210228" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="10405453" STOP_POS="10455973" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="14450836" STOP_POS="14501356" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="10704196" STOP_POS="10750564" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_39457950</CITATION_ID>
    <DESCRIPTION>The homozygous Ngly1 mutant rats are littermates of cross of heterozygotesNgly1 mutant rats . The mutations created by CRISPR/Cas9 contained  2.6 kb  deletions in exon 11 and exon 12 and a 3' flanking region of the Ngly1. Two single-guideRNA (sgRNA) sequences targeting sites upstream (5'-sgRNA;5'-cagaggaattgtgatagtacagg-3')anddownstream(3'-sgRNA; 5'-ccagttattcataccatggtaaa-3') of the exon 11, exon 12 and a 3'flanking region of the ratNgly1genome, respectively. By the time of deposition, this strain was crossed twice to Crl:CD (SD). "Homozygous rats are obtained by crossing between heterozygous rats.
Maintain the strain by crossing between heterozygous rats or by backcrossing to Crl:CD (SD) rats.
Homozygous rats, both females and males, have no record of pregnancy and reproduction. They are more likely to be infertile."</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>40818253</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Dyrk1a&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Generated with support from the Simons Foundation Autism Research Initiative (&lt;a href=https://www.sfari.org/resource/rat-models/&gt;SFARI&lt;/a&gt;); MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE> Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_40818253</CITATION_ID>
    <DESCRIPTION>The rat strain was produced by injecting  CRISPR/Cas9  targeting rat Dyrk1a into Crl:LE embryos. The result is a 14-bp deletion in exon 3</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>40818401</RGD_ID>
    <STRAIN_SYMBOL>M520/NRrrcMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2024-08-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_40818401</CITATION_ID>
    <DESCRIPTION>To N 1951 from Heston at F51. Developed by Curtis at Columbia University Institute for Cancer Research, 1920; to Heston, 1949 at F49. It was then sent to Rat Resource and Research Center (RRRC). Medical College of Wisconsin received live animals from cryo-resuscitated pairs at RRRC in 2009.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>40924649</RGD_ID>
    <STRAIN_SYMBOL>Beta IIM</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>School of Medicine at Rosario, Argentina</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_40924649</CITATION_ID>
    <DESCRIPTION>Nine inbred lines developed from random-bred colony maintained by B. Houssay since 1948. Inbreeding and upward selection of body weight and fertility were performed in every line.  Groups of rats from lines 'b' were separated in 1958  and raised at the School of Medicine at Rosario. In 1976, some degree of overweight was found in the original 'b' group and in 1980, the obesity group was identified as Beta line.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>40924650</RGD_ID>
    <STRAIN_SYMBOL>Alpha IIM</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>School of Medicine at Rosario, Argentina</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_40924650</CITATION_ID>
    <DESCRIPTION>Nine inbred lines developed from random-bred colony maintained by B. Houssay since 1948. Inbreeding and upward selection of body weight and fertility were performed in every line.  Groups of rats from lines 'b' and 'alpha' were separated in 1958 and 1972 respectively and raised at the School of Medicine at Rosario. This line alpha (Alpha IIM)  ), obtained from the F1 'a' X 'd', was used as control for the obese Beta line (RGD:40924649).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>40924656</RGD_ID>
    <STRAIN_SYMBOL>BN.ZUC-&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2021-01-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13432153</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116389200" STOP_POS="116389200" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120597857" STOP_POS="120597857" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_40924656</CITATION_ID>
    <DESCRIPTION>Established as  congenics by introducing fa from 13M/Vc to BN/Crl</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>40924661</RGD_ID>
    <STRAIN_SYMBOL>LA-&lt;i&gt;cp&lt;/i&gt;/NRll</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;cp&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11570565</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="121409735" STOP_POS="121593201" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="116294409" STOP_POS="116477904" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="120503475" STOP_POS="120682281" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="124380327" STOP_POS="124556585" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="122320075" STOP_POS="122503449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_40924661</CITATION_ID>
    <DESCRIPTION>This corpulent  rat used by Rudolph L Leibel's laboratory was developed at the National Institutes of Health (NIH). It was a  congenic strain initially derived by mating a male Koletsky rat that was heterozygous for the corpulent gene (cp/ +) to a female Lister Albany/NIH (LAIN) rat. This congenic carrying the recessive Leprcp (RGD:11570565) identified in  in the obese spontaneously hypertensive Koletsky rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41404646</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lrp5&lt;sup&gt;em1Vari&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrp5&lt;sup&gt;em1Vari&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>41404647</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="210243499" STOP_POS="210346886" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="200814247" STOP_POS="200917581" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="218816833" STOP_POS="218920147" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="225689353" STOP_POS="225793075" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="206102750" STOP_POS="206206350" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41404646</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a  18-bp deletion of exon 2 in the rat Lrp5 gene of Crl:SD embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41404648</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lrp5&lt;sup&gt;em2Vari&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrp5&lt;sup&gt;em2Vari&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>41404650</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="210243499" STOP_POS="210346886" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="200814247" STOP_POS="200917581" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="218816833" STOP_POS="218920147" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="225689353" STOP_POS="225793075" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="206102750" STOP_POS="206206350" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41404648</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a  22-bp deletion at the sgRNA2  site of exon 2 in the rat Lrp5 gene of Crl:SD embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41404651</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lrp5&lt;sup&gt;em3Vari&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrp5&lt;sup&gt;em3Vari&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>41404652</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="210243499" STOP_POS="210346886" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="200814247" STOP_POS="200917581" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="218816833" STOP_POS="218920147" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="225689353" STOP_POS="225793075" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="206102750" STOP_POS="206206350" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41404651</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce an
inversion coupled with small deletions in the exon 2 at both the sgRNA1 (11 bp) and sgRNA2 sites (3 bp)  in the rat Lrp5 gene of Crl:SD embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41404660</RGD_ID>
    <STRAIN_SYMBOL>GK/Jpe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Neurosciences and Cell Biology of  Coimbra, University of Coimbra, Coimbra, Portugal</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41404660</CITATION_ID>
    <DESCRIPTION>The Goto-Kakizaki (GK) rat is a non-obese Wistar substrain which develops Type 2 diabetes mellitus early in life. The model was developed by Goto and Kakizaki at Tohoku University, Sendai, Japan in 1975. The GK line was established by repeated inbreeding from Wistar rats selected at the upper limit of normal distribution for glucose tolerance. Repeated selection of rats with tendency to lowest glucose tolerance resulted in clear-cut glucose intolerance after five generations.Until the end of 1980s,</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41404661</RGD_ID>
    <STRAIN_SYMBOL>W/Jpe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Neurosciences and Cell Biology of Coimbra, University of Coimbra, Coimbra, Portugal</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41404661</CITATION_ID>
    <DESCRIPTION>Inbred Wistar rats maintained at Center for Neurosciences and Cell Biology of Coimbra, University of Coimbra, Coimbra, Portugal</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41404705</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Shank3&lt;sup&gt;em1Bux&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>SAGE Labs (Boyertown, PA).</ORIGINATION>
    <SOURCE>Mount Sinai Medical Center, New York NY 10029 USA</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Shank3&lt;sup&gt;em1Bux&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>41404706</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="122448323" STOP_POS="122518623" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="120568707" STOP_POS="120630796" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="130474278" STOP_POS="130534679" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="130159246" STOP_POS="130220171" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="127817026" STOP_POS="127877875" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41404705</CITATION_ID>
    <DESCRIPTION>The mutant rats were generated using zinc-finger nuclease (ZFN) technology to target exon 6 of the ankyrin repeat domain of rat Shank3. The resulting  mutant has a 68-base pair deletion in exon 6 leading to a premature stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41404723</RGD_ID>
    <STRAIN_SYMBOL>DA.W-&lt;i&gt;Ncf1&lt;sup&gt;W&lt;/sup&gt;&lt;/i&gt;/Rhd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Section for Medical Inflammation Research, Lund University, Lund, Sweden.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ncf1&lt;sup&gt;W&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>41404724</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41404723</CITATION_ID>
    <DESCRIPTION>The Wistar Ncf1 (Ncf1W) allele was backcrossed to the DA background for 10 generations</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41408337</RGD_ID>
    <STRAIN_SYMBOL>DA.F344-Dpp4&lt;sup&gt;DPPIV&lt;/sup&gt;/SvH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hannover Medical School, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dpp4&lt;sup&gt;DPPIV&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12792942</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="67370794" STOP_POS="67452422" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="46962233" STOP_POS="47043870" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="48291055" STOP_POS="48372672" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="54957146" STOP_POS="55038628" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="44279255" STOP_POS="44360283" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41408337</CITATION_ID>
    <DESCRIPTION>Generation of the congenic strain was started with an initial cross between F344/Crl(Wiga)SvH-Dpp4m females, homozygous for the loss-of-function mutation in the Dpp4 gene on RNO3  and a DA/Ztm wild type male rat. The DP4 deficient
congenic DA strain is maintained via brother=sister mating</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41408339</RGD_ID>
    <STRAIN_SYMBOL>WI.SD-&lt;i&gt;Pclo&lt;sup&gt;Tn(sb-B-Geo)Fkh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Texas Southwestern Medical Center, Dallas TX</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pclo&lt;sup&gt;Tn(sb-B-Geo)Fkh&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>41408340</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="20646604" STOP_POS="21005171" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="19691439" STOP_POS="20050015" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="16454904" STOP_POS="17058921" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="16428814" STOP_POS="17031648" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="15911051" STOP_POS="16269090" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41408339</CITATION_ID>
    <DESCRIPTION>The Sprague-Dawley transposon mutagenesis spermatogonial gene trap library  was screen to generate rats with a disrupted Pclo gene in Wistar rat background.  The transposon element was integrated into exon 3 of the Pclo genomic sequence, leading to a premature stop in the reading frame.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41410881</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Grm2&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Transposagen Biopharmaceutical</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Grm2&lt;sup&gt;em1&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>41410882</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="116158810" STOP_POS="116171857" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="107280099" STOP_POS="107293159" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="115344999" STOP_POS="115358628" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="114705123" STOP_POS="114718193" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="111837086" STOP_POS="111850133" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41410881</CITATION_ID>
    <DESCRIPTION>This mutant rat strain was produced by Transposagen Biopharmaceutical and available in mGluR2+/- breeding pairs. The genome modification created a premature stop codon insertion that causes a nonsense mutation at amino acid C407, deleting the transmembrane and intracellular domains of the receptor and rendering the gene nonfunctional.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41412170</RGD_ID>
    <STRAIN_SYMBOL>BBDR/RhwMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee WI</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41412170</CITATION_ID>
    <DESCRIPTION>This strain was given to Medical College of Wisconsin by Ake Lernmark and maintained there.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41412172</RGD_ID>
    <STRAIN_SYMBOL>BBDR.BBDP-(&lt;i&gt;D4Mit6-D4Mit24&lt;/i&gt;)/RhwMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, Milwaukee, WI, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="76647384" STOP_POS="78882945" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="77307388" STOP_POS="79575658" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="141978848" STOP_POS="144249450" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="75732943" STOP_POS="78039637" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41412172</CITATION_ID>
    <DESCRIPTION>The lymphopenia locus from diabetic proned BBDP rat was transferred onto the genome of diabetic-resistant BB rat by marker-assisted selection in nine cycles of cross-intercross breeding. This congenic strain  from Ake Lernmark,  Laboratory, University of Washington, Seattle, Washington to  Medical College of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41412186</RGD_ID>
    <STRAIN_SYMBOL>BBDP/Wor</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41412186</CITATION_ID>
    <DESCRIPTION>Diabetic prone BB rats. The Biobreeding rats (BB) spontaneously developed autoimmune diabetes mellitus were found  in a closed colony of outbred WI (Wistar) rats at the Bio-Breeding Laboratories, Ottawa, Ontario in 1974. In 1977, Butler et al. began inbreeding BB rats at the University of Massachusetts Medical Center
(laboratory code Wor) with 300 breeders purchased from the Bio-Breeding Laboratories. In 1978, during inbreding, pathogen-free rodent barrier system was introduced and  and 2 strains were produced: disease prone (DP) and disease resistant (DR) by selected progenies were diabetic (DP) or remained diabtes free (DR).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>41457452</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Prdm14&lt;sup&gt;em10Nips&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis, Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi, JAPAN</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2021-02-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prdm14&lt;sup&gt;em10Nips&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>41457453</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="10864137" STOP_POS="10876666" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="6082163" STOP_POS="6092712" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="5710076" STOP_POS="5730560" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="10550222" STOP_POS="10570255" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_41457452</CITATION_ID>
    <DESCRIPTION>Prdm14 mutation was induced by introducing ribonucleic complexes (crRNA, tract RNA and Cas9 protein) into Crlj:WI rat embryos using electroporator. The resulting mutation is a 4412-bp deletion in exon 1 to 4. Homozygous Prdm14 knocked-out rats have the germ cell-deficient phenotype.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>42721973</RGD_ID>
    <STRAIN_SYMBOL>LEW/SsNArc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_42721973</CITATION_ID>
    <DESCRIPTION>This strain is now maintained at Animal Resources Centre in Canning Vale, WA 6970 AUSTRALIA. The LEW rats were received from National Institutes of Health, Bethesda MD, USA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>42721974</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Nek8&lt;sup&gt;lpk&lt;/sup&gt;&lt;/i&gt;/Arc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nek8&lt;sup&gt;lpkArc&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>42721975</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="63558940" STOP_POS="63570954" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="63060868" STOP_POS="63073546" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="65404489" STOP_POS="65439059" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="66196993" STOP_POS="66230588" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="64458886" STOP_POS="64470044" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_42721974</CITATION_ID>
    <DESCRIPTION>The Lewis Polycystic Kidney (LPK) rat is a spontaneous mutant identified in the LEW colony (LEW/SsNArc)  maintained at Animal Resources Centre in Canning Vale, WA 6970 AUSTRALIA. The causal gene is identified as a non-synonymous mutation R650C in the NIMA (never in mitosis gene a)- related kinase 8 ( Nek8) gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>42721977</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Pde6b&lt;sup&gt;em1Baek&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Asan Institute for Life Sciences, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pde6b&lt;sup&gt;em1Baek&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>42721979</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="1468302" STOP_POS="1511435" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="1323310" STOP_POS="1366450" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="2328690" STOP_POS="2371913" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="2327104" STOP_POS="2370811" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="1871037" STOP_POS="1914170" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_42721977</CITATION_ID>
    <DESCRIPTION>Cpf1 mRNA (50 ng per uL) and CRISPR RNA (100 ng per uL) were co-microinjected into the cytoplasm of pronuclear stage embryos; surviving embryos were transplanted into the oviducts of pseudo-pregnant surrogate mothers to generate live animals. A Pde6b-mutant rat line with an 11-bp deletion in exon 1 was established. Western blot analysis confirmed deficiency of Pde6b protein in the homozygous mutant retina, indicating successful generation of Pde6b-deficient rats with Cpf1-mediated gene targeting.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>42722004</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(HIV)1Hsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_42722004</CITATION_ID>
    <DESCRIPTION>Noninfectious clone containing gag-pol-deleted HIV-1 provirus under the viral LTR promoter  was microinjected into fertilized one-cell Sprague�Dawley � Fisher 344/NHsd F1. Female founder  with opaque cataracts was mating with wil-type Fischer 344/NHsd. 
Tg rats from line 1 contained 20�25 copies.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>45073130</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Fmr1&lt;sup&gt;em1Mzhe&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The laboratory animal center of Peking University.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fmr1&lt;sup&gt;em1Mzhe&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>124715480</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="152284857" STOP_POS="152322686" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="147240239" STOP_POS="147278057" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="154684924" STOP_POS="154722369" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="154756031" STOP_POS="154793782" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_45073130</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to introduce deletions/mutations in exon 4 of the rat Fmr1 gene of  outbred Sprague-
Dawley  embryos. The resulting mutation is a deletion of five amino acids and a G-A mutation in the Fmr1 gene. This genetic modification results in a frame-shift starting from the second Agenet-like 2 domain in the Fmr1 protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>45073133</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Pon1&lt;sup&gt;em1Lizh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Laboratory Animal Science of Peking Union Medical College</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pon1&lt;sup&gt;em1Lizh&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>124715481</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="34261312" STOP_POS="34292327" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="33294737" STOP_POS="33325759" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="30249749" STOP_POS="30276297" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="30156712" STOP_POS="30183204" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="29936314" STOP_POS="29964821" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_45073133</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce  a 342-bp deletion in exon 4 of rat PON1 gene in Sprague-
Dawley  embryos. The destruction of Pon1 gene caused the absence of the the  expression of Pon1 mRNA, protein in liver, spleen and thymus in the Pon1 homozygous knock-out rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>53621137</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Wnt1-cre/ERT2)AppscRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=868&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-01-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00868</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was injected to the Crl:CD(SD)embryo to  induce the knock-in Cre-ERT2 cassette at the 3' end of Wnt1 gene linked by 2A peptide. This model is used to lineage tracing of neural crest cells  by tissue specific  expression of creERT2</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>56677892</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(GFAP-cre/ERT2)AppscRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=876&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-01-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00876</CITATION_ID>
    <DESCRIPTION>The 'docking site ready (DSR)' rat strain, or TARGAT /TM rat strain was generated using CRISPR/Cas9. With integrase, these TARGAT/DSR rats are used as embryo donors. TARGATT rat embryos will be microinjected with a mixture of TARGATT Cre DNA  constructs containing human GFAP promoter,  a fluorescent reporter mCherry in the Cre cassette linked by a T2A sequence. The astrocyte tissue-specific expression of a CreERT2 is also tamoxifen-dependent.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>58366897</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Tie2-cre/ERT2)AppscRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=877&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-01-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00877</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was injected to the Crl:CD(SD)embryo to  induce the knock-in Cre-ERT2 cassette at the 3' end of Tie2 gene linked by 2A peptide. This model is used to lineage tracing of vascular endothelial cells  by tissue specific  expression of creERT2</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>124713544</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Cyp27b1&lt;sup&gt;em1Thka&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp27b1&lt;sup&gt;em1Thka&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>124713545</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="64756626" STOP_POS="64761570" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="62869340" STOP_POS="62876242" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="70333150" STOP_POS="70340006" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="70512763" STOP_POS="70517707" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_124713544</CITATION_ID>
    <DESCRIPTION>This strain was established by injecting Jcl:Wistar embryo with CRISPR/Cas9 system to delete the cysteine at position 462 in exon 8, which is the 5th ligand of heme iron and an active center of Cyp27b1. The resulting mutation is a 25 amino acid deletion (75 bp deletion) in the target site. The mutant was maintained with CE-2 formula diet (CLEA Japan, Inc., Tokyo, Japan) containing 1.15% calcium and 2,100 IU vitamin D3/kg diet. Homozygotes Cyp27b1 mutants were maintained by mating of heterozygotes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>124713546</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Vdr&lt;sup&gt;em1Thka&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Vdr&lt;sup&gt;em1Thka&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>124713547</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="130864764" STOP_POS="130916757" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="128987981" STOP_POS="129037677" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="139344452" STOP_POS="139394138" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="139536241" STOP_POS="139585928" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="136567614" STOP_POS="136617280" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_124713546</CITATION_ID>
    <DESCRIPTION>This strain was established by injecting Jcl:Wistar embryo with CRISPR/Cas9 system to disrupt the array
near the arginine codon (CGC) at position 270 of the Vdr gene. This resulted in changing arginine codon to Leu at p.270 of the Vdr gene. They were allowed food and water ad libitum and fed a CE-2 formula diet ( CLEA Japan, Inc., Tokyo, Japan) containing 1.15% calcium and 2,100 IU vitamin D3/kg diet. The Vdr (R270L)  rats for analysis were fed an F-2 formula diet (Oriental Yeast
Co., Tokyo, Japan) containing 0.74% calcium and 2000 IU vitamin D/kg diet12 after weaning because the CE-2
diet partially reversed their rickets symptoms. Homozygotes Vdr(R270L mutants were maintained bymating of heterozygotes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>124713548</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Vdr&lt;sup&gt;em2Thka&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Vdr&lt;sup&gt;em2Thka&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>124713550</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="130864764" STOP_POS="130916757" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="128987981" STOP_POS="129037677" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="139344452" STOP_POS="139394138" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="139536241" STOP_POS="139585928" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="136567614" STOP_POS="136617280" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_124713548</CITATION_ID>
    <DESCRIPTION>This strain was established by injecting Jcl:Wistar embryo with CRISPR/Cas9 system to disrupt the array
near the arginine codon (CGC) at position 270 of the Vdr gene. This resulted in 1bp deletion and caused premature stop at p266  of the Vdr gene. They were allowed food and water ad libitum and fed a CE-2 formula diet ( CLEA Japan, Inc., Tokyo, Japan) containing 1.15% calcium and 2,100 IU vitamin D3/kg diet. The Vdr knock out rats for analysis were fed an F-2 formula diet (Oriental Yeast Co., Tokyo, Japan) containing 0.74% calcium and 2000 IU vitamin D/kg diet12 after weaning because the CE-2diet partially reversed their rickets symptoms. Homozygotes Vdr knock out mutants were maintained by mating of heterozygotes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>125093746</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Disc1&lt;sup&gt;em1Rst&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin-Madison School of Medicine and Public Health</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Disc1&lt;sup&gt;em1Rst&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>125093747</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="69911548" STOP_POS="70120970" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="53014201" STOP_POS="53223617" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="57818838" STOP_POS="58069992" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="68529791" STOP_POS="68769050" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="55265116" STOP_POS="55449375" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_125093746</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a  371-bp deletion of exon 2 in the rat Disc1 gene of one-cell Crl:SD embryos. This deletion caused non-sense mutation and early termination of translation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>125097486</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nr3c1&lt;sup&gt;em1Jhrmn&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, United States</ORIGINATION>
    <SOURCE>Strain deposited with the RRRC</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nr3c1&lt;sup&gt;em1Jhrmn&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>125097487</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="31522783" STOP_POS="31644508" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="31271681" STOP_POS="31393320" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="31728373" STOP_POS="32704022" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="31408742" STOP_POS="32348480" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="32371496" STOP_POS="32459145" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_125097486</CITATION_ID>
    <DESCRIPTION>CRISPR-mediated knock in of loxP sites flanking Glucocorticoid Receptor exon 3 via Homology Directed Repair (HDR)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>125097491</RGD_ID>
    <STRAIN_SYMBOL>WI;WDB-&lt;i&gt;Prdm14&lt;sup&gt;tm1(H2BVenus)Nips&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis, Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki, Aichi 444-8787, JAPAN</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2021-04-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prdm14&lt;sup&gt;tm1(H2BVenus)Nips&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126781696</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="10864137" STOP_POS="10876666" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="6082163" STOP_POS="6092712" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="5710076" STOP_POS="5730560" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="10550222" STOP_POS="10570255" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_125097491</CITATION_ID>
    <DESCRIPTION>Targeting vector was designed to replace 1st and 4th exons encoding DNA-binding domain of Prdm14 locus with H2BVenus.  The vector was introduced into WDB/Nips-ES1/Nips (RGD ID:10054010) embryonic stem cells by electroporation . Targeted ES cells were injected into Crlj:WI blastocysts to produce chimeric rats. The chimeric rats were crossed with Crlj:WI rats to produce heterozygous founder rats. These rat strains are being maintained by crossing the founder rats with Crlj:WI rats.
Homozygous Prdm14 knocked-in rats have the germ cell-deficient phenotype.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>125097492</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Sall1&lt;sup&gt;em1Nips&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis, Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki, Aichi 444-8787, JAPAN.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2021-04-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sall1&lt;sup&gt;em1Nips&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126781694</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="34179316" STOP_POS="34196278" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="18005782" STOP_POS="18022705" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="23387737" STOP_POS="23405025" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="34377838" STOP_POS="34395131" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="19277337" STOP_POS="19293298" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_125097492</CITATION_ID>
    <DESCRIPTION>Sall1 mutation was induced by injecting a mix of two pX330 expressing Cas9 and sgRNA targeting the sequence into Crlj:WI rat embryos. The resulting mutation is a 4456-bp deletion in exon 2 to 3. Homozygous Sall1 knocked-out rats had the anephric phenotype at E21.5, and died at postnatal Day-1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>125097494</RGD_ID>
    <STRAIN_SYMBOL>WI;WDB-&lt;i&gt;Sall1&lt;sup&gt;tm4(tdTomato)Nips&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis, Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi 444-8787, JAPAN</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2021-04-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Sall1&lt;sup&gt;tm4(tdTomato)Nips&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126781695</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="34179316" STOP_POS="34196278" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="18005782" STOP_POS="18022705" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="23387737" STOP_POS="23405025" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="34377838" STOP_POS="34395131" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="19277337" STOP_POS="19293298" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_125097494</CITATION_ID>
    <DESCRIPTION>Targeting vector was designed to replace 2nd and 3rd exons encoding DNA-binding domain of Sall1 locus with tdTomato.  The vector was introduced into WDB/Nips-ES1/Nips (RGD ID:10054010) embryonic stem cells by electroporation.Targeted ES cells were injected into Crlj:WI blastocysts to produce chimeric rats. The chimeric rats were crossed with Crlj:WI rats to produce heterozygous founder rats..These rat strains are being maintained by crossing the founder rats with Crlj:WI rats. Homozygous Sall1 knocked-in rats had the anephric phenotype at E21.5, and died at postnatal Day-1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>125097496</RGD_ID>
    <STRAIN_SYMBOL>Iar:WIC</STRAIN_SYMBOL>
    <FULL_NAME>Iar:Wistar-Imamichi</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.iar.or.jp/gp_rat/wi_rat/index.html&gt; Institute for Animal Reproduction in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.iar.or.jp/gp_rat/wi_rat/index.html&gt; Institute for Animal Reproduction in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Metabolism; Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_125097496</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>125097497</RGD_ID>
    <STRAIN_SYMBOL>WIC;WI;WDB-&lt;i&gt;Kiss1&lt;sup&gt;tm8Nips&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, Japan, National Institute for Physiological Sciences, Okazaki Aichi, JAPAN</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2021-04-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kiss1&lt;sup&gt;tm8Nips&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126781693</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="47327159" STOP_POS="47332759" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="44775106" STOP_POS="44780707" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="50529506" STOP_POS="50537603" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="55582365" STOP_POS="55590432" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="46244786" STOP_POS="46247288" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_125097497</CITATION_ID>
    <DESCRIPTION>This strain was made by electroporation of WDB/Nips-ES1/Nips (RGD ID:10054010) embryonic stem (ES) cells with a targeting vector. A targeting vector was designed to insert two loxP sites encompassing exons 2 and 3 of the Kiss1 gene coding for 52-amino acid rat kisspeptin-1 (Kiss1) and a neomycin-resistance gene into the Kiss1 locus in rat ES cells via homologous recombination. Targeted ES cells were injected into Crlj:WI blastocysts to produce chimeric rats. The chimeric rats were crossed with Iar:Wistar-Imamichi rats to produce heterozygous founder rats. This rat strain is being maintained by crossing the founder rat with Iar:Wistar-Imamichi rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126777684</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Mkx&lt;sup&gt;em1Asah&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mkx&lt;sup&gt;em1Asah&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126777685</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="59772113" STOP_POS="59851160" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="55077073" STOP_POS="55156877" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="60537615" STOP_POS="60553284" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="62321329" STOP_POS="62332471" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="63631540" STOP_POS="63710138" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126777684</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 genome editing system targeting exon 2 of rat Mkx gene was injected to  the Wistar embryo to generate this knock out rat strain with 14- bp deletion causing frameshift mutation in the gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126777687</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Dnd1&lt;sup&gt;ter&lt;/sup&gt;&lt;/i&gt;/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute for Laboratory Animal Science, Hannover Medical School (MHH), Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dnd1&lt;sup&gt;ter&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150340622</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="28652712" STOP_POS="28655336" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="28378692" STOP_POS="28381316" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="29608588" STOP_POS="29611212" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="29312395" STOP_POS="29315019" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="29464691" STOP_POS="29467315" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126777687</CITATION_ID>
    <DESCRIPTION>A spontaneous mutation (ter) leading to the formation of congenital ovarian and testicular tumors was detected in the WKY/Ztm rat strain. Sequence analysis detected a point mutation in exon 4 of the rat Dnd1, which introduces a premature stop codon assumed to cause a truncation of the Dnd1 protein. This recessive ter mutation has a complete penetrance of teratocarcinogenesis and infertility of both sexes in homozygous genotype.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126779578</RGD_ID>
    <STRAIN_SYMBOL>LOU/MWsl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Experimental Immunology Unite Faculty of Medicine Clos Chapelle aux Champs 30.56 Bruxelles 1200
BELGIUM</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126779578</CITATION_ID>
    <DESCRIPTION>A substrain of LOU/M maintained in the laboratory of Dr.  H. Bazin at Universite de Louvain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126779586</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Csf1r&lt;sup&gt;tm(EGFP)+/-&lt;/sup&gt;&lt;/i&gt;/Tset</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Edinburgh, United Kingdom</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Csf1r&lt;sup&gt;tm(EGFP)Tset&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126781692</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="56834152" STOP_POS="56860804" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="54546673" STOP_POS="54590418" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="56414493" STOP_POS="56458300" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="55662670" STOP_POS="55689297" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="57080324" STOP_POS="57107295" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126779586</CITATION_ID>
    <DESCRIPTION>Targeting vector was designed to disrupt the first exon encoding of Csf1r gene with a drug selection cassette by homologous recombination in Rat ESC clone DAK31-C2. Sprague-Dawley females were used as embryo donors and pseudo-pregnant recipients</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126779587</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Csf1r&lt;sup&gt;tm(EGFP)+/-&lt;/sup&gt;&lt;/i&gt;/Hume</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Microbiology, University of Queensland, Brisbane, Queensland 4072
Australia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Csf1r&lt;sup&gt;tm(EGFP)Tset&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126781692</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="56834152" STOP_POS="56860804" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="54546673" STOP_POS="54590418" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="56414493" STOP_POS="56458300" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="55662670" STOP_POS="55689297" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="57080324" STOP_POS="57107295" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126779587</CITATION_ID>
    <DESCRIPTION>Heterozygotes "SD-Csf1rtm(EGFP)+/-/Tset" were back-crossed for  at  least 7  generations to  the  inbred dark agouti (DA) background from the Animal Resource Centre, Western Australia.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126779591</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Csf1r&lt;sup&gt;tm(EGFP)-/-&lt;/sup&gt;&lt;/i&gt;/Tset</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Edinburgh, United Kingdom</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Csf1r&lt;sup&gt;tm(EGFP)Tset&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126781692</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="56834152" STOP_POS="56860804" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="54546673" STOP_POS="54590418" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="56414493" STOP_POS="56458300" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="55662670" STOP_POS="55689297" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="57080324" STOP_POS="57107295" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126779591</CITATION_ID>
    <DESCRIPTION>Targeting vector was designed to disrupt the first exon encoding of Csf1r gene with a drug selection cassette by homologous recombination in Rat ESC clone DAK31-C2. Sprague-Dawley females were used as embryo donors and pseudo-pregnant recipients. The homozygotes were obtained by crossing of heterozygotes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126779592</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Csf1r&lt;sup&gt;tm(EGFP)-/-&lt;/sup&gt;&lt;/i&gt;/Hume</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Microbiology, University of Queensland, Brisbane, Queensland 4072
Australia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Csf1r&lt;sup&gt;tm(EGFP)Tset&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126781692</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="56834152" STOP_POS="56860804" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="54546673" STOP_POS="54590418" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="56414493" STOP_POS="56458300" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="55662670" STOP_POS="55689297" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="57080324" STOP_POS="57107295" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126779592</CITATION_ID>
    <DESCRIPTION>Heterozygotes "SD-Csf1rtm(EGFP)+/-/Tset" were back-crossed for  at  least 7  generations to  the  inbred dark agouti (DA) background from the Animal Resource Centre, Western Australia.  The homozygotes were obtained by crossing of heterozygotes</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126781838</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(PDGFB-cre/ERT2)AppscRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=869&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2024-01-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00869</CITATION_ID>
    <DESCRIPTION>The 'docking site ready (DSR)' rat strain, or TARGAT /TM rat strain was generated using CRISPR/Cas9. With integrase, these TARGAT/DSR rats are used as embryo donors. TARGATT rat embryos will be microinjected with a mixture of TARGATT Cre DNA  constructs containing human PDGFB promoter,  a fluorescent reporter mCherry in the Cre cassette linked by a T2A sequence. The brain tissue-specific expression of a CreERT2 is also tamoxifen-dependent.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126781839</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Olfr16-cre/ERT2)AppscRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=870&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2024-01-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00870</CITATION_ID>
    <DESCRIPTION>The 'docking site ready (DSR)' rat strain, or TARGAT /TM rat strain was generated using CRISPR/Cas9. With integrase, these TARGAT/DSR rats are used as embryo donors. TARGATT rat embryos will be microinjected with a mixture of TARGATT Cre DNA  constructs containing mouse Olfr16 (MOR23) promoter,  a fluorescent reporter mCherry in the Cre cassette linked by a T2A sequence. The Olfactory sensory neuronal lineage tissue-specific expression of a CreERT2 is also tamoxifen-dependent.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126781841</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Mnx1-cre/ERT2)AppscRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=872&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryorecovery (as of 2024-01-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00872</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was injected to the Crl:CD(SD)embryo to  induce the knock-in Cre-ERT2 cassette at the 3' end of Mnx1 (HB9) gene linked by 2A peptide. This model is used to lineage tracing of motor neurons  by tissue specific  expression of creERT2</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126781842</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Drd1-cre/ERT2)AppscRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=873&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryorecovery (as of 2024-01-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00873</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was injected to the Crl:CD(SD)embryo to  induce the knock-in Cre-ERT2 cassette at the 3' end of Drd1 (Drd1a) gene linked by 2A peptide. This model is used to lineage tracing of dopamine D1 receptor expressing neurons</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126781843</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Gad1-cre/ERT2)AppscRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=874&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryorecovery (as of 2024-01-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00874</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was injected to the Crl:CD(SD)embryo to  induce the knock-in Cre-ERT2 cassette at the 3' end of Gad1 (Gad67) gene linked by 2A peptide. This model is used to lineage tracing of glutamate decarboxylase 1 expressing cells such as GABAergic neurons, islet cells and spermatocytes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126781844</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(SMHC-cre/ERT2)AppscRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=878&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-01-04)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00878</CITATION_ID>
    <DESCRIPTION>This mutant strain was created by injecting embryos from 'docking site ready (DSR)' rat strains. The DSR rat strain, or TARGAT /TM rat strain was generated using CRISPR/Cas9. The DSR embryos were microinjected with integrase, a mixture of TARGATT Cre DNA constructs containing rabbit smooth muscle myosin heavy chain (SMHC) gene promoter, and a fluorescent reporter mCherry in the Cre cassette linked by a T2A sequence. The vascular smooth muscle tissue-specific expression of a CreERT2 is tamoxifen-dependent."</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126781845</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-GFP-LacZ)AppscRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=879&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00879</CITATION_ID>
    <DESCRIPTION>A transgenic line carrying random insertion of transgene cassette CAG-LSL-GFP-LacZ (LSL: loxp-Stop-Loxp). It is used as a Cre reporter/test line expressing GFP and lacZ. Used as  lineage tracing tool rat line by mating with tissue specific cre or cre/ERT2 line</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126790464</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ube3a&lt;sup&gt;em1Jue&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ube3a&lt;sup&gt;em1Jue&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126790465</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="119204244" STOP_POS="119297097" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="110070260" STOP_POS="110161675" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="116586901" STOP_POS="116678161" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="117745283" STOP_POS="117834011" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="110729142" STOP_POS="110816491" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126790464</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 genome editing system was injected into fertilized Sprague-Dawley rat embryos and inserted
into a surrogate. Two genomic RNAs (gRNAs) were designed to target the 5&amp;#697;-end of the Ube3a gene (upstream of the Ube3a coding sequence) and two gRNAs target sequences downstream of Ube3a. gRNA pairs were used on each end of the deletion to maximize the probability of a complete deletion of the 90-kb region encompassing the Ube3a gene. The 90 kb deletion in Ube3a was confirmed by genome sequencing. Only pups with maternal inheritance of the deletion carried traits for model of Angleman Syndrome.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126790469</RGD_ID>
    <STRAIN_SYMBOL>F344.Cg-&lt;i&gt;Foxn1&lt;sup&gt;rnu-/-&lt;/sup&gt;&lt;/i&gt;/Jcl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/en/products/immunodeficiency/item_a0020&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/en/products/immunodeficiency/item_a0020&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-04-22)</AVAILABILITY>
    <RESEARCH_USE>Immuno deficiency</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126790469</CITATION_ID>
    <DESCRIPTION>This congenic strain was established as a strain with the genetic background of F344/N onto which a segment from the nude rat containing the &lt;i&gt;Foxn1&lt;sup&gt;rnu&lt;/sup&gt;&lt;/i&gt; was transferred. Originally, hairless mutant (&lt;i&gt;rnu&lt;/i&gt;) was observed in a colony of outbred hooded rats maintained at the Rowett Research Institute in Scotland. Backcrossing started at Central Institute for Experimental Animals in 1979 and thereafter the subline was transported to CLEA Japan, Inc for production and supply of these rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126790472</RGD_ID>
    <STRAIN_SYMBOL>F344.Cg-&lt;i&gt;Foxn1&lt;sup&gt;rnu-/+&lt;/sup&gt;&lt;/i&gt;/Jcl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/en/products/immunodeficiency/item_a0020&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/en/products/immunodeficiency/item_a0020&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-04-22)</AVAILABILITY>
    <RESEARCH_USE>Immuno deficiency</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126790472</CITATION_ID>
    <DESCRIPTION>This congenic strain was established as a strain with the genetic background of F344/N onto which a segment from the nude rat containing the &lt;i&gt;Foxn1&lt;sup&gt;rnu&lt;/sup&gt;&lt;/i&gt; was transferred. Originally, hairless mutant (&lt;i&gt;rnu&lt;/i&gt;) was observed in a colony of outbred hooded rats maintained at the Rowett Research Institute in Scotland. Backcrossing started at Central Institute for Experimental Animals in 1979 and thereafter the subline was transported to CLEA Japan, Inc for production and supply of these rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126790496</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Shank2&lt;sup&gt;em13Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Shank2&lt;sup&gt;em13Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126790499</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="208575144" STOP_POS="209020300" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="199146210" STOP_POS="199590962" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="217149156" STOP_POS="217593950" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="222118530" STOP_POS="224450737" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="204399856" STOP_POS="204855474" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126790496</CITATION_ID>
    <DESCRIPTION>The Shank2 KO rat line 13  was generated by zinc finger nuclease technology targeting exon 31 for deletion . Line 13 has a 437 bp deletion around and including the entire exon 31, thereby causing a frameshift and premature stop codon in all three known isoforms of the rat Shank2 mRNA</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126790511</RGD_ID>
    <STRAIN_SYMBOL>Jcl:WIST</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href =https://www.clea-japan.com/en/products/outbred/item_a0370&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-04-23)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126790511</CITATION_ID>
    <DESCRIPTION>CLEA Japan, Inc., Taconic Farms Inc. (USA), and Taconic Europe (Denmark) created the Global Alliance for Laboratory Animal Standardization (GALASTM) agreement in collaboration with the Central Institute for Experimental Animals to promote the international standardization of outbred stocks usable for safety testing in the field of toxicity and pharmacology. Based on these activities,Wistar Hannover GALAS rats are derived from the Han:WIST strain from the Zentral Institut fur Versuchstierzucht (ZfV) (Hannover, Germany). In 1989, 156 pairs were introduced from ZfV to the Institute for Biomedical Research (IBM) in Switzerland (IBM underwent a structural change [name change] to BRL Ltd. and RCC Ltd.). At and after the end of 1998, RCC Ltd. gave more than 50 pairs of pedigreed BrlHan:WIST rats to each GALAS member to use as seed rats for the Wistar Hannover GALAS strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126790547</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Rin1&lt;sup&gt;em1-/-Hcz&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Histology and Embryology, Basic Medical College, China Medical University, Shenyang 110122, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Rin1&lt;sup&gt;em1Hcz&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126790548</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="211785107" STOP_POS="211789755" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="202355729" STOP_POS="202362731" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="220335036" STOP_POS="220342319" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="227359504" STOP_POS="227364152" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="207671502" STOP_POS="207676150" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126790547</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting TALEN targeting the sequence of ratRin1 into SD embryos. The resulting mutation is a knock out of the gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126848737</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt; Msh6&lt;sup&gt;m1Hubr&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hubrecht Laboratory, Centre for Biomedical Genetics, 3584 CT Utrecht, The Netherlands. Hera Biolabs, Taconic.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Msh6&lt;sup&gt;m1Hubr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126848738</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="12316190" STOP_POS="12333505" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="6562631" STOP_POS="6579995" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="11644565" STOP_POS="11662389" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="21616672" STOP_POS="21634338" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="11525292" STOP_POS="11542592" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126848737</CITATION_ID>
    <DESCRIPTION>The Msh6 knockout mutant rat line was generated by target-selected ENU-driven mutagenesis on Crl:WI rats. The founder rat carried an ENU-induced premature stop codon in exon 4 of the Msh6 gene was bred to obtain homozygous animals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126848740</RGD_ID>
    <STRAIN_SYMBOL>SDT.Cg-&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt;/JttJcl</STRAIN_SYMBOL>
    <FULL_NAME>SDT fatty</FULL_NAME>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/en/products/diabetes/item_a0150&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/en/products/diabetes/item_a0150&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-05-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126848740</CITATION_ID>
    <DESCRIPTION>&lt;i&gt;Lepr&lt;sup&gt;fa&lt;/sup&gt;&lt;/i&gt; allele from ZDF was introgressed into SDT rats using the speed congenic method. The newly establised congenic strain of a SDT rat for Leprfa was maintained by intercross between fa-heterozygous littermates in Japan CLEA Inc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126848751</RGD_ID>
    <STRAIN_SYMBOL>RCS-&lt;i&gt;Mertk&lt;sup&gt;rdy&lt;/sup&gt;p&lt;/i&gt;/LavJcl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/dcms_media/other/p0020_RCSRat.pdf&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/dcms_media/other/p0020_RCSRat.pdf&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-04-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mertk&lt;sup&gt;&lt;i&gt;rdy&lt;/i&gt;&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>40902839</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126848751</CITATION_ID>
    <DESCRIPTION>This strain maintained at Japan JCLEA is homozygous  at the pink eye (p) locus and homozygous for a deletion in the Mertk gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126848763</RGD_ID>
    <STRAIN_SYMBOL>ODS-&lt;i&gt;Gulo&lt;sup&gt;od+/+&lt;/sup&gt;/ShiJcl</STRAIN_SYMBOL>
    <FULL_NAME>Osteogenic disorder Shionagi rat, wild type</FULL_NAME>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/en/products/other_disease/item_a0250&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/en/products/other_disease/item_a0250&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-04-29)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126848763</CITATION_ID>
    <DESCRIPTION>This is the wild type control for ODS-Gulood/od/ShiJcl (RGD:4140404) .  Dr. Susumu Makino and his colleagues found several animals that had gait abnormalities among Wistar rats maintained  at Shionogi Co. They named these animals osteogenic disorder (OD) rats because they exhibited prominent bone and joint abnormalities and systemic bleeding. Subsequent studies revealed that these symptoms were derived from an ascorbic acid (vitamin C) deficiency arising from defective gulonolactone oxidase (GLO) activity. This characteristic was confirmed to be the result of a mutation involving the autosomal single recessive gene od. Scurvy due to L-gulonolactone oxidase deficincy; phenotype normalizes if supplied with ascorbic acid 300mg/kg/d. od/od rats are more susceptible to dental caries as compared with +/+ rats, in only amoun parous females.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126848776</RGD_ID>
    <STRAIN_SYMBOL>RCS-&lt;i&gt;Mertk&lt;sup&gt;rdy+&lt;/sup&gt;p&lt;/i&gt;/LavJcl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/dcms_media/other/p0020_RCSRat.pdf&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/dcms_media/other/p0020_RCSRat.pdf&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-04-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126848776</CITATION_ID>
    <DESCRIPTION>This strain maintained at Japan JCLEA is homozygous  at the pink eye (p) locus and homozygous for wild type  Mertk gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126848777</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(HRAS)128NccJcl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/en/products/genetically_modified/item_a0203&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/en/products/genetically_modified/item_a0203&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-04-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126848777</CITATION_ID>
    <DESCRIPTION>Hras128 is a transgenic rat, introduced human proto-type c-Ha-ras gene to Jcl:SD rat fertilized egg by Dr. Hiroyuki Tsuda, Natl. Cancer Center, in 1998. The strain has been kept by CLEA Japan from its creation and supplied to the related research organization after concluded an agreement with Natl. Cancer Center and Japan Science and Technology Agency (JST). This strain is carrying three copies of the human c-Ha-ras proto-oncogene, including its own promoter region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126848778</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-KRAS*G12V)301Jcl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href =https://www.clea-japan.com/en/products/genetically_modified/item_a0206&gt; CLEA Japan, Inc&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href =https://www.clea-japan.com/en/products/genetically_modified/item_a0206&gt; CLEA Japan, Inc&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-04-30)</AVAILABILITY>
    <RESEARCH_USE>Oncology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126848778</CITATION_ID>
    <DESCRIPTION>The transgene consisting of CAG promoter/loxP/neomycin resistant gene casette/lox/Ha-Kras*G12V (KrasV12) was injected into embryos of SD rat (RGD:8547938). This strain was generated at CLEA Japan,Inc. This strain is introduced 3 copies of hemagglutinin (HA) epitope tag connected HA-K-rasv12 gene expression cassette by using Cre/loxP system for controlling term/location expression of human mutated form K-rasv12 gene (changing glycine to valine at the 12 amino acid sequence) that normally floxed rat does not express K-rasv12 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126848793</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Gper1&lt;sup&gt;em1Bj-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo College of Medicine and life Sciences OH</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gper1&lt;sup&gt;em1Bj&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>151347865</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="20331073" STOP_POS="20336527" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="15217217" STOP_POS="15222679" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="17309122" STOP_POS="17315267" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="19296086" STOP_POS="19301691" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="15718615" STOP_POS="15719893" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126848793</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas 9 was utilized to delete rat Gper1 gene in the one-cell embryos of SS/Jr rats. RNA validation performed via deletion
PCR using a sense primer at the 5' end and an antisense primer at the 3' end showed a deletion PCR product of 544
bps versus wild-type PCR product of 1484 bps. The homozygous founders had  complete deletion of Gper1 was confirmed by DNA sequenching.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126848794</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Zbtb16&lt;sup&gt;em1Ipcv+/-&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biology and Medical Genetics, Charles University, Prague</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Zbtb16&lt;sup&gt;em1Ipcv&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150340624</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="57885886" STOP_POS="58073507" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="48989376" STOP_POS="49177011" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="52980226" STOP_POS="53146765" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="51573252" STOP_POS="51740759" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="51931530" STOP_POS="52094813" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126848794</CITATION_ID>
    <DESCRIPTION>TALEN was used  to target Zbtb16 (Plzf )in the SHR and one founder with a deletion of G at position 93 of the coding sequence (c.93delG) was identified. That deletion resulted in a frameshift downstream glycine 31 (p.Gly31fs). The frameshift mutation caused the incorporation of 20 aberrant amino acids downstream of the deleted G, followed by a stop codon.  The founder  was bred with SHR to generate more heterozygous animals. The  homozygous animals die perinatally because of multiple developmental abnormalities.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126848804</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Trpc4&lt;sup&gt;Tn(sb)1Bni&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratorium voor Fysiologie, Campus Gasthuisberg, KU Leuven, B-3000 Leuven
Belgium</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpc4&lt;sup&gt;Tn(sb)Tngen&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126848808</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="140457841" STOP_POS="140629556" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="138307676" STOP_POS="138476856" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="143433102" STOP_POS="143605757" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="163115873" STOP_POS="163282223" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="143350286" STOP_POS="143485716" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126848804</CITATION_ID>
    <DESCRIPTION>The Sleeping Beauty transposon system was used to insert the sleeping beauty transposon into the first intron of the rat Trpc4 gene. Trpc4 knock-out (510 bp) and wild-type allele (905 bp) were confirmed  using PCR and gel electrophoresis</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126908010</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Kcnk3&lt;sup&gt;em1Ang-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnk3&lt;sup&gt;em1Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126908015</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="31483129" STOP_POS="31519061" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="25761487" STOP_POS="25799153" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="27154274" STOP_POS="27190209" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="36969843" STOP_POS="37005778" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="25745923" STOP_POS="25782144" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126908010</CITATION_ID>
    <DESCRIPTION>The homozygous Kcnk3 mutant rats are littermates of cross of heterozygotesKcnk3 mutant rats . The mutation created by CRISPR/Cas9 contained  a 94- bp  deletion  in exon1 of  resulted a premature stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126908013</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Kcnk3&lt;sup&gt;em1Ang-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kcnk3&lt;sup&gt;em1Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126908015</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="31483129" STOP_POS="31519061" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="25761487" STOP_POS="25799153" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="27154274" STOP_POS="27190209" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="36969843" STOP_POS="37005778" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="25745923" STOP_POS="25782144" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126908013</CITATION_ID>
    <DESCRIPTION>The heterozygous Kcnk3 mutant rats were created by CRISPR/Cas9. The mutated allele contained  a 94- bp  deletion  in exon1 of  resulted a premature stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925134</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Il36rn&lt;sup&gt;tm1(Myh6-cre)Mhzh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Nanjing University Model Animal Center.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il36rn&lt;sup&gt;tm1(Myh6-cre)Mhzh&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126925161</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="27442679" STOP_POS="27449306" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="7044419" STOP_POS="7051016" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="1385256" STOP_POS="1392275" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="1378833" STOP_POS="1385430" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="2530402" STOP_POS="2536999" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925134</CITATION_ID>
    <DESCRIPTION>This line was produced by mating rats carrying Il36rnf/f allele and Myh6-cre-allele. The expression of Il36rn was knockout in cardiomyocytes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925135</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Il1rl2&lt;sup&gt;tm1(Myh6-cre)Mhzh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Nanjing University Model Animal Center.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il1rl2&lt;sup&gt;tm1(Myh6-cre)Mhzh&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126925159</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="50087271" STOP_POS="50134225" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="42591658" STOP_POS="42639351" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="47044870" STOP_POS="47093679" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="46733619" STOP_POS="46778352" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="39492187" STOP_POS="39537792" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925135</CITATION_ID>
    <DESCRIPTION>This line was produced by mating rats carrying IIl1rl2f/f allele and Myh6-cre-allele. The expression of Il1rl2 was knockout in cardiomyocytes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925136</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Mstn&lt;sup&gt;em1Cqin&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mstn&lt;sup&gt;em1Cqin&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>151347430</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="55944513" STOP_POS="55950913" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="48452533" STOP_POS="48458933" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="53310977" STOP_POS="53315804" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="52977371" STOP_POS="52982198" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="45426831" STOP_POS="45431658" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925136</CITATION_ID>
    <DESCRIPTION>ZFN constructs were designed to target the genomic region of rat Mstn exon 1. A ZFN construct engineered to target bp 277 to 281 of rat Mstn was used for the rat embryo injection.  The # 6 founder was found to have sequence changed from GATCA to AGTC, resulting in a frame shift mutation within the open reading frame and generate an early termination codon, resulting in a truncated 109 amino acid peptide (wild type is 376). ZFN mutant founders were backcrossed to Spargue Dawley rats to get heterozygous offsprings which were intercrossed and offsprings maintained as homozygous and heterozygous breeders.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925137</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ogdh&lt;sup&gt;em1Yuyi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory Animal Center of Zhengzhou university</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ogdh&lt;sup&gt;em1Yuyi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126925168</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="85363949" STOP_POS="85431405" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="81150021" STOP_POS="81217479" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="86414924" STOP_POS="86481903" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="87376110" STOP_POS="87442862" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="87022994" STOP_POS="87090768" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925137</CITATION_ID>
    <DESCRIPTION>The TALEN systems targeting Ogdh were injected to Sprague Dawley one cell embryos and an 8-bp deletion was identified in one founder animal. No homozygous rats were obtained from mating of heterozygotes that suggests embryonic lethal for the homozygotic mutant.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925138</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ubd&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Cardiovascular Medicine, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi 330006</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ubd&lt;sup&gt;em1&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126925166</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="1390734" STOP_POS="1392685" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="1385487" STOP_POS="1387438" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="1876175" STOP_POS="1878126" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="3917777" STOP_POS="3919728" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="1475944" STOP_POS="1477895" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925138</CITATION_ID>
    <DESCRIPTION>This Ubd (FAT10) knockout rat strain was generated using  theCRISPR-Cas9 technique in a Sprague Dawley (SD) background. The knockout allele has a 911 bp deletion of exon 2, leading to a truncated protein of Ubd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925139</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Dnmt1&lt;sup&gt;tm1(Myh6-cre)Cqin&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Beijing Engineering Research Center for Experimental Animal Models of Human Diseases, Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences and Peking Union Medical College (ZLF18003), Beijing, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dnmt1&lt;sup&gt;tm1(Myh6-cre)Cqin&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126925165</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="27716797" STOP_POS="27763405" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="19440611" STOP_POS="19486659" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="21922515" STOP_POS="21968495" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="21978830" STOP_POS="22024656" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="19926995" STOP_POS="19973256" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925139</CITATION_ID>
    <DESCRIPTION>To specifically knockout Dnmt1 in the myocardium, Cre-loxP system was used by crossing alpha -MHC-Cre rats with Dnmt1 cKO rats. Dnmt1+/- offspring positive for the alpha MHC-Cre transgene (double-positive) were selected. In the second round of crossbreeding, the double-positive rats were crossed with Dnmt1 cKO rats, and Dnmt1-/- offspring positive for the alpha MHC-Cre transgene were obtained as myocardium-specific Dnmt1-KO rats</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925196</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Slc6a3&lt;sup&gt;m1Span&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Central Institute of Mental Health
Department of Psychopharmacology
Central Institute of Mental Health
Mannheim,</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc6a3&lt;sup&gt;m1Span&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126925197</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="31537990" STOP_POS="31578962" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="29709443" STOP_POS="29750413" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="32323011" STOP_POS="32363983" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="33745060" STOP_POS="33788878" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="30516568" STOP_POS="30557540" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925196</CITATION_ID>
    <DESCRIPTION>This strain was identified in the N-ethyl-N-nitrosourea (ENU)-driven target-selected mutagenesis screen. A point mutation in the Slc6a3 (DAT) coding sequence (exon 3) with a T/G transversion at nucleotide position 471 was identified in a male rat. This nucleotide exchange leads to substitution of an asparagine amino acid residue by a lysine residue at position 157 (N157K) in the SLC6A3 (DAT) protein, which introduces new positive charge into the amino acid sequence.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925212</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt; Drd1&lt;sup&gt;m1Hubr&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hubrecht Laboratory, Centre for Biomedical Genetics, 3584 CT Utrecht, The Netherlands.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Drd1&lt;sup&gt;m1Hubr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126925213</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="10545488" STOP_POS="10550029" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="10540440" STOP_POS="10544971" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="11099736" STOP_POS="11104352" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="13211031" STOP_POS="13215581" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="16655926" STOP_POS="16658161" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925212</CITATION_ID>
