# RGD-PIPELINE: ftp-file-extracts # MODULE: genes build 2022-04-18 # GENERATED-ON: 2023/05/19 # PURPOSE: information about active Chinchilla genes extracted from RGD database # SPECIES: Chinchilla lanigera (long-tailed chinchilla) NCBI:txid34839 # CONTACT: rgd.data@mcw.edu # FORMAT: tab delimited text # NOTES: multiple values in a single column are separated by ';' # ### Mar 11 2020 added Ensembl map positions ### Jan 18 2021 discontinued columns: UNIGENE_ID, TIGR_ID, SPLICE_RGD_ID, SPLICE_SYMBOL ### Apr 18 2022 added export of canonical proteins in column 27 # #COLUMN INFORMATION: # (First 38 columns are in common between all species) # #1 GENE_RGD_ID the RGD_ID of the gene #2 SYMBOL official gene symbol #3 NAME gene name #4 GENE_DESC gene description (if available) #5 (UNUSED) blank #6 CHROMOSOME_1.0 chromosome for reference assembly build 1.0 #7 (UNUSED) blank #8 FISH_BAND fish band information #9 (UNUSED) blank #10 (UNUSED) blank #11 (UNUSED) blank #12 START_POS_1.0 start position for reference assembly build 1.0 #13 STOP_POS_1.0 stop position for reference assembly build 1.0 #14 STRAND_1.0 strand information for reference assembly build 1.0 #15 (UNUSED) blank #16 (UNUSED) blank #17 (UNUSED) blank #18 CURATED_REF_RGD_ID RGD_ID of paper(s) used to curate gene #19 CURATED_REF_PUBMED_ID PUBMED_ID of paper(s) used to curate gene #20 UNCURATED_PUBMED_ID PUBMED ids of papers associated with the gene at NCBI but not used for curation #21 NCBI_GENE_ID NCBI Gene ID #22 UNIPROT_ID UniProtKB id(s) #23 GENE_REFSEQ_STATUS gene RefSeq Status (from NCBI) #24 GENBANK_NUCLEOTIDE GenBank Nucleotide ID(s) #25 (UNUSED) blank #26 GENBANK_PROTEIN GenBank Protein ID(s) #27 CANONICAL_PROTEIN UniProt canonical protein(s) #28 MARKER_RGD_ID RGD_ID(s) of markers associated with given gene #29 MARKER_SYMBOL marker symbol #30 OLD_SYMBOL old symbol alias(es) #31 OLD_NAME old name alias(es) #32 QTL_RGD_ID RGD_ID(s) of QTLs associated with given gene #33 QTL_SYMBOL QTL symbol #34 NOMENCLATURE_STATUS nomenclature status #35 (UNUSED) blank #36 (UNUSED) blank #37 GENE_TYPE gene type #38 ENSEMBL_ID Ensembl Gene ID #39 CHROMOSOME_ENSEMBL chromosome for primary Ensembl assembly #40 START_POS_ENSEMBL start position for primary Ensembl assembly #41 STOP_POS_ENSEMBL stop position for primary Ensembl assembly #42 STRAND_ENSEMBL strand information for primary Ensembl assembly # GENE_RGD_ID SYMBOL NAME GENE_DESC (UNUSED) CHROMOSOME_1.0 (UNUSED) FISH_BAND (UNUSED) (UNUSED) (UNUSED) START_POS_1.0 STOP_POS_1.0 STRAND_1.0 (UNUSED) (UNUSED) (UNUSED) CURATED_REF_RGD_ID CURATED_REF_PUBMED_ID UNCURATED_PUBMED_ID NCBI_GENE_ID UNIPROT_ID GENE_REFSEQ_STATUS GENBANK_NUCLEOTIDE (UNUSED) GENBANK_PROTEIN CANONICAL_PROTEIN MARKER_RGD_ID MARKER_SYMBOL OLD_SYMBOL OLD_NAME QTL_RGD_ID QTL_SYMBOL NOMENCLATURE_STATUS (UNUSED) (UNUSED) GENE_TYPE ENSEMBL_ID CHROMOSOME_ENSEMBL START_POS_ENSEMBL STOP_POS_ENSEMBL STRAND_ENSEMBL 8699520 Trnae-uuc transfer RNA glutamic acid (anticodon UUC) This record serves to anchor the annotations of this class of tRNAs at multiple locations on the chinchilla, long-tailed genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMe NW_004955518;NW_004955533;NW_004955404;NW_004955468;NW_004955467 2739880;3278389;51044487;13117506;8514521 2739951;3278460;51044558;13117577;8514592 -;+;-;+;+ 101978830 MODEL AGCD01004542;AGCD01051452;AGCD01052199;AGCD01067784;AGCD01070411 trna 8699521 Tex30 testis expressed 30 ASSOCIATED WITH Anal Atresia, Hypospadias, and Penoscrotal Inversion (ortholog); Evans Syndrome, Immunodeficiency, and Premature Immunosenescence associated with Tripeptidyl-Peptidase II Deficiency (ortholog); genetic disease (ortholog) NW_004955404 8390635 8394761 + 9068941 102002987 A0A8C2ULU9 MODEL AGCD01003352;GBDI01294125;GBDI01294139;XM_005374029 XP_005374086 protein-coding ENSCLAG00000002020 NW_004955404 8390625 8396625 + 8699530 LOC102003375 mortality factor 4-like protein 1 pseudogene NW_004955532 142317 143401 + 102003375 MODEL AGCD01070101 APPROVED pseudo 8699537 Entrep1 endosomal transmembrane epsin interactor 1 ENCODES a protein that exhibits ubiquitin ligase activator activity (ortholog); INVOLVED IN CXCL12-activated CXCR4 signaling pathway (ortholog); negative adaptation of signaling pathway (ortholog); receptor internalization (ortholog); ASSOCIATED WITH genetic disease (ortholog); prostate cancer (ortholog); FOUND IN early endosome membrane (ortholog); late endosome membrane (ortholog); plasma membrane (ortholog) NW_004955434 3615284 3704014 - 9068941 102004633 A0A8C2VCE4 MODEL AGCD01032137;AGCD01032138;AGCD01032139;AGCD01032140;AGCD01032141;GBBH01142742;GBCB01007711;XM_005388562 XP_005388619 Fam189a2 family with sequence similarity 189 member A2;family with sequence similarity 189, member A2 APPROVED protein-coding ENSCLAG00000007506 NW_004955434 3615182 3704014 - 8699552 LOC102004795 zinc finger CCCH domain-containing protein 14-like NW_004955466 12129671 12131134 - 102004795 MODEL AGCD01051113 pseudo 8699553 LOC102005362 olfactory receptor 51I2 NW_004955414 21355079 21356017 + 9068941 102005362 A0A8C2YV97 MODEL AGCD01015416;XM_005380086 XP_005380143 APPROVED protein-coding ENSCLAG00000017983 NW_004955414 21355079 21356017 + 8699556 Ephx2 epoxide hydrolase 2 ENCODES a protein that exhibits epoxide hydrolase activity (ortholog); lipid phosphatase activity (ortholog); lysophosphatidic acid phosphatase activity (ortholog); INVOLVED IN cholesterol homeostasis (ortholog); dephosphorylation (ortholog); epoxide metabolic process (ortholog); PARTICIPATES IN acetylsalicylic acid pharmacodynamics pathway; antipyrine drug pathway; arachidonic acid metabolic pathway; ASSOCIATED WITH acute kidney failure (ortholog); Acute Lung Injury (ortholog); atherosclerosis (ortholog); FOUND IN cytosol (ortholog); peroxisome (ortholog) NW_004955403 49999563 50038800 + 9068941;7240710 102005434 A0A8C2W371 MODEL AGCD01002954;AGCD01002955;GBBH01062366;XM_005373744 XP_005373801 bifunctional epoxide hydrolase 2;epoxide hydrolase 2, cytoplasmic APPROVED protein-coding ENSCLAG00000014569 NW_004955403 49999563 50041572 + 8699581 Znf385a zinc finger protein 385A ENCODES a protein that exhibits mRNA 3'-UTR binding (ortholog); p53 binding (ortholog); INVOLVED IN apoptotic process (ortholog); DNA damage response (ortholog); hemostasis (ortholog); PARTICIPATES IN p53 signaling pathway; ASSOCIATED WITH genetic disease (ortholog); FOUND IN chromatin (ortholog); cytosol (ortholog); dendrite (ortholog) NW_004955458 1610245 1631639 - 9068941 102006215 A0A8C2VVK9 MODEL AGCD01047194;AGCD01047195;AGCD01047196;AGCD01047197;GBDI01122147;XM_005397220;XM_005397223;XM_013521015;XM_013521016;XM_013521017 XP_005397277;XP_005397280;XP_013376469;XP_013376470;XP_013376471 protein-coding ENSCLAG00000012440 NW_004955458 1610245 1631639 - 8699603 Pank4 pantothenate kinase 4 (inactive) ENCODES a protein that exhibits pantothenate kinase activity (ortholog); ASSOCIATED WITH cataract (ortholog); Cataract 49 (ortholog); chromosome 1p36 deletion syndrome (ortholog) NW_004955486 8703236 8716017 + 9068941 102006465 A0A8C2V8L4 MODEL AGCD01059154;AGCD01059155;GBBH01065796;XM_005404165;XM_005404166 XP_005404222;XP_005404223 pantothenate kinase 4 APPROVED protein-coding ENSCLAG00000006749 NW_004955486 8702909 8716377 + 8699634 LOC102006723 uncharacterized LOC102006723 NW_004955576 651455 652726 - 102006723 MODEL AGCD01075304;GBDF01286939;XR_265073 ncrna 8699639 LOC102008539 sodium- and chloride-dependent transporter XTRP3A-like NW_004955420 26201378 26228005 + 102008539 A0A8C2VXL1 MODEL AGCD01021392;AGCD01021393;AGCD01021394;AGCD01021395;GBCQ01102604;XM_013513346 XP_013368800 APPROVED protein-coding ENSCLAG00000015187 NW_004955420 26201547 26227686 + 8699652 Lig1 DNA ligase 1 ENCODES a protein that exhibits DNA ligase activity (ortholog); INVOLVED IN base-excision repair (ortholog); DNA repair (ortholog); DNA replication (ortholog); PARTICIPATES IN mismatch repair pathway; nucleotide excision repair pathway; ASSOCIATED WITH epilepsy with generalized tonic-clonic seizures (ortholog); genetic disease (ortholog); Immunodeficiency 96 (ortholog); FOUND IN intracellular membrane-bounded organelle (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955609 118442 160009 + 9068941 102008805 A0A8C2UG12 MODEL AGCD01077052;GBDF01051840;XM_005414919;XM_005414920;XM_005414923 XP_005414976;XP_005414977;XP_005414980 ligase I, DNA, ATP-dependent APPROVED protein-coding ENSCLAG00000000346 NW_004955609 126278 160063 + 8699697 LOC102010809 protein FAM161A pseudogene NW_004955419 28597487 28599260 - 102010809 MODEL AGCD01020469 APPROVED pseudo 8699698 LOC102011408 zinc finger protein 354A NW_004955408 1675669 1691620 + 9068941 102011408 A0A8C2YT50 MODEL AGCD01007971;AGCD01007972;AGCD01007973;GBCB01038314;GBCB01038318;XM_013507993 XP_013363447 Znf354a APPROVED protein-coding ENSCLAG00000014648 NW_004955408 1675684 1691058 + 8699706 Dnaaf11 dynein axonemal assembly factor 11 INVOLVED IN axonemal dynein complex assembly (ortholog); cerebrospinal fluid circulation (ortholog); cilium movement (ortholog); ASSOCIATED WITH benign neonatal seizures (ortholog); Charcot-Marie-Tooth disease type 4 (ortholog); genetic disease (ortholog); FOUND IN apical cytoplasm (ortholog); cilium (ortholog); cytoplasm (ortholog) NW_004955461 7204165 7311524 - 9068941 102012512 A0A8C2UQ33 MODEL AGCD01048917;GBDI01260030;XM_005398014;XM_005398015;XM_005398016;XM_013521348 XP_005398071;XP_005398072;XP_005398073;XP_013376802 Lrrc6 leucine rich repeat containing 6 APPROVED protein-coding ENSCLAG00000001275 NW_004955461 7204339 7312241 - 8699729 Gpnmb glycoprotein nmb ENCODES a protein that exhibits heparin binding (ortholog); integrin binding (ortholog); receptor ligand activity (ortholog); INVOLVED IN bone mineralization (ortholog); cell adhesion (ortholog); cell-cell signaling (ortholog); ASSOCIATED WITH acute kidney failure (ortholog); Acute Liver Failure (ortholog); Breast Neoplasms (ortholog); FOUND IN cytoplasmic vesicle (ortholog); membrane (ortholog); plasma membrane (ortholog) NW_004955410 25554279 25583368 + 9068941 102013481 A0A8C2UYH5 MODEL AGCD01011159;AGCD01011160;AGCD01011161;GBDK01002119;XM_005377395;XM_013510586 XP_005377452;XP_013366040 glycoprotein (transmembrane) nmb;transmembrane glycoprotein NMB APPROVED protein-coding ENSCLAG00000004706 NW_004955410 25553973 25582500 + 8699748 Stra8 stimulated by retinoic acid 8 INVOLVED IN activation of meiosis (ortholog); cellular response to retinoic acid (ortholog); male germ-line stem cell asymmetric division (ortholog); ASSOCIATED WITH genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN cytoplasm (ortholog); male germ cell nucleus (ortholog); nucleus (ortholog) NW_004955494 7408479 7444154 - 9068941 102013942 A0A8C2YJ84 MODEL AGCD01061552;GBDF01074324;XM_005405489;XM_005405490;XM_005405491;XM_005405492 XP_005405546;XP_005405547;XP_005405548;XP_005405549 stimulated by retinoic acid gene 8 protein homolog protein-coding ENSCLAG00000001947 NW_004955494 7408421 7444383 - 8699771 Hps4 HPS4 biogenesis of lysosomal organelles complex 3 subunit 2 ENCODES a protein that exhibits guanyl-nucleotide exchange factor activity (ortholog); protein dimerization activity (ortholog); protein homodimerization activity (ortholog); INVOLVED IN blood coagulation (ortholog); lysosome organization (ortholog); melanocyte differentiation (ortholog); ASSOCIATED WITH Albinism (ortholog); cataract 23 (ortholog); genetic disease (ortholog); FOUND IN BLOC-3 complex (ortholog); cytoplasm (ortholog); cytoplasmic vesicle (ortholog) NW_004955455 1048946 1076097 - 9068941;7240710 102014319 A0A8C2YPJ3 MODEL AGCD01045568;GBDI01296596;XM_005396143;XM_013520383;XM_013520384;XM_013520385;XM_013520386;XM_013520387 XP_005396200;XP_013375837;XP_013375838;XP_013375839;XP_013375840;XP_013375841 HPS4, biogenesis of lysosomal organelles complex 3 subunit 2;Hermansky-Pudlak syndrome 4 APPROVED protein-coding ENSCLAG00000009568 NW_004955455 1049992 1073950 - 8699800 LOC102014967 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 4-like NW_004955817 12639 13506 - 102014967 MODEL AGCD01078405 pseudo 8699801 Dlx1 distal-less homeobox 1 ENCODES a protein that exhibits chromatin binding (ortholog); DNA binding (ortholog); DNA-binding transcription factor activity, RNA polymerase II-specific (ortholog); INVOLVED IN cellular response to BMP stimulus (ortholog); cellular response to transforming growth factor beta stimulus (ortholog); cerebral cortex GABAergic interneuron differentiation (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); Craniofacial Abnormalities (ortholog); FOUND IN cytosol (ortholog); intracellular membrane-bounded organelle (ortholog); nucleoplasm (ortholog) NW_004955449 2920705 2924667 - 9068941 102015676 A0A8C2UQW0 MODEL AGCD01041839;GBCC01012740;XM_005393218 XP_005393275 homeobox protein DLX-1 protein-coding ENSCLAG00000002722 NW_004955449 2920478 2924667 - 8699813 LOC102015854 uncharacterized LOC102015854 NW_004955489 8966832 8998732 + 102015854 MODEL AGCD01060025;GBDK01379970;XR_264026 ncrna 8699819 Smarce1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 ENCODES a protein that exhibits N-acetyltransferase activity (ortholog); nuclear receptor binding (ortholog); RNA binding (ortholog); INVOLVED IN chromatin remodeling (ortholog); negative regulation of DNA-templated transcription (ortholog); neurogenesis (ortholog); PARTICIPATES IN SWI/SNF family mediated chromatin remodeling pathway; ASSOCIATED WITH adenoid cystic carcinoma (ortholog); Coffin-Siris syndrome (ortholog); Coffin-Siris syndrome 5 (ortholog); FOUND IN nBAF complex (ortholog); npBAF complex (ortholog); nucleoplasm (ortholog) NW_004955451 15129619 15147487 - 9068941;7240710 102016124 A0A8C2W079;A0A8C2W5N4 MODEL AGCD01043596;AGCD01043597;GBDF01044017;GBDK01004228;XM_005394363 XP_005394420 SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 protein-coding ENSCLAG00000015303 NW_004955451 15129132 15147488 - 8699839 Six1 SIX homeobox 1 ENCODES a protein that exhibits chromatin binding (ortholog); DNA binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); INVOLVED IN anatomical structure development (ortholog); aorta morphogenesis (ortholog); branching involved in ureteric bud morphogenesis (ortholog); ASSOCIATED WITH 22q11 Deletion Syndrome (ortholog); autosomal dominant nonsyndromic deafness (ortholog); autosomal dominant nonsyndromic deafness 23 (ortholog); FOUND IN nucleolus (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955466 8961597 8966069 + 9068941;7240710 102016994 A0A8C2UW41 MODEL AGCD01051010;AGCD01051011;GBDI01084435;XM_005399176 XP_005399233 homeobox protein SIX1 protein-coding ENSCLAG00000003638 NW_004955466 8961597 8966069 + 8699845 Prodh2 proline dehydrogenase 2 ENCODES a protein that exhibits oxidoreductase activity, acting on the CH-NH group of donors (ortholog); ASSOCIATED WITH Brugada syndrome 5 (ortholog); Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog) NW_004955468 2747870 2754621 + 9068941;7240710 102017216 A0A8C2W6F3 MODEL AGCD01051834;AGCD01051835;GBCQ01009142;XM_005399947 XP_005400004 probable proline dehydrogenase 2;proline dehydrogenase (oxidase) 2 APPROVED protein-coding ENSCLAG00000015709 NW_004955468 2747862 2754592 + 8699859 LOC102017533 uncharacterized LOC102017533 NW_004955452 15825925 15829234 - 102017533 MODEL AGCD01044500;GBDF01153842;XR_001236006;XR_001236007 ncrna 8699863 Pla2g4f phospholipase A2 group IVF ENCODES a protein that exhibits calcium-dependent phospholipase A2 activity (ortholog); lysophospholipase activity (ortholog); phospholipase A2 activity (ortholog); INVOLVED IN arachidonic acid secretion (ortholog); cellular response to antibiotic (ortholog); cellular response to organic cyclic compound (ortholog); ASSOCIATED WITH Bloom syndrome (ortholog); colorectal cancer (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); ruffle membrane (ortholog) NW_004955416 8876560 8889764 - 9068941 102017867 A0A8C2V3B5 MODEL AGCD01017071;GBBH01062799;XM_005381324;XM_005381325;XM_013512650 XP_005381381;XP_005381382;XP_013368104 cytosolic phospholipase A2 zeta;phospholipase A2, group IVF APPROVED protein-coding ENSCLAG00000006702 NW_004955416 8873356 8889940 - 8699890 Ssu72 SSU72 homolog, RNA polymerase II CTD phosphatase ENCODES a protein that exhibits RNA polymerase II CTD heptapeptide repeat phosphatase activity (ortholog); INVOLVED IN mRNA polyadenylation (ortholog); PARTICIPATES IN RNA polymerase II transcription pathway; ASSOCIATED WITH chromosome 1p36 deletion syndrome (ortholog); congenital myasthenic syndrome 8 (ortholog); dilated cardiomyopathy 1LL (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog) NW_004955486 9317078 9338414 + 9068941 102018734 A0A8C2VVL6 MODEL AGCD01059176;GBDF01003615;XM_005404212 XP_005404269 RNA polymerase II subunit A C-terminal domain phosphatase SSU72;SSU72 RNA polymerase II CTD phosphatase homolog APPROVED protein-coding ENSCLAG00000013921 NW_004955486 9317078 9338414 + 8699899 Acads acyl-CoA dehydrogenase short chain ENCODES a protein that exhibits acyl-CoA dehydrogenase activity (ortholog); butyryl-CoA dehydrogenase activity (ortholog); fatty-acyl-CoA binding (ortholog); INVOLVED IN butyrate catabolic process (ortholog); fatty acid beta-oxidation using acyl-CoA dehydrogenase (ortholog); response to glucocorticoid (ortholog); PARTICIPATES IN 3-hydroxy-3-methylglutaryl-CoA lyase deficiency pathway; 3-hydroxyacyl-CoA dehydrogenase deficiency pathway; 3-hydroxyisobutyric aciduria pathway; ASSOCIATED WITH congestive heart failure (ortholog); developmental and epileptic encephalopathy 1 (ortholog); genetic disease (ortholog); FOUND IN centrosome (ortholog); mitochondrial matrix (ortholog); mitochondrial membrane (ortholog) NW_004955455 10928560 10942748 - 9068941;7240710 102019142 A0A8C2VAW3 MODEL AGCD01045967;AGCD01045968;GBBH01207722;GBDF01118831;XM_013520359 XP_013375813 acyl-CoA dehydrogenase, C-2 to C-3 short chain;short-chain specific acyl-CoA dehydrogenase, mitochondrial APPROVED protein-coding ENSCLAG00000008872 NW_004955455 10928560 10942926 - 8699912 Fads2 fatty acid desaturase 2 ENCODES a protein that exhibits stearoyl-CoA 9-desaturase activity (ortholog); PARTICIPATES IN alpha-linolenic acid metabolic pathway; linoleic acid metabolic pathway; ASSOCIATED WITH bipolar disorder (ortholog); Chemical and Drug Induced Liver Injury (ortholog); Colorectal Neoplasms (ortholog) NW_004955511 5827797 5842745 - 9068941 102020363 A0A8C2V8J2 MODEL AGCD01066587;GBDJ01003271;XM_013506432 XP_013361886 protein-coding ENSCLAG00000008171 NW_004955511 5827797 5842760 - 8699929 Utp25 UTP25 small subunit processome component INVOLVED IN embryonic organ development (ortholog); positive regulation of embryonic development (ortholog); protein catabolic process (ortholog); ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); Hirschsprung's disease (ortholog); FOUND IN nucleolus (ortholog) NW_004955489 2362290 2387162 - 9068941 102020572 A0A8C2UV33;A0A8C2UV36 MODEL AGCD01059868;AGCD01059869;GBCE01136335;XM_005404524 XP_005404581 Diexf UTP25 small subunit processor component;UTP25, small subunit processor component;digestive organ expansion factor homolog;digestive organ expansion factor homolog (zebrafish) APPROVED protein-coding ENSCLAG00000004405 NW_004955489 2339745 2387103 - 8699945 LOC102021923 malonyl-CoA decarboxylase, mitochondrial NW_004955564 281274 328682 - 102021923 A0A8C2UH59;A0A8C2UJB9 MODEL AGCD01074195;AGCD01074196;AGCD01074197;AGCD01074198;GBDI01256173;XM_005413231;XM_005413232;XM_005413233;XM_005413234;XM_005413235;XM_005413236;XM_013509208 XP_005413288;XP_005413289;XP_005413290;XP_005413291;XP_005413292;XP_005413293;XP_013364662 Mlycd;Osgin1 malonyl-CoA decarboxylase;oxidative stress induced growth inhibitor 1;oxidative stress-induced growth inhibitor 1 APPROVED protein-coding ENSCLAG00000000686;ENSCLAG00000000688 NW_004955564;NW_004955564 281052;314177 285762;328610 -;- 8699973 Adcy10 adenylate cyclase 10 ENCODES a protein that exhibits adenylate cyclase activity (ortholog); ATPase binding (ortholog); bicarbonate binding (ortholog); INVOLVED IN cAMP biosynthetic process (ortholog); cellular response to inorganic substance (ortholog); epithelial cilium movement involved in extracellular fluid movement (ortholog); PARTICIPATES IN adenine phoshoribosyltransferase deficiency pathway; adenosine monophosphate deaminase deficiency pathway; adenylosuccinate lyase deficiency pathway; ASSOCIATED WITH Cardiomegaly (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN apical part of cell (ortholog); apical plasma membrane (ortholog); astrocyte end-foot (ortholog) NW_004955462 9196984 9278850 + 9068941;7240710 102022369 A0A8C2YLG5 MODEL AGCD01049333;AGCD01049334;AGCD01049335;GBDF01086065;XM_013521435;XM_013521436 XP_013376889;XP_013376890 adenylate cyclase 10 (soluble);adenylate cyclase 10, soluble;adenylate cyclase type 10 APPROVED protein-coding ENSCLAG00000005189 NW_004955462 9207314 9278621 + 8700011 Dctn3 dynactin subunit 3 INVOLVED IN cytoskeleton-dependent cytokinesis (ortholog); microtubule-based process (ortholog); PARTICIPATES IN mitochondria transport pathway; ASSOCIATED WITH acromesomelic dysplasia, Maroteaux type (ortholog); anauxetic dysplasia (ortholog); distal arthrogryposis type 1A (ortholog); FOUND IN centrosome (ortholog); cytosol (ortholog); dynactin complex (ortholog) NW_004955472 1511984 1521148 + 9068941 102022382 A0A8C2ULA0;A0A8C2UQZ0 MODEL AGCD01053397;AGCD01053398;GBDI01005417;XM_005401050;XM_005401053 XP_005401107;XP_005401110 dynactin 3 (p22) APPROVED protein-coding ENSCLAG00000001399 NW_004955472 1511937 1521494 + 8700035 LOC102022452 ubiquitin thioesterase OTUB1-like NW_004955403 808314 811093 - 102022452 MODEL AGCD01001708 pseudo 8700049 LOC102023286 uncharacterized LOC102023286 NW_004955430 22267648 22322758 + 102023286 MODEL AGCD01029783;AGCD01029784;AGCD01029785;AGCD01029786;GBBH01020885;XR_261436 ncrna 8700055 LOC102023600 uncharacterized LOC102023600 NW_004955483 8636126 8641695 + 102023600 MODEL AGCD01057841;GBCB01042012;XR_263871;XR_263873 ncrna 8700066 Ubl3 ubiquitin like 3 ASSOCIATED WITH genetic disease (ortholog) NW_004955431 15991559 16046647 + 9068941 102024601 A0A8C2UU12 MODEL AGCD01030365;AGCD01030366;GBDF01009170;XM_013515870 XP_013371324 ubiquitin-like 3;ubiquitin-like protein 3 APPROVED protein-coding ENSCLAG00000003772 NW_004955431 15992353 16046647 + 8700080 LOC102026855 heterogeneous nuclear ribonucleoprotein C-like NW_004955415 14284575 14285556 - 102026855 MODEL AGCD01016295 APPROVED pseudo 8700081 Cacna1c calcium voltage-gated channel subunit alpha1 C ENCODES a protein that exhibits alpha-actinin binding (ortholog); calmodulin binding (ortholog); enzyme binding (ortholog); INVOLVED IN adult walking behavior (ortholog); axon development (ortholog); calcium ion import (ortholog); PARTICIPATES IN acebutolol pharmacodynamics pathway; adrenergic beta receptor agonist and beta-blocker pharmacodynamics pathway; amiodarone pharmacodynamics pathway; ASSOCIATED WITH acute stress disorder (ortholog); alcohol dependence (ortholog); Alzheimer's disease (ortholog); FOUND IN axon cytoplasm; basal pole of outer hair cell; basolateral plasma membrane NW_004955454 4573647 5199046 + 9068941;7240710;11556226;11554335 10408625;12845523 102026943 A0A8C2VW34;A0A8C2VW42;A0A8C2VWI0;A0A8C2VYW2;A0A8C2W178;A0A8C2W354;A0A8C2YT72;A0A8C2YT73 MODEL AGCD01045125;AGCD01045126;AGCD01045127;AGCD01045128;AGCD01045129;AGCD01045130;AGCD01045131;AGCD01045132;GBCE01065707;XM_005395963;XM_013520117;XM_013520118;XM_013520119;XM_013520120;XM_013520121;XM_013520122;XM_013520123;XM_013520124;XM_013520125;XM_013520126;XM_013520127;XM_013520128;XM_013520129 XP_005396020;XP_013375571;XP_013375572;XP_013375573;XP_013375574;XP_013375575;XP_013375576;XP_013375577;XP_013375578;XP_013375579;XP_013375580;XP_013375581;XP_013375582;XP_013375583 calcium channel, voltage-dependent, L type, alpha 1C subunit;voltage-dependent L-type calcium channel subunit alpha-1C APPROVED protein-coding ENSCLAG00000014730 NW_004955454 4490923 5198506 + 8700144 Ccdc198 coiled-coil domain containing 198 NW_004955466 11331799 11369866 - 102026959 A0A8C2UTQ0 MODEL AGCD01051087;AGCD01051088;AGCD01051089;GBCQ01007372;XM_005399205;XM_005399206;XM_005399207 XP_005399262;XP_005399263;XP_005399264 LOC102026959 chromosome unknown open reading frame, human C14orf105;uncharacterized protein C14orf105 homolog APPROVED protein-coding ENSCLAG00000002962 NW_004955466 11334430 11369894 - 8700157 Brdt bromodomain testis associated ENCODES a protein that exhibits histone binding (ortholog); histone reader activity (ortholog); lysine-acetylated histone binding (ortholog); INVOLVED IN chromatin remodeling (ortholog); male meiosis I (ortholog); male meiotic nuclear division (ortholog); PARTICIPATES IN histone modification pathway; ASSOCIATED WITH azoospermia (ortholog); genetic disease (ortholog); oligospermia (ortholog); FOUND IN nucleus (ortholog) NW_004955423 2434146 2498523 - 9068941 102027081 A0A8C2V2M7 MODEL AGCD01023473;AGCD01023474;AGCD01023475;AGCD01023476;AGCD01023477;GBDF01048977;XM_005385061;XM_013514358;XM_013514359 XP_005385118;XP_013369812;XP_013369813 bromodomain, testis-specific APPROVED protein-coding ENSCLAG00000006404 NW_004955423 2431192 2494906 - 8700190 Opn1sw opsin 1, short wave sensitive INVOLVED IN cellular response to UV-A (ortholog); PARTICIPATES IN retinoid cycle metabolic pathway; visual phototransduction pathway; ASSOCIATED WITH atrial fibrillation (ortholog); blue color blindness (ortholog); genetic disease (ortholog); FOUND IN cell body (ortholog); cone photoreceptor outer segment (ortholog); cytosol (ortholog) NW_004955479 9573594 9576668 - 9068941;7240710 102029511 A0A8C2V2K1 MODEL AGCD01056482;GBDF01236722;XM_005402383 XP_005402440 opsin 1 (cone pigments), short-wave-sensitive;short-wave-sensitive opsin 1 APPROVED protein-coding ENSCLAG00000006304 NW_004955479 9573594 9576668 - 8700199 Clta clathrin light chain A ENCODES a protein that exhibits clathrin heavy chain binding (ortholog); GTPase binding (ortholog); peptide binding (ortholog); INVOLVED IN clathrin coat assembly (ortholog); endocytosis (ortholog); PARTICIPATES IN Arf family mediated signaling pathway; clathrin-dependent synaptic vesicle endocytosis; ASSOCIATED WITH acromesomelic dysplasia, Maroteaux type (ortholog); anauxetic dysplasia (ortholog); COVID-19 (ortholog); FOUND IN clathrin coat (ortholog); clathrin complex (ortholog); clathrin-coated pit (ortholog) NW_004955472 96958 117230 - 9068941 102029957 A0A8C2UL02 MODEL AGCD01053314;AGCD01053315;GBBH01000318;GBDI01022015;XM_013522981 XP_013378435 clathrin, light chain A APPROVED protein-coding ENSCLAG00000001549 NW_004955472 97235 117144 - 8700206 LOC102030444 nucleolar RNA helicase 2 pseudogene NW_004955424 22944390 22945553 + 102030444 MODEL AGCD01024995 APPROVED pseudo 8700207 Dync2i2 dynein 2 intermediate chain 2 ENCODES a protein that exhibits dynein light chain binding (ortholog); INVOLVED IN cilium assembly (ortholog); intraciliary retrograde transport (ortholog); ASSOCIATED WITH asphyxiating thoracic dystrophy (ortholog); asphyxiating thoracic dystrophy 3 (ortholog); developmental and epileptic encephalopathy (ortholog); FOUND IN axoneme (ortholog); centriole (ortholog); centrosome (ortholog) NW_004955570 1076498 1086629 - 9068941;7240710 102030680 A0A8C2YJX3 MODEL AGCD01074785;AGCD01074786;GBDJ01014754;XM_005413560;XM_013509405;XM_013509406;XM_013509407;XM_013509408;XM_013509409 XP_005413617;XP_013364859;XP_013364860;XP_013364861;XP_013364862;XP_013364863 Wdr34 WD repeat domain 34;WD repeat-containing protein 34 APPROVED protein-coding ENSCLAG00000002947 NW_004955570 1076568 1086613 - 8700225 Col22a1 collagen type XXII alpha 1 chain ASSOCIATED WITH genetic disease (ortholog); intracranial aneurysm (ortholog); lung small cell carcinoma (ortholog) NW_004955461 12596449 12870853 - 9068941 102003950 A0A8C2URA5 MODEL AGCD01049020;AGCD01049021;AGCD01049022;AGCD01049023;AGCD01049024;GBCB01111979;GBCB01111980;XM_013521350 XP_013376804 collagen alpha-1(XXII) chain;collagen, type XXII, alpha 1 APPROVED protein-coding ENSCLAG00000002922 NW_004955461 12597488 12848410 - 8700292 Bmpr2 bone morphogenetic protein receptor type 2 ENCODES a protein that exhibits BMP binding (ortholog); BMP receptor activity (ortholog); cadherin binding (ortholog); INVOLVED IN anterior/posterior pattern specification (ortholog); aortic valve development (ortholog); artery development (ortholog); PARTICIPATES IN Bone morphogenetic proteins signaling pathway; ASSOCIATED WITH asthma (ortholog); autoimmune lymphoproliferative syndrome type 2B (ortholog); Autoimmune Lymphoproliferative Syndrome, Type V (ortholog); FOUND IN adherens junction (ortholog); apical plasma membrane (ortholog); axon (ortholog) NW_004955457 12235780 12315680 - 9068941;7240710 102004042 A0A8C2V577;A0A8C2V7Q2 MODEL AGCD01047005;AGCD01047006;GBCB01060551;GBDF01280157;XM_013520738 XP_013376192 bone morphogenetic protein receptor type-2;bone morphogenetic protein receptor, type II (serine/threonine kinase) APPROVED protein-coding ENSCLAG00000006272 NW_004955457 12235780 12316727 - 8700307 LOC102005079 uncharacterized LOC102005079 NW_004955437 3889822 3896136 - 102005079 MODEL AGCD01034353;AGCD01034354;GBDF01014278;XR_001235105;XR_001235106;XR_261849;XR_261850 ncrna 8700315 Sfrp2 secreted frizzled related protein 2 ENCODES a protein that exhibits endopeptidase activator activity (ortholog); enzyme activator activity (ortholog); fibronectin binding (ortholog); INVOLVED IN anterior/posterior pattern specification (ortholog); apoptotic process (ortholog); BMP signaling pathway (ortholog); PARTICIPATES IN Wnt signaling, canonical pathway; ASSOCIATED WITH Breast Neoplasms (ortholog); Colorectal Neoplasms (ortholog); genetic disease (ortholog); FOUND IN collagen-containing extracellular matrix (ortholog); extracellular space (ortholog) NW_004955471 8103937 8112596 - 9068941 102006653 A0A8C2UXM9 MODEL AGCD01053178;AGCD01053179;GBBH01060570;GBDJ01000856;XM_005400928 XP_005400985 secreted frizzled-related protein 2 APPROVED protein-coding ENSCLAG00000004916 NW_004955471 8103783 8112321 - 8700322 Foxh1 forkhead box H1 ENCODES a protein that exhibits bHLH transcription factor binding (ortholog); co-SMAD binding (ortholog); DNA binding (ortholog); INVOLVED IN anterior/posterior pattern specification (ortholog); aorta morphogenesis (ortholog); axial mesoderm development (ortholog); PARTICIPATES IN transforming growth factor-beta Smad dependent signaling pathway; ASSOCIATED WITH agnathia-otocephaly complex (ortholog); Brown-Vialetto-Van Laere syndrome 2 (ortholog); Conotruncal Cardiac Defects (ortholog); FOUND IN activin responsive factor complex (ortholog); chromatin (ortholog); nucleus (ortholog) NW_004955454 3094015 3096060 - 9068941 102007189 A0A8C2VTB3 MODEL AGCD01045051;GBDF01073904;XM_005395891 XP_005395948 forkhead box protein H1 protein-coding ENSCLAG00000013202 NW_004955454 3094033 3095512 - 8700329 LOC102007304 zinc finger protein 354B NW_004955408 1507667 1520239 - 9068941 102007304 A0A8C2VYY3 MODEL AGCD01007961;AGCD01007962;GBCB01038326;GBCE01165511;XM_005376027;XM_013507968 XP_005376084;XP_013363422 Znf354b zinc finger protein 354A APPROVED protein-coding ENSCLAG00000013514 NW_004955408 1508180 1515608 - 8700349 LOC102008106 uncharacterized LOC102008106 NW_004955482 4507858 4511301 + 102008106 MODEL AGCD01057294;GBDF01156183;XR_001230999 ncrna 8700353 Klhdc8a kelch domain containing 8A ASSOCIATED WITH autistic disorder (ortholog); familial adult myoclonic epilepsy 5 (ortholog); gastrointestinal stromal tumor (ortholog) NW_004955406 41080154 41087381 - 9068941 102008180 A0A8C2W400 MODEL AGCD01006670;GBCQ01093234;XM_005375356 XP_005375413 kelch domain-containing protein 8A protein-coding ENSCLAG00000015610 NW_004955406 41077925 41087574 - 8700366 LOC102008833 olfactory receptor 1F12 NW_004955465 13529663 13530604 + 102008833 MODEL AGCD01050613;XM_005398956 XP_005399013 APPROVED protein-coding 8700369 Tsga13 testis specific 13 ASSOCIATED WITH genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog) NW_004955410 36964398 36982042 + 9068941 102009259 A0A8C2VME3 MODEL AGCD01011441;AGCD01011442;GBDF01010268;XM_005377551;XM_005377552;XM_005377553;XM_013510641 XP_005377608;XP_005377609;XP_005377610;XP_013366095 testis specific, 13 APPROVED protein-coding ENSCLAG00000011601 NW_004955410 36967791 36981957 + 8700387 Dgkz diacylglycerol kinase zeta ENCODES a protein that exhibits ATP-dependent diacylglycerol kinase activity (ortholog); enzyme inhibitor activity (ortholog); kinase activity (ortholog); INVOLVED IN diacylglycerol metabolic process (ortholog); glycerolipid metabolic process (ortholog); lipid phosphorylation (ortholog); ASSOCIATED WITH congenital disorder of glycosylation type IIc (ortholog); Developmental Disabilities (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); glutamatergic synapse (ortholog); lamellipodium (ortholog) NW_004955422 1658237 1687000 - 9068941 102009511 A0A8C2W0J8;A0A8C2W0L8;A0A8C2W5F8 MODEL AGCD01022468;AGCD01022469;GBDI01006776;XM_005384031;XM_005384033;XM_005384035;XM_005384038;XM_013514024 XP_005384088;XP_005384090;XP_005384092;XP_005384095;XP_013369478 diacylglycerol kinase, zeta APPROVED protein-coding ENSCLAG00000016057 NW_004955422 1657926 1695404 - 8700440 Srbd1 S1 RNA binding domain 1 ASSOCIATED WITH genetic disease (ortholog); Lynch syndrome (ortholog) NW_004955441 12374940 12642295 - 9068941 102009549 A0A8C2VBI0;A0A8C2VDM7 MODEL AGCD01037121;AGCD01037122;AGCD01037123;AGCD01037124;AGCD01037125;AGCD01037126;AGCD01037127;AGCD01037128;AGCD01037129;AGCD01037130;AGCD01037131;GBCB01074860;XM_013517546;XM_013517547;XM_013517548;XM_013517549;XM_013517550;XM_013517551;XM_013517552 XP_013373000;XP_013373001;XP_013373002;XP_013373003;XP_013373004;XP_013373005;XP_013373006 S1 RNA-binding domain-containing protein 1 protein-coding ENSCLAG00000008623 NW_004955441 12375565 12606923 - 8700475 Zmat3 zinc finger matrin-type 3 INVOLVED IN positive regulation of apoptotic process (ortholog); ASSOCIATED WITH Currarino syndrome (ortholog); genetic disease (ortholog); Nerve Degeneration (ortholog); FOUND IN nucleoplasm (ortholog); plasma membrane (ortholog) NW_004955420 8270026 8301313 - 9068941 102009723 A0A8C2VYS1 MODEL AGCD01020713;GBBH01043845;XM_005383032;XM_005383033;XM_005383034;XM_013513603 XP_005383089;XP_005383090;XP_005383091;XP_013369057 zinc finger matrin-type protein 3;zinc finger, matrin-type 3 APPROVED protein-coding ENSCLAG00000013464 NW_004955420 8274395 8298224 - 8700490 Pdap1 PDGFA associated protein 1 ASSOCIATED WITH genetic disease (ortholog); high grade glioma (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN cytosol (ortholog); plasma membrane (ortholog) NW_004955460 15072667 15083329 - 9068941 102010133 A0A8C2V6N1 MODEL AGCD01048768;GBBH01031562;XM_005397946 XP_005398003 28 kDa heat- and acid-stable phosphoprotein protein-coding ENSCLAG00000007628 NW_004955460 15072667 15083329 - 8700500 Zng1a Zn regulated GTPase metalloprotein activator 1A ENCODES a protein that exhibits GTPase activity (ortholog); zinc chaperone activity (ortholog); INVOLVED IN intracellular zinc ion homeostasis (ortholog); kidney development (ortholog); protein maturation (ortholog); ASSOCIATED WITH CAKUT (ortholog); chromosome 9p deletion syndrome (ortholog); COVID-19 (ortholog); FOUND IN nucleus (ortholog) NW_004955434 4732584 4780990 - 102010514 A0A8C2UXG7 MODEL AGCD01032168;AGCD01032169;GBDI01293047;XM_005388584 XP_005388641 Cbwd1;Cbwd2;LOC102010514 COBW domain containing 1;COBW domain containing 2;COBW domain-containing protein 2 APPROVED protein-coding ENSCLAG00000005076 8700530 Tp53i13 tumor protein p53 inducible protein 13 INVOLVED IN negative regulation of cell cycle (ortholog); response to organic cyclic compound (ortholog); response to UV (ortholog); ASSOCIATED WITH Developmental Disease (ortholog); genetic disease (ortholog); neurofibromatosis 1 (ortholog); FOUND IN cytoplasm (ortholog) NW_004955481 3681495 3685051 - 9068941 102010584 A0A8C2V6K5 MODEL AGCD01056911;GBCE01029826;XM_005402678 XP_005402735 tumor protein p53-inducible protein 13 protein-coding ENSCLAG00000006219 NW_004955481 3681724 3685051 - 8700541 Prickle3 prickle planar cell polarity protein 3 ASSOCIATED WITH autistic disorder (ortholog); congenital disorder of glycosylation type IIm (ortholog); genetic disease (ortholog); FOUND IN mitochondrion (ortholog) NW_004955543 662438 673386 - 9068941 102010947 A0A8C2UZD2 MODEL AGCD01071598;GBBH01101699;XM_005411332 XP_005411389 prickle homolog 3;prickle-like protein 3 APPROVED protein-coding ENSCLAG00000003916 NW_004955543 662438 673662 - 8700554 LOC102011543 DCN1-like protein 1 pseudogene NW_004955484 8471459 8472600 - 102011543 MODEL AGCD01058384 APPROVED pseudo 8700555 LOC102012146 3-alpha-hydroxysteroid sulfotransferase-like NW_004955609 372015 408109 - 102012146 A0A8C2YIB2 MODEL AGCD01077059;AGCD01077060;GBDI01156067;XM_005414932 XP_005414989 protein-coding ENSCLAG00000000602 8700566 Rnf38 ring finger protein 38 ENCODES a protein that exhibits ubiquitin protein ligase activity (ortholog); INVOLVED IN male gonad development (ortholog); protein ubiquitination (ortholog); ASSOCIATED WITH acromesomelic dysplasia, Maroteaux type (ortholog); distal arthrogryposis type 1A (ortholog); frontotemporal dementia and/or amyotrophic lateral sclerosis-6 (ortholog); FOUND IN nucleoplasm (ortholog); nucleus (ortholog); sperm flagellum (ortholog) NW_004955419 29903917 30063705 + 9068941 102012435 A0A8C2VTB0;A0A8C2VVD3;A0A8C2W0P5 MODEL AGCD01020515;AGCD01020516;AGCD01020517;AGCD01020518;AGCD01020519;AGCD01020520;AGCD01020521;AGCD01020522;AGCD01020523;GBDF01054162;XM_005382901;XM_005382902;XM_005382903;XM_005382904;XM_005382905;XM_005382906;XM_005382907;XM_005382908;XM_005382909;XM_005382910;XM_005382911;XM_005382912 XP_005382958;XP_005382959;XP_005382960;XP_005382961;XP_005382962;XP_005382963;XP_005382964;XP_005382965;XP_005382966;XP_005382967;XP_005382968;XP_005382969 E3 ubiquitin-protein ligase RNF38 protein-coding ENSCLAG00000013858 NW_004955419 29993358 30063705 + 8700604 H3f3b H3 histone, family 3B ENCODES a protein that exhibits nucleosomal DNA binding (ortholog); RNA polymerase II cis-regulatory region sequence-specific DNA binding (ortholog); RNA polymerase II core promoter sequence-specific DNA binding (ortholog); INVOLVED IN cell population proliferation (ortholog); embryo implantation (ortholog); male gonad development (ortholog); PARTICIPATES IN histone modification pathway; ASSOCIATED WITH Animal Mammary Neoplasms (ortholog); Bryant-Li-Bhoj Neurodevelopmental Syndrome 2 (ortholog); carcinoma (ortholog); FOUND IN chromosome, telomeric region (ortholog); nucleosome (ortholog); nucleus (ortholog) NW_004955506 6475336 6478781 + 9068941 102012783 Q6QN07 PROVISIONAL AGCD01065426;AY533212;FB335718;GBDF01023456;HH767057;NM_001282367 AAS59415;CAR80825;CBX84296;NP_001269296 H3 histone, family 3B (H3.3B);histone H3.3;uncharacterized protein LOC102012783 APPROVED protein-coding ENSCLAG00000009278 NW_004955506 6474727 6482244 + 8700617 LOC102013904 zinc finger protein OZF-like NW_004955406 41519064 41522379 + 102013904 MODEL AGCD01006685 pseudo 8700618 LOC102014035 ral guanine nucleotide dissociation stimulator-like NW_004955413 4784689 4789519 + 102014035 MODEL AGCD01013628;GBDF01155508;XM_005378864 XP_005378921 protein-coding 8700629 LOC102014528 lysine-rich nucleolar protein 1-like NW_004955452 3249546 3256640 + 102014528 MODEL AGCD01043917;XM_013519455 XP_013374909 protein-coding 8700630 LOC102014582 uncharacterized LOC102014582 NW_004955497 1976079 1981871 + 102014582 MODEL AGCD01062484;GBDF01225528;XR_001231438 ncrna ENSCLAG00000025607 8700638 Cdh12 cadherin 12 ASSOCIATED WITH genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); Prostatic Neoplasms (ortholog) NW_004955426 9652418 10610762 - 9068941 102015218 A0A8C2VRV0 MODEL AGCD01026253;AGCD01026254;AGCD01026255;AGCD01026256;AGCD01026257;AGCD01026258;AGCD01026259;AGCD01026260;AGCD01026261;AGCD01026262;AGCD01026263;AGCD01026264;AGCD01026265;AGCD01026266;AGCD01026267;AGCD01026268;AGCD01026269;AGCD01026270;AGCD01026271;AGCD01026272;AGCD01026273;AGCD01026274;AGCD01026275;AGCD01026276;GBDK01336238;XM_005386141 XP_005386198 cadherin 12, type 2 (N-cadherin 2);cadherin-12 APPROVED protein-coding ENSCLAG00000013527 NW_004955426 9651959 10059415 - 8700656 LOC102015821 uncharacterized LOC102015821 NW_004955412 13142327 13160782 + 102015821 MODEL AGCD01012829;GBDF01278571;XR_001232884;XR_001232885;XR_001232886;XR_259991 ncrna 8700662 Aldh16a1 aldehyde dehydrogenase 16 family member A1 ASSOCIATED WITH developmental and epileptic encephalopathy 12 (ortholog); genetic disease (ortholog); gout (ortholog) NW_004955559 1376862 1390861 - 9068941 102016644 A0A8C2V043 MODEL AGCD01073641;AGCD01073642;GBCQ01035042;XM_005412882;XM_013509018 XP_005412939;XP_013364472 aldehyde dehydrogenase 16 family, member A1;aldehyde dehydrogenase family 16 member A1 APPROVED protein-coding ENSCLAG00000004135 NW_004955559 1376977 1390841 - 8700684 LOC102016648 uncharacterized LOC102016648 NW_004955447 7681151 7713953 + 102016648 MODEL AGCD01040821;GBDF01223785;XR_262414 ncrna 8700689 Slc33a1 solute carrier family 33 member 1 ASSOCIATED WITH cataract (ortholog); Congenital Cataracts, Hearing Loss, and Neurodegeneration (ortholog); Developmental Disabilities (ortholog) NW_004955448 6885153 6905641 - 9068941;7240710 102016652 A0A8C2V5Z8 MODEL AGCD01041396;GBDI01172474;XM_005393070;XM_005393071 XP_005393127;XP_005393128 acetyl-coenzyme A transporter 1;solute carrier family 33 (acetyl-CoA transporter), member 1 APPROVED protein-coding ENSCLAG00000007266 NW_004955448 6885153 6905631 - 8700706 Otos otospiralin INVOLVED IN sensory perception of sound (ortholog); ASSOCIATED WITH Bethlem Myopathy 1 (ortholog); chromosome 2q37 deletion syndrome (ortholog); D-2-hydroxyglutaric aciduria 1 (ortholog) NW_004955542 1128036 1129445 + 9068941 102018649 A0A8C2UPL5 MODEL AGCD01071489;GBCC01000940;XM_005411167 XP_005411224 protein-coding ENSCLAG00000001765 NW_004955542 1128036 1129445 + 8700718 LOC102020150 olfactory receptor 5D18-like NW_004955511 4966254 4966832 + 102020150 MODEL AGCD01066541;GBBH01201753;XM_005408081 XP_005408138 protein-coding 8700722 Sike1 suppressor of IKBKE 1 ENCODES a protein that exhibits protein kinase binding (ortholog); small GTPase binding (ortholog); ASSOCIATED WITH genetic disease (ortholog); hereditary spastic paraplegia 47 (ortholog); RASopathy (ortholog) NW_004955435 18066428 18076422 - 9068941 102022534 A0A8C2V228;A0A8C2V4F2 MODEL AGCD01033383;AGCD01033384;GBCQ01129412;XM_005389015;XM_013516466 XP_005389072;XP_013371920 protein-coding ENSCLAG00000005344 NW_004955435 18066428 18077127 - 8700733 LOC102022645 25-hydroxycholesterol 7-alpha-hydroxylase ENCODES a protein that exhibits oxysterol 7-alpha-hydroxylase activity (ortholog); INVOLVED IN B cell chemotaxis (ortholog); bile acid biosynthetic process (ortholog); circadian rhythm (ortholog); PARTICIPATES IN bile acid biosynthetic pathway; cerebrotendinous xanthomatosis pathway; congenital bile acid synthesis defect pathway; ASSOCIATED WITH adenocarcinoma (ortholog); cholestasis (ortholog); congenital bile acid synthesis defect (ortholog) NW_004955444 14274818 14446068 + 9068941;7240710 102022645 A0A8C2UNQ9 MODEL AGCD01039118;AGCD01039119;AGCD01039120;AGCD01039121;AGCD01039122;GBBH01005355;GBCQ01011879;XM_013518189 XP_013373643 APPROVED protein-coding ENSCLAG00000002352 NW_004955444 14275345 14444426 + 8700742 LOC102023101 uncharacterized LOC102023101 NW_004955403 1477883 1487353 + 102023101 MODEL AGCD01001723;GBDJ01318496;XM_013514706 XP_013370160 uncharacterized protein LOC102023101 protein-coding 8700751 LOC102023532 uncharacterized LOC102023532 NW_004955442 14977428 14983811 - 102023532 MODEL AGCD01037853;GBDI01024349;XR_262149 ncrna 8700755 LOC102023920 uncharacterized LOC102023920 NW_004955422 16265263 16269498 + 102023920 MODEL AGCD01022894;GBDF01193207;XR_260890 ncrna 8700760 LOC102024039 RNA exonuclease 1 homolog pseudogene NW_004955431 8914638 8931636 - 102024039 MODEL AGCD01030148;AGCD01030149;XM_005387663 APPROVED pseudo 8700766 Smim18 small integral membrane protein 18 ASSOCIATED WITH genetic disease (ortholog) NW_004955463 7057648 7071593 + 9068941 102024774 A0A8C2UME6 MODEL AGCD01049709;AGCD01049710;GBBH01116730;XM_005398367;XM_013521494;XM_013521495 XP_005398424;XP_013376948;XP_013376949 protein-coding ENSCLAG00000000790 NW_004955463 7063211 7075702 + 8700775 Stat5a signal transducer and activator of transcription 5A ENCODES a protein that exhibits DNA binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); DNA-binding transcription factor activity (ortholog); INVOLVED IN activated T cell proliferation (ortholog); B cell differentiation (ortholog); cell population proliferation (ortholog); PARTICIPATES IN erythropoietin signaling pathway; granulocyte-macrophage colony-stimulating factor signaling pathway; interleukin-12 signaling pathway; ASSOCIATED WITH Acute-Phase Reaction (ortholog); adenocarcinoma (ortholog); Animal Mammary Neoplasms (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955451 16305363 16319219 + 9068941 102026935 A0A8C2W181;A0A8C2W956;A0A8C2YU78 MODEL AGCD01043668;AGCD01043669;GBDJ01139839;GBDK01144004;XM_013519303 XP_013374757 protein-coding ENSCLAG00000016243 8700796 LOC102027136 uncharacterized LOC102027136 NW_004955403 35908296 35923201 - 102027136 MODEL AGCD01002526;GBDF01211604;XR_259227;XR_259228 ncrna 8700804 LOC102028162 solute carrier family 22 member 5 NW_004955408 3768414 3799399 + 9068941;7240710 102028162 A0A8C2VQ44;A0A8C2YRX9;A0A8C2YRY2 MODEL AGCD01008076;AGCD01008077;GBCQ01036146;GBCQ01036168;XM_005376099 XP_005376156 Slc22a5 solute carrier family 22 (organic cation/carnitine transporter), member 5 APPROVED protein-coding ENSCLAG00000012924 NW_004955408 3768336 3799089 + 8700833 LOC102028286 olfactory receptor 6K3-like NW_004955468 10597680 10598627 - 102028286 A0A8C2W891 MODEL AGCD01052090;XM_005400158 XP_005400215 protein-coding ENSCLAG00000017875 8700836 Rps26 ribosomal protein S26 ENCODES a protein that exhibits mRNA binding (ortholog); structural constituent of ribosome (ortholog); INVOLVED IN cytoplasmic translation (ortholog); negative regulation of RNA splicing (ortholog); PARTICIPATES IN ribosome biogenesis pathway; translation pathway; ASSOCIATED WITH anemia (ortholog); bone marrow disease (ortholog); Diamond-Blackfan anemia (ortholog); FOUND IN cytoplasmic side of rough endoplasmic reticulum membrane (ortholog); cytosolic small ribosomal subunit (ortholog); polysomal ribosome (ortholog) NW_004955458 3632675 3634565 + 9068941;7240710 102028616 A0A8C2VC62;A0A8C2VEE6;A0A8C2VHI9 MODEL AGCD01047328;AY533229;GBCB01007464;GBDJ01017907;XM_005415267 AAS59431;XP_005415324 40S ribosomal protein S26 protein-coding ENSCLAG00000009250 NW_004955458 3632699 3634566 + 8700843 LOC102028772 cytoskeleton-associated protein 2 pseudogene NW_004955424 20618151 20619511 - 102028772 MODEL AGCD01024867 APPROVED pseudo 8700844 Minpp1 multiple inositol-polyphosphate phosphatase 1 ENCODES a protein that exhibits bisphosphoglycerate 3-phosphatase activity (ortholog); inositol-1,3,4,5,6-pentakisphosphate 3-phosphatase activity (ortholog); inositol-1,4,5,6-tetrakisphosphate 6-phosphatase activity (ortholog); PARTICIPATES IN inositol metabolic pathway; inositol phosphate metabolic pathway; ASSOCIATED WITH Arsenic Poisoning (ortholog); Follicular Thyroid Cancer (ortholog); genetic disease (ortholog) NW_004955425 5329968 5359634 - 7240710;9068941 102028773 A0A8C2VGI7 MODEL AGCD01025341;AGCD01025342;GBDI01161263;XM_005385892;XM_005385893 XP_005385949;XP_005385950 multiple inositol polyphosphate phosphatase 1 protein-coding ENSCLAG00000010519 NW_004955425 5330957 5359551 - 8700856 Aars1 alanyl-tRNA synthetase 1 ENCODES a protein that exhibits alanine-tRNA ligase activity (ortholog); amino acid binding (ortholog); aminoacyl-tRNA editing activity (ortholog); INVOLVED IN alanyl-tRNA aminoacylation (ortholog); cerebellar Purkinje cell layer development (ortholog); negative regulation of neuron apoptotic process (ortholog); PARTICIPATES IN alanine metabolic pathway; lactic acidosis pathway; primary hyperoxaluria type 1 pathway; ASSOCIATED WITH adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ortholog); autosomal dominant dyskeratosis congenita 6 (ortholog); Charcot-Marie-Tooth disease (ortholog); FOUND IN cytosol (ortholog) NW_004955484 3090678 3115224 - 9068941;7240710 102028968 A0A8C2UW47 MODEL AGCD01058154;GBCE01054191;XM_005403471;XM_013503929 XP_005403528;XP_013359383 Aars alanine--tRNA ligase, cytoplasmic;alanyl-tRNA synthetase APPROVED protein-coding ENSCLAG00000004366 NW_004955484 3089235 3115230 - 8700881 Nif3l1 NGG1 interacting factor 3 like 1 ENCODES a protein that exhibits identical protein binding (ortholog); RNA polymerase II-specific DNA-binding transcription factor binding (ortholog); INVOLVED IN negative regulation of transcription by RNA polymerase II (ortholog); neuron differentiation (ortholog); positive regulation of DNA-templated transcription (ortholog); ASSOCIATED WITH genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); Pulmonary Arterial Hypertension (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog) NW_004955403 628069 640703 - 9068941 102029137 A0A8C2VUE7 MODEL AGCD01001698;AGCD01001699;GBCE01152519;XM_005373231;XM_013511808 XP_005373288;XP_013367262 NIF3 NGG1 interacting factor 3-like 1;NIF3-like protein 1 APPROVED protein-coding ENSCLAG00000013524 NW_004955403 628924 640703 - 8700891 Nfkbia NFKB inhibitor alpha ENCODES a protein that exhibits enzyme binding (ortholog); heat shock protein binding (ortholog); identical protein binding (ortholog); INVOLVED IN B cell receptor signaling pathway (ortholog); cellular response to cytokine stimulus (ortholog); cellular response to organic cyclic compound (ortholog); PARTICIPATES IN adenosine signaling pathway; ceramide signaling pathway; interleukin-23 signaling pathway; ASSOCIATED WITH acute necrotizing pancreatitis (ortholog); Adenoviridae Infections (ortholog); alcoholic hepatitis (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleus (ortholog) NW_004955409 25691673 25695151 + 9068941;7240710 102029373 A0A8C2VMV0 MODEL AGCD01010129;AGCD01010130;GBCE01000163;XM_005376922 XP_005376979 NF-kappa-B inhibitor alpha;nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha APPROVED protein-coding ENSCLAG00000011667 NW_004955409 25691534 25697520 + 8700900 ATP6 ATP synthase F0 subunit 6 MT 7932 8612 + 15822207 M9NW06 REVIEWED JX312692 AFQ55782;YP_008080750 APPROVED protein-coding ENSCLAG00000000022 MT 7932 8612 + 8700901 LOC102003877 chromosome unknown open reading frame, human C16orf47 NW_004955484 5772487 5791070 - 102003877 MODEL AGCD01058271;XM_005415398 XP_005415455 protein-coding 8700907 LOC102003927 PRAME family member 20-like NW_004955615 78379 80979 - 102003927 MODEL AGCD01077249;XM_013510138 XP_013365592 APPROVED protein-coding 8700916 LOC102004612 uncharacterized LOC102004612 NW_004955422 13845624 13851380 - 102004612 MODEL AGCD01022839;GBCE01145779;XR_001233893;XR_260876 ncrna 8700923 Kcnk7 potassium two pore domain channel subfamily K member 7 ASSOCIATED WITH Aicardi-Goutieres Syndrome 3 (ortholog); Bardet-Biedl syndrome (ortholog); genetic disease (ortholog) NW_004955422 19666974 19670449 + 9068941 102005052 A0A8C2W471 MODEL AGCD01023026;GBCB01035404;XM_005384475 XP_005384532 potassium channel subfamily K member 7;potassium channel, subfamily K, member 7;potassium channel, two pore domain subfamily K, member 7 APPROVED protein-coding ENSCLAG00000015744 NW_004955422 19666974 19670449 + 8700930 Myh4 myosin heavy chain 4 ENCODES a protein that exhibits double-stranded RNA binding (ortholog); INVOLVED IN muscle contraction (ortholog); muscle structure development (ortholog); response to activity (ortholog); ASSOCIATED WITH genetic disease (ortholog); proximal myopathy and ophthalmoplegia (ortholog); Right Ventricular Hypertrophy (ortholog); FOUND IN myofibril (ortholog) NW_004955467 6719572 6744147 + 9068941 102005352 A0A8C2VK36 MODEL AGCD01051422;GBCB01088370;XM_005399365 XP_005399422 myosin, heavy chain 4, skeletal muscle;myosin-4 APPROVED protein-coding ENSCLAG00000010433 8700974 LOC102005496 probable ATP-dependent RNA helicase DDX41 pseudogene NW_004955433 1844022 1845319 - 102005496 MODEL AGCD01031371 APPROVED pseudo 8700975 LOC102005618 UPF0061 protein ETA_18310-like NW_004955429 2822671 2866918 + 102005618 A0A8C2UY30 MODEL AGCD01028439;AGCD01028440;AGCD01028441;AGCD01028442;AGCD01028443;GBBH01006669;GBCQ01067969;XM_005386894 XP_005386951 APPROVED protein-coding ENSCLAG00000004989 8700998 Tex44 testis expressed 44 ASSOCIATED WITH Joubert syndrome 22 (ortholog); Perlman syndrome (ortholog); FOUND IN cytoplasm (ortholog) NW_004955453 4108596 4110610 - 9068941 102007083 MODEL AGCD01044678;GBDF01007868;XM_005395707 XP_005395764 CUNH2orf57;LOC102007083 chromosome unknown open reading frame, human C2orf57;uncharacterized protein C2orf57 homolog APPROVED protein-coding 8701002 Arpc1b actin related protein 2/3 complex subunit 1B ENCODES a protein that exhibits actin filament binding (ortholog); protein-containing complex binding (ortholog); structural constituent of cytoskeleton (ortholog); INVOLVED IN Arp2/3 complex-mediated actin nucleation (ortholog); response to estradiol (ortholog); response to estrogen (ortholog); PARTICIPATES IN insulin responsive facilitative sugar transporter mediated glucose transport pathway; platelet-derived growth factor signaling pathway; Rab family mediated signaling pathway; ASSOCIATED WITH combined immunodeficiency (ortholog); Experimental Liver Cirrhosis (ortholog); gastritis (ortholog); FOUND IN Arp2/3 protein complex (ortholog); tubulobulbar complex (ortholog) NW_004955460 15055753 15069093 + 9068941 102007091 A0A8C2V7W4 MODEL AGCD01048767;AGCD01048768;GBBH01000811;GBDF01088644;XM_013521227 XP_013376681 actin related protein 2/3 complex, subunit 1B, 41kDa;actin-related protein 2/3 complex subunit 1B APPROVED protein-coding ENSCLAG00000006996 NW_004955460 15055480 15069093 + 8701022 Yme1l1 YME1 like 1 ATPase ENCODES a protein that exhibits ATP-dependent peptidase activity (ortholog); INVOLVED IN cell population proliferation (ortholog); mitochondrial protein catabolic process (ortholog); mitochondrial protein processing (ortholog); ASSOCIATED WITH dilated cardiomyopathy (ortholog); genetic disease (ortholog); long QT syndrome (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrion (ortholog); nuclear body (ortholog) NW_004955429 2550611 2572472 - 9068941 102009090 A0A8C2V1C4 MODEL AGCD01028430;GBDF01051277;GBDJ01017421;XM_013515518 XP_013370972 ATP-dependent zinc metalloprotease YME1L1;YME1-like 1 ATPase APPROVED protein-coding ENSCLAG00000005859 NW_004955429 2549954 2572889 - 8701041 Ntf3 neurotrophin 3 ENCODES a protein that exhibits chemoattractant activity (ortholog); growth factor activity (ortholog); nerve growth factor binding (ortholog); INVOLVED IN activation of GTPase activity (ortholog); activation of protein kinase B activity (ortholog); axon guidance (ortholog); ASSOCIATED WITH Alzheimer's disease (ortholog); asthma (ortholog); atrial heart septal defect 1 (ortholog); FOUND IN cytoplasmic vesicle (ortholog); synapse (ortholog) NW_004955413 3207669 3273371 + 9068941 102009266 A0A8C2W3H5 MODEL AGCD01013568;GBBH01041463;XM_005378750 XP_005378807 neurotrophin-3 protein-coding ENSCLAG00000016065 NW_004955413 3207123 3273491 + 8701050 Dhrsx dehydrogenase/reductase X-linked INVOLVED IN positive regulation of autophagy (ortholog); ASSOCIATED WITH autistic disorder (ortholog); FOUND IN extracellular region (ortholog) NW_004955499 1360636 1471141 - 9068941 102010069 MODEL AGCD01063348;AGCD01063349;AGCD01063350;AGCD01063351;AGCD01063352;AGCD01063353;AGCD01063354;AGCD01063355;GBCB01024741;GBDF01253653;XM_005406518;XM_013505592 XP_005406575;XP_013361046 dehydrogenase/reductase (SDR family) X-linked;dehydrogenase/reductase SDR family member on chromosome X APPROVED protein-coding 8701060 LOC102011405 chromodomain Y-like protein pseudogene NW_004955407 28152182 28153855 - 102011405 MODEL AGCD01007576 APPROVED pseudo 8701061 LOC102011427 chromosome unknown open reading frame, human C19orf12 INVOLVED IN apoptotic process (ortholog); autophagy (ortholog); mitochondrial calcium ion homeostasis (ortholog); ASSOCIATED WITH Developmental Disabilities (ortholog); dystonia (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); endoplasmic reticulum (ortholog); mitochondrial membrane (ortholog) NW_004955468 7903438 7914038 + 9068941;7240710 102011427 A0A8C2YTM0 MODEL AGCD01052015;AGCD01052016;GBCB01022853;XM_005400110 XP_005400167 protein-coding ENSCLAG00000015360 NW_004955468 7903432 7914038 + 8701075 Ccdc92 coiled-coil domain containing 92 ENCODES a protein that exhibits identical protein binding (ortholog); ASSOCIATED WITH Coronary Disease (ortholog); genetic disease (ortholog); type 2 diabetes mellitus (ortholog); FOUND IN centriole (ortholog); centrosome (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955482 5196238 5206210 + 9068941 102011990 A0A8C2VET9 MODEL AGCD01057323;GBDF01006230;XM_005403014;XM_005403015;XM_005403016;XM_013503548 XP_005403071;XP_005403072;XP_005403073;XP_013359002 coiled-coil domain-containing protein 92 protein-coding ENSCLAG00000008502 NW_004955482 5197515 5206210 + 8701098 Usb1 U6 snRNA biogenesis phosphodiesterase 1 ENCODES a protein that exhibits 3'-5'-RNA exonuclease activity (ortholog); poly(U)-specific exoribonuclease activity, producing 3' uridine cyclic phosphate ends (ortholog); INVOLVED IN RNA splicing (ortholog); snRNA 3'-end processing (ortholog); U6 snRNA 3'-end processing (ortholog); ASSOCIATED WITH Bardet-Biedl syndrome (ortholog); developmental and epileptic encephalopathy (ortholog); early infantile epileptic encephalopathy (ortholog); FOUND IN intercellular bridge (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955433 15572884 15580108 + 9068941 102012016 A0A8C2VCD3 MODEL AGCD01031760;GBCB01056320;GBDF01010131;XM_005388505;XM_013516252;XM_013516253 XP_005388562;XP_013371706;XP_013371707 U6 snRNA biogenesis 1;U6 snRNA phosphodiesterase APPROVED protein-coding ENSCLAG00000007363 NW_004955433 15572881 15579509 + 8701106 Scimp SLP adaptor and CSK interacting membrane protein ENCODES a protein that exhibits molecular adaptor activity (ortholog); INVOLVED IN cellular response to molecule of fungal origin (ortholog); positive regulation of cytokine production involved in immune response (ortholog); positive regulation of dendritic cell cytokine production (ortholog); ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog); head and neck cancer (ortholog); FOUND IN filopodium (ortholog); immunological synapse (ortholog); leading edge membrane (ortholog) NW_004955467 10547706 10578355 - 9068941 102012180 A0A8C2YR29 MODEL AGCD01051575;AGCD01051576;AGCD01051577;GBDI01384955;XM_013522267;XM_013522268 XP_013377721;XP_013377722 protein-coding ENSCLAG00000011695 NW_004955467 10547294 10578387 - 8701115 Soat2 sterol O-acyltransferase 2 ENCODES a protein that exhibits cholesterol binding (ortholog); cholesterol O-acyltransferase activity (ortholog); fatty-acyl-CoA binding (ortholog); INVOLVED IN cholesterol efflux (ortholog); cholesterol metabolic process (ortholog); cholesterol storage (ortholog); PARTICIPATES IN kidney failure pathway; ASSOCIATED WITH arteriosclerosis (ortholog); celiac disease (ortholog); cholelithiasis (ortholog); FOUND IN brush border (ortholog); endoplasmic reticulum (ortholog); endoplasmic reticulum membrane (ortholog) NW_004955458 383123 394003 + 9068941 102012287 A0A8C2VU03 MODEL AGCD01047122;AGCD01047123;GBCQ01096818;XM_005397145;XM_005397147;XM_005397148;XM_005397150;XM_005397151;XM_013521027;XM_013521028 XP_005397202;XP_005397204;XP_005397205;XP_005397207;XP_005397208;XP_013376481;XP_013376482 protein-coding ENSCLAG00000014123 NW_004955458 382892 394749 + 8701161 Hnmt histamine N-methyltransferase ENCODES a protein that exhibits histamine N-methyltransferase activity (ortholog); N-methyltransferase activity (ortholog); INVOLVED IN histamine catabolic process (ortholog); histamine metabolic process (ortholog); hyperosmotic response (ortholog); PARTICIPATES IN histidine metabolic pathway; histidinemia pathway; homocysteine metabolic pathway; ASSOCIATED WITH asthma (ortholog); atopic dermatitis (ortholog); autosomal recessive intellectual developmental disorder 51 (ortholog); FOUND IN centrosome (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955440 5084198 5137577 + 9068941;7240710 102012366 A0A8C2ULR3 MODEL AGCD01036271;GBDJ01186894;XM_005390770;XM_005390771;XM_005390772;XM_013517507;XM_013517508 XP_005390827;XP_005390828;XP_005390829;XP_013372961;XP_013372962 protein-coding ENSCLAG00000001523 NW_004955440 5084081 5139348 + 8701178 Lrrn4cl LRRN4 C-terminal like ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); Larsen-like syndrome B3GAT3 type (ortholog) NW_004955599 514328 516684 + 9068941 102012387 A0A8C2UFL3 MODEL AGCD01076654;GBDI01220215;XM_005414782 XP_005414839 protein-coding ENSCLAG00000000228 NW_004955599 504370 517989 + 8701184 Tom1l2 target of myb1 like 2 membrane trafficking protein ENCODES a protein that exhibits clathrin binding (ortholog); protein kinase binding (ortholog); INVOLVED IN negative regulation of mitotic nuclear division (ortholog); signal transduction (ortholog); ASSOCIATED WITH autistic disorder (ortholog); Birt-Hogg-Dube syndrome (ortholog); common variable immunodeficiency 2 (ortholog) NW_004955577 93877 153381 + 9068941 102013775 A0A8C2UGT1;A0A8C2UIS1;A0A8C2UJH8;A0A8C2ULP7;A0A8C2ULT9 MODEL AGCD01075379;AGCD01075380;AGCD01075381;GBCB01003076;XM_013509625;XM_013509627;XM_013509628;XM_013509629;XR_001232462 XP_013365079;XP_013365081;XP_013365082;XP_013365083 TOM1-like protein 2;target of myb1-like 2 APPROVED protein-coding ENSCLAG00000000273 NW_004955577 93480 153437 + 8701212 Tmem200c transmembrane protein 200C ASSOCIATED WITH chromosome 18p deletion syndrome (ortholog); intellectual disability (ortholog) NW_004955402 5235381 5248845 + 9068941 102014100 MODEL AGCD01000131;AGCD01000132;AGCD01000133;GBDF01042126;XM_005373144 XP_005373201 protein-coding 8701226 LOC102014248 olfactory receptor 6F1-like NW_004955418 30394643 30395602 + 102014248 MODEL AGCD01019515;XM_005382375 XP_005382432 APPROVED protein-coding 8701229 Capn7 calpain 7 ENCODES a protein that exhibits endopeptidase activity (ortholog); MIT domain binding (ortholog); INVOLVED IN positive regulation of epithelial cell migration (ortholog); proteolysis (ortholog); self proteolysis (ortholog); ASSOCIATED WITH 3p deletion syndrome (ortholog); genetic disease (ortholog); FOUND IN centrosome (ortholog); cytosol (ortholog) NW_004955430 2269274 2307801 - 9068941 102014700 A0A8C2V0Z8 MODEL AGCD01029162;GBBH01149851;GBDF01192466;XM_005387313 XP_005387370 calpain-7 APPROVED protein-coding ENSCLAG00000006072 NW_004955430 2269274 2308713 - 8701260 LOC102015185 60S acidic ribosomal protein P0 pseudogene NW_004955467 10206250 10209516 - 102015185 MODEL AGCD01051553 APPROVED pseudo 8701261 Septin11 septin 11 INVOLVED IN regulation of synapse organization (ortholog); ASSOCIATED WITH autosomal recessive cerebellar ataxia (ortholog); genetic disease (ortholog); Kabuki Syndrome 1 (ortholog); FOUND IN GABA-ergic synapse (ortholog); glutamatergic synapse (ortholog); postsynapse (ortholog) NW_004955433 1606246 1691819 + 9068941 102015657 A0A8C2V152;A0A8C2V153;A0A8C2V1L8;A0A8C2V682 MODEL AGCD01031365;AGCD01031366;GBCE01031455;XM_005388189;XM_005388190;XM_013516164;XM_013516165;XM_013516166;XR_001234733;XR_001234734 XP_005388246;XP_005388247;XP_013371618;XP_013371619;XP_013371620 Sept11 septin-11 APPROVED protein-coding ENSCLAG00000006114 NW_004955433 1606261 1691812 + 8701279 Sec62 SEC62 homolog, preprotein translocation factor INVOLVED IN post-translational protein targeting to endoplasmic reticulum membrane (ortholog); post-translational protein targeting to membrane, translocation (ortholog); ASSOCIATED WITH autosomal dominant dyskeratosis congenita 1 (ortholog); Fanconi syndrome (ortholog); genetic disease (ortholog); FOUND IN membrane (ortholog) NW_004955420 219909 247471 + 9068941 102015850 A0A8C2VJ28 MODEL AGCD01020538;AGCD01020539;GBDI01002283;XM_005382962 XP_005383019 SEC62 homolog;translocation protein SEC62 APPROVED protein-coding ENSCLAG00000010122 8701297 LOC102015958 zinc finger protein 208-like NW_004955482 102076 193169 - 9068941 102015958 MODEL AGCD01057161;AGCD01057162;AGCD01057163;AGCD01057164;AGCD01057165;GBCE01005323;XM_005402935 XP_005402992 Znf26 zinc finger protein 26 PROVISIONAL protein-coding 8701315 LOC102017401 uncharacterized LOC102017401 NW_004955447 9620021 9623327 + 102017401 MODEL AGCD01040865;GBDF01045016;XR_001235711;XR_262416;XR_262417 ncrna 8701326 LOC102018017 olfactory receptor 2J3-like NW_004955524 45694 46627 + 102018017 MODEL AGCD01068663;XM_013507226 XP_013362680 protein-coding 8701327 LOC102018834 uncharacterized LOC102018834 NW_004955485 1420370 1427704 - 102018834 MODEL AGCD01058479;GBCE01148220;XR_263904 ncrna 8701332 Csdc2 cold shock domain containing C2 ENCODES a protein that exhibits RNA binding (ortholog); transcription factor binding (ortholog); ASSOCIATED WITH adenylosuccinase lyase deficiency (ortholog); common variable immunodeficiency 4 (ortholog); genetic disease (ortholog) NW_004955413 27079280 27090082 + 9068941 102020234 A0A8C2W2T7 MODEL AGCD01014491;AGCD01014492;GBCE01171981;XM_005379354 XP_005379411 cold shock domain containing C2, RNA binding;cold shock domain-containing protein C2 APPROVED protein-coding ENSCLAG00000016705 NW_004955413 27079280 27090082 + 8701340 Tspan5 tetraspanin 5 ENCODES a protein that exhibits enzyme binding (ortholog); INVOLVED IN positive regulation of Notch signaling pathway (ortholog); protein localization to plasma membrane (ortholog); protein maturation (ortholog); ASSOCIATED WITH genetic disease (ortholog); prostate cancer (ortholog); FOUND IN actin cytoskeleton (ortholog); nucleoplasm (ortholog); plasma membrane (ortholog) NW_004955405 8725761 8759784 - 9068941 102020520 A0A8C2V274;A0A8C2YM91 MODEL AGCD01004751;GBCQ01094713;GBDF01221548;XM_013517460 XP_013372914 tetraspanin-5 protein-coding ENSCLAG00000006295 NW_004955405 8725761 8759785 - 8701356 LOC102021214 interferon regulatory factor 8 pseudogene NW_004955409 1904386 1909564 + 102021214 MODEL AGCD01009184 APPROVED pseudo 8701357 Chrac1 chromatin accessibility complex subunit 1 INVOLVED IN chromatin remodeling (ortholog); nucleosome assembly (ortholog); regulation of DNA replication (ortholog); PARTICIPATES IN ISWI family mediated chromatin remodeling pathway; ASSOCIATED WITH genetic disease (ortholog); FOUND IN pericentric heterochromatin (ortholog) NW_004955461 14184318 14189645 + 9068941 102023235 A0A8C2UKA5 MODEL AGCD01049048;GBBH01119368;XM_005398053;XM_013521311 XP_005398110;XP_013376765 chromatin accessibility complex 1;chromatin accessibility complex protein 1 APPROVED protein-coding ENSCLAG00000001356 NW_004955461 14185737 14189645 + 8701364 LOC102023285 olfactory receptor 4C46-like NW_004955511 165034 165966 + 102023285 MODEL AGCD01066321;XM_005408180 XP_005408237 protein-coding 8701367 Vps37d VPS37D subunit of ESCRT-I ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); genetic disease (ortholog); FOUND IN ESCRT I complex (ortholog) NW_004955456 14064197 14067571 - 9068941 102025211 MODEL AGCD01046632;GBCE01185982;XM_005396773 XP_005396830 VPS37D, ESCRT-I subunit;vacuolar protein sorting 37 homolog D (S. cerevisiae);vacuolar protein sorting-associated protein 37D APPROVED protein-coding 8701375 Tasor2 transcription activation suppressor family member 2 ASSOCIATED WITH genetic disease (ortholog); hypoparathyroidism-deafness-renal disease syndrome (ortholog); schizophrenia (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog) NW_004955421 22381295 22448115 + 9068941 102025253 A0A8C2V4P6;A0A8C2VA34 MODEL AGCD01022134;AGCD01022135;AGCD01022136;GBDF01085789;XM_005383842;XM_005383843;XM_005383844;XM_005383845;XM_005383846;XM_005383847;XM_013513662;XM_013513663;XM_013513664 XP_005383899;XP_005383900;XP_005383901;XP_005383902;XP_005383903;XP_005383904;XP_013369116;XP_013369117;XP_013369118 Fam208b family with sequence similarity 208 member B;family with sequence similarity 208, member B APPROVED protein-coding ENSCLAG00000006738 NW_004955421 22401983 22447453 + 8701410 Trappc5 trafficking protein particle complex subunit 5 ASSOCIATED WITH familial hemophagocytic lymphohistiocytosis 5 (ortholog); genetic disease (ortholog); mucolipidosis type IV (ortholog); FOUND IN TRAPP complex (ortholog) NW_004955563 1600027 1601685 - 9068941 102026581 A0A8C2UVE0 MODEL AGCD01074153;GBBH01000859;XM_005413166;XM_005413167;XM_005413168;XM_013509161 XP_005413223;XP_005413224;XP_005413225;XP_013364615 trafficking protein particle complex 5 APPROVED protein-coding ENSCLAG00000002743 NW_004955563 1600027 1601649 - 8701422 LOC102026870 uncharacterized LOC102026870 NW_004955419 20421628 20427552 + 102026870 MODEL AGCD01020242;GBDF01013846;XR_260647 ncrna 8701428 Tex12 testis expressed 12 INVOLVED IN meiotic DNA repair synthesis (ortholog); synaptonemal complex assembly (ortholog); ASSOCIATED WITH BH4-deficient hyperphenylalaninemia A (ortholog); Chromosome 11, Partial Trisomy 11q (ortholog); genetic disease (ortholog); FOUND IN central element (ortholog); chromosome (ortholog); synaptonemal complex (ortholog) NW_004955412 13829637 13834481 + 9068941 102028391 A0A8C2VU92 MODEL AGCD01012846;GBCQ01024502;XM_005378113;XM_005378115;XM_005378116;XM_005378117;XM_013511042;XM_013511044 XP_005378170;XP_005378172;XP_005378173;XP_005378174;XP_013366496;XP_013366498 protein-coding ENSCLAG00000014098 NW_004955412 13831353 13834481 + 8701449 Adam9 ADAM metallopeptidase domain 9 ENCODES a protein that exhibits collagen binding (ortholog); integrin binding (ortholog); laminin binding (ortholog); INVOLVED IN amyloid precursor protein catabolic process (ortholog); cell adhesion (ortholog); cell adhesion mediated by integrin (ortholog); PARTICIPATES IN epidermal growth factor/neuregulin signaling pathway; ASSOCIATED WITH Alzheimer's disease (ortholog); cervix uteri carcinoma in situ (ortholog); cone-rod dystrophy (ortholog); FOUND IN basolateral plasma membrane (ortholog); cell surface (ortholog); cytoplasm (ortholog) NW_004955463 14545425 14646498 + 9068941;7240710 102029159 A0A8C2UP18 MODEL AGCD01049912;AGCD01049913;AGCD01049914;GBCB01026114;XM_005398463 XP_005398520 disintegrin and metalloproteinase domain-containing protein 9 protein-coding ENSCLAG00000000971 NW_004955463 14545589 14645419 + 8701483 Neo1 neogenin 1 ENCODES a protein that exhibits BMP receptor binding (ortholog); cadherin binding (ortholog); co-receptor binding (ortholog); INVOLVED IN intracellular iron ion homeostasis (ortholog); multicellular organismal-level iron ion homeostasis (ortholog); myoblast fusion (ortholog); ASSOCIATED WITH Bardet-Biedl syndrome (ortholog); Bloom syndrome (ortholog); Brugada syndrome 8 (ortholog); FOUND IN cell surface (ortholog); Golgi apparatus (ortholog); growth cone (ortholog) NW_004955450 4191168 4324997 - 9068941 102029578 A0A8C2V1D1 MODEL AGCD01042457;AGCD01042458;AGCD01042459;AGCD01042460;GBDF01119486;XM_013518999;XM_013519000;XM_013519001;XM_013519002;XM_013519003 XP_013374453;XP_013374454;XP_013374455;XP_013374456;XP_013374457 neogenin protein-coding ENSCLAG00000004747 NW_004955450 4191168 4375896 - 8701516 LOC102029858 aldo-keto reductase family 1 member B10 pseudogene NW_004955478 10537415 10548336 + 102029858 MODEL AGCD01056134 APPROVED pseudo 8701517 LOC102030009 cytochrome c oxidase subunit 7B2, mitochondrial INVOLVED IN spermatogenesis (ortholog); ASSOCIATED WITH genetic disease (ortholog); hepatocellular carcinoma (ortholog) NW_004955443 1650087 1768318 + 9068941 102030009 MODEL AGCD01038139;AGCD01038140;AGCD01038141;AGCD01038142;AGCD01038143;GBDF01004752;XM_005391898;XM_005391899;XM_013518038 XP_005391955;XP_005391956;XP_013373492 APPROVED protein-coding 8701527 LOC102030423 ATP synthase F(0) complex subunit B1, mitochondrial pseudogene NW_004955483 339393 341271 - 102030423 MODEL AGCD01057606 APPROVED pseudo 8701528 Rlbp1 retinaldehyde binding protein 1 ENCODES a protein that exhibits 11-cis retinal binding (ortholog); PARTICIPATES IN altered retinoid cycle metabolic pathway; retinitis pigmentosa pathway; retinoid cycle metabolic pathway; ASSOCIATED WITH Alpers-Huttenlocher syndrome (ortholog); Bloom syndrome (ortholog); Bothnia retinal dystrophy (ortholog); FOUND IN cell body (ortholog); centrosome (ortholog); cytosol (ortholog) NW_004955416 15862510 15873261 + 9068941;7240710 102003653 A0A8C2YQ96 MODEL AGCD01017346;GBDF01112309;XM_005381557;XM_005381558;XM_005381559 XP_005381614;XP_005381615;XP_005381616 retinaldehyde-binding protein 1 protein-coding ENSCLAG00000010583 NW_004955416 15862426 15873327 + 8701549 LOC102003845 E3 ubiquitin-protein ligase XIAP pseudogene NW_004955462 10272846 10275300 + 102003845 MODEL AGCD01049360 APPROVED pseudo 8701550 St7l suppression of tumorigenicity 7 like INVOLVED IN negative regulation of cell growth (ortholog); ASSOCIATED WITH genetic disease (ortholog); hereditary spastic paraplegia 47 (ortholog) NW_004955435 15938815 16048237 - 9068941 102004968 A0A8C2V988;A0A8C2VD52 MODEL AGCD01033291;AGCD01033292;AGCD01033293;GBCC01027959;XM_005388963;XM_013516414;XM_013516415;XM_013516416;XM_013516417;XM_013516418 XP_005389020;XP_013371868;XP_013371869;XP_013371870;XP_013371871;XP_013371872 suppressor of tumorigenicity 7 protein-like protein-coding ENSCLAG00000007732 NW_004955435 15979927 16048036 - 8701572 Mydgf myeloid derived growth factor INVOLVED IN negative regulation of apoptotic process (ortholog); positive regulation of angiogenesis (ortholog); positive regulation of endothelial cell proliferation (ortholog); ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog); Keloid (ortholog); FOUND IN endoplasmic reticulum (ortholog); extracellular region (ortholog); extracellular space (ortholog) NW_004955495 4320532 4330921 + 9068941 102006043 A0A8C2W1I5 MODEL AGCD01061912;AGCD01061913;AGCD01061914;GBDF01000136;XM_005405787;XM_005405788 XP_005405844;XP_005405845 myeloid-derived growth factor APPROVED protein-coding ENSCLAG00000016185 NW_004955495 4320540 4330921 + 8701590 LOC102006758 olfactory receptor 147-like NW_004955412 25230240 25240655 + 102006758 A0A8C2W8Y3 MODEL AGCD01013141;XM_005378417;XM_013510987 XP_005378474;XP_013366441 protein-coding ENSCLAG00000017941 8701593 Itga2b integrin subunit alpha 2b ENCODES a protein that exhibits extracellular matrix binding (ortholog); fibrinogen binding (ortholog); identical protein binding (ortholog); INVOLVED IN cell-matrix adhesion (ortholog); positive regulation of leukocyte migration (ortholog); PARTICIPATES IN abciximab pharmacodynamics pathway; ephrin - ephrin receptor bidirectional signaling axis; eptifibatide pharmacodynamics pathway; ASSOCIATED WITH carotid artery thrombosis (ortholog); Cerebral Hemorrhage (ortholog); Endotoxemia (ortholog); FOUND IN cell surface (ortholog); external side of plasma membrane (ortholog); extracellular exosome (ortholog) NW_004955451 17381323 17392122 - 9068941;7240710 102007079 A0A8C2W2Z3 MODEL AGCD01043747;AGCD01043748;AGCD01043749;GBDI01168281;GBDK01190451;XM_013519265 XP_013374719 integrin alpha-IIb;integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41) APPROVED protein-coding ENSCLAG00000016572 NW_004955451 17382779 17391859 - 8701629 Alg11 ALG11 alpha-1,2-mannosyltransferase ASSOCIATED WITH chromosome 13q14 deletion syndrome (ortholog); congenital disorder of glycosylation (ortholog); congenital disorder of glycosylation Ip (ortholog) NW_004955431 5297477 5320653 + 9068941;7240710 102007144 A0A8C2V200 MODEL AGCD01030019;GBDF01195619;XM_005387615;XM_005387616;XM_013515772;XM_013515773;XR_001234601 XP_005387672;XP_005387673;XP_013371226;XP_013371227 ALG11, alpha-1,2-mannosyltransferase;GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase APPROVED protein-coding ENSCLAG00000005320 NW_004955431 5297715 5306590 + 8701648 Rfc3 replication factor C subunit 3 ENCODES a protein that exhibits ATP-dependent activity, acting on DNA (ortholog); DNA binding (ortholog); DNA clamp loader activity (ortholog); INVOLVED IN DNA replication (ortholog); positive regulation of DNA-directed DNA polymerase activity (ortholog); response to organophosphorus (ortholog); PARTICIPATES IN mismatch repair pathway; nucleotide excision repair pathway; ASSOCIATED WITH genetic disease (ortholog); FOUND IN Ctf18 RFC-like complex (ortholog); DNA replication factor C complex (ortholog) NW_004955431 12071465 12084570 - 9068941 102007456 A0A8C2UYJ0 MODEL AGCD01030254;GBCB01075231;XM_005387702 XP_005387759 replication factor C (activator 1) 3, 38kDa APPROVED protein-coding ENSCLAG00000003664 NW_004955431 12069204 12084577 - 8701661 LOC102007925 calmodulin-A pseudogene NW_004955430 14879789 14880358 + 102007925 MODEL AGCD01029580;XM_005387538 APPROVED pseudo 8701664 LOC102009258 uncharacterized LOC102009258 NW_004955410 7298409 7299909 + 102009258 MODEL AGCD01010712;GBDK01133796;XR_259823;XR_259824 ncrna 8701672 LOC102009351 olfactory receptor 1361-like NW_004955408 1568710 1569651 + 102009351 MODEL AGCD01007965;XM_005376033 XP_005376090 protein-coding 8701675 Eef1a2 eukaryotic translation elongation factor 1 alpha 2 ENCODES a protein that exhibits protein kinase binding (ortholog); translation elongation factor activity (ortholog); INVOLVED IN positive regulation of apoptotic process (ortholog); positive regulation of lipid kinase activity (ortholog); response to electrical stimulus (ortholog); ASSOCIATED WITH Alzheimer's disease (ortholog); autistic disorder (ortholog); autosomal dominant intellectual developmental disorder 38 (ortholog); FOUND IN cytoplasm (ortholog); eukaryotic translation elongation factor 1 complex (ortholog); neuronal cell body (ortholog) NW_004955528 717338 726383 + 9068941 102010729 A0A8C2V5P6 MODEL AGCD01069544;AGCD01069545;GBCB01005764;GBDF01110613;XM_005409964 XP_005410021 elongation factor 1-alpha 2 protein-coding ENSCLAG00000006710 NW_004955528 717338 729692 + 8701687 Itfg1 integrin alpha FG-GAP repeat containing 1 ASSOCIATED WITH genetic disease (ortholog); glycogen storage disease IXb (ortholog) NW_004955474 7800984 8020891 + 9068941 102010994 A0A8C2YNG3 MODEL AGCD01054530;AGCD01054531;AGCD01054532;AGCD01054533;AGCD01054534;AGCD01054535;AGCD01054536;AGCD01054537;AGCD01054538;AGCD01054539;GBCB01043723;GBDF01119170;XM_005401409 XP_005401466 protein-coding ENSCLAG00000007967 NW_004955474 7801203 8020961 + 8701712 LOC102012802 uncharacterized LOC102012802 NW_004955541 36527 43417 + 102012802 MODEL AGCD01071344;GBDI01026247;XM_005410957;XM_013507937;XM_013507938 XP_005411014;XP_013363391;XP_013363392 uncharacterized protein LOC102012802 protein-coding ENSCLAG00000029069 8701722 Chchd1 coiled-coil-helix-coiled-coil-helix domain containing 1 ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); fibrillar center (ortholog); mitochondrion (ortholog) NW_004955437 18117090 18118586 - 9068941 102013006 A0A8C2VPK4 MODEL AGCD01034774;GBDK01143051;XM_005389962 XP_005390019 coiled-coil-helix-coiled-coil-helix domain-containing protein 1 protein-coding ENSCLAG00000012183 NW_004955437 18116923 18118670 - 8701729 Cep19 centrosomal protein 19 INVOLVED IN cilium assembly (ortholog); microtubule anchoring at centrosome (ortholog); vesicle targeting, trans-Golgi to periciliary membrane compartment (ortholog); ASSOCIATED WITH autistic disorder (ortholog); Bardet-Biedl syndrome (ortholog); chromosome 3q29 microdeletion syndrome (ortholog); FOUND IN centriole (ortholog); centrosome (ortholog); ciliary basal body (ortholog) NW_004955420 12823663 12829598 - 9068941;7240710 102014673 A0A8C2VR77 MODEL AGCD01020897;GBDF01225980;XM_005383140;XM_005383141 XP_005383197;XP_005383198 centrosomal protein 19kDa;centrosomal protein of 19 kDa APPROVED protein-coding ENSCLAG00000013341 NW_004955420 12823889 12825337 - 8701738 LOC102015309 olfactory receptor 52K1 NW_004955414 20126801 20127745 + 9068941 102015309 A0A8C2W695 MODEL AGCD01015358;XM_005380048 XP_005380105 APPROVED protein-coding ENSCLAG00000017936 NW_004955414 20126801 20127745 + 8701743 LOC102015473 ATP-dependent zinc metalloprotease YME1L1 NW_004955826 3824 15193 - 102015473 MODEL AGCD01078430;AGCD01078431;GBDF01051276;XM_005415123;XM_005415125;XM_013510198 XP_005415180;XP_005415182;XP_013365652 APPROVED protein-coding 8701757 LOC102016623 60S ribosomal protein L7-like NW_004955508 3685302 3686073 + 102016623 MODEL AGCD01065828 pseudo 8701758 LOC102016793 uncharacterized LOC102016793 NW_004955411 14391251 14392054 - 102016793 MODEL AGCD01011917;GBDF01047924;XR_001232836 ncrna 8701763 LOC102016893 olfactory receptor 2AP1-like NW_004955458 3035041 3035971 + 102016893 MODEL AGCD01047268;XM_013520864 XP_013376318 protein-coding 8701766 Oma1 OMA1 zinc metallopeptidase ENCODES a protein that exhibits metalloendopeptidase activity (ortholog); INVOLVED IN cristae formation (ortholog); diet induced thermogenesis (ortholog); energy homeostasis (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrial membrane (ortholog); mitochondrion (ortholog) NW_004955464 1305802 1393190 + 9068941 102017854 A0A8C2V9F6 MODEL AGCD01049946;AGCD01049947;AGCD01049948;AGCD01049949;GBDI01260850;XM_005398492;XM_005398493;XM_005398494;XM_005398495;XM_005398496;XM_005398497;XR_001236706;XR_263188 XP_005398549;XP_005398550;XP_005398551;XP_005398552;XP_005398553;XP_005398554 metalloendopeptidase OMA1, mitochondrial protein-coding ENSCLAG00000006571 NW_004955464 1305802 1393788 + 8701808 Vps16 VPS16 core subunit of CORVET and HOPS complexes ENCODES a protein that exhibits actin binding (ortholog); actin filament binding (ortholog); INVOLVED IN autophagosome maturation (ortholog); endosome to lysosome transport (ortholog); viral entry into host cell (ortholog); ASSOCIATED WITH Dystonia 30 (ortholog); genetic disease (ortholog); Huntington's disease-like 1 (ortholog); FOUND IN actin filament (ortholog); AP-3 adaptor complex (ortholog); axon (ortholog) NW_004955415 13791611 13813500 + 9068941 102018920 A0A8C2VK38;A0A8C2VNB4 MODEL AGCD01016269;GBDF01123714;XM_005380766 XP_005380823 VPS16, CORVET/HOPS core subunit;vacuolar protein sorting 16 homolog (S. cerevisiae);vacuolar protein sorting-associated protein 16 homolog APPROVED protein-coding ENSCLAG00000010899 NW_004955415 13791611 13813500 + 8701837 Cpn1 carboxypeptidase N subunit 1 ENCODES a protein that exhibits carboxypeptidase activity (ortholog); INVOLVED IN bradykinin catabolic process (ortholog); protein catabolic process (ortholog); response to glucocorticoid (ortholog); PARTICIPATES IN kallikrein-kinin cascade pathway; ASSOCIATED WITH carboxypeptidase N deficiency (ortholog); genetic disease (ortholog); FOUND IN extracellular space (ortholog) NW_004955507 5926508 5952515 - 9068941;7240710 102019517 A0A8C2UTR9 MODEL AGCD01065693;GBDK01395401;XM_005407682;XM_013506245 XP_005407739;XP_013361699 carboxypeptidase N catalytic chain;carboxypeptidase N, polypeptide 1 APPROVED protein-coding ENSCLAG00000003686 NW_004955507 5926508 5952559 - 8701850 LOC102020532 olfactory receptor 6C74-like NW_004955458 2708299 2716739 + 102020532 MODEL AGCD01047240 pseudo 8701851 Osbpl3 oxysterol binding protein like 3 ENCODES a protein that exhibits cholesterol binding (ortholog); ASSOCIATED WITH genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN cytosol (ortholog); nuclear membrane (ortholog); perinuclear endoplasmic reticulum (ortholog) NW_004955410 26804475 26968985 - 9068941 102022370 A0A8C2VB66;A0A8C2VDC0;A0A8C2VGG6 MODEL AGCD01011203;AGCD01011204;AGCD01011205;AGCD01011206;GBCE01123093;GBCQ01151566;XM_013510601 XP_013366055 oxysterol binding protein-like 3;oxysterol-binding protein-related protein 3 APPROVED protein-coding ENSCLAG00000008517 NW_004955410 26804410 26888470 - 8701884 LOC102022446 solute carrier family 25 member 46 pseudogene NW_004955402 17208998 17210219 + 102022446 MODEL AGCD01000500 APPROVED pseudo 8701894 LOC102023932 uncharacterized LOC102023932 NW_004955497 4837987 4866672 + 102023932 MODEL AGCD01062586;GBDF01305446;XR_264206 ncrna 8701900 LOC102024345 uncharacterized LOC102024345 NW_004955421 2482992 2490133 - 102024345 MODEL AGCD01021630;AGCD01021631;GBDF01236551;XR_260784 ncrna 8701905 LOC102024423 uncharacterized LOC102024423 NW_004955453 14383498 14394719 - 102024423 MODEL AGCD01044864;GBDF01252476;XR_001236145;XR_001236146;XR_262734;XR_262735 ncrna 8701912 Il4i1 interleukin 4 induced 1 ENCODES a protein that exhibits L-amino-acid oxidase activity (ortholog); INVOLVED IN L-phenylalanine catabolic process (ortholog); negative regulation of T cell activation (ortholog); negative regulation of T cell mediated immune response to tumor cell (ortholog); PARTICIPATES IN Canavan disease pathway; glycine N-methyltransferase deficiency pathway; homocystinuria pathway; ASSOCIATED WITH genetic disease (ortholog); Striatonigral Degeneration, Infantile (ortholog); FOUND IN acrosomal vesicle (ortholog); extracellular region (ortholog); immunological synapse (ortholog) NW_004955559 1012634 1047051 + 9068941 102025183 A0A8C2V5L1;A0A8C2V7X2;A0A8C2VAN3 MODEL AGCD01073626;GBDF01006554;XM_005412805;XM_005412806;XM_005412808;XM_013508954;XM_013508955;XM_013508956;XM_013508957;XM_013508958;XM_013508959;XM_013508960;XM_013508961;XM_013508962;XM_013508963;XM_013508964;XM_013508965 XP_005412862;XP_005412863;XP_005412865;XP_013364408;XP_013364409;XP_013364410;XP_013364411;XP_013364412;XP_013364413;XP_013364414;XP_013364415;XP_013364416;XP_013364417;XP_013364418;XP_013364419 L-amino-acid oxidase protein-coding ENSCLAG00000007325 NW_004955559 1034917 1047034 + 8701934 LOC102025191 60S ribosomal protein L23a pseudogene NW_004955578 358817 360090 + 102025191 MODEL AGCD01075477 APPROVED pseudo 8701935 Cspg4 chondroitin sulfate proteoglycan 4 ENCODES a protein that exhibits collagen binding (ortholog); coreceptor activity (ortholog); protein kinase binding (ortholog); INVOLVED IN glial cell migration (ortholog); intracellular signal transduction (ortholog); negative regulation of neuron projection development (ortholog); ASSOCIATED WITH acute lymphoblastic leukemia (ortholog); autistic disorder (ortholog); Bloom syndrome (ortholog); FOUND IN cell projection (ortholog); nucleoplasm (ortholog); plasma membrane (ortholog) NW_004955450 2631310 2663118 + 9068941 102025198 A0A8C2V210 MODEL AGCD01042392;AGCD01042393;GBCE01123444;XM_005393500 XP_005393557 protein-coding ENSCLAG00000005743 NW_004955450 2631327 2662269 + 8701952 Klf12 KLF transcription factor 12 ENCODES a protein that exhibits DNA binding (ortholog); DNA-binding transcription factor activity (ortholog); DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); INVOLVED IN negative regulation of transcription by RNA polymerase II (ortholog); positive regulation of transcription by RNA polymerase II (ortholog); regulation of DNA-templated transcription (ortholog); ASSOCIATED WITH chromosome 13q14 deletion syndrome (ortholog); genetic disease (ortholog); schizophrenia (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog) NW_004955404 32715636 33127525 + 9068941 102025205 A0A8C2UUE2;A0A8C2V028 MODEL AGCD01004053;AGCD01004054;AGCD01004055;AGCD01004056;AGCD01004057;AGCD01004058;GBDI01055813;XM_005374183;XM_013516591;XM_013516595;XM_013516598 XP_005374240;XP_013372045;XP_013372049;XP_013372052 Krueppel-like factor 12;Kruppel like factor 12;Kruppel-like factor 12 APPROVED protein-coding ENSCLAG00000004020 NW_004955404 32854754 33118361 + 8701964 Cimap2 ciliary microtubule associated protein 2 ENCODES a protein that exhibits mitochondrial ribosome binding (ortholog); INVOLVED IN positive regulation of cell population proliferation (ortholog); positive regulation of oxidative phosphorylation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN mitochondrion (ortholog) NW_004955464 4571161 4589879 - 9068941 102025445 A0A8C2VH91 MODEL AGCD01049992;GBDF01122493;XM_005398511 XP_005398568 LOC102025445;Lexm chromosome unknown open reading frame, human C1orf177;lymphocyte expansion molecule;uncharacterized protein C1orf177 homolog APPROVED protein-coding ENSCLAG00000010705 NW_004955464 4571830 4589777 - 8701978 LOC102025454 olfactory receptor 51A4-like NW_004955414 20541489 20544230 - 102025454 MODEL AGCD01015380 pseudo 8701979 LOC102025546 uncharacterized LOC102025546 NW_004955408 14226420 14232243 + 102025546 MODEL AGCD01008390;GBDF01084981;XR_259684 ncrna 8701983 LOC102026622 olfactory receptor 150-like NW_004955412 24978525 24979450 + 102026622 MODEL AGCD01013133 pseudo 8701984 Lrfn4 leucine rich repeat and fibronectin type III domain containing 4 INVOLVED IN regulation of postsynaptic density assembly (ortholog); regulation of presynapse assembly (ortholog); synaptic membrane adhesion (ortholog); ASSOCIATED WITH Aicardi-Goutieres Syndrome 3 (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN cell surface (ortholog); GABA-ergic synapse (ortholog); glutamatergic synapse (ortholog) NW_004955422 18524786 18527916 - 9068941 102027866 A0A8C2W1C4 MODEL AGCD01022950;GBBH01150721;XM_005384362 XP_005384419 leucine-rich repeat and fibronectin type-III domain-containing protein 4 protein-coding ENSCLAG00000016291 NW_004955422 18524786 18527916 - 8701990 Ece1 endothelin converting enzyme 1 ENCODES a protein that exhibits endopeptidase activity (ortholog); identical protein binding (ortholog); protein homodimerization activity (ortholog); INVOLVED IN axonogenesis involved in innervation (ortholog); blood vessel diameter maintenance (ortholog); bradykinin catabolic process (ortholog); PARTICIPATES IN endothelin signaling pathway; ASSOCIATED WITH 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (ortholog); acute kidney failure (ortholog); Alzheimer's disease (ortholog); FOUND IN early endosome (ortholog); endosome (ortholog); external side of plasma membrane (ortholog) NW_004955452 1653783 1704619 - 9068941;7240710 102028052 A0A8C2VMP9;A0A8C2VUX6 MODEL AGCD01043860;GBBH01031129;GBDI01008837;XM_005394714 XP_005394771 endothelin-converting enzyme 1 protein-coding ENSCLAG00000012254 NW_004955452 1651316 1751489 - 8702021 Ankrd2 ankyrin repeat domain 2 ENCODES a protein that exhibits chromatin binding (ortholog); protein kinase B binding (ortholog); RNA polymerase II-specific DNA-binding transcription factor binding (ortholog); INVOLVED IN myotube differentiation (ortholog); negative regulation of myoblast differentiation (ortholog); negative regulation of myotube differentiation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); euchromatin (ortholog); I band (ortholog) NW_004955507 3678009 3686967 + 9068941 102028215 A0A8C2UTM6 MODEL AGCD01065632;GBCQ01044645;XM_005407614;XR_264378 XP_005407671 ankyrin repeat domain 2 (stretch responsive muscle);ankyrin repeat domain-containing protein 2 APPROVED protein-coding ENSCLAG00000002245 NW_004955507 3677858 3687979 + 8702038 LOC102028566 vesicle-associated membrane protein 714-like NW_004955433 6388632 6443700 + 102028566 A0A8C2YMB4 MODEL AGCD01031533;AGCD01031534;AGCD01031535;AGCD01031536;AGCD01031537;AGCD01031538;GBDF01162678;XM_005388224;XM_005388225;XM_005388226;XM_005388227;XM_005388228 XP_005388281;XP_005388282;XP_005388283;XP_005388284;XP_005388285 vesicle-associated membrane protein 7-like;vesicle-associated membrane protein 712-like APPROVED protein-coding ENSCLAG00000006377 8702059 LOC102028787 60S ribosomal protein L36a-like NW_004955519 2803335 2804519 + 102028787 MODEL AGCD01067942;XM_005409209 pseudo 8702063 Bltp2 bridge-like lipid transfer protein family member 2 ASSOCIATED WITH genetic disease (ortholog); prostate cancer (ortholog) NW_004955481 4509840 4544706 + 9068941 102029080 A0A8C2VA20 MODEL AGCD01056943;GBCE01116508;GBCQ01065420;XM_005402743 XP_005402800 Kiaa0100 KIAA0100 ortholog APPROVED protein-coding ENSCLAG00000008465 NW_004955481 4509799 4544706 + 8702109 LOC102029554 proline-rich protein 2-like NW_004955437 3579235 3586547 - 102029554 MODEL AGCD01034325;AGCD01034326;GBCB01117887;XM_013516730 XP_013372184 APPROVED protein-coding 8702116 LOC102030049 nibrin pseudogene NW_004955409 16158130 16160312 + 102030049 MODEL AGCD01009710 APPROVED pseudo 8702117 Alg13 ALG13 UDP-N-acetylglucosaminyltransferase subunit INVOLVED IN negative regulation of TORC1 signaling (ortholog); regulation of synaptic plasticity (ortholog); ASSOCIATED WITH autistic disorder (ortholog); congenital disorder of glycosylation (ortholog); developmental and epileptic encephalopathy 1 (ortholog); FOUND IN cytoplasm (ortholog) NW_004955490 4069866 4140494 - 9068941;7240710 102030323 A0A8C2UQQ4;A0A8C2UTL8 MODEL AGCD01060180;AGCD01060181;AGCD01060182;GBCE01134171;XM_005404636;XM_005404639;XM_005404642;XM_013504527;XM_013504528;XM_013504529;XM_013504530;XM_013504531;XM_013504532;XM_013504533;XM_013504534 XP_005404693;XP_005404696;XP_005404699;XP_013359981;XP_013359982;XP_013359983;XP_013359984;XP_013359985;XP_013359986;XP_013359987;XP_013359988 ALG13, UDP-N-acetylglucosaminyltransferase subunit;UDP-N-acetylglucosamine transferase subunit ALG13 homolog;putative bifunctional UDP-N-acetylglucosamine transferase and deubiquitinase ALG13 APPROVED protein-coding ENSCLAG00000002938 NW_004955490 4069494 4140532 - 8702169 Ltb4r leukotriene B4 receptor ENCODES a protein that exhibits leukotriene B4 receptor activity (ortholog); leukotriene receptor activity (ortholog); INVOLVED IN leukotriene signaling pathway (ortholog); signal transduction (ortholog); PARTICIPATES IN G protein mediated signaling pathway; ASSOCIATED WITH otitis media; Anaphylaxis (ortholog); arteriosclerosis (ortholog) NW_004955409 35984757 35991492 - 9068941;11553910 20433028 102003215 A0A8C2W5Z5 MODEL AGCD01010438;GBBH01214872;XM_005377015;XM_005377016 XP_005377072;XP_005377073 BLT1 leukotriene B4 receptor 1 protein-coding ENSCLAG00000017796 NW_004955409 35984933 35985976 - 8702178 LOC102003807 uncharacterized LOC102003807 NW_004955546 1036841 1042659 - 102003807 MODEL AGCD01072038;GBDF01208163;XR_264887 ncrna 8702184 Sftpc surfactant protein C ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN cellular response to mechanical stimulus (ortholog); cellular response to nitric oxide (ortholog); circadian rhythm (ortholog); ASSOCIATED WITH adult respiratory distress syndrome (ortholog); asthma (ortholog); bacterial pneumonia (ortholog); FOUND IN alveolar lamellar body (ortholog); cytoplasm (ortholog); extracellular region (ortholog) NW_004955403 45649149 45651421 + 9068941;7240710 102004547 A0A8C2WC17 MODEL AGCD01002825;GBDK01013470;XM_005373651;XM_005373652 XP_005373708;XP_005373709 pulmonary surfactant-associated protein C protein-coding ENSCLAG00000017002 NW_004955403 45649122 45651837 + 8702196 LOC102004673 uncharacterized LOC102004673 NW_004955406 23278454 23287251 - 102004673 MODEL AGCD01006169;GBDK01311017;XR_001230927;XR_259505 ncrna 8702201 LOC102005642 T-complex protein 1 subunit theta pseudogene NW_004955443 13804351 13806658 - 102005642 MODEL AGCD01038484 APPROVED pseudo 8702202 Cep112 centrosomal protein 112 INVOLVED IN receptor localization to synapse (ortholog); ASSOCIATED WITH genetic disease (ortholog); spermatogenic failure 44 (ortholog); FOUND IN centrosome (ortholog); inhibitory synapse (ortholog); plasma membrane (ortholog) NW_004955478 5065925 5583624 - 9068941 102005929 A0A8C2UQR5;A0A8C2URC9;A0A8C2UTM9;A0A8C2UWC6;A0A8C2YJX7 MODEL AGCD01055864;AGCD01055865;AGCD01055866;AGCD01055867;AGCD01055868;AGCD01055869;AGCD01055870;AGCD01055871;AGCD01055872;AGCD01055873;AGCD01055874;AGCD01055875;AGCD01055876;AGCD01055877;AGCD01055878;AGCD01055879;GBDK01264291;XM_005402139;XM_005402140;XM_005402141;XM_005402146;XM_013503230;XM_013503231 XP_005402196;XP_005402197;XP_005402198;XP_005402203;XP_013358684;XP_013358685 centrosomal protein 112kDa;centrosomal protein of 112 kDa APPROVED protein-coding ENSCLAG00000002941 NW_004955478 5065603 5583522 - 8702252 LOC102006202 uncharacterized LOC102006202 