    <DESCRIPTION>The Drd1 mutant rat line was generated by target-selected ENU-driven mutagenesis on outbred Wistar  rats. Sequencing of genomic target sequences in progeny from mutagenized rats  revealed an ENU-induced missense mutation in Drd1.  The mutation  resulted in an isoleucine to serine exchange (Drd1I116S) in helix III of the protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925756</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cryba1&lt;sup&gt;Nuc1Dbsa&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Johns Hopkins University School of Medicine
The Wilmer Eye Institute
The Johns Hopkins University School of Medicine
Baltimore</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cryba1&lt;sup&gt;Nuc1Dbsa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126925758</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="63106465" STOP_POS="63113020" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="62608373" STOP_POS="62614726" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="65160777" STOP_POS="65167504" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="66458061" STOP_POS="66480390" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="63758929" STOP_POS="63765451" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925756</CITATION_ID>
    <DESCRIPTION>This spontaneous mutation was identified in the offspring of pregnant Sprague-Dawley rats purchased from Taconic Farms. This mutant exhibited abnormal eye phenotype including nuclear cataracts and was called Nuc1 rat. Sequencing of the mutant allele revealed a 27 base pair insertion in exon 6 of Cryba1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925949</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Myh7b&lt;sup&gt;em1Blar+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Beijing Laboratory
Animal Research Center of Chinese Academy of
Medical Sciences.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Myh7b&lt;sup&gt;em1Blar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126925953</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="164537211" STOP_POS="164582441" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="144076911" STOP_POS="144122714" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="151105038" STOP_POS="151150621" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="157472519" STOP_POS="157518151" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="146115687" STOP_POS="146139441" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925949</CITATION_ID>
    <DESCRIPTION>The Myh7b knockout SD rats were generated using the CRISPR/Cas9 system targeting exon 2, resulting 7 bases deletion of exon 2 and generated a new termination codon TGA in exon 3. The heterzygous Myh7b+/- rats were crossed to generate littermate controls. The birth ratio of wild type (WT):Myh7b+/-:Myh7b-/- was
approximately 1:2:1, indicating that Myh7b-/- did not cause fetal death.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925952</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Myh7b&lt;sup&gt;em1Blar-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Beijing Laboratory
Animal Research Center of Chinese Academy of
Medical Sciences.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Myh7b&lt;sup&gt;em1Blar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126925953</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="164537211" STOP_POS="164582441" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="144076911" STOP_POS="144122714" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="151105038" STOP_POS="151150621" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="157472519" STOP_POS="157518151" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="146115687" STOP_POS="146139441" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925952</CITATION_ID>
    <DESCRIPTION>The Myh7b knockout SD rats were generated using the CRISPR/Cas9 system targeting exon 2, resulting 7 bases deletion of exon 2 and generated a new termination codon TGA in exon 3. The heterzygous Myh7b+/- rats were crossed to generate littermate controls. The birth ratio of wild type (WT):Myh7b+/-:Myh7b-/- was
approximately 1:2:1, indicating that Myh7b-/- did not cause fetal death.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925978</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ercc6&lt;sup&gt;em1Cgen&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Key Laboratory of Neurological Function and Health, School of Basic Medical Science, Guangzhou Medical University, Guangzhou 511436, China.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ercc6&lt;sup&gt;em1Cgen&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126925980</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="7771311" STOP_POS="7841895" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="7810692" STOP_POS="7810692" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="8779715" STOP_POS="8779715" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="10699983" STOP_POS="10770565" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="8024881" STOP_POS="8091587" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925978</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was designed to introduce an in-frame amino acid substitution (R571X. CGA &gt; TGA). A silent mutation (ACC to ACG) was also introduced to prevent the binding and re-cutting of the sequence by gRNA after HDR. Founder animals harboring the expected single-nucleotide substitution were bred to produce heterozygous and homozygous rats.The heterozygous rats had phenotypes similar to the wild type littermates.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925992</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cftr&lt;sup&gt;em1Ang&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>INSERM 1151 INEM Universite de Paris Paris France.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cftr&lt;sup&gt;em1Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126925993</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="47600638" STOP_POS="47600640" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="46634751" STOP_POS="46634753" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="42766671" STOP_POS="42766673" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="42281040" STOP_POS="42448571" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="43874852" STOP_POS="44041870" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925992</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system targeting at exon 12 to create deletion  at codon F508 was injected to the male pronucleus of the fertalized one-cell stage embryos collected from Crl:SD. The donor DNA generated a codon deletion at F508 and the creation of one NdeI restriction site for sequencing identification.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126925994</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cftr&lt;sup&gt;em2Ang&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>INSERM 1151 INEM Universite de Paris Paris France.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cftr&lt;sup&gt;em2Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126925995</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="47562650" STOP_POS="47562652" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="46596759" STOP_POS="46596761" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="42728679" STOP_POS="42728681" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="42281040" STOP_POS="42448571" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="43874852" STOP_POS="44041870" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126925994</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system targeting at exon 3 to create gene knock out was injected to the male pronucleus of the fertalized one-cell stage embryos collected from Crl:SD. The donor DNA generated a frameshift and the creation of one XbaI restriction site and a premature stop codon. Two knockout founders ( referred as MUKORAT8.3 and  MUKORAT 6.4) exhibit no difference in phenotypes and were pooled for study.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126928141</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;F8&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;/Novo-Tg(ITGA2B-F8*)Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Blood Research Institute
8733 W Watertown Plank Road
Milwaukee, WI 53226</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>F8&lt;i&gt;&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>11531096</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126928141</CITATION_ID>
    <DESCRIPTION>This transgenic was produced by crossing the SD transgenic rat  carrying  Lentivirus constructs containing the  2bF8 vector [B-domain deleted human FVIII under control of ITGA2B (IIb) promoter] with an F8 knockout rat SD-F8em1Sage-/-/Novo (RGD:11531091). This transgenic rat strain expressed B-domain deleted human F8 under the control of ITGA2B promoter in the absence of rat F8 product.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126928146</RGD_ID>
    <STRAIN_SYMBOL>ACI.Cg.-&lt;i&gt;Cdkn1b&lt;sup&gt;em1Musc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Transgenic and Gene Function Core, Medical University of South Carolina, Charleston, South Carolina, United States of America</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cdkn1b&lt;sup&gt;em1Musc&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126928147</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="169491273" STOP_POS="169496500" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="167760067" STOP_POS="167765177" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="168689043" STOP_POS="168694159" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="232962218" STOP_POS="232967323" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="171841705" STOP_POS="171846506" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126928146</CITATION_ID>
    <DESCRIPTION>The CRISPR-Cas9 system  targeted to exon 2 of the rat Cdkn1b was injected to zygotes derived from the Sprague-Dawley outbred rat strain. Two mutations with the highest potential impact on Cdkn1b function were transferred through the germline showing a 32-bp deletion (DEL-32, em1Musc) and a 65-bp deletion (DEL-65, em4Musc), both disrupting the open reading frame of the Cdkn1b gene. The selected mutations were breded to the ACI inbred strain for future study. This mutant strain ACI.Cg.-&lt;i&gt;Cdkn1b&lt;sup&gt;em1Musc&lt;/sup&gt;&lt;/i&gt; harbors 32-bp deletion of Cdkn1b exhibits same phenotype as the em4Musc with 65-bp deletion</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>126928150</RGD_ID>
    <STRAIN_SYMBOL>ACI.Cg.-&lt;i&gt;Cdkn1b&lt;sup&gt;em4Musc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Transgenic and Gene Function Core, Medical University of South Carolina, Charleston, South Carolina, United States of America</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cdkn1b&lt;sup&gt;em4Musc&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>126928151</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="169491273" STOP_POS="169496500" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="167760067" STOP_POS="167765177" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="168689043" STOP_POS="168694159" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="232962218" STOP_POS="232967323" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="171841705" STOP_POS="171846506" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_126928150</CITATION_ID>
    <DESCRIPTION>The CRISPR-Cas9 system  targeted to exon 2 of the rat Cdkn1b was injected to zygotes derived from the Sprague-Dawley outbred rat strain. Two mutations with the highest potential impact on Cdkn1b function were transferred through the germline showing a 32-bp deletion (DEL-32, em1Musc) and a 65-bp deletion (DEL-65, em4Musc), both disrupting the open reading frame of the Cdkn1b gene. The selected mutations were breded to the ACI inbred strain for future study. This mutant strain ACI.Cg.-&lt;i&gt;Cdkn1b&lt;sup&gt;em4Musc&lt;/sup&gt;&lt;/i&gt; harbors 65-bp deletion of Cdkn1b exhibits same phenotype as the em1Musc with 32-bp deletion</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127284837</RGD_ID>
    <STRAIN_SYMBOL>GK/Wnsm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wales College of Medicine (Cardiff, UK)</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127284837</CITATION_ID>
    <DESCRIPTION>The Goto-Kakizaki (GK) rat is a non-obese Wistar substrain which develops Type 2 diabetes mellitus early in life. The model was developed by Goto and Kakizaki at Tohoku University, Sendai, Japan in 1975. The GK line was established by repeated inbreeding from Wistar rats selected at the upper limit of normal distribution for glucose tolerance. Repeated selection of rats with tendency to lowest glucose tolerance resulted in clear-cut glucose intolerance after five generations. This GK/Wnsm colony was established at the University of Wales College of Medicine (Cardiff, UK) after received breeding
pairs provided by Professor Y Goto (Tohoku University School of Medicine, Sendai, Japan).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127284865</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Nppc&lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/nbr&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/nbr&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nppc&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127284866</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="94767986" STOP_POS="94772186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="87320051" STOP_POS="87324251" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="93731436" STOP_POS="93735636" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="93458753" STOP_POS="93462953" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="85434254" STOP_POS="85438454" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127284865</CITATION_ID>
    <DESCRIPTION>This strain was established by injecting Zinc-finger nucleases (ZFNs)  to F344/Stm pronuclear  stage embryos. Selected  ZFNs were designed to target exon 1 of rat Nppc, which encodes the N-terminus of natriuretic peptide precursor C
(target sequence: CGAAGCCAAGCCCGGGACaccaccGAAGGTGGGTGCTGTCGCG; nucleotides 179 - 221, NC_005108.4). The injected F344/Stm embryos  were transferred into the oviducts of pseudopregnant rats. Four lines of knockout strains were estaglished. This F344-&lt;i&gt;Nppc&lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;  strain ( delta 6)  was deduced to generate a two a.a. deletion (a.a. 28 and 29, Pro and Pro, NP_446202, at nucleotides 198 - 203, NM_053750.1).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127284868</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Nppc&lt;sup&gt;em2Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/nbr&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/nbr&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nppc&lt;sup&gt;em2Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127284869</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="94767986" STOP_POS="94772186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="87320051" STOP_POS="87324251" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="93731436" STOP_POS="93735636" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="93458753" STOP_POS="93462953" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="85434254" STOP_POS="85438454" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127284868</CITATION_ID>
    <DESCRIPTION>This strain was established by injecting Zinc-finger nucleases (ZFNs)  to F344/Stm pronuclear  stage embryos. Selected  ZFNs were designed to target exon 1 of rat Nppc, which encodes the N-terminus of natriuretic peptide precursor C
(target sequence: CGAAGCCAAGCCCGGGACaccaccGAAGGTGGGTGCTGTCGCG; nucleotides 179 - 221, NC_005108.4). The injected F344/Stm embryos  were transferred into the oviducts of pseudopregnant rats. Four lines of knockout strains were estaglished. This F344-&lt;i&gt;Nppc&lt;sup&gt;em2Kyo&lt;/sup&gt;&lt;/i&gt;  strain ( delta 9)  was deduced to generate one amino-acid substitution (a.a. 26, from Gly to Ala, NP_446202, at nucleotides 192 - 194,
NM_053750.1) and a three amino-acid deletion (a.a. 27 - 29, Thr, Pro and Pro, NP_446202, at nucleotides 193 - 201, NM_053750.1), within the N-terminal portion of the full-length Nppc</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127284870</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Nppc&lt;sup&gt;em3Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/nbr&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/nbr&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nppc&lt;sup&gt;em3Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127284871</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="94767986" STOP_POS="94772186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="87320051" STOP_POS="87324251" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="93731436" STOP_POS="93735636" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="93458753" STOP_POS="93462953" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="85434254" STOP_POS="85438454" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127284870</CITATION_ID>
    <DESCRIPTION>This strain was established by injecting Zinc-finger nucleases (ZFNs)  to F344/Stm pronuclear  stage embryos. Selected  ZFNs were designed to target exon 1 of rat Nppc, which encodes the N-terminus of natriuretic peptide precursor C
(target sequence: CGAAGCCAAGCCCGGGACaccaccGAAGGTGGGTGCTGTCGCG; nucleotides 179 - 221, NC_005108.4). The injected F344/Stm embryos  were transferred into the oviducts of pseudopregnant rats. Four lines of knockout strains were estaglished. This F344-&lt;i&gt;Nppc&lt;sup&gt;em3Kyo&lt;/sup&gt;&lt;/i&gt;  strain ( delta 11)was deduced to generated a frame shift and a premature stop codon (at nucleotides 275 - 277, NM_053750.1)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127284872</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Nppc&lt;sup&gt;em4Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/nbr&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/nbr&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nppc&lt;sup&gt;em4Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127284873</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="94767986" STOP_POS="94772186" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="87320051" STOP_POS="87324251" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="93731436" STOP_POS="93735636" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="93458753" STOP_POS="93462953" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="85434254" STOP_POS="85438454" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127284872</CITATION_ID>
    <DESCRIPTION>This strain was established by injecting Zinc-finger nucleases (ZFNs)  to F344/Stm pronuclear  stage embryos. Selected  ZFNs were designed to target exon 1 of rat Nppc, which encodes the N-terminus of natriuretic peptide precursor C
(target sequence: CGAAGCCAAGCCCGGGACaccaccGAAGGTGGGTGCTGTCGCG; nucleotides 179 - 221, NC_005108.4). The injected F344/Stm embryos  were transferred into the oviducts of pseudopregnant rats. Four lines of knockout strains were estaglished. This F344-&lt;i&gt;Nppc&lt;sup&gt;em4Kyo&lt;/sup&gt;&lt;/i&gt;  strain ( delta 774) had a massive deletion within the Nppc gene that included the translation initiation site. Quantitative RT-PCR revealed that the expression of Nppc mRNA in the brain was drastically decreased in homozygous delta 774 mutant rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127284883</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Aqp4&lt;sup&gt;em1Hrt&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Anatomy and Histology, School of Basic Medical Sciences, Peking University, Beijing, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Aqp4&lt;sup&gt;em1Hrt&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127284884</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="6782389" STOP_POS="6799034" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="6507903" STOP_POS="6524558" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="6766009" STOP_POS="6782757" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="6720759" STOP_POS="6737703" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="6626313" STOP_POS="6642766" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127284883</CITATION_ID>
    <DESCRIPTION>The transcription activator-like effector nuclease (TALEN)-mediated knockout approach was applied to generate Aqp4-deficient rats. The synthesized  TALENs against the following sequences: (5&amp;#8242;-CACAGCAGAGTTCCTGG-3&amp;#8242;) for the sense strand and (5&amp;#8242;-GGATCCCACGCTGAGCA-3&amp;#8242;) for the antisense strand. The founder animal lacking three base pairs was crossed with wild-type rat to produced the F1 generration and the heterozygous offspring of F1 were corssed to produce mutant strains and confirmed by sequencing analysis of PCR products of modified genome region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127285380</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Mir31&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Cancer Biology and Genetics, Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210;</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127285380</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce the gene knockout of Mir31 in the Sprague Dawley embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127285404</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Cfb&lt;sup&gt;em1Tja&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre for Genomic and Experimental Medicine, MRC Institute for Genetics and Molecular Medicine, Edinburgh, United Kingdom</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cfb&lt;sup&gt;em1Tja&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127285405</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="3975271" STOP_POS="3981138" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="3970643" STOP_POS="3976510" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="4536206" STOP_POS="4542073" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="6616005" STOP_POS="6621872" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127285404</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting exon 6 of rat complement factor b (Cfb) (target sequence: CCCCTCGGGCTCCATGaatatcTACATGGTGCTGGATG),into SHR/NCrl rat embryos. The resulting mutation is a 19-bp deletion.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127285409</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abcc8&lt;sup&gt;em1Cgen&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Endocrinology, Shandong University, Jinan, China</ORIGINATION>
    <SOURCE>Cyagen Biosciences Inc., Guangzhou, China</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Abcc8&lt;sup&gt;em1Cgen&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127285598</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="105734992" STOP_POS="105816272" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="96598568" STOP_POS="96679563" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="102110708" STOP_POS="102191287" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="103194473" STOP_POS="103275508" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="96622574" STOP_POS="96703723" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127285409</CITATION_ID>
    <DESCRIPTION>TALEN system targeting the rat Abcc8 (sulfonylurea receptor 1, SUR1 ) gene was injected into Crl:CD(SD) embryos. This strain carries a 16-bp deletion corresponding to CCT CAC GGG GCT TCTG compared with wild-type rats is homozygous. No Abcc8 protein was detected in the liver and muscle tissues.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127285661</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Adgrl3&lt;sup&gt;em1Huyc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pediatrics, University of Cincinnati College of Medicine, Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Adgrl3&lt;sup&gt;em1Huyc&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127285662</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="27109219" STOP_POS="27110314" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="26754683" STOP_POS="26755778" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="28786591" STOP_POS="28787686" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="28183727" STOP_POS="29040121" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="28385112" STOP_POS="28854677" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127285661</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to to delete exon 3 of the rat Adgrl3 (Lphn3). Two sgRNAs
targeting the sequences flanking exon 3 (GTCCCTTGCCAGTACATCTC and CCTAGTGTTGTGTTCTGCTA),Cas9 mRNA with the CRISPR/Cas9 reagents was injected into fertilized eggs. Genotyping of founder rats was confirmed by PCR genotyping using three
primers: 1. AAAGGGTCATAGCATCCGGC, 2. CTAACGTGGCTTTTTGTCTTCT, and 3. GCTCGACAGACAGTGTGGAT. The WT band occurs at ~320 bp and KO band at ~452 bp.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127285810</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Trpa1&lt;sup&gt;em1Gne&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Neuroscience, Genentech, 1 DNA Way, South San Francisco, CA 94080 USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Trpa1&lt;sup&gt;em1Gne&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127285812</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="9163060" STOP_POS="9217325" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="4379862" STOP_POS="4434133" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="3783247" STOP_POS="3836485" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="3764339" STOP_POS="3818781" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="3531163" STOP_POS="3584401" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127285810</CITATION_ID>
    <DESCRIPTION>This Trpa1-deleted Sprague Dawley strain was generated by using CRISPR/Cas9. Rats harboring a 7282&amp;#8201;bp deletion spanning Trpa1 exons 19 through 24, corresponding to genomic position RGSC 6.0/rn6 chr5:3,818,620-3,825,901 were identified.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127338473</RGD_ID>
    <STRAIN_SYMBOL>WM/Nem</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The research institute of Environmental Medicine, Nagoya University.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127338473</CITATION_ID>
    <DESCRIPTION>This Strain was from the National Institute of Genetics., Mishima, Japan to the research institute of Environmental Medicine, Nagoya University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127338474</RGD_ID>
    <STRAIN_SYMBOL>BDIX/Nem</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127338474</CITATION_ID>
    <DESCRIPTION>This strain was maintained in Germany and was transferred to Japan by Dr. Tanaka of Aichi Cancer Center. Thereafter, this strain was transferred to Research Institute of Environmental Medicine, Nagoya University in 1973</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127345097</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Muc1&lt;sup&gt;em1Cgen&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Cyagen Biosciences Inc., Guangzhou, China</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Muc1&lt;sup&gt;em1Cgen&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127345099</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="176933312" STOP_POS="176938497" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="174635989" STOP_POS="174640738" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="188543137" STOP_POS="188547874" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="207957206" STOP_POS="207962396" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="181399482" STOP_POS="181403640" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127345097</CITATION_ID>
    <DESCRIPTION>The Muc1 knock out Sprague Dawley rats were produced by targeted gene mutation at rat Muc1 gene. The deletion was made by microinjection of TALENs and located in the exon 1 of rat Muc1 gene (Gen Bank: NM_012602.1). Genotyping was performed by PCR of tail DNA using primers specific for the rat MUC1 gene with forward primer 5&amp;#8242;-CTAGCAAGCCTAAAAGGTGAGAGGT-3&amp;#8242; and reverse primer 5&amp;#8242;-ACGAAGAGCATTTGCCTACTC-3&amp;#8242;, followed by DNA sequencing analysis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127345123</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Angptl8&lt;sup&gt;em1Kyo-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical Innovation Center Kyoto University Graduate School of Medicine, Kyoto, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1335  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Angptl8&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127345127</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="28653044" STOP_POS="28653050" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="20376951" STOP_POS="20376957" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="22857028" STOP_POS="22857034" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="22910979" STOP_POS="22913005" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="20948070" STOP_POS="20950087" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127345123</CITATION_ID>
    <DESCRIPTION>This line #1 Angptl8 knock out (KO) rats were generated using the CRISPR/Cas9 system containing 
 two guide RNAs (gRNAs) targeting exons 2 and 3 in the rat Angptl8 gene. A mixture of transcribed Cas9 and gRNAs was microinjected into F344/Stm rat zygotes [National BioResource Project rat number: 0140) provided by the National BioResource Project for the Rat in Japan. Two lines of rats heterozygous for Angptl8 (lines #1 and #2). Male and female Het rats were intercrossed to obtain homozygous Angptl8 KO rats. Rats were genotyped by PCR with the following primers, 5'-CATCTGTTGAGCAGGCAGAA-3' (sense) and 5'-GTTCAGTGGTGGCTTCCTTC-3' (antisense) for line #1. A 7-bp deletion mutation was identified in line #1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127345124</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Angptl8&lt;sup&gt;em1Kyo+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical Innovation Center Kyoto University Graduate School of Medicine, Kyoto, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1335  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Angptl8&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127345127</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="28653044" STOP_POS="28653050" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="20376951" STOP_POS="20376957" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="22857028" STOP_POS="22857034" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="22910979" STOP_POS="22913005" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="20948070" STOP_POS="20950087" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127345124</CITATION_ID>
    <DESCRIPTION>This line #1 Angptl8 heterozygous rats  were generated using the CRISPR/Cas9 system containing 
 two guide RNAs (gRNAs) targeting exons 2 and 3 in the rat Angptl8 gene. A mixture of transcribed Cas9 and gRNAs was microinjected into F344/Stm rat zygotes [National BioResource Project rat number: 0140) provided by the National BioResource Project for the Rat in Japan. Two lines of rats heterozygous for Angptl8 (lines #1 and #2). Male and female Het rats were intercrossed to obtain homozygous Angptl8 KO rats. Rats were genotyped by PCR with the following primers, 5'-CATCTGTTGAGCAGGCAGAA-3'(sense) and 5'-GTTCAGTGGTGGCTTCCTTC-3' (antisense) for line #1. A 7-bp deletion mutation was identified in line #1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127345125</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Angptl8&lt;sup&gt;em2Kyo-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical Innovation Center Kyoto University Graduate School of Medicine, Kyoto, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1336  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Angptl8&lt;sup&gt;em2Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127345128</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127345125</CITATION_ID>
    <DESCRIPTION>This line #2 Angptl8 knock out (KO) rats were generated using the CRISPR/Cas9 system containing 
 two guide RNAs (gRNAs) targeting exons 2 and 3 in the rat Angptl8 gene. A mixture of transcribed Cas9 and gRNAs was microinjected into F344/Stm rat zygotes [National BioResource Project rat number: 0140) provided by the National BioResource Project for the Rat in Japan. Two lines of rats heterozygous for Angptl8 (lines #1 and #2). Male and female Het rats were intercrossed to obtain homozygous Angptl8 KO rats. Rats were genotyped by PCR with the following primers5'-GGGTGAGCAAAGCTGACCTA-3' (sense) and 5'-GAGTAAACCCACCAGGCTCA-3' (antisense) for line #2. A 980-bp deletion in the ANGPTL8 gene was identified in line # 2, resulting in a premature termination codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>127345126</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Angptl8&lt;sup&gt;em2Kyo+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical Innovation Center Kyoto University Graduate School of Medicine, Kyoto, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1336  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Angptl8&lt;sup&gt;em2Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>127345128</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_127345126</CITATION_ID>
    <DESCRIPTION>This line #2 Angptl8 heterozygous rats were generated using the CRISPR/Cas9 system containing 
 two guide RNAs (gRNAs) targeting exons 2 and 3 in the rat Angptl8 gene. A mixture of transcribed Cas9 and gRNAs was microinjected into F344/Stm rat zygotes [National BioResource Project rat number: 0140) provided by the National BioResource Project for the Rat in Japan. Two lines of rats heterozygous for Angptl8 (lines #1 and #2). Male and female Het rats were intercrossed to obtain homozygous Angptl8 KO rats. Rats were genotyped by PCR with the following primers5'-GGGTGAGCAAAGCTGACCTA-3' (sense) and 5'-GAGTAAACCCACCAGGCTCA-3' (antisense) for line #2. A 980-bp deletion in the ANGPTL8 gene was identified in line # 2, resulting in a premature termination codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735334</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Wfs1&lt;sup&gt;em1Ptsn&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biomedicine and Translational Medicine, Department of Physiology, University of Tartu,</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Wfs1&lt;sup&gt;em1Ptsn&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>149735335</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="78035205" STOP_POS="78059718" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="73810478" STOP_POS="73834993" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="78640707" STOP_POS="78665224" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="78606172" STOP_POS="78630689" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="79379680" STOP_POS="79404003" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735334</CITATION_ID>
    <DESCRIPTION>Rat Wfs1 exon 5-specific zinc-finger nucleases (ZNFs) and microinjection-ready mRNA were injected to embryos harvested from female Sprague-Dawley rats (Crl: CD(SD) )rats. Thereafter, microinjected egg cells were transferred to the oviduct of pseudopregnant Sprague-Dawley recipients.Three different Wfs1 mutant rat lines were created: Wfs1&lt;sup&gt;em1&lt;/sup&gt; ( Wfs1-ex5-KO232), Wfs1&lt;sup&gt;em2&lt;/sup&gt; (Wfs1-ex5-KO266) and Wfs1&lt;sup&gt;em3&lt;/sup&gt; (Wfs1-ex5-INS244). Wfs1&lt;sup&gt;em1&lt;/sup&gt; rats carry a  184 bp deletion,  resulting 27 amino acids deletion in exon 5 (aa212-238) and a new GCC codon(alanine).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735336</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Wfs1&lt;sup&gt;em2Ptsn&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biomedicine and Translational Medicine, Department of Physiology, University of Tartu,</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Wfs1&lt;sup&gt;em2Ptsn&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>149735337</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="78035205" STOP_POS="78059718" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="73810478" STOP_POS="73834993" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="78640707" STOP_POS="78665224" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="78606172" STOP_POS="78630689" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="79379680" STOP_POS="79404003" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735336</CITATION_ID>
    <DESCRIPTION>Rat Wfs1 exon 5-specific zinc-finger nucleases (ZNFs) and microinjection-ready mRNA were injected to embryos harvested from female Sprague-Dawley rats (Crl: CD(SD) )rats. Thereafter, microinjected egg cells were transferred to the oviduct of pseudopregnant Sprague-Dawley recipients.Three different Wfs1 mutant rat lines were created: Wfs1&lt;sup&gt;em1&lt;/sup&gt; ( Wfs1-ex5-KO232), Wfs1&lt;sup&gt;em2&lt;/sup&gt; (Wfs1-ex5-KO266) and Wfs1&lt;sup&gt;em3&lt;/sup&gt; (Wfs1-ex5-INS244). Wfs1&lt;sup&gt;em2&lt;/sup&gt; rats carry a 27 amino acids deletion in exon 5 (aa212-238).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735338</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Wfs1&lt;sup&gt;em3Ptsn&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Biomedicine and Translational Medicine, Department of Physiology, University of Tartu,</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Wfs1&lt;sup&gt;em3Ptsn&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>149735339</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="78035205" STOP_POS="78059718" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="73810478" STOP_POS="73834993" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="78640707" STOP_POS="78665224" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="78606172" STOP_POS="78630689" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="79379680" STOP_POS="79404003" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735338</CITATION_ID>
    <DESCRIPTION>Rat Wfs1 exon 5-specific zinc-finger nucleases (ZNFs) and microinjection-ready mRNA were injected to embryos harvested from female Sprague-Dawley rats (Crl: CD(SD) )rats. Thereafter, microinjected egg cells were transferred to the oviduct of pseudopregnant Sprague-Dawley recipients.Three different Wfs1 mutant rat lines were created: Wfs1&lt;sup&gt;em1&lt;/sup&gt; ( Wfs1-ex5-KO232), Wfs1&lt;sup&gt;em2&lt;/sup&gt; (Wfs1-ex5-KO266) and Wfs1&lt;sup&gt;em3&lt;/sup&gt; (Wfs1-ex5-INS244). Wfs1&lt;sup&gt;em3&lt;/sup&gt; rats carry a substitution in exon 5 of the Wfs1 gene, which is predicted to result in a substitution of LQK (aa 224-226)
into YCMNTI in the WFS1 protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735356</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Wnt1-cre/ERT2)Appsc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>Deposited at &lt;a href=http://www.rrrc.us/Strain/?x=868&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-07-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735356</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was injected to the Crl:CD(SD)embryo to  induce the knock-in Cre-ERT2 cassette at the 3' end of Wnt1 gene linked by 2A peptide. This model is used to lineage tracing of neural crest cells  by tissue specific  expression of creERT2</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735357</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(PDGFB-cre/ERT2)Appsc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>Deposited at &lt;a href=http://www.rrrc.us/Strain/?x=869&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2021-07-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735357</CITATION_ID>
    <DESCRIPTION>The 'docking site ready (DSR)' rat strain, or TARGAT /TM rat strain was generated using CRISPR/Cas9. With integrase, these TARGAT/DSR rats are used as embryo donors. TARGATT rat embryos will be microinjected with a mixture of TARGATT Cre DNA  constructs containing human PDGFB promoter,  a fluorescent reporter mCherry in the Cre cassette linked by a T2A sequence. The brain tissue-specific expression of a CreERT2 is also tamoxifen-dependent.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735358</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Olfr16-cre/ERT2)Appsc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>Deposited at &lt;a href=http://www.rrrc.us/Strain/?x=870&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2021-07-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735358</CITATION_ID>
    <DESCRIPTION>The 'docking site ready (DSR)' rat strain, or TARGAT /TM rat strain was generated using CRISPR/Cas9. With integrase, these TARGAT/DSR rats are used as embryo donors. TARGATT rat embryos will be microinjected with a mixture of TARGATT Cre DNA  constructs containing mouse Olfr16 (MOR23) promoter,  a fluorescent reporter mCherry in the Cre cassette linked by a T2A sequence. The Olfactory sensory neuronal lineage tissue-specific expression of a CreERT2 is also tamoxifen-dependent.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735359</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Mnx1-cre/ERT2)Appsc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>Deposited at  at &lt;a href=http://www.rrrc.us/Strain/?x=872&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryorecovery (as of 2024-01-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735359</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was injected to the Crl:CD(SD)embryo to  induce the knock-in Cre-ERT2 cassette at the 3' end of Mnx1 (HB9) gene linked by 2A peptide. This model is used to lineage tracing of motor neurons  by tissue specific  expression of creERT2</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735361</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Drd1-cre/ERT2)Appsc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>deposited at &lt;a href=http://www.rrrc.us/Strain/?x=873&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryorecovery (as of 2021-07-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735361</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was injected to the Crl:CD(SD)embryo to  induce the knock-in Cre-ERT2 cassette at the 3' end of Drd1 (Drd1a) gene linked by 2A peptide. This model is used to lineage tracing of dopamine D1 receptor expressing neurons</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735362</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Gad1-cre/ERT2)Appsc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>Deposited at &lt;a href=http://www.rrrc.us/Strain/?x=874&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryorecovery (as of 2021-07-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735362</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was injected to the Crl:CD(SD)embryo to  induce the knock-in Cre-ERT2 cassette at the 3' end of Gad1 (Gad67) gene linked by 2A peptide. This model is used to lineage tracing of glutamate decarboxylase 1 expressing cells such as GABAergic neurons, islet cells and spermatocytes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735363</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(GFAP-cre/ERT2)Appsc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>deposited at &lt;a href=http://www.rrrc.us/Strain/?x=876&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-07-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735363</CITATION_ID>
    <DESCRIPTION>The 'docking site ready (DSR)' rat strain, or TARGAT /TM rat strain was generated using CRISPR/Cas9. With integrase, these TARGAT/DSR rats are used as embryo donors. TARGATT rat embryos will be microinjected with a mixture of TARGATT Cre DNA  constructs containing human GFAP promoter,  a fluorescent reporter mCherry in the Cre cassette linked by a T2A sequence. The astrocyte tissue-specific expression of a CreERT2 is also tamoxifen-dependent.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735364</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Tie2-cre/ERT2)Appsc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>deposited at &lt;a href=http://www.rrrc.us/Strain/?x=877&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-07-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735364</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was injected to the Crl:CD(SD)embryo to  induce the knock-in Cre-ERT2 cassette at the 3' end of Tie2 gene linked by 2A peptide. This model is used to lineage tracing of vascular endothelial cells  by tissue specific  expression of creERT2</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735365</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(SMHC-cre/ERT2)Appsc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>deposited at &lt;a href=http://www.rrrc.us/Strain/?x=878&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-07-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735365</CITATION_ID>
    <DESCRIPTION>The 'docking site ready (DSR)' rat strain, or TARGAT /TM rat strain was generated using CRISPR/Cas9. With integrase, these TARGAT/DSR rats are used as embryo donors. TARGATT rat embryos will be microinjected with a mixture of TARGATT Cre DNA  constructs containing rabbit smooth muscle myosin heavy chain (SMHC) gene promoter,  a fluorescent reporter mCherry in the Cre cassette linked by a T2A sequence. The Olfactory sensory neuronal lineage tissue-specific expression of a CreERT2 is also tamoxifen-dependent.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735366</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(CAG-GFP-LacZ)Appsc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Applied StemCell, Inc., Milpitas, CA, USA</ORIGINATION>
    <SOURCE>Deposited at &lt;a href=http://www.rrrc.us/Strain/?x=879&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735366</CITATION_ID>
    <DESCRIPTION>A transgenic line carrying random insertion of transgene cassette CAG-LSL-GFP-LacZ (LSL: loxp-Stop-Loxp). It is used as a Cre reporter/test line expressing GFP and lacZ. Used as  lineage tracing tool rat line by mating with tissue specific cre or cre/ERT2 line</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735371</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;C3&lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1145 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1145 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>advanced_intercross_line</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2021-07-20)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>C3&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>149735372</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735371</CITATION_ID>
    <DESCRIPTION>ZFN constructs specific for the rat C3 gene were designed to target bases 1803-1841 (NCBI reference sequence: NM_016994) of C3 (target sequence: cagggggcccgagtgggctagtggctgtggacaagggg) by Sigma-Aldrich (Tokyo, Japan).  The ZFN systems were injected into the pronucleus of SHR/Izm embryos. The DNA of 10 day old pups was extracted and screened for ZFN-induced mutations. Briefly, DNA extracted from ear tissue was amplified using primers flanking the target sequence (forward primer: 5'-ACTCTTCCCTGTCTTGCGTC-3'; reverse primer: 5'-AATAGAGGCCACCAATGCAC-3'). This mutant revealed a 9-base frameshift deletion of bases 1815-1824 (ggctagtgg).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735516</RGD_ID>
    <STRAIN_SYMBOL>LL/MavRrrcAek</STRAIN_SYMBOL>
    <FULL_NAME>Lyon hypotensive</FULL_NAME>
    <ORIGINATION>Department of Pharmacology, University of Iowa, Iowa</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-08-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735516</CITATION_ID>
    <DESCRIPTION>In 1969 outbred Sprague-Dawley rats were selected for high systolic blood pressure using an indirect plethysmographic technique in pre-warmed unrestrained conscious rats. Three pairs were originally selected, and selection was continued with brother x sister mating. Strain LN was maintained as a normotensive control, and LL as a hypotensive strain. The strain from Rat Resource &amp; Research Center was  maintained at Department of Pharmacology, University of Iowa</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735517</RGD_ID>
    <STRAIN_SYMBOL>LEXF10A/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735517</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of  LEXF10A/Stm now maintained at Medical College of Wisconsin. The parent strain was derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735518</RGD_ID>
    <STRAIN_SYMBOL>HXB4/IpcvMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu &gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu &gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735518</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of  HXB4/Ipcv now maintained at Medical College of Wisconsin. The parent strain was derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735519</RGD_ID>
    <STRAIN_SYMBOL>HXB31/IpcvMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735519</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of HXB31/Ipcv now maintained at Medical College of Wisconsin. The parent strain was derived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735520</RGD_ID>
    <STRAIN_SYMBOL>HXB2/IpcvMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735520</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of  HXB2/Ipcv now maintained at Medical College of Wisconsin. The parent strain was derived from founder strains SHR/OlaIpcv and BN-Lx/Cub.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735521</RGD_ID>
    <STRAIN_SYMBOL>HXB20/IpcvMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu &gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu &gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735521</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of  HXB20/Ipcv now maintained at Medical College of Wisconsin. The parent strain wasDerived from founder strains SHR/OlaIpcv and BN-Lx/Cub</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735530</RGD_ID>
    <STRAIN_SYMBOL>BXH2/CubMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735530</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of  BXH2/Cub now maintained at Medical College of Wisconsin. The parent strain was derived from founder strains BN-Lx/Cub and SHR/OlaIpcv</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735533</RGD_ID>
    <STRAIN_SYMBOL>BXH3/CubMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735533</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of  BXH3/Cub now maintained at Medical College of Wisconsin. The parent strain was derived from founder strains BN-Lx/Cub and SHR/OlaIpcv.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735557</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Pdyn-cre)2-9Koba</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Kazuto Kobayashi  Fukushima Medical University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1332&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2024-01-26)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735557</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting a modified BAC, in which a Cre recombinase was inserted into the third exon of the rat Pdyn gene, into rat zygotes (Iar:Long-Evans, RGD:18337282). This strain is a transgenic rat that expresses Cre recombinase under the control of the Pdyn gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735558</RGD_ID>
    <STRAIN_SYMBOL>F344.LEA-Ugl/Okt</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1333&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1333&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-07-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735558</CITATION_ID>
    <DESCRIPTION>A congenic strain in which the ugl locus of LEA/Tohm rats was introduced into F344/NSlc rats. "This strain is homozygous for the ugl locus, which contains a 13 bp deletion in the Ctns gene.Cystinosis model rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735559</RGD_ID>
    <STRAIN_SYMBOL>F344.LEA-Idao/Okt</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1334&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1334&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-07-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735559</CITATION_ID>
    <DESCRIPTION>A congenic strain in which the Idao locus of LEA/Tohm rats was introduced into F344/NSlc rats. "This strain is homozygous for the Idao locus, which contains a 54.1 kb deletion in the Dao gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735560</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Gad1&lt;sup&gt;em15Yyan&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Gunma University Graduate School of Medicine</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1331&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-07-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gad1&lt;sup&gt;em15Yyan&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>149735561</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="75777260" STOP_POS="75818099" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="55386152" STOP_POS="55386442" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="56861440" STOP_POS="56902139" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="63479963" STOP_POS="63519879" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="52789370" STOP_POS="52830038" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735560</CITATION_ID>
    <DESCRIPTION>Knockout rats carry  a 291 bp deletion, including  exon-6  of  Gad1 gene  using the CRISPR/Cas9. Glutamate decarboxylase (GAD; there are two isoforms, GAD65 and GAD67) is an enzyme that synthesizes the neurotransmitter GABA. In this strain, the Gad1 gene encoding GAD67 was knocked out. In homozygous rats, low body weight at 3 weeks and impaired spatial learning memory were observed. Some homozygous rats die as juveniles. This strain is maintained in heterozygotes.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735562</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Gad2&lt;sup&gt;em24Yyan&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Gunma University Graduate School of Medicine</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1328&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-07-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gad2&lt;sup&gt;em24Yyan&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>149735563</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="89671718" STOP_POS="89734246" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="84763740" STOP_POS="84764054" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="89171576" STOP_POS="89234770" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="90851699" STOP_POS="90914893" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="96259430" STOP_POS="96321857" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735562</CITATION_ID>
    <DESCRIPTION>Knockout rats in which the Gad2 gene was disrupted using the TALEN. In this strain, the Gad2 gene encoding GAD65 was knocked out. In homozygous rats, a high rate of epileptic seizures was observed at 2 to 3 weeks of age.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735570</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Atg16l1&lt;sup&gt;em8Rrrc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>RRRC</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-07-23)</AVAILABILITY>
    <RESEARCH_USE>Inflammatory Bowel Disease, autophagy</RESEARCH_USE>
    <ALLELES>Atg16l1&lt;sup&gt;em8Rrrc&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>149735571</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="9" START_POS="95869839" STOP_POS="95905354" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="9" START_POS="88420737" STOP_POS="88457530" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="9" START_POS="94879876" STOP_POS="94915231" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="9" START_POS="94599174" STOP_POS="94634551" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="9" START_POS="86712122" STOP_POS="86747370" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735570</CITATION_ID>
    <DESCRIPTION>CRISPR-Cas9-mediated knock-in of a single base pair polymorphism of guanine to alanine in exon 10, resulting in a threonine to alanine substitution at amino acid position 299 in the rat. Mimics the same nucleotide substitution for the threonine to alanine substitution at amino acid position 300 in humans (T300A), Homozygosity for this allele is embryonic lethal.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735895</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(Col2a1-luc,-mCherry)RmptRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=942&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=942&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Skeletal Regenerative Medicine</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00942</CITATION_ID>
    <DESCRIPTION>Random insertion of transgene consisting of firefly luciferase-T2A-mCherry driven by regulatory elements of rat Col2a1, for conditional expression in chondrogenic cells. Both reporters are expressed by chondrogenic cells, leading to bioluminescence within regions of active chondrogenesis upon injecting rats with D-luciferin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735896</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(Col2a1-luc,-mCherry)Rmpt</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This transgenic was created by Dr. Ryan Porter at  University of Arkansas for Medical Sciences.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=942&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Skeletal Regenerative Medicine</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735896</CITATION_ID>
    <DESCRIPTION>Random insertion of transgene consisting of firefly luciferase-T2A-mCherry driven by regulatory elements of rat Col2a1, for conditional expression in chondrogenic cells. Both reporters are expressed by chondrogenic cells, leading to bioluminescence within regions of active chondrogenesis upon injecting rats with D-luciferin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735897</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Cacna1a&lt;sup&gt;gry&lt;/sup&gt;&lt;/i&gt;/Okym</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1164 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1164 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-07-29)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735897</CITATION_ID>
    <DESCRIPTION>This strain is derived from GRY/Idr (GRY/Idr has the M251K mutation in the Cacna1a gene) provided from NBRP-Rat. 
GRY/Idr was backcrossed to F344/NSlc.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735898</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Myh7b&lt;sup&gt;em1Blar+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Beijing Laboratory
Animal Research Center of Chinese Academy of
Medical Sciences.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735898</CITATION_ID>
    <DESCRIPTION>This is the homozygous wild type littermate from crossing of heterozygous SD-Myh7b mutants.  The Myh7b knockout SD rats were generated using the CRISPR/Cas9 system targeting exon 2, resulting 7 bases deletion of exon 2 and generated a new termination codon TGA in exon 3. The heterzygous Myh7b+/- rats were crossed to generate littermate controls. The birth ratio of wild type (WT):Myh7b+/-:Myh7b-/- was
approximately 1:2:1, indicating that Myh7b-/- did not cause fetal death.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>149735906</RGD_ID>
    <STRAIN_SYMBOL>RCCHan:WIST</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_149735906</CITATION_ID>
    <DESCRIPTION>Wistar Hannover rats are derived from the Han:WIST strain from the Zentral Institut fur Versuchstierzucht (ZfV) (Hannover, Germany). In 1989, 156 pairs were introduced from ZfV to the Institute for Biomedical Research (IBM) in Switzerland (IBM underwent a structural change [name change] to BRL Ltd. and RCC Ltd.)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150340617</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;rs197197017 -rs198445122&lt;/i&gt;)/Utx</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Texas, Houston, TX</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="155609738" STOP_POS="191324766" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="146197289" STOP_POS="181894275" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="156969388" STOP_POS="198720287" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150340617</CITATION_ID>
    <DESCRIPTION>A congenic strain made by introducing B2 fragment (a segment of chromosome 1, 154.7 Mb - 203 Mb)  from SHR/Utx into SHRSP/BbbUtx.The B2 fragment contains wild-type Stim1 as confirmed by sequencing.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150340629</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Tgfb1&lt;sup&gt;em3Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>SS-&lt;i&gt;Tgfb1&lt;sup&gt;em3Mcwi+&lt;/sup&gt;/Tgfb1&lt;sup&gt;em3Mcwi+&lt;/sup&gt;&lt;/i&gt;</FULL_NAME>
    <ORIGINATION>PhysGen Knockouts</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150340629</CITATION_ID>
    <DESCRIPTION>ZFN mutant founders were backcrossed with SS/JrHsdMcwi to get heterozygous offsprings which were intercrossed to produce homozygous wild type  and heterozygous mutant littermates.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150404267</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Myo15a&lt;sup&gt;ci2&lt;/sup&gt;&lt;/i&gt;/Ztm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Laboratory Animal Science, Hannover Medical School, Hannover, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Myo15a&lt;sup&gt;ci2&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150404269</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="45776907" STOP_POS="45835473" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="45277619" STOP_POS="45335953" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="46840098" STOP_POS="46897362" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="46595676" STOP_POS="46660835" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="46742535" STOP_POS="46798928" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150404267</CITATION_ID>
    <DESCRIPTION>LEW/Ztm-ci2 rat is an animal model for syndromal deafness that arose from a spontaneous mutation. Base substitution (T-&gt;C) in exon 56 of Myo15, leading to an amino acid exchange from leucine (Leu) to proline (Pro) within the carboxy-terminal MyTH4 domain in the proteins' tail region.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429598</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Vwf&lt;sup&gt;em4Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://rgd.mcw.edu/rgdweb/models/allModels.html&gt;Rat Genetic Models&lt;/a&gt;, through Versiti Blood Research Institute</ORIGINATION>
    <SOURCE>&lt;a href=http://rgd.mcw.edu/rgdweb/models/allModels.html&gt;Rat Genetic Models&lt;/a&gt;, through Versiti Blood Research Institute</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Type I von Willebrand Disease</RESEARCH_USE>
    <ALLELES>Vwf&lt;sup&gt;em4Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150429599</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="160042900" STOP_POS="160177757" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="158360152" STOP_POS="158491539" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="158085059" STOP_POS="158219525" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="225098521" STOP_POS="225229257" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="161723415" STOP_POS="161854766" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429598</CITATION_ID>
    <DESCRIPTION>The rat strain was created via CRISPR/Cas9  targeting  the VWF gene in DahlSS/Mcw (SS/JrHsdMcwi ) rat embryos.  The resulting rat strain has a 13bp deletion in the untranslated region of Exon 52 of the VWF gene (g.158491511 - 158491523 on chromosome 4, Assembly: mRatBN7.2)  The 13-bp deletion happens to be in the region where the polyadenylation signal resides (AAUAAA).  The resulting mRNA is not polyadenylated and has trouble with transport from the nucleus to the cytoplasm.  The result is a phenotype that is similar to a Type I von Willebrand Disease, being a partial quantitative deficiency of the circulating VWF protein.  Some mRNA must make it through to translation, because low levels of VWF protein are detectable via ELISA (&lt;10%). Both homozygous pairs and heterozygous pairs were used for breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429601</RGD_ID>
    <STRAIN_SYMBOL>MWF.SHR-(&lt;i&gt;D6Rat1-D6Rat30&lt;/i&gt;)/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Freie Universitdt Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="143944560" STOP_POS="143944780" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="47370564" STOP_POS="137801795" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="49695264" STOP_POS="144745573" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="58374821" STOP_POS="153672040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="48631043" STOP_POS="144152572" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429601</CITATION_ID>
    <DESCRIPTION>The congenic MWF.SHR-(&lt;i&gt;D6Rat1-D6Rat30&lt;/i&gt;)/Rkb  was generated by transfer of different nested SHR/FubRkb segments onto the MWF/FubRkb background. For this procedure, male and female rats of the MWF-6SHR (RGD:1641831) breeding, that were homozygous for all MWF chromosomes except RNO6 and heterozygous for RNO6, were intercrossed. Eight congenics were generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429602</RGD_ID>
    <STRAIN_SYMBOL>MWF.SHR-(&lt;i&gt;D6Rat1-D6Rat106&lt;/i&gt;)/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Freie Universitdt Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="143944560" STOP_POS="143944780" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="65531555" STOP_POS="137801795" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="68781170" STOP_POS="144745573" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="78348236" STOP_POS="153672040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="68036028" STOP_POS="144152572" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429602</CITATION_ID>
    <DESCRIPTION>The congenic MWF.SHR-(&lt;i&gt;D6Rat1-D6Rat106&lt;/i&gt;)/Rkb  was generated by transfer of different nested SHR/FubRkb segments onto the MWF/FubRkb background. For this procedure, male and female rats of the MWF-6SHR (RGD:1641831) breeding, that were homozygous for all MWF chromosomes except RNO6 and heterozygous for RNO6, were intercrossed. Eight congenics were generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429603</RGD_ID>
    <STRAIN_SYMBOL>MWF.SHR-(&lt;i&gt;D6Rat1-D6Mit8&lt;/i&gt;)/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Freie Universitdt Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="99437079" STOP_POS="143944780" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="93701310" STOP_POS="137801795" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="97949772" STOP_POS="144745573" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="107370981" STOP_POS="153672040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="97561873" STOP_POS="144152572" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429603</CITATION_ID>
    <DESCRIPTION>The congenic MWF.SHR-(&lt;i&gt;D6Rat1-D6Mit8&lt;/i&gt;)/Rkb  was generated by transfer of different nested SHR/FubRkb segments onto the MWF/FubRkb background. For this procedure, male and female rats of the MWF-6SHR (RGD:1641831) breeding, that were homozygous for all MWF chromosomes except RNO6 and heterozygous for RNO6, were intercrossed. Eight congenics were generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429604</RGD_ID>
    <STRAIN_SYMBOL>MWF.SHR-(&lt;i&gt;D6Rat1-D6Rat121&lt;/i&gt;)/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Freie Universitdt Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="143944560" STOP_POS="143944780" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="95760211" STOP_POS="137801795" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="100120078" STOP_POS="144745573" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="109506414" STOP_POS="153672040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="99651951" STOP_POS="144152572" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429604</CITATION_ID>
    <DESCRIPTION>The congenic MWF.SHR-(&lt;i&gt;D6Rat1-D6Rat121&lt;/i&gt;)/Rkb  was generated by transfer of different nested SHR/FubRkb segments onto the MWF/FubRkb background. For this procedure, male and female rats of the MWF-6SHR (RGD:1641831) breeding, that were homozygous for all MWF chromosomes except RNO6 and heterozygous for RNO6, were intercrossed. Eight congenics were generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429605</RGD_ID>
    <STRAIN_SYMBOL>MWF.SHR-(&lt;i&gt;D6Rat1-D6Mgh4&lt;/i&gt;)/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Freie Universitdt Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="143944560" STOP_POS="143944780" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="104085867" STOP_POS="137801795" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="108154445" STOP_POS="144745573" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="117391806" STOP_POS="153672040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="108503674" STOP_POS="144152572" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429605</CITATION_ID>
    <DESCRIPTION>The congenic MWF.SHR-(&lt;i&gt;D6Rat1-D6Mgh4&lt;/i&gt;)/Rkb  was generated by transfer of different nested SHR/FubRkb segments onto the MWF/FubRkb background. For this procedure, male and female rats of the MWF-6SHR (RGD:1641831) breeding, that were homozygous for all MWF chromosomes except RNO6 and heterozygous for RNO6, were intercrossed. Eight congenics were generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429606</RGD_ID>
    <STRAIN_SYMBOL>MWF.SHR-(&lt;i&gt;D6Rat1-D6Rat81&lt;/i&gt;)/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Freie Universitdt Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="113082045" STOP_POS="143944780" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="107351142" STOP_POS="137801795" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="111715478" STOP_POS="144745573" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="120994890" STOP_POS="153672040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="111967597" STOP_POS="144152572" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429606</CITATION_ID>
    <DESCRIPTION>The congenic MWF.SHR-(&lt;i&gt;D6Rat1-D6Rat81&lt;/i&gt;)/Rkb  was generated by transfer of different nested SHR/FubRkb segments onto the MWF/FubRkb background. For this procedure, male and female rats of the MWF-6SHR (RGD:1641831) breeding, that were homozygous for all MWF chromosomes except RNO6 and heterozygous for RNO6, were intercrossed. Eight congenics were generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429607</RGD_ID>
    <STRAIN_SYMBOL>MWF.SHR-(&lt;i&gt;D6Rat1-D6Rat115&lt;/i&gt;)/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Freie Universitdt Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="117568674" STOP_POS="143944780" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="111837996" STOP_POS="137801795" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="116576030" STOP_POS="144745573" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="125802476" STOP_POS="153672040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="116550201" STOP_POS="144152572" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429607</CITATION_ID>
    <DESCRIPTION>The congenic MWF.SHR-(&lt;i&gt;D6Rat1-D6Rat115&lt;/i&gt;)/Rkb  was generated by transfer of different nested SHR/FubRkb segments onto the MWF/FubRkb background. For this procedure, male and female rats of the MWF-6SHR (RGD:1641831) breeding, that were homozygous for all MWF chromosomes except RNO6 and heterozygous for RNO6, were intercrossed. Eight congenics were generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429608</RGD_ID>
    <STRAIN_SYMBOL>MWF.SHR-(&lt;i&gt;D6Rat1-D6Rat184&lt;/i&gt;)/Rkb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Freie Universitdt Berlin, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="122236101" STOP_POS="143944780" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="116506292" STOP_POS="137801795" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="121224054" STOP_POS="144745573" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="130448688" STOP_POS="153672040" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="121381065" STOP_POS="144152572" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429608</CITATION_ID>
    <DESCRIPTION>The congenic MWF.SHR-(&lt;i&gt;D6Rat1-D6Rat184&lt;/i&gt;)/Rkb  was generated by transfer of different nested SHR/FubRkb segments onto the MWF/FubRkb background. For this procedure, male and female rats of the MWF-6SHR (RGD:1641831) breeding, that were homozygous for all MWF chromosomes except RNO6 and heterozygous for RNO6, were intercrossed. Eight congenics were generated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429614</RGD_ID>
    <STRAIN_SYMBOL>FHH-Tg(CAG-Add3)McwiRoman</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pharmacology and Toxicology, University of Mississippi Medical Center, Jackson, Mississippi</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Add3</ALLELES>
    <ALLELE_RGD_IDS>2043</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429614</CITATION_ID>
    <DESCRIPTION>A full-length rat wild type Add3 cDNA obtained from an expression plasmid pCMV6-entry-Add3 purchased from Origene (Rockville, MD) was inserted in a sleeping beauty transposon vector. The expression of wild type ADD3 in the transposon vector was driven
by a CAG promoter. The construct was injected into the pronucleus ofoocytes collected from female FHH/EurMcwi rats along with SB100 transposase mRNA. A single-transgene insertion was identified on chromosome 10, which is located .64 kbp away from the protein shisa-6 homolog precursor at its 59 end and .360 kbp away from the phosphoinositide-interacting protein at the 3 prime end. Heterozygous founders were intercrossed to derive a homozygous transgenic line that was used for studies.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429615</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Add3&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;/ Roman</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pharmacology and Toxicology, University of Mississippi Medical Center, Jackson, Mississippi</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2021-09-09)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Add3&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150429617</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="262152722" STOP_POS="262260504" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="252147341" STOP_POS="252255126" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="273854195" STOP_POS="273961982" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="281267424" STOP_POS="281375203" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="259347673" STOP_POS="259455407" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429615</CITATION_ID>
    <DESCRIPTION>ZFN system was used to Knock out the rat Add3 gene of Crl:SD rat embryos.The ZFN mRNA was injected into the pronucleus of fertilized SpragueDawley embryos and transferred to the oviduct of pseudopregnant females. PCR genotyping  of tail biopsies confirmed a 14-bp deletion using  forward primer 5'-GCCCCCATGAGTCACTACAC-3' and reverse primer 5'-GCTACAGGAAGCATCTCCTGTG-3'. Founders with Add3 deletion were backcrossed to the parental strain to generate heterozygous F1 rats. Heterozygous F1 siblings were then intercrossed to derive a homozygous KO line used</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429618</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Add3&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt; /Roman</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pharmacology and Toxicology, University of Mississippi Medical Center, Jackson, Mississippi</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Add3&lt;sup&gt;em2Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150429619</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="262152722" STOP_POS="262260504" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="252147341" STOP_POS="252255126" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="273854195" STOP_POS="273961982" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="281267424" STOP_POS="281375203" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="259347673" STOP_POS="259455407" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429618</CITATION_ID>
    <DESCRIPTION>ZFN system was used to Knock out the rat Add3 gene of  FHH-Chr 1BN/Mcwi rat embryos.The ZFN mRNA was
injected into the pronucleus of fertilized FHH-Chr 1BN/Mcwi embryos and transferred to the oviduct of pseudopregnant
females. PCR genotyping  of tail biopsies confirmed a 68-bp deletion using  forward primer 5'-GCCCCCATGAGTCACTACAC-3' and reverse primer 5'-GCTACAGGAAGCATCTCCTGTG-3'. Founders with Add3 deletion were backcrossed to the parental strain
to generate heterozygous F1 rats. Heterozygous F1 siblings were then intercrossed to derive a homozygous KO line used</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429634</RGD_ID>
    <STRAIN_SYMBOL>F344 -&lt;i&gt;Aspa&lt;sup&gt;em34Kyo&lt;/sup&gt;  Hcn1&lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Laboratory Animals, Graduate School of Medicine, Kyoto University, Yoshidakonoe-cho, Sakyo-ku, Kyoto
606-8501, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Aspa&lt;sup&gt;em34Kyo&lt;/sup&gt;|Hcn1&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11564348|150429632</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="51531189" STOP_POS="51531195" METHOD="8"/>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="58433303" STOP_POS="58433318" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="57934804" STOP_POS="57934819" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="49798369" STOP_POS="49798375" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="50399472" STOP_POS="50399478" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="59882494" STOP_POS="59882509" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="59578788" STOP_POS="59627450" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="68473431" STOP_POS="68874494" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="49525949" STOP_POS="49939066" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="60178509" STOP_POS="60199207" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429634</CITATION_ID>
    <DESCRIPTION>F344-Aspaem34Kyo (RGD:11564349) and F344-Hcn1em1Kyo (RGD:38676253) rats
from the National BioResource Project-Rat
were intercrossed to produce F1 hybrids and then to obtain F2 progeny.