NW_004955452 4902765 4908470 + 102006202 MODEL AGCD01044001;GBCC01009101;XR_262655 ncrna 8702256 LOC102006994 cytochrome c oxidase subunit 7A2, mitochondrial pseudogene NW_004955412 10686073 10686348 + 102006994 MODEL AGCD01012776 APPROVED pseudo 8702257 Dda1 DET1 and DDB1 associated 1 INVOLVED IN protein polyubiquitination (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN Cul4-RING E3 ubiquitin ligase complex (ortholog) NW_004955524 912752 920714 - 9068941 102007049 A0A8C2V845;A0A8C2V8B8 MODEL AGCD01068725;AGCD01068726;GBDK01139764;XM_005409525;XM_005409526;XM_005409527;XM_013507242;XM_013507243;XM_013507244;XM_013507245;XM_013507246 XP_005409582;XP_005409583;XP_005409584;XP_013362696;XP_013362697;XP_013362698;XP_013362699;XP_013362700 DET1- and DDB1-associated protein 1 protein-coding ENSCLAG00000008060 NW_004955524 914106 920677 - 8702276 LOC102008196 NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 3 pseudogene NW_004955410 6003925 6016151 - 102008196 MODEL AGCD01010695 APPROVED pseudo 8702277 Krt84 keratin 84 ENCODES a protein that exhibits structural constituent of skin epidermis (ortholog); INVOLVED IN regulation of keratinocyte differentiation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN intermediate filament cytoskeleton (ortholog); keratin filament (ortholog) NW_004955547 2729046 2737142 - 9068941 102008577 A0A8C2URJ4 MODEL AGCD01072294;XM_005411940;XM_013508447 XP_005411997;XP_013363901 keratin 84, type II;keratin, type II cuticular Hb4 APPROVED protein-coding ENSCLAG00000001540 NW_004955547 2729046 2737142 - 8702289 Elk3 ETS transcription factor ELK3 ENCODES a protein that exhibits DNA binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); DNA-binding transcription factor activity (ortholog); INVOLVED IN angiogenesis (ortholog); negative regulation of DNA-templated transcription (ortholog); positive regulation of DNA-templated transcription (ortholog); ASSOCIATED WITH Breast Neoplasms (ortholog); congenital chylothorax (ortholog); diastolic heart failure (ortholog); FOUND IN cytoplasm (ortholog); mitochondrion (ortholog); nucleoplasm (ortholog) NW_004955405 32526911 32559580 + 9068941 102009344 A0A8C2W1F8;A0A8C2W3Y4 MODEL AGCD01005334;GBDJ01136162;XM_005374495;XM_013518514;XM_013518521;XR_259422 XP_005374552;XP_013373968;XP_013373975 ELK3, ETS transcription factor;ELK3, ETS-domain protein (SRF accessory protein 2);ETS domain-containing protein Elk-3 APPROVED protein-coding ENSCLAG00000014957 NW_004955405 32526673 32557197 + 8702310 Tex28 testis expressed 28 ASSOCIATED WITH adrenoleukodystrophy (ortholog); autistic disorder (ortholog); Barth syndrome (ortholog) NW_004955580 781339 791284 - 9068941;7240710 102009777 MODEL AGCD01075622;XM_005414223 XP_005414280 protein-coding 8702316 Habp4 hyaluronan binding protein 4 ENCODES a protein that exhibits SUMO binding (ortholog); INVOLVED IN cellular response to mechanical stimulus (ortholog); negative regulation of DNA binding (ortholog); PML body organization (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); FOUND IN Cajal body (ortholog); cytoplasm (ortholog); cytoplasmic stress granule (ortholog) NW_004955422 23449175 23475919 - 9068941 102010273 A0A8C2YUM3 MODEL AGCD01023190;GBDK01134940;XM_005384698;XM_005384699 XP_005384755;XP_005384756 intracellular hyaluronan-binding protein 4 protein-coding ENSCLAG00000016858 NW_004955422 23450251 23475984 - 8702337 Pgp phosphoglycolate phosphatase ENCODES a protein that exhibits ADP phosphatase activity (ortholog); glycerol-3-phosphatase activity (ortholog); magnesium ion binding (ortholog); INVOLVED IN glycerol biosynthetic process (ortholog); glycerophospholipid metabolic process (ortholog); negative regulation of gluconeogenesis (ortholog); ASSOCIATED WITH autosomal dominant polycystic kidney disease (ortholog); developmental and epileptic encephalopathy 1 (ortholog); endometrial carcinoma (ortholog) NW_004955442 15051149 15053123 + 9068941 102011702 A0A8C2W1T6 MODEL AGCD01037855;AGCD01037856;GBBH01186797;GBDF01006244;XM_013517733 XP_013373187 protein-coding ENSCLAG00000016428 NW_004955442 15051183 15052289 + 8702344 Rps23 ribosomal protein S23 ENCODES a protein that exhibits structural constituent of ribosome (ortholog); INVOLVED IN cytoplasmic translation (ortholog); maintenance of translational fidelity (ortholog); ribosomal small subunit biogenesis (ortholog); PARTICIPATES IN ribosome biogenesis pathway; translation pathway; ASSOCIATED WITH Brachycephaly, Trichomegaly, and Developmental Delay (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN cytoplasmic side of rough endoplasmic reticulum membrane (ortholog); cytosol (ortholog); cytosolic ribosome (ortholog) NW_004955418 28106333 28108276 + 9068941 102011769 P62298 PROVISIONAL AGCD01019428;AY533228;GBDF01010421;NM_001282369 AAS59430;NP_001269298;P62298 40S ribosomal protein S23 protein-coding ENSCLAG00000004798 NW_004955418 28106333 28108271 + 8702352 LOC102011889 KATNB1-like protein 1 NW_004955426 24920133 24920909 - 102011889 MODEL AGCD01026698 APPROVED pseudo 8702353 LOC102012107 uncharacterized LOC102012107 NW_004955504 1489501 1499030 + 102012107 MODEL AGCD01064841;GBDI01349444;XR_264287 ncrna 8702358 LOC102013611 olfactory receptor 14K1-like NW_004955418 30363345 30372168 + 102013611 MODEL AGCD01019514;AGCD01019515;XM_013512882 XP_013368336 protein-coding 8702359 Eml6 EMAP like 6 ASSOCIATED WITH genetic disease (ortholog); keratoconus (ortholog) NW_004955424 28125287 28461646 - 9068941 102014262 A0A8C2VQH1;A0A8C2VVJ1 MODEL AGCD01025147;AGCD01025148;AGCD01025149;AGCD01025150;AGCD01025151;AGCD01025152;AGCD01025153;AGCD01025154;AGCD01025155;AGCD01025156;AGCD01025157;AGCD01025158;AGCD01025159;AGCD01025160;AGCD01025161;AGCD01025162;AGCD01025163;AGCD01025164;AGCD01025165;AGCD01025166;AGCD01025167;AGCD01025168;GBDF01277097;XM_013514622;XM_013514623;XM_013514624;XM_013514625;XM_013514626;XR_001234170 XP_013370076;XP_013370077;XP_013370078;XP_013370079;XP_013370080 echinoderm microtubule associated protein like 6;echinoderm microtubule-associated protein-like 6 APPROVED protein-coding ENSCLAG00000012421 NW_004955424 28127825 28462003 - 8702408 Amer3 APC membrane recruitment protein 3 ASSOCIATED WITH genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); schizophrenia (ortholog) NW_004955459 267754 277422 + 9068941 102014424 MODEL AGCD01047931;GBDF01117001;XM_005397547;XM_013521051;XR_263003;XR_263004 XP_005397604;XP_013376505 protein-coding 8702424 LOC102014832 uncharacterized LOC102014832 NW_004955440 5909959 5927193 + 102014832 MODEL AGCD01036285;GBDF01123806;XR_001235246;XR_262009 ncrna 8702432 Ncam2 neural cell adhesion molecule 2 ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN axonal fasciculation (ortholog); ASSOCIATED WITH Alzheimer's disease (ortholog); amenorrhea (ortholog); genetic disease (ortholog); FOUND IN axon (ortholog); nuclear body (ortholog); plasma membrane (ortholog) NW_004955407 21730331 22220664 + 9068941 102014868 A0A8C2VDE4;A0A8C2VDH3;A0A8C2VDH5 MODEL AGCD01007371;AGCD01007372;AGCD01007373;AGCD01007374;AGCD01007375;AGCD01007376;AGCD01007377;AGCD01007378;AGCD01007379;AGCD01007380;AGCD01007381;AGCD01007382;AGCD01007383;GBBH01154784;XM_005375584;XM_005375585 XP_005375641;XP_005375642 protein-coding ENSCLAG00000009655 NW_004955407 21730434 22215377 + 8702457 Sparcl1 SPARC like 1 INVOLVED IN regulation of synapse organization (ortholog); synaptic membrane adhesion (ortholog); ASSOCIATED WITH autosomal dominant polycystic kidney disease (ortholog); endometriosis (ortholog); epilepsy (ortholog); FOUND IN extracellular matrix of synaptic cleft (ortholog); glutamatergic synapse (ortholog) NW_004955474 2352662 2387237 + 9068941 102015104 A0A8C2UVK5 MODEL AGCD01054289;AGCD01054290;AGCD01054291;GBDJ01018536;XM_005401335;XM_013502717 XP_005401392;XP_013358171 SPARC-like 1 (hevin);SPARC-like protein 1 APPROVED protein-coding ENSCLAG00000004209 NW_004955474 2370237 2391285 + 8702472 Gng13 G protein subunit gamma 13 ENCODES a protein that exhibits G-protein beta-subunit binding (ortholog); INVOLVED IN phospholipase C-activating G protein-coupled receptor signaling pathway (ortholog); sensory perception of taste (ortholog); ASSOCIATED WITH epilepsy (ortholog); genetic disease (ortholog); idiopathic generalized epilepsy (ortholog); FOUND IN dendrite (ortholog); heterotrimeric G-protein complex (ortholog) NW_004955442 16408295 16414608 + 9068941 102015247 A0A8C2VS13 MODEL AGCD01037900;GBDF01083589;XM_005391602;XM_005391603;XM_005391604 XP_005391659;XP_005391660;XP_005391661 guanine nucleotide binding protein (G protein), gamma 13;guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-13 APPROVED protein-coding ENSCLAG00000013499 NW_004955442 16408295 16414608 + 8702485 Hspa5 heat shock protein family A (Hsp70) member 5 ENCODES a protein that exhibits ATP binding (ortholog); ATP hydrolysis activity (ortholog); enzyme binding (ortholog); INVOLVED IN cellular response to antibiotic (ortholog); cellular response to calcium ion (ortholog); cellular response to cAMP (ortholog); PARTICIPATES IN codeine and morphine pharmacodynamics pathway; codeine and morphine pharmacokinetics pathway; etoposide pharmacodynamics pathway; ASSOCIATED WITH Acute Experimental Pancreatitis (ortholog); Acute Lung Injury (ortholog); asbestosis (ortholog); FOUND IN cell surface (ortholog); COP9 signalosome (ortholog); cytoplasm (ortholog) NW_004955419 3055420 3060208 + 9068941 102015520 A0A8C2YPQ6 MODEL AGCD01019701;GBDF01006448;XM_005382466 XP_005382523 heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) APPROVED protein-coding ENSCLAG00000009815 NW_004955419 3055420 3062131 + 8702498 Gsx1 GS homeobox 1 ENCODES a protein that exhibits DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); RNA polymerase II cis-regulatory region sequence-specific DNA binding (ortholog); sequence-specific DNA binding (ortholog); INVOLVED IN adenohypophysis development (ortholog); hypothalamus development (ortholog); neuron fate commitment (ortholog); ASSOCIATED WITH genetic disease (ortholog) NW_004955497 7167915 7169177 + 9068941 102015741 A0A8C2UW38 MODEL AGCD01062660;XM_005406377 XP_005406434 protein-coding ENSCLAG00000004357 NW_004955497 7167915 7169177 + 8702502 LOC102015849 uncharacterized LOC102015849 NW_004955419 26437701 26446195 - 102015849 MODEL AGCD01020409;GBDF01144301;XR_260658 ncrna 8702508 LOC102016500 charged multivesicular body protein 5 pseudogene NW_004955428 13744889 13782648 + 102016500 MODEL AGCD01027962;AGCD01027963 APPROVED pseudo 8702509 Rigi RNA sensor RIG-I ENCODES a protein that exhibits ATP hydrolysis activity (ortholog); double-stranded DNA binding (ortholog); double-stranded RNA binding (ortholog); INVOLVED IN antiviral innate immune response (ortholog); cellular response to exogenous dsRNA (ortholog); cytosolic pattern recognition receptor signaling pathway (ortholog); ASSOCIATED WITH acromesomelic dysplasia, Maroteaux type (ortholog); Disease Progression (ortholog); distal arthrogryposis type 1A (ortholog); FOUND IN actin cytoskeleton (ortholog); bicellular tight junction (ortholog); cytoplasm (ortholog) NW_004955472 3093895 3135524 + 9068941 102017119 A0A8C2UUC2 MODEL AGCD01053503;AGCD01053504;GBBH01063676;XM_013522945 XP_013378399 Ddx58 DEAD (Asp-Glu-Ala-Asp) box polypeptide 58;DExD/H-box helicase 58;probable ATP-dependent RNA helicase DDX58 APPROVED protein-coding ENSCLAG00000002351 NW_004955472 3093939 3133987 + 8702530 Exosc5 exosome component 5 ENCODES a protein that exhibits RNA exonuclease activity (ortholog); INVOLVED IN defense response to virus (ortholog); DNA deamination (ortholog); exonucleolytic catabolism of deadenylated mRNA (ortholog); PARTICIPATES IN ribosome biogenesis pathway; ASSOCIATED WITH Carpenter Syndrome 2 (ortholog); CEREBELLAR ATAXIA, BRAIN ABNORMALITIES, AND CARDIAC CONDUCTION DEFECTS (ortholog); congenital hypoplastic anemia (ortholog); FOUND IN cytosol (ortholog); euchromatin (ortholog); exosome (RNase complex) (ortholog) NW_004955555 328130 334106 - 9068941 102017167 A0A8C2UKW9 MODEL AGCD01073024;GBBH01163376;XM_005412347 XP_005412404 exosome complex component RRP46 protein-coding ENSCLAG00000001186 NW_004955555 326698 334106 - 8702540 Il22ra2 interleukin 22 receptor subunit alpha 2 ENCODES a protein that exhibits interleukin-22 binding (ortholog); interleukin-22 receptor activity (ortholog); INVOLVED IN negative regulation of inflammatory response (ortholog); regulation of tyrosine phosphorylation of STAT protein (ortholog); ASSOCIATED WITH familial Behcet-like autoinflammatory syndrome (ortholog); genetic disease (ortholog); immunodeficiency 27A (ortholog); FOUND IN cytosol (ortholog) NW_004955436 22208267 22219667 + 9068941 102019953 A0A8C2VAG3 MODEL AGCD01034087;XM_005389281 XP_005389338 interleukin 22 receptor, alpha 2;interleukin-22 receptor subunit alpha-2 APPROVED protein-coding ENSCLAG00000008741 NW_004955436 22211175 22220566 + 8702549 LOC102020599 uncharacterized LOC102020599 NW_004955515 3783964 3807130 - 102020599 MODEL AGCD01067303;AGCD01067304;AGCD01067305;GBDF01304550;XR_264524 ncrna 8702555 Prkaa2 protein kinase AMP-activated catalytic subunit alpha 2 ENCODES a protein that exhibits AMP-activated protein kinase activity (ortholog); ATP binding (ortholog); chromatin binding (ortholog); INVOLVED IN cellular response to calcium ion (ortholog); cellular response to glucose starvation (ortholog); cellular response to glucose stimulus (ortholog); PARTICIPATES IN adenosine monophosphate-activated protein kinase (AMPK) signaling pathway; vascular endothelial growth factor signaling pathway; ASSOCIATED WITH Cardiomegaly (ortholog); cardiomyopathy (ortholog); cerebral malaria (ortholog); FOUND IN apical plasma membrane (ortholog); axon (ortholog); cytoplasm (ortholog) NW_004955464 2996608 3062197 - 9068941 102021219 A0A8C2YLN7 MODEL AGCD01049967;AGCD01049968;AGCD01049969;GBCB01001848;XM_005398501;XM_013521596 XP_005398558;XP_013377050 5'-AMP-activated protein kinase catalytic subunit alpha-2 APPROVED protein-coding ENSCLAG00000005475 NW_004955464 3003837 3062197 - 8702571 LOC102021276 disintegrin and metalloproteinase domain-containing protein 5-like NW_004955536 3528401 3648035 - 102021276 A0A8C2UPA9 MODEL AGCD01070827;AGCD01070828;AGCD01070829;AGCD01070830;GBDF01008700;XM_005410548;XM_005410549;XM_013507719;XM_013507720 XP_005410605;XP_005410606;XP_013363173;XP_013363174 protein-coding ENSCLAG00000001686 8702598 Srek1ip1 SREK1 interacting protein 1 ASSOCIATED WITH genetic disease (ortholog); Neurodevelopmental Disorders (ortholog) NW_004955446 4230559 4267331 + 9068941 102021718 A0A8C2USD1 MODEL AGCD01040034;GBDF01047867;XM_005392633 XP_005392690 SREK1-interacting protein 1 APPROVED protein-coding ENSCLAG00000003592 NW_004955446 4230720 4262904 + 8702607 LOC102022022 olfactory receptor 4K2-like NW_004955550 506630 507583 - 102022022 A0A8C2YV08 MODEL AGCD01072509;XM_005412132 XP_005412189 protein-coding ENSCLAG00000017427 NW_004955550 506636 507586 - 8702610 LOC102022290 uncharacterized LOC102022290 NW_004955418 7276604 7378661 + 102022290 MODEL AGCD01018886;AGCD01018887;AGCD01018888;AGCD01018889;AGCD01018890;GBDF01261954;XR_260543 ncrna 8702615 Galnt14 polypeptide N-acetylgalactosaminyltransferase 14 ASSOCIATED WITH genetic disease (ortholog); Hydrops Fetalis (ortholog); intestinal volvulus (ortholog) NW_004955469 12650191 12865779 - 9068941 102022488 A0A8C2W556;A0A8C2W9G2 MODEL AGCD01052585;AGCD01052586;AGCD01052587;GBDI01278263;XM_005400557;XM_005400558;XM_005400559 XP_005400614;XP_005400615;XP_005400616 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 14 (GalNAc-T14) APPROVED protein-coding ENSCLAG00000016568 NW_004955469 12649071 12866010 - 8702642 Dyrk1b dual specificity tyrosine phosphorylation regulated kinase 1B ENCODES a protein that exhibits protein kinase activity (ortholog); transcription coactivator activity (ortholog); INVOLVED IN adipose tissue development (ortholog); myoblast fusion (ortholog); positive regulation of DNA-templated transcription (ortholog); ASSOCIATED WITH abdominal obesity-metabolic syndrome 3 (ortholog); Carpenter Syndrome 2 (ortholog); congenital hypoplastic anemia (ortholog); FOUND IN chromosome (ortholog); nucleoplasm (ortholog) NW_004955578 1187128 1195574 + 9068941;7240710 102022981 A0A8C2UK08 MODEL AGCD01075511;GBDF01008859;XM_005414085;XM_005414086;XM_005414087;XM_005414088;XM_005414089;XM_005414090 XP_005414142;XP_005414143;XP_005414144;XP_005414145;XP_005414146;XP_005414147 dual specificity tyrosine-phosphorylation-regulated kinase 1B;dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1B APPROVED protein-coding ENSCLAG00000000674 NW_004955578 1187742 1195574 + 8702681 Atf7 activating transcription factor 7 ENCODES a protein that exhibits DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); enzyme binding (ortholog); mitogen-activated protein kinase binding (ortholog); INVOLVED IN heart development (ortholog); hematopoietic progenitor cell differentiation (ortholog); hepatocyte apoptotic process (ortholog); ASSOCIATED WITH colorectal cancer (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN nucleoplasm (ortholog); RNA polymerase II transcription regulator complex (ortholog) NW_004955458 803738 898847 - 9068941 102023878 A0A8C2VDC3 MODEL AGCD01047154;AGCD01047155;AGCD01047156;GBCB01056445;XM_005397189;XM_005397190 XP_005397246;XP_005397247 cyclic AMP-dependent transcription factor ATF-7 protein-coding ENSCLAG00000009615 NW_004955458 803738 898967 - 8702700 Coq4 coenzyme Q4 ASSOCIATED WITH developmental and epileptic encephalopathy (ortholog); Developmental Disease (ortholog); early infantile epileptic encephalopathy (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrion (ortholog); protein-containing complex (ortholog) NW_004955570 837216 846653 + 9068941 102024062 A0A8C2URY3 MODEL AGCD01074769;GBDJ01131032;XM_005413536 XP_005413593 coenzyme Q4 homolog;ubiquinone biosynthesis protein COQ4 homolog, mitochondrial APPROVED protein-coding ENSCLAG00000001766 NW_004955570 837216 846653 + 8702711 LOC102025057 RBPJ-interacting and tubulin-associated protein 1-like NW_004955445 6768638 6786308 + 102025057 MODEL AGCD01039514;AGCD01039515;AGCD01039516;AGCD01039517;AGCD01039518;XM_013518238 XP_013373692 APPROVED protein-coding 8702712 Per2 period circadian regulator 2 ENCODES a protein that exhibits DNA-binding transcription factor binding (ortholog); histone deacetylase binding (ortholog); histone methyltransferase binding (ortholog); INVOLVED IN chromatin remodeling (ortholog); circadian regulation of gene expression (ortholog); circadian regulation of translation (ortholog); ASSOCIATED WITH advanced sleep phase syndrome (ortholog); advanced sleep phase syndrome 1 (ortholog); Alcoholic Intoxication (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955542 2331547 2369011 + 9068941;7240710 102025287 A0A8C2UWA7 MODEL AGCD01071518;AGCD01071519;GBBH01061747;GBDI01080968;XM_005411189 XP_005411246 period circadian clock 2;period circadian protein homolog 2 APPROVED protein-coding ENSCLAG00000004749 NW_004955542 2338099 2371274 + 8702771 Hdac9 histone deacetylase 9 ENCODES a protein that exhibits DNA-binding transcription factor binding (ortholog); histone deacetylase activity (ortholog); histone deacetylase binding (ortholog); INVOLVED IN cellular response to insulin stimulus (ortholog); cholesterol homeostasis (ortholog); determination of adult lifespan (ortholog); PARTICIPATES IN histone modification pathway; ASSOCIATED WITH genetic disease (ortholog); middle cerebral artery infarction (ortholog); Osteoarthritis, Hip (ortholog); FOUND IN cytoplasm (ortholog); histone methyltransferase complex (ortholog); nucleus (ortholog) NW_004955410 21046312 21932029 + 9068941 102025552 A0A8C2V7K0;A0A8C2V7K4;A0A8C2VCP1;A0A8C2YNE8;A0A8C2YNE9 MODEL AGCD01011056;AGCD01011057;AGCD01011058;AGCD01011059;AGCD01011060;AGCD01011061;AGCD01011062;AGCD01011063;AGCD01011064;AGCD01011065;AGCD01011066;GBDF01088540;XM_005377344;XM_005377345;XM_005377349;XM_005377350;XM_005377351;XM_013510571 XP_005377401;XP_005377402;XP_005377406;XP_005377407;XP_005377408;XP_013366025 protein-coding ENSCLAG00000007911 NW_004955410 21245562 21932023 + 8702834 LOC102026603 uncharacterized LOC102026603 NW_004955455 15424473 15437401 - 102026603 MODEL AGCD01046107;GBDJ01385206;XR_262862 ncrna 8702839 Tbl2 transducin beta like 2 ENCODES a protein that exhibits phosphoprotein binding (ortholog); protein kinase binding (ortholog); translation initiation factor binding (ortholog); INVOLVED IN cellular response to glucose starvation (ortholog); cellular response to hypoxia (ortholog); endoplasmic reticulum unfolded protein response (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); COVID-19 (ortholog); FOUND IN endoplasmic reticulum (ortholog) NW_004955456 14128847 14134314 + 9068941 102027612 A0A8C2VUM2 MODEL AGCD01046634;GBDF01044026;XM_005396782 XP_005396839 transducin (beta)-like 2;transducin beta-like protein 2 APPROVED protein-coding ENSCLAG00000013573 NW_004955456 14128188 14134314 + 8702850 LOC102029415 oocyte zinc finger protein XlCOF6-like NW_004955499 218603 226070 - 102029415 A0A8C2UF52 MODEL AGCD01063201;GBDF01248845;XM_013505560 XP_013361014 APPROVED protein-coding ENSCLAG00000000042 8702851 LOC102004199 trace amine-associated receptor 9 NW_004955436 13004804 13005842 + 9068941 102004199 A0A8C2VAB7 MODEL AGCD01033849;XM_005415376 XP_005415433 Taar9 trace amine associated receptor 9 APPROVED protein-coding ENSCLAG00000008728 NW_004955436 13004804 13005842 + 8702855 LOC102004259 phosphoacetylglucosamine mutase pseudogene NW_004955465 13182009 13183562 + 102004259 MODEL AGCD01050592 APPROVED pseudo 8702856 Znf750 zinc finger protein 750 ENCODES a protein that exhibits DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); promoter-specific chromatin binding (ortholog); INVOLVED IN epidermis development (ortholog); negative regulation of epithelial to mesenchymal transition (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM (ortholog); genetic disease (ortholog); Seborrhea-Like Dermatitis with Psoriasiform Elements (ortholog); FOUND IN nucleus (ortholog) NW_004955506 352616 360802 + 9068941;7240710 102004503 A0A8C2UW58 MODEL AGCD01065218;GBBH01214381;XM_005407180 XP_005407237 protein-coding ENSCLAG00000004435 NW_004955506 352552 363003 + 8702863 Garnl3 GTPase activating Rap/RanGAP domain like 3 ASSOCIATED WITH developmental and epileptic encephalopathy (ortholog); developmental and epileptic encephalopathy 31 (ortholog); early infantile epileptic encephalopathy (ortholog) NW_004955419 1190059 1332553 - 9068941 102004710 A0A8C2VWB5;A0A8C2VYU3;A0A8C2W0S8 MODEL AGCD01019644;AGCD01019645;AGCD01019646;GBDF01256859;GBDI01309723;XM_005382431 XP_005382488 GTPase activating Rap/RanGAP domain-like 3;GTPase-activating Rap/Ran-GAP domain-like protein 3 APPROVED protein-coding ENSCLAG00000014036 NW_004955419 1190344 1332553 - 8702923 Ss18l1 SS18L1 subunit of BAF chromatin remodeling complex INVOLVED IN dendrite development (ortholog); positive regulation of dendrite morphogenesis (ortholog); positive regulation of DNA-templated transcription (ortholog); ASSOCIATED WITH amyotrophic lateral sclerosis (ortholog); genetic disease (ortholog); FOUND IN condensed chromosome, centromeric region (ortholog); cytosol (ortholog); kinetochore (ortholog) NW_004955528 1849457 1881138 - 9068941 102004749 A0A8C2USY9 MODEL AGCD01069574;GBCB01004872;XM_005410035;XM_005410036;XM_005410037;XM_013507508;XM_013507509;XM_013507510;XR_264698 XP_005410092;XP_005410093;XP_005410094;XP_013362962;XP_013362963;XP_013362964 SS18L1, nBAF chromatin remodeling complex subunit;calcium-responsive transactivator;synovial sarcoma translocation gene on chromosome 18-like 1 APPROVED protein-coding ENSCLAG00000003078 NW_004955528 1849462 1870872 - 8702945 LOC102005316 NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial pseudogene NW_004955445 11834175 11839386 - 102005316 MODEL AGCD01039717;XM_005392425 APPROVED pseudo 8702957 Arpc1a actin related protein 2/3 complex subunit 1A PARTICIPATES IN insulin responsive facilitative sugar transporter mediated glucose transport pathway; Rab family mediated signaling pathway; ASSOCIATED WITH genetic disease (ortholog); pancreatic cancer (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN muscle cell projection membrane (ortholog) NW_004955460 15022663 15050955 + 9068941 102006751 A0A8C2V5H1;A0A8C2V7S8 MODEL AGCD01048767;GBDF01050144;XM_005397933 XP_005397990 actin related protein 2/3 complex, subunit 1A, 41kDa;actin-related protein 2/3 complex subunit 1A APPROVED protein-coding ENSCLAG00000006964 NW_004955460 15023221 15051115 + 8702971 Tmem120a transmembrane protein 120A ENCODES a protein that exhibits monoatomic ion channel activity (ortholog); INVOLVED IN detection of mechanical stimulus involved in sensory perception of pain (ortholog); fat cell differentiation (ortholog); monoatomic ion transmembrane transport (ortholog); ASSOCIATED WITH Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB (ortholog); cytochrome P450 oxidoreductase deficiency (ortholog); genetic disease (ortholog); FOUND IN plasma membrane (ortholog) NW_004955456 14748666 14754270 - 9068941 102007195 A0A8C2V3Y1 MODEL AGCD01046650;GBDK01090011;XM_005396805 XP_005396862 protein-coding ENSCLAG00000005891 NW_004955456 14747621 14754270 - 8702991 LOC102007924 olfactory receptor 5B12-like NW_004955511 3402858 3403802 + 102007924 A0A8C2WCP6 MODEL AGCD01066460;XM_005408265 XP_005408322 protein-coding ENSCLAG00000017573 8702994 Abcc12 ATP binding cassette subfamily C member 12 ASSOCIATED WITH bone marrow disease (ortholog); Drug-Related Side Effects and Adverse Reactions (ortholog); genetic disease (ortholog); FOUND IN endoplasmic reticulum (ortholog) NW_004955474 7166148 7238013 + 9068941 102008402 A0A8C2V923 MODEL AGCD01054515;AGCD01054516;GBDF01120114;XM_005401403;XM_005401404;XM_005401405;XM_005401406 XP_005401460;XP_005401461;XP_005401462;XP_005401463 ATP-binding cassette, sub-family C (CFTR/MRP), member 12;multidrug resistance-associated protein 9 APPROVED protein-coding ENSCLAG00000006887 NW_004955474 7166150 7238033 + 8703039 Numbl NUMB like endocytic adaptor protein INVOLVED IN adherens junction organization (ortholog); axonogenesis (ortholog); cytokine-mediated signaling pathway (ortholog); ASSOCIATED WITH Carpenter Syndrome 2 (ortholog); congenital hypoplastic anemia (ortholog); craniosynostosis (ortholog); FOUND IN cytoplasm (ortholog); glutamatergic synapse (ortholog) NW_004955578 636298 661566 + 9068941 102009899 A0A8C2UGB4;A0A8C2UGB9;A0A8C2UL73 MODEL AGCD01075490;AGCD01075491;GBBH01019159;XM_005414036;XM_005414037 XP_005414093;XP_005414094 numb homolog (Drosophila)-like APPROVED protein-coding ENSCLAG00000000433 NW_004955578 636282 661566 + 8703055 Polr1h RNA polymerase I subunit H PARTICIPATES IN RNA polymerase I transcription pathway; ASSOCIATED WITH Experimental Neoplasms (ortholog); megacolon (ortholog); Stomach Neoplasms (ortholog) NW_004955583 191252 195563 + 9068941 102010006 A0A8C2UT06 MODEL AGCD01075801;AGCD01075802;GBDF01080016;XM_005414292;XM_005414293 XP_005414349;XP_005414350 Znrd1 DNA-directed RNA polymerase I subunit RPA12;zinc ribbon domain containing 1 APPROVED protein-coding ENSCLAG00000003830 NW_004955583 191564 195358 + 8703074 Spmip9 sperm microtubule inner protein 9 ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog) NW_004955424 296514 305141 - 9068941 102011332 A0A8C2VDN2 MODEL AGCD01024170;AGCD01024171;GBDF01007131;XM_005385378;XM_005385379;XM_013514595;XM_013514596 XP_005385435;XP_005385436;XP_013370049;XP_013370050 Tex37 testis expressed 37 APPROVED protein-coding ENSCLAG00000008169 NW_004955424 295268 304328 - 8703091 Tmem143 transmembrane protein 143 INVOLVED IN hematopoietic progenitor cell differentiation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN mitochondrion (ortholog) NW_004955559 2097010 2116027 + 9068941 102012135 A0A8C2UX03;A0A8C2V2A8 MODEL AGCD01073691;GBCB01041014;XM_005412958 XP_005413015 protein-coding ENSCLAG00000004634 NW_004955559 2096373 2116021 + 8703103 Htr7 5-hydroxytryptamine receptor 7 ENCODES a protein that exhibits G protein-coupled serotonin receptor activity (ortholog); neurotransmitter receptor activity (ortholog); INVOLVED IN adenylate cyclase-activating serotonin receptor signaling pathway (ortholog); behavioral response to pain (ortholog); detection of mechanical stimulus involved in sensory perception of pain (ortholog); PARTICIPATES IN serotonin signaling pathway via receptors engaging G alphas protein family; ASSOCIATED WITH alcohol use disorder (ortholog); amnestic disorder (ortholog); anxiety disorder (ortholog); FOUND IN axon terminus (ortholog); dendrite (ortholog); neuronal cell body (ortholog) NW_004955425 2321420 2420420 + 9068941 102012876 A0A8C2YQU0 MODEL AGCD01025258;AGCD01025259;AGCD01025260;AGCD01025261;AGCD01025262;AGCD01025263;GBDF01050691;GBDF01050693;XM_005385841;XM_005385842;XM_005385844 XP_005385898;XP_005385899;XP_005385901 5-hydroxytryptamine (serotonin) receptor 7, adenylate cyclase-coupled APPROVED protein-coding ENSCLAG00000011360 NW_004955425 2321420 2420530 + 8703124 Crtc3 CREB regulated transcription coactivator 3 INVOLVED IN energy homeostasis (ortholog); lipid catabolic process (ortholog); macrophage activation (ortholog); ASSOCIATED WITH Bloom syndrome (ortholog); colorectal cancer (ortholog); D-2-hydroxyglutaric aciduria 2 (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955416 14672291 14768879 + 9068941 102013291 A0A8C2VHR9 MODEL AGCD01017282;AGCD01017283;GBBH01006313;GBDI01182296;XM_013512506 XP_013367960 CREB-regulated transcription coactivator 3 protein-coding ENSCLAG00000010334 NW_004955416 14672291 14765893 + 8703142 Ubxn2b UBX domain protein 2B INVOLVED IN establishment of mitotic spindle orientation (ortholog); negative regulation of protein localization to centrosome (ortholog); positive regulation of mitotic centrosome separation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN spindle pole centrosome (ortholog) NW_004955454 16929816 16978706 + 9068941 102015372 A0A8C2VJG8 MODEL AGCD01045536;AGCD01045537;AGCD01045538;AGCD01045539;AGCD01045540;GBDK01404414;XM_005396089;XM_005396090;XM_005396092;XM_013520208;XM_013520209 XP_005396146;XP_005396147;XP_005396149;XP_013375662;XP_013375663 UBX domain-containing protein 2B protein-coding ENSCLAG00000011369 NW_004955454 16929917 16956588 + 8703164 Psmb6 proteasome 20S subunit beta 6 ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); mitochondrion (ortholog) NW_004955467 10220435 10222470 + 9068941 102015495 A0A8C2YQX4 MODEL AGCD01051555;GBDJ01010777;XM_005399601 XP_005399658 proteasome (prosome, macropain) subunit, beta type, 6;proteasome subunit beta 6;proteasome subunit beta type-6 APPROVED protein-coding ENSCLAG00000011492 NW_004955467 10220285 10222659 + 8703174 Cmtm4 CKLF like MARVEL transmembrane domain containing 4 ASSOCIATED WITH autosomal dominant dyskeratosis congenita 6 (ortholog); cataract 5 multiple types (ortholog); genetic disease (ortholog) NW_004955433 23189925 23245722 - 9068941 102016191 A0A8C2V259 MODEL AGCD01031955;GBBH01142816;XM_013516195 XP_013371649 CKLF-like MARVEL transmembrane domain containing 4;CKLF-like MARVEL transmembrane domain-containing protein 4 APPROVED protein-coding ENSCLAG00000006181 NW_004955433 23189925 23245728 - 8703183 LOC102016810 uncharacterized LOC102016810 NW_004955482 9604236 9611654 + 102016810 MODEL AGCD01057574;GBDF01128151;XR_001230966;XR_001230967 ncrna 8703187 LOC102017830 WAP four-disulfide core domain protein 18-like NW_004955451 195886 200393 + 102017830 A0A8C2VN69 MODEL AGCD01042928;GBCC01009398;XM_005393904;XM_005393905 XP_005393961;XP_005393962 protein-coding ENSCLAG00000012435 8703196 Lypd6b LY6/PLAUR domain containing 6B ENCODES a protein that exhibits acetylcholine receptor regulator activity (ortholog); ASSOCIATED WITH genetic disease (ortholog) NW_004955440 14865736 15028655 + 9068941 102018030 A0A8C2UST8 MODEL AGCD01036481;AGCD01036482;AGCD01036483;AGCD01036484;GBBH01114673;XM_013517509 