Rats homozygous for both Aspa and Hcn1 knockout
alleles were selected from among F2 progeny and were
used to generate the F344-Aspaem34Kyo/Hcn1em1Kyo double-
knockout strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429707</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cyp2c11&lt;sup&gt;em1Nju&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp2c11&lt;sup&gt;em1Nju&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150429708</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="246175216" STOP_POS="246211445" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="236762719" STOP_POS="236799069" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="257676172" STOP_POS="258004428" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="265418158" STOP_POS="265454574" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="243281320" STOP_POS="243320945" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429707</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system containing two pairs of single guide RNA
(sgRNA) primers: sgRNA1 (forward primer: 59-GCTACTG-
TAACTGACATGTT-39; reverse primer: 59-AACATGTCAGTTACAGTAGC-
39) and sgRNA2 (forward primer: 59-TCAAGGGTAAACTCAGACTG-39;
reverse primer: 59-CAGTCTGAGTTTACCCTTGA-39), was injected to Sprague-Dawley rat one-cell embryos. The F0 pups were screened by genomic DNA sequencing to identify heterozygous CYP2C11+/2 founders.This mutant strain carries a two base pairs (GT) 
insertion  into exon 6 of CYP2C11 and resulting  in the knockout allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429760</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;rs198233821-rs198932221&lt;/i&gt;)/Utx</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Texas, Houston, TX</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="137337812" STOP_POS="144493456" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="131516676" STOP_POS="138350465" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="137021260" STOP_POS="145293041" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429760</CITATION_ID>
    <DESCRIPTION>A congenic strain made by introducing  IgH haplotype block (a segment of chr6:146,030,387 to 154,214,590 ,Rn5 assembly of the rat genome).  from SHR-B2 (SHR/Utx) into SHR-A3 (SHRSP/BbbUtx). The igH block contains  sequences that are highly divergent between of SHR-A3   and SHR-B2 .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429814</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gnal&lt;sup&gt;em1Hpng+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Huu Phuc Nguyen,	Institute of Medical Genetics and Applied Genomics, University of Tuebingen;  Core Facility Transgenic Animals, University Clinics Tuebingen, Tuebingen, Germany</ORIGINATION>
    <SOURCE>&lt;a href=https://www.infrafrontier.eu/emma/strain-details/?q=14800&gt;European Mouse Mutant Archive(EMMA)&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-09-04)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gnal&lt;sup&gt;em1Hpng&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>150429816</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="62892257" STOP_POS="63032510" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="60622311" STOP_POS="60762599" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="62805406" STOP_POS="62946133" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="61991738" STOP_POS="62131420" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="63595606" STOP_POS="63735803" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429814</CITATION_ID>
    <DESCRIPTION>The heterozygousGnal mutant rats were created by CRISPR/Cas9. Guide RNA sequences targeting the first exon of the rat Gnal gene isoform 2 were designed.  The mutated allele contained  a 13- bp  deletion  in exon1 that corresponded to
position 34 to 46 downstream of the translation start point ATG of the
Gnal splicing variant 2 was detected resulting in an early stop at position
150 and producing a truncated protein with 50 amino acids .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429815</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gnal&lt;sup&gt;em1Hpng+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Core Facility Transgenic Animals, University Clinics Tuebingen, Tuebingen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429815</CITATION_ID>
    <DESCRIPTION>The homozygous wild type  Gnal rats were littermates of  SD-Gnalem1Hpng+/- (RGD:150429814) created by CRISPR/Cas9. The heterozygous mutants carried one copy of  mutated allele contained  a 13- bp  deletion  in exon1 that corresponded to position 34 to 46 downstream of the translation start point ATG of theGnal splicing variant 2 was detected resulting in an early stop at position150 and producing a truncated protein with 50 amino acids .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429817</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gnal&lt;sup&gt;em1Hpng-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Core Facility Transgenic Animals, University Clinics Tuebingen, Tuebingen, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gnal&lt;sup&gt;em1Hpng&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>150429816</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="62892257" STOP_POS="63032510" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="60622311" STOP_POS="60762599" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="62805406" STOP_POS="62946133" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="61991738" STOP_POS="62131420" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="63595606" STOP_POS="63735803" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429817</CITATION_ID>
    <DESCRIPTION>Thehomozygous Gnal mutant rats were created by CRISPR/Cas9. Guide RNA sequences targeting the first exon of the rat Gnal gene isoform 2 were designed.  The mutated allele contained  a 13- bp  deletion  in exon1 that corresponded to
position 34 to 46 downstream of the translation start point ATG of the
Gnal splicing variant 2 was detected resulting in an early stop at position
150 and producing a truncated protein with 50 amino acids. Only 5% of homozygous Gnal knockout mice could survive till maturity</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429818</RGD_ID>
    <STRAIN_SYMBOL>BN/HsdMcwiRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=562&gt;Rat Resource &amp; Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=562&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2021-09-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00562</CITATION_ID>
    <DESCRIPTION>Inbred from a single pair of SsN line rats obtained from Harlan Sprague Dawley (Alabama colony). Maintained at the Medical College of Wisconsin since 1995. To confirm homozygosity, the strain was tested with 200 microsatellite markers (genome-wide scan at 20cM) all of which were homozygous for all regions tested (Cowley et al. 2000, Physiol. Genomics. 2:107-115). This strain was maintained at RRRC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429825</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Scn9a*&lt;sup&gt;tm1Amgn&lt;/sup&gt;&lt;/i&gt;/Crl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This Sprague Dawley (SD) rat model was designed by Amgen, adapted and executed by SAGE Labs, Sigma-Aldrich.</ORIGINATION>
    <SOURCE>Charles River Laboratories</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Scn9a*&lt;sup&gt;tm1Amgn&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150429827</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="71553185" STOP_POS="71701377" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="51145148" STOP_POS="51293342" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="52583953" STOP_POS="52664209" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="59207264" STOP_POS="59286961" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="48438725" STOP_POS="48518893" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429825</CITATION_ID>
    <DESCRIPTION>Exon 25 of the rat Scn9a gene was replaced with the human SCN9A exon counterpart (exon 26) using ZFN technology. The mRNAs of the active ZFN pair targets middle region of the exon (CACCATCATGGTTCTTATAtgcctcAACATGGTAA CCATGATG, ZFN binding sites in uppercase).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429828</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Tspo&lt;sup&gt;em1Vpl&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>McGill University and Genome Quebec Innovation Centre (Montreal, Canada)</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tspo&lt;sup&gt;em1Vpl&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150429831</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="116600214" STOP_POS="116610461" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="114720188" STOP_POS="114730450" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="124460358" STOP_POS="124470610" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="124449361" STOP_POS="124459090" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="121597084" STOP_POS="121599342" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429828</CITATION_ID>
    <DESCRIPTION>Tspo-targeted genome editing in Sprague Dawley  rats embryos  by microinjecting
 with optimized and customized ZFNs designed for targeted gene KO. Locus-specific PCR was performed to identify Rat5  founders using
the following primer pairs: CKOZFN-F: 50-AGAGCATACTCTTGCCGTCG-30 and CKOZFN-R:50-ACTCCTAAAGGGGTTGCAGG-30; Normal PCRs generated 362 bp for the WT and
273 bp for the mutant,(89 bp deletion).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429830</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Tspo&lt;sup&gt;em2Vpl&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>McGill University and Genome Quebec Innovation Centre (Montreal, Canada)</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tspo&lt;sup&gt;em2Vpl&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150429832</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="116600214" STOP_POS="116610461" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="114720188" STOP_POS="114730450" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="124460358" STOP_POS="124470610" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="124449361" STOP_POS="124459090" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="121597084" STOP_POS="121599342" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429830</CITATION_ID>
    <DESCRIPTION>Tspo-targeted genome editing in Sprague Dawley rats embryos by microinjecting with optimized and customized ZFNs designed for targeted gene KO. Locus-specific PCR was performed to identify Rat7  founders using the following primer pairs: COMPOZr-1kbF: 50-CCTGGATATGCTGTGTCCCC-30 and COMPOZr-1kbR: 50-TGATGGGTCATTTGTGCCCT-30. Normal PCRs generated 818 bp for WT and 652 bp for the mutant (166 bp deletion).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429960</RGD_ID>
    <STRAIN_SYMBOL>WIC-&lt;i&gt;Wwox&lt;sup&gt;lde&lt;/sup&gt;&lt;/i&gt;/Fta</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory of Veterinary Physiology, Nippon Veterinary and Life Science University, Tokyo</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Wwox&lt;sup&gt;lde&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150429961</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="59338402" STOP_POS="60269323" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="42432141" STOP_POS="43360278" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="46761353" STOP_POS="47695247" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="57582172" STOP_POS="58503008" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="44516391" STOP_POS="44829849" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429960</CITATION_ID>
    <DESCRIPTION>Established from a closed colony of Wistar-Imamichi (WIC) rats as a spontaneous mutant exhibiting severe dwarfism, short lifespan (early postnatal lethality), and high incidence of epileptic seizures. Mutant rats showed growth retardation after 3 d of age, and at 21 d their weight was about 56% that of normal rats. Sequencing of the full-length Wwox transcript identified a 13-bp deletion in exon 9 in lde/lde rats. This mutation causes a frame shift, resulting in aberrant amino acid sequences at the C-terminal.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429963</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Pmch&lt;sup&gt;m1Hubr&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hubrecht Laboratory, Centre for Biomedical Genetics, 3584 CT Utrecht, The Netherlands. Hera Biolabs, Taconic.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pmch&lt;sup&gt;m1Hubr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150429964</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="24399404" STOP_POS="24400720" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="22511934" STOP_POS="22513250" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="28655206" STOP_POS="28656522" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="28764993" STOP_POS="28766309" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="24778133" STOP_POS="24779449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429963</CITATION_ID>
    <DESCRIPTION>The Pmch mutant rat line was generated by target-selected ENU-driven mutagenesis, and high-throughput resequencing of genomic target sequences in progeny from mutagenized rats (Wistar/Crl background) revealed an ENU-induced premature stop codon in exon 1(K50X) of Pmch in a rat. The heterozygous mutant rat was backcrossed to wild-type Wistar background for six generations to eliminate confounding effects from background mutations induced by ENU.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429965</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Apoa4&lt;sup&gt;em1Bcgen&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Beijing Biocytogen Co., Ltd. (Beijing, China).</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Apoa4&lt;sup&gt;em1Bcgen&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150429966</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="55436268" STOP_POS="55436275" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="46539572" STOP_POS="46539579" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="50537472" STOP_POS="50537479" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="49163055" STOP_POS="49165333" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="49233142" STOP_POS="49233431" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429965</CITATION_ID>
    <DESCRIPTION>TALEN system targeting the rat Apoa4 gene was injected to Sprague Dawley embryos. An 8 bp deletion was induced within the coding region of Apoa4 gene, which results in a frameshift and gene knockout. The genotypes were confirmed by PCR analysis followed by Sanger sequencing and agarose electrophoresis (PCR forward primer: 5&amp;#8242;-TATCCCAACTCCAACATCATCCA-3&amp;#8242;, reverse primer: 5&amp;#8242;-TCGCAGTCTGATCCCACTTACTT-3&amp;#8242;). The knockout allele generated a band at 237&amp;#8201;bp, while the wild-type allele was at 245&amp;#8201;bp.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150429988</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(EEF1A1-Wars2)Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Wars2</ALLELES>
    <ALLELE_RGD_IDS>1593417</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150429988</CITATION_ID>
    <DESCRIPTION>This strain was derived by microinjecting fertilized eggs with a mix of the Sleeping Beauty construct containing BN Wars2 cDNA under control of the universal EF-1Î± (human EEF1A1) promoter and mRNA of the SB100X transposase (Ivics et al. 2014). Transgenic rats were detected using PCR with the following primers: Wars2-F 5'-TGT GCT ACA AGT CCA CAC AC-3' and Wars2-R 5'-GCA GAA GGG TCA CGA AGA GA-3'.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150517549</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D2Rat46- D2Mco48&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="170857550" STOP_POS="170857716" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="168559501" STOP_POS="168559667" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="182194909" STOP_POS="182195074" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="201609408" STOP_POS="201609573" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="34115408" STOP_POS="34116469" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="174932771" STOP_POS="190428097" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="29853888" STOP_POS="29855558" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150517549</CITATION_ID>
    <DESCRIPTION>This SS congenic carries the chromosomal fragment from  the spontaneously hypertensive rat (SHR). Recombinant  Progeny  Testing  (RPT)  was  used  to  fine-map  the  proteinuria  locus.  The congenic was developed from the recombinant families by fixing the transferred genomic interval (D2Rat46- D2Mco48) in the homozygous SHR/SHR state</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150517550</RGD_ID>
    <STRAIN_SYMBOL>SS.SHR-(&lt;i&gt;D2Rat127- D2Rat230&lt;/i&gt;)/Mco</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Toledo Toledo, Ohio</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="176357002" STOP_POS="176357179" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="204650681" STOP_POS="204650836" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="177914620" STOP_POS="177914774" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150517550</CITATION_ID>
    <DESCRIPTION>This SS congenic carries the chromosomal fragment from  the spontaneously hypertensive rat (SHR). Recombinant  Progeny  Testing  (RPT)  was  used  to  fine-map  the  proteinuria  locus.  The congenic was developed from the recombinant families by fixing the transferred genomic interval (D2Rat127- D2Rat230) in the homozygous SHR/SHR state</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150519895</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gfap&lt;sup&gt;em1Mes+/-&lt;/sup&gt;&lt;/i&gt; /Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=932&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=932&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gfap&lt;sup&gt;em1Mes&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150519905</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="88352987" STOP_POS="88361661" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="87852891" STOP_POS="87861631" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="90990762" STOP_POS="90999435" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="90763150" STOP_POS="90771823" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="92059881" STOP_POS="92068555" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00932</CITATION_ID>
    <DESCRIPTION>The targeted mutation in the rat GFAP gene was based on the severity and frequency of the R239H mutation in human disease. The CRISPR/Cas9 system was used to mediated knockin of point mutation (R237H) to Sprague-Dawley embryos. The current background srain is Crl:CD (SD). This mutant strain serves as a model for Alexander disease. knockins have post-weaning failure to thrive and ~10% mortality by 12 weeks, but afterwards are viable and can breed .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150519896</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gfap&lt;sup&gt;em2Mes&lt;/sup&gt;&lt;/i&gt; /Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=931&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=931&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gfap&lt;sup&gt;em2Mes&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150519906</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="88352987" STOP_POS="88361661" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="87852891" STOP_POS="87861631" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="90990762" STOP_POS="90999435" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="90763150" STOP_POS="90771823" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="92059881" STOP_POS="92068555" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00931</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 mediated single nucleotide deletion resulting in a frameshift  that creates a premature stop and generates a null allele. This strain serves as a model for Alexander disease - nulls are of interest for traumatic brain injury and many other studies of CNS disease and astrocyte response.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150519899</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Prkar1b&lt;sup&gt;em1Tua&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Animal Science
Faculty of Agriculture
Tokyo University of Agriculture
1737 Funako
Atsugi
Kanagawa
243-0034
Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prkar1b&lt;sup&gt;em1Tua&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150519902</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="20606066" STOP_POS="20738766" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="15492233" STOP_POS="15624942" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="17614536" STOP_POS="17713567" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="19611694" STOP_POS="19708682" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="16025867" STOP_POS="16131129" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150519899</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system containing guide RNAs targeting exon 2 and intron 2  were introduced into the F344/Stm embryos using a super electroporator NEPA 2. This mutant strain F344-&lt;i&gt;Prkar1b&lt;sup&gt;em1Tua&lt;/sup&gt;&lt;/i&gt; carried  a 2-bp frameshift insertion in exon2 creating a premature stop codon in the Prkar1b transcripts. Expression levels of Prkar1b transcripts and protein are significantly decreased in the mutants.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150519901</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Prkar1b&lt;sup&gt;em2Tua&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Animal Science
Faculty of Agriculture
Tokyo University of Agriculture
1737 Funako
Atsugi
Kanagawa
243-0034
Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Prkar1b&lt;sup&gt;em2Tua&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150519903</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="20606066" STOP_POS="20738766" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="15492233" STOP_POS="15624942" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="17614536" STOP_POS="17713567" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="19611694" STOP_POS="19708682" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="16025867" STOP_POS="16131129" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150519901</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system containing guide RNAs targeting exon 2 and intron 2  were introduced into the F344/Stm embryos using a super electroporator NEPA 2. This mutant strain F344-&lt;i&gt;Prkar1b&lt;sup&gt;em2Tua&lt;/sup&gt;&lt;/i&gt; carried  a 13-bp frameshift deletion in exon2 creating a premature stop codon in the Prkar1b transcripts. Expression levels of Prkar1b transcripts and protein are significantly decreased in the mutants.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520049</RGD_ID>
    <STRAIN_SYMBOL>WBN-&lt;i&gt;Ht&lt;/i&gt;/Kob</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520049</CITATION_ID>
    <DESCRIPTION>The hairless rat was orginially found in JCL:Wistar rats at Ishikawa Laboratory Animal company, Saitama, Japan. Thereafter, hairless rats were backcrossed with WBN rats for 8 generations and the congenic strain of hairless rats has been established with a background of WBN at the company.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520052</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Mlycd&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>Please contact: mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520052</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Mlycd gene of SS/JrHsdMcwi rat embryos. This resulted in a global knock-out of the rat  Mlycd gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520162</RGD_ID>
    <STRAIN_SYMBOL>Kwl:Wistar</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href="https://kwl-a.co.jp/rat/"&gt;Kiwa Laboratory Animals Co., Ltd. Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href="https://kwl-a.co.jp/rat/"&gt;Kiwa Laboratory Animals Co., Ltd. Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520162</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>150520182</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;ROSA26&lt;sup&gt;em1(CAG-tdTomato)Rrrc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=938&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=938&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2023-08-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00938 </CITATION_ID>
    <DESCRIPTION>The DNA construct was made by replacing ZsGreen with TdTomato in plasmid pCAG-loxP-STOP-loxP-ZsGreen (Addgene plasmid #51269, donated by Pawel Pelczar). CRISPR/Cas9 genome editing technology was used to knock in the DNA construct into the rat ROSA26 locus in the embryos from outbred BluHsd:LE. Reporter line that can be crossed with Cre-expressing strains. In presence of Cre, the floxed "STOP" upstream of the TdTomato gene is deleted allowing expression of the red fluorescent TdTomato protein. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520183</RGD_ID>
    <STRAIN_SYMBOL>BDIX.BDIV-&lt;i&gt;Mss1c/ZteRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=904&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=904&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00904</CITATION_ID>
    <DESCRIPTION>strain haboring on a BDIX background a 22,3 MB BDIV Fragment called Mss1c which covers part of the Mss1 fragment. Homozygous rats of both sexes display resistence towards ENU-induced development of PNS tumors in terms of survival time and incidence.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520185</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ldlr&lt;sup&gt;em1Dlli&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ldlr&lt;sup&gt;em1Dlli&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150520193</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="28546191" STOP_POS="28569075" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="20270020" STOP_POS="20292981" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="22750425" STOP_POS="22773305" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="22804325" STOP_POS="22827199" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="20824040" STOP_POS="20846920" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520185</CITATION_ID>
    <DESCRIPTION>Zygotes of SD rats were microinjected with CRISPR/Cas9 system  targeting Ldlr . This mutant possesses a 118-bp deletion from No.22759599bp to 22759716bp in the Ldlr gene (NC_005107.4), resulting in a termination codon TAG, and deletion
of 768 amino acids of Ldlr.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520186</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Apoe&lt;sup&gt;em1Dlli&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shanghai Key Laboratory of Regulatory Biology East China Normal University, Shanghai, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520186</CITATION_ID>
    <DESCRIPTION>carried a 130 bp deletion from No.80613571bp to 80613700bp in Apoe gene (NC_005100.4), resulting in a termination codon TAA, and deletion of 231 amino acids of ApoE.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520187</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Apoe&lt;sup&gt;em1Dlli&lt;/sup&gt;Ldlr&lt;sup&gt;em1Ldlr&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520187</CITATION_ID>
    <DESCRIPTION>This  Apoe/Ldlr double knock-out  (DKO) was derived from cross-breeding of SD-Apoeem1Dlli (RGD:150520186) and SD-Ldlrem1Dlli (150520185).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520189</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Apoe&lt;sup&gt;em1Ejt&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Purdue Center for Cancer Research, 201 South University Street, Purdue University, West 
Lafayette, Indiana, 47907, United States</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Apoe&lt;sup&gt;em1Ejt&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150520190</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="88482390" STOP_POS="88482405" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="79354425" STOP_POS="79354440" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="80613395" STOP_POS="80613410" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="81878372" STOP_POS="81882298" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="79003634" STOP_POS="79006387" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520189</CITATION_ID>
    <DESCRIPTION>The  mutant rat strain was produced by injecting TALEN  system  targeting the exon 4 of rat Apoe into Sprague Dawley (Hsd:SD) embryos. This mutant rat has a 16-bp deletion in the gene third coding exon) located on chromosome 1; frameshift mutation resulted (p.Glu178fs)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520204</RGD_ID>
    <STRAIN_SYMBOL>SHR/OlaIpcv-mt&lt;sup&gt;LEW/Ipcv&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>conplastic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520204</CITATION_ID>
    <DESCRIPTION>Mitochodrial genome of SHR/OlaIpcv was selectively replaced by LEW/Ipcv to create this conplastic strain using the supersonic breeding strategy; these have the mitochondrial genome of LEW/Ipcv on SHR/OlaIpcv nuclear genetic background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520205</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Gja8&lt;/i&gt;&lt;sup&gt;m1+/-Cub&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Biology, Charles University in Prague, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gja8&lt;sup&gt;m1Cub&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12791992</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="187179668" STOP_POS="187181284" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="184492360" STOP_POS="184492360" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="199052374" STOP_POS="199052374" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="218536831" STOP_POS="218538447" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520205</CITATION_ID>
    <DESCRIPTION>This strain is derived from SHR/OlaIpcv where a spontaneous mutation was observed in the NH&lt;sub&gt;2&lt;/sub&gt;-terminal cytosolic domain of Cx50, L7Q. The connexin50 mutation in heterozygous state affects significantly the lipid profile and the oxidative stress parameters in SHR rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520206</RGD_ID>
    <STRAIN_SYMBOL>SHR-Tg(EEF1A1-Folr1 )Ipcv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520206</CITATION_ID>
    <DESCRIPTION>Generated by microinjecting SHR/OlaIpcv zygotes with wild type Folr1 cDNA  from BN-Lx/Cub under control of EF-1Î± (human EEF1A1)  universal promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520207</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;ROSA26&lt;sup&gt;em1(AttP)Davis&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Rat Resource and Research Center (RRRC)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2021-11-05)</AVAILABILITY>
    <RESEARCH_USE>Tool rat for creating other trasngenic rat models</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00939</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to introduce 2 AttP landing sites in the ROSA26 locus of F344/NHsd rat embryos. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520208</RGD_ID>
    <STRAIN_SYMBOL>ACI-&lt;i&gt;Pvt1&lt;sup&gt;em1Shul&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shull Lab, Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-11-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520208</CITATION_ID>
    <DESCRIPTION>Using CRISPR/Cas9, exon 1b of the Pvt1 gene was excised from the ACI/SegHsd genome in a 1165bp deletion.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520209</RGD_ID>
    <STRAIN_SYMBOL>ACI-&lt;i&gt;Pvt1&lt;sup&gt;em1Shul&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shull Lab, Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison. </ORIGINATION>
    <SOURCE>This strain is now maintained at Rat Resource and Research Center.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520209</CITATION_ID>
    <DESCRIPTION>The ACI-&lt;i&gt;Pvt1&lt;sup&gt;em1Shul&lt;/sup&gt;&lt;/i&gt; was created using CRISPR/Cas9 by Shull laboratory at UW madison. The  exon 1b of the Pvt1 gene was excised from the ACI/SegHsd genome in a 1165bp deletion.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520210</RGD_ID>
    <STRAIN_SYMBOL>ACI-&lt;i&gt;Pvt1&lt;sup&gt;em2Shul&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shull Lab, Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-11-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520210</CITATION_ID>
    <DESCRIPTION>Using CRISPR/Cas9, a 568bp region of the Pvt1 gene was deleted from the ACI genome including all of exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520211</RGD_ID>
    <STRAIN_SYMBOL>ACI-&lt;i&gt;Pvt1&lt;sup&gt;em2Shul&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The strain was created at Shull Lab, Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison. </ORIGINATION>
    <SOURCE>This strain is maintained at Rat Resource and Research Center.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2021-11-09)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520211</CITATION_ID>
    <DESCRIPTION>Using CRISPR/Cas9, a 568bp region of the Pvt1 gene was deleted from the ACI genome including all of exon 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520212</RGD_ID>
    <STRAIN_SYMBOL>ACI-&lt;i&gt;Pvt1&lt;sup&gt;em3Shul&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shull Lab, Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-11-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520212</CITATION_ID>
    <DESCRIPTION>using CRISPR/Cas9, exon 8 of the pvt1 gene was deleted from the ACI genome. Resulting in a total excision of 588bp.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520213</RGD_ID>
    <STRAIN_SYMBOL>ACI-&lt;i&gt;Pvt1&lt;sup&gt;em3Shul&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The strain was created at Shull Lab, Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison. </ORIGINATION>
    <SOURCE>This strain is maintained at Rat Resource and Research Center.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-11-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520213</CITATION_ID>
    <DESCRIPTION>using CRISPR/Cas9, exon 8 of the pvt1 gene was deleted from the ACI genome. Resulting in a total excision of 588bp.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520214</RGD_ID>
    <STRAIN_SYMBOL>ACI-&lt;i&gt;Pvt1&lt;sup&gt;em4Shul&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shull Lab, Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-11-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520214</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 was used to delete miR1208 in a 763bp excision in ACI rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520215</RGD_ID>
    <STRAIN_SYMBOL>ACI-&lt;i&gt;Pvt1&lt;sup&gt;em4Shul&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The strain was created at Shull Lab, Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison. </ORIGINATION>
    <SOURCE>This strain is maintained at Rat Resource and Research Center.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520215</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 was used to delete miR1208 in a 763bp excision in ACI rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520216</RGD_ID>
    <STRAIN_SYMBOL>ACI-&lt;i&gt;Pvt1&lt;sup&gt;em5Shul&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shull Lab, Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-11-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520216</CITATION_ID>
    <DESCRIPTION>Using CRISPR/Cas9, a suspected enhancer of miR1208 was deleted in a 8315bp excision in ACI rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520217</RGD_ID>
    <STRAIN_SYMBOL>ACI-&lt;i&gt;Pvt1&lt;sup&gt;em5Shul&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The strain was created at Shull Lab, Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison. </ORIGINATION>
    <SOURCE>This strain is maintained at Rat Resource and Research Center.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520217</CITATION_ID>
    <DESCRIPTION>Using CRISPR/Cas9, a suspected enhancer of miR1208 was deleted in a 8315bp excision in ACI rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520220</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ccdc39&lt;sup&gt;em1Jgn&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Cincinnati Children's Hospital Medical Center, Cincinnati, OH</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ccdc39&lt;sup&gt;em1Jgn&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150521525</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="118593881" STOP_POS="118631584" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="116665651" STOP_POS="116703354" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="120278605" STOP_POS="120367829" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="139933049" STOP_POS="139971476" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="120117112" STOP_POS="120154958" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520220</CITATION_ID>
    <DESCRIPTION>The CRISPR/Case9 system was desgined to create the progressive hydrocephalus (prh) mutation in Sprague Dawley rats. The homozygous rat carries  chr2:g.120305679A&gt;T change that creates a splice site (Ccdc39c.916+2T ) mutation in the rat Ccdc39 gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150520221</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Slco1b2&lt;sup&gt;em1Myliu&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shanghai Key Laboratory of Regulatory Biology, Institute of Biomedical Sciences and School of Life Sciences, East China Normal University, Shanghai 200241, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slco1b2&lt;sup&gt;em1Myliu&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150521524</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="176282577" STOP_POS="176355557" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="174551463" STOP_POS="174619988" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="175814118" STOP_POS="175881775" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="240035313" STOP_POS="240103015" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="179045586" STOP_POS="179118680" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150520221</CITATION_ID>
    <DESCRIPTION>The Sprague Dawley embryos were injected with CRISPR/Case9 system targeting the first exon of the rat Slco1b2 gene. A Slco1b2 knockout was created with 11-bp deletion.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521538</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Uox&lt;sup&gt;em1Cya&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Yunnan University of Traditional Chinese Medicine,and Kunming Medical University, Kunming, Yunnan, China.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Uox&lt;sup&gt;em1Cya&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150521540</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="238147130" STOP_POS="238183320" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="235486867" STOP_POS="235523053" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="252452282" STOP_POS="252488497" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="270978811" STOP_POS="271015097" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="244795552" STOP_POS="244832143" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150521538</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system targeting exons 2 to 4 was injected into Sprague Dawley embryos. The resulting mutation was complete deletion of exons 2, 3 and 4.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521556</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Trpm4&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory of Biological Psychology, Brain and Cognition, 
Katholieke Universiteit Leuven (KUL), Tiensestraat 102, 

3000 Leuven, Belgium</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150521556</CITATION_ID>
    <DESCRIPTION>Trpm4 gene specific  Zinc finger constructs directed against exons 18-19, which 
contain the coding sequence for TM3-5 and the pore region of  the  TRPM4  protein,  were  injected  in  zygotes  from  Sprague-Dawley rats. This  mutant rat with a 514 bp deletion  which includes completely removes exon 18 and a piece of exon 19 from the Trpm4 gene, plus the intron 18-19. The  deletion  was  confirmed  via  genomic  
sequencing and western blotting.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521559</RGD_ID>
    <STRAIN_SYMBOL>LEW.SD-&lt;i&gt;CD8a&lt;sup&gt;m1Trg&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Texas Southwestern Medical Center, 5323</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150521559</CITATION_ID>
    <DESCRIPTION>Male SD rats were treated with the mutagen N-ethyl-N-nitrosourea (60
mg/kg intraperitoneally) at ages 9 and 10 weeks. A heterozygous mutant founder carrying a T to C transition that encoded a substitution of a proline residue (CCA) for a highly conserved serine residue (TCA) at amino acid position 94 was identified. This mutant male was mated to a LEW female and phenotyping by the expression of CD8a and CD8ab.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521599</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Tshr&lt;sup&gt;em1Mlit&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Animal Center of Tongji University; Tongji University School of Medicine, Shanghai, 200065, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tshr&lt;sup&gt;em1Mlit&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150521600</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="116072321" STOP_POS="116206009" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="110341585" STOP_POS="110475297" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="115170290" STOP_POS="115306871" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="124509406" STOP_POS="124561916" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="115024999" STOP_POS="115162531" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150521599</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system targeting exon 10 of the rat Tshr gene was injected into Sprague Dawley embryos to create this mutant strain. The strain was homozygous  with 5 bp deletion (CACGC) which introduces frameshift at residue 449 and a stop codon at 478 (P449fsX478).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521602</RGD_ID>
    <STRAIN_SYMBOL>OFA(SD)-&lt;i&gt;Dsg4&lt;sup&gt;hr&lt;/sup&gt;&lt;/i&gt;/Crl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Iffa Credo (L'Arbresle Cedex, France; www.criver.com/ ico/iffa_reachus.html).</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dsg4&lt;sup&gt;hr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150521603</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="11995902" STOP_POS="12032908" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="11720844" STOP_POS="11757927" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="12056113" STOP_POS="12092858" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="11853980" STOP_POS="11888828" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="12173507" STOP_POS="12209833" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150521602</CITATION_ID>
    <DESCRIPTION>This Iffa Credo ( IC)  hairless strain  was a spontaneous recessive mutant identified in a colony of   Crl:OFA(SD) at 1974. A large intracellular out-of-frame deletion in Dsg4 of IC mutant rats was identified. The intragenic deletion spanning exons 2?10 that results in a significant down-regulation of Dsg4 message.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521604</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Tnfrsf14&lt;sup&gt;em1Tja&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was created by Tim Aitman at University of Edinburgh.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=796&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2021-11-11)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00796</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeted sequence into WKY/Cruk rat embryos. The resulting mutation 77 has a stop codon, 15 amino acids from the ZFN-binding site, that resulted in a 490 amino acids (54 kDa) truncated protein, 198 amino acids smaller than the WT protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521605</RGD_ID>
    <STRAIN_SYMBOL>W/Lnne</STRAIN_SYMBOL>
    <FULL_NAME>Audiogenic Wistar rat</FULL_NAME>
    <ORIGINATION>Norberto Garcia-Cairasco at University of Sao Paulo</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>audiogenic seizures</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150521605</CITATION_ID>
    <DESCRIPTION>Wistar rats maintained at the  animal  facility  of  the  Ribeirao  Preto  School  of Medicine at the University of Sao Paulo, Brazil, were tested for audiogenic seizures, using as criteria an SI and the L1 (ref. RGD:14695082). The WAR colony foundation stock was produced  by  mating  animals  displaying  at  least procursive behaviors in three consecutive  tests,  one  every  4  days  (two  males  and four females). Each couple produced two or three lit-ters,  from  which  selected  individuals  displaying  the highest SI and shortest L1 were mated, at adult age,with their fathers and mothers. From the second generation on, brother  and sister matings were done, in a ratio of one male to two females, selected accordingto the criteria above.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521606</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lrp5&lt;sup&gt;em2Vari&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=880&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=880&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrp5&lt;sup&gt;em2Vari&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>41404650</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="210243499" STOP_POS="210346886" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="200814247" STOP_POS="200917581" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="218816833" STOP_POS="218920147" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="225689353" STOP_POS="225793075" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="206102750" STOP_POS="206206350" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00880</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a  22-bp deletion at the sgRNA2  site of exon 2 in the rat Lrp5 gene of Crl:SD embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521608</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lrp5&lt;sup&gt;em3Vari&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=881&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=881&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrp5&lt;sup&gt;em3Vari&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>41404652</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="210243499" STOP_POS="210346886" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="200814247" STOP_POS="200917581" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="218816833" STOP_POS="218920147" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="225689353" STOP_POS="225793075" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="206102750" STOP_POS="206206350" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00881</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce an
inversion coupled with small deletions in the exon 2 at both the sgRNA1 (11 bp) and sgRNA2 sites (3 bp)  in the rat Lrp5 gene of Crl:SD embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521610</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lrp5&lt;sup&gt;em1Vari&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=867&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=867&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lrp5&lt;sup&gt;em1Vari&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>41404647</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="210243499" STOP_POS="210346886" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="200814247" STOP_POS="200917581" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="218816833" STOP_POS="218920147" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="225689353" STOP_POS="225793075" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="206102750" STOP_POS="206206350" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00867</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a  18-bp deletion of exon 2 in the rat Lrp5 gene of Crl:SD embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521611</RGD_ID>
    <STRAIN_SYMBOL>BDIX.BDIV-&lt;i&gt;D6Mit8-D6Rat229&lt;/i&gt;/ZteRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cell Biology (Cancer Research) of Duisburg-Essen University Medical School, Essen, Germany</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=899&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00899</CITATION_ID>
    <DESCRIPTION>The BDIX.BDIV-&lt;i&gt;D6Mit8-D6Rat229&lt;/i&gt;/Zte congenic strain was produced by crossing BDIX (tumor-susceptible) and BDIV (tumor resistant) and then selecting for strains carrying homozygous segments of the BDIV chromosome on a BDIX background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521612</RGD_ID>
    <STRAIN_SYMBOL>BDIX.BDIV-&lt;i&gt;Mss1b/ZteRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=905&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=905&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00905</CITATION_ID>
    <DESCRIPTION>strain haboring on a BDIX background two BDIV Fragments generated by a double recombination, 37,3 and 20,0 Mb long,Mss1b1 and Mss1b2 both covering parts of the Mss1 fragment. Homozygous rats of both sexes display susceptibility towards ENU-induced development of PNS tumors in terms of survival time and incidence. Through the Mss1b1 and Mss1b2 fragments and the Mss1c fragment the Mss1 locus was fine-mapped between 82.9 and 85.2Mb</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521613</RGD_ID>
    <STRAIN_SYMBOL>BDIX.BDIV-&lt;i&gt;D6Mit1-D6Mgh2&lt;/i&gt;/ZteRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cell Biology (Cancer Research) of Duisburg-Essen University Medical School, Essen, Germany.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=901&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00901</CITATION_ID>
    <DESCRIPTION>The BDIX.BDIV-&lt;i&gt;D6Mit1-D6Mgh2&lt;/i&gt;/Zte congenic strain was produced by crossing BDIX (tumor-susceptible) and BDIV (tumor resistant) and then selecting for strains carrying homozygous segments of the BDIV chromosome on a BDIX background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521614</RGD_ID>
    <STRAIN_SYMBOL>BDIX.BDIV-&lt;i&gt;D10Got1-D10Rat45&lt;/i&gt;/ZteRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cell Biology (Cancer Research) of Duisburg-Essen University Medical School, Essen, Germany</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=902&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00902</CITATION_ID>
    <DESCRIPTION>The BDIX.BDIV-&lt;i&gt;D10Got1-D10Rat45&lt;/i&gt;/Zte congenic strain was produced by crossing BDIX (tumor-susceptible) and BDIV (tumor resistant) and then selecting for strains carrying homozygous segments of the BDIV chromosome on a BDIX background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521616</RGD_ID>
    <STRAIN_SYMBOL>BDIX.BDIV-&lt;i&gt;D10Mit3-D10Mgh16&lt;/i&gt;/ZteRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cell Biology (Cancer Research) of Duisburg-Essen University Medical School, Essen, Germany</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=903&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-11-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00903</CITATION_ID>
    <DESCRIPTION>The BDIX.BDIV-&lt;i&gt;D10Mit3-D10Mgh16&lt;/i&gt;/Zte congenic strain was produced by crossing BDIX (tumor-susceptible) and BDIV (tumor resistant) and then selecting for strains carrying homozygous segments of the BDIV chromosome on a BDIX background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521617</RGD_ID>
    <STRAIN_SYMBOL>BDIX/IfzRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Duisburg-Essen University Medical School, Essen, Germany</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=900&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00900</CITATION_ID>
    <DESCRIPTION>BDIX/IFZ rats have been inbred in the Institute of Cell Biology, Essen and later in the Central Animal Facility,Essen for about 45 years. The BDIX/Ifz rats are extremely susceptible to ENU-induced development of tumors of the peripheral and central nervous system.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521619</RGD_ID>
    <STRAIN_SYMBOL>BDIV/lfzRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=898&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=898&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00898</CITATION_ID>
    <DESCRIPTION>Substrain of BDIV, from cross between BDI and BDII single mating pair, with selection for coat color alleles (Druckrey 1971). BDIV/IFZ rats have been inbred in the Institute of Cell Biology, Essen and later in the Central Animal Facility for about 45 years. BDIX/Ifz rats are extremely resistant to ENU-induced development of tumors of the peripheral nervous System.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521659</RGD_ID>
    <STRAIN_SYMBOL>FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;-&lt;i&gt;Dusp5&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=922&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=922&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2021-11-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150521659</CITATION_ID>
    <DESCRIPTION>This strain was produced by injecting ZFNs targeting the following sequence CAGGGCAGCCGC-CACtggcaGAAGCTGCGGGAGGA in exon 1 of the rat Dusp5 gene into FHH-Chr 1&lt;sup&gt;BN&lt;/sup&gt;/Mcwi embryos. The resulting mutation is a 14 bp deletion and a 3 bp insertion between nucleotides 449 and 464 in Dusp5 mRNA that creates a frame shift mutation which is predicted to introduce a premature stop codon at amino acid 121.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521660</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(DIO-mCherry)2Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>A Rrrc substrain available at &lt;a href=http://www.rrrc.us/Strain/?x=687&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>A Rrrc substrain available at &lt;a href=http://www.rrrc.us/Strain/?x=687&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150521660</CITATION_ID>
    <DESCRIPTION>The transgene contains Cre recombinase reporter rat expressing mCherry driven by the EF1 alpha promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521661</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(DIO-mCherry)2OttcRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=928&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=928&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00928 </CITATION_ID>
    <DESCRIPTION>The transgene contains Cre recombinase reporter rat expressing mCherry driven by the EF1 alpha promoter. Expresses mCherry in cells of the brain transduced with a Cre-expression virus. Currently in SD background generated by backcrossing to LE-Tg(DIO-mCherry)2Ottc</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521675</RGD_ID>
    <STRAIN_SYMBOL>BN/NHsdShul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shull Lab, Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-11-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150521675</CITATION_ID>
    <DESCRIPTION>Inbred substrain derived from BN/SsNHsd(RGD:10008)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521676</RGD_ID>
    <STRAIN_SYMBOL>ACI/SegHsdShul</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shull Lab, Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-11-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150521676</CITATION_ID>
    <DESCRIPTION>Inbred substrain of ACI of ACI derived from ACI/SegHsd</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521677</RGD_ID>
    <STRAIN_SYMBOL>BN/HsdShulRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This substrain is transferred from Shull Lab, Department of Oncology, McArdle Laboratory for Cancer Research, University of Wisconsin-Madison to Rat Reource &amp; Research Center in 2021.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150521677</CITATION_ID>
    <DESCRIPTION>Inbred substrain derived from BN/SsNHsd(RGD:10008)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150521708</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Tbc1d1&lt;sup&gt;Tn(sb)1Fkh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Texas Southwestern Medical Center, Dallas TX</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tbc1d1&lt;sup&gt;Tn(sb)1Fkh&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150521709</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="44289241" STOP_POS="44489246" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="43936820" STOP_POS="44135133" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="45598753" STOP_POS="45797650" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="45404208" STOP_POS="45603325" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="46594874" STOP_POS="46781813" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150521708</CITATION_ID>
    <DESCRIPTION>The Sleeping Beauty transposon-mediated mutagenesis was used to knock out the rat Tbc1d1 gene in in rat spermatogonial stem cells from Sprague Dawley.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150523755</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ighm&lt;sup&gt;em1Ang&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Platform Rat Transgenesis IBiSA-CNRS, Nantes, France.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ighm&lt;sup&gt;em1Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150523756</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150523755</CITATION_ID>
    <DESCRIPTION>The mutation in this rat strain (line 19) comprised a 64 bp deletion of  the IgM CH1 domain  and generation of a stop codon. This strain carries deletion in both alleles has 
truncated Cmu.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150523757</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ighm&lt;sup&gt;em2Ang&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Platform Rat Transgenesis IBiSA-CNRS, Nantes, France.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ighm&lt;sup&gt;em2Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150523758</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150523757</CITATION_ID>
    <DESCRIPTION>Microinjection of Sprague-Dawley rat zygotes with ZFN mRNA specific for the JH locus resulted in the generation of a mutant animal with a 2465 bp DNA deletion, spanning the entire locus</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150523775</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(HLA-B*2705,B2M)&lt;sup&gt;Tg/0&lt;/sup&gt;21-3Reh Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=916&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2022-03-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00916</CITATION_ID>
    <DESCRIPTION>This strain was made by pronuclear injection into LEW/Crl embryos. The embryos were co-injected with DNA fragments containing the HLA-B*2705 human gene  and the human beta-2-microglobulin gene.   The strain carries 20 copies of HLA-B*2705 and 15 copies of the human beta-2-microglobulin gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150523778</RGD_ID>
    <STRAIN_SYMBOL>LEW-Tg(B2M)283-2RehRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=917&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=917&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2022-03-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00917</CITATION_ID>
    <DESCRIPTION>This strain carries 35 copies of genomic human B2-microglobulin gene. When crossed with the 21-3 line (RRRC:00 916), the F1 males develop a spontaneous disease mimicking human spondyloarthritis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150523780</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Erap1&lt;sup&gt;em1Reh&lt;/sup&gt;&lt;/i&gt;2786/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=918&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=918&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2021-11-19)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00918</CITATION_ID>
    <DESCRIPTION>The ZFN mRNA targeting exon 2 of Erap1 was microinjected into both the pronuclei and the cytoplasm of fertilized LEW eggs. This strain was heterozygous for a 2-bp deletion within the targeted AGGAGA sequence of Erap1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150523781</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Erap1&lt;sup&gt;em1Reh&lt;/sup&gt;&lt;/i&gt;2786</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Texas Southwestern Medical Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150523781</CITATION_ID>
    <DESCRIPTION>The ZFN mRNA targeting exon 2 of Erap1 was microinjected into both the pronuclei and the cytoplasm of fertilized LEW eggs. This strain was heterozygous for a 2-bp deletion within the targeted AGGAGA sequence of Erap1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150524338</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(ERAP1*)2793RehRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=919&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=919&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2021-11-29)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00919</CITATION_ID>
    <DESCRIPTION>This transgenic rat carrying  the human " II or *002" allele of ERAP1 under mouse H-2K promoter control.  The construct was made by Dr. Edd James, University of Southampton, UK.  The II allele is generally considered to be a risk allele for ankylosing spondylitisThe original background strain is SD and the current background strain is mixed Lewis x SD.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150526804</RGD_ID>
    <STRAIN_SYMBOL>AZK/Misiv</STRAIN_SYMBOL>
    <FULL_NAME>Azman Kamal rats</FULL_NAME>
    <ORIGINATION>Forest Research Institute Malaysia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2021-12-01)</AVAILABILITY>
    <RESEARCH_USE>Wound healing</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150526804</CITATION_ID>
    <DESCRIPTION>The rat was derived from inbreeding of  Sprague Dawley rats for 3 years.  Because of longer inbreeding process we  got SD progenies without fur. So, this rat is used for wound healing study in our facility.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150526809</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ar&lt;sup&gt;tfm&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Donated by Cynthia Jordan from Michigan State University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=940&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00940</CITATION_ID>
    <DESCRIPTION>This spontaneous mutant strain was originally derived from  King Holtzman background and now maintained in Sprague Dawley background. A single nucleotide mutation was identified in the androgen receptor gene. The tfm males are sterile so the mutation is carried via females who breed normally.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150527860</RGD_ID>
    <STRAIN_SYMBOL>BDIX/OrlIco</STRAIN_SYMBOL>
    <FULL_NAME>BDIX Rats</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150527860</CITATION_ID>
    <DESCRIPTION>Rats selected in 1937 by H. Druckrey in Berlin from a strain of yellow coated, pink-eyed rats. It is part of a series of BD I to X strains produced at Max Planck Institute, Freiburg and was introduced to France in 1971 to the INSERM unit, Immunology Laboratory, Dijon where it was maintained in strict brother-sister inbreeding. Developed and studied by Dr. Ms. Martin, CNRS/CSEAL, Orleans (Orl)  acquired by IFFA CREDO later (Ico).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150573816</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nkx3-1&lt;sup&gt;em1Pjhak+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Laboratory Animal Medicine
College of Veterinary Medicine
Seoul National University</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nkx3-1&lt;sup&gt;em1Pjhak&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150573819</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="50883661" STOP_POS="50886253" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="44473851" STOP_POS="44476443" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="51065316" STOP_POS="51067908" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="54796102" STOP_POS="54798694" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="49743313" STOP_POS="49745905" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150573816</CITATION_ID>
    <DESCRIPTION>A pair of TALENs targeting coding region of  rat Nkx3-1gene was electroporated into SD zygotes to create NKx3-1 mutants. The resulting mutation was indel  mutation with sequences loss beyond TALEN recognition resulting a premature termination codon of the protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>150573818</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nkx3-1&lt;sup&gt;em1Pjhak-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Laboratory Animal Medicine
College of Veterinary Medicine
Seoul National University</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nkx3-1&lt;sup&gt;em1Pjhak&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150573819</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="50883661" STOP_POS="50886253" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="44473851" STOP_POS="44476443" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="51065316" STOP_POS="51067908" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="54796102" STOP_POS="54798694" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="49743313" STOP_POS="49745905" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_150573818</CITATION_ID>
    <DESCRIPTION>A pair of TALENs targeting coding region of  rat Nkx3-1gene was electroporated into SD zygotes to create NKx3-1 mutants. The resulting mutation was indel  mutation with sequences loss beyond TALEN recognition resulting a premature termination codon of the protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151347605</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ddah1&lt;sup&gt;em1Ywxu&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Cardiovascular Department, Shanghai Tenth People's Hospital, Tongji University, School of Medicine, Shanghai, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ddah1&lt;sup&gt;em1Ywxu&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>151347606</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="237327812" STOP_POS="237460624" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="234667499" STOP_POS="234800322" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="251634368" STOP_POS="251766009" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="270160842" STOP_POS="270289319" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="243932221" STOP_POS="244069832" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_151347605</CITATION_ID>
    <DESCRIPTION>CRISPR-Cas9 technique was used to generate DDAH1-/- rats on Sprague-Dawley background. Genome deletion in exon 1 was confirmed by PCR analysis with the primers:DDAH1-F (5'-GCGCTGCTCTCGGGAAGA-3') and DDAH1-R (5'-GGGTGATGAGGGCGGTCT-3').</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151347873</RGD_ID>
    <STRAIN_SYMBOL>Slc:ZUC-&lt;I&gt;Lepr&lt;sup&gt;fa+&lt;/sup&gt;&lt;/I&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Zucker lean rats</FULL_NAME>
    <ORIGINATION>Japan SLC, Inc. (Hamamatsu, Japan)</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr</ALLELES>
    <ALLELE_RGD_IDS>3001</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_151347873</CITATION_ID>
    <DESCRIPTION>The Zucker lean rats were siblings of Zucker fatty rats.  They were used as lean controls for Zucker fatty rats studies. This strain was available at Japan SLC, Inc. (Hamamatsu, Japan.)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151356741</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Alb-TAg)Mlcr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>McArdle Laboratory for Cancer Research, Medical School, University of Wisconsin, Madison, Wisconsin 53706-1599, USA.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_151356741</CITATION_ID>
    <DESCRIPTION>This transgenic strain was generated by microinjection into outbred Sprague-Dawley from Harlan Sprague-Dawley (Hsd:SD) fertilized eggs and carries simian virus T Antigen drived by the enhancer/promoter region of the mouse albumin gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151356945</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;ROSA26&lt;sup&gt;em1(EF1a-TetR, Fos-iCre)&lt;/sup&gt;&lt;/i&gt;/Bhope</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIDA IRP (Hope lab).</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_151356945</CITATION_ID>
    <DESCRIPTION>Two  DNA expression constructs, the bacterial tetracyclin repressor (TetR) under the expression control of human EF1a promoter and  the improved Cre recombinase (iCre) under Fos promoter were joined in an antiparallel orientation in one rat ROSA26 targeting cassette.  The  DNA construct, together with CRISPR /Cas9 system, was injected to one cell Long-Evans (Crl:LE) rat embryos and founders were identified and bred for 8 generations at at NIDA IRP (Hope lab).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151356946</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;ROSA26&lt;sup&gt;em1(EEF1A1-TetR, Fos-iCre)&lt;/sup&gt;&lt;/i&gt;/BhopeRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=953&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=953&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00953</CITATION_ID>
    <DESCRIPTION>Two  DNA expression constructs, the bacterial tetracyclin repressor (TetR) under the expression control of human EEF1A1 promoter and  the improved Cre recombinase (iCre) under Fos promoter were joined in an antiparallel orientation in one rat ROSA26 targeting cassette.  ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature. The  DNA construct, together with CRISPR /Cas9 system, was injected to one cell Long-Evans (Crl:LE) rat embryos and founders were identified and bred for 8 generations at at NIDA IRP (Hope lab).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151356950</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(Fos-LacZ)BhopeRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=952&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=952&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00952</CITATION_ID>
    <DESCRIPTION>The lacZ gene was inserted between NcoI and SalI sites in exon 4 of the murine Fos gene . The linearized DNA was then microinjected into fertilized rat oocytes and line 1-8 was chosen for continuation.  Initial SD rats were then bred onto Wistar background for &gt;10 generations at NIDA IRP (Bruce Hope lab)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151356957</RGD_ID>
    <STRAIN_SYMBOL>Sah:SD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>North Terrace
Adelaide
SA
5000
Australia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_151356957</CITATION_ID>
    <DESCRIPTION>Sprague-Dawley maintained at South Australian Health and Medical Research Institute</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151356958</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cftr&lt;sup&gt;em1Apb&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Organization: Australian Phenomics Facility, Australian National University</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cftr&lt;sup&gt;em1Apb&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>151660342</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="47600638" STOP_POS="47600640" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="46634751" STOP_POS="46634753" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="42766671" STOP_POS="42766673" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="42281040" STOP_POS="42448571" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="43874852" STOP_POS="44041870" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_151356958</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to target exon 11 to create a deletion  at codon F508 which was injected into Sprague-Dawley one-cell
embryos (C076 line). One rat
had an allele that contained the desired homology-directed
repair edited TTT deletion and was designated the
Phe508del founder (c.1522_1524delTTT).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151356959</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cftr&lt;sup&gt;em2Apb&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Organization: Australian Phenomics Facility, Australian National University</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cftr&lt;sup&gt;em2Apb&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>151660343</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="47600630" STOP_POS="47600637" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="46634743" STOP_POS="46634750" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="42766663" STOP_POS="42766670" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="42281040" STOP_POS="42448571" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="43874852" STOP_POS="44041870" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_151356959</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to target exon 11 and create a deletion at codon F508, which was injected into Sprague-Dawley one-cell
embryos (C076 line). A rat with an 8-bp deletion upstream of the TTT site
(c.1514_1521delATATCATC) was used to establish the KO strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151356971</RGD_ID>
    <STRAIN_SYMBOL>RjOrl:LE</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://janvier-labs.com/en/fiche_produit/long-evans_rat/&gt;Janvier&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://janvier-labs.com/en/fiche_produit/long-evans_rat/&gt;Janvier&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2022-02-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_151356971</CITATION_ID>
    <DESCRIPTION>This model was developed by Dr Long and Dr Evans in 1915. The LONG EVANS rat is the result of a cross between a female albino from the WISTAR Institute and a wild male (Rattus norvegicus) captured near Berkeley and offspring selection.