XP_013372963 ly6/PLAUR domain-containing protein 6B protein-coding ENSCLAG00000002017 NW_004955440 15014264 15027648 + 8703205 Ilrun inflammation and lipid regulator with UBA-like and NBR1-like domains INVOLVED IN negative regulation of defense response to virus (ortholog); negative regulation of DNA binding (ortholog); negative regulation of protein localization to nucleus (ortholog); ASSOCIATED WITH JMP syndrome (ortholog); FOUND IN centrosome (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955437 2697998 2769998 - 9068941 102018326 A0A8C2VGZ3;A0A8C2VK95 MODEL AGCD01034284;AGCD01034285;GBDF01007654;GBDK01126877;XM_005389532 XP_005389589 LOC102018326 chromosome unknown open reading frame, human C6orf106;uncharacterized protein C6orf106 homolog APPROVED protein-coding ENSCLAG00000010022 NW_004955437 2694945 2769998 - 8703224 LOC102018739 non-histone chromosomal protein HMG-14 pseudogene NW_004955422 17353812 17357226 + 102018739 MODEL AGCD01022920;AGCD01022921 APPROVED pseudo 8703225 Alkbh1 alkB homolog 1, histone H2A dioxygenase ENCODES a protein that exhibits 2-oxoglutarate-dependent dioxygenase activity (ortholog); class I DNA-(apurinic or apyrimidinic site) endonuclease activity (ortholog); ferrous iron binding (ortholog); INVOLVED IN DNA dealkylation involved in DNA repair (ortholog); DNA demethylation (ortholog); DNA repair (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN endoplasmic reticulum (ortholog); mitochondrion (ortholog); nucleoplasm (ortholog) NW_004955438 1531114 1556483 - 9068941 102019107 A0A8C2VYD7 MODEL AGCD01034986;GBDK01361284;XM_005390212;XM_013517181 XP_005390269;XP_013372635 alkB, alkylation repair homolog 1;alkylated DNA repair protein alkB homolog 1 APPROVED protein-coding ENSCLAG00000014129 NW_004955438 1531114 1556481 - 8703235 Sall1 spalt like transcription factor 1 ENCODES a protein that exhibits beta-catenin binding (ortholog); chromatin binding (ortholog); cis-regulatory region sequence-specific DNA binding (ortholog); INVOLVED IN adrenal gland development (ortholog); branching involved in ureteric bud morphogenesis (ortholog); embryonic digestive tract development (ortholog); ASSOCIATED WITH CAKUT (ortholog); chronic kidney disease (ortholog); Congenital Abnormalities (ortholog); FOUND IN chromocenter (ortholog); cytoplasm (ortholog); heterochromatin (ortholog) NW_004955433 9146074 9161171 - 9068941;7240710 102019424 A0A8C2V8N4 MODEL AGCD01031610;GBDI01327095;XM_005388281 XP_005388338 sal-like 1;sal-like protein 1;spalt-like transcription factor 1 APPROVED protein-coding ENSCLAG00000006380 NW_004955433 9144748 9161171 - 8703253 LOC102020141 general transcription factor IIH subunit 1 pseudogene NW_004955501 6162583 6163797 + 102020141 MODEL AGCD01064181 APPROVED pseudo 8703254 LOC102020282 serine/threonine-protein kinase N2-like NW_004955529 1397769 1402834 + 102020282 MODEL AGCD01069683 pseudo 8703255 Gprasp1 G protein-coupled receptor associated sorting protein 1 INVOLVED IN endosome to lysosome transport (ortholog); G protein-coupled receptor catabolic process (ortholog); ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN cytosol (ortholog) NW_004955548 132373 137817 + 9068941 102020290 A0A8C2WA81 MODEL AGCD01072319;GBDI01177597;XM_005411968 XP_005412025 G-protein coupled receptor-associated sorting protein 1 protein-coding ENSCLAG00000017431 NW_004955548 133425 137468 + 8703262 CUNH1orf127 chromosome unknown C1orf127 homolog INVOLVED IN determination of left/right symmetry (ortholog); heart development (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease type 2 (ortholog); chromosome 1p36 deletion syndrome (ortholog); Familial Atrial Fibrillation 6 (ortholog) NW_004955486 2691850 2717340 + 9068941 102020345 A0A8C2UZK7;A0A8C2V0W5;A0A8C2V3A9 MODEL AGCD01059006;GBDF01112771;XM_005404305 XP_005404362 LOC102020345 chromosome unknown open reading frame, human C1orf127;uncharacterized protein C1orf127 homolog APPROVED protein-coding ENSCLAG00000005018 NW_004955486 2674528 2717568 + 8703278 LOC102020472 olfactory receptor 5W2-like NW_004955511 5001133 5002068 + 102020472 MODEL AGCD01066542;XM_005408082 XP_005408139 protein-coding 8703281 Slc7a4 solute carrier family 7 member 4 ASSOCIATED WITH autistic disorder (ortholog); chromosome 22q11.2 deletion syndrome, distal (ortholog); chromosome 22q11.2 microduplication syndrome (ortholog) NW_004955442 19258901 19263317 + 9068941 102020617 A0A8C2VTI0;A0A8C2W0X3 MODEL AGCD01038045;GBDF01126826;XM_005391817;XM_005391818 XP_005391874;XP_005391875 cationic amino acid transporter 4;solute carrier family 7, member 4 APPROVED protein-coding ENSCLAG00000013920 NW_004955442 19258796 19263317 + 8703293 Rgs7bp regulator of G protein signaling 7 binding protein INVOLVED IN G protein-coupled receptor signaling pathway (ortholog); regulation of postsynaptic membrane potential (ortholog); PARTICIPATES IN dopamine signaling pathway via D1 family of receptors; dopamine signaling pathway via D2 family of receptors; G protein mediated signaling pathway via Galphai family; ASSOCIATED WITH genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN axon (ortholog); cytoplasm (ortholog); dendritic shaft (ortholog) NW_004955446 4354689 4451269 - 9068941 102022648 A0A8C2YKF1 MODEL AGCD01040034;AGCD01040035;AGCD01040036;AGCD01040037;GBDJ01301600;XM_005392636 XP_005392693 APPROVED protein-coding ENSCLAG00000003654 NW_004955446 4359906 4451315 - 8703303 Idh2 isocitrate dehydrogenase (NADP(+)) 2 ENCODES a protein that exhibits isocitrate dehydrogenase (NADP+) activity (ortholog); INVOLVED IN NADP biosynthetic process (ortholog); negative regulation of glial cell migration (ortholog); negative regulation of glial cell proliferation (ortholog); ASSOCIATED WITH 2-hydroxyglutaric aciduria (ortholog); acute myeloid leukemia (ortholog); acute myocardial infarction (ortholog); FOUND IN cytosol (ortholog); mitochondrion (ortholog); peroxisome (ortholog) NW_004955416 15197611 15212919 + 9068941;7240710 102023150 A0A8C2YSP4 MODEL AGCD01017308;AGCD01017309;GBCQ01003629;XM_005381533;XM_005381534 XP_005381590;XP_005381591 isocitrate dehydrogenase (NADP(+)) 2, mitochondrial;isocitrate dehydrogenase 2 (NADP+), mitochondrial;isocitrate dehydrogenase [NADP], mitochondrial APPROVED protein-coding ENSCLAG00000014007 NW_004955416 15197366 15223363 + 8703320 Srsf4 serine and arginine rich splicing factor 4 ENCODES a protein that exhibits sequence-specific mRNA binding (ortholog); INVOLVED IN hematopoietic progenitor cell differentiation (ortholog); negative regulation of mRNA splicing, via spliceosome (ortholog); response to insulin (ortholog); PARTICIPATES IN spliceosome pathway; ASSOCIATED WITH acute myeloid leukemia (ortholog); clear cell renal cell carcinoma (ortholog); colon adenocarcinoma (ortholog); FOUND IN nuclear speck (ortholog) NW_004955452 8143850 8174830 - 9068941 102023221 A0A8C2VGN3 MODEL AGCD01044211;GBDJ01016011;XM_005394977;XM_013519479;XM_013519480 XP_005395034;XP_013374933;XP_013374934 serine/arginine-rich splicing factor 4 APPROVED protein-coding ENSCLAG00000009008 NW_004955452 8142500 8174869 - 8703342 Haus2 HAUS augmin like complex subunit 2 INVOLVED IN centrosome cycle (ortholog); spindle assembly (ortholog); ASSOCIATED WITH Bloom syndrome (ortholog); colorectal cancer (ortholog); genetic disease (ortholog); FOUND IN centrosome (ortholog); HAUS complex (ortholog); mitotic spindle microtubule (ortholog) NW_004955416 9237713 9252920 + 9068941 102023691 A0A8C2VL09 MODEL AGCD01017081;GBDF01005291;XM_005381346 XP_005381403 HAUS augmin-like complex subunit 2;HAUS augmin-like complex, subunit 2 APPROVED protein-coding ENSCLAG00000011815 NW_004955416 9237731 9252561 + 8703352 LOC102023819 melanoma-associated antigen 10-like NW_004955498 4467730 4468548 - 102023819 MODEL AGCD01063000 pseudo 8703353 LOC102023989 ubiquitin-conjugating enzyme E2 variant 2-like NW_004955462 10852436 10854575 + 102023989 MODEL AGCD01049373;XM_005398313 XP_005398370 protein-coding 8703358 LOC102025031 prostaglandin F synthase 1-like NW_004955429 664039 699169 + 102025031 A0A8C2VGZ4;A0A8C2VJ38;A0A8C2VKM7;A0A8C2VLP9 MODEL AGCD01028369;AGCD01028370;AGCD01028371;AGCD01028372;AGCD01028373;GBDF01207576;XM_005386862;XM_005386863;XM_005386864 XP_005386919;XP_005386920;XP_005386921 protein-coding ENSCLAG00000010130 8703376 LOC102026108 uncharacterized LOC102026108 NW_004955416 24569709 24571723 + 102026108 MODEL AGCD01017570;GBDF01210261;XR_001233280;XR_001233281 ncrna 8703384 LOC102026610 uncharacterized LOC102026610 NW_004955409 25163737 25192309 + 102026610 MODEL AGCD01010107;AGCD01010108;GBDF01177040;XR_259795 ncrna 8703390 LOC102028320 tetraspanin-11 NW_004955429 18777421 18822829 - 102028320 A0A8C2VFA9 MODEL AGCD01028921;AGCD01028922;AGCD01028923;GBCQ01010048;GBDJ01355119;XM_005387138;XM_005387139;XM_005387140;XM_013515458;XR_001234511;XR_261360 XP_005387195;XP_005387196;XP_005387197;XP_013370912 APPROVED protein-coding ENSCLAG00000009091 8703413 Acad10 acyl-CoA dehydrogenase family member 10 ASSOCIATED WITH genetic disease (ortholog) NW_004955482 8282530 8327511 + 9068941 102028967 A0A8C2VRE8 MODEL AGCD01057515;GBDF01160099;XM_005403170;XM_013503680;XM_013503681;XM_013503682;XM_013503683 XP_005403227;XP_013359134;XP_013359135;XP_013359136;XP_013359137 acyl-CoA dehydrogenase family, member 10 APPROVED protein-coding ENSCLAG00000012691 NW_004955482 8288032 8327161 + 8703441 Mtmr2 myotubularin related protein 2 ENCODES a protein that exhibits identical protein binding (ortholog); phosphatidylinositol phosphate phosphatase activity (ortholog); phosphatidylinositol-3,5-bisphosphate 3-phosphatase activity (ortholog); INVOLVED IN dendritic spine maintenance (ortholog); dephosphorylation (ortholog); myelin assembly (ortholog); ASSOCIATED WITH ataxia telangiectasia (ortholog); Charcot-Marie-Tooth disease (ortholog); Charcot-Marie-Tooth disease type 4 (ortholog); FOUND IN axon (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955412 693743 764377 - 9068941;7240710 102029489 A0A8C2VKU0;A0A8C2VR76 MODEL AGCD01012494;AGCD01012495;AGCD01012496;GBCE01135603;GBDF01008769;XM_005377950 XP_005378007 myotubularin-related protein 2 protein-coding ENSCLAG00000011747 NW_004955412 693743 750154 - 8703468 Ercc6 ERCC excision repair 6, chromatin remodeling factor ENCODES a protein that exhibits ATP binding (ortholog); ATP-dependent activity, acting on DNA (ortholog); ATP-dependent chromatin remodeler activity (ortholog); INVOLVED IN base-excision repair (ortholog); DNA damage checkpoint signaling (ortholog); DNA damage response (ortholog); PARTICIPATES IN altered nucleotide excision repair pathway; nucleotide excision repair pathway; ASSOCIATED WITH age related macular degeneration 5 (ortholog); arthrogryposis multiplex congenita (ortholog); cataract (ortholog); FOUND IN B-WICH complex (ortholog); nuclear body (ortholog); nucleolus (ortholog) NW_004955556 745175 812215 + 9068941;7240710 102029672 A0A8C2ULD8 MODEL AGCD01073179;GBCE01126926;XM_005412569 XP_005412626 DNA excision repair protein ERCC-6;excision repair cross-complementation group 6;excision repair cross-complementing rodent repair deficiency, complementation group 6 APPROVED protein-coding ENSCLAG00000000850 NW_004955556 748231 813133 + 8703493 Eps15l1 epidermal growth factor receptor pathway substrate 15 like 1 ASSOCIATED WITH genetic disease (ortholog); FOUND IN clathrin coat of coated pit (ortholog) NW_004955524 1264035 1309394 + 9068941 102029784 A0A8C2UUD5;A0A8C2UZE9 MODEL AGCD01068741;AGCD01068742;GBCE01030448;XM_013507228;XM_013507229;XM_013507230;XM_013507231 XP_013362682;XP_013362683;XP_013362684;XP_013362685 epidermal growth factor receptor pathway substrate 15-like 1;epidermal growth factor receptor substrate 15-like 1 APPROVED protein-coding ENSCLAG00000003824 NW_004955524 1272565 1309294 + 8703523 Angel1 angel homolog 1 ENCODES a protein that exhibits eukaryotic initiation factor 4E binding (ortholog); protein domain specific binding (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); FOUND IN cis-Golgi network (ortholog); cytosol (ortholog); endoplasmic reticulum (ortholog) NW_004955438 776213 805020 - 9068941 102004006 A0A8C2VPH0 MODEL AGCD01034963;GBDF01001997;XM_005390162;XM_005390163;XM_005390164;XM_005390165;XM_005390166;XM_013517174 XP_005390219;XP_005390220;XP_005390221;XP_005390222;XP_005390223;XP_013372628 angel homolog 1 (Drosophila) APPROVED protein-coding ENSCLAG00000012161 NW_004955438 776213 797948 - 8703550 LOC102005651 uncharacterized LOC102005651 NW_004955449 5758290 5762221 + 102005651 MODEL AGCD01041942;XR_262490 ncrna 8703555 Syf2 SYF2 pre-mRNA splicing factor INVOLVED IN embryonic organ development (ortholog); gastrulation (ortholog); in utero embryonic development (ortholog); PARTICIPATES IN spliceosome pathway; ASSOCIATED WITH encephalitis (ortholog); genetic disease (ortholog); FOUND IN catalytic step 2 spliceosome (ortholog); nuclear speck (ortholog); nucleus (ortholog) NW_004955452 4850049 4856647 - 9068941 102005883 A0A8C2V9P9 MODEL AGCD01043996;GBCB01007303;XM_005394818 XP_005394875 SYF2 homolog, RNA splicing factor;SYF2 pre-mRNA-splicing factor;pre-mRNA-splicing factor SYF2 APPROVED protein-coding ENSCLAG00000008474 NW_004955452 4848659 4857114 - 8703566 LOC102006253 elongation factor 1-alpha 1-like NW_004955420 25364489 25376572 + 102006253 MODEL AGCD01021353;AGCD01021354 pseudo 8703567 Armc6 armadillo repeat containing 6 INVOLVED IN hematopoietic progenitor cell differentiation (ortholog); ASSOCIATED WITH genetic disease (ortholog); Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 (ortholog); progressive myoclonus epilepsy 8 (ortholog); FOUND IN cytosol (ortholog) NW_004955524 2695720 2709163 - 9068941 102006492 A0A8C2VFD5 MODEL AGCD01068829;GBBH01226770;XM_005409610;XM_005409611 XP_005409667;XP_005409668 armadillo repeat-containing protein 6 protein-coding ENSCLAG00000008215 NW_004955524 2692758 2709262 - 8703582 LOC102006777 olfactory receptor 2G6 NW_004955418 29618805 29621581 - 102006777 A0A8C2YV45 MODEL AGCD01019475;XM_005382357 XP_005382414 APPROVED protein-coding ENSCLAG00000017632 NW_004955418 29620628 29621581 - 8703585 Aftph aftiphilin ENCODES a protein that exhibits clathrin binding (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN AP-1 adaptor complex (ortholog); cytosol (ortholog); Golgi apparatus (ortholog) NW_004955424 19835911 19899878 - 9068941 102007915 A0A8C2VQW9;A0A8C2VTN4 MODEL AGCD01024837;AGCD01024838;GBCQ01008748;XM_005385699;XM_005385701 XP_005385756;XP_005385758 protein-coding ENSCLAG00000012032 NW_004955424 19834702 19877751 - 8703607 LOC102007969 maestro heat-like repeat-containing protein family member 7 NW_004955406 37107660 37135900 + 102007969 A0A8C2YR03 MODEL AGCD01006571;GBDF01021853;XM_013522084 XP_013377538 APPROVED protein-coding ENSCLAG00000011608 8703608 Sox15 SRY-box transcription factor 15 ENCODES a protein that exhibits chromatin binding (ortholog); DNA binding (ortholog); DNA-binding transcription factor activity, RNA polymerase II-specific (ortholog); INVOLVED IN cell differentiation (ortholog); myoblast development (ortholog); negative regulation of striated muscle tissue development (ortholog); ASSOCIATED WITH atrial fibrillation (ortholog); common variable immunodeficiency (ortholog); congenital disorder of glycosylation If (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog); transcription regulator complex (ortholog) NW_004955467 9333620 9335498 + 9068941 102008611 A0A8C2V776 MODEL AGCD01051497;GBDI01384127;XM_005399474;XM_005399475 XP_005399531;XP_005399532 SRY (sex determining region Y)-box 15;SRY-box 15 APPROVED protein-coding ENSCLAG00000007796 NW_004955467 9333643 9335498 + 8703620 Plin5 perilipin 5 ENCODES a protein that exhibits identical protein binding (ortholog); lipase binding (ortholog); INVOLVED IN lipid droplet organization (ortholog); lipid storage (ortholog); mitochondrion localization (ortholog); ASSOCIATED WITH amenorrhea (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955495 4406590 4414783 + 9068941 102008639 A0A8C2W2N6 MODEL AGCD01061922;GBCB01043643;XM_013505191;XM_013505192 XP_013360645;XP_013360646 Plin4 perilipin 4;perilipin-5 APPROVED protein-coding ENSCLAG00000015835 NW_004955495 4407246 4416848 + 8703642 Hexd hexosaminidase D ENCODES a protein that exhibits beta-N-acetylhexosaminidase activity (ortholog); hexosaminidase activity (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); extracellular vesicle (ortholog); nucleus (ortholog) NW_004955506 702828 719733 - 9068941 102008874 A0A8C2V9L1;A0A8C2VBW5 MODEL AGCD01065234;GBDJ01234157;XM_005407196;XM_013506081;XM_013506082;XM_013506083;XM_013506084 XP_005407253;XP_013361535;XP_013361536;XP_013361537;XP_013361538 Hexdc hexosaminidase (glycosyl hydrolase family 20, catalytic domain) containing APPROVED protein-coding ENSCLAG00000008098 NW_004955506 702919 718572 - 8703664 Ckm creatine kinase, M-type ENCODES a protein that exhibits creatine kinase activity (ortholog); INVOLVED IN phosphocreatine biosynthetic process (ortholog); PARTICIPATES IN creatine metabolic pathway; ASSOCIATED WITH Acute Coronary Syndrome (ortholog); Colonic Neoplasms (ortholog); genetic disease (ortholog); FOUND IN extracellular space (ortholog) NW_004955555 2318072 2330733 - 9068941 102009326 A0A8C2YJG3 MODEL AGCD01073144;AGCD01073145;GBDJ01231000;XM_005412510 XP_005412567 creatine kinase M-type;creatine kinase, muscle APPROVED protein-coding ENSCLAG00000002240 NW_004955555 2318072 2336811 - 8703676 Hcfc2 host cell factor C2 INVOLVED IN negative regulation of transcription by RNA polymerase II (ortholog); PARTICIPATES IN RNA polymerase II transcription initiation pathway; ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); MLL1 complex (ortholog) NW_004955405 38729700 38758398 + 9068941 102009455 A0A8C2VDC9;A0A8C2VIM8 MODEL AGCD01005484;AGCD01005485;GBDF01082212;XM_005374584;XM_005374585;XM_005374586;XM_013518889 XP_005374641;XP_005374642;XP_005374643;XP_013374343 host cell factor 2 protein-coding ENSCLAG00000009125 NW_004955405 38730054 38760115 + 8703700 Ptpn11 protein tyrosine phosphatase non-receptor type 11 ENCODES a protein that exhibits cadherin binding (ortholog); cell adhesion molecule binding (ortholog); D1 dopamine receptor binding (ortholog); INVOLVED IN atrioventricular canal development (ortholog); axonogenesis (ortholog); Bergmann glial cell differentiation (ortholog); PARTICIPATES IN epidermal growth factor/neuregulin signaling pathway; erythropoietin signaling pathway; fibroblast growth factor signaling pathway; ASSOCIATED WITH acute myeloid leukemia (ortholog); acute promyelocytic leukemia (ortholog); adenocarcinoma (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog); plasma membrane raft (ortholog) NW_004955482 8934734 9031230 + 9068941;7240710 102009502 A0A8C2YSZ3 MODEL AGCD01057558;AGCD01057559;AGCD01057560;GBDF01081705;XM_005403196;XM_005403197;XM_005403198;XM_013503715;XM_013503717 XP_005403253;XP_005403254;XP_005403255;XP_013359169;XP_013359171 tyrosine-protein phosphatase non-receptor type 11 APPROVED protein-coding ENSCLAG00000014414 NW_004955482 8934306 9035203 + 8703728 Rrbp1 ribosome binding protein 1 INVOLVED IN signal transduction (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN endoplasmic reticulum (ortholog); endoplasmic reticulum membrane (ortholog) NW_004955415 26601707 26634747 - 9068941 102010154 A0A8C2W4K7 MODEL AGCD01016600;AGCD01016601;GBBH01001406;XM_013512263 XP_013367717 ribosome-binding protein 1 protein-coding ENSCLAG00000017033 NW_004955415 26602123 26634726 - 8703756 Bche butyrylcholinesterase ENCODES a protein that exhibits acetylcholinesterase activity (ortholog); choline binding (ortholog); cholinesterase activity (ortholog); INVOLVED IN choline metabolic process (ortholog); learning (ortholog); negative regulation of cell population proliferation (ortholog); PARTICIPATES IN heroin pharmacodynamics pathway; heroin pharmacokinetics pathway; irinotecan pharmacodynamics pathway; ASSOCIATED WITH Acholinesterasemia (ortholog); Alzheimer's disease (ortholog); amnestic disorder (ortholog); FOUND IN endoplasmic reticulum (ortholog); endoplasmic reticulum lumen (ortholog); extracellular space (ortholog) NW_004955448 15327374 15396827 - 9068941 102010751 A0A8C2YJ75;G3M684 MODEL AGCD01041663;AGCD01041664;GBDJ01278447;JN633046;XM_005393137;XM_005393138;XM_013518684 AEO94791;XP_005393194;XP_005393195;XP_013374138 cholinesterase protein-coding ENSCLAG00000001890 NW_004955448 15329273 15396970 - 8703767 LOC102010843 kallikrein-2-like NW_004955559 416199 433647 - 102010843 MODEL AGCD01073584;AGCD01073585;AGCD01073586;GBDJ01062263;GBDJ01062266;XM_005412758 XP_005412815 protein-coding 8703787 LOC102011736 uncharacterized LOC102011736 NW_004955456 6662166 6678865 - 102011736 MODEL AGCD01046375;GBDF01041115;XR_001236334 ncrna 8703793 LOC102011867 josephin-1-like NW_004955417 14417553 14418271 + 102011867 MODEL AGCD01018204 pseudo 8703794 Shisa8 shisa family member 8 ASSOCIATED WITH adenylosuccinase lyase deficiency (ortholog); common variable immunodeficiency 4 (ortholog); genetic disease (ortholog) NW_004955413 27328632 27330304 - 9068941 102012751 A0A8C2W0S2 MODEL AGCD01014501;AGCD01014502;GBBH01127137;GBDI01328292;XM_013511364 XP_013366818 putative protein shisa-8 protein-coding ENSCLAG00000016102 8703803 Arl3 ADP ribosylation factor like GTPase 3 ENCODES a protein that exhibits GDP binding (ortholog); GTP binding (ortholog); GTPase activity (ortholog); INVOLVED IN cilium assembly (ortholog); Golgi to plasma membrane transport (ortholog); intraciliary transport (ortholog); ASSOCIATED WITH autosomal recessive polycystic kidney disease (ortholog); genetic disease (ortholog); JOUBERT SYNDROME 35 (ortholog); FOUND IN axoneme (ortholog); centrosome (ortholog); ciliary basal body (ortholog) NW_004955485 7739556 7772582 + 9068941 102013508 A0A8C2UM41 MODEL AGCD01058674;AGCD01058675;GBDK01131229;XM_005403829 XP_005403886 ADP-ribosylation factor-like 3;ADP-ribosylation factor-like protein 3 APPROVED protein-coding ENSCLAG00000001055 NW_004955485 7733211 7775687 + 8703813 Bmpr1b bone morphogenetic protein receptor type 1B ENCODES a protein that exhibits ATP binding (ortholog); BMP binding (ortholog); BMP receptor activity (ortholog); INVOLVED IN BMP signaling pathway (ortholog); bone development (ortholog); camera-type eye development (ortholog); PARTICIPATES IN Bone morphogenetic proteins signaling pathway; ASSOCIATED WITH acromesomelic dysplasia, Hunter-Thompson type (ortholog); acromesomelic dysplasia-3 (ortholog); asthma (ortholog); FOUND IN dendrite (ortholog); neuronal cell body (ortholog); plasma membrane (ortholog) NW_004955405 5408171 5784930 + 9068941;7240710 102013791 A0A8C2YPP2;A0A8C2YPP3 MODEL AGCD01004682;AGCD01004683;AGCD01004684;AGCD01004685;AGCD01004686;AGCD01004687;GBDI01326385;XM_013517414;XM_013517415;XM_013517416;XM_013517418;XM_013517428;XM_013517431;XM_013517434;XM_013517436;XM_013517437 XP_013372868;XP_013372869;XP_013372870;XP_013372872;XP_013372882;XP_013372885;XP_013372888;XP_013372890;XP_013372891 bone morphogenetic protein receptor type-1B;bone morphogenetic protein receptor, type IB APPROVED protein-coding ENSCLAG00000009761 NW_004955405 5700162 5787957 + 8703873 Dlc1 DLC1 Rho GTPase activating protein ENCODES a protein that exhibits GTPase activator activity (ortholog); phospholipase binding (ortholog); SH2 domain binding (ortholog); INVOLVED IN actin cytoskeleton organization (ortholog); activation of cysteine-type endopeptidase activity involved in apoptotic process (ortholog); activation of phospholipase C activity (ortholog); PARTICIPATES IN Rho/Rac/Cdc42 mediated signaling pathway; ASSOCIATED WITH amenorrhea (ortholog); colon carcinoma (ortholog); colorectal cancer (ortholog); FOUND IN actin filament (ortholog); caveola (ortholog); cortical actin cytoskeleton (ortholog) NW_004955463 3599415 3981187 + 9068941;7240710 102014429 A0A8C2UMH4;A0A8C2UQ55;A0A8C2USF3;A0A8C2UTH2 MODEL AGCD01049591;AGCD01049592;AGCD01049593;AGCD01049594;AGCD01049595;AGCD01049596;AGCD01049597;AGCD01049598;AGCD01049599;AGCD01049600;GBCE01115032;XM_005398346;XM_013521500;XM_013521501;XM_013521502 XP_005398403;XP_013376954;XP_013376955;XP_013376956 deleted in liver cancer 1;rho GTPase-activating protein 7 APPROVED protein-coding ENSCLAG00000002202 NW_004955463 3598985 3990849 + 8703909 LOC102014659 uncharacterized LOC102014659 NW_004955469 8587811 8588814 - 102014659 MODEL AGCD01052476;GBDF01187430;XR_263440 ncrna 8703913 Col20a1 collagen type XX alpha 1 chain ASSOCIATED WITH autosomal dominant nocturnal frontal lobe epilepsy (ortholog); benign familial infantile seizures 6 (ortholog); developmental and epileptic encephalopathy (ortholog) NW_004955528 847416 878741 - 9068941 102015343 A0A8C2URD6;A0A8C2UUS3 MODEL AGCD01069547;GBCB01080248;XM_013507451;XM_013507452;XM_013507453;XM_013507454;XM_013507455;XM_013507456;XM_013507457;XR_001231982 XP_013362905;XP_013362906;XP_013362907;XP_013362908;XP_013362909;XP_013362910;XP_013362911 collagen alpha-1(XX) chain;collagen, type XX, alpha 1 APPROVED protein-coding ENSCLAG00000002569 8703970 Sdf2l1 stromal cell derived factor 2 like 1 ENCODES a protein that exhibits ATPase binding (ortholog); misfolded protein binding (ortholog); protein-folding chaperone binding (ortholog); INVOLVED IN cellular response to misfolded protein (ortholog); chaperone cofactor-dependent protein refolding (ortholog); ER-associated misfolded protein catabolic process (ortholog); PARTICIPATES IN codeine and morphine pharmacodynamics pathway; codeine and morphine pharmacokinetics pathway; etoposide pharmacodynamics pathway; ASSOCIATED WITH chromosome 22q11.2 deletion syndrome, distal (ortholog); Crohn's disease (ortholog); DiGeorge syndrome (ortholog); FOUND IN endoplasmic reticulum (ortholog); endoplasmic reticulum chaperone complex (ortholog); membrane (ortholog) NW_004955442 17468302 17470296 - 9068941 102015353 A0A8C2VX76 MODEL AGCD01037955;GBCB01077176;XM_005391702 XP_005391759 stromal cell-derived factor 2-like 1;stromal cell-derived factor 2-like protein 1 APPROVED protein-coding ENSCLAG00000015053 NW_004955442 17468302 17470296 - 8703977 LOC102015560 RNA-binding protein 7 pseudogene NW_004955434 16063246 16064603 - 102015560 MODEL AGCD01032511 APPROVED pseudo 8703978 Znf658 zinc finger protein 658 ENCODES a protein that exhibits transcription cis-regulatory region binding (ortholog); INVOLVED IN cellular response to zinc ion (ortholog); negative regulation of DNA-templated transcription (ortholog); ribosome biogenesis (ortholog); ASSOCIATED WITH genetic disease (ortholog); skin disease (ortholog) NW_004955422 24194458 24218504 + 9068941 102015733 MODEL AGCD01023216;AGCD01023217;GBDF01179520;XM_005384714;XM_013514253;XM_013514254;XM_013514255 XP_005384771;XP_013369707;XP_013369708;XP_013369709 protein-coding 8703987 LOC102016661 kelch-like protein 12 NW_004955452 13484193 13486084 - 102016661 MODEL AGCD01044421 APPROVED pseudo 8703988 Rangap1 Ran GTPase activating protein 1 ENCODES a protein that exhibits GTPase activator activity (ortholog); RNA binding (ortholog); small GTPase binding (ortholog); INVOLVED IN activation of GTPase activity (ortholog); cellular response to peptide hormone stimulus (ortholog); cellular response to vasopressin (ortholog); PARTICIPATES IN CRM1 export pathway; ASSOCIATED WITH adenylosuccinase lyase deficiency (ortholog); Carotid Artery Injuries (ortholog); common variable immunodeficiency 4 (ortholog); FOUND IN aggresome (ortholog); axon cytoplasm (ortholog); cytoplasm (ortholog) NW_004955413 26869487 26894192 - 9068941 102016691 A0A8C2W4W8 MODEL AGCD01014485;GBDJ01275353;XM_005379343;XM_005379344;XM_013511354 XP_005379400;XP_005379401;XP_013366808 ran GTPase-activating protein 1 protein-coding ENSCLAG00000017330 NW_004955413 26867812 26890284 - 8704011 LOC102016946 DNA polymerase epsilon subunit 3 pseudogene NW_004955521 4203300 4203697 + 102016946 MODEL AGCD01068255 APPROVED pseudo 8704012 Celf3 CUGBP Elav-like family member 3 ENCODES a protein that exhibits 7SK snRNA binding (ortholog); RNA binding (ortholog); INVOLVED IN flagellated sperm motility (ortholog); ncRNA transcription (ortholog); nuclear body organization (ortholog); ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); immunodeficiency 42 (ortholog); FOUND IN cytoplasm (ortholog); nuclear body (ortholog); nucleus (ortholog) NW_004955589 700965 715684 + 9068941 102016965 A0A8C2UIR7;A0A8C2UJ16;A0A8C2YIA8;A0A8C2YIB3 MODEL AGCD01076181;GBBH01095116;XM_005414558;XM_005414559;XM_005414561;XM_005414562;XM_005414563;XM_005414565 XP_005414615;XP_005414616;XP_005414618;XP_005414619;XP_005414620;XP_005414622 CUGBP, Elav-like family member 3 APPROVED protein-coding ENSCLAG00000000586 NW_004955589 701767 713179 + 8704051 Nnat neuronatin INVOLVED IN establishment of localization in cell (ortholog); insulin secretion (ortholog); neuron differentiation (ortholog); ASSOCIATED WITH Aicardi-Goutieres Syndrome 5 (ortholog); focal epilepsy (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog) NW_004955445 19121164 19125514 - 9068941 102017518 A0A8C2VI43;A0A8C2VQ20 MODEL AGCD01039911;GBDI01278731;XM_005392555;XM_005392556;XM_013518350 XP_005392612;XP_005392613;XP_013373804 protein-coding ENSCLAG00000010875 NW_004955445 19121164 19125514 - 8704062 LOC102019544 40S ribosomal protein S6 pseudogene NW_004955568 1456206 1472192 + 102019544 MODEL AGCD01074545 APPROVED pseudo 8704063 Maged1 MAGE family member D1 ENCODES a protein that exhibits identical protein binding (ortholog); transcription coactivator activity (ortholog); INVOLVED IN circadian regulation of gene expression (ortholog); negative regulation of DNA-templated transcription (ortholog); negative regulation of epithelial cell proliferation (ortholog); ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); Stocco Dos Santos type X-linked intellectual disability (ortholog); FOUND IN chromatin (ortholog); nucleus (ortholog); protein-containing complex (ortholog) NW_004955543 2939960 3052442 + 9068941 102019960 A0A8C2UPN3;A0A8C2USI4;A0A8C2UUY6;A0A8C2UVB1 MODEL AGCD01071667;AGCD01071668;AGCD01071669;AGCD01071670;AGCD01071671;GBDI01136995;XM_005411362;XM_005411363;XM_013508174 XP_005411419;XP_005411420;XP_013363628 LOC102019960 melanoma-associated antigen D1 APPROVED protein-coding ENSCLAG00000002620 NW_004955543 2975259 3052504 + 8704083 LOC102020382 uncharacterized LOC102020382 NW_004955439 14686866 14703870 + 102020382 MODEL AGCD01035985;GBBH01173721;XR_261991 ncrna 8704094 Dnajc19 DnaJ heat shock protein family (Hsp40) member C19 INVOLVED IN genitalia development (ortholog); regulation of cardiolipin metabolic process (ortholog); visual perception (ortholog); PARTICIPATES IN presequence pathway of mitochondrial protein import; ASSOCIATED WITH 3-methylglutaconic aciduria (ortholog); 3-methylglutaconic aciduria type 3 (ortholog); 3-methylglutaconic aciduria type 5 (ortholog); FOUND IN inner mitochondrial membrane protein complex (ortholog); matrix side of mitochondrial inner membrane (ortholog); mitochondrial inner membrane (ortholog) NW_004955420 9974466 9978789 - 9068941;7240710 102020673 A0A8C2VJ01;A0A8C2VJ06;A0A8C2VL93;A0A8C2VN19;A0A8C2VPF4;A0A8C2VQQ7 MODEL AGCD01020772;GBDI01061774;XM_005383071;XM_005383072 XP_005383128;XP_005383129 DnaJ (Hsp40) homolog, subfamily C, member 19;mitochondrial import inner membrane translocase subunit TIM14 APPROVED protein-coding ENSCLAG00000011246 NW_004955420 9953045 9978789 - 8704109 Gorasp2 golgi reassembly stacking protein 2 INVOLVED IN establishment of protein localization to plasma membrane (ortholog); Golgi organization (ortholog); organelle assembly (ortholog); ASSOCIATED WITH genetic disease (ortholog); split hand-foot malformation 5 (ortholog); FOUND IN endoplasmic reticulum membrane (ortholog); Golgi apparatus (ortholog); Golgi medial cisterna (ortholog) NW_004955449 3857097 3886100 - 9068941 102022345 A0A8C2V1I4 MODEL AGCD01041868;AGCD01041869;GBDI01078948;XM_005393241 XP_005393298 Golgi reassembly-stacking protein 2;golgi reassembly stacking