The LONG EVANS rat is small and resistant to oncogenesis. This strain is widely used in behavioral, learning, ageing (visual acuity less affected than that of albino strains), addiction - especially to alcohol - studies.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151356985</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(cFos-eGFP)Bhope</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>NIDA IRP (Hope lab)</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_151356985</CITATION_ID>
    <DESCRIPTION>This LE transgenic rats were created by injecting the cfos-eGFP construct to pronuclei of fertilized eggs obtained from Long Evans females. The 5 prime end of the transgenic DNA construct contained mouse genomic cFos (indluding the promoter and all exon and intron sequences) was fused with eGFP (including poly(A) tail derived from the IRES (phosphorylated-internal ribosomal entry site) of the EGFP Clontech (Cambridge, UK) vector. A single founder animal was identified. All subsequent breeding used hemizygous cfos-GFP male rats paired with wild-type Long Evans female rats obtained from Charles River Laboratories. Rats were bred on Long-Evans background for 13 generations at NIDA IRP (Hope lab).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151356988</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(cFos-eGFP)BhopeRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=954&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=954&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00954</CITATION_ID>
    <DESCRIPTION>This transgenic was created by Dr.  Bruce Hope at  at NIDA IRP and donated to RRRC in 2022. The transgenic rats were created by injecting the cfos-eGFP construct to pronuclei of fertilized eggs obtained from Long Evans females. The 5 prime end of the transgenic DNA construct contained mouse genomic cFos (indluding the promoter and all exon and intron sequences) was fused with eGFP (including poly(A) tail derived from the IRES (phosphorylated-internal ribosomal entry site) of the EGFP Clontech (Cambridge, UK) vector. A single founder animal was identified. All subsequent breeding used hemizygous cfos-GFP male rats paired with wild-type Long Evans female rats obtained from Charles River Laboratories. Rats were bred on Long-Evans background for 13 generations</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151664748</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Slc9a6 &lt;sup&gt;em1Moro&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Organization: Dr. Eric Morrow at  Brown University
70 Ship Street, Box G-E4
Providence
RI
02912
USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc9a6 &lt;sup&gt;em1Moro&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>151664749</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="139468045" STOP_POS="139524111" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="134443830" STOP_POS="134443831" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="158979081" STOP_POS="159045019" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="153620082" STOP_POS="153675717" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="141146237" STOP_POS="141201234" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01017</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant. Guide RNA sequence is the following: 5'-CGGCTGTGTAACCCTGATGA-3'. Cas9-mediated cleavage at exon 7 in the Slc9a6 locus resulted in the insertion of 2 bp (TT) generating frameshift and a premature stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151665324</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Ucp2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>contact MCW Rat Distribution at   &lt;a href=mailto:mcwcustomrats@mcw.edu&gt;  mcwcustomrats@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2022-03-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_151665324</CITATION_ID>
    <DESCRIPTION>Generated by CRISPR/Cas9 mutagenesis of SS/JrHsdMcwi rats by Aron Geurts. The resulting mutation is a 23-bp deletion (rn7: chr1:154,842,967-154,842,989)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151665772</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Tfap2c&lt;sup&gt;em1(tdTomato)Nips&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi 444-8787, Japan. or Division of Mammalian Embryology, Center for Stem Cell Biology and Regenerative Medicine, The Institute for Medical Science, The University of Tokyo, Tokyo108-8639, Japan.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2022-04-01)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_151665772</CITATION_ID>
    <DESCRIPTION>The targeting vector was designed to replace the stop codon of Tfap2c with T2A-tdTomato. The adeno-associated virus carrying the targeting vector was infected to Crlj:WI (RGD ID: 2312504) rat 1 cell zygotes followed by the introduction of CRISPR/Cas9 ribonucleoprotein complex by electroporation. After incubation overnight, the zygotes were transferred into oviducts of pseudo-pregnant rats. The pups were judged correct gene-targeting by genomic PCR. These rat strains are being maintained by crossing the founder rats with Crlj:WI rats. The tdTomato fluorescence faithfully label Tfap2c expressing cells.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151667414</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Ckm&lt;sup&gt;tm1(cre)&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=951&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_151667414</CITATION_ID>
    <DESCRIPTION>This model expresses cre-recombinase under the control of the endogenous Ckm (creatine kinase, M-type) promoter. Cre was targeted to the rat Ckm gene of LE embryos through CRISP/Cas9 system genome editing system.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>151893484</RGD_ID>
    <STRAIN_SYMBOL>SS-Tg(CAG-Fh)A1Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>contact MCW Rat Distribution at   &lt;a href=mailto:mcwcustomrats@mcw.edu&gt;  mcwcustomrats@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2022-04-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_151893484</CITATION_ID>
    <DESCRIPTION>This is a transgenic model  created using Sleeping Beauty system. The transgenic animals are overexpressing fumarate hydratase (Fh) under the control of the ubiquitous CAG promoter in the Dahl salt-sensitive strain background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152975964</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;F8&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Blood Research Institute 8733 W Watertown Plank Road Milwaukee, WI 53226</ORIGINATION>
    <SOURCE>Contact MCW Rat Distribution at   &lt;a href=mailto:mcwcustomrats@mcw.edu&gt;  mcwcustomrats@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_152975964</CITATION_ID>
    <DESCRIPTION>Full gene inversion of the rat F8 gene introduced by CRISPR/Cas9, to DahlSS background rats.  This inversion causes a premature stop codon 3 amino acids into the protein.  F8 activity in rats, homozygous for the mutation, is undetectable.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152975965</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;F8&lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;-Tg(ITGA2B-F8*)Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Blood Research Institute 8733 W Watertown Plank Road Milwaukee, WI 53226</ORIGINATION>
    <SOURCE>contact MCW Rat Distribution at   &lt;a href=mailto:mcwcustomrats@mcw.edu&gt;  mcwcustomrats@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_152975965</CITATION_ID>
    <DESCRIPTION>This transgenic was produced by crossing the SS transgenic rat  carrying  Lentivirus constructs containing the  2bF8 vector [B-domain deleted human FVIII under control of ITGA2B (IIb) promoter] with an F8 knockout rat SS-F8em2Mcwi (RGD:152975964). This transgenic rat strain expressed B-domain deleted human F8 under the control of ITGA2B promoter in the absence of rat F8 product.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152977766</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Drd2-IL2RA/YFP*)1Koba</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1337  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1337  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2022-07-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_152977766</CITATION_ID>
    <DESCRIPTION>Background strain: Iar:LE (Institute for Animal Reproduction) ( RGD:18337282). This strain was generated by injecting a modified BAC, in which a fusion protein created from the human IL2R alpha-subunit gene (IL2RA) and YFP* (enhanced yellow fluorescent protein,Venus) was inserted into the second exon of the rat Drd2 gene, into fertilized eggs of Long-Evans rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152977768</RGD_ID>
    <STRAIN_SYMBOL>WIC-Tg(Oprk1-YFP*)1Utthe</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1338 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1338 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_152977768</CITATION_ID>
    <DESCRIPTION>The KOR-Venus construct consisting of  promoter of rat Oprk1 (opioid receptor, kappa 1) fused with Venus fluorescent protein, was introduced into fertilized eggs of Wistar rats (Crlj:WI, Charles River Japan). They were then crossed with Wistar-Imamichi rats (Iar:Wistar-Imamichi, Institute for Animal Reproduction) to maintain the strain. Transgenic rats expressing the fluorescent protein Venus under the control of the Oprk1 promoter. This strain is heterozygous.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152985526</RGD_ID>
    <STRAIN_SYMBOL>WIC-&lt;i&gt;Cdkn2a&lt;sup&gt;em1Kyhs&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1339&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1339&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_152985526</CITATION_ID>
    <DESCRIPTION>A 7-bp deletion in exon 1 of the Cdkn2a (p16) gene was introduced by the CRISPR/Cas9. Genetic background is Iar:Wistar-Imamichi (Institute for Animal Reproduction) (RGD:125097496). Introducing the deletion mutation in the Cdkn2a (p16) gene into the background of DMD rats (muscular dystrophy model rats) improves muscle pathology.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152985692</RGD_ID>
    <STRAIN_SYMBOL>WAG-&lt;i&gt;Cd247&lt;sup&gt;em9Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Genome Editing Rat Resource Center, Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2022-06-08)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_152985692</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 mutagenesis was used to knockout Cd247 in the WAG/RijCmcr (WAG) strain. A single guide RNA (sgRNA) targeting the Cd247 exon 2 sequence GATGGAATCCTCTTCATCTACGG (protospacer adjacent motif in bold) was injected along with SpCas9 protein into one-cell WAG embryos. A founder offspring harboring a 17-bp frame-shift indel mutation deleting GAATCCTCTTCATCTAC (rn6.0 chr13:84,064,185-84,064,201) was identified and confirmed by Sanger sequencing. The frameshift mutation is predicted to cause a premature truncation of the normal 165 amino acid protein coding sequence after only 37 amino acids, lacking most of the transmembrane and the entirety of the external cellular protein domains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152995284</RGD_ID>
    <STRAIN_SYMBOL>W/Nov</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_152995284</CITATION_ID>
    <DESCRIPTION>Substrain of Wistar, now bred at the Institute of Cytology and Genetics, Russian Academy of Sciences (Novosibirsk)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152998993</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ager &lt;sup&gt;em2Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>contact MCW Rat Distribution at   &lt;a href=mailto:mcwcustomrats@mcw.edu&gt;  mcwcustomrats@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2022-07-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_152998993</CITATION_ID>
    <DESCRIPTION>This model was produced at the Medical College of Wisconsin using CRISPR/Cas9 in the Crl:SD strain. The resulting mutation is a 1-bp insertion in the third exon of the Ager gene. rn6.0:chr20:4,150,403-4,150,403 ins T</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152998995</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ager &lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>contact MCW Rat Distribution at   &lt;a href=mailto:mcwcustomrats@mcw.edu&gt;  mcwcustomrats@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2022-07-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_152998995</CITATION_ID>
    <DESCRIPTION>This model was generated at the Medical College of Wisconsin by CRISPR/Cas9 in Crl:SD strain. The resulting mutation is a 16-bp deletion in the third exon of Ager. rn6.0:chr20:4,150,397-4,150,412.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152998996</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Adh5&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>contact MCW Rat Distribution at   &lt;a href=mailto:mcwcustomrats@mcw.edu&gt;  mcwcustomrats@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2022-07-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_152998996</CITATION_ID>
    <DESCRIPTION>This model was generated at the Medical College of Wisconsin by CRISPR/Cas9 mutagenesis in Crl:SD strain and harbors a 16-bp deletion in exon 3 of Adh5. rn6.0:chr2:226,979,096-226,979,111.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152999000</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Fxn&lt;sup&gt; em2Fara-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>This strain has been deposited with RRRC</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fxn&lt;sup&gt; em2Fara&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>152999006</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="231300457" STOP_POS="231323989" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="221874007" STOP_POS="221897543" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="242123975" STOP_POS="242152834" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="249400435" STOP_POS="249426597" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="227647092" STOP_POS="227671081" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_152999000</CITATION_ID>
    <DESCRIPTION>Heterozygous KO of the Fxn gene obtained by targeting exon 4 with CRISPR/Cas9 system</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152999001</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Fxn&lt;sup&gt; em1Fara-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>This strain has been deposited with RRRC.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fxn&lt;sup&gt; em1Fara&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>152999004</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="231300457" STOP_POS="231323989" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="221874007" STOP_POS="221897543" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="242123975" STOP_POS="242152834" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="249400435" STOP_POS="249426597" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="227647092" STOP_POS="227671081" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_152999001</CITATION_ID>
    <DESCRIPTION>Exon 4 of the rat Fxn gene was targeted for homologous recombination to introduce loxP sites using CRISPR/Cas9</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152999002</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Fxn&lt;sup&gt; em2Fara-/+&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=961&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fxn&lt;sup&gt; em2Fara&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>152999006</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="231300457" STOP_POS="231323989" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="221874007" STOP_POS="221897543" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="242123975" STOP_POS="242152834" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="249400435" STOP_POS="249426597" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="227647092" STOP_POS="227671081" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00961</CITATION_ID>
    <DESCRIPTION>Heterozygous KO of the Fxn gene obtained by targeting exon 4 with CRISPR/Cas9 system</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152999003</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Fxn&lt;sup&gt; em1Fara-/+&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=960&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=960&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fxn&lt;sup&gt; em1Fara&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>152999004</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="231300457" STOP_POS="231323989" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="221874007" STOP_POS="221897543" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="242123975" STOP_POS="242152834" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="249400435" STOP_POS="249426597" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="227647092" STOP_POS="227671081" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00960</CITATION_ID>
    <DESCRIPTION>Exon 4 of the rat Fxn gene was targeted for homologous recombination to introduce loxP sites using CRISPR/Cas9</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>152999023</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Aif1&lt;sup&gt;tm(EGFP)Apps&lt;/sup&gt;&lt;/i&gt;/Mmmc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Pharmacology, University of Maryland School of Medicine, Baltimore, Maryland 21201</ORIGINATION>
    <SOURCE>&lt;a href=https://www.rrrc.us/Strain/?x=965&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-05-21)</AVAILABILITY>
    <RESEARCH_USE>Study of effects of disease, injury, and aging on microglia</RESEARCH_USE>
    <ALLELES>Aif1&lt;sup&gt;tm(EGFP)Apps&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>152999024</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="3651435" STOP_POS="3657341" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="3646784" STOP_POS="3652670" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="5161350" STOP_POS="5167176" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="7234609" STOP_POS="7240454" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="3714428" STOP_POS="3716327" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00965</CITATION_ID>
    <DESCRIPTION>Applied StemCell, Inc (Milpitas, CA) was contracted to generate the Iba1-EGFP knock-in rat model using
CRISPR/Cas9 technology in the Sprague Dawley rat strain. The donor construct inserted consisted of the
EGFP coding sequence (minus the first ATG), followed by the 22 amino acid sequence of the porcine
teschovirus-1 2A (P2A) self-cleaving peptide, and then the first exon of the rat Iba1 gene immediately
downstream of the translational start site. Guide RNA with the following sequence: 5'- TACCCTGCAAATCCTTGCTCTGG-3' targeting the Iba1 gene just
downstream of the translational start site were used.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>153297754</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gsap&lt;sup&gt;em2mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dr. Troy Stevens, University of Southern Alabama</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2022-07-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_153297754</CITATION_ID>
    <DESCRIPTION>This strain was produced at the Medical College of Wisconsin using CRISPR Cas9 mutagenesis in the Crl:SD strain. A CRISPR SpCas9/sgRNA targeting the GTCCTTTGCAGTCCCTGCCG sequence within exon 15 of Gsap and a 5-bp indel (rn72: chr4:13,849,488-13,849,492) was identified.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>153298963</RGD_ID>
    <STRAIN_SYMBOL>Taiep/JosvRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=963&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=963&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00963</CITATION_ID>
    <DESCRIPTION>These mutants were found in Sprague-Dawley rats at University of Puebla in 1989 and donated by John Svaren to RRRC now are maintained at RRRC</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>153323320</RGD_ID>
    <STRAIN_SYMBOL>MR/NRrrc</STRAIN_SYMBOL>
    <FULL_NAME>Maudsely reactive</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=00173&gt;Rat Resource and Research Center&lt;/a&gt;, &lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=00173&gt;Rat Resource and Research Center&lt;/a&gt;, &lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryorecovery (as of 2023-10-25)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00173</CITATION_ID>
    <DESCRIPTION>Origin: as for MNR except selection was for high defecation response in the open field. To Harrington in 1965 at F25 and to NIH in 1964 at F18+ (Hansen et al 1982). Now is available at  Rat Resource &amp; Research Center</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>153323324</RGD_ID>
    <STRAIN_SYMBOL>FXLE12/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_153323324</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>153344518</RGD_ID>
    <STRAIN_SYMBOL>FXLE15/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_153344518</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.  This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>153344519</RGD_ID>
    <STRAIN_SYMBOL>LEXF1C/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_153344519</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>153344520</RGD_ID>
    <STRAIN_SYMBOL>LEXF6B/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_153344520</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj.  This substrain was maintained at Medical College of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155260360</RGD_ID>
    <STRAIN_SYMBOL>COP/HsdUwmRrrc</STRAIN_SYMBOL>
    <FULL_NAME>Copenhagen</FULL_NAME>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=966&gt;Rat Resource and Research Center&lt;/a&gt;, &lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=966&gt;Rat Resource and Research Center&lt;/a&gt;, &lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-25)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00966</CITATION_ID>
    <DESCRIPTION>Donated from Michael Gould/Jim Shull at University of Wisconsin Madison to Rat Resource &amp; Research Center,</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155260361</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Sycp1-Cas9-eGFP)SynblRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=968&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=968&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2022-10-06)</AVAILABILITY>
    <RESEARCH_USE>Genetics, Reproductive Biology, Gene Conversion, Active Genetics</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00968</CITATION_ID>
    <DESCRIPTION>This project entailed generation of a novel rat strain in which a P2A-Cas9-T2A-EGFP coding sequence was inserted at the stop codon of the rat Sycp1 gene for co-expression of Cas9 and EGFP under the control of the Sycp1 regulatory elements. Animals express Cas9 in the testis in the spermatogonial layer and in meiosis stages with 4N DNA content. Strain catalyzes high levels of Active Genetic Gene conversion when paired with certain Active Genetic cassettes.   ROBUST AND EFFICIENT ACTIVE GENETICS GENE CONVERSION IN THE RAT AND MOUSE Chenyen Lai, Oscar Alvarez, Kristen Read, Don van Fossan,Christopher M Conner, Shannon Xaing-Ru Xu, Dale O. Cowley, Valentino Gantz, David R. Webb, Kurt Jarnagin
URL: Doi:10.1101/2022.08.30.505951</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155260362</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Ddx4-Cas9)SynblRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=969&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=969&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Genetics, Reproductive Biology, Gene Conversion, Active Genetics</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00969</CITATION_ID>
    <DESCRIPTION>rat strain designed to express Cas9 under the control of the rat Ddx4 (Vasa) regulatory elements while also retaining expression of Ddx4. The strategy entailed insertion of a P2A sequence followed by human-codon-optimized Cas9 coding sequences with nuclear localization signals near the C-terminus of the rat Ddx4 (Vasa) gene.  Animals express Cas9 in the testis in the spermatogonial layer and in meiosis stages with 4N DNA content. Strain catalyzes high levels of Active Genetic Gene conversion when paired with certain Active Genetic cassettes. ROBUST AND EFFICIENT ACTIVE GENETICS GENE CONVERSION IN THE RAT AND MOUSE Chenyen Lai, Oscar Alvarez, Kristen Read, Don van Fossan,Christopher M Conner, Shannon Xaing-Ru Xu, Dale O. Cowley, Valentino Gantz, David R. Webb, Kurt Jarnagin URL: Doi:10.1101/2022.08.30.505951 
URL: Doi:10.1101/2022.08.30.505951</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155260363</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Cyp2e1-CYP2E1*-Cas9)SynblRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>RRRC</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2022-10-06)</AVAILABILITY>
    <RESEARCH_USE>Genetics, Reproductive Biology, Gene Conversion, Active Genetics, Drug Metabolism, Cyp450</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155260363</CITATION_ID>
    <DESCRIPTION>rat strain in which the rat Cyp2e1 gene is humanized by insertion of a human CYP2E1 minigene (CYP2E1*) insert at the native start codon. The insert also included a CRISPR/Cas9 gene drive element to enable super-Mendelian inheritance of the modified allele when crossed to a rat expressing Cas9 in the germline. ROBUST AND EFFICIENT ACTIVE GENETICS GENE CONVERSION IN THE RAT AND MOUSE Chenyen Lai, Oscar Alvarez, Kristen Read, Don van Fossan,Christopher M Conner, Shannon Xaing-Ru Xu, Dale O. Cowley, Valentino Gantz, David R. Webb, Kurt Jarnagin URL: Doi:10.1101/2022.08.30.505951 URL: Doi:10.1101/2022.08.30.505951 
URL: URL: Doi:10.1101/2022.08.30.505951</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155260364</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Cyp3a23-3a1-Cyp3A4*-Cas9)SynblRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=970&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=970&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2022-10-06)</AVAILABILITY>
    <RESEARCH_USE>Genetics, Reproductive Biology, Gene Conversion, Active Genetics, Drug Metabolism, Cyp450</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00970</CITATION_ID>
    <DESCRIPTION>rat strain in which the rat Cyp3a1 gene (Cyp3a23-3a1, RGD:628626) was inactivated by insertion of a human CYP3A4 minigene (Cyp3A4*) and the linked rat Cyp3a2 locus was simultaneously mutated by CRISPR-mediated indel introduction. Strain contains Indel 8 at the Rat 3A2 locus (55 kb away), The CYP3A4 minigene included a CRISPR/Cas9 gene drive element to enable super-Mendelian inheritance.   Strain contains and Active Genetic cassette which encodes a gRNA targeting the Rat 3A1 and 3A2 translation initiation site. ROBUST AND EFFICIENT ACTIVE GENETICS GENE CONVERSION IN THE RAT AND MOUSE Chenyen Lai, Oscar Alvarez, Kristen Read, Don van Fossan,Christopher M Conner, Shannon Xaing-Ru Xu, Dale O. Cowley, Valentino Gantz, David R. Webb, Kurt Jarnagin URL: Doi:10.1101/2022.08.30.505951 URL: Doi:10.1101/2022.08.30.505951 
URL: URL: Doi:10.1101/2022.08.30.505951</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155260365</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Sycp1-Cas9-eGFP)Synbl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Created by Dr. Kurt Jarnagin at Synbal, Inc.San Diego, CA, USA</ORIGINATION>
    <SOURCE>Donated to Rat Resource &amp; Research Center</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2022-10-06)</AVAILABILITY>
    <RESEARCH_USE>Genetics, Reproductive Biology, Gene Conversion, Active Genetics</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155260365</CITATION_ID>
    <DESCRIPTION>This project entailed generation of a novel rat strain in which a P2A-Cas9-T2A-EGFP coding sequence was inserted at the stop codon of the rat Sycp1 gene for co-expression of Cas9 and EGFP under the control of the Sycp1 regulatory elements. Animals express Cas9 in the testis in the spermatogonial layer and in meiosis stages with 4N DNA content. Strain catalyzes high levels of Active Genetic Gene conversion when paired with certain Active Genetic cassettes.   ROBUST AND EFFICIENT ACTIVE GENETICS GENE CONVERSION IN THE RAT AND MOUSE Chenyen Lai, Oscar Alvarez, Kristen Read, Don van Fossan,Christopher M Conner, Shannon Xaing-Ru Xu, Dale O. Cowley, Valentino Gantz, David R. Webb, Kurt Jarnagin
URL: Doi:10.1101/2022.08.30.505951</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155260366</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Ddx4-Cas9)Synbl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Created by Dr. Kurt Jarnagin at Synbal, Inc.San Diego, CA, USA</ORIGINATION>
    <SOURCE> Donated to Rat Resource &amp; Research Center</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Genetics, Reproductive Biology, Gene Conversion, Active Genetics</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155260366</CITATION_ID>
    <DESCRIPTION>rat strain designed to express Cas9 under the control of the rat Ddx4 (Vasa) regulatory elements while also retaining expression of Ddx4. The strategy entailed insertion of a P2A sequence followed by human-codon-optimized Cas9 coding sequences with nuclear localization signals near the C-terminus of the rat Ddx4 (Vasa) gene.  Animals express Cas9 in the testis in the spermatogonial layer and in meiosis stages with 4N DNA content. Strain catalyzes high levels of Active Genetic Gene conversion when paired with certain Active Genetic cassettes. ROBUST AND EFFICIENT ACTIVE GENETICS GENE CONVERSION IN THE RAT AND MOUSE Chenyen Lai, Oscar Alvarez, Kristen Read, Don van Fossan,Christopher M Conner, Shannon Xaing-Ru Xu, Dale O. Cowley, Valentino Gantz, David R. Webb, Kurt Jarnagin URL: Doi:10.1101/2022.08.30.505951 
URL: Doi:10.1101/2022.08.30.505951</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155260367</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Cyp2e1-CYP2E1*-Cas9)Synbl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Created by Dr. Kurt Jarnagin at Synbal, Inc.San Diego, CA, USA</ORIGINATION>
    <SOURCE>Donated to Rat Resource &amp; Research Center</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2022-10-06)</AVAILABILITY>
    <RESEARCH_USE>Genetics, Reproductive Biology, Gene Conversion, Active Genetics, Drug Metabolism, Cyp450</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155260367</CITATION_ID>
    <DESCRIPTION>rat strain in which the rat Cyp2e1 gene is humanized by insertion of a human CYP2E1 minigene (CYP2E1*) insert at the native start codon. The insert also included a CRISPR/Cas9 gene drive element to enable super-Mendelian inheritance of the modified allele when crossed to a rat expressing Cas9 in the germline. ROBUST AND EFFICIENT ACTIVE GENETICS GENE CONVERSION IN THE RAT AND MOUSE Chenyen Lai, Oscar Alvarez, Kristen Read, Don van Fossan,Christopher M Conner, Shannon Xaing-Ru Xu, Dale O. Cowley, Valentino Gantz, David R. Webb, Kurt Jarnagin URL: Doi:10.1101/2022.08.30.505951 URL: Doi:10.1101/2022.08.30.505951 
URL: URL: Doi:10.1101/2022.08.30.505951</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155260368</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Cyp3a23-3a1-Cyp3A4*-Cas9)Synb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Created by Dr. Kurt Jarnagin at Synbal, Inc.San Diego, CA, USA</ORIGINATION>
    <SOURCE>Donated to Rat Resource &amp; Research Center</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2022-10-06)</AVAILABILITY>
    <RESEARCH_USE>Genetics, Reproductive Biology, Gene Conversion, Active Genetics, Drug Metabolism, Cyp450</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155260368</CITATION_ID>
    <DESCRIPTION>rat strain in which the rat Cyp3a1 gene (Cyp3a23-3a1, RGD:628626) was inactivated by insertion of a human CYP3A4 minigene (Cyp3A4*) and the linked rat Cyp3a2 locus was simultaneously mutated by CRISPR-mediated indel introduction. Strain contains Indel 8 at the Rat 3A2 locus (55 kb away), The CYP3A4 minigene included a CRISPR/Cas9 gene drive element to enable super-Mendelian inheritance.   Strain contains and Active Genetic cassette which encodes a gRNA targeting the Rat 3A1 and 3A2 translation initiation site. ROBUST AND EFFICIENT ACTIVE GENETICS GENE CONVERSION IN THE RAT AND MOUSE Chenyen Lai, Oscar Alvarez, Kristen Read, Don van Fossan,Christopher M Conner, Shannon Xaing-Ru Xu, Dale O. Cowley, Valentino Gantz, David R. Webb, Kurt Jarnagin URL: Doi:10.1101/2022.08.30.505951 URL: Doi:10.1101/2022.08.30.505951 
URL: URL: Doi:10.1101/2022.08.30.505951</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155269039</RGD_ID>
    <STRAIN_SYMBOL>WI;WDB-&lt;i&gt;ROSA26&lt;sup&gt;tm1(H2B-tdTomato)&lt;/sup&gt;&lt;/i&gt;/Nips</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi, JAPAN</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2022-10-11)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155269039</CITATION_ID>
    <DESCRIPTION>PCR products of the human H2BC11 (H2B-6), tdTomato, splice acceptor sequence, and IRES-Neor-SV40pA were inserted into the NheI site of prROSA26-1 with an in-fusion cloning kit. The final tdTomato-H2B-6 targeting vector was linearized by SalI digestion. The vector was introduced into WDB/Nips-ES1/Nips (RGD ID:10054010) embryonic stem cells by electroporation. Targeted ES cells were injected into Crlj:WI (RGD ID: 2312504) blastocysts to produce chimeric rats. The chimeric rats were crossed with Crlj:WI rats to produce heterozygous founder rats.These rat strains are being maintained by crossing the founder rats with Crlj:WI rats. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155269040</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(CAG-ACE2)057Bryd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Deposited at &lt;a href=http://www.rrrc.us/Strain/?x=946&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2022-10-11)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00946</CITATION_ID>
    <DESCRIPTION>The human ACE2 gene was placed under control of the synthetic CAG promoter which allows ubiquitous expression of the gene. Based on droplet digital PCR analysis, the strain carries only 1 copy of the transgene. The integration site is unknown. These rats express the human ACE2 gene. The encoded protein is a functional receptor for the spike glycoprotein of several human coronaviruses including SARS-CoV-2, the causative agent of coronavirus disease-2019 (COVID-19).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155269102</RGD_ID>
    <STRAIN_SYMBOL>McwiWfsmAap:HS</STRAIN_SYMBOL>
    <FULL_NAME>Heterogeneous stock</FULL_NAME>
    <ORIGINATION>Dr. Abraham Palmer laboratory at UCSD</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155269102</CITATION_ID>
    <DESCRIPTION>This HS is maintained and distributed from Dr. Palmer's laboratory at UCSD. The colony from Wake Forest maintained by Dr. Solberg Woods's laboratory was sent to Dr. Palmer's laboratory at University of California San Diego Department of Psychiatry in 2022. The Wake Forest HS rats were derived from NMcwi:HS at the Medical College of Wisconsin and maintained at Wake Forest Baptist Medical Center starting in 2017.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155598601</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Bmal1&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Bmal1&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>155598603</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="176834431" STOP_POS="176834488" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="167399921" STOP_POS="167399978" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="178107159" STOP_POS="178107216" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="185007527" STOP_POS="185105413" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="171062181" STOP_POS="171162426" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155598601</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a  58-base pair deletion in exon 6 in the rat Bmal1 gene of Crl:SD embryos. The deletion caused a premature stop codon in exon 6 resulting in a severe truncation of the Bmal1 protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155630631</RGD_ID>
    <STRAIN_SYMBOL>CD-&lt;i&gt;Ctns&lt;sup&gt;em2Vjupk&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Vernon Jansen Unit, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ctns&lt;sup&gt;em2Vjupk&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>155630632</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="58300069" STOP_POS="58315725" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="57801551" STOP_POS="57817213" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="59749250" STOP_POS="59772475" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="59488895" STOP_POS="59503993" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="60060254" STOP_POS="60075352" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155630631</CITATION_ID>
    <DESCRIPTION>The mutant rat was produced by injecting  Crl:CD(SD)  zygotes with gRNA +Cas9 ribonucleoprotein complex targeting exon 3 of rat Ctns. The founder of this strain possessed  a 2-bp insertion which results in frameshift and pre-mature stop truncated protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155630633</RGD_ID>
    <STRAIN_SYMBOL>CD-&lt;i&gt;Ctns&lt;sup&gt;em3Vjupk&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Vernon Jansen Unit, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ctns&lt;sup&gt;em3Vjupk&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>155630634</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="58300069" STOP_POS="58315725" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="57801551" STOP_POS="57817213" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="59749250" STOP_POS="59772475" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="59488895" STOP_POS="59503993" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="60060254" STOP_POS="60075352" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155630633</CITATION_ID>
    <DESCRIPTION>The mutant rat was produced by injecting  Crl:CD(SD)  zygotes with gRNA +Cas9 ribonucleoprotein complex targeting exon 3 of rat Ctns. The founder of this strain possessed  a 8-bp insertion which results in frameshift and pre-mature stop truncated protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155630635</RGD_ID>
    <STRAIN_SYMBOL>CD-&lt;i&gt;Ctns&lt;sup&gt;em4Vjupk&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Vernon Jansen Unit, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ctns&lt;sup&gt;em4Vjupk&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>155630636</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="58300069" STOP_POS="58315725" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="57801551" STOP_POS="57817213" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="59749250" STOP_POS="59772475" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="59488895" STOP_POS="59503993" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="60060254" STOP_POS="60075352" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155630635</CITATION_ID>
    <DESCRIPTION>The mutant rat was produced by injecting  Crl:CD(SD)  zygotes with gRNA +Cas9 ribonucleoprotein complex targeting exon 3 of rat Ctns. The founder of this strain possessed  a 7-bp deletion which results in frameshift and pre-mature stop truncated protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155631259</RGD_ID>
    <STRAIN_SYMBOL>Taiep</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Departamento de Ciencias Fisiologicas, Universidad Autonoma de Puebla, Mexico.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155631259</CITATION_ID>
    <DESCRIPTION>These mutants were found in Sprague-Dawley rats at University of Puebla in 1989. A spontaneous neurological mutation was detected in a colony of Sprague Dawley rats. The animals developed a progressive neurological syndrome characterized by tremor (which appeared at the age of 1 month), ataxia (at 4 months), immobility episodes (after 5-6 months), audiogenic seizures and hindlimb paralysis (after 10 months). Cross breeding experiments indicate that this is an autosomal recessive mutation, The rat line was named taiep (tremor, ataxia, tonic immobility episodes, epilepsy and paralysis) rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155631261</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Brca1&lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Kyoto University
Institute of Laboratory Animals Graduate School of Medicine Yoshida Konoe-cho, Skyo-ku, Kyoto 606-8501
JAPAN</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Brca1&lt;sup&gt;em1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>155631262</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="86917693" STOP_POS="86978012" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="86417441" STOP_POS="86477762" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="89394821" STOP_POS="89455093" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="89192653" STOP_POS="89252760" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="90513630" STOP_POS="90572676" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155631261</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to generate this mutant; sgRNA+Cas9 targeting exon 4 of rat Brca1was injected to fertilized eggs of Jcl:SD rats (Clea Japan). The founder animal carried c.188T&gt;A (p.L63X) was mated to closed-colony Jcl:SD rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155631278</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Flna&lt;sup&gt;em1Ang&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Transgenic Rats and ImmunoPhenomic (TRIP) facility in Nantes (France).</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Flna&lt;sup&gt;em1Ang&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>155631280</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="157159051" STOP_POS="157185559" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="152007758" STOP_POS="152034266" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="156460785" STOP_POS="156487245" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="152200936" STOP_POS="152227391" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="160362334" STOP_POS="160385626" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155631278</CITATION_ID>
    <DESCRIPTION>This mutant strain was generated by electroporating rat zygotes with  CRISPRs/Cas9 system targeting exon12 of rat Flna into Crl:SD embryo. This mutant strain carries P637Q knock in the gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155631285</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(MECP2 )Chnsr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155631285</CITATION_ID>
    <DESCRIPTION>PAC671D9 (AF031078) DNA containing all the exons of human MECP2 was injected to SD embryos to generate MECP2 duplication rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155631289</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Pde6b&lt;sup&gt;em1Cgen&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Cyagen Biosciences Inc, Santa Clara, CA, USA</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pde6b&lt;sup&gt;em1Cgen&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>155631290</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="1468302" STOP_POS="1511435" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="1323310" STOP_POS="1366450" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="2328690" STOP_POS="2371913" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="2327104" STOP_POS="2370811" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="1871037" STOP_POS="1914170" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155631289</CITATION_ID>
    <DESCRIPTION>This mutant strain was generated by microinjecting CRISPRs/Cas9 system targeting rat Pde6b. Pde6b  knock out rat was successfully created.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155631293</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Pde3a&lt;sup&gt;em1Bdr&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbr'ck-Center for Molecular Medicine (MDC) in the Helmholtz Association, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pde3a&lt;sup&gt;em1Bdr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>155631294</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="175904276" STOP_POS="176170531" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="174172804" STOP_POS="174443944" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="175431904" STOP_POS="175703844" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="239659270" STOP_POS="239921900" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="178658896" STOP_POS="178930417" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155631293</CITATION_ID>
    <DESCRIPTION>The rat mutant was generated by pronuclear microinjection of Sprague-Dawley rat zygotes with a mixture of Cas9/Cas9  system to target the region in the rat Pde3a gene homologous to the human T445N mutation. The rat model exhibits a 9-bp deletion within the conserved 15-bp regulatory  region that  leads to the loss of 3 amino acids (aa 441-443 analogous to human PDE3A aa 444-446).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155631295</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Pde3a&lt;sup&gt;em2Bdr&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbr'ck-Center for Molecular Medicine (MDC) in the Helmholtz Association, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pde3a&lt;sup&gt;em2Bdr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>155631296</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="175904276" STOP_POS="176170531" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="174172804" STOP_POS="174443944" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="175431904" STOP_POS="175703844" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="239659270" STOP_POS="239921900" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="178658896" STOP_POS="178930417" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155631295</CITATION_ID>
    <DESCRIPTION>The rat mutant was generated by pronuclear microinjection of Sprague-Dawley rat zygotes with a mixture of Cas9/Cas9  system to target the region in the rat Pde3a gene homologous to the human T445N mutation. The rat model exhibits a 20-bp deletion within the conserved 15-bp regulatory  region that  leads to n a frameshift and thus in a truncated and functionally deleted protein (functional DEL).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155631298</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Pde3a&lt;sup&gt;em3Bdr&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Max-Delbr'ck-Center for Molecular Medicine (MDC) in the Helmholtz Association, Berlin, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pde3a&lt;sup&gt;em3Bdr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>155631299</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="175904276" STOP_POS="176170531" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="174172804" STOP_POS="174443944" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="175431904" STOP_POS="175703844" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="239659270" STOP_POS="239921900" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="178658896" STOP_POS="178930417" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155631298</CITATION_ID>
    <DESCRIPTION>The rat mutant was generated by pronuclear microinjection of Sprague-Dawley rat zygotes with a mixture of Cas9/Cas9  system to target the catalytic domain in the rat Pde3a gene. The model has a  carriesa CGT to TGD missense mutation and results in R862C  substitutions in the protein</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155641233</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Rho*P23H)1Lav</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;,&lt;a href=http://www.rrrc.us/Strain/?x=639&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://ophthalmology.ucsf.edu/matthew-lavail-phd-retinal-degeneration-rat-model-resource/&gt; Retinal Degeneration Rat Model Resource &lt;/a&gt;,&lt;a href=http://www.rrrc.us/Strain/?x=639&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155641233</CITATION_ID>
    <DESCRIPTION>This transgenic strain carries a copy of mouse Rhodopsin gene with a proline to histidine substitution at codon 23 (c.68C&gt;A).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155641235</RGD_ID>
    <STRAIN_SYMBOL>WMI/Eer</STRAIN_SYMBOL>
    <FULL_NAME>WKY most immobile</FULL_NAME>
    <ORIGINATION>Dept. of Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, Chicago, Illinois</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=973&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00973</CITATION_ID>
    <DESCRIPTION>3 pairs of WKY males and females with highest immobility and lowest climbing scores in the forced swim test were mated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155641237</RGD_ID>
    <STRAIN_SYMBOL>WLI/Eer</STRAIN_SYMBOL>
    <FULL_NAME>WKY least immobile</FULL_NAME>
    <ORIGINATION>Dept. of Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, Chicago, Illinois</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=967&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00967</CITATION_ID>
    <DESCRIPTION>3 pairs of WKY males and females with lowest immobility and highest climbing scores in the forced swim test were mated.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155641239</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;rs65785750-rs13452155&lt;/i&gt;)/OpazRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Massachusetts. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=612&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2022-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00612</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing SS/JrHsd and SR/JrHsd parental strains</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155641240</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;rs65785750-rs106808193&lt;/i&gt;)/OpazRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Massachusetts. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=613&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2022-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="106658272" STOP_POS="140009902" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="101612333" STOP_POS="134724733" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="105452223" STOP_POS="140120264" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00613</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing SS/JrHsd and SR/JrHsd parental strains</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155641241</RGD_ID>
    <STRAIN_SYMBOL>SS.SR-(&lt;i&gt;rs105019230-D17Rat44&lt;/i&gt;)/OpazRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Massachusetts. </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=616&gt;Rat Resource and Research Center&lt;/a&gt;.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2022-11-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="59237618" STOP_POS="75066472" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="54542464" STOP_POS="70156904" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="57343133" STOP_POS="73981731" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="75653544" STOP_POS="75653670" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="81612361" STOP_POS="81612488" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00616</CITATION_ID>
    <DESCRIPTION>Congenic strain which was generated using the speed congenic strategy by backcrossing SS/JrHsd and SR/JrHsd parental strains.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155641245</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Oprm1-icre)1Ottc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This rat was produced by &lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=975&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2023-12-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00975</CITATION_ID>
    <DESCRIPTION>Targeted knock-in adding a T2A-iCre to the Oprm1 (mu opioid receptor) in this cre recombinase reporter SD rat</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155641246</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(Cx3cr1-cre/ERT2)3OttcRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=927&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155641246</CITATION_ID>
    <DESCRIPTION>The transgene of LE-Tg(Cx3cr1-cre)3Ottc (RGD: 13441557) was crossed onto  Fischer344 background by backcrossing  the hybrid to Fischer344 and select for the presence of transgene. The donor LE transgenic  was generated by microinjection of LE embyos with a BAC DNA containing the Cx3cr1-cre/ERT2 transgene which is composed of cre/ERT2 recombinase gene driven by the rat genomic Cx3cr1promoter.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155641247</RGD_ID>
    <STRAIN_SYMBOL>F344.LE-ROSA26 &lt;sup&gt;em1(LTR-nLuc)Ottc&lt;/sup&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>now deposited at &lt;a href=http://www.rrrc.us/Strain/?x=926&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00926</CITATION_ID>
    <DESCRIPTION>The mutated ROSA26 locus  of  LE-(ROSA)26 em1(LTR-nLuc)Ottc (RGD:13208223) was crossed onto  Fischer344 background by backcrossing  the hybrid to Fischer344 and select for the presence of mutated locus. The LE donor is CRISPR/Case9 knock-in strain that  has cre recombinase-dependent expression of nanoluciferase under the control of HIV LTR promoter inserted to the rat ROSA26 locus. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155641248</RGD_ID>
    <STRAIN_SYMBOL>SD-ROSA26&lt;sup&gt;em1(LTR-nLuc)Ottc&lt;/sup&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was created by &lt;a href=http://irp.drugabuse.gov/OTTC/index.php&gt;Optogenetics and Transgenic Technology Core&lt;/a&gt;.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=925&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00925</CITATION_ID>
    <DESCRIPTION>The CRISPR/Case9 knock-in rats have cre recombinase-dependent expression of  nanoluciferase under the control of HIV LTR promoter inserted to the rat ROSA26 locus. ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155641251</RGD_ID>
    <STRAIN_SYMBOL>F344-Tg(CAG-ACE2)057BrydRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=946&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=946&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2022-11-04)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00946</CITATION_ID>
    <DESCRIPTION>The human ACE2 gene was placed under control of the synthetic CAG promoter which allows ubiquitous expression of the gene. Based on droplet digital PCR analysis, the strain carries only 1 copy of the transgene. The integration site is unknown. These rats express the human ACE2 gene. The encoded protein is a functional receptor for the spike glycoprotein of several human coronaviruses including SARS-CoV-2, the causative agent of coronavirus disease-2019 (COVID-19).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155663364</RGD_ID>
    <STRAIN_SYMBOL>SD-Del(Yp)1Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2022-11-11)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155663364</CITATION_ID>
    <DESCRIPTION>CRISPR guide RNAs flanking Sry4a and Sry1 (Sry) on the Y-chromosome were injected into Crl:SD strain embryos. Chromosomal deletions have not been explicitly defined.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155663365</RGD_ID>
    <STRAIN_SYMBOL>CD-Tg(RNECO-180E22)208Arno</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Art Arnold laboratory, University of California Los Angeles</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155663365</CITATION_ID>
    <DESCRIPTION>This transgenic model line 208 was made by injecting bacterial artificial chromosome (BAC) RNECO-180E22, into Crl:CD(SD) strain embryos. The BAC clone RNECO-180E22, a kind gift of Helen Skaletsky, is  derived from Rattus norvegicus strain SHR chromosome Y.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155663366</RGD_ID>
    <STRAIN_SYMBOL>CD-Tg(RNECO-180E22)424Arno</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Art Arnold laboratory, University of California Los Angeles</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155663366</CITATION_ID>
    <DESCRIPTION>This transgenic model line 424 was made by injecting bacterial artificial chromosome (BAC) RNECO-180E22, into Crl:CD(SD) strain embryos. The BAC clone RNECO-180E22, a kind gift of Helen Skaletsky, is  derived from Rattus norvegicus strain SHR chromosome Y.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155663367</RGD_ID>
    <STRAIN_SYMBOL>CD-Tg(RNECO-180E22)733Arno</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Art Arnold laboratory, University of California Los Angeles</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155663367</CITATION_ID>
    <DESCRIPTION>This transgenic model line 733 was made by injecting bacterial artificial chromosome (BAC) RNECO-180E22, into Crl:CD(SD) strain embryos. The BAC clone RNECO-180E22, a kind gift of Helen Skaletsky, is  derived from Rattus norvegicus strain SHR chromosome Y.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155663368</RGD_ID>
    <STRAIN_SYMBOL>CD-Tg(RNECO-180E22)737Arno</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Art Arnold laboratory, University of California Los Angeles</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155663368</CITATION_ID>
    <DESCRIPTION>This transgenic model line 737 was made by injecting bacterial artificial chromosome (BAC) RNECO-180E22, into Crl:CD(SD) strain embryos. The BAC clone RNECO-180E22, a kind gift of Helen Skaletsky, is  derived from Rattus norvegicus strain SHR chromosome Y.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155663559</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gcg&lt;sup&gt;tm1(iCre)Lrina&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was created by Dr. Linda Rinaman PhD at Florida State University</ORIGINATION>
    <SOURCE>Strain has been deposited to RRRC(RRRC:00983, RGD:155663560)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2022-11-28)</AVAILABILITY>
    <RESEARCH_USE>Neuroscience, diabetes, metabolic syndrome, obesity, anxiety</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155663559</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 technology was used to insert an IRES for iCre expression after the final coding sequence of exon 6 of the rat Gcg gene, before the 3' UTR.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155663560</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gcg&lt;sup&gt;tm1(iCre)Lrina&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was created by Dr.  Linda Rinaman PhD at Florida State University, and now deposited at  &lt;a href=http://www.rrrc.us/Strain/?x=983&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=983&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Neuroscience, diabetes, metabolic syndrome, obesity, anxiety</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00983</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 technology was used to insert an IRES for iCre expression after the final coding sequence of exon 6 of the rat Gcg gene, before the 3' UTR.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155663675</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(ChAT-cre)5.1Deis</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=658&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2022-12-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155663675</CITATION_ID>
    <DESCRIPTION>Cre gene was introduced immediately before the ATG of the mouse choline acetyltransferase (Chat) gene in BAC RP23-246B12. This strain is estimated to carry 6 copies of the transgene at the integration site.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782877</RGD_ID>
    <STRAIN_SYMBOL>SHRSP/NgskMeltw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Life Sciences in Molecular Embryological &amp; DNA Methylation Lab at National Chung Hsing University, Taiwan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2022-12-07)</AVAILABILITY>
    <RESEARCH_USE>Chronic kidney disease; Hypertension; Proteinuria; Stroke</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782877</CITATION_ID>
    <DESCRIPTION>Imported from Kyoto University in 2010, now maintained at Molecular Embryological &amp; DNA Methylation Lab at National Chung Hsing University, Taiwan.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782879</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat26-D3Mgh30)&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="91609794" STOP_POS="151080115" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="95176716" STOP_POS="158417703" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="101798743" STOP_POS="164637442" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="90573349" STOP_POS="153262477" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782879</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-3BN/Mcwi, rats from F1 were intercrossed and genotyped to select the congenic strain carrying  introgressed chromosome 3 from SS to BN.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782880</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Arb3-D3Rat93)( D3Rat78-D3Rat1)&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="32287733" STOP_POS="97485741" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="165398679" STOP_POS="165398925" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="77029705" STOP_POS="77029923" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="144938577" STOP_POS="168026850" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="7140238" STOP_POS="79875036" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="152506537" STOP_POS="176418101" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="12491255" STOP_POS="86583789" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="159184511" STOP_POS="180128021" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="7547341" STOP_POS="75411665" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="146830639" STOP_POS="170016653" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782880</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-3BN/Mcwi, rats from F1 were intercrossed and genotyped to select the congenic strain carrying introgressed chromosome 3 from SS to BN.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782881</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat222-D3Rat218)&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="99740665" STOP_POS="145746396" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="79285268" STOP_POS="125293758" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="82222060" STOP_POS="131051652" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="88924451" STOP_POS="137527624" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="77727907" STOP_POS="126079458" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782881</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-3BN/Mcwi, rats from F1 were intercrossed and genotyped to select the congenic strain carrying  introgressed chromosome 3 from SS to BN.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782883</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat222-D3Got42)&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="100822652" STOP_POS="111696569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="80367329" STOP_POS="91241711" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="83300114" STOP_POS="94807225" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="89999731" STOP_POS="101431576" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="78808731" STOP_POS="90197018" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782883</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed withSS-Chr3BN.SS-(D3Rat222-D3Rat218)/Mcwi (jq strain)
, rats from F1 were backcrossed to SS/JrHsdMcwi  to select   the congenic strains carrying  subregion of jq to BN chromosome 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782884</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat222-D3Mco33)&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="100822652" STOP_POS="117752947" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="80367329" STOP_POS="97298391" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="83300114" STOP_POS="101902734" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="89999731" STOP_POS="108500874" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="78808731" STOP_POS="96185250" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782884</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed withSS-Chr3BN.SS-(D3Rat222-D3Rat218)/Mcwi (jq strain), rats from F1 were backcrossed to SS/JrHsdMcwi  to select   the congenic strains carrying  subregion of jq to BN chromosome 3..</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782885</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-(D3Rat36-D3Rat156)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="100822652" STOP_POS="143966100" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="80367329" STOP_POS="123513386" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="83300114" STOP_POS="129166212" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="89999731" STOP_POS="135651688" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="78808731" STOP_POS="124269028" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782885</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-3BN/Mcwi, rats from F1 were intercrossed and genotyped to select the congenic strain carrying  introgressed chromosome 3 from SS to BN.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782907</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Synpo&lt;sup&gt;em1Kmh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by  Masaaki (Masa) Kuwajima, PhD   (masa@mail.clm.utexas.edu). Strains were produced at Kristen Harris Laboratory, Department of Neuroscience, Center for Learning and Memory, University of Texas at Austin</ORIGINATION>
    <SOURCE>This strain is deposited at &lt;a href=http://www.rrrc.us/Strain/?x=964&gt;Rat Resource and Research Center&lt;/a&gt;,</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2025-05-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00964</CITATION_ID>
    <DESCRIPTION>Exons 2 and 3 were deleted to eliminate all known Synaptopodin isoforms in rat  by CRISPR/Cas9 system in the outbred LE embryos.  It is similar to RRRC strain #1025 (LE-Synpoem2Kmh) (RGD:616335891), has a different mutation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782909</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-(D3Arb22 - D3Mgh30)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="135287266" STOP_POS="151080115" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="142174160" STOP_POS="158417703" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="148587087" STOP_POS="164637442" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="136541408" STOP_POS="153262477" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782909</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-3BN/Mcwi, rats from F1 were intercrossed and genotyped to select the congenic strain carrying  introgressed chromosome 3 from SS to BN.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782910</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-(D3Rat154 - D3Mgh30)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="144739217" STOP_POS="144739363" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="124286544" STOP_POS="151080115" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="129958906" STOP_POS="158417703" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="136438243" STOP_POS="164637442" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="125060606" STOP_POS="153262477" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782910</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-3BN/Mcwi, rats from F1 were intercrossed and genotyped to select the congenic strain carrying  introgressed chromosome 3 from SS to BN.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782911</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-(D3Rat26 - D3Rat14)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="147308445" STOP_POS="147308590" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="91609794" STOP_POS="126854898" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="95176716" STOP_POS="132567457" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="101798743" STOP_POS="139030095" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="90573349" STOP_POS="127698688" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782911</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-3BN/Mcwi, rats from F1 were intercrossed and genotyped to select the congenic strain carrying  introgressed chromosome 3 from SS to BN.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782912</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-(D3Rat26 - D3Rat5)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="167012663" STOP_POS="167012824" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="91609794" STOP_POS="146592883" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="95176716" STOP_POS="154416795" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="101798743" STOP_POS="161185522" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="90573349" STOP_POS="148643323" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782912</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-3BN/Mcwi, rats from F1 were intercrossed and genotyped to select the congenic strain carrying  introgressed chromosome 3 from SS to BN.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782913</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-(D3Rat12 - D3Mgh30)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="147616381" STOP_POS="147616569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="127162703" STOP_POS="151080115" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="132875075" STOP_POS="158417703" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="139333901" STOP_POS="164637442" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="127988419" STOP_POS="153262477" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782913</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-3BN/Mcwi, rats from F1 were intercrossed and genotyped to select the congenic strain carrying  introgressed chromosome 3 from SS to BN.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782914</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-(D3Rat217- D3Mgh30)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="153746295" STOP_POS="153746477" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="133293002" STOP_POS="151080115" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="140077066" STOP_POS="158417703" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="146499815" STOP_POS="164637442" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="134491977" STOP_POS="153262477" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782914</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-3BN/Mcwi, rats from F1 were intercrossed and genotyped to select the congenic strain carrying  introgressed chromosome 3 from SS to BN.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155782915</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-(D3Rat26 - D3Rat217)/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="153746295" STOP_POS="153746477" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="91609794" STOP_POS="133293184" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="95176716" STOP_POS="140077247" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="101798743" STOP_POS="146499996" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="90573349" STOP_POS="134492553" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155782915</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed with SS-3BN/Mcwi, rats from F1 were intercrossed and genotyped to select the congenic strain carrying  introgressed chromosome 3 from SS to BN.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791425</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 3&lt;sup&gt;BN&lt;/sup&gt;.&lt;i&gt;Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790633</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66398567" STOP_POS="66398585" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791425</CITATION_ID>
    <DESCRIPTION>The IL2Rg gene was targeted in the SS/JrHsdMcwi rat by
TALEN injection into single-cell rat embryos. Once established, a homozygous (RGD:12790632)  female rat from the SSIL2Rg line was intercrossed with a homozygous SS.BN3 (RGD:1358154) male to yield heterozygous SS.BN3IL2Rg offspring (F1),
followed by brother-sister mating to yield homozygous SS.