protein 2, 55kDa APPROVED protein-coding ENSCLAG00000006221 NW_004955449 3854682 3886100 - 8704123 LOC102023192 uncharacterized LOC102023192 NW_004955437 3136338 3136884 - 102023192 MODEL AGCD01034298;GBDF01194081;XR_001235054 ncrna 8704128 LOC102023842 zinc finger protein OZF-like NW_004955532 259427 307861 - 102023842 MODEL AGCD01070111;AGCD01070112;AGCD01070113;GBDF01011091;XM_005410144;XM_005410145;XM_013507658;XM_013507659;XM_013507660 XP_005410201;XP_005410202;XP_013363112;XP_013363113;XP_013363114 zinc finger protein 14-like;zinc finger protein 709-like APPROVED protein-coding 8704138 LOC102023954 arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 pseudogene NW_004955543 959137 960309 + 102023954 MODEL AGCD01071608 APPROVED pseudo 8704139 LOC102024173 testis-specific serine/threonine-protein kinase 1-like NW_004955446 5256392 5257796 - 102024173 MODEL AGCD01040061;GBDK01384059;XM_005392640 XP_005392697 protein-coding 8704144 Nkapd1 NKAP domain containing 1 ENCODES a protein that exhibits identical protein binding (ortholog); ASSOCIATED WITH ataxia telangiectasia (ortholog); BH4-deficient hyperphenylalaninemia A (ortholog); Carney-Stratakis syndrome (ortholog) NW_004955412 13755704 13765047 + 9068941 102025100 A0A8C2VMS6 MODEL AGCD01012845;GBDF01120750;XM_005378101;XM_005378102;XM_005378103;XM_013511040;XM_013511041 XP_005378158;XP_005378159;XP_005378160;XP_013366494;XP_013366495 LOC102025100 chromosome unknown open reading frame, human C11orf57;uncharacterized protein C11orf57 homolog APPROVED protein-coding ENSCLAG00000012317 NW_004955412 13755817 13765047 + 8704161 Mamdc4 MAM domain containing 4 ASSOCIATED WITH Adams-Oliver Syndrome 5 (ortholog); autosomal dominant intellectual developmental disorder 8 (ortholog); autosomal dominant nocturnal frontal lobe epilepsy 5 (ortholog); FOUND IN endosome (ortholog) NW_004955513 4932596 4941330 + 9068941 102026249 A0A8C2VCN2 MODEL AGCD01066944;GBDI01093135;XM_013506638 XP_013362092 apical endosomal glycoprotein protein-coding ENSCLAG00000007572 NW_004955513 4933927 4941160 + 8704192 Ca12 carbonic anhydrase 12 ENCODES a protein that exhibits carbonate dehydratase activity (ortholog); INVOLVED IN chloride ion homeostasis (ortholog); estrous cycle (ortholog); ASSOCIATED WITH Bloom syndrome (ortholog); colon adenocarcinoma (ortholog); colorectal adenocarcinoma (ortholog); FOUND IN apical plasma membrane (ortholog); basolateral plasma membrane (ortholog) NW_004955450 11927730 11975553 + 9068941;7240710 102026927 A0A8C2VE25 MODEL AGCD01042685;GBBH01177179;XM_013518981 XP_013374435 carbonic anhydrase XII APPROVED protein-coding ENSCLAG00000009814 NW_004955450 11943340 11975928 + 8704213 LOC102027976 uncharacterized LOC102027976 NW_004955417 29729033 29734861 - 102027976 MODEL AGCD01018606;GBDJ01063877;XR_260516;XR_260517 ncrna 8704220 Rpl21 ribosomal protein L21 ENCODES a protein that exhibits structural constituent of ribosome (ortholog); PARTICIPATES IN ribosome biogenesis pathway; translation pathway; ASSOCIATED WITH genetic disease (ortholog); hypotrichosis (ortholog); hypotrichosis 12 (ortholog); FOUND IN cytosolic large ribosomal subunit (ortholog); cytosolic ribosome (ortholog); ribosome (ortholog) NW_004955497 6676584 6681776 + 9068941 102030442 A0A8C2UYU7;Q6QN05 PROVISIONAL AGCD01062643;AGCD01062644;AY533214;GBCQ01004975;NM_001282366 AAS59417;NP_001269295;Q6QN05 60S ribosomal protein L21 protein-coding ENSCLAG00000003656 NW_004955497 6678965 6681419 + 8704236 LOC102004604 olfactory receptor 1N1-like NW_004955419 5180021 5180950 - 102004604 MODEL AGCD01019787;XM_013513100 XP_013368554 protein-coding 8704237 Gprin3 GPRIN family member 3 ASSOCIATED WITH autosomal dominant polycystic kidney disease (ortholog); genetic disease (ortholog) NW_004955405 253917 265309 - 102005103 A0A8C2YV42 MODEL AGCD01004555;GBDF01115743;XM_013517274 XP_013372728 G protein-regulated inducer of neurite outgrowth 3 protein-coding ENSCLAG00000017649 NW_004955405 254105 256414 - 8704246 Siglec5 sialic acid binding Ig like lectin 5 ENCODES a protein that exhibits monosaccharide binding (ortholog); sialic acid binding (ortholog); INVOLVED IN regulation of endocytosis (ortholog); ASSOCIATED WITH Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog); FOUND IN lysosome (ortholog) NW_004955558 932981 945623 + 9068941 102005310 MODEL AGCD01073406;AGCD01073407;GBBH01003474;GBDF01009380;XM_013508882 XP_013364336 sialic acid binding Ig-like lectin 5;sialic acid-binding Ig-like lectin 5 APPROVED protein-coding 8704247 LOC102005408 nucleosome assembly protein 1-like 1 pseudogene NW_004955515 171191 172070 + 102005408 MODEL AGCD01067185 APPROVED pseudo 8704248 Ssbp2 single stranded DNA binding protein 2 ASSOCIATED WITH bipolar disorder (ortholog); genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN cytoplasm (ortholog) NW_004955418 28562735 28813541 + 9068941 102005473 A0A8C2UXW1;A0A8C2YLB8 MODEL AGCD01019442;AGCD01019443;AGCD01019444;AGCD01019445;GBDF01111104;XM_013512973 XP_013368427 single-stranded DNA binding protein 2;single-stranded DNA-binding protein 2 APPROVED protein-coding ENSCLAG00000004986 NW_004955418 28633753 28808117 + 8704269 Rnase13 ribonuclease A family member 13 (inactive) ASSOCIATED WITH Brain-Lung-Thyroid Syndrome (ortholog); genetic disease (ortholog); purine nucleoside phosphorylase deficiency (ortholog) NW_004955550 1786550 1800191 - 9068941 102005753 A0A8C2UM99 MODEL AGCD01072588;GBCB01100056;XM_005412091;XM_005412093;XM_005412094 XP_005412148;XP_005412150;XP_005412151 probable inactive ribonuclease-like protein 13;ribonuclease, RNase A family, 13 (non-active) APPROVED protein-coding ENSCLAG00000001669 NW_004955550 1786550 1800191 - 8704283 Clk2 CDC like kinase 2 ENCODES a protein that exhibits identical protein binding (ortholog); protein serine/threonine kinase activity (ortholog); protein tyrosine kinase activity (ortholog); INVOLVED IN negative regulation of gluconeogenesis (ortholog); peptidyl-tyrosine phosphorylation (ortholog); protein autophosphorylation (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease type 2 (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN nuclear body (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955545 1716294 1727187 - 9068941 102006076 A0A8C2YKK3 MODEL AGCD01071869;GBCE01054181;XM_005411600;XM_005411602;XM_013508341 XP_005411657;XP_005411659;XP_013363795 CDC-like kinase 2;dual specificity protein kinase CLK2 APPROVED protein-coding ENSCLAG00000003873 NW_004955545 1716294 1725185 - 8704306 LOC102007330 ATP synthase F(0) complex subunit B1, mitochondrial pseudogene NW_004955414 4403610 4404427 - 102007330 MODEL AGCD01014865 APPROVED pseudo 8704307 Ptpn6 protein tyrosine phosphatase non-receptor type 6 ENCODES a protein that exhibits cell adhesion molecule binding (ortholog); cytokine receptor binding (ortholog); natural killer cell lectin-like receptor binding (ortholog); INVOLVED IN B cell receptor signaling pathway (ortholog); cell differentiation (ortholog); cellular response to macrophage colony-stimulating factor stimulus (ortholog); PARTICIPATES IN angiotensin II signaling pathway via AT2 receptor; epidermal growth factor/neuregulin signaling pathway; erythropoietin signaling pathway; ASSOCIATED WITH anogenital venereal wart (ortholog); autism spectrum disorder (ortholog); calcinosis (ortholog); FOUND IN alpha-beta T cell receptor complex (ortholog); apical dendrite (ortholog); cell-cell junction (ortholog) NW_004955413 4525954 4547177 + 9068941 102009165 A0A8C2VUM1;A0A8C2VWJ6;A0A8C2VZU0 MODEL AGCD01013621;GBCQ01152113;XM_005378847;XM_005378848 XP_005378904;XP_005378905 tyrosine-protein phosphatase non-receptor type 6 APPROVED protein-coding ENSCLAG00000013644 NW_004955413 4525954 4547177 + 8704332 LOC102009750 H-2 class II histocompatibility antigen, E-S beta chain pseudogene NW_004955433 10616032 10617329 + 102009750 MODEL AGCD01031633 APPROVED pseudo 8704333 LOC102011284 uncharacterized LOC102011284 NW_004955460 12592756 12593305 - 102011284 MODEL AGCD01048661;GBDF01041740;XR_263061 ncrna 8704337 Gipc2 GIPC PDZ domain containing family member 2 ENCODES a protein that exhibits identical protein binding (ortholog); ASSOCIATED WITH genetic disease (ortholog) NW_004955423 15113049 15183211 - 9068941 102011331 A0A8C2YKQ0 MODEL AGCD01023794;AGCD01023795;AGCD01023796;GBDF01156626;XM_013514544;XM_013514545;XM_013514546;XM_013514547;XR_001234123 XP_013369998;XP_013369999;XP_013370000;XP_013370001 GIPC PDZ domain containing family, member 2;PDZ domain-containing protein GIPC2 APPROVED protein-coding ENSCLAG00000004082 NW_004955423 15119566 15161798 - 8704359 LOC102012479 uncharacterized LOC102012479 NW_004955559 461354 469388 - 102012479 MODEL AGCD01073586;GBDK01094411;XM_013508927;XM_013508928;XM_013508929;XM_013508930;XM_013508931;XM_013508932;XM_013508933;XM_013508934 XP_013364381;XP_013364382;XP_013364383;XP_013364384;XP_013364385;XP_013364386;XP_013364387;XP_013364388 uncharacterized protein LOC102012479 protein-coding 8704375 Ccar2 cell cycle and apoptosis regulator 2 ENCODES a protein that exhibits enzyme binding (ortholog); enzyme inhibitor activity (ortholog); RNA polymerase II complex binding (ortholog); INVOLVED IN mitochondrial fragmentation involved in apoptotic process (ortholog); negative regulation of catalytic activity (ortholog); negative regulation of cell growth (ortholog); ASSOCIATED WITH Conotruncal Cardiac Defects (ortholog); genetic disease (ortholog); Wallerian Degeneration (ortholog); FOUND IN chromatin (ortholog); cytoplasm (ortholog); DBIRD complex (ortholog) NW_004955403 46027997 46042154 + 9068941 102013241 A0A8C2VYY9 MODEL AGCD01002849;GBDF01085278;XM_005373683;XM_005373684;XM_005373685 XP_005373740;XP_005373741;XP_005373742 Kiaa1967 cell cycle and apoptosis regulator protein 2 APPROVED protein-coding ENSCLAG00000014299 NW_004955403 46027998 46042154 + 8704406 Hoxb9 homeobox B9 ENCODES a protein that exhibits RNA polymerase II transcription regulatory region sequence-specific DNA binding (ortholog); sequence-specific double-stranded DNA binding (ortholog); INVOLVED IN anterior/posterior pattern specification (ortholog); cell chemotaxis (ortholog); embryonic skeletal system development (ortholog); ASSOCIATED WITH Acute Erythroleukemia (ortholog); Breast Neoplasms (ortholog); genetic disease (ortholog); FOUND IN nucleoplasm (ortholog); RNA polymerase II transcription regulator complex (ortholog) NW_004955451 12616465 12616926 + 9068941 102015274 MODEL AGCD01043414;GBDF01267242;GBDJ01193876;XM_013519051 XP_013374505 homeobox protein Hox-B9 APPROVED protein-coding 8704413 Chd4 chromodomain helicase DNA binding protein 4 ENCODES a protein that exhibits ATP hydrolysis activity (ortholog); ATP-dependent chromatin remodeler activity (ortholog); DNA-binding transcription factor binding (ortholog); INVOLVED IN chromatin remodeling (ortholog); double-strand break repair via homologous recombination (ortholog); histone deacetylation (ortholog); PARTICIPATES IN CHD family mediated chromatin remodeling pathway; ASSOCIATED WITH autistic disorder (ortholog); brain disease (ortholog); breast cancer (ortholog); FOUND IN centrosome (ortholog); cerebellar granule cell to Purkinje cell synapse (ortholog); chromosome, telomeric region (ortholog) NW_004955413 4191619 4228225 - 9068941 102015302 A0A8C2YRF7 MODEL AGCD01013601;AGCD01013602;AGCD01013603;AGCD01013604;GBDK01016911;XM_005378770;XM_013511310;XM_013511311;XM_013511312 XP_005378827;XP_013366764;XP_013366765;XP_013366766 chromodomain-helicase-DNA-binding protein 4 protein-coding ENSCLAG00000012244 NW_004955413 4191619 4228225 - 8704459 LOC102015418 uncharacterized LOC102015418 NW_004955424 21476497 21490967 + 102015418 MODEL AGCD01024898;GBDF01074469;XR_001234201;XR_261092 ncrna 8704464 Son SON DNA and RNA binding protein ENCODES a protein that exhibits RNA binding (ortholog); RS domain binding (ortholog); INVOLVED IN microtubule cytoskeleton organization (ortholog); mitotic cytokinesis (ortholog); mRNA processing (ortholog); ASSOCIATED WITH adenoid cystic carcinoma (ortholog); amyotrophic lateral sclerosis type 1 (ortholog); autosomal dominant intellectual developmental disorder 7 (ortholog); FOUND IN nuclear speck (ortholog) NW_004955407 32974656 33007073 + 9068941 102016237 A0A8C2VL40;A0A8C2VN07;A0A8C2VT71 MODEL AGCD01007692;AGCD01007693;GBDF01053041;XM_013504280;XM_013504282;XM_013504287;XM_013504291;XM_013504293 XP_013359734;XP_013359736;XP_013359741;XP_013359745;XP_013359747 APPROVED protein-coding ENSCLAG00000011776 NW_004955407 32974725 33006297 + 8704481 Znf81 zinc finger protein 81 ASSOCIATED WITH autistic disorder (ortholog); congenital disorder of glycosylation type IIm (ortholog); genetic disease (ortholog) NW_004955516 215370 312684 - 9068941;7240710 102016836 A0A8C2UK83 MODEL AGCD01067371;AGCD01067372;AGCD01067373;AGCD01067374;AGCD01067375;AGCD01067376;AGCD01067377;AGCD01067378;AGCD01067379;AGCD01067380;AGCD01067381;GBDI01314200;XM_005408944;XM_013506907 XP_005409001;XP_013362361 protein-coding ENSCLAG00000001537 NW_004955516 219262 248215 - 8704490 Lcat lecithin-cholesterol acyltransferase ENCODES a protein that exhibits 1-alkyl-2-acetylglycerophosphocholine esterase activity (ortholog); apolipoprotein A-I binding (ortholog); phosphatidylcholine-sterol O-acyltransferase activity (ortholog); INVOLVED IN cholesterol homeostasis (ortholog); cholesterol metabolic process (ortholog); cholesterol transport (ortholog); PARTICIPATES IN reverse cholesterol transport pathway; ASSOCIATED WITH arteriosclerosis (ortholog); autosomal dominant dyskeratosis congenita 6 (ortholog); end stage renal disease (ortholog); FOUND IN extracellular space (ortholog); high-density lipoprotein particle (ortholog) NW_004955484 8772692 8776122 + 9068941;7240710 102017239 A0A8C2V8K0 MODEL AGCD01058396;GBDF01235122;XM_005403602;XM_013503882 XP_005403659;XP_013359336 phosphatidylcholine-sterol acyltransferase protein-coding ENSCLAG00000007185 NW_004955484 8772692 8776122 + 8704500 LOC102018063 uncharacterized LOC102018063 NW_004955460 12992444 12996471 - 102018063 MODEL AGCD01048666;GBDK01027678;XR_001236498;XR_001236499 ncrna 8704505 Ube2l6 ubiquitin conjugating enzyme E2 L6 ENCODES a protein that exhibits ISG15 transferase activity (ortholog); ubiquitin binding (ortholog); ubiquitin-like protein transferase activity (ortholog); INVOLVED IN innate immune response (ortholog); ISG15-protein conjugation (ortholog); modification-dependent protein catabolic process (ortholog); ASSOCIATED WITH genetic disease (ortholog); Human Influenza (ortholog); intellectual disability (ortholog) NW_004955511 2522850 2528926 - 9068941 102018753 A0A8C2UT39 MODEL AGCD01066410;GBDJ01081009;XM_005407999 XP_005408056 ubiquitin-conjugating enzyme E2L 6;ubiquitin/ISG15-conjugating enzyme E2 L6 APPROVED protein-coding ENSCLAG00000003829 NW_004955511 2522850 2528926 - 8704512 Ncdn neurochondrin INVOLVED IN bone resorption (ortholog); neuron projection development (ortholog); regulation of neuronal synaptic plasticity (ortholog); ASSOCIATED WITH cerebellar ataxia (ortholog); Charcot-Marie-Tooth disease dominant intermediate C (ortholog); epilepsy (ortholog); FOUND IN axon (ortholog); cytosol (ortholog); dendrite (ortholog) NW_004955452 13650016 13659382 + 9068941 102019768 A0A8C2VA41;A0A8C2YNW8 MODEL AGCD01044429;GBDF01120972;XM_005395148;XM_005395149;XM_005395150;XM_005395151;XM_013519573 XP_005395205;XP_005395206;XP_005395207;XP_005395208;XP_013375027 protein-coding ENSCLAG00000008627 NW_004955452 13649539 13659436 + 8704538 Pxylp1 2-phosphoxylose phosphatase 1 ENCODES a protein that exhibits phosphatase activity (ortholog); INVOLVED IN chondroitin sulfate proteoglycan biosynthetic process (ortholog); glycosaminoglycan biosynthetic process (ortholog); positive regulation of heparan sulfate proteoglycan biosynthetic process (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN Golgi apparatus (ortholog) NW_004955508 4390647 4449782 - 9068941 102020038 A0A8C2UY16 MODEL AGCD01065866;GBDJ01388065;XM_005407772;XM_005407773;XM_013506265;XM_013506266;XM_013506267;XM_013506268;XM_013506269;XM_013506270;XM_013506271;XM_013506272;XM_013506273;XM_013506274;XM_013506275;XM_013506276;XM_013506277 XP_005407829;XP_005407830;XP_013361719;XP_013361720;XP_013361721;XP_013361722;XP_013361723;XP_013361724;XP_013361725;XP_013361726;XP_013361727;XP_013361728;XP_013361729;XP_013361730;XP_013361731 Acpl2 acid phosphatase-like 2 APPROVED protein-coding ENSCLAG00000005226 NW_004955508 4390455 4449782 - 8704578 Fancb FA complementation group B INVOLVED IN cellular response to camptothecin (ortholog); cellular response to ketone (ortholog); cellular response to organic cyclic compound (ortholog); ASSOCIATED WITH autistic disorder (ortholog); breast cancer (ortholog); Fanconi anemia (ortholog); FOUND IN chromatin (ortholog); Fanconi anaemia nuclear complex (ortholog) NW_004955519 3337138 3364963 + 9068941;7240710 102020044 A0A8C2UUT8 MODEL AGCD01067957;AGCD01067958;AGCD01067959;GBDF01033497;XM_013506977 XP_013362431 Fanconi anemia complementation group B;Fanconi anemia, complementation group B APPROVED protein-coding ENSCLAG00000004329 NW_004955519 3343446 3363814 + 8704588 Apcdd1l APC down-regulated 1 like ASSOCIATED WITH genetic disease (ortholog) NW_004955445 1025597 1070385 + 9068941 102020172 MODEL AGCD01039328;AGCD01039329;GBBH01147400;GBCE01148194;XM_013518260 XP_013373714 adenomatosis polyposis coli down-regulated 1-like APPROVED protein-coding 8704596 LOC102020626 uncharacterized LOC102020626 NW_004955451 15331564 15337087 + 102020626 MODEL AGCD01043605;GBDJ01052134;XR_001235959;XR_001235960 ncrna 8704601 Bard1 BRCA1 associated RING domain 1 ENCODES a protein that exhibits protein heterodimerization activity (ortholog); protein homodimerization activity (ortholog); RNA binding (ortholog); INVOLVED IN cellular response to follicle-stimulating hormone stimulus (ortholog); cellular response to ionizing radiation (ortholog); cellular response to organic cyclic compound (ortholog); ASSOCIATED WITH brain disease (ortholog); Breast Cancer, Familial (ortholog); breast carcinoma (ortholog); FOUND IN BRCA1-A complex (ortholog); BRCA1-B complex (ortholog); BRCA1-BARD1 complex (ortholog) NW_004955457 1187942 1258475 + 9068941;7240710 102020764 A0A8C2YN81 MODEL AGCD01046721;AGCD01046722;GBDF01159748;XM_005396916 XP_005396973 BRCA1-associated RING domain protein 1 protein-coding ENSCLAG00000007649 NW_004955457 1187942 1253803 + 8704622 Cenpk centromere protein K INVOLVED IN positive regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH castration-resistant prostate carcinoma (ortholog); genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN nucleus (ortholog) NW_004955446 3531702 3583914 + 9068941 102021058 A0A8C2UXP1 MODEL AGCD01040022;GBDF01226475;XM_005392631 XP_005392688 protein-coding ENSCLAG00000003322 NW_004955446 3531702 3583914 + 8704636 Shf Src homology 2 domain containing F PARTICIPATES IN platelet-derived growth factor signaling pathway; ASSOCIATED WITH AGAT deficiency (ortholog); Bloom syndrome (ortholog); colorectal cancer (ortholog) NW_004955409 8219295 8227877 + 9068941 102021316 A0A8C2VE78;A0A8C2VFF3;A0A8C2VKR9 MODEL AGCD01009387;GBDJ01390482;XM_013510314;XM_013510315 XP_013365768;XP_013365769 SH2 domain-containing adapter protein F protein-coding ENSCLAG00000009719 NW_004955409 8201663 8227921 + 8704659 Mif4gd MIF4G domain containing ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN cap-dependent translational initiation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); Golgi apparatus (ortholog); histone mRNA stem-loop binding complex (ortholog) NW_004955553 2128410 2133519 - 9068941 102022861 A0A8C2VAL3 MODEL AGCD01072923;AGCD01072924;GBCB01024532;XM_005412282;XM_005412283;XM_005412284;XM_005412285 XP_005412339;XP_005412340;XP_005412341;XP_005412342 protein-coding ENSCLAG00000006875 NW_004955553 2128410 2132667 - 8704678 Llph LLP homolog, long-term synaptic facilitation factor ENCODES a protein that exhibits basal RNA polymerase II transcription machinery binding (ortholog); INVOLVED IN dendrite extension (ortholog); positive regulation of dendritic spine development (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN chromosome (ortholog); nucleolus (ortholog) NW_004955458 12785194 12791918 - 9068941 102023233 A0A8C2VZL7 MODEL AGCD01047789;GBDF01120063;XM_005397449;XM_005397450;XM_005397451;XM_013520895 XP_005397506;XP_005397507;XP_005397508;XP_013376349 LLP homolog, long-term synaptic facilitation;LLP homolog, long-term synaptic facilitation (Aplysia) APPROVED protein-coding ENSCLAG00000015620 NW_004955458 12785194 12791915 - 8704693 Ssh3 slingshot protein phosphatase 3 ASSOCIATED WITH Aicardi-Goutieres Syndrome 3 (ortholog); genetic disease (ortholog); intellectual disability (ortholog) NW_004955422 18149846 18158257 - 9068941 102023610 A0A8C2YU74 MODEL AGCD01022938;GBBH01118306;XM_005384351;XM_005384352;XM_005384353 XP_005384408;XP_005384409;XP_005384410 protein-coding ENSCLAG00000016225 NW_004955422 18147149 18158254 - 8704724 Tsnaxip1 translin associated factor X interacting protein 1 ASSOCIATED WITH autosomal dominant dyskeratosis congenita 6 (ortholog); genetic disease (ortholog); prostate cancer (ortholog); FOUND IN cytoplasm (ortholog) NW_004955484 8868022 8889089 - 9068941 102024010 A0A8C2V1I0 MODEL AGCD01058398;AGCD01058399;AGCD01058400;GBDK01187927;XM_005403624;XM_005403625;XM_013503887;XM_013503888 XP_005403681;XP_005403682;XP_013359341;XP_013359342 translin-associated factor X interacting protein 1;translin-associated factor X-interacting protein 1 APPROVED protein-coding ENSCLAG00000006090 NW_004955484 8864786 8888983 - 8704748 Serpinb12 serpin family B member 12 ENCODES a protein that exhibits serine-type endopeptidase inhibitor activity (ortholog); INVOLVED IN hematopoietic progenitor cell differentiation (ortholog); ASSOCIATED WITH chromosome 18q deletion syndrome (ortholog); genetic disease (ortholog); multiple congenital anomalies-hypotonia-seizures syndrome 1 (ortholog); FOUND IN cornified envelope (ortholog) NW_004955402 47338874 47361485 + 9068941 102024072 A0A8C2YPX5 MODEL AGCD01001180;GBDI01178459;XM_005373030 XP_005373087 serpin B12;serpin peptidase inhibitor, clade B (ovalbumin), member 12 APPROVED protein-coding ENSCLAG00000010100 NW_004955402 47342151 47360030 + 8704761 LOC102024327 cytokine receptor common subunit beta-like NW_004955413 23468980 23472461 - 102024327 MODEL AGCD01014332;GBDI01259559;XM_005379176;XR_260099 XP_005379233 protein-coding 8704777 Myo1b myosin IB ENCODES a protein that exhibits actin binding (ortholog); actin filament binding (ortholog); ATP binding (ortholog); INVOLVED IN actin filament bundle assembly (ortholog); actin filament organization (ortholog); actin filament-based movement (ortholog); ASSOCIATED WITH colorectal cancer (ortholog); genetic disease (ortholog); Hepatomegaly (ortholog); FOUND IN actin filament (ortholog); apical part of cell (ortholog); brush border (ortholog) NW_004955403 7826058 7966457 - 9068941 102024867 A0A8C2VPW0;A0A8C2VRZ3;A0A8C2VX23;A0A8C2YRW3 MODEL AGCD01001865;GBDI01259767;XM_005373287;XM_005373288;XM_005373291;XM_013512219 XP_005373344;XP_005373345;XP_005373348;XP_013367673 unconventional myosin-Ib protein-coding ENSCLAG00000012867 NW_004955403 7826058 7966624 - 8704821 LOC102026295 uncharacterized LOC102026295 NW_004955456 3401369 3403585 - 102026295 MODEL AGCD01046271;GBDI01312868;XR_001236351;XR_001236352;XR_262876 ncrna 8704832 Bace1 beta-secretase 1 ENCODES a protein that exhibits amyloid-beta binding (ortholog); aspartic-type endopeptidase activity (ortholog); endopeptidase activity (ortholog); INVOLVED IN amyloid precursor protein catabolic process (ortholog); amyloid-beta formation (ortholog); amyloid-beta metabolic process (ortholog); ASSOCIATED WITH Alzheimer's disease (ortholog); CD3epsilon deficiency (ortholog); Chromosome 11, Partial Trisomy 11q (ortholog); FOUND IN axon (ortholog); cell surface (ortholog); cytoplasmic vesicle (ortholog) NW_004955412 18596643 18620089 - 9068941 102026730 A0A8C2YS57;A0A8C2YS60 MODEL AGCD01012945;GBDJ01018816;XM_005378205 XP_005378262 beta-site APP-cleaving enzyme 1 APPROVED protein-coding ENSCLAG00000013254 NW_004955412 18596643 18620362 - 8704858 Serpinb8 serpin family B member 8 ENCODES a protein that exhibits serine-type endopeptidase inhibitor activity (ortholog); INVOLVED IN epithelial cell-cell adhesion (ortholog); negative regulation of endopeptidase activity (ortholog); ASSOCIATED WITH chromosome 18q deletion syndrome (ortholog); genetic disease (ortholog); multiple congenital anomalies-hypotonia-seizures syndrome 1 (ortholog); FOUND IN cytosol (ortholog) NW_004955402 47761900 47781281 + 9068941 102026819 A0A8C2VBM4 MODEL AGCD01001193;GBDJ01355314;XM_005373037;XM_005373038;XM_005373039;XM_013511271 XP_005373094;XP_005373095;XP_005373096;XP_013366725 serpin B8;serpin peptidase inhibitor, clade B (ovalbumin), member 8 APPROVED protein-coding ENSCLAG00000008433 NW_004955402 47763322 47781523 + 8704874 LOC102028179 olfactory receptor 52A1 ASSOCIATED WITH delta beta-thalassemia (ortholog); genetic disease (ortholog) NW_004955414 21134193 21135131 - 9068941 102028179 A0A8C2YV92 MODEL AGCD01015407;XM_005380075 XP_005380132 APPROVED protein-coding ENSCLAG00000017984 NW_004955414 21134193 21135131 - 8704877 LOC102028532 cytochrome b561 ENCODES a protein that exhibits transmembrane monodehydroascorbate reductase activity (ortholog); INVOLVED IN ascorbate homeostasis (ortholog); intracellular iron ion homeostasis (ortholog); ASSOCIATED WITH genetic disease (ortholog); Orthostatic Hypotension 2 (ortholog); FOUND IN chromaffin granule membrane (ortholog) NW_004955478 8362190 8366947 + 9068941 102028532 A0A8C2UYG1 MODEL AGCD01056023;AGCD01056024;GBBH01031184;GBDF01278544;XM_005402225;XM_013503197 XP_005402282;XP_013358651 APPROVED protein-coding ENSCLAG00000005085 8704905 LOC102028621 zinc finger and SCAN domain-containing protein 29-like NW_004955410 10591936 10671606 + 102028621 MODEL AGCD01010796;GBBH01182187;GBCB01089004;XM_005377267 XP_005377324 APPROVED protein-coding 8704911 LOC102028625 lymphoid-restricted membrane protein-like NW_004955413 20134003 20227710 + 102028625 MODEL AGCD01014210;AGCD01014211;AGCD01014212;GBDI01212292;XM_013511444;XM_013511445 XP_013366898;XP_013366899 APPROVED protein-coding 8704952 LOC102029210 olfactory receptor 8H1-like NW_004955511 1038327 1039277 + 102029210 MODEL AGCD01066354;XM_005407952 XP_005408009 protein-coding 8704955 LOC102029380 uncharacterized LOC102029380 NW_004955465 12004627 12005993 - 102029380 MODEL AGCD01050539;GBDF01208481;XR_263271 ncrna 8704959 LOC102029518 C-C chemokine receptor type 1 NW_004955420 25759430 25764447 + 102029518 A0A8C2W6B9 MODEL AGCD01021369;GBCQ01017077;XM_005383455 XP_005383512 Ccr1 chemokine (C-C motif) receptor 1 APPROVED protein-coding ENSCLAG00000017981 8704965 Cfap95 cilia and flagella associated protein 95 FOUND IN cytoplasm (ortholog); plasma membrane (ortholog) NW_004955434 3193250 3267992 - 9068941 102030467 A0A8C2V4I3 MODEL AGCD01032129;AGCD01032130;GBDI01245825;XM_005388557;XR_001234830;XR_001234831 XP_005388614 CUNH9orf135;LOC102030467 chromosome unknown C9orf135 homolog;chromosome unknown open reading frame, human C9orf135;uncharacterized protein C9orf135 homolog APPROVED protein-coding ENSCLAG00000007041 NW_004955434 3190776 3267922 - 8704975 Raph1 Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 INVOLVED IN axon extension (ortholog); ASSOCIATED WITH autoimmune lymphoproliferative syndrome type 2B (ortholog); Autoimmune Lymphoproliferative Syndrome, Type V (ortholog); common variable immunodeficiency 1 (ortholog); FOUND IN cell leading edge (ortholog); cytosol (ortholog); nuclear body (ortholog) NW_004955457 11394572 11462617 + 9068941 102030500 A0A8C2USB7;A0A8C2YK34 MODEL AGCD01046968;AGCD01046969;AGCD01046970;GBDF01154438;XM_013520695;XM_013520696;XM_013520697;XM_013520698;XM_013520699;XM_013520700 XP_013376149;XP_013376150;XP_013376151;XP_013376152;XP_013376153;XP_013376154 ras-associated and pleckstrin homology domains-containing protein 1 protein-coding ENSCLAG00000003175 8704996 Tmem108 transmembrane protein 108 INVOLVED IN cellular response to brain-derived neurotrophic factor stimulus (ortholog); dendrite extension (ortholog); dentate gyrus development (ortholog); ASSOCIATED WITH alkaptonuria (ortholog); genetic disease (ortholog); nephronophthisis (ortholog); FOUND IN axon (ortholog); early endosome (ortholog); endosome membrane (ortholog) NW_004955501 5148821 5475073 - 9068941 102003157 A0A8C2V0Q4;A0A8C2V2Y1 MODEL AGCD01064152;AGCD01064153;AGCD01064154;AGCD01064155;AGCD01064156;GBDK01321678;XM_005406820;XM_005406821;XM_013505802;XM_013505803;XM_013505804;XM_013505805;XM_013505806;XM_013505807;XM_013505808 XP_005406877;XP_005406878;XP_013361256;XP_013361257;XP_013361258;XP_013361259;XP_013361260;XP_013361261;XP_013361262 protein-coding ENSCLAG00000005981 NW_004955501 5147375 5468417 - 8705018 Fscn2 fascin actin-bundling protein 2, retinal INVOLVED IN eye photoreceptor cell development (ortholog); ASSOCIATED WITH auditory system disease (ortholog); genetic disease (ortholog); Leber congenital amaurosis (ortholog); FOUND IN actin cytoskeleton (ortholog); stereocilium (ortholog) NW_004955506 1526830 1533775 - 9068941;7240710 102004952 A0A8C2VXM1 MODEL AGCD01065269;GBDF01163107;XM_005407276 XP_005407333 fascin homolog 2, actin-bundling protein, retinal;fascin-2 APPROVED protein-coding ENSCLAG00000014531 NW_004955506 1526830 1533775 - 8705029 Tektip1 tektin bundle interacting protein 1 ASSOCIATED WITH Neurodevelopmental Disorders (ortholog) NW_004955495 5504867 5507412 + 102005485 A0A8C2VCY7 MODEL AGCD01062009;GBDI01020557;XM_005405875;XM_005405876 XP_005405932;XP_005405933 CUNH19orf71;LOC102005485 chromosome unknown C19orf71 homolog;chromosome unknown open reading frame, human C19orf71;uncharacterized protein C19orf71 homolog APPROVED protein-coding ENSCLAG00000009360 NW_004955495 5505349 5507412 + 8705041 Tomm5 translocase of outer mitochondrial membrane 5 PARTICIPATES IN beta-barrel pathway of mitochondrial protein import; carrier pathway of mitochondrial protein import; presequence pathway of mitochondrial protein import; ASSOCIATED WITH acromesomelic dysplasia, Maroteaux type (ortholog); distal arthrogryposis type 1A (ortholog); frontotemporal dementia and/or amyotrophic lateral sclerosis-6 (ortholog); FOUND IN mitochondrial outer membrane translocase complex (ortholog); mitochondrion (ortholog) NW_004955419 28897328 28900289 + 9068941 102006133 MODEL AGCD01020479;GBCQ01035619;XM_005382876 XP_005382933 mitochondrial import receptor subunit TOM5 homolog;translocase of outer mitochondrial membrane 5 homolog (yeast) APPROVED protein-coding 8705053 Prlh prolactin releasing hormone ENCODES a protein that exhibits neuropeptide hormone activity (ortholog); prolactin-releasing peptide receptor binding (ortholog); INVOLVED IN autonomic nervous system development (ortholog); eating behavior (ortholog); energy reserve metabolic process (ortholog); PARTICIPATES IN obesity pathway; ASSOCIATED WITH Bethlem Myopathy 1 (ortholog); chromosome 2q37 deletion syndrome (ortholog); D-2-hydroxyglutaric aciduria 1 (ortholog); FOUND IN cytoplasm (ortholog) NW_004955542 2765578 2768057 - 9068941 102008030 A0A8C2UNV2 MODEL AGCD01071537;GBDK01287743;XM_005411227 XP_005411284 prolactin-releasing peptide protein-coding ENSCLAG00000002598 NW_004955542 2765566 2766371 - 8705060 LOC102008726 peptidyl-prolyl cis-trans isomerase FKBP11 pseudogene NW_004955481 3772130 3773131 + 102008726 MODEL AGCD01056916 APPROVED pseudo 8705061 LOC102009225 uncharacterized LOC102009225 NW_004955549 375942 379270 + 102009225 MODEL AGCD01072423;GBDF01288013;XR_264913 ncrna 8705067 Rab10 RAB10, member RAS oncogene family ENCODES a protein that exhibits GDP binding (ortholog); GDP-dissociation inhibitor binding (ortholog); GTP binding (ortholog); INVOLVED IN antigen processing and presentation (ortholog); axonogenesis (ortholog); cellular