BN3IL2Rg offspring by the F3 generation. This strain is Immunodeficient Ilrg (X-SCID) mutant consomic line.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791426</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat26-D3Rat218)&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791426</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed withSS-Chr3BN.SS-(D3Rat222-D3Rat218)/Mcwi (jq strain), rats from F1 were backcrossed to SS/JrHsdMcwi  to select   the congenic strains carrying  subregion of jq to BN chromosome 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791427</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat160-D3Rat218)&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791427</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed withSS-Chr3BN.SS-(D3Rat222-D3Rat218)/Mcwi (jq strain), rats from F1 were backcrossed to SS/JrHsdMcwi  to select   the congenic strains carrying  subregion of jq to BN chromosome 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791428</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat164-D3Rat218)&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791428</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed withSS-Chr3BN.SS-(D3Rat222-D3Rat218)/Mcwi (jq strain), rats from F1 were backcrossed to SS/JrHsdMcwi  to select   the congenic strains carrying  subregion of jq to BN chromosome 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791429</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Mgh13-D3Rat218)&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791429</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed withSS-Chr3BN.SS-(D3Rat222-D3Rat218)/Mcwi (jq strain), rats from F1 were backcrossed to SS/JrHsdMcwi  to select   the congenic strains carrying  subregion of jq to BN chromosome 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791430</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat 86 to D3Rat218 )&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin. </ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791430</CITATION_ID>
    <DESCRIPTION>SS/JrHsdMcwi were crossed withSS-Chr3BN.SS-(D3Rat222-D3Rat218)/Mcwi (jq strain), rats from F1 were backcrossed to SS/JrHsdMcwi  to select   the congenic strains carrying  subregion of jq to BN chromosome 3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791431</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Arb3-D3Rat93)( D3Rat78-D3Rat1).Il2rg&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790633</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="32287733" STOP_POS="97485741" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="165398679" STOP_POS="165398925" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="77029705" STOP_POS="77029923" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="144938577" STOP_POS="168026850" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="7140238" STOP_POS="79875036" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="152506537" STOP_POS="176418101" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="12491255" STOP_POS="86583789" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="159184511" STOP_POS="180128021" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="7547341" STOP_POS="75411665" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="146830639" STOP_POS="170016653" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791431</CITATION_ID>
    <DESCRIPTION>Immunodeficient congenic line developed by intercross of SS-Chr 3BN.SS-(D3Arb3-D3Rat93)( D3Rat78-D3Rat1)/Mcwi (RGD:155782880) withSS-Il2rgem1Mcwi (RGD:12790632) to  breed  the Il2rg (X-SCID) mutation into this background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791432</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat26-D3Mgh30).Il2rg&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790633</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="91609794" STOP_POS="151080115" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="95176716" STOP_POS="158417703" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="101798743" STOP_POS="164637442" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="90573349" STOP_POS="153262477" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791432</CITATION_ID>
    <DESCRIPTION>Immunodeficient congenic line developed by intercross of SS-Chr3BN.SS-(D3Rat26-D3Mgh30)/Mcwi(RGD:155782879)
withSS-Il2rgem1Mcwi (RGD:12790632) to  breed  the Il2rg (X-SCID) mutation into this background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791433</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat222-D3Rat218).Il2rg&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790633</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="99740665" STOP_POS="145746396" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="79285268" STOP_POS="125293758" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="82222060" STOP_POS="131051652" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="88924451" STOP_POS="137527624" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="77727907" STOP_POS="126079458" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791433</CITATION_ID>
    <DESCRIPTION>Immunodeficient congenic line developed by intercross of SS-Chr3BN.SS-(D3Rat222-D3Rat218)/Mcwi(RGD:155782881)
withSS-Il2rgem1Mcwi (RGD:12790632) to  breed  the Il2rg (X-SCID) mutation into this background.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791434</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat222-D3Got42).Il2rg&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790633</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="99740665" STOP_POS="111696569" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="79285268" STOP_POS="91241711" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="82222060" STOP_POS="94807225" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="88924451" STOP_POS="101431576" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="77727907" STOP_POS="90197018" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791434</CITATION_ID>
    <DESCRIPTION>Immunodeficient subcongenic line developed by intercross SS-Chr 3BN.SS-(D3Rat222-D3Rat218).Il2rgem1Mcwi/Mcwi (RGD:155791433) heterozygous congenic, Il2rg null mutant (X-SCID) lines. .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791435</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat222-D3Mco33).Il2rg&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790633</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="99740665" STOP_POS="117752947" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="79285268" STOP_POS="97298391" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="82222060" STOP_POS="101902734" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="88924451" STOP_POS="108500874" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="77727907" STOP_POS="96185250" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791435</CITATION_ID>
    <DESCRIPTION>Immunodeficient subcongenic line developed by intercross SS-Chr 3BN.SS-(D3Rat222-D3Rat218).Il2rgem1Mcwi/Mcwi (RGD:155791433) heterozygous congenic, Il2rg null mutant (X-SCID) lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791436</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat26-D3Rat218).Il2rg&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790633</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="145746177" STOP_POS="145746396" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="91609794" STOP_POS="125293758" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="95176716" STOP_POS="131051652" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="101798743" STOP_POS="137527624" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="90573349" STOP_POS="126079458" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791436</CITATION_ID>
    <DESCRIPTION>Immunodeficient subcongenic line developed by intercross SS-Chr 3BN.SS-(D3Rat222-D3Rat218).Il2rgem1Mcwi/Mcwi (RGD:155791433) heterozygous congenic, Il2rg null mutant (X-SCID) lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791437</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat160-D3Rat218).Il2rg&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790633</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="138688338" STOP_POS="145746396" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="118235304" STOP_POS="125293758" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="123558901" STOP_POS="131051652" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="130058246" STOP_POS="137527624" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="118692155" STOP_POS="126079458" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791437</CITATION_ID>
    <DESCRIPTION>Immunodeficient subcongenic line developed by intercross SS-Chr 3BN.SS-(D3Rat222-D3Rat218).Il2rgem1Mcwi/Mcwi (RGD:155791433) heterozygous congenic, Il2rg null mutant (X-SCID) lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791438</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat164-D3Rat218).Il2rg&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790633</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66398567" STOP_POS="66398585" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791438</CITATION_ID>
    <DESCRIPTION>Immunodeficient subcongenic line developed by intercross SS-Chr 3BN.SS-(D3Rat222-D3Rat218).Il2rgem1Mcwi/Mcwi (RGD:155791433) heterozygous congenic, Il2rg null mutant (X-SCID) lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791439</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Mgh13-D3Rat218).Il2rg&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790633</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66398567" STOP_POS="66398585" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791439</CITATION_ID>
    <DESCRIPTION>Immunodeficient subcongenic line developed by intercross SS-Chr 3BN.SS-(D3Rat222-D3Rat218).Il2rgem1Mcwi/Mcwi (RGD:155791433) heterozygous congenic, Il2rg null mutant (X-SCID) lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791440</RGD_ID>
    <STRAIN_SYMBOL>SS-Chr 3&lt;sup&gt;BN&lt;/sup&gt;.SS-&lt;i&gt;(D3Rat 86-D3Rat218).Il2rg&lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by Dr. Amit Joshi Medical College of Wisconsin.</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu for availability.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il2rg&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12790633</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66398567" STOP_POS="66398585" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791440</CITATION_ID>
    <DESCRIPTION>Immunodeficient subcongenic line developed by intercross SS-Chr 3BN.SS-(D3Rat222-D3Rat218).Il2rgem1Mcwi/Mcwi (RGD:155791433) heterozygous congenic, Il2rg null mutant (X-SCID) lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155791645</RGD_ID>
    <STRAIN_SYMBOL>BN/NOlaHsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Harlan Sprague Dawley, Inc., Indianapolis, IN</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155791645</CITATION_ID>
    <DESCRIPTION>In 1980, from National Institutes of Health, Bethesda, USA (BN/SsN, RGD:61115)
 to OLAC (now Envigo).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155804258</RGD_ID>
    <STRAIN_SYMBOL>BN/Rij</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155804258</CITATION_ID>
    <DESCRIPTION>inbred Brown Norway (BN) rat strain produced in the Rijswijk colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155888488</RGD_ID>
    <STRAIN_SYMBOL>MWF/SimwMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin, &lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2023-02-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155888488</CITATION_ID>
    <DESCRIPTION>A colony of inbred Munich Wistar Fromter (MWF) rats maintained at the Medical College of Wisconsin since 2014, more than 20 breeding generations. Imported from a colony at Indiana University maintained more than 20 years; originally obtained from Roland Blatz at the University of California, San Diego</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155888489</RGD_ID>
    <STRAIN_SYMBOL>MWF/Simw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Indiana University</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2023-02-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_155888489</CITATION_ID>
    <DESCRIPTION>A colony of Munich Wistar Fromter (MWF) rats maintained at Indiana University over 20 years, originally obtained from Roland Blatz at the University of California, San Diego</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155900755</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Chrna6&lt;sup&gt;em1Slot&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>The laboratory  has deposited these strains with the &lt;a href=http://www.rrrc.us/Strain/?x=984&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2023-02-09)</AVAILABILITY>
    <RESEARCH_USE>Drug Addiction, Nicotine/Tobacco Addiction</RESEARCH_USE>
    <ALLELES>Chrna6&lt;sup&gt;em1Slot&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>155900756</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="71400615" STOP_POS="71407315" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="64697741" STOP_POS="64704441" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="68860018" STOP_POS="68866718" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="68486608" STOP_POS="68493308" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="69012201" STOP_POS="69018901" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00984</CITATION_ID>
    <DESCRIPTION>Using CRISPR/Cas9 genomic engineering in rats via homologous end-joining in fertilized embryos, we have knocked'in a humanized CHRNA6 3'UTR in place of the natural CHRNA6 3'UTR of the Sprague Dawley rat line. This new genetically modified CHRNA6C123G humanized rat line carries a  homozygous GG nucleotide modification at position 123 within the CHRNA6 gene 3'UTR.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>155900757</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Chrna6&lt;sup&gt;em2Slot&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>The laboratory  has deposited these strains with the &lt;a href=http://www.rrrc.us/Strain/?x=985&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2023-12-19)</AVAILABILITY>
    <RESEARCH_USE>Drug Addiction, Nicotine/Tobacco Addiction</RESEARCH_USE>
    <ALLELES>Chrna6&lt;sup&gt;em2Slot&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>155900759</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="16" START_POS="71400615" STOP_POS="71407315" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="16" START_POS="64697741" STOP_POS="64704441" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="16" START_POS="68860018" STOP_POS="68866718" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="16" START_POS="68486608" STOP_POS="68493308" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="16" START_POS="69012201" STOP_POS="69018901" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00985</CITATION_ID>
    <DESCRIPTION>Using CRISPR/Cas9 genomic engineering in rats via homologous end-joining in fertilized embryos, we have knocked'in a humanized CHRNA6 3'UTR in place of the natural CHRNA6 3'UTR of the Sprague Dawley rat line. This new genetically modified CHRNA6C123G humanized rat line carries a homozygous CC nucleotide modification at position 123 within the CHRNA6 gene 3'UTR.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156212871</RGD_ID>
    <STRAIN_SYMBOL>HSRA/Ummc</STRAIN_SYMBOL>
    <FULL_NAME>heterogeneous stock-derived renal agenesis rat</FULL_NAME>
    <ORIGINATION>Michael Garrett, University of Mississippi Medical Center</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2023-02-14)</AVAILABILITY>
    <RESEARCH_USE>Renal agenesis, CAKUT, altered neprhogenesis</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156212871</CITATION_ID>
    <DESCRIPTION>An inbred strain derived from the Heterogeneous Stock by selective inbreeding more than 20 generations for spontaneous renal agenesis.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156340304</RGD_ID>
    <STRAIN_SYMBOL>MWF/HsdMcwi</STRAIN_SYMBOL>
    <FULL_NAME>Munich Wistar Fromter</FULL_NAME>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156340304</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of from substrain of Munich Wistar stock, inbred by Harlan Sprague Dawley and  now maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156354230</RGD_ID>
    <STRAIN_SYMBOL>PVG/SeacMcwi</STRAIN_SYMBOL>
    <FULL_NAME>Piebald Virol Glaxo</FULL_NAME>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2024-08-06)</AVAILABILITY>
    <RESEARCH_USE>Immunology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156354230</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of  from Seac Yoshitomi, LTD., Fukuoka, Japan. and maintained at Medical College of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156362762</RGD_ID>
    <STRAIN_SYMBOL>RCS/LavRrrcMcwi</STRAIN_SYMBOL>
    <FULL_NAME>royal college of surgeons rat</FULL_NAME>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2024-08-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156362762</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of from RCS/LavRrrc and maintained at Medical College of Wisconsin. Originally developed before 1965 by Sidman from stock obtained from Sorsby of the Royal College of Surgeons, London. Then to University of California- San Francisco, School of Medicine, deposited to Rat Resource &amp; Research Center.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156368567</RGD_ID>
    <STRAIN_SYMBOL>BDIX/NemOdaMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2024-08-06)</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156368567</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of from BDIX/NemOda and maintained at Medical college of Wisconsin. This strain was maintained in Germany and was transferred to Japan by Dr. Tanaka of Aichi Cancer Center. Thereafter, this strain was transferred to Research Institute of Environmental Medicine, Nagoya University in 1973 and to Department of Agricultural, Nagoya University in 1992.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156403001</RGD_ID>
    <STRAIN_SYMBOL>BUF/MnaMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2024-08-06)</AVAILABILITY>
    <RESEARCH_USE>Cancer; Urology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156403001</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of from BUF/Mna and maintained at Medical College of Wisconsin. BUF strain originated from Heston 1946 from Buffalo stock of H. Morris. To NIH in 1950 at F10.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156406412</RGD_ID>
    <STRAIN_SYMBOL>HTX/KyoMcwi</STRAIN_SYMBOL>
    <FULL_NAME>hydrocephalus texas</FULL_NAME>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2024-08-06)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156406412</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of from  HTX/Kyo and maintained at Medical College of Wisconsin.1981 by Kohn from institutional albino rats of unknown origin at University of Texas. From Juntendo University to Kyoto University in 1992.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156420138</RGD_ID>
    <STRAIN_SYMBOL>MR/HarMcwi</STRAIN_SYMBOL>
    <FULL_NAME>Maudsely reactive</FULL_NAME>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156420138</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of MR/Har now maintained at Medical College of Wisconsin. This strain has been selected for high open-field defecation (a test of emotional reactivity). The underlying genetic basis for this phenotype is not known. Originally selected by Broadhurst in 1954 for high open-field defacation (OFD) response in an open field. By Broadhurst to Harrington at the University of Northern Iowa at generation 25 in 1965.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156420139</RGD_ID>
    <STRAIN_SYMBOL>MNS/NMcwi</STRAIN_SYMBOL>
    <FULL_NAME>Milan normotensive strain</FULL_NAME>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2024-08-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156420139</CITATION_ID>
    <DESCRIPTION>These are re-derived rats of MNS/N now maintained at Medical College of Wisconsin. Origin: Wistar rats with brother x sister mating and selection for low systolic blood pressure as a normotensive control for MHS.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156420144</RGD_ID>
    <STRAIN_SYMBOL>HXB1/IpcvMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156420144</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock HXB1/Ipcv provided by Pravenec and Kren from the Prague colonies, maintained at Medical college of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156420145</RGD_ID>
    <STRAIN_SYMBOL>HXB7/IpcvMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156420145</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock HXB7/Ipcv provided by Pravenec and Kren from the Prague colonies, maintained at Medical college of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156420146</RGD_ID>
    <STRAIN_SYMBOL>HXB13/IpcvMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156420146</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock HXB13/Ipcv provided by Pravenec and Kren from the Prague colonies, maintained at Medical college of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156420147</RGD_ID>
    <STRAIN_SYMBOL>HXB17/IpcvMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156420147</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock provided by Pravenec and Kren from the Prague colonies, maintained at Medical college of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156420148</RGD_ID>
    <STRAIN_SYMBOL>HXB18/IpcvMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156420148</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock HXB18/Ipcv provided by Pravenec and Kren from the Prague colonies, maintained at Medical college of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156420149</RGD_ID>
    <STRAIN_SYMBOL>HXB23/IpcvMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156420149</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock HXB23/Ipcv provided by Pravenec and Kren from the Prague colonies, maintained at Medical college of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156420150</RGD_ID>
    <STRAIN_SYMBOL>BXH6/CubMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156420150</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock BXH6/Cub provided by Dr. Kren from Charles University, Department of Biology, Prague, Czech Republic, maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156420151</RGD_ID>
    <STRAIN_SYMBOL>ZDF-&lt;i&gt;Lepr&lt;sup&gt;fa/+&lt;/sup&gt;&lt;/i&gt;/Crl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.criver.com/products-services/find-model/zdf-rat-lean-fa?region=3611&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/zdf-rat-lean-fa?region=3611&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>coisogenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156420151</CITATION_ID>
    <DESCRIPTION>This is the control model for the ZDF-Leprfa/Crl.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156420152</RGD_ID>
    <STRAIN_SYMBOL>Mlac:WR</STRAIN_SYMBOL>
    <FULL_NAME>Wistar rats</FULL_NAME>
    <ORIGINATION>&lt;a href=https://nlac.mahidol.ac.th/en/index.php/mlacwr/&gt; National Laboratory Animal Center, Mahidol University Thailand&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://nlac.mahidol.ac.th/en/index.php/mlacwr/&gt; National Laboratory Animal Center, Mahidol University Thailand&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156420152</CITATION_ID>
    <DESCRIPTION>This outbred Wistar was maintained at National Laboratory Animal Center (NLAC), Thailand. All animals were housed at the Chulalongkorn University Laboratory Animal Center (CULAC) .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156420153</RGD_ID>
    <STRAIN_SYMBOL>Mlac:SD</STRAIN_SYMBOL>
    <FULL_NAME>Sprague Dawley rats</FULL_NAME>
    <ORIGINATION>&lt;a href=https://nlac.mahidol.ac.th/en/index.php/mlacwr/&gt; National Laboratory Animal Center, Mahidol University Thailand&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://nlac.mahidol.ac.th/en/index.php/mlacwr/&gt; National Laboratory Animal Center, Mahidol University Thailand&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156420153</CITATION_ID>
    <DESCRIPTION>This outbred Sprague Dawley  was maintained at National Laboratory Animal Center (NLAC), Thailand. All animals were housed at the Chulalongkorn University Laboratory Animal Center (CULAC) .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430076</RGD_ID>
    <STRAIN_SYMBOL>LEXF1A/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430076</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430077</RGD_ID>
    <STRAIN_SYMBOL>LEXF2A/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430077</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430078</RGD_ID>
    <STRAIN_SYMBOL>LEXF2B/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430078</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430079</RGD_ID>
    <STRAIN_SYMBOL>LEXF2C/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430079</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430080</RGD_ID>
    <STRAIN_SYMBOL>LEXF3/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE>Diabetes Obesity; Cancer</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430080</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430081</RGD_ID>
    <STRAIN_SYMBOL>LEXF4/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430081</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430082</RGD_ID>
    <STRAIN_SYMBOL>LEXF5/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430082</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430083</RGD_ID>
    <STRAIN_SYMBOL>LEXF7A/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430083</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430085</RGD_ID>
    <STRAIN_SYMBOL>LEXF7B/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430085</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430086</RGD_ID>
    <STRAIN_SYMBOL>LEXF7C/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430086</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430087</RGD_ID>
    <STRAIN_SYMBOL>LEXF8A/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430087</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430089</RGD_ID>
    <STRAIN_SYMBOL>LEXF8D/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430089</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430090</RGD_ID>
    <STRAIN_SYMBOL>LEXF9/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430090</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430091</RGD_ID>
    <STRAIN_SYMBOL>LEXF10B/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430091</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430092</RGD_ID>
    <STRAIN_SYMBOL>LEXF10C/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430092</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430093</RGD_ID>
    <STRAIN_SYMBOL>LEXF11/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430093</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430094</RGD_ID>
    <STRAIN_SYMBOL>FXLE13/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430094</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430095</RGD_ID>
    <STRAIN_SYMBOL>FXLE14/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430095</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430099</RGD_ID>
    <STRAIN_SYMBOL>FXLE16/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430099</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430100</RGD_ID>
    <STRAIN_SYMBOL>FXLE17/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430100</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430101</RGD_ID>
    <STRAIN_SYMBOL>FXLE18/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430101</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430102</RGD_ID>
    <STRAIN_SYMBOL>FXLE19/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430102</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430103</RGD_ID>
    <STRAIN_SYMBOL>FXLE21/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430103</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430104</RGD_ID>
    <STRAIN_SYMBOL>FXLE22/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430104</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430105</RGD_ID>
    <STRAIN_SYMBOL>FXLE23/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430105</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430106</RGD_ID>
    <STRAIN_SYMBOL>FXLE24/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430106</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430107</RGD_ID>
    <STRAIN_SYMBOL>FXLE25/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430107</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430108</RGD_ID>
    <STRAIN_SYMBOL>FXLE26/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430108</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/Stm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430109</RGD_ID>
    <STRAIN_SYMBOL>FXLE20/StmMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430109</CITATION_ID>
    <DESCRIPTION>This strain is derived from systematic breeding of the F2 generation between LE/Stm and F344/DuCrlj. This substrain was maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430110</RGD_ID>
    <STRAIN_SYMBOL>BXH12/CubMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430110</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock BXH12-1/Cub provided by Dr. Kren from Charles University, Department of Biology, Prague, Czech Republic, maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430169</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Mecp2&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;/Hsd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.envigo.com/model/hsdsage-sd-mecp2em1sage&gt; ENVIGO&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.envigo.com/model/hsdsage-sd-mecp2em1sage&gt; ENVIGO&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2023-02-22)</AVAILABILITY>
    <RESEARCH_USE>Autism, Rett syndrome, Cognition</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430169</CITATION_ID>
    <DESCRIPTION>The MeCP2 KO rat model was originally created at SAGE Labs,
Inc. in St. Louis, MO and distributed out of the Boyertown, PA
facility. The line continues to be maintained through the original
SAGE Labs animal inventory acquired by Envigo. The ZFN mutant rat strain was produced by injecting zinc finger nuclease targeting rat Mecp2 into Sprague Dawley embryos. This mutant rat has a knockout of the methyl CpG binding protein 2 (Mecp2).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430327</RGD_ID>
    <STRAIN_SYMBOL>FSL</STRAIN_SYMBOL>
    <FULL_NAME>Flinders Sensitive Line Rat</FULL_NAME>
    <ORIGINATION>Karolinska Institutet,  Stockholm Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430327</CITATION_ID>
    <DESCRIPTION>Flinders Sensitive Line Rat (FSL) was selectively bred from outbred Sprague Dawley for increased response an anticholinesterase agent. The FSL rat
partially resembles depressed individuals with phenotypes of  reduced appetite and psychomotor function but exhibits normal hedonic
responses and cognitive function.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156430328</RGD_ID>
    <STRAIN_SYMBOL>FRL</STRAIN_SYMBOL>
    <FULL_NAME>Flinders Resistant Line Rat</FULL_NAME>
    <ORIGINATION>Karolinska Institutet,  Stockholm Sweden</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156430328</CITATION_ID>
    <DESCRIPTION>Flinders Resistant Line Rat (FRL) was selectively bred from outbred Sprague Dawley for less response to an anticholinesterase agent than FSL. FRL is not more resistant to the anticholinesterase agent compared to other outbred rats. The FSL rat
partially resembles depressed individuals with phenotypes of  reduced appetite and psychomotor function but exhibits normal hedonic
responses and cognitive function.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156431061</RGD_ID>
    <STRAIN_SYMBOL>LH-&lt;i&gt;C17h6orf52&lt;sup&gt;em1Aek&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dr. Anne Kwitek at the Medical College of Wisconsin</ORIGINATION>
    <SOURCE>Currently live colony with Dr. Anne Kwitek at the Medical College of Wisconsin. Being cryopreserved and the live colony will not be available.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2026-01-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>C17h6orf52&lt;sup&gt;em1Aek&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>630350568</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="23968510" STOP_POS="23968510" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="23753359" STOP_POS="23776251" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="21600326" STOP_POS="21615888" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="23581681" STOP_POS="23595498" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="29733271" STOP_POS="29746771" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156431061</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to introduce a T insertion  in exon 1 of C17h6orf52  gene causing a frameshift and predicated early truncation of the translated protein in an embryo from LH/MavRrrcAek (RGD:10755352)  through electroporation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156451369</RGD_ID>
    <STRAIN_SYMBOL>HAD</STRAIN_SYMBOL>
    <FULL_NAME>high-alcohol-drinking</FULL_NAME>
    <ORIGINATION>Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156451369</CITATION_ID>
    <DESCRIPTION>These high-alcohol-drinking rats were developed by selective breeding from the heterogeneous N/N  (N:NIH) strain . 8 inbred rat strains were intercrossed for alcohol preference and consumption.Within-family selection and a rotational breeding design were employed to reduce inbreeding and to allow maintenance of non-inbred replicate lines</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>156451370</RGD_ID>
    <STRAIN_SYMBOL>LAD</STRAIN_SYMBOL>
    <FULL_NAME>low-alcohol-drinking</FULL_NAME>
    <ORIGINATION>Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_156451370</CITATION_ID>
    <DESCRIPTION>These low-alcohol-drinking were developed by selective breeding from the heterogeneous strain  N:NIH (RGD:728185). 8 inbred rat strains were intercrossed for alcohol preference and consumption. Within-family selection and a rotational breeding design were employed to reduce inbreeding and to allow maintenance of non-inbred replicate lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>158013766</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Akt1&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute for Reproductive and Developmental Sciences, Department of Pathology
&amp; Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS
66160, USA.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Akt1&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>158013767</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="137534810" STOP_POS="137555131" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="131717680" STOP_POS="131719011" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="137218398" STOP_POS="137239970" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="146225955" STOP_POS="146247008" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="137640482" STOP_POS="137657552" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00891</CITATION_ID>
    <DESCRIPTION>This Akt mutant strain was created in zygotes from Holtzman Sprague-Dawley.  Guided RNAs targeting exon 4 (target sequence: GCCGTTTGAGTCCATCAGCC; nucleotides 356-375) and exon 7 (target sequence: TTGTCATGGAGTACGCCAAT;
nucleotides 712-731) of the Akt1 gene (NM_033230.3) were injected to the embryos to create  a1332-bp deletion from exon 4 to exon7, resulting a premature stop of the protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>288084580</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Txn1&lt;sup&gt;m1Kyo&lt;/sup&gt; &lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>age dependent mitochondrial cytopathy rat</FULL_NAME>
    <ORIGINATION>Division of Animal Genetics, Laboratory Animal Research Center, Institute of Medical Science, The University of Tokyo, Tokyo 108-8639, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_288084580</CITATION_ID>
    <DESCRIPTION>This mutation Phe54Leu  is an autosomal dominant mutation that appeared in  a stock of F344/NSlc rats that had been mutagenized with N-ethyl-N-nitrosourea (ENU). Rats heterozygous for Txn1 (Txn1 /+) exhibited running seizures only in its juvenile stage. The rat called Adem rat, exhibited age dependent mitochondrial cytopathy (Adem). The rats were backcrossed for more than ten generations on the F344/NSlc inbred background to ensure other mutations induced by ENU was reduced. The causative gene was identified as a missense substitution (c. 160 T &gt; C, p. Phe54Leu) in exon 3 of Txn1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>288084582</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Txn1 &lt;sup&gt;em1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Division of Animal Genetics, Laboratory Animal Research Center, Institute of Medical Science, The University of Tokyo, Tokyo 108-8639, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_288084582</CITATION_ID>
    <DESCRIPTION>This CRISPR/Cas9 induced mutation Phe54Leu is induced  in embryos of F344/NSlc.  The genome editing system targeting exon 3 of Txn1 gene ( (c. 160 T &gt; C) was delivered into  embryos by electroporation. The two-cell stage embryos  were transferred into the oviducts of pseudopregnant females.  The rat called Txn1-F54L  rat, replicates Adem rats (RGD:288084580) which carried Phe54Leu mutation in the same gene.These two strains exhibit similar phenotype.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>291492855</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Prp-DISC1)Uhg</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Center for Behavioral Neuroscience, Institute of Experimental Psychology, Heinrich-Heine University D�sseldorf, D�sseldorf, Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_291492855</CITATION_ID>
    <DESCRIPTION>Transgenic Sprague Dawley rats were generated by injecting the linearized
fragment of the CosSHa.tet vector containing the full-length, non-mutant
human DISC1 as transgene with the polymorphisms F607 and C704, under the control of the Syrian hamster prion protein promoter, into pronuclei of Sprague Dawley rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329322880</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Mertk&lt;sup&gt;em1Cgen&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Cyagen Biosciences (Guangzhou) Inc.Building D, 3rd Floor, 3 Juquan Road, Science City, Guangzhou, 510663, China</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2023-04-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329322880</CITATION_ID>
    <DESCRIPTION>The gRNA to rat Mertk gene, and Cas9 mRNA were co-injected into fertilized rat eggs to generate targeted knockout offspring. F0 founder animals were identified by PCR followed by sequence analysis, which were bred to wildtype rat to test germline transmission and F1 animal generation. This strain was derived from founder 6# carrying a 13934 deletion which included exons 3 to 5.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329333019</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Spon2&lt;sup&gt;em1Holi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Spon2&lt;sup&gt;em1Holi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>329333021</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="81713070" STOP_POS="81742510" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="77505695" STOP_POS="77518001" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="82815158" STOP_POS="82824529" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="83501025" STOP_POS="83510376" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329333019</CITATION_ID>
    <DESCRIPTION>This Spon2 knockout mutant was produced by injecting TALENs targeting exon 2 of rat Spon2 into Sprague Dawley embryos. Founder #4-1 (a1) carrying a 22-bp deletion was chosen  to produce heterozygous and homozygous rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329812004</RGD_ID>
    <STRAIN_SYMBOL>Ibd:WI</STRAIN_SYMBOL>
    <FULL_NAME>Wistar rats</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329812004</CITATION_ID>
    <DESCRIPTION>The Wistar rats maintained at The Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw, Poland</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329845586</RGD_ID>
    <STRAIN_SYMBOL>W;WIAR-&lt;i&gt;Izumo1&lt;sup&gt;em1Osb&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Osaka University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1340&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-12-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Izumo1&lt;sup&gt;em1Osb&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>329845587</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="105227603" STOP_POS="105233357" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="96090817" STOP_POS="96096893" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="101603222" STOP_POS="101608977" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="102682319" STOP_POS="102682325" METHOD="8"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="96090118" STOP_POS="96095872" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329845586</CITATION_ID>
    <DESCRIPTION>Izumo1 KO strain was established by CRISPR/Cas9 system using inbred WIAR (RGD:2304222) (SLC, Inc.). sgRNA:GGTGGCTGCAATAAAGACTT, PAM sequence：TGG. A 7-bp deletion（CTTTGGA）after start codon (Met) in exon2 of Izumo1 gene was detected. After establishment of WIAR background KO rats, this strain was mated with Slc:Wistar (RGD:2314928), hence this mutant is in mix background.Izumo1-deficient male rats are infertile. In female rats, no specific phenotype is observed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329845597</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Col4a5&lt;sup&gt;em1Matsu&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Division of Molecular Genetics, Shigei Medical Research Institute, 2117 Yamada, Minami-ku, Okayama, 701-0202, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1341&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2023-05-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Col4a5&lt;sup&gt;em1Matsu&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>329969888</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="109907251" STOP_POS="110111214" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="105118762" STOP_POS="105322699" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="112769595" STOP_POS="112983720" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="111226503" STOP_POS="111437171" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="36918697" STOP_POS="37130659" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329845597</CITATION_ID>
    <DESCRIPTION>Genome editing was performed using the rGONAD method to produce three different lines of KO rats  due to three different genome mutations thus different in protein expression predication. The genetic background is WKY/NCrlCrlj (Charles River Laboratories Japan) (RGD:61119). Tandem STOP codons were designed to integrate into 27 bases after the first ATG in the rat Col4a5 gene This em1 mutant carries a premature stop coden after 9 amino acids due to the insertion of a 20 bp stop codon. Col4a5 KO rats have urinary protein and hematuria from early on, and males begin to die at 18 weeks of age and all die by 28 weeks of age.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329845599</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Col4a5&lt;sup&gt;em2Matsu&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Division of Molecular Genetics, Shigei Medical Research Institute, 2117 Yamada, Minami-ku, Okayama, 701-0202, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1342&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Col4a5&lt;sup&gt;em2Matsu&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>329969892</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="109907251" STOP_POS="110111214" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="105118762" STOP_POS="105322699" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="112769595" STOP_POS="112983720" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="111226503" STOP_POS="111437171" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="36918697" STOP_POS="37130659" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329845599</CITATION_ID>
    <DESCRIPTION>Genome editing was performed using the rGONAD method to produce three different lines of KO rats  due to three different genome mutations thus different in protein expression predication. The genetic background is WKY/NCrlCrlj (Charles River Laboratories Japan) (RGD:61119). Tandem STOP codons were designed to integrate into 27 bases after the first ATG in the rat Col4a5 gene This em2 mutant carries a premature stop coden after 15 amino acids due to insertion of a 42bp stop codon. Col4α5 em2 rats have urinary protein and hematuria from early on, and males begin to die at 18 weeks of age and all die by 28 weeks of age.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329845600</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Col4a5&lt;sup&gt;em3Matsu&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Division of Molecular Genetics, Shigei Medical Research Institute, 2117 Yamada, Minami-ku, Okayama, 701-0202, Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1343&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Col4a5&lt;sup&gt;em3Matsu&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>329969893</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="109907251" STOP_POS="110111214" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="105118762" STOP_POS="105322699" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="112769595" STOP_POS="112983720" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="111226503" STOP_POS="111437171" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="36918697" STOP_POS="37130659" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329845600</CITATION_ID>
    <DESCRIPTION>Genome editing was performed using the rGONAD method to produce three different lines of KO rats  due to three different genome mutations thus different in protein expression predication. The genetic background is WKY/NCrlCrlj (Charles River Laboratories Japan) (RGD:61119). Tandem STOP codons were designed to integrate into 27 bases after the first ATG in the rat Col4a5 gene This em3 mutant carries a deletion of 56 base pairs containing the first methioine. Col4α5 em3 ratshave urinary protein and hematuria from early on, and males begin to die at 18 weeks of age and all die by 28 weeks of age.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329848962</RGD_ID>
    <STRAIN_SYMBOL>SHRSP.SHR-(&lt;i&gt;D1Got82-D1Rat97&lt;/i&gt;)/Izm</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1344&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1344&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="79969446" STOP_POS="81169607" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="81241080" STOP_POS="82453948" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="82503596" STOP_POS="83715456" METHOD="1 - by flanking markers"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="79624016" STOP_POS="80868564" METHOD="1 - by flanking markers"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329848962</CITATION_ID>
    <DESCRIPTION>A subcongenic strain generated by backcrossing SHRSP.SHR-(D1Mgh5-D1Got87)/Izm (NBRP Rat No.0709, RGD:7411707) to SHRSP/Izm. A segment of the QTL region of chromosome 1 involved in salt-induced stroke (Niiya et al. Sci Rep. 2018; 8; 9403) has been exchanged.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329848994</RGD_ID>
    <STRAIN_SYMBOL>WIC.WDB-&lt;i&gt;Kiss1&lt;sup&gt;tm1(tdTomato)Nurep&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1345&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1345&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-06-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329848994</CITATION_ID>
    <DESCRIPTION>Kiss1 knockout rats were generated by K.I. Maeda (The University of Tokyo), H. Tsukamura, Y. Uenoyama, N. Inoue (Nagoya University), and M. Hirabayashi (National Institute for Physiological Sciences). The targeting vector (tdTomato/puromycin N-acetyl transferase) was introduced by electroporation targeting the Kiss1 gene in ES cells (WDB/Nips-ES1/Nips). Crossed with and maintained by the Wistar-Imamichi rats (Iar:Wistar-Imamichi, Institute for Animal Reproduction).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329848995</RGD_ID>
    <STRAIN_SYMBOL>WIC;WDB-&lt;i&gt;Kiss1&lt;sup&gt;tm1Nurep&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1346&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1346&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-06-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329848995</CITATION_ID>
    <DESCRIPTION>The kisspeptin gene (Kiss1) is knocked out conditonally by the Cre recombinase. This strain was generated by K.I. Maeda (The University of Tokyo), H. Tsukamura, Y. Uenoyama, N. Inoue (Nagoya University), and M. Hirabayashi (National Institute for Physiological Sciences) for the purpose of producing conditional knockout rats of the Kiss1 gene in the hypothalamus. The targeting vector (loxP, Kiss1[exons 2 and 3], PGK promoter-neo, loxP) was introduced by electroporation targeting the Kiss1 gene in ES cells (WDB/Nips-ES1/Nips). Crossed with and maintained by the Wistar-Imamichi rats (Iar:Wistar-Imamichi, Institute for Animal Reproduction).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329848998</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Drd2-cre)487-3Koba</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1249&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1249&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-06-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329848998</CITATION_ID>
    <DESCRIPTION>This strain is established by injection of modified BAC (cre gene was inserted into the exon 2 of rat Drd2 gene) into Long-Evans rat's fertile eggs. 
Detailed information of BAC: Drd2, CH230-11B15 from the CHORI-230 Female Brown Norway rat BAC Library (BACPAC Resources Center, Children?s Hospital Oakland Research Institute)"</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329848999</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Drd2-cre)490-9Koba</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1348&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1348&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-06-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329848999</CITATION_ID>
    <DESCRIPTION>This strain is established by injection of modified BAC (cre gene was inserted into the exon 2 of rat Drd2 gene) into Long-Evans rat's fertile eggs. "</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329849003</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Pvalb&lt;sup&gt;em2(cre)Koba&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1347&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1347&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329849003</CITATION_ID>
    <DESCRIPTION>A complex of Cas9 protein and gRNA was introduced into Iar:LE fertilized rat eggs by electroporation. Combi-CRISPR (Yoshimi K. et al.) was used to induce knock-in. Knock-in rats were selected and crossed with wild-type rats to establish this strain. Sequence features: the intron just before the fourth exon of the Pvalb gene (intron 3) is deleted by NHEJ after double-strand break by one base compared to the wild-type. ---ttggcgggccagaacctcagggg---(wild-type) ---ttggcgggccagaacc-cagggg---(knock-in)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329849006</RGD_ID>
    <STRAIN_SYMBOL>LE;LEH-&lt;i&gt;Ednrb&lt;sup&gt;sl&lt;/sup&gt;&lt;/i&gt;/Kwb</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1349&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1349&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2023-06-08)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ednrb&lt;sup&gt;sl&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10755424</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329849006</CITATION_ID>
    <DESCRIPTION>LEH/Hkv (NBRP Rat No. 0802 aka. RGD:6480220) was resuscitated from frozen embryos and heterozygous male was obtained.
The heterozygous male was mated with female Long-Evans rats (Crlj:LE), and the resulting offspring were deposited to NBRP.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329849009</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Tyr&lt;sup&gt;C&lt;/sup&gt;Kit&lt;sup&gt;H&lt;/sup&gt;/Hkv&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1350&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1350&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-06-09)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kit|Tyr</ALLELES>
    <ALLELE_RGD_IDS>620568|1589755</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="32901615" STOP_POS="32978895" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150527687" STOP_POS="150622857" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="32547459" STOP_POS="32624694" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="141115036" STOP_POS="141210207" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="35072131" STOP_POS="35149638" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="151012598" STOP_POS="151106802" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157322968" STOP_POS="157416594" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="34901860" STOP_POS="34979384" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143641257" STOP_POS="143746315" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="34906043" STOP_POS="34984819" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329849009</CITATION_ID>
    <DESCRIPTION>F344-TyrC KitH/Kyo (Black F344, NBRP Rat No. 0768, aka RGD:11040971), carrying 1) point mutation in the exon 2 (896G&gt;A, p.R229H) of Tyrosinase (Tyr) gene (albino phenotype) and 2) retrotransposon insertion (7-bp) in kit gene (hooded phenotype) induced  was crossed with F344/NSlc (Japan SLC, Inc.). Then, from the F2 generation, Tyr as a wild-type homozygous (confirmed by sequence) and Kit as a hooded homozygous (confirmed by phenotype) were selected.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329849010</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Tyr&lt;sup&gt;C&lt;/sup&gt;Kit&lt;sup&gt;H&lt;/sup&gt;&lt;/i&gt;.LEA-(&lt;i&gt;Tel-D17Got10&lt;/i&gt;)/Hkv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1351&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1351&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-06-09)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Kit|Tyr</ALLELES>
    <ALLELE_RGD_IDS>620568|1589755</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="32901615" STOP_POS="32978895" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150527687" STOP_POS="150622857" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="32547459" STOP_POS="32624694" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="141115036" STOP_POS="141210207" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="35072131" STOP_POS="35149638" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="151012598" STOP_POS="151106802" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="34901860" STOP_POS="34979384" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157322968" STOP_POS="157416594" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="34906043" STOP_POS="34984819" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143641257" STOP_POS="143746315" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329849010</CITATION_ID>
    <DESCRIPTION>A congenic strain in which a chromosome 17 fragment of LEA rats (provided by Dr. Tadashi Okamura) was introduced into the F344-TyrC KitH (NBRP Rat No. 0768).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329849011</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Fos&lt;sup&gt;em1Yossi&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1352&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1352&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-06-09)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329849011</CITATION_ID>
    <DESCRIPTION>SD rats (Slc:SD) in which the c-Fos gene (ENSRNOG00000008015) was disrupted by the CRISPR/Cas9 system. Two guide RNAs and Cas9 protein were injected into the pronucleus of fertilized eggs of SD rats. After injection, they were transferred into the oviducts of the recipient rats and born. The founder rat (line 12) showed abnormal teeth, and PCR and sequencing analysis revealed that 1,067 bases including Exon 1 were deleted. The founder rat were mated with SD rats and bred.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329849114</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ghrh&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ghrh&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>329853764</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="166412763" STOP_POS="166432519" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="145992762" STOP_POS="146012528" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="153453801" STOP_POS="153453810" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="158251824" STOP_POS="158270812" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="148027235" STOP_POS="148046352" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329849114</CITATION_ID>
    <DESCRIPTION>The CRISPR/SpCas9 system was used to introduce a 10-bp deletion (rn6: chr3:153,453,801-153,453,810) in exon 3 of the Ghrh gene in Crl:SD Sprague Dawley embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329951704</RGD_ID>
    <STRAIN_SYMBOL>ACI.BBDP-(&lt;i&gt;RT1&lt;sup&gt;u&lt;/sup&gt;&lt;/i&gt;)/Sunn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Sunnybrook Research Institute, Toronto, Ontario, Canada.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=790&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2023-07-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00790</CITATION_ID>
    <DESCRIPTION>1 BBDP regions [Iddm1(RT1u) was introgressed into the ACI/SegHsd background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329951705</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cited2&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=807&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=807&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm; Cryorecovery (as of 2023-07-10)</AVAILABILITY>
    <RESEARCH_USE>hypoxia</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00807</CITATION_ID>
    <DESCRIPTION>Deletion of coding sequence (Exon 2) using CRISPR/Cas9</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329951706</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Adrm1&lt;sup&gt;em1Uok&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=861&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=861&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2023-07-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00861</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9-mediated deletion of ATG start site in Exon 2 of Adrm1 gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329955364</RGD_ID>
    <STRAIN_SYMBOL>WKY-Tg(CD68-GFP)Kjw</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Kevin Woollard at Imperial College London</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>glomerulonephritis</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329955364</CITATION_ID>
    <DESCRIPTION>Transgene insertion (human CD68-GFP) using Sleeping Beauty transposon system on Wistar Kyoto rats. Rat monocyte/macrophage reporter strain on a WKY background which has susceptibility to experimental glomerulonephritis. GFP expression occurs exclusively within blood monocytes and tissue macrophages.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329955365</RGD_ID>
    <STRAIN_SYMBOL>WKY-Tg(CD68-GFP)KjwRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Develop by Kevin Woollard at Imperial College London</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=866&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryorecovery (as of 2023-07-11)</AVAILABILITY>
    <RESEARCH_USE>glomerulonephritis</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00866</CITATION_ID>
    <DESCRIPTION>Transgene insertion (human CD68-GFP) using Sleeping Beauty transposon system on Wistar Kyoto rats. Rat monocyte/macrophage reporter strain on a WKY background which has susceptibility to experimental glomerulonephritis. GFP expression occurs exclusively within blood monocytes and tissue macrophages.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329955449</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Serpina6&lt;sup&gt;em1Glha&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Rats were originally  bred and maintained at the Center for Disease Modeling.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=930&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryorecovery (as of 2023-07-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Serpina6&lt;sup&gt;em1Glha&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>329955453</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="128544828" STOP_POS="128555064" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="122787486" STOP_POS="122787538" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="127523948" STOP_POS="127534178" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="136742720" STOP_POS="136752950" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="127911618" STOP_POS="127921851" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329955449</CITATION_ID>
    <DESCRIPTION>A CRISPR/cas9 strategy was employed by Sage Labs, to generate Charles River Sprague Dawley rats with a 53 base pair deletion within SerpinA6. The single guide RNA (sgRNA) targeted sequences within exon 2 of SerpinA6, encoding amino acid residues within the amino-terminal region of the mature Serpina6, also known as corticosteroid-binding globulin (CBG) polypeptide. The resulting 53 base pair deletion removed codons for residues Pro40-Thr57, with a frameshift after Ser39, resulting in a unique 14 residue sequence followed by a TGA stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329955451</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Serpina6&lt;sup&gt;em1Glha&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Rats were originally  bred and maintained at the Center for Disease Modeling.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=930&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryorecovery (as of 2023-07-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Serpina6&lt;sup&gt;em1Glha&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>329955453</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="128544828" STOP_POS="128555064" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="122787486" STOP_POS="122787538" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="127523948" STOP_POS="127534178" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="136742720" STOP_POS="136752950" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="127911618" STOP_POS="127921851" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00930</CITATION_ID>
    <DESCRIPTION>A CRISPR/cas9 strategy was employed by Sage Labs, to generate Charles River Sprague Dawley rats with a 53 base pair deletion within SerpinA6. The single guide RNA (sgRNA) targeted sequences within exon 2 of SerpinA6, encoding amino acid residues within the amino-terminal region of the mature Serpina6, also known as corticosteroid-binding globulin (CBG) polypeptide. The resulting 53 base pair deletion removed codons for residues Pro40-Thr57, with a frameshift after Ser39, resulting in a unique 14 residue sequence followed by a TGA stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329955459</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;P2rx7&lt;sup&gt;em1Tja&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Imperial College London</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>P2rx7&lt;sup&gt;em1Tja&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>329955460</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="39550531" STOP_POS="39594984" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="33900615" STOP_POS="33900616" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="39353613" STOP_POS="39396042" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="41242368" STOP_POS="41808755" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="35074025" STOP_POS="35117152" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329955459</CITATION_ID>
    <DESCRIPTION>A global P2RX7KO on a WKYbackground was created at Imperial College London using zinc finger nuclease
(ZFN) technology to generate a 2 base pair insertion in exon 10 of P2rx7</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329955557</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ace2&lt;sup&gt;em1(ACE2)Prem&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Deposited this strain with the Rat Resource and Research Center: (RRRC), 4011 Discovery Drive, Columbia, MO 65201. Phone: (573) 884-6076 Fax: 573-882-9857</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2023-07-17)</AVAILABILITY>
    <RESEARCH_USE>COVID-19 research.</RESEARCH_USE>
    <ALLELES>ACE2</ALLELES>
    <ALLELE_RGD_IDS>1347174</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329955557</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 knock-in of the human ACE2 transgene into the endogenous locus of the rat Ace2 gene. Single integration of hACE2, with expression driven by the endogenous rat Ace2 promoter. Provides a more natural expression pattern (versus abundant overexpression as seen in prior models).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329969882</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Myh6-cre)Lizh</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Key Laboratory of Human Disease
Comparative Medicine, NHFPC, Institute of
Laboratory Animal Science, Peking Union
Medicine College, Chinese Academy of
Medical Sciences,</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329969882</CITATION_ID>
    <DESCRIPTION>The heart-specific cre expression plasmid (alpha-MHC-Cre) was produced by inserting the cre coding sequence downstream of the a-MHC (Mgh6) promoter in the a-MHC expression vector. The a-MHC-Cre transgenic rat was generated by microinjection of linearized alpha-MHC-Cre plasmid to Sprague Dawley embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329969883</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Trim44&lt;sup&gt;em1Lizh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Key Laboratory of Human Disease Comparative Medicine, NHFPC, Institute of Laboratory Animal Science, Peking Union Medicine College, Chinese Academy of Medical Sciences,</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329969883</CITATION_ID>
    <DESCRIPTION>A pair of synthetic oligonucleotides for sgRNA (sgRNA1, CCTTGCCGCTTTAAGTGACTC; sgRNA2, CCATGTTGGGAGCATTGCCTA) were annealed and then cloned into the pUC57-sgRNA expression vector, and the floxed plasmid donor was cloned into the pGSI plasmid. Both the Cas9 and sgRNA expression plasmids were linearized and used as templates for in vitro transcription. A mixture of the donor vector (4Ã¢â¬â¦ng/ul), Cas9 mRNA (25Ã¢â¬â¦ng/ul), and sgRNAs (10Ã¢â¬â¦ng/ul each) was microinjected into both the cytoplasm and male pronucleus of the fertilized eggs. The injected zygotes were then transferred to pseudopregnant SD rats, which then carried them to parturition. This is called conditional knockout Trim44 (Trim44 cKO).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>329969885</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Trim44&lt;sup&gt;em1Lizh&lt;/sup&gt;&lt;/i&gt;,Tg(Myh6-cre)Lizh</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Key Laboratory of Human Disease Comparative Medicine, NHFPC, Institute of Laboratory Animal Science, Peking Union Medicine College, Chinese Academy of Medical Sciences,</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_329969885</CITATION_ID>
    <DESCRIPTION>The conditional Trim44  knockout (Trim44 cKO, SD-Trim44em1Lizh, RGD:329969883) was bred with the Î±-MHC-Cre tool rat (SD-Tg(Myh6-cre)Lizh, RGD:329969882) to generate cardiac-specific Trim44 knockout which had the Trim44flox/flox/Î±-MHC-Cre genotype.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401717572</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Mpo&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2023-08-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mpo&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>401717573</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="73092124" STOP_POS="73102057" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="72595923" STOP_POS="72595933" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="75087892" STOP_POS="75098260" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="75004128" STOP_POS="75014496" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="76085872" STOP_POS="76097012" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401717572</CITATION_ID>
    <DESCRIPTION>CRISPR/SpCas9 system using sgRNA targeting the sequence CAGGGCCACGTGCAGATAGTCGG was used to introduce an 11-bp deletion (rn7: chr10:72,595,923-72,595,933) in exon 4 of the Mpo gene in Crl:SD strain rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401795481</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Nanos3&lt;sup&gt;em1(tdTomato)Nips&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi 444-8787, Japan. or Division of Mammalian Embryology, Center for Stem Cell Biology and Regenerative Medicine, The Institute for Medical Science, The University of Tokyo, Tokyo108-8639, Japan.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2023-09-11)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nanos3&lt;sup&gt;em1(tdTomato)Nips&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>401795483</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="19" START_POS="40889531" STOP_POS="40893699" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="19" START_POS="23978465" STOP_POS="23988933" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="19" START_POS="25284907" STOP_POS="25288680" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="19" START_POS="36262007" STOP_POS="36265766" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="19" START_POS="25669353" STOP_POS="25672779" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401795481</CITATION_ID>
    <DESCRIPTION>The targeting vector was designed to replace the stop codon of Nanos3 with T2A-2xtdTomato. The adeno-associated virus carrying the targeting vector was infected to Crlj:WI (RGD ID: 2312504) rat 1 cell zygotes followed by the introduction of CRISPR/Cas9 ribonucleoprotein complex by electroporation. After incubation overnight, the zygotes were transferred into oviducts of pseudo-pregnant rats. The pups were judged correct gene-targeting by genomic PCR. These rat strains are being maintained by crossing the founder rats with Crlj:WI rats. The tdTomato fluorescence faithfully label Nanos3 expressing cells.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401795484</RGD_ID>
    <STRAIN_SYMBOL>CD-&lt;i&gt;Slc30a10&lt;sup&gt;em1Sommu&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The strain was submitted by Dr. Somshuvra Mukhopadhyay from the University of Texas at Austin.</ORIGINATION>
    <SOURCE>The strain will be deposited to &lt;a href=http://www.rrrc.us/Strain/?x=996&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-09-11)</AVAILABILITY>
    <RESEARCH_USE>neuroscience, toxicology, metal homeostasis, physiology, manganese toxicity</RESEARCH_USE>
    <ALLELES>Slc30a10&lt;sup&gt;em1Sommu&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>401795485</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="13" START_POS="99529664" STOP_POS="99584442" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="13" START_POS="96998143" STOP_POS="97048076" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="13" START_POS="103396295" STOP_POS="103406759" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="13" START_POS="108048948" STOP_POS="108083821" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="13" START_POS="101474867" STOP_POS="101492180" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401795484</CITATION_ID>
    <DESCRIPTION>Exon 1 of Slc30a10 was targeted using CRISPR/Cas9 in the Crl:CD(SD) embryos . A mosiac founder that transmitted a 248 bp deletion in exon 1 of Slc30a10 leading to an out of frame mutation after amino acid 22 was bred to a CD rat to select for the above deletion and establish the line.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401799619</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Acr3-EGFP)Nips</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Section of Mammalian Transgenesis Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki Aichi 444-8787, Japan. or Division of Mammalian Embryology, Center for Stem Cell Biology and Regenerative Medicine, The Institute for Medical Science, The University of Tokyo, Tokyo108-8639, Japan.</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2023-09-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401799619</CITATION_ID>
    <DESCRIPTION>This transgenic strain was created by intracytoplasmic sperm injection (ICSI) mediated  DNA transfer. Linearized Acr3-EGFP plasmid DNA (Nakanishi et al., FEBS Lett. 1999; 0.1 micrograms/ml) is mixed with sperm heads of Slc:SD rats for 2 min. The sperm head is microinjected into ovulated oocytes of Slc:SD rat (RGD ID:12910483) and incubated overnight prior to embryo transfer to pseudopregnant females. Resultant pups are examined for correct gene-targeting by genomic PCR, and maintained by crossing the founder with Slc:SD rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401824639</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Fah&lt;sup&gt;em3Mcwi&lt;/sup&gt;Il2rg&lt;sup&gt;em2Mcwi&lt;/sup&gt;Rag1&lt;sup&gt;em6Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin,  Aron Geurts, ageurts@mcw.edu.</ORIGINATION>
    <SOURCE>availability contact: robcopenhaver@yecuris.com</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-11-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fah&lt;sup&gt;em3Mcwi&lt;/sup&gt;|Il2rg&lt;sup&gt;em2Mcwi&lt;/sup&gt;|Rag1&lt;sup&gt;em6Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10002790|10002792|629096379</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70435340" STOP_POS="70439052" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="147957931" STOP_POS="147980708" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="108372087" STOP_POS="108383184" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66398582" STOP_POS="66398582" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="146713663" STOP_POS="146736339" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="91206394" STOP_POS="91217491" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71165378" STOP_POS="71169078" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72017856" STOP_POS="72021516" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="147640316" STOP_POS="147662920" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="97866048" STOP_POS="97877145" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="86780782" STOP_POS="86791878" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="140851975" STOP_POS="140876187" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89342055" STOP_POS="89345715" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401824639</CITATION_ID>
    <DESCRIPTION>Produced by injection of CRISPR/Cas9 targeting the genomic sequence GGTGAGATCCTTTGAAAAGG in Rag1 into double homozygous embryos with knockout of Fah and Il2rg produced following multiple generations of intercrossing strains SD-Il2rgem2Mcwi (RGDID:10002794) and SD-Fahem3Mcw (RGDID: 10002791).   The resulting CRISPR-induced mutation in Rag1 deletes 25-bp (rn7: chr3:87,923,384-87,923,408) and inserts 17 bp (ACCCTAAACAGCTGTGC) for a net 8-bp deletion.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401824640</RGD_ID>
    <STRAIN_SYMBOL>SD.SD-&lt;i&gt;Fah&lt;sup&gt;em3Mcwi&lt;/sup&gt;Il2rg&lt;sup&gt;em2Mcwi&lt;/sup&gt;Rag1&lt;sup&gt;em6Mcwi&lt;/sup&gt;/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin,  Aron Geurts, ageurts@mcw.edu.</ORIGINATION>
    <SOURCE>Availability contact: robcopenhaver@yecuris.com</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-09-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fah&lt;sup&gt;em3Mcwi&lt;/sup&gt;|Il2rg&lt;sup&gt;em2Mcwi&lt;/sup&gt;|Rag1&lt;sup&gt;em6Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>10002790|10002792|629096379</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401824640</CITATION_ID>
    <DESCRIPTION>This  model was made by taking RGD:401824639 (Fah, Il2rg, and Rag1 triple knockout model) and backcrossing to Crl:SD, then intercrossing multiple generations again until all three gene alleles were homozygous again.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401827145</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Pink1&lt;sup&gt;em1Davis&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>The rat is deposited at Rat Resource and Research Center (RRRC).