response to antibiotic (ortholog); PARTICIPATES IN insulin responsive facilitative sugar transporter mediated glucose transport pathway; Rab family mediated signaling pathway; ASSOCIATED WITH genetic disease (ortholog); Tatton-Brown-Rahman syndrome (ortholog); FOUND IN cilium (ortholog); endoplasmic reticulum membrane (ortholog); endoplasmic reticulum tubular network (ortholog) NW_004955469 8057235 8138983 + 9068941 102009369 A0A8C2VK51 MODEL AGCD01052446;AGCD01052447;AGCD01052448;AGCD01052449;AGCD01052450;AGCD01052451;AGCD01052452;GBDF01090181;XM_005400418 XP_005400475 ras-related protein Rab-10 protein-coding ENSCLAG00000010979 NW_004955469 8057235 8138983 + 8705077 Scara5 scavenger receptor class A member 5 ENCODES a protein that exhibits ferritin receptor activity (ortholog); INVOLVED IN cellular response to heat (ortholog); endocytosis (ortholog); intracellular iron ion homeostasis (ortholog); ASSOCIATED WITH autosomal dominant nocturnal frontal lobe epilepsy (ortholog); benign familial infantile seizures 6 (ortholog); genetic disease (ortholog); FOUND IN cell surface (ortholog); plasma membrane (ortholog) NW_004955403 50386212 50486335 - 9068941 102009566 A0A8C2YTZ0 MODEL AGCD01002966;GBDJ01137248;XM_005373759 XP_005373816 scavenger receptor class A, member 5;scavenger receptor class A, member 5 (putative) APPROVED protein-coding ENSCLAG00000015896 NW_004955403 50386125 50486361 - 8705090 Scn1b sodium voltage-gated channel beta subunit 1 ENCODES a protein that exhibits sodium channel inhibitor activity (ortholog); sodium channel regulator activity (ortholog); voltage-gated sodium channel activity (ortholog); INVOLVED IN axon guidance (ortholog); cardiac conduction (ortholog); cardiac muscle cell action potential involved in contraction (ortholog); PARTICIPATES IN alfentanil pharmacodynamics pathway; bupivacaine pharmacodynamics pathway; buprenorphine pharmacodynamics pathway; ASSOCIATED WITH benign epilepsy with centrotemporal spikes (ortholog); Brugada syndrome (ortholog); Brugada syndrome 5 (ortholog); FOUND IN intercalated disc (ortholog); node of Ranvier (ortholog); plasma membrane (ortholog) NW_004955468 4375517 4383383 + 9068941;7240710 102009704 A0A8C2VWX5 MODEL AGCD01051908;GBDI01008492;GBDJ01353495;XM_013522375 XP_013377829 sodium channel subunit beta-1;sodium channel, voltage gated, type I beta subunit;sodium channel, voltage-gated, type I, beta subunit APPROVED protein-coding ENSCLAG00000014191 NW_004955468 4375157 4383502 + 8705101 LOC102011438 octapeptide-repeat protein T2-like NW_004955414 22365294 22365779 - 102011438 MODEL AGCD01015455;XM_005380507 XP_005380564 protein-coding 8705104 LOC102011493 uncharacterized LOC102011493 NW_004955403 2475409 2479214 + 102011493 MODEL AGCD01001736;GBDF01280925;XR_001234362 ncrna 8705109 Mrpl48 mitochondrial ribosomal protein L48 ASSOCIATED WITH 3-methylglutaconic aciduria type 7b (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN mitochondrial large ribosomal subunit (ortholog); mitochondrial ribosome (ortholog); mitochondrion (ortholog) NW_004955414 17670909 17727308 - 9068941 102012753 A0A8C2W0X7 MODEL AGCD01015248;AGCD01015249;GBCB01022765;XM_005379938 XP_005379995 39S ribosomal protein L48, mitochondrial protein-coding ENSCLAG00000014653 NW_004955414 17670909 17727491 - 8705121 LOC102012823 inositol-3-phosphate synthase 1-like NW_004958180 30 610 + 102012823 MODEL AGCD01081576;GBBH01061916;XM_005415238 XP_005415295 protein-coding 8705126 Abhd5 abhydrolase domain containing 5, lysophosphatidic acid acyltransferase ENCODES a protein that exhibits 1-acylglycerol-3-phosphate O-acyltransferase activity (ortholog); lipase activator activity (ortholog); lysophosphatidic acid acyltransferase activity (ortholog); INVOLVED IN lipid metabolic process (ortholog); negative regulation of sequestering of triglyceride (ortholog); phosphatidic acid biosynthetic process (ortholog); ASSOCIATED WITH autosomal recessive congenital ichthyosis 1 (ortholog); colon adenocarcinoma (ortholog); congenital muscular dystrophy-dystroglycanopathy type A8 (ortholog); FOUND IN cytosol (ortholog); intracellular membrane-bounded organelle (ortholog); lipid droplet (ortholog) NW_004955420 27484500 27508360 - 9068941;7240710 102013938 A0A8C2VYN4;A0A8C2VYQ1 MODEL AGCD01021454;GBDF01266672;XM_005383485 XP_005383542 1-acylglycerol-3-phosphate O-acyltransferase ABHD5;abhydrolase domain containing 5 APPROVED protein-coding ENSCLAG00000015503 NW_004955420 27482709 27508360 - 8705137 LOC102014663 uncharacterized LOC102014663 NW_004955474 2353119 2366287 - 102014663 MODEL AGCD01054289;AGCD01054290;AGCD01054291;GBDF01295636;XR_001230725;XR_001230727;XR_001230728;XR_001230729;XR_001230730 ncrna 8705148 LOC102015547 26S proteasome non-ATPase regulatory subunit 10-like NW_004955503 7733146 7733943 - 102015547 MODEL AGCD01064799 pseudo 8705149 Rps6kl1 ribosomal protein S6 kinase like 1 ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog) NW_004955523 645444 659004 + 9068941 102015659 A0A8C2UV02 MODEL AGCD01068474;GBDF01251184;XM_005409384;XM_005409385 XP_005409441;XP_005409442 ribosomal protein S6 kinase-like 1 APPROVED protein-coding ENSCLAG00000004091 NW_004955523 645444 658535 + 8705171 Fads6 fatty acid desaturase 6 ASSOCIATED WITH genetic disease (ortholog) NW_004955553 1759435 1774691 - 9068941 102015896 A0A8C2YL38 MODEL AGCD01072899;GBDK01013629;XM_005412260 XP_005412317 protein-coding ENSCLAG00000004663 NW_004955553 1759435 1775063 - 8705181 LOC102016496 uncharacterized LOC102016496 NW_004955426 22212445 22224220 - 102016496 MODEL AGCD01026613;AGCD01026614;GBDF01006654;XR_261217 ncrna 8705185 Pot1 protection of telomeres 1 ENCODES a protein that exhibits 8-hydroxy-2'-deoxyguanosine DNA binding (ortholog); DEAD/H-box RNA helicase binding (ortholog); G-rich single-stranded DNA binding (ortholog); INVOLVED IN chromosome organization (ortholog); DNA duplex unwinding (ortholog); establishment of protein localization to telomere (ortholog); ASSOCIATED WITH Cerebroretinal Microangiopathy with Calcifications and Cysts 3 (ortholog); cholecystitis (ortholog); chromosomal disease (ortholog); FOUND IN chromosome, telomeric region (ortholog); nuclear telomere cap complex (ortholog); nucleoplasm (ortholog) NW_004955479 6140599 6230512 - 9068941 102018183 A0A8C2UW33 MODEL AGCD01056377;AGCD01056378;AGCD01056379;GBDF01156854;XM_005402344;XM_005402345;XM_005402346;XM_013503293;XR_001230883 XP_005402401;XP_005402402;XP_005402403;XP_013358747 protection of telomeres protein 1 protein-coding ENSCLAG00000004448 NW_004955479 6140501 6209031 - 8705218 LOC102018215 60S ribosomal protein L7 pseudogene NW_004955521 4288386 4289394 - 102018215 MODEL AGCD01068259 APPROVED pseudo 8705219 LOC102018738 reactive oxygen species modulator 1 pseudogene NW_004955493 7585489 7586094 - 102018738 MODEL AGCD01061202;XM_005405270 APPROVED pseudo 8705224 Alk ALK receptor tyrosine kinase ENCODES a protein that exhibits heparin binding (ortholog); identical protein binding (ortholog); protein tyrosine kinase activity (ortholog); INVOLVED IN adult behavior (ortholog); brain development (ortholog); energy homeostasis (ortholog); ASSOCIATED WITH anaplastic large cell lymphoma (ortholog); Brain Neoplasms (ortholog); Breast Neoplasms (ortholog); FOUND IN plasma membrane (ortholog); protein-containing complex (ortholog) NW_004955469 11049373 11751235 - 9068941;7240710 102019052 A0A8C2V793;A0A8C2V795;A0A8C2VCC7 MODEL AGCD01052554;AGCD01052555;AGCD01052556;AGCD01052557;AGCD01052558;AGCD01052559;AGCD01052560;AGCD01052561;AGCD01052562;AGCD01052563;AGCD01052564;AGCD01052565;AGCD01052566;GBCQ01044578;XM_005400546 XP_005400603 ALK tyrosine kinase receptor;anaplastic lymphoma receptor tyrosine kinase APPROVED protein-coding ENSCLAG00000007813 NW_004955469 11047048 11548233 - 8705257 Nfrkb nuclear factor related to kappaB binding protein ENCODES a protein that exhibits protease binding (ortholog); INVOLVED IN chromatin remodeling (ortholog); positive regulation of DNA repair (ortholog); positive regulation of DNA-templated transcription (ortholog); PARTICIPATES IN INO80 family mediated chromatin remodeling pathway; ASSOCIATED WITH Chromosome 11, Partial Trisomy 11q (ortholog); Dwarfism (ortholog); genetic disease (ortholog); FOUND IN Ino80 complex (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955412 30817151 30848992 - 9068941 102019156 A0A8C2W352 MODEL AGCD01013312;GBDF01225318;XM_005378552;XM_005378553;XM_013511175;XM_013511176;XM_013511177 XP_005378609;XP_005378610;XP_013366629;XP_013366630;XP_013366631 protein-coding ENSCLAG00000015352 NW_004955412 30813769 30849001 - 8705295 Rnf216 ring finger protein 216 ENCODES a protein that exhibits ubiquitin protein ligase activity (ortholog); INVOLVED IN proteasome-mediated ubiquitin-dependent protein catabolic process (ortholog); protein catabolic process, modulating synaptic transmission (ortholog); protein K48-linked ubiquitination (ortholog); ASSOCIATED WITH genetic disease (ortholog); Gordon Holmes syndrome (ortholog); hypogonadotropic hypogonadism 7 with or without anosmia (ortholog); FOUND IN cytosol (ortholog); glutamatergic synapse (ortholog); nucleoplasm (ortholog) NW_004955460 10423736 10578421 - 9068941;7240710 102019894 A0A8C2VGV7 MODEL AGCD01048584;AGCD01048585;AGCD01048586;AGCD01048587;AGCD01048588;AGCD01048589;GBBH01228789;GBCB01074954;XM_013521126 XP_013376580 E3 ubiquitin-protein ligase RNF216 protein-coding ENSCLAG00000009524 NW_004955460 10425885 10551295 - 8705314 Samm50 SAMM50 sorting and assembly machinery component INVOLVED IN cristae formation (ortholog); mitochondrial respiratory chain complex assembly (ortholog); protein insertion into mitochondrial outer membrane (ortholog); PARTICIPATES IN beta-barrel pathway of mitochondrial protein import; ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); non-alcoholic fatty liver disease (ortholog); FOUND IN membrane (ortholog); mitochondrial outer membrane (ortholog); mitochondrion (ortholog) NW_004955413 28901124 28925093 + 9068941 102020647 A0A8C2W4M3 MODEL AGCD01014572;GBDF01046690;XM_005379452 XP_005379509 sorting and assembly machinery component 50 homolog APPROVED protein-coding ENSCLAG00000017226 NW_004955413 28901124 28925093 + 8705338 Ctc1 CST telomere replication complex component 1 ENCODES a protein that exhibits G-rich strand telomeric DNA binding (ortholog); single-stranded DNA binding (ortholog); telomeric DNA binding (ortholog); INVOLVED IN bone marrow development (ortholog); chromosome organization (ortholog); DNA damage response (ortholog); ASSOCIATED WITH Autosomal Recessive Dyskeratosis Congenita (ortholog); brain disease (ortholog); calcinosis (ortholog); FOUND IN chromosome, telomeric region (ortholog); CST complex (ortholog); cytosol (ortholog) NW_004955467 8673069 8700730 + 9068941 102021327 A0A8C2YSW3;A0A8C2YSW6 MODEL AGCD01051466;GBDJ01339470;XM_005399422;XM_005399423;XM_005399425 XP_005399479;XP_005399480;XP_005399482 CST complex subunit CTC1;CTS telomere maintenance complex component 1 APPROVED protein-coding ENSCLAG00000014305 NW_004955467 8673128 8702165 + 8705375 Vmac vimentin type intermediate filament associated coiled-coil protein ASSOCIATED WITH genetic disease (ortholog); FOUND IN type III intermediate filament (ortholog) NW_004955495 3553025 3556726 - 9068941 102021777 A0A8C2VMA5 MODEL AGCD01061862;GBDJ01239546;XM_005405750;XM_005405751 XP_005405807;XP_005405808 APPROVED protein-coding ENSCLAG00000012168 NW_004955495 3554567 3555973 - 8705385 LOC102021910 olfactory receptor 10C1-like NW_004955524 278339 279310 + 102021910 MODEL AGCD01068674;XM_005409658 XP_005409715 protein-coding 8705388 LOC102022326 uncharacterized LOC102022326 NW_004955538 1051081 1056074 - 102022326 MODEL AGCD01071043;GBDF01261166;XR_264794 ncrna 8705394 Il10 interleukin 10 ENCODES a protein that exhibits cytokine activity (ortholog); interleukin-10 receptor binding (ortholog); protein dimerization activity (ortholog); INVOLVED IN branching involved in labyrinthine layer morphogenesis (ortholog); cellular response to antibiotic (ortholog); cellular response to estradiol stimulus (ortholog); PARTICIPATES IN Interleukin-10 signaling pathway; interleukin-4 signaling pathway; ASSOCIATED WITH abdominal aortic aneurysm (ortholog); Actinic Cheilitis (ortholog); Acute Experimental Pancreatitis (ortholog); FOUND IN extracellular space (ortholog) NW_004955406 42307789 42312255 - 9068941;7240710 102022355 A0A8C2VZ06 MODEL AGCD01006700;GBDJ01151912;XM_005375404 XP_005375461 interleukin-10 protein-coding ENSCLAG00000013410 NW_004955406 42307664 42312779 - 8705403 Rpap2 RNA polymerase II associated protein 2 ENCODES a protein that exhibits RNA polymerase II CTD heptapeptide repeat phosphatase activity (ortholog); INVOLVED IN snRNA transcription (ortholog); PARTICIPATES IN RNA polymerase II transcription pathway; ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleolus (ortholog) NW_004955423 2062163 2195351 - 9068941 102022401 A0A8C2V3Z7;A0A8C2V7S2 MODEL AGCD01023467;AGCD01023468;AGCD01023469;AGCD01023470;GBDF01220283;XM_005385045;XM_013514463;XM_013514464;XM_013514465;XM_013514466;XM_013514467;XM_013514468;XM_013514469;XR_001234092;XR_001234093;XR_001234094 XP_005385102;XP_013369917;XP_013369918;XP_013369919;XP_013369920;XP_013369921;XP_013369922;XP_013369923 putative RNA polymerase II subunit B1 CTD phosphatase RPAP2 protein-coding ENSCLAG00000006291 NW_004955423 2101780 2195390 - 8705432 LOC102022930 calmodulin-4-like NW_004955421 22194729 22195647 - 102022930 MODEL AGCD01022128;GBCC01008059;XM_005383839 XP_005383896 protein-coding 8705437 Cdca2 cell division cycle associated 2 INVOLVED IN chromosome segregation (ortholog); positive regulation of protein dephosphorylation (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease type 2E (ortholog); COVID-19 (ortholog); genetic disease (ortholog); FOUND IN chromosome (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955403 48374276 48417130 + 9068941 102023316 A0A8C2YR89;A0A8C2YR96 MODEL AGCD01002918;AGCD01002919;AGCD01002920;GBDF01004693;XM_005373713;XM_005373714;XM_005373715;XM_013514099 XP_005373770;XP_005373771;XP_005373772;XP_013369553 cell division cycle-associated protein 2 protein-coding ENSCLAG00000011981 NW_004955403 48375287 48419955 + 8705466 LOC102024286 olfactory receptor 11G2-like NW_004955550 750775 751537 + 102024286 MODEL AGCD01072520 pseudo 8705467 Alkbh3 alkB homolog 3, alpha-ketoglutarate dependent dioxygenase ENCODES a protein that exhibits 2-oxoglutarate-dependent dioxygenase activity (ortholog); cytosine C-5 DNA demethylase activity (ortholog); DNA-N1-methyladenine dioxygenase activity (ortholog); INVOLVED IN cell population proliferation (ortholog); DNA dealkylation involved in DNA repair (ortholog); DNA repair (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); FOUND IN cytosol (ortholog); mitochondrion (ortholog); nucleoplasm (ortholog) NW_004955422 3660504 3695352 - 9068941 102024809 A0A8C2W771 MODEL AGCD01022526;AGCD01022527;GBCB01024527;XM_005384082;XM_005384083 XP_005384139;XP_005384140 alkB homolog 3, alpha-ketoglutarate-dependent dioxygenase;alkB homolog 3, alpha-ketoglutaratedependent dioxygenase;alkB, alkylation repair homolog 3;alpha-ketoglutarate-dependent dioxygenase alkB homolog 3 APPROVED protein-coding ENSCLAG00000016579 NW_004955422 3657765 3695409 - 8705484 Ttc33 tetratricopeptide repeat domain 33 ASSOCIATED WITH genetic disease (ortholog); Neurodevelopmental Disorders (ortholog) NW_004955426 25017351 25075164 - 9068941 102024820 A0A8C2VBB8 MODEL AGCD01026701;GBCQ01098236;XM_005386241;XM_005386242 XP_005386298;XP_005386299 tetratricopeptide repeat protein 33 protein-coding ENSCLAG00000009002 NW_004955426 25017351 25075039 - 8705499 Znf180 zinc finger protein 180 ASSOCIATED WITH ethylmalonic encephalopathy (ortholog); genetic disease (ortholog) NW_004955555 1733657 1749131 - 9068941 102025399 MODEL AGCD01073098;GBCE01179425;XM_005415272 XP_005415329 protein-coding 8705508 Pcdh10 protocadherin 10 INVOLVED IN cell adhesion (ortholog); homophilic cell adhesion via plasma membrane adhesion molecules (ortholog); ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog) NW_004955428 9433478 9495260 - 9068941 102026240 A0A8C2UXQ8;A0A8C2V008;A0A8C2V2V7;A0A8C2V3Q8 MODEL AGCD01027836;AGCD01027837;GBDF01264237;XM_005386714;XM_005386716;XM_005386717;XR_261296;XR_261297 XP_005386771;XP_005386773;XP_005386774 protocadherin-10 protein-coding ENSCLAG00000005145 NW_004955428 9433478 9495305 - 8705529 Tmem139 transmembrane protein 139 ASSOCIATED WITH genetic disease (ortholog); Neoplasm Invasiveness (ortholog) NW_004955494 369309 371526 - 9068941 102026538 A0A8C2UN99 MODEL AGCD01061376;GBCE01011410;XM_005405368;XM_005405369;XM_013505019 XP_005405425;XP_005405426;XP_013360473 protein-coding ENSCLAG00000001417 NW_004955494 369309 371516 - 8705540 Nme8 NME/NM23 family member 8 ENCODES a protein that exhibits microtubule binding (ortholog); INVOLVED IN cellular response to reactive oxygen species (ortholog); cilium assembly (ortholog); flagellated sperm motility (ortholog); ASSOCIATED WITH genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog); primary ciliary dyskinesia (ortholog); FOUND IN axoneme (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955460 5672768 5718707 - 9068941;7240710 102026949 A0A8C2V5V1 MODEL AGCD01048456;AGCD01048457;GBDF01052740;XM_005397749 XP_005397806 thioredoxin domain-containing protein 3 protein-coding ENSCLAG00000007392 NW_004955460 5680678 5718628 - 8705561 Jph3 junctophilin 3 INVOLVED IN exploration behavior (ortholog); learning (ortholog); locomotion (ortholog); ASSOCIATED WITH 16Q24.3 Microdeletion Syndrome (ortholog); autosomal recessive chronic granulomatous disease 4 (ortholog); CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO (ortholog); FOUND IN endoplasmic reticulum (ortholog); endoplasmic reticulum membrane (ortholog); junctional membrane complex (ortholog) NW_004955541 1969197 2020868 + 9068941;7240710 102027457 A0A8C2YJ81 MODEL AGCD01071398;GBBH01037412;XM_005411005 XP_005411062 junctophilin-3 protein-coding ENSCLAG00000001912 NW_004955541 1969194 2017588 + 8705570 Armcx4 armadillo repeat containing X-linked 4 ASSOCIATED WITH autistic disorder (ortholog); developmental and epileptic encephalopathy 9 (ortholog); isolated growth hormone deficiency type III (ortholog) NW_004955503 7603395 7613711 + 9068941 102027763 A0A8C2YJC4 MODEL AGCD01064796;GBDK01060405;XM_013505860 XP_013361314 armadillo repeat containing, X-linked 4;armadillo repeat-containing X-linked protein 4 APPROVED protein-coding ENSCLAG00000002088 NW_004955503 7606353 7613363 + 8705583 Caskin2 CASK interacting protein 2 ASSOCIATED WITH genetic disease (ortholog) NW_004955553 2353767 2367357 - 9068941 102027793 A0A8C2USY8;A0A8C2UVD0 MODEL AGCD01072935;GBCQ01038679;XM_005412298;XM_005412299;XM_013508626 XP_005412355;XP_005412356;XP_013364080 caskin-2 protein-coding ENSCLAG00000002735 NW_004955553 2353767 2367352 - 8705612 LOC102028284 olfactory receptor 145-like NW_004955412 25164135 25165092 - 102028284 A0A8C2W8P4 MODEL AGCD01013138;XM_005378648 XP_005378705 APPROVED protein-coding ENSCLAG00000018075 8705616 CUNH12orf40 chromosome unknown C12orf40 homolog ASSOCIATED WITH genetic disease (ortholog) NW_004955505 676988 763746 - 9068941 102029312 A0A8C2UKB6 MODEL AGCD01064961;GBDF01155084;XM_005407103;XM_005407106;XM_013505952;XM_013505953;XM_013505954;XM_013505955;XM_013505956 XP_005407160;XP_005407163;XP_013361406;XP_013361407;XP_013361408;XP_013361409;XP_013361410 LOC102029312 chromosome unknown open reading frame, human C12orf40;uncharacterized protein C12orf40 homolog APPROVED protein-coding ENSCLAG00000000532 NW_004955505 676679 706535 - 8705649 Trappc10 trafficking protein particle complex subunit 10 INVOLVED IN intra-Golgi vesicle-mediated transport (ortholog); ASSOCIATED WITH agnathia-otocephaly complex (ortholog); Arsenic Poisoning (ortholog); autistic disorder (ortholog); FOUND IN TRAPP complex (ortholog) NW_004955407 41271526 41347850 - 9068941 102029827 A0A8C2UWX7 MODEL AGCD01007863;AGCD01007864;GBCQ01072221;GBDF01089628;XM_005375874 XP_005375931 trafficking protein particle complex 10 APPROVED protein-coding ENSCLAG00000004935 NW_004955407 41271526 41347850 - 8705676 Mfsd14a major facilitator superfamily domain containing 14A INVOLVED IN acrosome assembly (ortholog); sperm mitochondrion organization (ortholog); spermatid development (ortholog); ASSOCIATED WITH genetic disease (ortholog); maple syrup urine disease (ortholog) NW_004955435 4810919 4831829 + 9068941 102003580 A0A8C2UYI9;A0A8C2V3Z9 MODEL AGCD01032855;GBCB01077165;GBDI01112507;XM_005388793;XM_013516437 XP_005388850;XP_013371891 Hiat1 hippocampus abundant transcript 1 APPROVED protein-coding ENSCLAG00000005104 NW_004955435 4810603 4830775 + 8705691 LOC102003728 uncharacterized LOC102003728 NW_004955454 12328311 12330494 + 102003728 MODEL AGCD01045409;XR_262791 ncrna ENSCLAG00000028517 8705695 LOC102004023 guanine deaminase-like NW_004955402 41170178 41171764 - 102004023 MODEL AGCD01001012 pseudo 8705696 LOC102004828 olfactory receptor 2A12 ASSOCIATED WITH genetic disease (ortholog) NW_004955491 418194 419126 + 9068941 102004828 MODEL AGCD01060334;XM_005404724 XP_005404781 APPROVED protein-coding 8705699 LOC102005028 FACT complex subunit SSRP1 pseudogene NW_004955469 10948388 10950687 - 102005028 MODEL AGCD01052552 APPROVED pseudo 8705700 LOC102005160 uncharacterized LOC102005160 NW_004955505 2073316 2169827 - 102005160 MODEL AGCD01064984;AGCD01064985;GBDF01195356;XR_001231571;XR_264302;XR_264303 ncrna ENSCLAG00000022574 8705710 LOC102005997 keratin-associated protein 20-2-like NW_004955407 30123405 30123560 + 102005997 MODEL AGCD01007628;XM_005375637 XP_005375694 protein-coding 8705713 Chka choline kinase alpha ENCODES a protein that exhibits ATP binding (ortholog); choline binding (ortholog); choline kinase activity (ortholog); INVOLVED IN CDP-choline pathway (ortholog); cellular response to glucose starvation (ortholog); choline metabolic process (ortholog); PARTICIPATES IN glycerophospholipid metabolic pathway; ASSOCIATED WITH Aicardi-Goutieres Syndrome 3 (ortholog); colon adenoma (ortholog); colon cancer (ortholog); FOUND IN cytosol (ortholog); lipid droplet (ortholog) NW_004955422 17710981 17766256 + 9068941 102006673 A0A8C2VX16;A0A8C2VYP7;A0A8C2W1D8 MODEL AGCD01022932;GBDF01051159;XM_005384285;XM_005384286 XP_005384342;XP_005384343 protein-coding ENSCLAG00000014223 NW_004955422 17710434 17766256 + 8705732 Tas2r3 taste 2 receptor member 3 ENCODES a protein that exhibits bitter taste receptor activity (ortholog); INVOLVED IN detection of chemical stimulus involved in sensory perception of bitter taste (ortholog); ASSOCIATED WITH genetic disease (ortholog); Hereditary Pancreatitis (ortholog); RASopathy (ortholog) NW_004955494 1799438 1800388 - 9068941 102006678 MODEL AGCD01061424;XM_005405533 XP_005405590 LOC102006678 taste receptor type 2 member 3 APPROVED protein-coding 8705735 Rassf9 Ras association domain family member 9 ENCODES a protein that exhibits enzyme binding (ortholog); protein domain specific binding (ortholog); INVOLVED IN intracellular transport (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); endosome (ortholog); recycling endosome (ortholog) NW_004955405 23677319 23711542 - 9068941 102006866 A0A8C2V6W4 MODEL AGCD01005133;AGCD01005134;GBDI01327913;XM_005374413 XP_005374470 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9;ras association domain-containing protein 9 APPROVED protein-coding ENSCLAG00000007610 NW_004955405 23677319 23711542 - 8705741 St3gal4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4 ENCODES a protein that exhibits beta-D-galactosyl-(1->3)-N-acetyl-beta-D-galactosaminide alpha-2,3- sialyltransferase (ortholog); beta-galactoside (CMP) alpha-2,3-sialyltransferase activity (ortholog); N-acetyllactosaminide alpha-2,3-sialyltransferase activity (ortholog); INVOLVED IN cognition (ortholog); glycolipid biosynthetic process (ortholog); glycoprotein biosynthetic process (ortholog); ASSOCIATED WITH adenoid cystic carcinoma (ortholog); Chromosome 11, Partial Trisomy 11q (ortholog); Dwarfism (ortholog) NW_004955412 27376270 27418770 + 9068941 102007098 A0A8C2W6A6 MODEL AGCD01013236;AGCD01013237;AGCD01013238;GBBH01157473;XM_005378516;XM_005378517;XM_005378518;XM_005378519;XM_013511052;XM_013511053;XM_013511054 XP_005378573;XP_005378574;XP_005378575;XP_005378576;XP_013366506;XP_013366507;XP_013366508 CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 4 protein-coding ENSCLAG00000016327 NW_004955412 27387039 27418770 + 8705779 LOC102007563 uncharacterized LOC102007563 NW_004955493 470268 489066 - 102007563 MODEL AGCD01060852;AGCD01060853;AGCD01060854;GBDJ01366389;XM_013504742 XP_013360196 uncharacterized protein LOC102007563 protein-coding 8705786 LOC102008073 39S ribosomal protein L47, mitochondrial pseudogene NW_004955411 8554284 8555056 + 102008073 MODEL AGCD01011730 APPROVED pseudo 8705787 CUNH16orf96 chromosome unknown C16orf96 homolog ASSOCIATED WITH epilepsy (ortholog); genetic disease (ortholog); idiopathic generalized epilepsy (ortholog) NW_004955442 12834662 12879308 - 102009323 A0A8C2YTH0;A0A8C2YTH1 MODEL AGCD01037747;AGCD01037748;GBDK01184197;XM_005391288;XM_005391289;XM_013517721;XM_013517722 XP_005391345;XP_005391346;XP_013373175;XP_013373176 LOC102009323 chromosome unknown open reading frame, human C16orf96;uncharacterized protein C16orf96 homolog APPROVED protein-coding ENSCLAG00000015157 NW_004955442 12839570 12879144 - 8705810 Cysrt1 cysteine rich tail 1 ENCODES a protein that exhibits identical protein binding (ortholog); ASSOCIATED WITH Adams-Oliver Syndrome 5 (ortholog); autosomal dominant intellectual developmental disorder 8 (ortholog); developmental and epileptic encephalopathy 14 (ortholog) NW_004955513 5223124 5224650 + 9068941 102010396 A0A8C2V5W9 MODEL AGCD01066963;GBDI01327324;XM_005408604 XP_005408661 UPF0574 protein C9orf169 homolog;cysteine-rich tail protein 1 APPROVED protein-coding ENSCLAG00000007413 NW_004955513 5223124 5224650 + 8705816 Kcnh5 potassium voltage-gated channel subfamily H member 5 ENCODES a protein that exhibits protein-containing complex binding (ortholog); transmembrane transporter binding (ortholog); INVOLVED IN regulation of G2/M transition of mitotic cell cycle (ortholog); ASSOCIATED WITH developmental and epileptic encephalopathy (ortholog); early infantile epileptic encephalopathy (ortholog); epilepsy (ortholog); FOUND IN cell surface (ortholog) NW_004955466 6704431 7042727 + 9068941 102010463 A0A8C2VGL2 MODEL AGCD01050932;AGCD01050933;AGCD01050934;AGCD01050935;AGCD01050936;AGCD01050937;AGCD01050938;AGCD01050939;AGCD01050940;AGCD01050941;GBCQ01085123;XM_005399159 XP_005399216 potassium channel, voltage gated eag related subfamily H, member 5;potassium voltage-gated channel, subfamily H (eag-related), member 5 APPROVED protein-coding ENSCLAG00000008714 NW_004955466 6704364 7040734 + 8705831 Ccnf cyclin F ENCODES a protein that exhibits anaphase-promoting complex binding (ortholog); INVOLVED IN negative regulation of centrosome duplication (ortholog); placenta development (ortholog); protein ubiquitination (ortholog); ASSOCIATED WITH amyotrophic lateral sclerosis (ortholog); autosomal dominant nonsyndromic deafness 65 (ortholog); autosomal recessive nonsyndromic deafness 86 (ortholog); FOUND IN cell junction (ortholog); centriole (ortholog); centrosome (ortholog) NW_004955442 14864935 14890802 - 9068941 102011053 A0A8C2YUW7 MODEL AGCD01037845;AGCD01037846;GBBH01183568;GBDF01001353;XM_013518018 XP_013373472 cyclin-F protein-coding ENSCLAG00000017219 NW_004955442 14865954 14890709 - 8705851 Igsf9 immunoglobulin superfamily member 9 ENCODES a protein that exhibits cell-cell adhesion mediator activity (ortholog); INVOLVED IN dendrite development (ortholog); homophilic cell adhesion via plasma membrane adhesion molecules (ortholog); regulation of synapse organization (ortholog); ASSOCIATED WITH autoimmune interstitial lung, joint, and kidney disease (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN axon (ortholog); dendrite (ortholog); inhibitory synapse (ortholog) NW_004955468 11722716 11741622 - 9068941 102011298 A0A8C2VRX6 MODEL AGCD01052137;GBDF01166084;XM_005400184;XM_005400186;XM_005400187 XP_005400241;XP_005400243;XP_005400244 immunoglobulin superfamily, member 9 APPROVED protein-coding ENSCLAG00000013469 NW_004955468 11722442 11740932 - 8705883 LOC102011583 uncharacterized LOC102011583 NW_004955436 8909255 8926076 + 102011583 MODEL AGCD01033752;AGCD01033753;AGCD01033754;GBDI01265317;XR_001234994;XR_261775;XR_261776 ncrna 8705892 Magi1 membrane associated guanylate kinase, WW and PDZ domain containing 1 ENCODES a protein that exhibits alpha-actinin binding (ortholog); INVOLVED IN positive regulation of cell-cell adhesion (ortholog); ASSOCIATED WITH adenoid cystic carcinoma (ortholog); genetic disease (ortholog); intrahepatic cholangiocarcinoma (ortholog); FOUND IN adherens junction (ortholog); cell junction (ortholog); cell periphery (ortholog) NW_004955517 54699 654398 + 9068941 102012118 A0A8C2UJ88;A0A8C2YIE4;A0A8C2YIE9 MODEL AGCD01067566;AGCD01067567;AGCD01067568;AGCD01067569;AGCD01067570;AGCD01067571;AGCD01067572;AGCD01067573;AGCD01067574;AGCD01067575;AGCD01067576;AGCD01067577;AGCD01067578;AGCD01067579;GBBH01166414;XM_005409004;XM_005409005;XM_005409007;XM_005409011;XM_013506940;XM_013506941;XM_013506942 XP_005409061;XP_005409062;XP_005409064;XP_005409068;XP_013362394;XP_013362395;XP_013362396 membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 protein-coding ENSCLAG00000000742 NW_004955517 55091 655638 + 8705945 LOC102012698 zinc finger protein 709-like NW_004955569 603589 617354 + 102012698 MODEL AGCD01074601;AGCD01074602;XM_013509369 XP_013364823 protein-coding 8705951 Nup42 nucleoporin 42 ENCODES a protein that exhibits nuclear export signal receptor activity (ortholog); INVOLVED IN protein export from nucleus (ortholog); ASSOCIATED WITH genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN cytosol (ortholog); nuclear envelope (ortholog); nucleoplasm (ortholog) NW_004955410 25487481 25515863 + 9068941 102012934 A0A8C2VD17 MODEL AGCD01011154;AGCD01011155;AGCD01011156;AGCD01011157;GBDF01043576;XM_005377393 XP_005377450 Nupl2 nucleoporin like 2;nucleoporin-like protein 2 APPROVED protein-coding ENSCLAG00000007547 NW_004955410 25487189 25518582 + 8705962 Sec11c SEC11 homolog C, signal peptidase complex subunit ENCODES a protein that exhibits serine-type endopeptidase activity (ortholog); INVOLVED IN signal peptide processing (ortholog); ASSOCIATED WITH genetic disease (ortholog); immunodeficiency 12 (ortholog); isolated microphthalmia 3 (ortholog); FOUND IN signal peptidase complex (ortholog) NW_004955402 43317038 43333816 + 9068941 102013128 A0A8C2VEQ2;A0A8C2VEQ6 MODEL AGCD01001070;GBDI01007992;XM_005372997 XP_005373054 SEC11 homolog C;signal peptidase complex catalytic subunit SEC11C APPROVED protein-coding ENSCLAG00000009984 NW_004955402 43316966 43334136 + 8705978 Pkia cAMP-dependent protein kinase inhibitor alpha ENCODES a protein that exhibits cAMP-dependent protein kinase inhibitor activity (ortholog); protein kinase A catalytic subunit binding (ortholog); INVOLVED IN negative regulation of cAMP-dependent protein kinase activity (ortholog); negative regulation of catalytic activity (ortholog); negative regulation of protein import into nucleus (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog) NW_004955444 2498785 2532881 - 9068941 102013561 A0A8C2YQ85 MODEL AGCD01038768;GBDK01234704;XM_005392066;XM_005392067;XM_013518200 XP_005392123;XP_005392124;XP_013373654 APPROVED protein-coding ENSCLAG00000010536 NW_004955444 2498288 2532881 - 8705988 LOC102013862 uncharacterized LOC102013862 NW_004955435 22115074 22120032 + 102013862 MODEL AGCD01033491;GBDF01153273;XR_001234904 ncrna 8705993 LOC102014188 uncharacterized LOC102014188 NW_004955448 18347215 18360566 + 102014188 MODEL AGCD01041746;GBCQ01112525;XR_262479 ncrna 8705998 LOC102014586 phospholipase DDHD2 