&lt;a href=http://www.rrrc.us/Strain/?x=1007&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2025-01-27)</AVAILABILITY>
    <RESEARCH_USE>Parkinson's research</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01007</CITATION_ID>
    <DESCRIPTION>The CRISPR-Cas9 system was used to delete the coding region (exons 1-8) of the Pink1 gene in NTac:SD embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401827899</RGD_ID>
    <STRAIN_SYMBOL>BXH13/CubMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo (as of 2023-10-24)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401827899</CITATION_ID>
    <DESCRIPTION>This recombinant inbred was originally derived from founder strains BN-Lx/Cub and SHR/OlaIpcv at Charles University, Department of Biology, Prague, Czech Republic. This substrain was maintained at the Medical College of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401900746</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Prl7b1&lt;sup&gt;tm1(cre)Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Kansas Medical Center</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1013&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2023-11-21)</AVAILABILITY>
    <RESEARCH_USE>Reproductive biology</RESEARCH_USE>
    <ALLELES>Prl7b1&lt;sup&gt;tm1(cre)Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>401900752</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="37410605" STOP_POS="37423139" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="37202058" STOP_POS="37214739" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="39153431" STOP_POS="39161644" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="41012487" STOP_POS="41020700" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="43783328" STOP_POS="43791541" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_001013</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce Cre recombinase downstream of the Prl7b1 start site.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401900748</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Prl7b1&lt;sup&gt;tm1(cre)Soar&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain is rederived at Rat Resource and Research Center </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1013&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2023-11-21)</AVAILABILITY>
    <RESEARCH_USE>Reproductive biology</RESEARCH_USE>
    <ALLELES>Prl7b1&lt;sup&gt;tm1(cre)Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>401900752</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="37410605" STOP_POS="37423139" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="37202058" STOP_POS="37214739" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="39153431" STOP_POS="39161644" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="41012487" STOP_POS="41020700" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="43783328" STOP_POS="43791541" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_001013</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce Cre recombinase downstream of the Prl7b1 start site.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401900749</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Prl7b1&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Kansas Medical Center</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1014&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2023-11-21)</AVAILABILITY>
    <RESEARCH_USE>Reproductive biology</RESEARCH_USE>
    <ALLELES>Prl7b1&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>401900751</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="37410605" STOP_POS="37423139" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="37202058" STOP_POS="37214739" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="39153431" STOP_POS="39161644" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="41012487" STOP_POS="41020700" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="43783328" STOP_POS="43791541" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_001014</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 272 bp deletion at the Prl7b1 locus</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401900750</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Prl7b1&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain is rederived at Rat Resource and Research Center </ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1014&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2023-11-21)</AVAILABILITY>
    <RESEARCH_USE>Reproductive biology</RESEARCH_USE>
    <ALLELES>Prl7b1&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>401900751</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="37410605" STOP_POS="37423139" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="37202058" STOP_POS="37214739" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="39153431" STOP_POS="39161644" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="41012487" STOP_POS="41020700" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="43783328" STOP_POS="43791541" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_001014</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 272 bp deletion at the Prl7b1 locus</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401901198</RGD_ID>
    <STRAIN_SYMBOL>SHHF&lt;i&gt;&lt;sup&gt;cp/cp&lt;/sup&gt;&lt;/i&gt;/MccGmiCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.criver.com/products-services/find-model/spontaneously-hypertensive-heart-failure-shhf-rat-obese?region=3611&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/spontaneously-hypertensive-heart-failure-shhf-rat-obese?region=3611&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401901198</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>401901199</RGD_ID>
    <STRAIN_SYMBOL>SHHF&lt;i&gt;&lt;sup&gt;cp/+&lt;/sup&gt;&lt;/i&gt;/MccGmiCrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://www.criver.com/products-services/find-model/spontaneously-hypertensive-heart-failure-shhf-rat-lean?region=3611&gt;Charles River Laboratories &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/spontaneously-hypertensive-heart-failure-shhf-rat-lean?region=3611&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401901199</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>401901201</RGD_ID>
    <STRAIN_SYMBOL>SHHF&lt;i&gt;&lt;sup&gt;cp/+&lt;/sup&gt;&lt;/i&gt;/Mcc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dr. McCune laboratory</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401901201</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>401901202</RGD_ID>
    <STRAIN_SYMBOL>SHHF&lt;i&gt;&lt;sup&gt;cp/cp&lt;/sup&gt;&lt;/i&gt;/Mcc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dr. McCune laboratory</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401901202</CITATION_ID>
    <DESCRIPTION/>
  </Strain>
  <Strain>
    <RGD_ID>401901286</RGD_ID>
    <STRAIN_SYMBOL>test8Dec</STRAIN_SYMBOL>
    <FULL_NAME>test8Dec</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>advanced_intercross_line</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401901286</CITATION_ID>
    <DESCRIPTION>test8Dec</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401938598</RGD_ID>
    <STRAIN_SYMBOL>SS-Del(2q)1Mcwi &lt;sup&gt;-/-&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>Please contact: mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2023-12-12)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401938598</CITATION_ID>
    <DESCRIPTION>Four single guide RNAs and SpCas9 targeting sequences ATGAAGTGCCTAGCTTCATT, GAAGCTAGGCACTTCATCTA, ATTCATAATGGGACACTCGA, and CCCAGCCTCAGATTCATAAT flanking a chromosome 2 region distal to Npr3 were targeted in SS/JrHsdMcwi embryos. A 29,508 bp deletion in chromosome 2 (rn6: chr2:61,845,176-61,874,684) resulted, along with an insertion of 3 nucleotides (TGG).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401938647</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Slc9a6 &lt;sup&gt;em1Moro&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dr. Eric Morrow at Brown University
70 Ship Street, Box G-E4
Providence
RI
02912
USA</ORIGINATION>
    <SOURCE>deposited at RRRC</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2023-12-18)</AVAILABILITY>
    <RESEARCH_USE>neurodevelopment/neurodegeneration</RESEARCH_USE>
    <ALLELES>Slc9a6 &lt;sup&gt;em1Moro&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>151664749</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="139468045" STOP_POS="139524111" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="134443830" STOP_POS="134443831" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="158979081" STOP_POS="159045019" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="153620082" STOP_POS="153675717" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="141146237" STOP_POS="141201234" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401938647</CITATION_ID>
    <DESCRIPTION>Crispr-Cas was used to introduce a 2bp insertion of TT to create a stop codon in exon 7 of SLC9a6 gene, causing termination of translation. The strain was rederived at RRRC.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401938650</RGD_ID>
    <STRAIN_SYMBOL>CD-&lt;i&gt;Slc30a10&lt;sup&gt;em1Sommu&lt;/sup&gt;&lt;/i&gt;/Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The strain was created by Dr. Somshuvra Mukhopadhyay from the University of Texas at Austin.</ORIGINATION>
    <SOURCE>The strain is rederived at &lt;a href=http://www.rrrc.us/Strain/?x=996&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm; Cryorecovery (as of 2023-12-19)</AVAILABILITY>
    <RESEARCH_USE>neuroscience, toxicology, metal homeostasis, physiology, manganese toxicity</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401938650</CITATION_ID>
    <DESCRIPTION>Exon 1 of Slc30a10 was targeted using CRISPR/Cas9 in the Crl:CD(SD) embryos . A mosiac founder that transmitted a 248 bp deletion in exon 1 of Slc30a10 leading to an out of frame mutation after amino acid 22 was bred to a CD rat to select for the above deletion and establish the line.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401938653</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ctns&lt;sup&gt;em1Odev&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Zurich - Institute of Physiology, Mechanisms of Inherited Kidney Disorders Group                                           Winterthurerstrasse 190 CH-8057 Zürich</ORIGINATION>
    <SOURCE>Contact Olivier Devuyst at Email: olivier.devuyst@uzh.ch, &lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1377 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-03-31)</AVAILABILITY>
    <RESEARCH_USE>Cystinosis</RESEARCH_USE>
    <ALLELES>Ctns&lt;sup&gt;em1Odev&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>401938654</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="58300069" STOP_POS="58315725" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="57810970" STOP_POS="57810981" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="59749250" STOP_POS="59772475" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="59488895" STOP_POS="59503993" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="60060254" STOP_POS="60075352" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401938653</CITATION_ID>
    <DESCRIPTION>The Ctns gen was deleted by oocyte injection of the CRISPER/Cas9 system (PolyGene AG, Zurich,Switzer-land). Two single guideRNAs(sgRNAs) targeting exon3 of Ctns were selected :CRISPR1a: ACCAACGTCAGCATTAC-CCT(TGG), CRISPR1b: CCATTTACCAGCTTCACAGT(GGG). This Ctns rat line harboring a deletion of 12bp and insertion of 8bp resultingin a premature stop codon in the exon3 of Ctns.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401940195</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ahr&lt;sup&gt;em1Iexas-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Osaka University, Faculty of Medicine, Institute of Experimental Animal Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ahr&lt;sup&gt;em1Iexas&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>401940199</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="57961423" STOP_POS="57998901" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="52263461" STOP_POS="52263470" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="54963990" STOP_POS="55001806" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="64589066" STOP_POS="64624078" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="54205104" STOP_POS="54240268" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401940195</CITATION_ID>
    <DESCRIPTION>The homozygous knockout rats were created using CRISPR/Cas9 gene editing to delete 10 bp of exon 2 of  Ahr in Sprague Dawley rats .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401940197</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ahr&lt;sup&gt;em1Iexas+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Osaka University, Faculty of Medicine, Institute of Experimental Animal Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Ahr&lt;sup&gt;em1Iexas&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>401940199</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="57961423" STOP_POS="57998901" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="52263461" STOP_POS="52263470" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="54963990" STOP_POS="55001806" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="64589066" STOP_POS="64624078" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="54205104" STOP_POS="54240268" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401940197</CITATION_ID>
    <DESCRIPTION>The Ahr heterozygous  rats were created using CRISPR/Cas9 gene editing to delete 10 bp of exon 2 of  Ahr in Sprague Dawley rats .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401940198</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Ahr&lt;sup&gt;em1Iexas+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Osaka University, Faculty of Medicine, Institute of Experimental Animal Sciences</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401940198</CITATION_ID>
    <DESCRIPTION>The Ahr wild type littermates from the cross of heterozygous Ahr  rats. The Ahr mutants were created using CRISPR/Cas9 gene editing to delete a portion of exon 2 of  Ahr in Sprague Dawley rats .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401959229</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Thy1-GCaMP6f)8Rrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Janelia Research Campus and Princeton University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1010&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Neuroscience</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01010</CITATION_ID>
    <DESCRIPTION>Pronuclear injection was used to introduce an expression cassette containing the Thy-1 enhancer and GCaMP6f protein coding sequence. GCaMP6f is a genetically encoded calcium indicator. It is a synthetic fusion of green fluorescent protein, calmodulin, and M13, a peptide sequence from myosin light-chain kinase. Reference ID: https://doi.org/10.1101/2023.08.17.553594</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401959407</RGD_ID>
    <STRAIN_SYMBOL>OlaHsd:LE</STRAIN_SYMBOL>
    <FULL_NAME>Long Evans</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>Envigo, UK and Netherlands</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Behaviour</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401959407</CITATION_ID>
    <DESCRIPTION>Medical Research Council, Mill Hill obtained LH stock from ICI, Alderley Edge in 1932 and have maintained closed colony since that time. 
From Medical Research Council, Mill Hill to OLAC (Harlan) in 1969. Harlan became Envigo in 2015, then Envigo was acquired by Inotiv in 2021</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401959606</RGD_ID>
    <STRAIN_SYMBOL>Cnc:SD</STRAIN_SYMBOL>
    <FULL_NAME>Sprague-Dawley</FULL_NAME>
    <ORIGINATION>R. Dawley, Sprague-Dawley Company,</ORIGINATION>
    <SOURCE>http://www.spfbiotech.com/product/ratdetail/10/75</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401959606</CITATION_ID>
    <DESCRIPTION>This strain was initiated by R. Dawley, Sprague-Dawley Company, Madison, Wisconsin in 1925. This strain was maintained by China National Center For Rodent Laboratory Animal. and  available from SPF biotech since 2018.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401960080</RGD_ID>
    <STRAIN_SYMBOL>Yxch:SD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Experimental Animal Center of Army Medical University (Chongqing, China).</ORIGINATION>
    <SOURCE>Experimental Animal Center of Army Medical University (Chongqing, China).</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401960080</CITATION_ID>
    <DESCRIPTION>Experimental Animal Center of Army Medical University (Chongqing, China).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401960101</RGD_ID>
    <STRAIN_SYMBOL>ZSF1-&lt;i&gt;Lepr&lt;sup&gt;fa/cp&lt;/sup&gt;&lt;/i&gt;/Crl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Genetic Models International, Indianapolis.</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/zsf1-rat?region=3611&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>hybrid</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lepr&lt;sup&gt;cp&lt;/sup&gt;|Lepr&lt;sup&gt;fa&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>11570565|13432153</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401960101</CITATION_ID>
    <DESCRIPTION>This F1 obese model was developed by crossing rat strains with two separate leptin receptor mutations (fa and facp),  In Charles River, they mate a Heterozygous ZDF (fa/+) with a Homozygous SHHF (cp/cp).This mating of ZDF and SHHF parent can produce obese ZSF1 (having fa and cp mutation from both parents) or lean ZSF1 (having just one copy of mutated Lepr, either cp or fa). The obese F1 develop insulin resistance, hyperglycaemia, and mild hypertension</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401960104</RGD_ID>
    <STRAIN_SYMBOL>ZSF1-&lt;i&gt;Lepr&lt;sup&gt;lean&lt;/sup&gt;&lt;/i&gt;/Crl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Genetic Models International, Indianapolis.</ORIGINATION>
    <SOURCE>&lt;a href=https://www.criver.com/products-services/find-model/zsf1-rat-lean?region=3611&gt;Charles River Laboratories &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>hybrid</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401960104</CITATION_ID>
    <DESCRIPTION>This F1 lean model was developed by crossing rat strains with two separate leptin receptor mutations (fa and cp). In Charles River, they mate a Heterozygous ZDF (fa/+) with a Homozygous  SHHF (cp/cp).This mating of  ZDF and SHHF parent can produce obese ZSF1 (having  fa and cp mutation from both parents) or lean ZSF1 (having just one copy of mutated Lepr, either cp or fa).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401976372</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Crh&lt;sup&gt;tm1(Cre)Kji&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was created by Dr. Karl Iremonger at the Centre for Neuroendocrinology, Department of Physiology, University of Otago, Dunedin, New Zealand</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401976372</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 technology was used to insert an IRES for Cre expression after the corticotropin-releasing hormone (Crh) gene and is expressed in cells that produce CRH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401976374</RGD_ID>
    <STRAIN_SYMBOL>NTacSam:SD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://http://www.samtako.com/bbs/board.php?bo_table=b1#&gt;Taconic&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401976374</CITATION_ID>
    <DESCRIPTION>This outbred Sprague Dawley was originally from Taconic and bred at SAMTAKO in Korea.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401976436</RGD_ID>
    <STRAIN_SYMBOL>Cnc:WI</STRAIN_SYMBOL>
    <FULL_NAME>Wistar rats</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.spfbiotech.com/product/ratdetail/10/74&gt;spfbiotech&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401976436</CITATION_ID>
    <DESCRIPTION>The Wistar rat is an outbred albino rat. This breed was developed at the Wistar Institute in 1906 for use in biological and medical research. The Wistar was maintained by China National Center For Rodent Laboratory Animal. and available from SPF biotech since 2019.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401976445</RGD_ID>
    <STRAIN_SYMBOL>HsdOla:LIS</STRAIN_SYMBOL>
    <FULL_NAME>Lister Hooded</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.inotivco.com/model/hsdola-lh&gt; inotiv&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401976445</CITATION_ID>
    <DESCRIPTION>Medical Research Council, Mill Hill obtained LH stock from ICI, Alderley Edge in 1932 and have maintained closed colony since that time.
From Medical Research Council, Mill Hill to OLAC (Harlan) in 1969. Harlan became Envigo in 2015, then Envigo was acquired by Inotiv in 2021.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>401976475</RGD_ID>
    <STRAIN_SYMBOL>CrlNifdc:CD(SD)</STRAIN_SYMBOL>
    <FULL_NAME>Sprague-Dawley</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://nrla.nifdc.org.cn/resource/zinfo.html?id=LJDm7HWNa+QBdY1tlGAACA==&amp;kjzybm=CSTR:15497.09.N2004&gt; National Rodent Laboratory Animal Resources Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_401976475</CITATION_ID>
    <DESCRIPTION>Originated in 1925 by Robert W. Dawley from a hybrid hooded male and a female Wistar rat. To CRL in 1950 from Sprague Dawley, Inc. Caesarean rederived in 1955 from original Charles River Sprague Dawley. colonies. In 1991, 8 colonies were selected to form the IGS Foundation Colony. Rederived into isolator foundation colony in 1997. IGS refers to animals bred using the CRL International Genetic Standard system. The Nifdc strain is available from ?National Rodent Laboratory Animal Resources Center? in China.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>404976869</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Tlr4&lt;sup&gt;em6Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2024-03-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Tlr4&lt;sup&gt;em6Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>404976870</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_404976869</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Tlr4 gene of Crl:SD rat embryos. The resulting mutation is a 14-bp deletion in exon 2; rn7:chr5:80,151,447-80,151,460.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>404976871</RGD_ID>
    <STRAIN_SYMBOL>DA/MolTacMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-03-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_404976871</CITATION_ID>
    <DESCRIPTION>A closed colony of DA/MolTac  (RRID:RGD_1566438) has been maintained at the Medical College of Wisconsin for more than 30 generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>404976872</RGD_ID>
    <STRAIN_SYMBOL>DA;CD-Tg(RNECO-180E22)733Arno/Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2024-03-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_404976872</CITATION_ID>
    <DESCRIPTION>CD-Tg(RNECO-180E22)733Arno, RGD:155663367 was backcrossed at the Medical College of Wisconsin to DA/MolTacMcwi for 6-7 generations before cryopreservation of sperm.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>404976873</RGD_ID>
    <STRAIN_SYMBOL>SS-Del(1q)2Mcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>Please contact: mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2024-03-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_404976873</CITATION_ID>
    <DESCRIPTION>Four single guide RNAs and SpCas9 targeting sequences CTTCATTGTATGAGCAGCCG, TTTGAAAGAGACAGCTGCCT, ACGCACGTCGGACAGTTCCA, and GGCTTATTGCGCACGCACGT flanking a chromosome 1 region were targeted in SS/JrHsdMcwi embryos. An 82-bp deletion in chromosome 1 (rn7: chr1:255,749,164-255,749,245) resulted.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405100226</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Fmr1&lt;sup&gt;em1Sidb&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>SAGE (Sigma Advanced Genetic Engineering) Labs</ORIGINATION>
    <SOURCE>Simons Initiative for the Developing Brain (SIDB), Institute for Neuroscience and Cardiovascular Research, University of Edinburgh, Edinburgh EH8 9XD, UK. Contact SIDB Scientific Officer for enquiries on rat distribution (sidbadm@ed.ac.uk).</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Fmr1&lt;sup&gt;em1Sidb&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>625813034</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="152284857" STOP_POS="152322686" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="147240239" STOP_POS="147278057" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="154684924" STOP_POS="154722369" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="154756031" STOP_POS="154793782" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405100226</CITATION_ID>
    <DESCRIPTION>Colony founders were produced by SAGE (Sigma Advanced Genetic Engineering) Labs using ZFN-mediated disruption of Fmr1  with a targeted construct containing coding sequence for eGFP; resulting founders did not express FMRP or eGFP.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405100723</RGD_ID>
    <STRAIN_SYMBOL>LE-ROSA26 &lt;sup&gt;em1(CAG-Ghsr)Ottc&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Optogenetics and Transgenic Technology Core</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1022&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-08-29)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01022</CITATION_ID>
    <DESCRIPTION>The CRISPR/Case9 knock-in of CAG-LSL-Ghsr (LSL: loxp-Stop-Loxp) to the ROSA 26 locus of LE rats has cre recombinase-dependent expression of  rat Ghsr under the control of CAG promoter.  ROSA26 is a synonym for rat Thumpd3-as1 (RGD:6491660) and is used as an official symbol for rat strain nomenclature.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405100724</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Pdyn&lt;sup&gt;em1(iCre)Ottc&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Optogenetics and Transgenic Technology Core</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1023&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2026-02-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01023</CITATION_ID>
    <DESCRIPTION>This mutant rat was produced by targeted knocking adding in IRES-iCre to the 3' end of Pdyn in LE rat using CRISPR/Cas9 method.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405100725</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Pdyn&lt;sup&gt;em(iCre)2Ottc&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Optogenetics and Transgenic Technology Core</ORIGINATION>
    <SOURCE>Optogenetics and Transgenic Technology Core</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405100725</CITATION_ID>
    <DESCRIPTION>This mutant rat was produced by targeted knocking adding in IRES-iCre to the 3' end of Pdyn in LE rat  using CRISPR/Cas9 method.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405649860</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Esr1&lt;sup&gt;em1Bra-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Genome Editing and Animal Models, University of Wisconin-Madison</ORIGINATION>
    <SOURCE>Department of Medicine, Division of Pulmonary, Critical Care, Sleep and Occupational Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Esr1&lt;sup&gt;em1Bra&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>405649861</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="43511685" STOP_POS="43904454" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="41106335" STOP_POS="41499104" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="41192029" STOP_POS="41594799" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="42534049" STOP_POS="42935434" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="35523680" STOP_POS="35759891" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405649860</CITATION_ID>
    <DESCRIPTION>Two target sequences (GCCGTGTTCAACTACCCCGAGGG and
GCTGCGCAAGTGTTACGAAGTGG) within the second and third exon, respectively, of the
coding sequence of Esr1 (the rat gene encoding ERα) were selected. gRNAs targeting these
sequences were synthesized via in vitro transcription. gRNAs (25 ng/ul each) were co-
microinjected with Cas9 protein (40 ng/ul) into Sprague-Dawley rat embryos, and embryos were
transferred into pseudo-pregnant recipients. Animals heterozygous for a 25 base pair deletion in Esr1 exon 3 were used to establish an ER alpha mutant colony and subsequent homozygous mutant offspring were obtained for study.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405650195</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Esr1&lt;sup&gt;em1Bra+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Genome Editing and Animal Models, University of Wisconin-Madison</ORIGINATION>
    <SOURCE>Department of Medicine, Division of Pulmonary, Critical Care, Sleep and Occupational Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405650195</CITATION_ID>
    <DESCRIPTION>This is the  wild type littermate from the crossing of heterozygous Esr1 mutant rats. This wild type littermate rat was used as a control for the homozygous mutant SD-Esr1em1-/- (RGD:405649860)  in estrogen receptor study.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405847397</RGD_ID>
    <STRAIN_SYMBOL>Wakil: bHR</STRAIN_SYMBOL>
    <FULL_NAME>High Responder</FULL_NAME>
    <ORIGINATION>The selectively bred High Responder (bHR) rat line was generated at the University of Michigan (Ann Arbor, MI USA).</ORIGINATION>
    <SOURCE>Laboratory of Dr. Huda Akil and Dr. Stanley Watson,
MBNI,
University of Michigan,
205 Zina Pitcher Pl. 
Ann Arbor, MI 48109
Please contact  hebda@med.umich.edu for availability or contact URL
https://medicine.umich.edu/dept/mni/elaine-k-hebda-bauer-phd</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-05-16)</AVAILABILITY>
    <RESEARCH_USE>Substance Use, Mood Disorder, Hyperactivity, Exploratory Behavior, Locomotor Behavior, Behavioral Disinhibition, Externalizing</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405847397</CITATION_ID>
    <DESCRIPTION>Dawley rats derived from three distinct breeding colonies. In the first generation, sib-matings were avoided by only breeding pairs of animals that were derived from different colonies.  At each generation, we maintain 12 litters for each of our selectively bred lines. Behavior response to a novel environment performed on adults was used as a criterion for selective breeding. Males and females with the highest scores from locomotion testing were bred together to generate the bred high-responder (bHR).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405847400</RGD_ID>
    <STRAIN_SYMBOL>Wakil: bLR</STRAIN_SYMBOL>
    <FULL_NAME>Low Responder</FULL_NAME>
    <ORIGINATION>The selectively bred Low Responder (bLR) rat line was generated at the University of Michigan (Ann Arbor, MI USA).</ORIGINATION>
    <SOURCE>Laboratory of Dr. Huda Akil and Dr. Stanley Watson,
MBNI,
University of Michigan,
205 Zina Pitcher Pl. 
Ann Arbor, MI 48109
Please contact  hebda@med.umich.edu for availability or contact URL
https://medicine.umich.edu/dept/mni/elaine-k-hebda-bauer-phd</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-05-16)</AVAILABILITY>
    <RESEARCH_USE>Substance Use, Mood Disorder, Hyperactivity, Exploratory Behavior, Locomotor Behavior, Behavioral Disinhibition, Externalizing</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405847400</CITATION_ID>
    <DESCRIPTION>Dawley rats derived from three distinct breeding colonies. In the first generation, sib-matings were avoided by only breeding pairs of animals that were derived from different colonies.  At each generation, we maintain 12 litters for each of our selectively bred lines. Behavior response to a novel environment performed on adults was used as a criterion for selective breeding. Males and females with the lowest scores from locomotion testing were bred together to generate the bred low-responder (bHR).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405849381</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Tti2&lt;sup&gt;em1Ipcv+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405849381</CITATION_ID>
    <DESCRIPTION>This Tti2 knockout rats were generated by microinjecting fertilized ova of SHR/OlaIpcv rats with the ZFN (Zinc Finger Nuclease) construct from Sigma-Aldrich. The construct was designed to target the first exon using the following sequence of ZFN binding (capital letters) and cutting site (small letters): TCTGACCCGGATCCAAGCaccaagGGTGGGTGGCAGGGC. DNA samples isolated from 452 rats born after microinjection with ZFN construct were amplified using primers flanking the target sequence: ZFN F: 5'-TACACTGTGATTGGCTGGGA-3' and ZFN R: 5'-GGCGCAGTGGAGTGATC-3'.   SHR-Tti2+/- with an 8 bp deletion (NM_001013883.1(Tti2):c.243_250delCGAGATCC; on the protein level: NP_001013905.1:p.Glu82Glyfs) has been selected for further analyses. The heterozygous founder was crossed with SHR and F1 rats were intercrossed. SHR-Tti2+/- heterozygotes were selected for breeding and phenotyping while their wild type littermates were used as controls.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405849382</RGD_ID>
    <STRAIN_SYMBOL>SHR-&lt;i&gt;Tti2&lt;sup&gt;em1Ipcv+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405849382</CITATION_ID>
    <DESCRIPTION>This is the wild type littermate of the Tti2 knockout rats. The knockout rats  were generated by microinjecting fertilized ova of SHR/OlaIpcv rats with the ZFN (Zinc Finger Nuclease) construct from Sigma-Aldrich. The construct was designed to target the first exon using the following sequence of ZFN binding (capital letters) and cutting site (small letters): TCTGACCCGGATCCAAGCaccaagGGTGGGTGGCAGGGC. DNA samples isolated from 452 rats born after microinjection with ZFN construct were amplified using primers flanking the target sequence: ZFN F: 5'-TACACTGTGATTGGCTGGGA-3' and ZFN R: 5'-GGCGCAGTGGAGTGATC-3'.   SHR-Tti2+/- with an 8 bp deletion (NM_001013883.1(Tti2):c.243_250delCGAGATCC; on the protein level: NP_001013905.1:p.Glu82Glyfs) has been selected for further analyses. The heterozygous founder was crossed with SHR and F1 rats were intercrossed. SHR-Tti2+/- heterozygotes were selected for breeding and this wild type littermates were used as controls.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405849385</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(DNMT3A&lt;sup&gt;+&lt;/sup&gt;) Feis</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shanghai Jiao Tong University
International Peace Maternity &amp; Child Health Hospital
Shanghai Key laboratory for Embryo?Original Adult Disease
School of Medicine
Shanghai Jiao Tong University
Shanghai
200030</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405849385</CITATION_ID>
    <DESCRIPTION>The hDNMT3A transgenic rats were established using zygote microinjection of a bacterial artificial chromosome (BAC). The RP11-159D24 BAC (NCBI-ID:223335, Homo sapiens, GRCh38.p2: Chr. 2: 25,202,642-25,410,145, total length: 207,504 bp) containing DNMT3A (GRCh38.p2: 25,232,961,25,342,590, total length: 109,630 bp) was injected into rat zygotes (Rattus norvegicus, Sprague-Dawley, SD). The offspring were identified with 8 PCR primer-pairs that were specific for the RP11-159D24 sequence to detect positive transgenic ones.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405849386</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(DNMT3A)&lt;sup&gt;-/-&lt;/sup&gt; Feis</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shanghai Jiao Tong University
International Peace Maternity &amp; Child Health Hospital
Shanghai Key laboratory for Embryo?Original Adult Disease
School of Medicine
Shanghai Jiao Tong University
Shanghai
200030</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405849386</CITATION_ID>
    <DESCRIPTION>This is the wild type littermate of the hDNMT3A transgenic rats which were established using zygote microinjection of a bacterial artificial chromosome (BAC). The RP11-159D24 BAC (NCBI-ID:223335, Homo sapiens, GRCh38.p2: Chr. 2: 25,202,642-25,410,145, total length: 207,504 bp) containing DNMT3A (GRCh38.p2: 25,232,961,25,342,590, total length: 109,630 bp) was injected into rat zygotes (Rattus norvegicus, Sprague-Dawley, SD). The offspring were identified with 8 PCR primer-pairs that were specific for the RP11-159D24 sequence to detect positive transgenic ones and wild type littermates that did not carry the human transgene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405849408</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Xdh&lt;sup&gt;em1Mcwi+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Xdh&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>14398480</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="27282319" STOP_POS="27344022" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="21530463" STOP_POS="21592172" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="25149570" STOP_POS="25211273" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="34996983" STOP_POS="35059195" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="21417685" STOP_POS="21590015" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405849408</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 7-bp deletion in exon 4 of rat Xdh gene in the SS/JrHsdMcwi embryos. This is a heterozygous strain which has decreased Xdh protein detected in the kidney cortex tissue as compared to the wild type littermate at 6-week old.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405849409</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Xdh&lt;sup&gt;em1Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405849409</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a 7-bp deletion in exon 4 of rat Xdh gene in the SS/JrHsdMcwi embryos. This is a wild type littermate used as the control for its  homozygous  or  heterozygous littermate.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405849411</RGD_ID>
    <STRAIN_SYMBOL>WKY-&lt;i&gt;Krtcap3&lt;sup&gt;em3Mcwi+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>MCW Gene Editing Rat Resource Center</ORIGINATION>
    <SOURCE>Contact MCW rat distribution at mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405849411</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to introduce a mutation in the Krtcap3  gene of WKY/Ncrlrat embryos. This is the wild type littermate (from heterozygous breeders) carrying wild type Krtcap3. This wild type mutant usually is used as an experimental control.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405850241</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Mir500 &lt;sup&gt;em1Cgen&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Cyagen Biosciences
19 South Dongcang Rd
Taicang
Jiangsu
215499
P. R. China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Mir500 &lt;sup&gt;em1Cgen&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>405850242</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="17930647" STOP_POS="17930726" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="15258778" STOP_POS="15258857" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="16121332" STOP_POS="16121411" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="16906456" STOP_POS="16906535" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405850241</CITATION_ID>
    <DESCRIPTION>Sprague Dawley rats by microinjection of TALENs in fertilized eggs (Cyagen Biosciences). Briefly, the rno-mir-500 gene (Gene ID: 100314112; MirBase accession no. MIMAT0005321), which was located on rat chromosome X, was selected as the TALEN target site. TALENs were constructed using the Golden Gate Assembly and confirmed by sequencing. The founder, which carried 8- bp deletion (GCACCTGG) in the both strands compared with the wild-type (WT) DNA sequence, were genotyped by PCR followed by DNA-sequencing analysis. After that, heterozygous F1 were produced by mating F0 with WT rats. Heterozygous F1 rats were determined and mated to produce homozygote mutant (mir-500−/−) and WT (mir-500+/+).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405850257</RGD_ID>
    <STRAIN_SYMBOL>Stock Tc(HSA21)1Yakaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1360&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;,

&lt;a href=https://www.rrrc.us/Strain/?x=1021&gt; Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transchromosomal</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-02-03)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology, Ophthalmology, Cancer, Immunology, Internal Organ, Behavior, Hematology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01021</CITATION_ID>
    <DESCRIPTION>Chimeric rats were generated using rBLK2i-1 (WDB/Nips-ES1/Nips, RGD: 10054010) to which human chromosome 21 was introduced. They were then backcrossed with Wistar rats (Crlj:WI) for more than 10 generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405855876</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Foxo4&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute for Reproductive and Developmental Sciences, Department of Pathology
&amp; Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS
66160, USA.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=957&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Foxo4&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>405855878</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="70425218" STOP_POS="70432120" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="66385241" STOP_POS="66392115" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="71155284" STOP_POS="71162158" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="72007762" STOP_POS="72014636" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="89332278" STOP_POS="89338835" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405855876</CITATION_ID>
    <DESCRIPTION>This Foxo4 mutant strain was created in zygotes from Holtzman Sprague-Dawley.  Guided RNAs targeting exon 2 (target sequence: CCAGATATACGAATGGATGGTCC; nucleotides 517-539) and exon 3 (target sequence: GTTCATCAAGGTACATAACGAGG; nucleotides 631-653) of the Foxo4 gene (NM_001106943.1)) were injected to the embryos to create  a 3096-bp deletion including the 3' part of exon 2 and 5' part of exon 3, and resulting a premature stop of the protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405855877</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Foxo4&lt;sup&gt;em1Soar+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute for Reproductive and Developmental Sciences, Department of Pathology
&amp; Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS
66160, USA.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405855877</CITATION_ID>
    <DESCRIPTION>This is the wild type littermate from crossing of  heterozygous mutant female rats with wild-type male rats to generate hemizygous null male rats and wild type mutant.  Foxo4 mutant strain (RGD:405855876) was created in zygotes from Holtzman Sprague-Dawley.  Guided RNAs targeting exon 2 (target sequence: CCAGATATACGAATGGATGGTCC; nucleotides 517-539) and exon 3 (target sequence: GTTCATCAAGGTACATAACGAGG; nucleotides 631-653) of the Foxo4 gene (NM_001106943.1)) were injected to the embryos to create  a 3096-bp deletion including the 3' part of exon 2 and 5' part of exon 3, and resulting a premature stop of the protein.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405878045</RGD_ID>
    <STRAIN_SYMBOL>ACI</STRAIN_SYMBOL>
    <FULL_NAME>August x Copenhagen Irish</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405878045</CITATION_ID>
    <DESCRIPTION>Curtiss and Dunning 1926 at the Columbia University Institute for Cancer Research, after accidental mating between an August male with an Irish coat and a COP (Copenhagen2331)female. This is the parent to ACI substrains sent to Heston 1945 at F30, to National Institutes of Health 1950 at F41. Subsequent sublines from Dunning or NIH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405878046</RGD_ID>
    <STRAIN_SYMBOL>BUF</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405878046</CITATION_ID>
    <DESCRIPTION>This strain derived by Heston 1946 from Buffalo stock of H. Morris, to. It is the parental strains to several BUF substrains maintained in other institutions.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405878047</RGD_ID>
    <STRAIN_SYMBOL>HTX</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405878047</CITATION_ID>
    <DESCRIPTION>D. F. Kohn, Inst. of Comparative Medicine,Columbia University established this strain from institutional albino rats of unknown origin at University of Texas. This HTX is the parent to HTX substrains maintained in other institutions.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405878048</RGD_ID>
    <STRAIN_SYMBOL>LH</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405878048</CITATION_ID>
    <DESCRIPTION>In 1969 outbred Sprague-Dawley rats were selected for high systolic blood pressure using an indirect plethysmographic technique in pre-warmed unrestrained conscious rats. Three pairs were originally selected, and selection was continued with brother x sister mating. Strain LN was maintained as a normotensive control, and LL as a hypotensive strain. (see Vincent et al 1984, and Vincent and Sassard, 1994 for reviews). This LH is the parent to LH substrains maintained in other institutions.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405878049</RGD_ID>
    <STRAIN_SYMBOL>LL</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405878049</CITATION_ID>
    <DESCRIPTION>This the hypotensive strain established from the selective breeding In 1969.  Outbred Sprague-Dawley rats were selected for systolic blood pressure trait using an indirect plethysmographic technique in pre-warmed unrestrained conscious rats. Three pairs were originally selected, and selection was continued with brother x sister mating. Strain LN was maintained as a normotensive control, and LH as a hypertensive strain. (see Vincent et al 1984, and Vincent and Sassard, 1994 for reviews).  This LL is the parent to LL substrains maintained in other institutions.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405878050</RGD_ID>
    <STRAIN_SYMBOL>LN</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405878050</CITATION_ID>
    <DESCRIPTION>This is the normotensive control strain established from the selective breeding In 1969.  Outbred Sprague-Dawley rats were selected for systolic blood pressure trait using an indirect plethysmographic technique in pre-warmed unrestrained conscious rats. Three pairs were originally selected, and selection was continued with brother x sister mating. Strain LH was maintained as a hypertensive strain, and LL as a hypotensive strain. (see Vincent et al 1984, and Vincent and Sassard, 1994 for reviews). This LN is the parent to LN substrains maintained in other institutions.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405878051</RGD_ID>
    <STRAIN_SYMBOL>MR</STRAIN_SYMBOL>
    <FULL_NAME>Maudsely reactive</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2024-07-09)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405878051</CITATION_ID>
    <DESCRIPTION>This strain has been selected for high open-field defecation (a test of emotional reactivity). The underlying genetic basis for this phenotype is not known. Originally selected by Broadhurst in 1954 for high open-field defacation (OFD) response in an open field. This MR is the parent to MR substrains maintained in other institutions.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405878052</RGD_ID>
    <STRAIN_SYMBOL>RCS</STRAIN_SYMBOL>
    <FULL_NAME>royal college of surgeons rat</FULL_NAME>
    <ORIGINATION/>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405878052</CITATION_ID>
    <DESCRIPTION>Originally developed before 1965 by Sidman from stock obtained from Sorsby of the Royal College of Surgeons, This RCS is the parent to RCS substrains maintained in other institutions.The RCS/LavRrrc substrain is available  from Rat Resource &amp; Research Center.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>405878082</RGD_ID>
    <STRAIN_SYMBOL>PD</STRAIN_SYMBOL>
    <FULL_NAME>polydactylous</FULL_NAME>
    <ORIGINATION>Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_405878082</CITATION_ID>
    <DESCRIPTION>Strain a highly inbred strain kept since 1969 at the Institute of Biology Medical Genetics, Charles University, Prague. Strain originated from Wistar rats exhibiting a spontaneous mutation which gave rise to the polydactyly-luxate syndrome.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407420261</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nme7&lt;sup&gt;em1Pdra+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory of Transgenic Models of Diseases, Institute of Molecular Genetics of the Czech Academy of Sciences,  Czech Republic.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_407420261</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 nuclease system was used to generate Sprague Dawley (SD) rats
with Nme7 gene knock-out. Two sets of guide (g)RNA were designed within the exon 4 of
the Nme7 gene. A knock-out founder with a 5-nucleotide deletion (TCGAA within the exon 4 of the Nme7 gene) 
creating a premature stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407420262</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Nme7&lt;sup&gt;em1Pdra-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory of Transgenic Models of Diseases, Institute of Molecular Genetics of the Czech Academy of Sciences,  Czech Republic.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_407420262</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 nuclease system was used to generate Sprague Dawley (SD) rats
with Nme7 gene knock-out. Two sets of guide (g)RNA were designed within the exon 4 of
the Nme7 gene. A knock-out founder with a 5-nucleotide deletion (TCGAA within the exon 4 of the Nme7 gene) 
creating a premature stop codon.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407431635</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Drd3&lt;sup&gt;em2(cre)Davis&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Created by Daniel Davis at University of Missouri for Section on Behavioral Neuroscience, NIMH.</ORIGINATION>
    <SOURCE>Deposited at RRRC.  Contact RRRC@missouri.edu  for availability.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-08-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_407431635</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 was used to insert CRE recombinase at DRD3 in rat embryos.This is line2, and line1 is "LE-DRD3em1(cre)Davis" (RGD:407431632). Both are created by Daniel Davis at University of Missouri for the Section on Behavioral Neuroscience at NIMH.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407431636</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Drd3&lt;sup&gt;em3(cre)Davis&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Created by Daniel Davis at University of Missouri for Section on Behavioral Neuroscience, NIMH.</ORIGINATION>
    <SOURCE>Deposited at RRRC.  Contact RRRC@missouri.edu  for availability.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-08-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_407431636</CITATION_ID>
    <DESCRIPTION>This rat model was generated using CRISPR-Cas9 technology insert a Cre-P2A cassette into the ATG start site of rat Drd3.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407431637</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Gal&lt;sup&gt;em2(cre)Davis&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Created by Daniel Davis at University of Missouri for Section on Behavioral Neuroscience, NIMH.</ORIGINATION>
    <SOURCE>Deposited at RRRC. Deposited at RRRC.  Contact RRRC@missouri.edu  for availability.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-08-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_407431637</CITATION_ID>
    <DESCRIPTION>This rat model was generated using CRISPR-Cas9 technology insert a Cre-P2A cassette into the ATG start site of rat Gal. Created by Daniel Davis at University of Missouri.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407445919</RGD_ID>
    <STRAIN_SYMBOL>Mmab:W</STRAIN_SYMBOL>
    <FULL_NAME>Wistar</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>Department for Breeding of Laboratory and Experimental Animals, Institute for Medical Research, Military Medical Academy, Belgrade</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-08-22)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_407445919</CITATION_ID>
    <DESCRIPTION>The outbred Wistar rats which bred and housed at the Military Medical Academy in Belgrade, Serbia</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407446370</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cyp2d&lt;sup&gt;em1Kg&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dr.  Kristin Grimsrud at University of California, Davis</ORIGINATION>
    <SOURCE>The rat strain is deposited to Rat Research and Resource Contact RRRC@missouri.edu for availability.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown (as of 2024-08-29)</AVAILABILITY>
    <RESEARCH_USE>Pharmacogenetics, drug studies</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01005</CITATION_ID>
    <DESCRIPTION>A ~58.0 kb deletion of the rat Cyp2d gene cluster (1-5) was created using the CRISPR-Cas9 system.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407446371</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cyp2d&lt;sup&gt;em2(CYP2D6)Kg&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Dr.  Kristin Grimsrud at University of California, Davis</ORIGINATION>
    <SOURCE>The rat strain is deposited to Rat Research and Resource Contact RRRC@missouri.edu for availability.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2024-08-29)</AVAILABILITY>
    <RESEARCH_USE>Pharmacogenetics, drug studies</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01006</CITATION_ID>
    <DESCRIPTION>A ~58.0 kb deletion of the rat Cyp2d gene cluster (1-5) was created using the CRISPR-Cas9 system. Subsequently, the human CYP2D6 gene (~6.2 kb) was inserted in place of the rat Cyp2d gene cluster.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407450403</RGD_ID>
    <STRAIN_SYMBOL>BN/Slacc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Shanghai laboratory animal center of the Chinese Academy of Sciences, Shanghai, China</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_407450403</CITATION_ID>
    <DESCRIPTION>Substrain of BN maintained at Shanghai laboratory animal center of the Chinese Academy of Sciences, Shanghai, China</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407450412</RGD_ID>
    <STRAIN_SYMBOL>Liuch:WI</STRAIN_SYMBOL>
    <FULL_NAME>Wistar rats</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>The Laboratory Animal Center of Zhejiang University</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_407450412</CITATION_ID>
    <DESCRIPTION>This outbred rat strain was derived from Wistar Institute. Now is maintained at the Laboratory Animal Center of Zhejiang University</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407450413</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Il6&lt;sup&gt;em1Yona-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Pharma Foods International Co., Ltd. (Kyoto, Japan)</ORIGINATION>
    <SOURCE>National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka 564-8565, Japan</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Il6&lt;sup&gt;em1Yona&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>407450416</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="5889999" STOP_POS="5894575" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="5214602" STOP_POS="5219178" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="3043231" STOP_POS="3047807" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="3095536" STOP_POS="3100112" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="456799" STOP_POS="461376" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_407450413</CITATION_ID>
    <DESCRIPTION>The Il6 knockout (KO) rats were generated using the CRISPR/Cas9 technique to induce a shift in the 
reading frame of the second exon of Il6 by KAC Co. Ltd (Kyoto, Japan). This strain carried a
118 bp deleted in the second exon of IL-6</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407450414</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Il6&lt;sup&gt;em1Yona+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Pharma Foods International Co., Ltd. (Kyoto, Japan)</ORIGINATION>
    <SOURCE>National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka 564-8565, Japan</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_407450414</CITATION_ID>
    <DESCRIPTION>The wild type rats were littermates of cross of heterozygous  Il6  mutant rats. The wild type littermates were used as experimental controls for the homozygous mutant SD-Il6em1Yona-/- (RGD:407450413) generated using the CRISPR/Cas9 technique to induce a 118 bp deletion  in the reading frame of the second exon of Il6 by KAC Co. Ltd (Kyoto, Japan).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407550225</RGD_ID>
    <STRAIN_SYMBOL>WKYLEWF1/Ebv</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology, Justus Liebig University, Giessen, Germany</ORIGINATION>
    <SOURCE>Department of Physiology, Justus Liebig University, Giessen, Germany</SOURCE>
    <STRAIN_TYPE>hybrid</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_407550225</CITATION_ID>
    <DESCRIPTION>This hybrid rat is a cross between a WKY female and a LEW male rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407570623</RGD_ID>
    <STRAIN_SYMBOL>Slacc:SD</STRAIN_SYMBOL>
    <FULL_NAME>Sprague-Dawley</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>Laboratory Animal Management Department, Shanghai Institute of Family Planning Science.</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_407570623</CITATION_ID>
    <DESCRIPTION>SD rats maintained at Laboratory Animal Management Department, Shanghai Institute of Family Planning Science..</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>407571697</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Nr3c1&lt;sup&gt;em1Jhrmn&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Strain deposited with the &lt;a href=http://www.rrrc.us/Strain/?x=1036&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nr3c1&lt;sup&gt;em1Jhrmn&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>125097487</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="31522783" STOP_POS="31644508" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="31271681" STOP_POS="31393320" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="31728373" STOP_POS="32704022" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="31408742" STOP_POS="32348480" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="32371496" STOP_POS="32459145" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01036</CITATION_ID>
    <DESCRIPTION>This LE mutant strain was produced by backcrossing SD-Nr3c1em1Jhrmn (RGD:125097486) to the LE background. SD-Nr3c1em1Jhrmn was produced by CRISPR-mediated knock in of loxP sites flanking Glucocorticoid Receptor exon 3 via Homology Directed Repair (HDR)</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>408364955</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Vdr&lt;sup&gt;em1Hfd&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hector DeLuca laboratory at UW-Madison</ORIGINATION>
    <SOURCE>This strain is deposited to Rat Resource and Research Center (RRRC)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2024-11-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Vdr&lt;sup&gt;em1Hfd&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>408364972</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="130864764" STOP_POS="130916757" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="129014788" STOP_POS="129014799" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="139344452" STOP_POS="139394138" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="139536241" STOP_POS="139585928" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="136567614" STOP_POS="136617280" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01033</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to introduce a  net 12-bp deletion in exon 3 of the VDR gene of Hsd:SD rat embryos

WT: GGAGGCAACAGCGGCCAGCACCTCCCTGCCCGACCCTGGTGACTTTGACCGGAACGTGcccccggatctgtgGAGTGTGTGGAGACCGAGCCAC 
KO: GGAGGCAACAGCGGCCAGCACCTCCCTGCCCGACCCTGGTGACTTTGACCGGAACGTGt--del---                               GAGTGTGTGGAGACCGAGCCAC</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>408364956</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Vdr&lt;sup&gt;em2Hfd&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hector DeLuca laboratory at UW-Madison</ORIGINATION>
    <SOURCE>Rat Resource and Research Center (RRRC); strain ID 1034</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2024-11-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01034</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to introduce deletion and insertion in exon 3 of the VDR gene of Hsd:SD rat embryos

WT: GGAGGCAACAGCGGCCAGCACCTCCCTGCccgaccCTGGTGACTTTGACCggaacgtgccccGGATCTGTGGAGTGTGTGGAGACCGAGCCAC
KO: GGAGGCAACAGCGGCCAGCACCTCCCTGCtggt– CTGGTGACTTTGACC------GGATCTGTGGAGTGTGTGGAGACCGAGCCAC</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>408364957</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Apc&lt;sup&gt;Pirc/Uwm&lt;/sup&gt;Vdr&lt;sup&gt;em3Hfd&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hector DeLuca laboratory at UW-Madison</ORIGINATION>
    <SOURCE>Rat Resource and Research Center (RRRC); strain ID 1033</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2024-11-05)</AVAILABILITY>
    <RESEARCH_USE>Colon cancer</RESEARCH_USE>
    <ALLELES>Apc&lt;sup&gt;Pirc&lt;/sup&gt;|Vdr&lt;sup&gt;em3Hfd&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>1554322|408364962</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="26190901" STOP_POS="26190901" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="129014788" STOP_POS="129014792" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="25916744" STOP_POS="25916744" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="27100213" STOP_POS="27100213" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="26725560" STOP_POS="26820837" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="139536241" STOP_POS="139585928" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="136567614" STOP_POS="136617280" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="26732147" STOP_POS="26790383" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01033</CITATION_ID>
    <DESCRIPTION>The F344-ApcPirc rat was generated previously by ENU mutagenesis (RGD ID 1641862). These fertilized rat embryos were used with the CRISPR/Cas9 system to introduce a 5-bp deletion (CCCCG) in exon 3 of the Vdr gene. This mutant was heterozygous for the Apc mutation and homozygous for the VDR deletion. 

WT: GGAGGCAACAGCGGCCAGCACCTCCCTGCCCGACCCTGGTGACTTTGACCGGAACGTGCCCCGGATCTGTGGAGTGTGTGGAGACCGAGCCAC
KO: GGAGGCAACAGCGGCCAGCACCTCCCTGCCCGACCCTGGTGACTTTGACCGGAACGTGG              ATCTGTGGAGTGTGTGGAGACCGAGCCAC</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>408364958</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cyp27b1&lt;sup&gt;em1Hfd&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hector DeLuca laboratory at UW-Madison</ORIGINATION>
    <SOURCE>Rat Resource and Research Center (RRRC); strain ID 1031</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2024-11-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp27b1&lt;sup&gt;em1Hfd&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>408364974</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="64756626" STOP_POS="64761570" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="62871377" STOP_POS="62871458" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="70333150" STOP_POS="70340006" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="70512763" STOP_POS="70517707" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01031</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to introduce a 82-bp deletion in exon 1 of the Cyp27b1 gene of Hsd:SD rat embryos

WT: CTCGCCTCCAGAGTCTTCCATCGAGTCCAACTGCCTTCTcagctgggcagtgactcggttctccggagtttatctgatatccctgggccctctacacctagcttcctggctgaactcttctGCAAAGGGGG

KO: CTCGCCTCCAGAGTCTTCCATCGAGTCCAACTGCCTTCT---                                                                                                                                                                                                 GCAAAGGGGG</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>408364959</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cyp27b1&lt;sup&gt;em2Hfd&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Hector DeLuca laboratory at UW-Madison</ORIGINATION>
    <SOURCE>Rat Resource and Research Center (RRRC); strain ID 1032</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2024-11-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Cyp27b1&lt;sup&gt;em2Hfd&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>408364975</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="64756626" STOP_POS="64761570" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="62871348" STOP_POS="62871376" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="70333150" STOP_POS="70340006" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="70512763" STOP_POS="70517707" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01032</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to introduce a 29-bp deletion in exon 1 of the Cyp27b1 gene of Hsd:SD rat embryos

WT: CTCGCCTCCAgagtcttccatcgagtccaactgccttctCAGCTGGGCAGTGACTCGGTTCTCCGGAGTTTATCTGATATCCCTGGGCCCTCTACACCTAGCTTCCTGGCTGAACTCTTCTGCAAAGGGGG
KO: CTCGCCTCCA-----                                                               CAGCTGGGCAGTGACTCGGTTCTCCGGAGTTTATCTGATATCCCTGGGCCCTCTACACCTAGCTTCCTGGCTGAACTCTTCTGCAAAGGGGG</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>408364982</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;C1ql3&lt;sup&gt;em1Lian&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Laboratory Animal Science, Peking Union Medicine College,</ORIGINATION>
    <SOURCE>National Human Disease Animal Model Resource Center, Beijing, China (https://namr.org.cn/Ldesc/1_1074)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2024-11-08)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>C1ql3&lt;sup&gt;em1Lian&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>408364987</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="81028418" STOP_POS="81038244" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="76119344" STOP_POS="76129170" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="80314186" STOP_POS="80320681" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="81939086" STOP_POS="81945581" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="87275167" STOP_POS="87285484" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_408364982</CITATION_ID>
    <DESCRIPTION>The C1ql3 knout rats were established using CRISPR/cas9 method. The exon 1 of C1ql3 was
targeted with two sgRNAs of (TCATC CTC ATC CCG GTG CTGG) and
(AAGGT GCT GAC AAG AGG GAGG), which, respectively, targeted on
the 5′ end and the 3′ end of exon 1.Wistar embryos born from Sprague Dawley pseudo-pregnant female were genotyped by polymerase chain reaction (PCR) with two
upstream primers of (5′-TCCAAAAG CAG ACA AGA GGATC-3′
and 5′-CTACTTCT TCA CCT ACC ACG TCCTG-3′)
and one downstream primer
(5′-GGCTTCTG AAA CCT TAT ACA TTCTCG-3′). This mutant carried a 631-bp deletion resulting a premature stop at 61 bp of the open reading frame.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>529435545</RGD_ID>
    <STRAIN_SYMBOL>Wakil:bHRbLRF1</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory of Dr. Huda Akil and Dr. Stanley Watson, MBNI, University of Michigan, 205 Zina Pitcher Pl. Ann Arbor, MI 48109</ORIGINATION>
    <SOURCE>Laboratory of Dr. Huda Akil and Dr. Stanley Watson, MBNI, University of Michigan, 205 Zina Pitcher Pl. Ann Arbor, MI 48109</SOURCE>
    <STRAIN_TYPE>hybrid</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_529435545</CITATION_ID>
    <DESCRIPTION>Offspring of a cross between the F37  Wakil: bHR (RGD:405847397) female and  Wakil  bLR (RGD:405847400) male rat.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>596938164</RGD_ID>
    <STRAIN_SYMBOL>CrlNctr:CD(SD)</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.criver.com/en-US/Pages/home.aspx&gt; Charles River Laboratories&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_596938164</CITATION_ID>
    <DESCRIPTION>A colony of outbred Crl:CD(SD) (RGD:734476)  maintained at National Center for Toxicological Research, FDA.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>597538479</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Eml1&lt;sup&gt;tish&lt;/sup&gt;&lt;/i&gt;/Scrb</STRAIN_SYMBOL>
    <FULL_NAME>tish rat</FULL_NAME>
    <ORIGINATION>University of Virginia, Charlottesville, VA, United States</ORIGINATION>
    <SOURCE>University of Virginia, Charlottesville, VA, United States</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Eml1&lt;sup&gt;tish&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>597538481</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="133048271" STOP_POS="133221642" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="127283968" STOP_POS="127457246" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="132367342" STOP_POS="132450488" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="141536753" STOP_POS="141619726" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="132825590" STOP_POS="132880169" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_597538479</CITATION_ID>
    <DESCRIPTION>The first tish animals were identified on the basis of postmortem
histological analyses during the course of unrelated experiments
using a strain of Sprague Dawley rats maintained at the University of Virginia. It is called tish (telencephalic internal structural heterotopia) rat.  The brain of this mutant animal exhibits a large region of heterotopic
gray matter that is located bilaterally beneath the neocortex. Mild to moderate 
ventriculomegaly is also observed in most tish animals.  
 A breeding colony was established by identifying living relatives
of deceased tish individuals, and then these relatives were
screened using magnetic resonance imaging (MRI). The tish is identified recessive to wild type by breeding. The mutation was identified as a 1215 bp deletion in the unannotated exon 1 of Eml1 genome (Rnor_6.0; ENSRNOG00000043143).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>597538592</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(SNCA&lt;sup&gt;&lt;/sup&gt;)Nuber</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>ARCND, BWH, Harvard Medical School
77 Avenue Louis Pasteur, Boston MA 02115 USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_597538592</CITATION_ID>
    <DESCRIPTION>For the generation of transgenic rats, the authors used a 190-kb fused AF163864 PAC/AC097478 BAC clone (Yamakado et al., 2012, PMID:22475625). It contained the entire human SNCA sequence (GenBank AF163864), with 30-kb upstream regulatory promoter sequences and a 45-kb flanking downstream region, cloned into pBACe3.6 vector as described previously. Transgenic rats were obtained by injecting the purified BAC fragment into fertilized Sprague–Dawley oocytes at a concentration of 1.5 µg/ml. A founder line displaying the highest integration number of BAC DNA construct was crossedbred to homozygosity.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>597830029</RGD_ID>
    <STRAIN_SYMBOL>Pha:WI</STRAIN_SYMBOL>
    <FULL_NAME>Wistar rats</FULL_NAME>
    <ORIGINATION>Breeding station Dobrá Voda, Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Science, Slovak Republic</ORIGINATION>
    <SOURCE>Breeding station Dobrá Voda, Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Science, Slovak Republic</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_597830029</CITATION_ID>
    <DESCRIPTION>The outbred Wistar rats are maintained at  Breeding station Dobrá Voda, Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Science, Slovak Republic.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>597830140</RGD_ID>
    <STRAIN_SYMBOL>BBDR.BBDP-&lt;i&gt;(Zfp786-Aoc1)&lt;/i&gt;/Ulund</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Celiac Disease and Diabetes Unit, Lund University, Lund, Sweden</ORIGINATION>
    <SOURCE>Celiac Disease and Diabetes Unit, Lund University, Lund, Sweden</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_597830140</CITATION_ID>
    <DESCRIPTION>This congenic strain was developed by intercross breeding using diabetic prone (DP) and diabetic resistant (DR) BB rats. This diabetes susceptible congenic rat strain carries Zfp786-Aoc1 genome fragment from DP and the other genomes are from DR.  Since Gimap4 and Gimap5 are within Zfp786-Aoc1 region, they are of DP origin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>597830141</RGD_ID>
    <STRAIN_SYMBOL>BBDR.BBDP-&lt;i&gt;(Gimap1-Aoc1)&lt;/i&gt;/Ulund</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Celiac Disease and Diabetes Unit, Lund University, Lund, Sweden</ORIGINATION>
    <SOURCE>Celiac Disease and Diabetes Unit, Lund University, Lund, Sweden</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_597830141</CITATION_ID>
    <DESCRIPTION>This diabetic resistant congenic strain was developed by sister-brother breeding of heterozygote  sBBM (BBDP.BBDR-(Zfp786-Aoc1)/Ulund, RGD:597830140 ). The congenic rat carries DP genome from Gimap1-Aoc1 where Gimap5 is located.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092487</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Cftr&lt;sup&gt;em1Wpick&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Missouri Columbia</ORIGINATION>
    <SOURCE>&lt;a href=https://www.rrrc.us/Strain/?x=1038&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-03-18)</AVAILABILITY>
    <RESEARCH_USE>study of cystic fibrosis</RESEARCH_USE>
    <ALLELES>Cftr&lt;sup&gt;em1Wpick&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>598092489</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="4" START_POS="47571723" STOP_POS="47571738" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="4" START_POS="46605832" STOP_POS="46605847" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="4" START_POS="42737752" STOP_POS="42737767" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="4" START_POS="42281040" STOP_POS="42448571" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="4" START_POS="43874852" STOP_POS="44041870" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01038</CITATION_ID>
    <DESCRIPTION>A targeted 16 bp deletion was made in Exon 3 of the rat Cftr gene using CRISPR-Cas9 technology.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092509</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lgals3&lt;sup&gt;em1Dfult&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Availability Contact Email: dfulton@augusta.edu at Augusta University</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2025-03-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lgals3&lt;sup&gt;em1Dfult&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419691</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="23099795" STOP_POS="23111731" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="20620083" STOP_POS="20632019" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="24153602" STOP_POS="24165537" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="28094344" STOP_POS="28106281" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="23327071" STOP_POS="23339006" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092509</CITATION_ID>
    <DESCRIPTION>Gal-3 KO rats were developed using CRISPR technology on the Sprague-Dawley background (Sage). CRISPR guides were selected targeting the fifth exon, and gene disruption was confirmed by genomic sequencing and immunoblot analysis for Gal-3 protein expression in lung tissue. PMCID: PMC6589585</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092510</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Pbk&lt;sup&gt;em1Dfult&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Availability Contact Email: dfulton@augusta.edu at Augusta University</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Sperm (as of 2025-03-21)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Pbk&lt;sup&gt;em1Dfult&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419692</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="15" START_POS="44198506" STOP_POS="44209572" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="15" START_POS="40022873" STOP_POS="40034014" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="15" START_POS="42489253" STOP_POS="42500377" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="15" START_POS="49092278" STOP_POS="49103401" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="15" START_POS="45227251" STOP_POS="45238096" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092510</CITATION_ID>
    <DESCRIPTION>we used CRISPR-Cas9 technology to generate a PBK KO rat. Cas9 editing of exon 4 in the rat PBK gene resulted in the insertion of a single “T” resulting in a frame shift and premature termination of the PBK protein. PMCID: PMC11650665</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092522</RGD_ID>
    <STRAIN_SYMBOL>DA-&lt;i&gt;Lyst&lt;sup&gt;bg&lt;/sup&gt;&lt;/i&gt;/Slc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Lyst gene mutation was identified in 1985 in DA rats maintained at Hamamatsu University School of Medicine since 1980.</ORIGINATION>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1353&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-03-25)</AVAILABILITY>
    <RESEARCH_USE>Hematology</RESEARCH_USE>
    <ALLELES>Lyst&lt;sup&gt;bg&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>598099555</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092522</CITATION_ID>
    <DESCRIPTION>Lyst gene mutation was identified in 1985 in DA rats maintained at Hamamatsu University School of Medicine since 1980. In 2000, it was provided to Japan SLC, Inc.The mutant beige protein was frameshift and prematured truncated at the 2594th amino acids due to 578 bp deletion (positions 7742-8319) caused by recombination between LINE1s (Long Interspersed Nuclear Element 1).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092524</RGD_ID>
    <STRAIN_SYMBOL>Slc:WSRC-&lt;i&gt;Kit&lt;sup&gt;Ws&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Yagi Memorial Park in Hiroshima, Japan</ORIGINATION>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1354 &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-03-25)</AVAILABILITY>
    <RESEARCH_USE>mast cell deficiency</RESEARCH_USE>
    <ALLELES>Kit&lt;sup&gt;Ws&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>12910763</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="14" START_POS="32901615" STOP_POS="32978895" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="14" START_POS="32554595" STOP_POS="32554606" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="14" START_POS="35079269" STOP_POS="35079280" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="14" START_POS="34901860" STOP_POS="34979384" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="14" START_POS="34906043" STOP_POS="34984819" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092524</CITATION_ID>
    <DESCRIPTION>In 1987, a Ws mutant (RGD:12910762) with a light-colored coat and large abdominal white spots was discovered in a colony of BN/fMai inbred rats that had been allocated to Yagi Memorial Park from the Institute of Laboratory Animals Graduate School of Medicine, Kyoto University. However, homozygous for the Ws mutation could not be obtained in BN inbred rats due to embryonic lethality. Therefore, they crossed with Donryu outbred rats and obtained homozygous by crossing F1 heterozygous. This strain was designated as WsRC and was supplied to Japan SLC, Inc. in 1993.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092525</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;C5ar1&lt;sup&gt;em22Taoki&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1355&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-25)</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension, Infectious, Pharmacology</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092525</CITATION_ID>
    <DESCRIPTION>This strain was established by CRISPR/Cas9 system in the Research Institute, National Cerebral and Cardiovascular Center. Genetic background is Slc:SD. guide RNA gRNA No1; ATAAGTAACGACAGCAGTGA gRNA No2; GAGTTTCACTCGGTCCACGA</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092526</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Rnf213&lt;sup&gt;em1Taoki&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1356&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-25)</AVAILABILITY>
    <RESEARCH_USE>Cardio Hypertension</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092526</CITATION_ID>
    <DESCRIPTION>This strain was established in 2020 using the CRISPR/Cas9 system at the Institute of Immunology Co., Ltd. In the same year, it was introduced to the Research Institute, National Cerebral and Cardiovascular Center. The genetic background is Slc:SD.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092574</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Hspa8&lt;sup&gt;em1Opu&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1379&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-27)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Hspa8&lt;sup&gt;em1Opu&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626467889</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="50080514" STOP_POS="50084376" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="41183397" STOP_POS="41187260" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="44989401" STOP_POS="44993261" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="43478238" STOP_POS="46006864" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="43784035" STOP_POS="43787760" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092574</CITATION_ID>
    <DESCRIPTION>The Hspa8 mutation (c.284T&gt;A) in the KK rat (NBRP Rat No. 0890)(RGD:598092575) was inserted into the F344/Jcl. Knocking in of the mutant allele was performed by lsODN-mediated knock-in with the CRISPR-Cas9 system. The gRNA and PAM sequences are gtgccacaagctattaaatatatgg (PAM: tgg) and ccatttatggatgggctctctccc (PAM: cca). In KI rats, each PAM sequence is replaced by a silent mutation. Two lines were obtained from founder rats. In line 1, there is one SNP in the intron where the upstream gRNA, but this is not related to the phenotype. This strain was produced with the support of the AdAMS (Advanced Animal Model Support).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092575</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Hspa8&lt;sup&gt;m1Kyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1378&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-03-27)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Hspa8&lt;sup&gt;m1Kyo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626467888</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="50080514" STOP_POS="50084376" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="41183397" STOP_POS="41187260" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="44989401" STOP_POS="44993261" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="43478238" STOP_POS="46006864" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="43784035" STOP_POS="43787760" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092575</CITATION_ID>
    <DESCRIPTION>This strain, called KK rats, in homozygous rats show gait abnormalities from around 5-6 weeks of age. Thereafter, the neurological symptoms progress rapidly, leading to emaciation and death. The mutant gene was named kk, as Kenta Kumafuji was the discoverer of the gait abnormality.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092577</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Hspa8&lt;sup&gt;em2Opu&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1380&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-27)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Hspa8&lt;sup&gt;em2Opu&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626467891</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="50080514" STOP_POS="50084376" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="41183397" STOP_POS="41187260" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="44989401" STOP_POS="44993261" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="43478238" STOP_POS="46006864" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="43784035" STOP_POS="43787760" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092577</CITATION_ID>
    <DESCRIPTION>The Hspa8 mutation (c.284T&gt;A) in the KK rat (NBRP Rat No. 0890) was inserted into the F344/Jcl. Knocking in of the mutant allele was performed by lsODN-mediated knock-in with the CRISPR-Cas9 system. The gRNA and PAM sequences are gtgccacaagctattaaatatatgg (PAM: tgg) and ccatttatggatgggctctctccc (PAM: cca). In KI rats, each PAM sequence is replaced by a silent mutation. Two lines were obtained from founder rats. In line 2, there are two SNPs in the intron where the upstream gRNA, but this is not related to the phenotype. This strain was produced with the support of the AdAMS (Advanced Animal Model Support).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092579</RGD_ID>
    <STRAIN_SYMBOL>LE-Tg(Tac1-cre)3-2Koba</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1374&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-27)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology, Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092579</CITATION_ID>
    <DESCRIPTION>Background strain: Long-Evans rat (Iar:Long-Evans). This strain was established by injection of modified BAC (cre gene was inserted into the exon 2 of rat Tac1 gene) into Long-Evans rat's fertiled eggs.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092582</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Calca&lt;sup&gt;em4(cre)Daiyi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1376&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-27)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology, Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092582</CITATION_ID>
    <DESCRIPTION>Genetic background is Iar:Long-Evans (Institute for Animal Reproduction). Cre and T2A were inserted into the start codon (methionine) of the second exon of the Calca gene using CRISPR/Cas9.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092583</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Sst&lt;sup&gt;em1(cre)Bfdi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1375&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-27)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology, Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092583</CITATION_ID>
    <DESCRIPTION>Cre was inserted at the start codon (methionine) of the somatostatin (Sst) gene. The Sst precursor is then expressed using the T2A peptide as a linker. Genetic background is Iar:Long-Evans (Institute for Animal Reproduction).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092585</RGD_ID>
    <STRAIN_SYMBOL>SD.LIS-&lt;i&gt;Actb&lt;sup&gt;tm1(CAG-GCaMP8)Ksak&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1372&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-27)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology, Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092585</CITATION_ID>
    <DESCRIPTION>The ES cell line derived from Lister Hooded rats (Seac:LIS), which was established by Prof. Sakimura at Department of Animal Model Development, Brain Research Institute, Niigata University, was used. Cloned ES cells established by introducing a vector of G8CaMP-flox stop at the 3'non-coding site of the Actb gene were injected into fertilized eggs of SD rats (Slc:SD) using a microinjection method.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092586</RGD_ID>
    <STRAIN_SYMBOL>SD.LIS-&lt;i&gt;ROSA26&lt;sup&gt;tm1(CAG-RCaMP2)Ksak&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1373&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-27)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology, Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092586</CITATION_ID>
    <DESCRIPTION>The ES cell line derived from Lister Hooded rats (Seac:LIS), which was established by Prof. Sakimura at Department of Animal Model Development, Brain Research Institute, Niigata University, was used. Cloned ES cells established by introducing a vector of RCaMP2-flox stop at the Rosa26 locus were injected into fertilized eggs of SD rats (Slc:SD) using a microinjection method. RCaMP2 stands for red calcium indicator (PMID: 25419959).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092588</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Th&lt;sup&gt;em2-2(cre)Koba&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1371&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-27)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology, Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092588</CITATION_ID>
    <DESCRIPTION>The T2A, nlsCre, and BGHpolyA are knocked in at the stop codon in the 13th exon of the tyrosine hydroxylase (TH) gene (NCBI Gene ID: 25085).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092591</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Th&lt;sup&gt;em2-1(cre)Koba&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1370&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-27)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology, Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092591</CITATION_ID>
    <DESCRIPTION>The T2A, nlsCre, and BGHpolyA are knocked in at the stop codon in the 13th exon of the tyrosine hydroxylase (TH) gene (NCBI Gene ID: 25085).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092592</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Th&lt;sup&gt;em1(cre)Koba&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1369&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-27)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology, Behavior</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092592</CITATION_ID>
    <DESCRIPTION>The T2A, nlsCre, and BGHpolyA are knocked in at the stop codon in the 13th exon of the tyrosine hydroxylase (TH) gene (NCBI Gene ID: 25085).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092593</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Gpr143&lt;sup&gt;em19Gosh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1358&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-28)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology, Ophthalmology, Cardio Hypertension, Behavior, Pharmacology</RESEARCH_USE>
    <ALLELES>Gpr143&lt;sup&gt;em19Gosh&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419681</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="25498601" STOP_POS="25523408" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="22002914" STOP_POS="22027720" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="23668363" STOP_POS="23693162" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="24084931" STOP_POS="24109730" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="42481440" STOP_POS="42506239" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092593</CITATION_ID>
    <DESCRIPTION>Deletion of exon1 of Gpr143 gene in Wistar rats (Charles River, Japan) by CRISPR/Cas9. Line No. is 19.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092595</RGD_ID>
    <STRAIN_SYMBOL>F344.VF-&lt;i&gt;Dop1a&lt;sup&gt;vf&lt;/sup&gt;&lt;/i&gt;/Omu</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1357&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-28)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology</RESEARCH_USE>
    <ALLELES>Dop1a&lt;sup&gt;vf&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419686</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092595</CITATION_ID>
    <DESCRIPTION>A congenic strain generated by backcrossing VF/Kyo rats (donor line, NBRP Rat No. 0022, RGD:1302674) to the F344/DuCrlCrlj (RGD:69643). This congenic strain carries the vacuole formation causing mutation (Dop1avf) in  Dopey1(Dop1a) from VF/Kyo strain.  It was generated at Osaka Metropolitan University.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092597</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Tmem130&lt;sup&gt;em1Taoki&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1359&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-28)</AVAILABILITY>
    <RESEARCH_USE>Cancer</RESEARCH_USE>
    <ALLELES>Tmem130&lt;sup&gt;em1Taoki&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419687</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="12" START_POS="14950784" STOP_POS="14976571" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="12" START_POS="9837055" STOP_POS="9862843" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="12" START_POS="11814071" STOP_POS="11840100" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="12" START_POS="13876610" STOP_POS="13900957" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="12" START_POS="10153114" STOP_POS="10177002" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092597</CITATION_ID>
    <DESCRIPTION>Generated with CRISPR/Cas9 system in the Research Institute, National Cerebral and Cardiovascular Center. Genetic background is Slc:SD. Guide RNA gRNA No1: GACCATCAGTAGTAAGACTA gRNA No2: GATTTCCAGGTACTCGGGACG</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092598</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Nox1&lt;sup&gt;em1Shmo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1361&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nox1&lt;sup&gt;em1Shmo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419688</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="101572338" STOP_POS="101625571" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="97279058" STOP_POS="97332291" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="104909328" STOP_POS="104932508" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="104742161" STOP_POS="104765479" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092598</CITATION_ID>
    <DESCRIPTION>A 29-base deletion was introduced into the first exon of the NADPH oxidase 1 (Nox1) gene of F344/DuCrj rats by CRISPR/Cas9. They were then backcrossed to F344/N (Japan SLC, Inc.).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092601</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Cybb&lt;sup&gt;em1Shmo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1362&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-28)</AVAILABILITY>
    <RESEARCH_USE>Hematology</RESEARCH_USE>
    <ALLELES>Cybb&lt;sup&gt;em1Shmo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419689</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="16030596" STOP_POS="16065065" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="13358101" STOP_POS="13392570" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="14578330" STOP_POS="14610049" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="15359405" STOP_POS="15391317" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="25514572" STOP_POS="25547181" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092601</CITATION_ID>
    <DESCRIPTION>A 7-base deletion was introduced into the first exon of the NADPH oxidase 2 (Nox2)(official symbol:Cybb) gene of F344/DuCrj rats by CRISPR/Cas9. They were then backcrossed to F344/N (Japan SLC, Inc.).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092602</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Nox4&lt;sup&gt;em1Shmo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1363&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Nox4&lt;sup&gt;em1Shmo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419690</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150313736" STOP_POS="150491480" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="140900886" STOP_POS="141078844" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="150796359" STOP_POS="150976186" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157106652" STOP_POS="157285107" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143415816" STOP_POS="143603554" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092602</CITATION_ID>
    <DESCRIPTION>A one-base insertion was introduced into the first exon of the NADPH oxidase 4 (Nox4) gene of F344/DuCrj rats by CRISPR/Cas9. They were then backcrossed to F344/N (Japan SLC, Inc.).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092603</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Cybb&lt;sup&gt;em1Shmo&lt;/sup&gt;&lt;/i&gt;&lt;i&gt;Nox1&lt;sup&gt;em1Shmo&lt;/sup&gt;&lt;/i&gt;&lt;i&gt;Nox4&lt;sup&gt;em1Shmo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1364&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-28)</AVAILABILITY>
    <RESEARCH_USE>Hematology</RESEARCH_USE>
    <ALLELES>Nox1&lt;sup&gt;em1Shmo&lt;/sup&gt;|Cybb&lt;sup&gt;em1Shmo&lt;/sup&gt;|Nox4&lt;sup&gt;em1Shmo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419688|626419689|626419690</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="16030596" STOP_POS="16065065" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="150313736" STOP_POS="150491480" METHOD="7"/>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="101572338" STOP_POS="101625571" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="97279058" STOP_POS="97332291" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="140900886" STOP_POS="141078844" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="13358101" STOP_POS="13392570" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="104909328" STOP_POS="104932508" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="14578330" STOP_POS="14610049" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="150796359" STOP_POS="150976186" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="15359405" STOP_POS="15391317" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="157106652" STOP_POS="157285107" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="104742161" STOP_POS="104765479" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="143415816" STOP_POS="143603554" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="25514572" STOP_POS="25547181" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092603</CITATION_ID>
    <DESCRIPTION>A 7-base deletion in the first exon of the NADPH oxidase 2 (Nox2) gene, a 29-base deletion in the first exon of the NADPH oxidase 1 (Nox1) gene, and a one-base insertion in the first exon of the NADPH oxidase 4 (Nox4) gene were introduced by CRISPR/Cas9 in the F344/DuCrj rats. They were then backcrossed to F344/N (Japan SLC, Inc.). This triple Nox knock rats were created by compound crossbreeding of single knockout rats (RGD:598092598, RGD:598092601, RGD:598092602).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092604</RGD_ID>
    <STRAIN_SYMBOL>F344.MES-&lt;i&gt;Cyba&lt;sup&gt;mes&lt;/sup&gt;&lt;/i&gt;/Shmo</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1365&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-28)</AVAILABILITY>
    <RESEARCH_USE>Hematology</RESEARCH_USE>
    <ALLELES>Cyba&lt;sup&gt;mesSdi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>13209000</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092604</CITATION_ID>
    <DESCRIPTION>The Cybames mutant allele (Cyba&lt;sup&gt;mes&lt;/sup&gt;) carried by MES rats was introduced by backcrossing to F344/N (Japan SLC, Inc.). The Cybames mutant allele is a 4-bp deletion in the splice sequence of the fourth intron of the Cyba gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092605</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Dbh-tTA,-cre)2_7Fusa</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1366&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-28)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology, Behavior,  Pharmacology, Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092605</CITATION_ID>
    <DESCRIPTION>This strain was established by a use of the BAC transgenic method with a technical support from the C.B.S.N resource (Dr. Kazuto Kobayashi, Fukushima Medical University, Dr. Yuchio Yanagawa, Gunma University Graduate School of Medicine). This transgenic rat was transported to The Jikei University School of Medicine, and cre recombinase expression was confirmed by crossing it with a reporter rat (NBRP Rat No: 0734). These rats are maintained in The Jikei University School of Medicine. Background strain: Crlj:WI.
Transgene: Dbh (dopamine beta-hydroxylase: rat), TetR (E.coli), VP16 protein minimal“F”-type activation domain (Herpes simplex virus), 2A (Thosea asigna virus), cre recombinase (P1 Phage), bGlobin polyA (rabbit), loxP (P1 phage). Detailed method (BAC transgenic method): a rat BAC clone was used (CH230-211J22). Combined mRNA for tTA and cre recombinase sequences is transcribed under the control of Dbh promoter. In translation step, the transcript is cut at the 2A peptide sequence, resulting in a separate protein production of tTA and Cre.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092606</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Dbh-tTA,-cre)5_4Fusa</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1367&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-28)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology, Behavior, Pharmacology, Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092606</CITATION_ID>
    <DESCRIPTION>This strain was established by a use of the BAC transgenic method with a technical support from the C.B.S.N resource (Dr. Kazuto Kobayashi, Fukushima Medical University, Dr. Yuchio Yanagawa, Gunma University Graduate School of Medicine). This transgenic rat was transported to The Jikei University School of Medicine, and cre recombinase expression was confirmed by crossing it with a reporter rat (NBRP Rat No: 0734). These rats are maintained in The Jikei University School of Medicine. Background strain: Crlj:WI.
Transgene: Dbh (dopamine beta-hydroxylase: rat), TetR (E.coli), VP16 protein minimal“F”-type activation domain (Herpes simplex virus), 2A (Thosea asigna virus), cre recombinase (P1 Phage), bGlobin polyA (rabbit), loxP (P1 phage). Detailed method (BAC transgenic method): a rat BAC clone was used (CH230-211J22). Combined mRNA for tTA and cre recombinase sequences is transcribed under the control of Dbh promoter. In translation step, the transcript is cut at the 2A peptide sequence, resulting in a separate protein production of tTA and Cre.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598092607</RGD_ID>
    <STRAIN_SYMBOL>W-Tg(Dbh-tTA,-cre)5_9Fusa</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=https://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1368&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-03-28)</AVAILABILITY>
    <RESEARCH_USE>Neurobiology, Behavior, Pharmacology, Development</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598092607</CITATION_ID>
    <DESCRIPTION>This strain was established by a use of the BAC transgenic method with a technical support from the C.B.S.N resource (Dr. Kazuto Kobayashi, Fukushima Medical University, Dr. Yuchio Yanagawa, Gunma University Graduate School of Medicine). This transgenic rat was transported to The Jikei University School of Medicine, and cre recombinase expression was confirmed by crossing it with a reporter rat (NBRP Rat No: 0734). These rats are maintained in The Jikei University School of Medicine. Background strain: Crlj:WI.
Transgene: Dbh (dopamine beta-hydroxylase: rat), TetR (E.coli), VP16 protein minimal“F”-type activation domain (Herpes simplex virus), 2A (Thosea asigna virus), cre recombinase (P1 Phage), bGlobin polyA (rabbit), loxP (P1 phage). Detailed method (BAC transgenic method): a rat BAC clone was used (CH230-211J22). Combined mRNA for tTA and cre recombinase sequences is transcribed under the control of Dbh promoter. In translation step, the transcript is cut at the 2A peptide sequence, resulting in a separate protein production of tTA and Cre.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598130079</RGD_ID>
    <STRAIN_SYMBOL>LEW-&lt;i&gt;Col7a1&lt;sup&gt;em1Jtol-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Division of Blood and Marrow Transplantation
Department of Pediatrics
University of Minnesota Medical School</ORIGINATION>
    <SOURCE>The strain is deposited  with RRRC (Rat Resource and Research Center)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2025-04-15)</AVAILABILITY>
    <RESEARCH_USE>Recessive Dystrophic Epidermolysis Bullosa; pediatric dermatologic disorders; dermatologic cancers.</RESEARCH_USE>
    <ALLELES>Col7a1&lt;sup&gt;em1Jtol&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419684</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="8" START_POS="118483364" STOP_POS="118515736" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="8" START_POS="109604877" STOP_POS="109637249" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="8" START_POS="117694441" STOP_POS="117726844" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="8" START_POS="117046218" STOP_POS="117078589" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="8" START_POS="113971207" STOP_POS="114003445" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598130079</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to introduce an 8-bp deletion in exon 1 of the Col7a1 gene of one-cell Lew/Crl rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598136401</RGD_ID>
    <STRAIN_SYMBOL>Wakil:bHRbLRF2</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Laboratory of Dr. Huda Akil and Dr. Stanley Watson, MBNI, University of Michigan, 205 Zina Pitcher Pl. Ann Arbor, MI 48109</ORIGINATION>
    <SOURCE>Laboratory of Dr. Huda Akil and Dr. Stanley Watson, MBNI, University of Michigan, 205 Zina Pitcher Pl. Ann Arbor, MI 48109</SOURCE>
    <STRAIN_TYPE>hybrid</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598136401</CITATION_ID>
    <DESCRIPTION>Selectively breeding rats for high or low locomotor activity in a novel environment (LocoScore) produced the bHR line (Wakil:bHR, RRID:RGD_405847397) and bLR line (Wakil:bLR, RRID:RGD_405847400), respectively (Stead. After 37 generations, 12 bHRs and 12 bLRs (F0) were chosen from 24 distinct families to crossbreed. The F1 offspring with similarly high or low LocoScores were then bred with each other to produce a re-emergence of diverse behavioral phenotypes in the F2 generation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598154594</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;C5ar1&lt;sup&gt;em1(C5AR1)Idor&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Michel Steiner, Idorsia Pharmaceuticals Ltd.    Hegenheimermattweg 91    4125 Allschwil     Switzerland</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1383  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-04-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598154594</CITATION_ID>
    <DESCRIPTION>Zinc fingers were designed and human C5aR1 cDNA was cloned into a pZFN plasmid and sequence verified. Subsequently, co-microinjection of a pair of ZFNs and the donor plasmid into the pronucleus of fertilized, one cell embryos was performed, generating HR-mediated KI animals. The entire process was performed at SAGE Labs, Horizon, (St Louis, USA). Sprague Dawley (Charles River) rat (Rattus norvegicus) C5aR1 (NCBI Gene ID: 113959, updated on 18-Oct-2012 Location : 1q12 Sequence : Chromosome: 1; NC_005100.3 (79452051..79458856, complement) mRNA join (1..&gt;34,5088..6806) /gene="C5ar1" CDS join(32..34,5088..6143) /gene="C5ar1") was replaced using zinc finger technology utilizing with the human C5aR1 cDNA by inserting the human cDNA into the 5’ end of the rat C5ar1 exon 2 locus using the ZFN Binding. Cut Site: CTTGGCCGTGTTCCTGGTaggagtTACCGGAAATGCCCTGGTG</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598154597</RGD_ID>
    <STRAIN_SYMBOL>W-&lt;i&gt;Mkx&lt;sup&gt;em2Asah&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1384  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-04-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598154597</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 genome editing system targeting exon 2 of rat Mkx gene was injected to  the Wistar embryo to generate this knock out rat strain with 7- bp deletion causing frameshift mutation in the gene.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598154598</RGD_ID>
    <STRAIN_SYMBOL>F344.W-&lt;i&gt;np&lt;/i&gt;/Shi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Shionogi and Company, Ltd.
Address: Koka-cho, Shiga. JAPAN</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1385  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-04-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598154598</CITATION_ID>
    <DESCRIPTION>In 1983, Wistar rats with pleural and ascites effusions and severe skin oedema were found at the Shionogi Pharmaceutical Co. The rats were named Nephrose Shionogi (NPS) because they showed nephrosis (F12). Breeding revealed that this phenotype was dominated by a autosomal recessive gene, np. NPS rats develop nephrosis at 4 weeks of age and die within 2 weeks. To prolong survival, NPS rats (np/+) were backcrossed with F344/Shi rats to generate the congenic strain (N12-13).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598154599</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Il2rg&lt;sup&gt;em1Larc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Tomoji Mashimo  The University of Tokyo, The Institute of Medical Science       4-6-1 Shirokanedai-Minatoku-Tokyoto    108-8639      Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1381  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-04-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598154599</CITATION_ID>
    <DESCRIPTION>This strain was generated at the Institute of Medical Science, University of Tokyo, by using CRISPR-Cas3. Microinjected into pronuclear-stage rat embryos of the F344/Jcl strain. The embryos were transferred into the oviducts of pseudopregnant females. A strain with a 1,869 bp deletion in the Il2rg gene was established from the resulting litters.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598154600</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Rag2&lt;sup&gt;em1Larc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Tomoji Mashimo  The University of Tokyo, The Institute of Medical Science       4-6-1 Shirokanedai-Minatoku-Tokyoto    108-8639      Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1381  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-04-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598154600</CITATION_ID>
    <DESCRIPTION>This strain was generated at the Institute of Medical Science, University of Tokyo, by using CRISPR-Cas3. Microinjected into pronuclear-stage rat embryos of the F344/Jcl strain. The embryos were transferred into the oviducts of pseudopregnant females. A strain with a 410 bp deletion in the Rag2 gene was established from the resulting litters.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598154602</RGD_ID>
    <STRAIN_SYMBOL>WIC;W-&lt;i&gt;Oprk1&lt;sup&gt;em1(cre)Nurep&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1386  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-04-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598154602</CITATION_ID>
    <DESCRIPTION>Oprk1-cre rats were generated by Dr. Hiroko Tsukamura, Dr. Yoshihisa Uenoyama, Dr. Naoko Inoue, Dr. Mayuko Nagae (Nagoya University) and Dr. Masumi Hirabayashi (National Institute for Physiological Sciences). The CRISPR/Cas9 and adeno-associated virus vector (Oprk1 [exon 4], T2A, Cre) were introduced into the pronuclear stage embryos of Wistar rats (Crlj:WI). It was maintained by mating with the Wistar-Imamichi rats (Iar:WIC) (RGD:125097496) or by sibling mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598154604</RGD_ID>
    <STRAIN_SYMBOL>ZFDM-&lt;i&gt;Lcn2&lt;sup&gt;em1Nyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1387  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-04-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598154604</CITATION_ID>
    <DESCRIPTION>"This knock-in rat was generated by injecting guide RNA, Cas9 protein, and ssODN targeting the Lcn2 gene into fertilized eggs of ZFDM rats. The Lcn2 gene of ZFDM rats has a nonsense mutation (c.409C&gt;T, p.Gln137X), but in this line, this mutation is replaced with the wild type sequence by homologous recombination with the introduced ssODN. The target sequence of the guide RNA is TGACTACGACTAGTTTGCCA. The ssODN sequence for inducing homologous recombination is AAGTGGCCGACACTGACTACGACCAGTTTGCCATGGTATTTTTCCAGAAGACCTCTGAAA.
"</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598154608</RGD_ID>
    <STRAIN_SYMBOL>ZFDM-&lt;i&gt;Lcn2&lt;sup&gt;em2Nyo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1388  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-04-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598154608</CITATION_ID>
    <DESCRIPTION>"This knock-in rat was generated by injecting guide RNA, Cas9 protein, and ssODN targeting the Lcn2 gene into fertilized eggs of ZFDM rats. The Lcn2 gene of ZFDM rats has a nonsense mutation (c.409C&gt;T, p.Gln137X), but in this line, this mutation is replaced with the wild type sequence by homologous recombination with the introduced ssODN. The target sequence of the guide RNA is TGACTACGACTAGTTTGCCA. The ssODN sequence for inducing homologous recombination is AAGTGGCCGACACTGACTACGACCAGTTTGCCATGGTATTTTTCCAGAAGACCTCTGAAA.
"</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598154611</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(TOR1A)Tot</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University Clinics Tuebingen, Core Facility Transgenic Animals
FORS/HIH
Otfried-Mueller-Str. 27
Tuebingen
72076
Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598154611</CITATION_ID>
    <DESCRIPTION>The  full length humanTOR1A  wild type gene including upstream and downstream flanking regions were inserted into a pUC19 vector. Following linearization and purification the transgenes were used to generate transgenic rats by microinjection of the DNA construct into the pronucleus of rat zygotes. Transgenic rats were kept on Sprague–Dawley background and bred as hemizygotes using standard procedures. Genotypes of offspring were determined by PCR and sequencing of DNA extracted from ear biopsies. Primer pair 5′-TAAAAATGTGTATCCGAGTGGAAAT (forward) and 5′-AAGGACTGAGTGTTGTTTCTTTTC (reverse) amplified a 230 bp segment within the coding sequence of exon 5 under the following conditions: 94 °C for 1 min, 60 °C for 1 min and 72 °C for 1 min, 40 cycles. Only lines that showed stable germline transmission of the transgenes were used for further analyses.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598154612</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(TOR1A&lt;sup&gt;DYT1&lt;/sup&gt;)Tot</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University Clinics Tuebingen, Core Facility Transgenic Animals
FORS/HIH
Otfried-Mueller-Str. 27
Tuebingen
72076
Germany</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598154612</CITATION_ID>
    <DESCRIPTION>The 16.25 kbps full length human DYT1 allele of TOR1A gene including upstream and downstream flanking regions were inserted into a pUC19 vector. Following linearization and purification the transgenes were used to generate transgenic rats by microinjection of the DNA construct into the pronucleus of rat zygotes. Transgenic rats were kept on Sprague–Dawley background and bred as hemizygotes using standard procedures. Genotypes of offspring were determined by PCR and sequencing of DNA extracted from ear biopsies. Primer pair 5′-TAAAAATGTGTATCCGAGTGGAAAT (forward) and 5′-AAGGACTGAGTGTTGTTTCTTTTC (reverse) amplified a 230 bp segment within the coding sequence of exon 5 under the following conditions: 94 °C for 1 min, 60 °C for 1 min and 72 °C for 1 min, 40 cycles. Only lines that showed stable germline transmission of the transgenes were used for further analyses.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598973841</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Apc&lt;sup&gt;Pirc&lt;/i&gt;&lt;/sup&gt;/UwmRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Wisconsin-Madison, Madison, Wisconsin</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=782&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-05-11)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Apc&lt;sup&gt;Pirc&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>1554322</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="26190901" STOP_POS="26190901" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="25916744" STOP_POS="25916744" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="27100213" STOP_POS="27100213" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="26725560" STOP_POS="26820837" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="26732147" STOP_POS="26790383" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598973841</CITATION_ID>
    <DESCRIPTION>ThPirc rats were generated by crossing male F344-ApcPirc/Uwm (RGD:1641862) Pirc rats with wild-type female rats obtained commercially from Envigo Laboratories (Indianapolis, IN, USA), i.e., F344/NHsd.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598973845</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gfap&lt;sup&gt;em1Mes+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Waisman Center, University of Wisconsin Madison</ORIGINATION>
    <SOURCE>The strain is now deposited at &lt;a href=http://www.rrrc.us/Strain/?x=932&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gfap&lt;sup&gt;em1Mes&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>150519905</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="88352987" STOP_POS="88361661" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="87852891" STOP_POS="87861631" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="90990762" STOP_POS="90999435" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="90763150" STOP_POS="90771823" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="92059881" STOP_POS="92068555" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598973845</CITATION_ID>
    <DESCRIPTION>The targeted mutation in the rat GFAP gene was based on the severity and frequency of the R239H mutation in human disease. The CRISPR/Cas9 system was used to mediated knockin of point mutation (R237H) to Sprague-Dawley embryos. The current background srain is Crl:CD (SD). This mutant strain serves as a model for Alexander disease. knockins have post-weaning failure to thrive and ~10% mortality by 12 weeks, but afterwards are viable and can breed .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>598973846</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gfap&lt;sup&gt;em1Mes+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Waisman Center, University of Wisconsin Madison</ORIGINATION>
    <SOURCE>The heterozygous mutant strain is now deposited at &lt;a href=http://www.rrrc.us/Strain/?x=932&amp;log=yes&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_598973846</CITATION_ID>
    <DESCRIPTION>These rats are wild type littermates of the  mutant where the rat GFAP gene was mutated based on the severity and frequency of the R239H mutation in human disease. The CRISPR/Cas9 system was used to mediated knockin of point mutation (R237H) to Sprague-Dawley embryos. The current background srain is Crl:CD (SD). This mutant strain serves as a model for Alexander disease. knockins have post-weaning failure to thrive and ~10% mortality by 12 weeks, but afterwards are viable and can breed .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616335891</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Synpo&lt;sup&gt;em2Kmh&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was submitted by  Masaaki (Masa) Kuwajima, PhD   (masa@mail.clm.utexas.edu). Strains were produced at Kristen Harris Laboratory, Department of Neuroscience, Center for Learning and Memory, University of Texas at Austin</ORIGINATION>
    <SOURCE>This strain is deposited at &lt;a href=http://www.rrrc.us/Strain/?x=1025&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-05-13)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01025</CITATION_ID>
    <DESCRIPTION>Exons 2 and 3 were deleted to eliminate all known Synaptopodin isoforms in the outbred  	Long Evans (Charles River 006). It is similar to RRRC strain #964 (LE-Synpoem1Kmh) (RGD:155782907), has a different mutation location upstream of exon 2.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616335894</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;ROSA26 &lt;sup&gt;em1(CAG-DdCBE-Mt-co3&lt;/sup&gt;&lt;/i&gt;/Ilas</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences and Peking Union
Medical College</ORIGINATION>
    <SOURCE>Rat Resource Center of China (www.ratresource.com)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_616335894</CITATION_ID>
    <DESCRIPTION>The knock in of "CAG-loxP-stop-loxP-DdCBE-Mt-co3" to ROSA26 was induced by CRISPR/Cas9 in SD embryos from Vital River. This ROSA 26 knock in construct  carrying DddA-derived cytosine base editor (DdCBE)linked to Mt-co3 was used to introduce premature stop codons in the rat Mt-co3 in mitochondrial genome in the presence of Cre recombinase.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616336063</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;ROSA26 &lt;sup&gt;em1(CAG-DdCBE-Mt-co3, NeuN-Cre&lt;/sup&gt;&lt;/i&gt;/Ilas</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences and Peking Union
Medical College</ORIGINATION>
    <SOURCE>Rat Resource Center of China (www.ratresource.com)</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_616336063</CITATION_ID>
    <DESCRIPTION>This rat strain with neuronal specific knock out of Mt-co3 was generated by crossing a rat neuron-specific Cre strain (NeuN-Cre) with SD-ROSA26 em1(CAG-loxP-stop-loxP-DdCBE-Mt-co3/Ilas. Compared with the controls, the neuron-specific Mt-co3 knock out rats were largely normal in the first postnatal month, but progressively developed ALS-like symptoms afterward.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616336064</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;ROSA26&lt;sup&gt;em11(CAG-EGFP,-mCherry)Larc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Tomoji Mashimo  The University of Tokyo, The Institute of Medical Science       4-6-1 Shirokanedai-Minatoku-Tokyoto    108-8639      Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1389  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>advanced_intercross_line</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-05-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_616336064</CITATION_ID>
    <DESCRIPTION>F344/Jcl rat fertilized eggs were microinjected and transplanted into the oviducts of pseudopregnant females. From the resulting offspring, rats with the CAG promoter-loxP-EGFP-loxP-polyA-mCherry sequence inserted into the ROSA26 gene were selected and established.EGFP is expressed throughout the body, and when the EGFP sequence is removed in the presence of cre recombinase, mCherry is expressed.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616336065</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;ROSA26&lt;sup&gt;em10(Alb-cre)Larc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was created at the Institute of Medical Science, University of Tokyo. Principle investigator is Masayuki Yamamoto  Tohoku University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1390  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-05-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_616336065</CITATION_ID>
    <DESCRIPTION>F344/Jcl rat fertilized eggs were microinjected and then transplanted into the oviducts of pseudopregnant females. From the resulting offspring, rats with the Alb promoter-Cre sequence inserted into the Rosa26 gene were selected and established. Although the Alb promoter is inserted, cre leakage is confirmed throughout the body.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616336066</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;ROSA26&lt;sup&gt;em20(Alb-cre)Larc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was created at the Institute of Medical Science, University of Tokyo. Principle investigator is Masayuki Yamamoto  Tohoku University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1391  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Extinct (as of 2025-05-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_616336066</CITATION_ID>
    <DESCRIPTION>F344/Jcl rat fertilized eggs were microinjected and then transplanted into the oviducts of pseudopregnant females. From the resulting offspring, rats with the Alb promoter-Cre sequence inserted into the ROSA26 gene were selected and established. The Alb promoter-Cre sequence is inserted in an inverted position.  	Cre is expressed specifically in the liver.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616336067</RGD_ID>
    <STRAIN_SYMBOL>F344-&lt;i&gt;Alb&lt;sup&gt;em4(cre)Larc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>This strain was created at the Institute of Medical Science, University of Tokyo. Principle investigator is Masayuki Yamamoto  Tohoku University</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1392  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-05-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_616336067</CITATION_ID>
    <DESCRIPTION>Fertilized eggs from F344/Jcl rats were microinjected and then transplanted into the oviducts of pseudopregnant females. From the resulting offspring, rats with the 2A-Cre sequence inserted into the Albumin gene were selected and established.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616336068</RGD_ID>
    <STRAIN_SYMBOL>LE.W-Tg(Dbh-tTA,-cre)2_7Fusa/Koba</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1393  &gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>congenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-05-14)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_616336068</CITATION_ID>
    <DESCRIPTION>This congenic strain was created by back crossing Long-Evans with The W-Tg(Dbh-tTA-2A-cre)2_7Fusa strain(RGD: 598092605) provided by Dr. Fusao Kato and Dr. Yukari Takahashi of the Jikei University School of Medicine. Background strain: Long-Evans (Institute for Animal Reproduction) Transgenes: DBH (rat), TetR (Escherichia coli), VP16 protein minimal "F"-type activation domain (Herpes simplex virus), 2A (Thosea asigna virus), Cre (P1 phage), bGlobin polyA (rabbit), loxP (P1 phage).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616362803</RGD_ID>
    <STRAIN_SYMBOL>sP</STRAIN_SYMBOL>
    <FULL_NAME>Sardinian alcohol-preferring rats</FULL_NAME>
    <ORIGINATION>University of Cagliari, Italy</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_616362803</CITATION_ID>
    <DESCRIPTION>The bidirectional breeding program of sP (Sardinian alcohol-preferring rats) and sNP (Sardinian non-alcohol-preferring) was begun in 1981 by Drs Fabio Fadda and Gian Luigi
Gessa, at the University of Cagliari, Italy.Selection of sP
and sNP rats started from a heterogeneous base population
of outbred Wistar rats purchased from Morini, San Polo d’Enza, RE,
Italy). The sP rats have alcohol preference in two-bottle chocice between water and 10% alcohol, while the sNP rats prefer water.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616362805</RGD_ID>
    <STRAIN_SYMBOL>sNP</STRAIN_SYMBOL>
    <FULL_NAME>Sardinian alcohol-non-preferring rats</FULL_NAME>
    <ORIGINATION>University of Cagliari, Italy</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_616362805</CITATION_ID>
    <DESCRIPTION>The bidirectional breeding program of sP (Sardinian alcohol-preferring rats) and sNP (Sardinian non-alcohol-preferring) was begun in 1981 by Drs Fabio Fadda and Gian Luigi
Gessa, at the University of Cagliari, Italy.Selection of sP
and sNP rats started from a heterogeneous base population
of outbred Wistar rats purchased from Morini, San Polo d’Enza, RE,
Italy). The sP rats have alcohol preference in two-bottle chocice between water and 10% alcohol, while the sNP rats prefer water.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616390066</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;CdCS&lt;sup&gt;em1Bcgen+/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME>Cri du Chat Syndrome rat</FULL_NAME>
    <ORIGINATION>The animal facility of the Chongqing Medical University.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_616390066</CITATION_ID>
    <DESCRIPTION>To generate the 5p15.2 deletion in the rat, two CRISPR gRNAs were designed at syntenic loci in the rat genome: ATGTCGATGTCTTGTTAGGGTGG at Chr.2:83120000 (RGSC 6.0/rn6) and GCTGAGATGGCTTTCAGAAATGG at Chr.2:84800000 (RGSC 6.0/rn6), which induced ≈1.68 Mb chromosomal deletion. The Biocytogen Transgenic and Gene Targeting core injected 50 ng uL−1 of each gRNAs and 100 ng uL−1 Cas9 RNA into single‐cell SD rat zygotes. Embryos were cultured overnight and transferred to pseudopregnant females. PCR was used to screen for the deletion. PCR was performed using genomic ear or tail DNA, and the following primer pair: Proximal Forward‐TTGCTCAGCTGTTAAGGGAAACTAT and Distal Reverse‐TCATCAAAATGCACCAAAAGTGCAA (these primers generate ≈485 bp product). PCR primers were used to detect the breakpoint on the undeleted 5p15.2 interval (wild‐type allele): Proximal Forward‐TTGCTCAGCTGTTAAGGGAAACTAT and Proximal Reverse‐GGAGTAAGTCAACTGACTAGGGGACA (these primers generate ≈618 bp product).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616572761</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;CdCS&lt;sup&gt;em1Bcgen+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The animal facility of the Chongqing Medical University.</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_616572761</CITATION_ID>
    <DESCRIPTION>This is the wild type littermate of SD-CdCSem1Bcgen+/- (RGD:616390066). The mutant CdCS rat has the 5p15.2 deletion in the genome and it a rat model for human Cri du Chat Syndrome .</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616572805</RGD_ID>
    <STRAIN_SYMBOL>HXB5/IpcvMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  contact Hybrid Rat Diversity Panel at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_616572805</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock HXB5/Ipcv provided by Pravenec and Kren from the Prague colonies, maintained at Medical college of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>616572806</RGD_ID>
    <STRAIN_SYMBOL>BXH10/CubMcwi</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;,  &lt;a href=mailto:HRDP@mcw.edu&gt; contact HRDP&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>recombinant_inbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_616572806</CITATION_ID>
    <DESCRIPTION>Embryo-rederived from breeder stock BXH10/Cub provided by Dr. Kren from Charles University, Department of Biology, Prague, Czech Republic, maintained at Medical College of Wisconsin</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>617148292</RGD_ID>
    <STRAIN_SYMBOL>SS-Del(2q)1Mcwi &lt;sup&gt;+/+&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>Please contact: mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-07-07)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_617148292</CITATION_ID>
    <DESCRIPTION>Four single guide RNAs and SpCas9 targeting sequences ATGAAGTGCCTAGCTTCATT, GAAGCTAGGCACTTCATCTA, ATTCATAATGGGACACTCGA, and CCCAGCCTCAGATTCATAAT flanking a chromosome 2 region distal to Npr3 were targeted in SS/JrHsdMcwi embryos. A 29,508 bp deletion in chromosome 2 (rn6: chr2:61,845,176-61,874,684) resulted, along with an insertion of 3 nucleotides (TGG).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>617154642</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Elovl4 &lt;sup&gt; em1cgen-/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Cyagen Bioscience Inc. (Santa Clara, CA). University of Oklahoma Health Sciences
Center, Oklahoma City, OK 73104, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_617154642</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 genetic editing approach was used to generate .a heterozygous Long-Evans rat model of human SCA34. The human Cas9 D10A (hCas9-D10A) nickase was used to knock-in the c.736T&gt;G mutation by targeting exon 6 of the rat Elovl4 (Ensembl: ENSRNOG00000009773) located on rat chromosome 8. The hCas9 mRNA, sgRNA(CCTTCCCCAAGTGGATGCAC), and single-strand oligonucleotide donor (ssODN: TTCCATGTGACCATTGGGCACACAGCACTGTCTCTCTACACCGACTGCCCCTTCCCCAAGGGGATGCACTGGGCTCTGATCGCCTATGCCATCAGCTTCATCTTCCTCTTCCTCAACTTCTAC) were co-injected into Long-Evans rat zygotes at the laboratories of Cyagen Bioscience Inc.The heterozygous  F0 rats  carrying c.736T&gt;G, p.W246G, mutation were bred with  with WT Long-Evans rats over several generations to breed out any potential off-target effects and to establish the heterozygous SCA34 Long-Evans rat model. Successfully generation of  homozygous SCA34 rats (MUT) by breeding heterozygous rats from the different F0 lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>617154644</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Elovl4 &lt;sup&gt; em1cgen-/-&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Cyagen Bioscience Inc. (Santa Clara, CA). University of Oklahoma Health Sciences
Center, Oklahoma City, OK 73104, USA</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_617154644</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 genetic editing approach was used to generate .a homozygous Long-Evans rat model of human SCA34. The human Cas9 D10A (hCas9-D10A) nickase was used to knock-in the c.736T&gt;G mutation by targeting exon 6 of the rat Elovl4 (Ensembl: ENSRNOG00000009773) located on rat chromosome 8. The hCas9 mRNA, sgRNA(CCTTCCCCAAGTGGATGCAC), and single-strand oligonucleotide donor (ssODN: TTCCATGTGACCATTGGGCACACAGCACTGTCTCTCTACACCGACTGCCCCTTCCCCAAGGGGATGCACTGGGCTCTGATCGCCTATGCCATCAGCTTCATCTTCCTCTTCCTCAACTTCTAC) were co-injected into Long-Evans rat zygotes at the laboratories of Cyagen Bioscience Inc.The heterozygous  F0 rats  carrying c.736T&gt;G, p.W246G, mutation were bred with  with WT Long-Evans rats over several generations to breed out any potential off-target effects and to establish the heterozygous SCA34 Long-Evans rat model. Successfully generation of  homozygous SCA34 rats (MUT) by breeding heterozygous rats from the different F0 lines.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>617212698</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Abca4&lt;sup&gt;em1Tuckr&lt;/sup&gt;&lt;i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Iowa Institute for Vision Research</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1035&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-07-16)</AVAILABILITY>
    <RESEARCH_USE>AMD (Age-related macular degeneration, retinitis pigmentosa (RP),cone-rod dystrophy (CRD) and Stargardt/Fundus Flavimaculatus disease (STGD/FFM)</RESEARCH_USE>
    <ALLELES>Abca4&lt;sup&gt;em1Tuckr&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>617212699</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="2" START_POS="212849470" STOP_POS="212986730" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="2" START_POS="210164813" STOP_POS="210302069" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="2" START_POS="225645539" STOP_POS="225783288" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="2" START_POS="243682218" STOP_POS="243818930" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="2" START_POS="218712663" STOP_POS="218849896" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01035</CITATION_ID>
    <DESCRIPTION>The rat Abca4 gene (Gene ID: 310836; GenBank accession number: NM_001107721.1) is located on rat chromosome 2. Exon 2 to exon 8 were selected as the target site for CRISPR/Cas9 modification on Sprague Dawley embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>617256277</RGD_ID>
    <STRAIN_SYMBOL>LE.SD-Tg(Camk2a-cre/ERT2)/Kmh</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Rat Resource and Research Center</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-07-23)</AVAILABILITY>
    <RESEARCH_USE>neuroscience</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_617256277</CITATION_ID>
    <DESCRIPTION>Cryopreserved sperm was obtained and recovered for SD-Tg(Camk2a-cre/ERT2)ZiRrrc (RRRC_00688; RGD ID: 13446407), and then back-crossed to the outbred Long-evans (LE) strain for 8 generations. This transgenic strain is a tamoxifen inducible Cre recombinase animal in the Long-evans strain, with targeted cre/ERT2 fusion protein expression in neural populations, and is suitable for crossing with loxP models also in the LE strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>617301241</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Slc5a9&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>Dr. Noreen Rossi, Contact Email: nrossi@wayne.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-07-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc5a9&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>617301244</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="5" START_POS="131937368" STOP_POS="131966405" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="5" START_POS="126730986" STOP_POS="126730989" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="5" START_POS="131836927" STOP_POS="131865218" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="5" START_POS="135659660" STOP_POS="135683248" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="5" START_POS="133455811" STOP_POS="133465217" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_617301241</CITATION_ID>
    <DESCRIPTION>Crl:SD embryos were injected with CRISPR-Cas9 using guide RNA targeting the sequence AGGTCATGGATCTTCCAGCC. A 4-bp deletion in exon 2 (rn7: chr5:126,730,986-126,730,989) resulted.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>617301243</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Slc5a10&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>Dr. Noreen Rossi, Contact Email: nrossi@wayne.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-07-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Slc5a10&lt;sup&gt;em1Mcwi&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>617301245</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="46851527" STOP_POS="46898460" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="46393272" STOP_POS="46393300" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="47949775" STOP_POS="47997802" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="47742919" STOP_POS="47789930" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="47831700" STOP_POS="47878552" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_617301243</CITATION_ID>
    <DESCRIPTION>Crl:SD embryos were injected with CRISPR-Cas9 using guide RNA targeting the sequence GAATACATTCAGAAGCGCTT. A 29-bp deletion in exon 5 (rn7: chr10:46,393,272-46,393,300) resulted.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>625776930</RGD_ID>
    <STRAIN_SYMBOL>Tc(HSA4-UGT2)Yakaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Chromosome Engineering Research Center, Tottori University, Yonago, 683-8503 Tottori, Japan</SOURCE>
    <STRAIN_TYPE>transchromosomal</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_625776930</CITATION_ID>
    <DESCRIPTION>Chimeric rats were generated using rBLK2i-1 (WDB/Nips-ES1/Nips, RGD: 10054010) to which human UGT2 cluster (10 coding genes: UGT2B4, UGT2B7, UGT2B10, UGT2B11, UGT2B15, UGT2B17, UGT2B28, UGT2A1, UGT2A2, and UGT2A3) was introduced. ES cells carrying the UGT2 chromosomal DNA were microinjected into the blastocoel cavity of Crlj:wi E4.5 blastocysts.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>625776931</RGD_ID>
    <STRAIN_SYMBOL>Tc(HSA7-CYP3A)Yakaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Chromosome Engineering Research Center, Tottori University, Yonago, 683-8503 Tottori, Japan</SOURCE>
    <STRAIN_TYPE>transchromosomal</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_625776931</CITATION_ID>
    <DESCRIPTION>Chimeric rats were generated using rBLK2i-1 (WDB/Nips-ES1/Nips, RGD: 10054010) to which human CYP3A cluster (4 coding genes: CYP3A4, CYP3A5, CYP3A7, and CYP3A43) was introduced. ES cells carrying the CYP3A chromosomal DNA were microinjected into the blastocoel cavity of Crlj:wi E4.5 blastocysts.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>625777899</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Ugt2&lt;sup&gt;em1Yakaz&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Chromosome Engineering Research Center, Tottori University, Yonago, 683-8503 Tottori, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_625777899</CITATION_ID>
    <DESCRIPTION>To produce Ugt2 cluster (∼762-kb) KO rats, two gRNAs with target sites upstream of Ugt2a1 and the coding region of Ugt2b31-like were injected into rat fertilized eggs.
 A knockout strain with Ugt2 cluster mutation carried concatenation of the genomic sequence upstream of Ugt2a1, a 102-bp insertion, and the Ugt2b31-like region. 
 The F2 homozygous rats showed decreased gemfibrozil glucuronidation activity in the liver. 
  The result suggested the functional deletion of rat Ugt2 genes in the Ugt2-KO rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>625777900</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Ugt2&lt;sup&gt;em1Yakaz&lt;/sup&gt;&lt;/i&gt;Tc(HSA4-UGT2)Yakaz/Yakaz</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Tottori University       86 Nishimachi    683-8503 Yonago-shi　Tottori     Japan</ORIGINATION>
    <SOURCE>&lt;a href=http://www.anim.med.kyoto-u.ac.jp/NBR/strains/Strains_d.aspx?StrainID=1395&gt; National BioResource Project for the Rat in Japan&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-08-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_625777900</CITATION_ID>
    <DESCRIPTION>Ugt2 (cluster) KO strain: The Ugt2 cluster was disrupted using the genome editing technology CRISPR/Cas9, and F1 rats (heterozygotes) were produced by crossing with Wistar (Crlj:WI) rats. The F1 rats were then crossed with each other to produce a homozygous strain. Ugt2 KO map Tc (UGT2-MAC) strain (Tc: transchromosomic): After introducing UGT2-MAC into rat ES cells (BLK2i-1), chimera rats were produced, which were then crossed with Wistar rats to produce F1 transmission rats, and further crossed with Wistar rats for several generations to produce strain rats. The MAC vector consists of the following genes: HPRT gene full length sequence, bovine growth hormone (BGH) polyA signal, b-actin promoter, b-globin insulator, CMV-IE enhancer, SV40 polyA signal, loxP sequence, FRT sequence, ampicillin resistance gene, neomycin resistance gene, kanamycin resistance gene, puromycin resistance gene, green fluorescent protein (GFP) gene and its mutants, PGK promoter, mouse chromosome 11 centromere region Tc (UGT2-MAC)-UGT2 strain: The strain was created by crossing the Tc(UGT2-MAC) strain with the Ugt2 (cluster) KO strain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>625777901</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Cyp3a&lt;sup&gt;em58Yakaz&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Chromosome Engineering Research Center, Tottori University, Yonago, 683-8503 Tottori, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_625777901</CITATION_ID>
    <DESCRIPTION>To produce Cyp3a (∼560-kb) KO rats, A pair of TALEN mRNAs targeting exon 5 of rat Cyp3a23/3a1 and Cyp3a2 were injected into rat fertilized eggs. A founder with  homozygous big deletion (BD) mutation from No. 58 line selected.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>625777902</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Cyp3a&lt;sup&gt;em65Yakaz&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Chromosome Engineering Research Center, Tottori University, Yonago, 683-8503 Tottori, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_625777902</CITATION_ID>
    <DESCRIPTION>To produce Cyp3a (∼560-kb) KO rats, A pair of TALEN mRNAs targeting exon 5 of rat Cyp3a23/3a1 and Cyp3a2 were injected into rat fertilized eggs. A founder with 9-bp deletion  mutation from No. 65 line selected.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>625777904</RGD_ID>
    <STRAIN_SYMBOL>WI-&lt;i&gt;Nr1i2&lt;sup&gt;em1Yakaz&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Chromosome Engineering Research Center, Tottori University, Yonago, 683-8503 Tottori, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_625777904</CITATION_ID>
    <DESCRIPTION>To produce Pxr  KO rats, A pair of TALEN mRNAs targeting Nr1i2 (Pxr) was injected into rat fertilized eggs.This strain was derived from a founder  harbouring a16 bp deletion (rPxr-KO).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626168247</RGD_ID>
    <STRAIN_SYMBOL>WI-Tg(Avp-CHRM3*-mCherry)Tuch</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Department of Physiology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu,
807-8555, Japan</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_626168247</CITATION_ID>
    <DESCRIPTION>A chimeric AVP-hM3Dq-mCherry BAC clone transgene construct was
purified for microinjections. hM3Dq is a modified form of the human M3 muscarinic  receptor (hM3; CHRM3*). It can be activated by the inert clozapine metabolite clozapine-N-oxide (CNO), engaging the Gq signaling pathway.The hM3Dq-mCherry sequence from the hM3Dq-mCherry cassette (Plasmid
#44361, Addgene, Cambridge, MA, USA) was used for the transgene.  Next, SV40 poly A sequence was framed to the hM3Dq-mCherry sequence. Finally, this
hM3Dq-mCherry-SV40 poly A cassette was introduced into the rat Avp gene in place of the genomic start
codon. Thus, hM3Dq-mCherry should be specifically expressed under the Avp promoter in the transgenic rat
brain.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626168248</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Csf1r&lt;sup&gt;em1Prdns&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Clare Pridans
Centre for Inflammation Research
Institute for Regeneration and Repair
The University of Edinburgh</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-08-28)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_626168248</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to delete the FIRE ( Fms intronic regulatory element) enhancer of the Csf1r gene of LE rat embryos</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626168255</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Thy1-APP&lt;sup&gt;DI&lt;/sup&gt;)BWevn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>William Van Nostrand, University Rhode Island</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=974&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2025-10-30)</AVAILABILITY>
    <RESEARCH_USE>Neurodegeneration, Alzheimer's Disease, Neurovascular degeneration</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00974</CITATION_ID>
    <DESCRIPTION>This novel transgenic rat produces low levels of human familial cerebral amyloid angiopath (CAA) Dutch/Iowa E22Q/D23N mutant amyloid beta protein in brain and recapitulates many of the pathologic aspects of human small-vessel CAA. A pcDNA3 vector containing 2.1 kb of human APP (isoform 770) cDNA was used to introduce the mutations Swedish K670N/M671L, Dutch E693Q, and Iowa D694N using the QuikChange kit.  The APP770-SwDI cDNA was amplified by PCR using primers containing the NheI five linker and SacII three linker. The PCR product of the APP770-SwDI was subcloned between exons II and IV of a Thy1.2 expression cassette using NheI and SacII restriction sites. The completed construct was microinjected into pronuclei of Sprague-Dawley single-cell embryos. Founder rats were identified by Southern blot analysis of tail DNA. Transgenic offspring were determined by PCR analysis of tail DNA. All subsequent analyses were performed with hemizygous transgenic rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626168261</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Peg3&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Michael Soares, University of Kansas Medical Center</ORIGINATION>
    <SOURCE>The strain is deposit at RRRC - University of Missouri</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-08-29)</AVAILABILITY>
    <RESEARCH_USE>Reproduction, developmental biology, cancer, etc</RESEARCH_USE>
    <ALLELES>Peg3&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419682</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="76130965" STOP_POS="76157774" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="67097874" STOP_POS="67124692" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="70210810" STOP_POS="70237450" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="65513912" STOP_POS="65526040" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_626168261</CITATION_ID>
    <DESCRIPTION>Crispr/Cas9 genome editing of the Peg3 gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626168268</RGD_ID>
    <STRAIN_SYMBOL>SD-Del&lt;i&gt;(Sult1a1-Spn)&lt;/i&gt;/YahIcsOrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Yann HERAULT, 	Translational Medicine and Neurogenetics, I.G.B.M.C.</ORIGINATION>
    <SOURCE>&lt;a href=https://www.infrafrontier.eu/emma/strain-details/?q=11821&gt;European Mouse Mutant Archive(EMMA)&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryorecovery (as of 2025-08-29)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Spn|Sult1a1</ALLELES>
    <ALLELE_RGD_IDS>3750|3767</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_626168268</CITATION_ID>
    <DESCRIPTION>Deletion of the genetic interval Sult1a1-Spn of Sprague Dawley rat: we targeted an extended sequence of the whole locus from one allele and the CRISPR/Cas9 system allowed us to remove the region encompassing 28 genes, orthologous to human.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626168271</RGD_ID>
    <STRAIN_SYMBOL>SD-Dp&lt;i&gt;(Sult1a1-Spn)&lt;/i&gt;/YahIcsOrl</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Yann HERAULT, 	Translational Medicine and Neurogenetics, I.G.B.M.C.</ORIGINATION>
    <SOURCE>&lt;a href=https://www.infrafrontier.eu/emma/strain-details/?q=11822&gt;European Mouse Mutant Archive(EMMA)&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryorecovery (as of 2025-08-29)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Spn|Sult1a1</ALLELES>
    <ALLELE_RGD_IDS>3750|3767</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_626168271</CITATION_ID>
    <DESCRIPTION>Sprague Dawley rat. Tandem duplication of the genetic interval between Sult1a1 and Spn genes using CRISPR/Cas9 engineering. We targeted the genetic interval borders from one allele and the CRISPR/Cas9 system allowed us to cut and transpose those sequences to the same locus on the second allele. Heterozygous animals are Overweight and hypoactivity.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626170595</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Syngap1&lt;sup&gt;em2Sidb&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Simons Initiative for the Developing Brain (SIDB), Institute for Neuroscience and Cardiovascular Research, University of Edinburgh, Edinburgh EH8 9XD, UK. Contact SIDB Scientific Officer for enquiries on rat distribution (sidbadm@ed.ac.uk).</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-09-02)</AVAILABILITY>
    <RESEARCH_USE>Autism Spectrum Disorder (ASD), Intellectual Disability (ID), Epilepsy</RESEARCH_USE>
    <ALLELES>Syngap1&lt;sup&gt;em2Sidb&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419668</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="5028226" STOP_POS="5058519" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="5026366" STOP_POS="5056659" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="5535434" STOP_POS="5564657" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="7594614" STOP_POS="7623865" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="5178523" STOP_POS="5208449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_626170595</CITATION_ID>
    <DESCRIPTION>This allele has a deletion of the C2/GAP domain of Syngap1 and was generated by Sigma Advanced Genetic Engineering (SAGE) Labs (St. Louis, MO, US). Zinc-ﬁnger nucleases (ZFNs) designed to target Syngap1 exons 8–12 were microinjected into the pronucleus of fertilized, single-cell Long Evans (LE) embryos. A 3,584-bp selective deletion and 3-bp insertion were conﬁrmed by sequencing, which resulted in a mutant protein that was 377 amino acids smaller than endogenous SYNGAP1.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626170599</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Syngap1&lt;sup&gt;em1Sidb&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Simons Initiative for the Developing Brain (SIDB), Institute for Neuroscience and Cardiovascular Research, University of Edinburgh, Edinburgh EH8 9XD, UK. Contact SIDB Scientific Officer for enquiries on rat distribution (sidbadm@ed.ac.uk).</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-09-02)</AVAILABILITY>
    <RESEARCH_USE>Autism Spectrum Disorder (ASD), Intellectual Disability (ID), Epilepsy</RESEARCH_USE>
    <ALLELES>Syngap1&lt;sup&gt;em1Sidb&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419667</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="20" START_POS="5028226" STOP_POS="5058519" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="20" START_POS="5026366" STOP_POS="5056659" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="20" START_POS="5535434" STOP_POS="5564657" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="20" START_POS="7594614" STOP_POS="7623865" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="20" START_POS="5178523" STOP_POS="5208449" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_626170599</CITATION_ID>
    <DESCRIPTION>This KO allele was generated by Sigma Advanced Genetic Engineering (SAGE) Labs (St. Louis, MO, US) by injecting CRISPR/Cas9 reagents and sgRNA targeting exon 8 (gtgcatagagcatgtcgtccAGG) into Long Evans (LE) zygotes. Founder #23 displayed a 2bp deletion and 1bp insertion, leading to a frameshift mutation in exon 8 of Syngap1, which prevents expression of the protein. Homozygous Syngap1 KO rats die perinatally, but heterozygous Syngap1 KO rats appear healthy and are fertile.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626170601</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Grin2a&lt;sup&gt;em1Sidb&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Simons Initiative for the Developing Brain (SIDB), Institute for Neuroscience and Cardiovascular Research, University of Edinburgh, Edinburgh EH8 9XD, UK. Contact SIDB Scientific Officer for enquiries on rat distribution (sidbadm@ed.ac.uk).</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-09-02)</AVAILABILITY>
    <RESEARCH_USE>neuronal development, epilepsy aphasia spectrum, developmental encephalopathy, epileptic encephalopathy</RESEARCH_USE>
    <ALLELES>Grin2a&lt;sup&gt;em1Sidb&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419669</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="6136458" STOP_POS="6560003" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="5629683" STOP_POS="6053262" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="5707806" STOP_POS="6123568" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="4523233" STOP_POS="4940912" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="5588229" STOP_POS="6004780" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_626170601</CITATION_ID>
    <DESCRIPTION>In collaboration with Horizon Discovery, we generated a CRISPR/Cas9-mediated deletion of a 1065bp region spanning Grin2a exon 8 (which encodes key pore forming domains of GluN2A) in Long Evans (LE) embryos, generating a KO allele.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626170603</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Cdkl5&lt;sup&gt;em1Sidb&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Simons Initiative for the Developing Brain (SIDB), Institute for Neuroscience and Cardiovascular Research, University of Edinburgh, Edinburgh EH8 9XD, UK. Contact SIDB Scientific Officer for enquiries on rat distribution (sidbadm@ed.ac.uk).</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-09-02)</AVAILABILITY>
    <RESEARCH_USE>Neurodevelopmental Disorder, Seizures, Neurodevelopmental Delay</RESEARCH_USE>
    <ALLELES>Cdkl5&lt;sup&gt;em1Sidb&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419670</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="37566320" STOP_POS="37796766" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="33757605" STOP_POS="33988075" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="35536396" STOP_POS="35773204" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="35864921" STOP_POS="36102409" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="55033499" STOP_POS="55228646" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_626170603</CITATION_ID>
    <DESCRIPTION>In collaboration with Horizon Discovery, CRISPR/Cas9 technology was used in Long Evans (LE) embryos to introduce a 10bp deletion in exon 8 of the Cdkl5 gene (Ensembl coordinates X:35,674,763–35,674,772, in the Rnor_6.0 genome assembly) which results in the introduction of an early stop codon in constitutive exon 9, leading to lack of CDKL5 protein expression.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626189117</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Foxn1&lt;sup&gt;rnu&lt;/sup&gt;&lt;/i&gt;Tg(Rho-S334X)3LavRrrc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>&lt;a href=http://www.rrrc.us/Strain/?x=539&gt;Rat Resource and Research Center&lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=539&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2025-09-03)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00539</CITATION_ID>
    <DESCRIPTION>This strain was created by crossing  “SD-Tg(Rho*S334X)3Lav, RGD: 1358302,”( also known as, SD-Tg(S334ter)3Lav , homozygous for a mutated mouse rhodopsin transgene Rho S334ter-3) with “NTac:NIH-Foxn1rnu, RGD: 7246928,” (also known as NTac:NIH-Whn (NIH nude) males (foxn1-/-). By selective breeding, all animals of this strain (RRRC#539) are homozygous for the rhodopsin mutation, and homo- or hemizygous for the foxn1 mutation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626189121</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Foxn1&lt;sup&gt;rnu&lt;/sup&gt;&lt;/i&gt;Tg((Rho-S334X)3,CAG-tdTomato)1010Mjsuc</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Seiler lab, UC Irvine; RRRC, University of Missouri (future strain #1055). Strain has been deposited with the  RRRC as future strain #1055.</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1055&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-09-03)</AVAILABILITY>
    <RESEARCH_USE>retinal degeneration (retinitis pigmentosa), retinal transplantation</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01055</CITATION_ID>
    <DESCRIPTION>Embryos from “SD-Foxn1rnuTg(Rho-S334X)3LavRrrc (RGD: 626189117)”, citation ID:RRID:RRRC_00539, were injected with the plasmid gene construct floxed TdTomato created by Envigo, coupled to the universal CAG promoter</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626419677</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gnal&lt;sup&gt;em2Hpng&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Huu Phuc Nguyen,	Institute of Medical Genetics and Applied Genomics, University of Tuebingen;  Core Facility Transgenic Animals, University Clinics Tuebingen, Tuebingen, Germany</ORIGINATION>
    <SOURCE>&lt;a href=https://www.infrafrontier.eu/emma/strain-details/?q=14794&gt;European Mouse Mutant Archive(EMMA)&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gnal&lt;sup&gt;em2Hpng&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419678</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="62892257" STOP_POS="63032510" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="60622311" STOP_POS="60762599" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="62805406" STOP_POS="62946133" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="61991738" STOP_POS="62131420" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="63595606" STOP_POS="63735803" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_626419677</CITATION_ID>
    <DESCRIPTION>Gnal knockout rats were generated by CRISPR/Cas9 technology. Exon1 of rat Gnal splicing variant 2 was targeted, resulting in a deletion of 1 base pair that corresponds to position 44 downstream of the translation start point ATG of the Gnal splicing variant 2. CRISPR technology details: self-synthesized Cas9 mRNA using px 330 vector, applying T7 transcription kit followed by Poly-Adenylation and Capping. No sequencing performed, whether Cas9 has been inserted into the rat genome is unknown. Homozygous:
Approximately 25% body weight reduction; Smaller body size; Hyperactivity; Better rotarod performance than wild-type littermates.Heterozygous:
No body weight change; No body size change; Hypo-activity; Worse rotarod performance than wild-type littermates.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626419679</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Gnal&lt;sup&gt;em3Hpng&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Huu Phuc Nguyen,	Institute of Medical Genetics and Applied Genomics, University of Tuebingen;  Core Facility Transgenic Animals, University Clinics Tuebingen, Tuebingen, Germany</ORIGINATION>
    <SOURCE>&lt;a href=https://www.infrafrontier.eu/emma/strain-details/?q=14799&gt;European Mouse Mutant Archive(EMMA)&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-09-05)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Gnal&lt;sup&gt;em3Hpng&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626419680</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="18" START_POS="62892257" STOP_POS="63032510" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="18" START_POS="60622311" STOP_POS="60762599" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="18" START_POS="62805406" STOP_POS="62946133" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="18" START_POS="61991738" STOP_POS="62131420" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="18" START_POS="63595606" STOP_POS="63735803" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_626419679</CITATION_ID>
    <DESCRIPTION>Crl:CD(SD)-KO(Gnal*135)44-178Hpng/Hpng rats were generated by CRISPR/Cas9 technology. A deletion of 135 base pairs, corresponding to position 44-178, downstream of the translation initiation start ATG of the Gnal splicing variant 2, results in a deletion mutation. CRISPR technology details: self-synthesized Cas9 mRNA using px 330 vector, applying T7 transcription kit followed by Poly-Adenylation and Capping. No sequencing performed, whether Cas9 has been inserted into the rat genome is unknown.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626469547</RGD_ID>
    <STRAIN_SYMBOL>Nifdc:WI</STRAIN_SYMBOL>
    <FULL_NAME>outbred Wistar</FULL_NAME>
    <ORIGINATION/>
    <SOURCE>Dr. Zhang guoxi, 
&lt;a href=https://nrla.nifdc.org.cn/resource/zinfo.html?id=LJDm7HWNa+QBdY1zpWQADw==&amp;kjzybm=CSTR:15497.09.N2003&gt; National Rodent Laboratory Animal Resources Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_626469547</CITATION_ID>
    <DESCRIPTION>This colony was introduced from Japan in 1994. The colony was maintained by rotational mating avoiding brother sister mating.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626469553</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Thbd&lt;sup&gt;em1Soar&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>KUMC: University of Kansas Medical Center</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1047&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-09-15)</AVAILABILITY>
    <RESEARCH_USE>Thrombosis and reproductive biology research</RESEARCH_USE>
    <ALLELES>Thbd&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626469576</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="156316526" STOP_POS="156320178" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="135863366" STOP_POS="135867018" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="142748673" STOP_POS="142752325" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="149159895" STOP_POS="149163547" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="137158955" STOP_POS="137162607" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01047</CITATION_ID>
    <DESCRIPTION>1316 bp deletion of the coding region of the Thbd gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626469555</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Phlda2&lt;sup&gt;em1Soar&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1048&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-09-15)</AVAILABILITY>
    <RESEARCH_USE>Reproduction, developmental biology</RESEARCH_USE>
    <ALLELES>Phlda2&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626469578</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="1" START_POS="208126302" STOP_POS="208127241" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="1" START_POS="198696897" STOP_POS="198699292" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="1" START_POS="216701345" STOP_POS="216704479" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="1" START_POS="223562616" STOP_POS="223564645" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="1" START_POS="203878093" STOP_POS="203879038" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01048</CITATION_ID>
    <DESCRIPTION>Crispr/Cas9 mediated 103 bp deletion within Exon 1 of the Phlda2 gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626469556</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Adm&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>KUMC: University of Kansas Medical Center</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1046&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE>Cardiovascular and reproductive research</RESEARCH_USE>
    <ALLELES>Adm&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626469800</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01046</CITATION_ID>
    <DESCRIPTION>Crispr/Cas9 mediated 206 bp deletion associated with Exon 2 and the second intron of the Adm gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626469557</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Taf7l&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>KUMC: University of Kansas Medical Center</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1045&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-09-15)</AVAILABILITY>
    <RESEARCH_USE>Reproductive biology research</RESEARCH_USE>
    <ALLELES>Taf7l&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626469801</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="101953508" STOP_POS="101968336" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="X" START_POS="97660222" STOP_POS="97675241" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="105292338" STOP_POS="105308554" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="105183229" STOP_POS="105199248" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="121935672" STOP_POS="121950719" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01045</CITATION_ID>
    <DESCRIPTION>Crispr/Cas9 mediated 110 bp deletion targeting Exon 3 of the Taf7l gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626469558</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Tfap2c&lt;sup&gt;em1Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>KUMC: University of Kansas Medical Center</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1039&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-09-15)</AVAILABILITY>
    <RESEARCH_USE>Embryonic and extraembryonic development</RESEARCH_USE>
    <ALLELES>Tfap2c&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626469802</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="181733524" STOP_POS="181742412" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="161315114" STOP_POS="161322998" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="170550314" STOP_POS="170558197" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="176625472" STOP_POS="176633355" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="163459283" STOP_POS="163467166" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01039</CITATION_ID>
    <DESCRIPTION>Crispr/Cas9 mediated 308 bpy deletion within Exon 4 of the Tfap2c gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626469560</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Tfap2c&lt;sup&gt;em2Soar&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>KUMC: University of Kansas Medical Center</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1040&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-09-15)</AVAILABILITY>
    <RESEARCH_USE>Investigation of a wide range of biological systems - dependent upon access to suitable cre recombinase rat strains</RESEARCH_USE>
    <ALLELES>Tfap2c&lt;sup&gt;em2Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626469803</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="3" START_POS="181733524" STOP_POS="181742412" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="3" START_POS="161315114" STOP_POS="161322998" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="3" START_POS="170550314" STOP_POS="170558197" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="3" START_POS="176625472" STOP_POS="176633355" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="3" START_POS="163459283" STOP_POS="163467166" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01040</CITATION_ID>
    <DESCRIPTION>Crispr/Cas9 mediated insertion of loxp sites flanking Exon 4 of the Tfap2c gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626469567</RGD_ID>
    <STRAIN_SYMBOL>BBDP</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1041&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-09-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01041</CITATION_ID>
    <DESCRIPTION>Diabetic prone BB rats. The Biobreeding rats (BB) spontaneously developed autoimmune diabetes mellitus were found in a closed colony of outbred WI (Wistar) rats at the Bio-Breeding Laboratories, Ottawa, Health Canada received the original stock from Bio-Breeding Laboratories after the company was out of business. The embryos preservation was through Charles River until donated to RRRC..</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626469568</RGD_ID>
    <STRAIN_SYMBOL>BBDR</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1042&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-09-16)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01042</CITATION_ID>
    <DESCRIPTION>Diabetic resistant (non diabetic)  BB rats. This is the control strain for BB rat diabetic prone. BBDR rats do not get disease. The Biobreeding rats (BB) rats were found in a closed colony of outbred WI (Wistar) rats at the Bio-Breeding Laboratories, Ottawa, Health Canada received the original stock from Bio-Breeding Laboratories after the company was out of business. The embryos preservation was through Charles River until donated to RRRC..</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>626469804</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Tbx21&lt;sup&gt;em1Sage&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The Tbx21 (T-beta) Knockout Rat model was originally created at SAGE Labs, Inc. in St. Louis, MO and distributed out of the Boyertown, PA facility. The line continues to be maintained through the original SAGE Labs animal inventory acquired by Envigo, then Envigo was acquired by Inotiv in 2021.</ORIGINATION>
    <SOURCE>&lt;a href=https://www.inotiv.com/research-model/hsdsage-sd-tbx21em1sage&gt; Inotiv&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-09-17)</AVAILABILITY>
    <RESEARCH_USE>acute and chronic human asthma, Crohn's disease, colitis, cancer metastasis, autoimmune disorders and inflammation.</RESEARCH_USE>
    <ALLELES>Tbx21&lt;sup&gt;em1Sage&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>626471108</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="82578751" STOP_POS="82595253" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="82082322" STOP_POS="82098831" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="85032799" STOP_POS="85049331" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="84822665" STOP_POS="84839295" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="85817743" STOP_POS="85834178" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_626469804</CITATION_ID>
    <DESCRIPTION>This is a Tbx21 knockout rat created using ZFN technology targeting exon 1 coding sequences 378-412. The resulting mutation is a 22-bp deletion (392-413).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>628359016</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Epas1&lt;sup&gt;em1Soar&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Kansas Medical Center</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1060&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-09-18)</AVAILABILITY>
    <RESEARCH_USE>Reproductive, Developmental Biology, Hypoxia</RESEARCH_USE>
    <ALLELES>Epas1&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>628359038</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="6" START_POS="13543252" STOP_POS="13626147" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="6" START_POS="7790236" STOP_POS="7871717" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="6" START_POS="10306508" STOP_POS="10385239" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="6" START_POS="20299603" STOP_POS="20379864" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="6" START_POS="10203108" STOP_POS="10297215" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01060</CITATION_ID>
    <DESCRIPTION>Crispr/Cas9 mediated 34 bp deletion within Exon 2 of the Epas1 gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>628359017</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Lifr&lt;sup&gt;em1Soar&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Kansas Medical Center</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1058&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-09-18)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Lifr&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>628359039</ALLELE_RGD_IDS>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01058</CITATION_ID>
    <DESCRIPTION>Crispr/Cas9 mediated 88bp deletion of Exon 2 of the Lifr gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>628359018</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Fstl3&lt;sup&gt;em1Soar&lt;/i&gt;&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Kansas Medical Center</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1059&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2025-09-18)</AVAILABILITY>
    <RESEARCH_USE>Reproduction, developmental biology</RESEARCH_USE>
    <ALLELES>Fstl3&lt;sup&gt;em1Soar&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>628359040</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="10574195" STOP_POS="10579844" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="9923574" STOP_POS="9929223" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="12806031" STOP_POS="12810556" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="12976235" STOP_POS="12980760" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="11438360" STOP_POS="11442885" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01059</CITATION_ID>
    <DESCRIPTION>Crispr/Cas9 mediated 3243 bp deletion affecting Exons 1-3 of the Fstl3 gene</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629006509</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(Thy1-APP&lt;sup&gt;D&lt;/sup&gt;)BWevn</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>William Van Nostrand, University Rhode Island</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=1051&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryorecovery (as of 2025-10-30)</AVAILABILITY>
    <RESEARCH_USE>Neurodegeneration, Alzheimer's Disease, Neurovascular degeneration</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01051</CITATION_ID>
    <DESCRIPTION>These rats produce human familial CAA Dutch E22Q mutant amyloid APPB2-protein in brain and develop arteriolar CAA type-2. The deposition of fibrillar APPB2 promotes arteriolar smooth muscle cell loss and cerebral microhemorrhages that can be detected by magnetic resonance imaging and confirmed by histopathology. Random integration of a transgene consisting of 2.1 kb of human APP (isoform 770) cDNA carrying the Dutch E693Q mutation cloned between exons II and IV of a Thy1.2 expression cassette. This leads to expression of chimeric mutant human A beta PP under control of the neuronal specific Thy1.2 promoter. The integration site of the transgene is unknown.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629006528</RGD_ID>
    <STRAIN_SYMBOL>ACI/EurMcwiRrrc</STRAIN_SYMBOL>
    <FULL_NAME>ACI (August × Copenhagen Irish)</FULL_NAME>
    <ORIGINATION>&lt;a href=https://rgd.mcw.edu/wg/hrdp_panel/ &gt; RGD HRDP&lt;/a&gt;, contact Hybrid Rat Diversity Program at 
 &lt;a href=mailto:HRDP@mcw.edu&gt;  HRDP@mcw.edu &lt;/a&gt;</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=284&gt;Rat Resource &amp; Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>inbred</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo; Cryopreserved Sperm (as of 2025-11-03)</AVAILABILITY>
    <RESEARCH_USE>Renal disease</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00284</CITATION_ID>
    <DESCRIPTION>substrain of ACI derived from ACI/EurMcwi donated to RRRC by Howard Jacob from Medical College of Wisconsin.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629006610</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(ACE2)955Bryd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Rat Resource and Research Center</ORIGINATION>
    <SOURCE>Deposited at &lt;a href=http://www.rrrc.us/Strain/?x=1001&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-11-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01001</CITATION_ID>
    <DESCRIPTION>Genetic Alteration(s):human ACE2 gene under expression of the human ACE2 promoter. Thirty (30) copies of the transgene are randomly integrated into an as yet unknown insertion site.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629006611</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(ACE2)058Bryd</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Rat Resource and Research Center</ORIGINATION>
    <SOURCE>Deposited at &lt;a href=http://www.rrrc.us/Strain/?x=1012&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Embryo (as of 2025-11-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01012</CITATION_ID>
    <DESCRIPTION>Genetic Alteration(s):human ACE2 gene under expression of the human ACE2 promoter. Eight copies of the transgene are randomly integrated into an as yet unknown insertion site.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629006637</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Antxr2 &lt;sup&gt;em1&lt;/sup&gt;&lt;/i&gt;/Vr</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical Research Center, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, 

Capital Medical University, Beijing, China</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629006637</CITATION_ID>
    <DESCRIPTION>ANTXR2 knock-out rats were generated using CRISPR/Cas9-mediated genome editing. Specifically, a 67 base pairs deletion in exon 1 of ANTXR2 was induced by 2 guide RNAs targeting sequences within exon 1. The guide RNA targeting vectors and Cas9 were co-injected into the fertilized Sprague  Dawley eggs to generate ANTXR2 knock-out rats. The pups were genotyped by PCR and confirmed by sequencing (forward primer: 5′-TTGGGTGGCTCTGAGCTTGGA-3′, reverse primer: 5′-AGGGGTCTAGGGGAGTGTGATAAAGA-3′).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629006641</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Per1&lt;sup&gt;em1Smoc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Cyagen Company (Jiangsu, China)</ORIGINATION>
    <SOURCE>National Institute on Drug Dependence and Beijing Key Laboratory on Drug Dependence Research, Peking University, Beijing, China</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Per1&lt;sup&gt;em1Smoc&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>629006643</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="54299002" STOP_POS="54313804" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="53800126" STOP_POS="53814963" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="55681761" STOP_POS="55696557" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="55424863" STOP_POS="55439853" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="55859851" STOP_POS="55868747" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629006641</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9 system was used to  generate rats with a deletion of the CRE site (Del_TGACGTCA) in the Per1
gene promoter Per1 gene in  Sprague Dawley (Charles River) rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629020173</RGD_ID>
    <STRAIN_SYMBOL>LE-&lt;i&gt;Drd2&lt;sup&gt;em1(Cre)Rrrc&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Rrrc</ORIGINATION>
    <SOURCE>&lt;a href=http://www.rrrc.us/Strain/?x=979&gt;Rat Resource and Research Center&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_00979</CITATION_ID>
    <DESCRIPTION>The Cre recombinase gene was knocked into exon 2 of the Drd2 gene using CRISPR/Cas9 genome editing.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629116668</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Slc6a9&lt;sup&gt;em1(cre)Mira&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>University of Texas at El Paso, Biological Sciences Department</ORIGINATION>
    <SOURCE>Rat Resource and Research Center</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals; Cryopreserved Embryo; Cryopreserved Sperm (as of 2025-12-09)</AVAILABILITY>
    <RESEARCH_USE>Neuroscience</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RRRC_01052</CITATION_ID>
    <DESCRIPTION>The knock-in rat line was engineered to express the iCRE recombinase under the SLC6A9 locus. It was generated in SD background and maintain in this background for many generations.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629136826</RGD_ID>
    <STRAIN_SYMBOL>SHR/OlaIpcv-mt&lt;sup&gt;F344/Crl&lt;/sup&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>conplastic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629136826</CITATION_ID>
    <DESCRIPTION>Mitochodrial genome of SHR/OlaIpcv was selectively replaced byF344/Crl to create this conplastic strain using the supersonic breeding strategy; these have the mitochondrial genome of F344/Crl on SHR/OlaIpcv nuclear genetic background</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629142768</RGD_ID>
    <STRAIN_SYMBOL>CD-&lt;i&gt;Dmd&lt;sup&gt;em1Gene&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Genethon in collaboration with Genoway (https://www.genoway.com/)</ORIGINATION>
    <SOURCE>Genethon; 1, bis rue de l’internationale23
91000 Evry, France</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>Dmd&lt;sup&gt;em1Gene&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>632518375</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="X" START_POS="51070098" STOP_POS="53437845" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="x" START_POS="48566517" STOP_POS="48567122" METHOD="8"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="X" START_POS="51149358" STOP_POS="53519271" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="X" START_POS="51475950" STOP_POS="53700033" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="X" START_POS="71501362" STOP_POS="71671414" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629142768</CITATION_ID>
    <DESCRIPTION>The model was generated using a single guide RNA-Cas9 targeted to exon 45 of the rat Dmd gene on a Sprague-Dawley (CD®(SD), Crl:CD(SD)) background. One male founder with a 606 bp deletion encompassing Dmd exon 45 and spanning from 207 bp into the 3’ region of intron 44 to 223 bp into the 5’ region of intron 45,including exon 45, was selected for phenotyping. The  heterozygous/hemizygous Dmd knock-out lines were used for breeding.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629142769</RGD_ID>
    <STRAIN_SYMBOL>CD-&lt;i&gt;Dmd&lt;sup&gt;em1Gene+/+&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Genethon in collaboration with Genoway (https://www.genoway.com/)</ORIGINATION>
    <SOURCE>Genethon; 1, bis rue de l’internationale23
91000 Evry, France</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629142769</CITATION_ID>
    <DESCRIPTION>The is the wild type litter mate for the Dmd mutant: CD-Dmdem1Gene (RGD:629142768),</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629142772</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rrg2&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>Custom Rats at Medical College of Wisconsin, Email: mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-12-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629142772</CITATION_ID>
    <DESCRIPTION>Cas9 and sgRNA targeting the sequence GCTTTGCAACTTGTGCAGCA were injected into SS embryos to mutate a CTCF binding site within the first intron of Golt1a. a 3-bp deletion rn6 chr13:50,545,341-50,545,343 resulted.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>629142773</RGD_ID>
    <STRAIN_SYMBOL>SS-&lt;i&gt;Rrg3&lt;sup&gt;em1Mcwi&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Medical College of Wisconsin</ORIGINATION>
    <SOURCE>Custom Rats at Medical College of Wisconsin, Email: mcwcustomrats@mcw.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Cryopreserved Sperm (as of 2025-12-30)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_629142773</CITATION_ID>
    <DESCRIPTION>Cas9 and sgRNA targeting the sequence GGGCATCTTCTGCCACCTAC were injected into SS embryos to mutate a CTCF binding site within the first intron of Ren. An 11-bp deletion rn6 chr13:50,509,649-50,509,659 resulted.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>630350396</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Dmd&lt;sup&gt;em1Ins&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>The “Institut Clinique de la Souris”–PHENO MIN</ORIGINATION>
    <SOURCE>Rats can be obtained through material transfer agreement by contacting the corresponding author at valentina.-
taglietti@inserm.fr and frederic.relaix@inserm.fr.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_630350396</CITATION_ID>
    <DESCRIPTION>Deletion of exons 45 to 47 of the rat Dmd gene by CRISPR/Cas9 was performed by using two pairs of sgRNAs on both sides of exons 45 and 47. The spCas9 and sgRNAs were electroporated in rat Sprague Dawley (RjHan:SD) fertilized oocytes. Genotyping PCR and sequencing were used to confirm the deletion of exons 45–47 in F0 founder animals.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>630350551</RGD_ID>
    <STRAIN_SYMBOL>LH-&lt;i&gt;C17h6orf52&lt;sup&gt;em2Aek&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Currently live colony with Dr. Anne Kwitek at the Medical College of Wisconsin. Being cryopreserved and the live colony will not be available.</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2026-01-14)</AVAILABILITY>
    <RESEARCH_USE>Metabolic syndrome</RESEARCH_USE>
    <ALLELES>C17h6orf52&lt;sup&gt;em2Aek&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>630350562</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="17" START_POS="23968511" STOP_POS="23982103" METHOD="8"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="17" START_POS="23753359" STOP_POS="23776251" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="17" START_POS="21600326" STOP_POS="21615888" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="17" START_POS="23581681" STOP_POS="23595498" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="17" START_POS="29733271" STOP_POS="29746771" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_630350551</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was used to delete the entire C17h6orf52 gene from LH/MavRrrcAek embryos. Deletion ranges on chromosome 17 from 23968511 to 23982103 in GRCr8 per NCBI blast - see attachment for sequence annotation.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>630350554</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Prnp&lt;sup&gt;em1Evm&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>This strain has been deposited with the RRRC</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2026-01-15)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_630350554</CITATION_ID>
    <DESCRIPTION>A deletion mutation was induced using CRISPR/Cas9 system in embryos of Spague-Dawley  rats from Charles  River.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>631721277</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Shank3&lt;sup&gt;em1Bcgen&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Beijing Biocytogen Co. Ltd., Beijing, China.</ORIGINATION>
    <SOURCE>zhangrong@bjmu.edu.cn at Department of Neurobiology, School of Basic Medical Sciences, Peking University, Beijing, China</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES>SD-&lt;i&gt;Shank3&lt;sup&gt;em1Bcgen&lt;/sup&gt;&lt;/i&gt;</ALLELES>
    <ALLELE_RGD_IDS>631721279</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="7" START_POS="122448323" STOP_POS="122518623" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="7" START_POS="120568707" STOP_POS="120630796" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="7" START_POS="130474278" STOP_POS="130534679" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="7" START_POS="130159246" STOP_POS="130220171" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="7" START_POS="127817026" STOP_POS="127877875" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_631721277</CITATION_ID>
    <DESCRIPTION>The mutant rats were generated using CRISPR/Cas9 technology to target upstream of exon 11 or downstream of exon 21 of rat Shank3. The resulting  mutant carried approximately 26 kb deletions with the removal of the Shank3 exon 11–21</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>632517841</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Oxtr&lt;sup&gt;em1(cre)Grin&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Prof. Dr. Valery Grinevich, Central Institute of Mental Health</ORIGINATION>
    <SOURCE>Availability Contact Email: alexander.bexter@zi-mannheim.de,Central Institute of Mental Health</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2026-01-28)</AVAILABILITY>
    <RESEARCH_USE>Used for Cre-dependent, cell-type-specific genetic manipulation of Oxtr-expressing neurons.</RESEARCH_USE>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_632517841</CITATION_ID>
    <DESCRIPTION>CRISPR/Cas9-mediated knock-in of an IRES-Cre cassette into the 3' UTR of the endogenous Oxtr gene. The line is maintained in the heterozygous state and preserves normal Oxtr expression.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>632518356</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Dbh&lt;sup&gt;em1(cre)Xyan&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>Shenzhen Institute of Advanced Technolog, Shenzhen, China</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_632518356</CITATION_ID>
    <DESCRIPTION>DBH-Cre knock-in (KI)  rats, developed on the Sprague
Dawley (SD) rat background, were generated using the CRISPR/Cas9
system. In this knock-in model, a gene cassette encod-
ing 2A peptide, fused to Cre recombinase  was introduced to
replace the TAA stop codon in exon 12 of the rat Dbh gene. Additionally, a
synonymous mutation p. T616= (ACG to ACA) was incorporated to pre-
vent gRNA binding and recutting of the sequence following
homology-directed repair. The gRNA targeting the rat DBH gene
(gRNA-B1: 5′-TTACTCAGTGTCTGCCTCCGTGG-3′), the donor vector con-
taining the “P2A-Cre” cassette, and a synonymous mutation p. T616=
(ACG to ACA), along with Cas9 mRNA, were co-injected into fertilized rat embryos. F0 founders. DBH-Cre KI rats were bred with wild-type SD rats (Guangdong Vital River Laboratory Animal Technology Co., Ltd.,
China).</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>632518357</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;(ROSA)26 Sor&lt;sup&gt;em1(CAG-tdTomato)Cya</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Cyagen Bioscience Inc., Guangzhou, China</ORIGINATION>
    <SOURCE>&lt;a href=https://www.cyagen.com/mouseatlas/CR003&gt;Cyagen&lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2026-02-06)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_632518357</CITATION_ID>
    <DESCRIPTION>The endonuclease mediated knock in of the   transgenic cassette, CAG-LSL-tdTomato in mouse (ROSA)26Sor, was created in Crl:CD (SD) rats.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>632518377</RGD_ID>
    <STRAIN_SYMBOL>NShjh:SD</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION/>
    <SOURCE>&lt;a href=http://www.jh-labanimal.site/myAppAIMED_ANIMALS_MODE16/AIMED_ANIMALS_MODE16.html/&gt;Shanghai Jihui Laboratory Animal Breeding Co., Ltd &lt;/a&gt;</SOURCE>
    <STRAIN_TYPE>outbred</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2026-02-10)</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_632518377</CITATION_ID>
    <DESCRIPTION>Shjh outbred SD rats were first obtained in 2017 from the NIH Animal Genetic Resource. The NIH stock originated from Sprague Dawley, Inc. in 1945 and has since been maintained as an outbred closed colony.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>632518398</RGD_ID>
    <STRAIN_SYMBOL>SD-&lt;i&gt;Mpo&lt;sup&gt;em1Lempo&lt;/sup&gt;&lt;/i&gt;</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Animal Modeling Core at the University of Missouri.</ORIGINATION>
    <SOURCE>Animal Modeling Core at the University of Missouri. Availability Contact Email: davisdaniel@missouri.edu</SOURCE>
    <STRAIN_TYPE>mutant</STRAIN_TYPE>
    <AVAILABILITY>Live Animals (as of 2026-02-12)</AVAILABILITY>
    <RESEARCH_USE>Inflammation, oxidative stress, and vascular disease</RESEARCH_USE>
    <ALLELES>Mpo&lt;sup&gt;em1Lempo&lt;/sup&gt;</ALLELES>
    <ALLELE_RGD_IDS>632518399</ALLELE_RGD_IDS>
    <POSITIONS>
      <POSITION ASSEMBLY="GRCr8" CHR="10" START_POS="73092124" STOP_POS="73102057" METHOD="7"/>
      <POSITION ASSEMBLY="mRatBN7.2" CHR="10" START_POS="72594883" STOP_POS="72608862" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_6.0" CHR="10" START_POS="75087892" STOP_POS="75098260" METHOD="7"/>
      <POSITION ASSEMBLY="Rnor_5.0" CHR="10" START_POS="75004128" STOP_POS="75014496" METHOD="7"/>
      <POSITION ASSEMBLY="RGSC v.3.4" CHR="10" START_POS="76085872" STOP_POS="76097012" METHOD="7"/>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_632518398</CITATION_ID>
    <DESCRIPTION>The CRISPR/Cas9 system was multiplexed to introduce a double strand brake at exon 3 and 14 to promote the removal of majority of the MPO gene in rat embryos.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>632522749</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(NR3C2*)Frje</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre de Recherche des Cordeliers, Inserm, Universit´e Paris Cit´e, Sorbonne Universit´e, Paris, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_632522749</CITATION_ID>
    <DESCRIPTION>This transgenic rat strain carrying human NR3C2 was developed on a Sprague-Dawley albino background. The transgene was constructed with the human NR3C2  (also know as MR)  under the proximal P1 promotor in the 5′-flanking regions of exons 1alpha.</DESCRIPTION>
  </Strain>
  <Strain>
    <RGD_ID>632522750</RGD_ID>
    <STRAIN_SYMBOL>SD-Tg(NR3C2*)&lt;sup&gt;-/-&lt;/sup&gt;Frje</STRAIN_SYMBOL>
    <FULL_NAME/>
    <ORIGINATION>Centre de Recherche des Cordeliers, Inserm, Universit´e Paris Cit´e, Sorbonne Universit´e, Paris, France</ORIGINATION>
    <SOURCE/>
    <STRAIN_TYPE>transgenic</STRAIN_TYPE>
    <AVAILABILITY>Unknown</AVAILABILITY>
    <RESEARCH_USE/>
    <ALLELES/>
    <ALLELE_RGD_IDS/>
    <POSITIONS>
    </POSITIONS>
    <CITATION_ID>RRID:RGD_632522750</CITATION_ID>
    <DESCRIPTION>This is the wild type littermate of the transgenic rat strain carrying human NR3C2 (RGD:632522749).</DESCRIPTION>
  </Strain>
</Strains>