pseudogene NW_004955502 6145208 6147408 + 102014586 MODEL AGCD01064394 APPROVED pseudo 8705999 Znf74 zinc finger protein 74 ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); chromosome 22q11.2 deletion syndrome, distal (ortholog); FOUND IN actin cytoskeleton (ortholog); nucleoplasm (ortholog) NW_004955442 18969061 18982193 + 9068941 102015354 MODEL AGCD01038026;AGCD01038027;GBBH01067162;XM_013518016 XP_013373470 protein-coding 8706008 Gsap gamma-secretase activating protein ENCODES a protein that exhibits amyloid-beta binding (ortholog); INVOLVED IN positive regulation of amyloid-beta formation (ortholog); regulation of proteolysis (ortholog); ASSOCIATED WITH Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB (ortholog); genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN trans-Golgi network (ortholog) NW_004955410 7740548 7810563 + 9068941 102015486 MODEL AGCD01010723;GBCE01057270;GBCQ01176435;XM_013510519 XP_013365973 protein-coding 8706043 Ndufa3 NADH:ubiquinone oxidoreductase subunit A3 INVOLVED IN mitochondrial respiratory chain complex I assembly (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN mitochondrial respiratory chain complex I (ortholog) NW_004955604 139844 141578 - 9068941 102015682 A0A8C2YID9 MODEL AGCD01076865;GBCE01007106;XM_005414866 XP_005414923 NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 3, 9kDa;NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 3 APPROVED protein-coding ENSCLAG00000000698 NW_004955604 139844 141578 - 8706051 LOC102015894 uncharacterized LOC102015894 NW_004955440 9879399 9883532 - 102015894 MODEL AGCD01036385;XR_001235270 ncrna 8706057 LOC102016572 granzyme B-like NW_004955409 35563970 35566671 + 102016572 MODEL AGCD01010426;XM_005377174 XP_005377231 protein-coding 8706064 Nalf2 NALCN channel auxiliary factor 2 ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); syndromic X-linked intellectual disability Lubs type (ortholog) NW_004955475 9024816 9052394 + 9068941 102017007 A0A8C2VCC2 MODEL AGCD01055054;AGCD01055055;AGCD01055056;GBBH01018923;GBBH01212781;XM_005401597 XP_005401654 Fam155b family with sequence similarity 155 member B;family with sequence similarity 155, member B;transmembrane protein FAM155B APPROVED protein-coding ENSCLAG00000009312 NW_004955475 9025628 9052438 + 8706071 Cdca5 cell division cycle associated 5 ENCODES a protein that exhibits protein-containing complex binding (ortholog); INVOLVED IN double-strand break repair (ortholog); mitotic cell cycle (ortholog); mitotic chromosome condensation (ortholog); ASSOCIATED WITH Bardet-Biedl syndrome (ortholog); COVID-19 (ortholog); genetic disease (ortholog); FOUND IN chromatin (ortholog); cytoplasm (ortholog); nucleoplasm (ortholog) NW_004955422 20114565 20129679 + 9068941 102017464 MODEL AGCD01023066;GBDK01415409;XM_005384519;XM_005384521;XM_013514192;XM_013514193;XM_013514194;XR_001233977;XR_001233978 XP_005384576;XP_005384578;XP_013369646;XP_013369647;XP_013369648 sororin APPROVED protein-coding 8706093 LOC102018861 uncharacterized LOC102018861 NW_004955547 1458211 1476533 - 102018861 MODEL AGCD01072224;AGCD01072225;GBDJ01374207;XR_001232216 ncrna 8706098 Ccdc18 coiled-coil domain containing 18 ASSOCIATED WITH genetic disease (ortholog); FOUND IN centriolar satellite (ortholog) NW_004955423 1357515 1423094 - 9068941 102019613 A0A8C2V211 MODEL AGCD01023433;AGCD01023434;GBDF01187769;XM_013514360 XP_013369814 coiled-coil domain-containing protein 18 protein-coding ENSCLAG00000004649 NW_004955423 1356298 1434413 - 8706130 Abca12 ATP binding cassette subfamily A member 12 ENCODES a protein that exhibits apolipoprotein A-I receptor binding (ortholog); lipid transporter activity (ortholog); signaling receptor binding (ortholog); INVOLVED IN ceramide metabolic process (ortholog); ceramide transport (ortholog); cholesterol efflux (ortholog); ASSOCIATED WITH autosomal recessive congenital ichthyosis (ortholog); autosomal recessive congenital ichthyosis 1 (ortholog); autosomal recessive congenital ichthyosis 4A (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); epidermal lamellar body (ortholog) NW_004955457 885941 1062713 + 9068941;7240710 102020422 A0A8C2V3A1 MODEL AGCD01046716;AGCD01046717;AGCD01046718;GBCQ01127755;XM_013520777 XP_013376231 ATP-binding cassette sub-family A member 12;ATP-binding cassette, sub-family A (ABC1), member 12 APPROVED protein-coding ENSCLAG00000006672 NW_004955457 879510 1062713 + 8706189 LOC102021213 YEATS domain-containing protein 4-like NW_004955460 13231488 13238875 - 102021213 MODEL AGCD01048675;AGCD01048676 pseudo 8706190 Kmt2b lysine methyltransferase 2B ENCODES a protein that exhibits histone H3K4 methyltransferase activity (ortholog); unmethylated CpG binding (ortholog); zinc ion binding (ortholog); INVOLVED IN DNA methylation-dependent heterochromatin formation (ortholog); maternal-to-zygotic transition of gene expression (ortholog); oocyte development (ortholog); PARTICIPATES IN histone modification pathway; ASSOCIATED WITH acute myeloid leukemia (ortholog); autism spectrum disorder (ortholog); autistic disorder (ortholog); FOUND IN histone methyltransferase complex (ortholog); MLL1/2 complex (ortholog); nucleus (ortholog) NW_004955468 2813183 2834326 - 9068941 102024207 A0A8C2YRC7 MODEL AGCD01051838;GBCE01008533;GBCE01008553;XM_013522393;XM_013522395 XP_013377847;XP_013377849 histone-lysine N-methyltransferase 2B;lysine (K)-specific methyltransferase 2B APPROVED protein-coding ENSCLAG00000012114 NW_004955468 2813496 2834326 - 8706237 Tsc22d2 TSC22 domain family member 2 INVOLVED IN response to osmotic stress (ortholog); ASSOCIATED WITH genetic disease (ortholog); glycogen storage disease XV (ortholog) NW_004955448 1639463 1678279 + 9068941 102024397 MODEL AGCD01041265;GBCE01089585;GBDI01261302;XM_013518634 XP_013374088 TSC22 domain family protein 2;TSC22 domain family, member 2 APPROVED protein-coding 8706244 Dsg2 desmoglein 2 ENCODES a protein that exhibits cell adhesion molecule binding (ortholog); INVOLVED IN bundle of His cell-Purkinje myocyte adhesion involved in cell communication (ortholog); cell adhesion (ortholog); desmosome organization (ortholog); ASSOCIATED WITH arrhythmogenic right ventricular cardiomyopathy (ortholog); arrhythmogenic right ventricular dysplasia 1 (ortholog); arrhythmogenic right ventricular dysplasia 10 (ortholog); FOUND IN apical plasma membrane (ortholog); cell junction (ortholog); desmosome (ortholog) NW_004955402 18826400 18876188 + 9068941;7240710 102024409 MODEL AGCD01000541;GBDI01013125;GBDK01278961;XM_005373161 XP_005373218 desmoglein-2 protein-coding 8706262 LOC102026775 26S protease regulatory subunit 4-like NW_004955508 3435725 3438075 - 102026775 MODEL AGCD01065811 pseudo 8706263 Ube2j2 ubiquitin conjugating enzyme E2 J2 ENCODES a protein that exhibits ubiquitin conjugating enzyme activity (ortholog); ubiquitin protein ligase binding (ortholog); INVOLVED IN positive regulation of protein targeting to mitochondrion (ortholog); ubiquitin-dependent ERAD pathway (ortholog); ASSOCIATED WITH chromosome 1p36 deletion syndrome (ortholog); congenital myasthenic syndrome 8 (ortholog); dilated cardiomyopathy 1LL (ortholog); FOUND IN endoplasmic reticulum (ortholog); ubiquitin ligase complex (ortholog) NW_004955486 9519467 9539666 + 9068941 102027309 A0A8C2V4U5;A0A8C2V739;A0A8C2VA85 MODEL AGCD01059188;AGCD01059189;GBCE01118406;XM_005404243;XM_005404244;XM_013504213;XM_013504214;XM_013504215;XM_013504216;XM_013504217;XM_013504218 XP_005404300;XP_005404301;XP_013359667;XP_013359668;XP_013359669;XP_013359670;XP_013359671;XP_013359672 ubiquitin-conjugating enzyme E2 J2;ubiquitin-conjugating enzyme E2, J2 APPROVED protein-coding ENSCLAG00000006776 NW_004955486 9524459 9540562 + 8706280 LOC102027482 nuclear body protein SP140-like protein NW_004955453 4735334 4878501 + 102027482 MODEL AGCD01044696;AGCD01044697;AGCD01044698;AGCD01044699;AGCD01044700;AGCD01044701;GBDJ01266082;XM_005395417;XM_005395418;XM_013519812;XM_013519813;XM_013519814;XM_013519815;XM_013519816;XM_013519817;XR_001236159;XR_001236160;XR_001236161;XR_001236162;XR_001236163;XR_001236164;XR_001236165;XR_001236166;XR_001236167;XR_001236168;XR_001236169;XR_001236170;XR_001236171;XR_001236172 XP_005395474;XP_005395475;XP_013375266;XP_013375267;XP_013375268;XP_013375269;XP_013375270;XP_013375271 LOC102028493 uncharacterized LOC102028493 PROVISIONAL protein-coding 8706301 LOC102027516 40S ribosomal protein S18-like NW_004955470 5582595 5583466 + 102027516 MODEL AGCD01052753 pseudo 8706302 Emd emerin ENCODES a protein that exhibits actin binding (ortholog); beta-tubulin binding (ortholog); INVOLVED IN cellular response to growth factor stimulus (ortholog); negative regulation of canonical Wnt signaling pathway (ortholog); negative regulation of fibroblast proliferation (ortholog); ASSOCIATED WITH adrenoleukodystrophy (ortholog); autistic disorder (ortholog); autosomal recessive limb-girdle muscular dystrophy type 2J (ortholog); FOUND IN cortical endoplasmic reticulum (ortholog); cytoplasm (ortholog); endoplasmic reticulum (ortholog) NW_004955580 864532 866904 - 9068941;7240710 102027697 A0A8C2UUU8 MODEL AGCD01075627;GBDK01089927;XM_005414187 XP_005414244 protein-coding ENSCLAG00000002874 NW_004955580 864532 866904 - 8706312 LOC102027707 keratin, type I cuticular Ha3-I-like NW_004955451 15735490 15740410 - 102027707 MODEL AGCD01043635;AGCD01043636;GBCB01128392;XM_005394396 XP_005394453 protein-coding 8706328 Klf9 KLF transcription factor 9 ENCODES a protein that exhibits DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); DNA-binding transcription factor activity (ortholog); RNA polymerase II transcription regulatory region sequence-specific DNA binding (ortholog); INVOLVED IN cellular response to cortisol stimulus (ortholog); cellular response to peptide (ortholog); cellular response to thyroid hormone stimulus (ortholog); ASSOCIATED WITH Body Weight (ortholog); diastolic heart failure (ortholog); endometriosis (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955434 2685416 2716669 + 9068941 102029218 A0A8C2V424 MODEL AGCD01032105;GBDK01095916;XM_005388555 XP_005388612 Krueppel-like factor 9;Kruppel like factor 9;Kruppel-like factor 9 APPROVED protein-coding ENSCLAG00000005123 NW_004955434 2685416 2716669 + 8706334 LOC102029879 40S ribosomal protein S12-like NW_004955426 3752953 3753829 - 102029879 MODEL AGCD01026083 pseudo 8706344 Mc2r melanocortin 2 receptor INVOLVED IN adenylate cyclase-activating G protein-coupled receptor signaling pathway (ortholog); placenta development (ortholog); PARTICIPATES IN G protein mediated signaling pathway via Galphas family; melanocortin system pathway; ASSOCIATED WITH Acute-Phase Reaction (ortholog); chromosome 18p deletion syndrome (ortholog); genetic disease (ortholog) NW_004955402 190513 225627 + 9068941;7240710 102004992 A0A8C2VJS8 MODEL AGCD01000011;AGCD01000012;GBDF01110673;XM_005372543 XP_005372600 adrenocorticotropic hormone receptor;melanocortin 2 receptor (adrenocorticotropic hormone) APPROVED protein-coding ENSCLAG00000011457 NW_004955402 190513 225627 + 8706350 LOC102005191 WW domain-binding protein 5-like NW_004955445 15861773 15862606 + 102005191 MODEL AGCD01039857 pseudo 8706351 LOC102005629 uncharacterized LOC102005629 NW_004955526 3115354 3136784 + 102005629 MODEL AGCD01069328;XR_264659 ncrna 8706358 Pdha1 pyruvate dehydrogenase E1 subunit alpha 1 ENCODES a protein that exhibits pyruvate dehydrogenase (acetyl-transferring) activity (ortholog); pyruvate dehydrogenase (NAD+) activity (ortholog); pyruvate dehydrogenase activity (ortholog); INVOLVED IN acetyl-CoA biosynthetic process from pyruvate (ortholog); PARTICIPATES IN citric acid cycle pathway; fumaric aciduria pathway; Leigh disease pathway; ASSOCIATED WITH autistic disorder (ortholog); Coffin-Lowry syndrome (ortholog); developmental and epileptic encephalopathy 2 (ortholog); FOUND IN catalytic complex (ortholog); mitochondrial pyruvate dehydrogenase complex (ortholog); mitochondrion (ortholog) NW_004955586 98492 114927 - 9068941;7240710 102005758 A0A8C2UFB7 MODEL AGCD01076020;AGCD01076021;GBBH01166354;XM_005414433 XP_005414490 pyruvate dehydrogenase (lipoamide) alpha 1;pyruvate dehydrogenase E1 alpha 1 subunit;pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial;pyruvate dehydrogenase alpha 1 APPROVED protein-coding ENSCLAG00000000108 NW_004955586 97172 114928 - 8706379 Pnpt1 polyribonucleotide nucleotidyltransferase 1 ENCODES a protein that exhibits 3'-5'-RNA exonuclease activity (ortholog); identical protein binding (ortholog); miRNA binding (ortholog); INVOLVED IN cellular response to interferon-beta (ortholog); cellular response to oxidative stress (ortholog); liver regeneration (ortholog); ASSOCIATED WITH autosomal recessive nonsyndromic deafness 70 (ortholog); combined oxidative phosphorylation deficiency 13 (ortholog); Developmental Disabilities (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); endoplasmic reticulum membrane (ortholog) NW_004955424 27407451 27449830 + 9068941;7240710 102006366 A0A8C2V1K8 MODEL AGCD01025116;AGCD01025117;GBBH01149997;XM_005385770;XM_013514724 XP_005385827;XP_013370178 polyribonucleotide nucleotidyltransferase 1, mitochondrial protein-coding ENSCLAG00000006240 NW_004955424 27407489 27448992 + 8706411 Cdk3 cyclin dependent kinase 3 INVOLVED IN DNA damage response (ortholog); G0 to G1 transition (ortholog); negative regulation of Notch signaling pathway (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cyclin-dependent protein kinase holoenzyme complex (ortholog) NW_004955506 6247146 6252083 - 9068941 102006371 A0A8C2VC11 MODEL AGCD01065405;GBDF01210937;XM_005407460;XM_005407461;XM_005407462;XM_005407463 XP_005407517;XP_005407518;XP_005407519;XP_005407520 cyclin-dependent kinase 3 APPROVED protein-coding ENSCLAG00000007409 NW_004955506 6247146 6252043 - 8706434 Ppp3r2 protein phosphatase 3 regulatory subunit B, beta ENCODES a protein that exhibits calcium-dependent protein serine/threonine phosphatase regulator activity (ortholog); INVOLVED IN penetration of zona pellucida (ortholog); PARTICIPATES IN calcineurin signaling pathway; ASSOCIATED WITH fructose-1,6-bisphosphatase deficiency (ortholog); genetic disease (ortholog); hereditary fructose intolerance syndrome (ortholog); FOUND IN calcineurin complex (ortholog); sperm flagellum (ortholog); sperm midpiece (ortholog) NW_004955419 24252772 24253730 + 9068941 102006666 A0A8C2VPC4 MODEL AGCD01020340;GBDF01003998;XM_005382792 XP_005382849 calcineurin subunit B type 2 APPROVED protein-coding ENSCLAG00000012103 8706439 LOC102006850 vomeronasal type-1 receptor 2-like NW_004955603 165496 166395 - 102006850 MODEL AGCD01076814;XM_005414836 XP_005414893 protein-coding 8706442 Ndufs2 NADH:ubiquinone oxidoreductase core subunit S2 ENCODES a protein that exhibits NADH dehydrogenase (ubiquinone) activity (ortholog); NADH dehydrogenase activity (ortholog); oxygen sensor activity (ortholog); INVOLVED IN cellular response to oxygen levels (ortholog); gliogenesis (ortholog); mitochondrial ATP synthesis coupled electron transport (ortholog); PARTICIPATES IN doxorubicin pharmacokinetics pathway; ASSOCIATED WITH autoimmune interstitial lung, joint, and kidney disease (ortholog); cardiomyopathy (ortholog); Experimental Diabetes Mellitus (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrial respiratory chain complex I (ortholog); mitochondrion (ortholog) NW_004955468 12961873 12971278 + 9068941;7240710 102007000 A0A8C2VR21;A0A8C2VYB1 MODEL AGCD01052194;GBCB01088834;XM_005400268 XP_005400325 NADH dehydrogenase (ubiquinone) Fe-S protein 2, 49kDa (NADH-coenzyme Q reductase);NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrial APPROVED protein-coding ENSCLAG00000013194 NW_004955468 12961915 12971095 + 8706460 Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 ENCODES a protein that exhibits GTPase activator activity (ortholog); phosphatidylinositol-3,4,5-trisphosphate binding (ortholog); phosphatidylinositol-3-phosphate binding (ortholog); INVOLVED IN cilium assembly (ortholog); negative regulation of dendritic spine development (ortholog); positive regulation of membrane tubulation (ortholog); PARTICIPATES IN Arf family mediated signaling pathway; ASSOCIATED WITH genetic disease (ortholog); juvenile rheumatoid arthritis (ortholog); pulmonary tuberculosis (ortholog); FOUND IN cell projection membrane (ortholog); cytosol (ortholog); dendritic spine (ortholog) NW_004955461 4813228 5083548 - 9068941 102007744 A0A8C2UJQ8;A0A8C2ULK1;A0A8C2YIV2 MODEL AGCD01048875;AGCD01048876;GBDF01249602;GBDK01182284;XM_013521324 XP_013376778 arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 protein-coding ENSCLAG00000001402 NW_004955461 4811069 5133257 - 8706504 Tmem248 transmembrane protein 248 ASSOCIATED WITH argininosuccinic aciduria (ortholog); genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog) NW_004955456 8730374 8762549 + 9068941 102008822 A0A8C2UYA4 MODEL AGCD01046499;AGCD01046500;AGCD01046501;GBBH01060920;GBDF01004951;XM_013520567 XP_013376021 protein-coding ENSCLAG00000005032 NW_004955456 8730038 8762549 + 8706521 Lrrc14 leucine rich repeat containing 14 ENCODES a protein that exhibits kinase binding (ortholog); INVOLVED IN negative regulation of NF-kappaB transcription factor activity (ortholog); negative regulation of toll-like receptor signaling pathway (ortholog); ASSOCIATED WITH Baller-Gerold syndrome (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog) NW_004955454 3142621 3146470 + 102010226 A0A8C2VFN9 MODEL AGCD01045057;GBDI01115994;XM_005395903;XM_005395907;XM_013520075;XM_013520076;XM_013520077;XM_013520078;XM_013520079;XM_013520080;XM_013520081;XM_013520082;XM_013520083 XP_005395960;XP_005395964;XP_013375529;XP_013375530;XP_013375531;XP_013375532;XP_013375533;XP_013375534;XP_013375535;XP_013375536;XP_013375537 leucine-rich repeat-containing protein 14 protein-coding ENSCLAG00000008753 NW_004955454 3142636 3146470 + 8706552 LOC102010577 fatty acid-binding protein, epidermal pseudogene NW_004955414 14243606 14244127 + 102010577 MODEL AGCD01015144 APPROVED pseudo 8706553 Tial1 TIA1 cytotoxic granule associated RNA binding protein like 1 ENCODES a protein that exhibits mRNA 3'-UTR AU-rich region binding (ortholog); mRNA 3'-UTR binding (ortholog); protein-RNA adaptor activity (ortholog); INVOLVED IN germ cell development (ortholog); negative regulation of cell population proliferation (ortholog); positive regulation of hippo signaling (ortholog); PARTICIPATES IN spliceosome pathway; ASSOCIATED WITH Disease Progression (ortholog); Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytoplasmic stress granule (ortholog); cytosol (ortholog) NW_004955551 370792 395836 - 9068941 102010637 A0A8C2UK13;A0A8C2UQG7 MODEL AGCD01072655;GBCQ01042559;XM_005412159;XM_005412160;XM_013508586;XM_013508587 XP_005412216;XP_005412217;XP_013364040;XP_013364041 TIA1 cytotoxic granule-associated RNA binding protein-like 1;nucleolysin TIAR APPROVED protein-coding ENSCLAG00000001273 NW_004955551 370792 395836 - 8706583 LOC102012203 dual specificity protein phosphatase 5-like NW_004955485 904628 909295 - 102012203 MODEL AGCD01058465;GBDK01430993;XM_005403917 XP_005403974 protein-coding 8706589 LOC102013096 probable E3 ubiquitin-protein ligase HECTD2 NW_004955493 1068126 1073096 + 102013096 MODEL AGCD01060877 APPROVED pseudo 8706591 Klf17 KLF transcription factor 17 ENCODES a protein that exhibits DNA-binding transcription factor activity (ortholog); DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); RNA polymerase II cis-regulatory region sequence-specific DNA binding (ortholog); INVOLVED IN gamete generation (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease dominant intermediate C (ortholog); developmental and epileptic encephalopathy (ortholog); early infantile epileptic encephalopathy (ortholog) NW_004955537 3637825 3648078 + 9068941 102013338 MODEL AGCD01070970;AGCD01070971;GBDF01085578;XM_005410712 XP_005410769 Krueppel-like factor 17;Kruppel like factor 17;Kruppel-like factor 17 APPROVED protein-coding 8706603 Pkn1 protein kinase N1 ENCODES a protein that exhibits chromatin binding (ortholog); histone binding (ortholog); histone deacetylase binding (ortholog); INVOLVED IN B cell apoptotic process (ortholog); B cell homeostasis (ortholog); epithelial cell migration (ortholog); ASSOCIATED WITH genetic disease (ortholog); Neointima (ortholog); FOUND IN cleavage furrow (ortholog); cytoplasm (ortholog); cytoplasmic vesicle (ortholog) NW_004955415 33040868 33062753 + 9068941 102014448 A0A8C2W967 MODEL AGCD01016747;AGCD01016748;GBDK01001917;XM_005381094;XM_005381095;XM_005381096;XM_005381097;XM_005381098;XM_013512169 XP_005381151;XP_005381152;XP_005381153;XP_005381154;XP_005381155;XP_013367623 serine/threonine-protein kinase N1 protein-coding ENSCLAG00000016252 NW_004955415 33043918 33063567 + 8706640 Hao2 hydroxyacid oxidase 2 ENCODES a protein that exhibits (S)-2-hydroxy-acid oxidase activity (ortholog); FMN binding (ortholog); identical protein binding (ortholog); INVOLVED IN fatty acid oxidation (ortholog); mandelate metabolic process (ortholog); ASSOCIATED WITH Chemical and Drug Induced Liver Injury (ortholog); cholestasis (ortholog); Experimental Liver Cirrhosis (ortholog); FOUND IN peroxisomal matrix (ortholog); peroxisome (ortholog) NW_004955435 22380395 22404426 + 9068941 102014823 A0A8C2V0G9 MODEL AGCD01033502;AGCD01033503;GBCQ01010091;XM_005389076;XM_005389077 XP_005389133;XP_005389134 hydroxyacid oxidase 2 (long chain) APPROVED protein-coding ENSCLAG00000005779 NW_004955435 22380388 22404052 + 8706654 Ndel1 nudE neurodevelopment protein 1 like 1 ENCODES a protein that exhibits alpha-tubulin binding (ortholog); beta-tubulin binding (ortholog); identical protein binding (ortholog); INVOLVED IN activation of GTPase activity (ortholog); canonical Wnt signaling pathway (ortholog); cell migration (ortholog); ASSOCIATED WITH genetic disease (ortholog); juvenile rheumatoid arthritis (ortholog); schizophrenia (ortholog); FOUND IN axon (ortholog); axon hillock (ortholog); cell body (ortholog) NW_004955467 8432806 8486563 - 9068941 102015823 A0A8C2VYZ1 MODEL AGCD01051450;AGCD01051451;GBCB01002091;XM_005399403;XM_005399405;XM_005399406;XM_005399407;XM_013522099 XP_005399460;XP_005399462;XP_005399463;XP_005399464;XP_013377553 nuclear distribution protein nudE-like 1;nudE neurodevelopment protein 1-like 1 APPROVED protein-coding ENSCLAG00000013523 NW_004955467 8432806 8468155 - 8706690 LOC102016615 glyceraldehyde-3-phosphate dehydrogenase-like NW_004955500 6543405 6544562 + 102016615 MODEL AGCD01063884;XR_264233 pseudo 8706693 Plscr3 phospholipid scramblase 3 ENCODES a protein that exhibits calcium ion binding (ortholog); calcium-dependent protein binding (ortholog); lead ion binding (ortholog); INVOLVED IN apoptotic process (ortholog); cardiolipin biosynthetic process (ortholog); cellular response to lipopolysaccharide (ortholog); ASSOCIATED WITH common variable immunodeficiency (ortholog); congenital myasthenic syndrome 2A (ortholog); dyskeratosis congenita (ortholog); FOUND IN cytosol (ortholog); mitochondrial inner membrane (ortholog); mitochondrion (ortholog) NW_004955467 9534462 9539738 + 9068941 102016998 A0A8C2VVC5 MODEL AGCD01051516;GBDI01305134;XM_005399507;XM_013522122 XP_005399564;XP_013377576 protein-coding ENSCLAG00000014430 NW_004955467 9535261 9539738 + 8706715 Tmem243 transmembrane protein 243 ASSOCIATED WITH genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog) NW_004955621 42121 50628 + 9068941 102017086 A0A8C2UGQ0 MODEL AGCD01077372;GBDF01085595;XM_005415014 XP_005415071 transmembrane protein 243, mitochondrial APPROVED protein-coding ENSCLAG00000000237 8706723 Gmps guanine monophosphate synthase ENCODES a protein that exhibits enzyme binding (ortholog); GMP synthase (glutamine-hydrolyzing) activity (ortholog); GMP synthase activity (ortholog); INVOLVED IN GMP biosynthetic process (ortholog); GMP salvage (ortholog); response to L-cysteine (ortholog); PARTICIPATES IN 2-hydroxyglutaric aciduria pathway; adenine phoshoribosyltransferase deficiency pathway; adenosine monophosphate deaminase deficiency pathway; ASSOCIATED WITH acute myelomonocytic leukemia (ortholog); Experimental Diabetes Mellitus (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog) NW_004955448 6931891 6984662 + 9068941;7240710 102017178 A0A8C2V7I7;A0A8C2V9P7;A0A8C2VCD4 MODEL AGCD01041397;AGCD01041398;GBDF01007582;XM_005393072;XM_005393073 XP_005393129;XP_005393130 GMP synthase [glutamine-hydrolyzing] APPROVED protein-coding ENSCLAG00000007499 NW_004955448 6932926 6984662 + 8706749 Prpf8 pre-mRNA processing factor 8 ENCODES a protein that exhibits K63-linked polyubiquitin modification-dependent protein binding (ortholog); INVOLVED IN cellular response to lipopolysaccharide (ortholog); cellular response to tumor necrosis factor (ortholog); mRNA splicing, via spliceosome (ortholog); PARTICIPATES IN retinitis pigmentosa pathway; spliceosome pathway; ASSOCIATED WITH Developmental Disease (ortholog); fundus dystrophy (ortholog); genetic disease (ortholog); FOUND IN catalytic step 2 spliceosome (ortholog); nucleus (ortholog); small nuclear ribonucleoprotein complex (ortholog) NW_004955481 1499634 1530670 + 9068941;7240710 102017981 A0A8C2UXE8 MODEL AGCD01056833;AGCD01056834;GBDF01002836;XM_005402612 XP_005402669 pre-mRNA-processing-splicing factor 8 protein-coding ENSCLAG00000004388 NW_004955481 1499634 1530670 + 8706796 LOC102018620 melanoma-associated antigen 8-like NW_004955498 2322033 2323007 - 102018620 MODEL AGCD01062784;XM_013505524 XP_013360978 protein-coding 8706800 LOC102018881 keratin, type I cytoskeletal 28 NW_004955451 15254864 15264012 - 9068941 102018881 A0A8C2VY45;A0A8C2VY60;A0A8C2VY67;A0A8C2VYM0;A0A8C2W0D4;A0A8C2YTL6 MODEL AGCD01043603;AGCD01043604;GBDK01170754;XM_005394373 XP_005394430 Krt28 keratin 28 APPROVED protein-coding ENSCLAG00000015353 NW_004955451 15216809 15264012 - 8706812 Mest mesoderm specific transcript INVOLVED IN regulation of lipid storage (ortholog); response to retinoic acid (ortholog); ASSOCIATED WITH Barth syndrome (ortholog); Childhood Schizophrenia (ortholog); genetic disease (ortholog); FOUND IN endoplasmic reticulum (ortholog) NW_004955479 11116705 11135061 + 9068941 102018927 A0A8C2V5M1 MODEL AGCD01056573;AGCD01056574;GBDF01042954;XM_005402446;XM_005402447 XP_005402503;XP_005402504 protein-coding ENSCLAG00000007263 NW_004955479 11122007 11135061 + 8706833 LOC102019044 serpin B6 NW_004955465 10220475 10248997 + 9068941;7240710 102019044 A0A8C2YJL0 MODEL AGCD01050504;AGCD01050505;AGCD01050506;GBCE01029516;XM_005398908;XM_005398909 XP_005398965;XP_005398966 Serpinb6 serpin peptidase inhibitor, clade B (ovalbumin), member 6 APPROVED protein-coding ENSCLAG00000002474 NW_004955465 10237018 10249050 + 8706847 LOC102019085 40S ribosomal protein S11-like NW_004955503 5228501 5228977 - 102019085 MODEL AGCD01064700 pseudo 8706848 Cct4 chaperonin containing TCP1 subunit 4 ENCODES a protein that exhibits protein folding chaperone (ortholog); INVOLVED IN binding of sperm to zona pellucida (ortholog); chaperone-mediated protein folding (ortholog); positive regulation of establishment of protein localization to telomere (ortholog); ASSOCIATED WITH genetic disease (ortholog); hereditary sensory neuropathy (ortholog); schizophrenia (ortholog); FOUND IN cell body (ortholog); centrosome (ortholog); chaperonin-containing T-complex (ortholog) NW_004955424 22088949 22108514 + 9068941 102019615 A0A8C2VUU3;A0A8C2YSW7 MODEL AGCD01024931;AGCD01024932;AGCD01024933;GBDF01009053;XM_005385733 XP_005385790 T-complex protein 1 subunit delta;chaperonin containing TCP1, subunit 4 (delta) APPROVED protein-coding ENSCLAG00000014321 NW_004955424 22088949 22108514 + 8706866 LOC102020499 uncharacterized LOC102020499 NW_004955574 228074 230012 + 102020499 MODEL AGCD01075093;GBCB01123138;XR_265057;XR_265058 ncrna 8706873 LOC102020558 olfactory receptor 52B4-like NW_004955414 20016773 20017717 + 102020558 MODEL AGCD01015350;XM_005380462 XP_005380519 protein-coding 8706876 Tmem88b transmembrane protein 88B ASSOCIATED WITH chromosome 1p36 deletion syndrome (ortholog); congenital myasthenic syndrome 8 (ortholog); dilated cardiomyopathy 1LL (ortholog) NW_004955486 9376707 9379315 - 9068941 102020571 A0A8C2VBK9 MODEL AGCD01059179;GBDF01040460;XM_005404219 XP_005404276 protein-coding ENSCLAG00000009079 NW_004955486 9376707 9379315 - 8706882 Mospd1 motile sperm domain containing 1 INVOLVED IN negative regulation of transcription by RNA polymerase II (ortholog); positive regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); syndromic X-linked intellectual disability Lubs type (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog); perinuclear region of cytoplasm (ortholog) NW_004955473 103541 127854 + 9068941 102022492 A0A8C2YIE8 MODEL AGCD01053832;GBBH01219182;XM_005401196 XP_005401253 motile sperm domain-containing protein 1 protein-coding ENSCLAG00000000760 NW_004955473 103356 129274 + 8706896 Pycr1 pyrroline-5-carboxylate reductase 1 ENCODES a protein that exhibits identical protein binding (ortholog); pyrroline-5-carboxylate reductase activity (ortholog); INVOLVED IN cellular response to oxidative stress (ortholog); obsolete negative regulation of hydrogen peroxide-induced cell death (ortholog); proline biosynthetic process (ortholog); ASSOCIATED WITH Autosomal Recessive Cutis Laxa (ortholog); autosomal recessive cutis laxa type IIB (ortholog); autosomal recessive cutis laxa type IIIB (ortholog); FOUND IN mitochondrion (ortholog) NW_004955506 1231874 1236550 + 9068941;7240710 102023056 A0A8C2V8V6 MODEL AGCD01065251;GBCB01119841;XM_005407242;XM_005407244;XM_013506062;XM_013506063 XP_005407299;XP_005407301;XP_013361516;XP_013361517 pyrroline-5-carboxylate reductase 1, mitochondrial protein-coding ENSCLAG00000007608 NW_004955506 1231863 1236550 + 8706913 Ube2v2 ubiquitin conjugating enzyme E2 V2 INVOLVED IN DNA double-strand break processing (ortholog); error-free postreplication DNA repair (ortholog); negative regulation of neuron apoptotic process (ortholog); ASSOCIATED WITH immunodeficiency 26 (ortholog); FOUND IN nucleoplasm (ortholog); nucleus (ortholog); UBC13-MMS2 complex (ortholog) NW_004955454 7951876 7998686 + 9068941 102023110 A0A8C2VHK4;A0A8C2YQG3;A0A8C2YQG7 MODEL AGCD01045315;GBDF01213661;XM_005396039 XP_005396096 ubiquitin-conjugating enzyme E2 variant 2 APPROVED protein-coding ENSCLAG00000010839 NW_004955454 7951876 7998686 + 8706926 Creg1 cellular repressor of E1A stimulated genes 1 INVOLVED IN autophagy (ortholog); endocytosis (ortholog); lysosomal lumen acidification (ortholog); ASSOCIATED WITH COVID-19 (ortholog); diastolic heart failure (ortholog); gastrointestinal stromal tumor (ortholog); FOUND IN endosome (ortholog); extracellular space (ortholog); lysosome (ortholog) NW_004955462 9440019 9451875 + 9068941 102023447 A0A8C2V0V7 MODEL AGCD01049338;GBBH01032942;XM_005398225;XM_005398226 XP_005398282;XP_005398283 cellular repressor of E1A-stimulated genes 1 APPROVED protein-coding ENSCLAG00000005740 NW_004955462 9439987 9455268 + 8706936 Apod apolipoprotein D ENCODES a protein that exhibits cholesterol binding (ortholog); INVOLVED IN glucose metabolic process (ortholog); lipid metabolic process (ortholog); negative regulation of cytokine production involved in inflammatory response (ortholog); ASSOCIATED WITH Alzheimer's disease (ortholog); Brain Injuries (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosolic ribosome (ortholog); dendrite (ortholog) NW_004955420 13553254 13570357 + 9068941 102024118 A0A8C2VK31 MODEL AGCD01020925;GBCE01000148;XM_005383177;XM_013513581 XP_005383234;XP_013369035 protein-coding ENSCLAG00000011471 NW_004955420 13553058 13573690 + 8706948 Pgap1 post-GPI attachment to proteins inositol deacylase 1 ENCODES a protein that exhibits phosphatidylinositol deacylase activity (ortholog); INVOLVED IN anterior/posterior axis specification (ortholog); embryonic pattern specification (ortholog); forebrain regionalization (ortholog); ASSOCIATED WITH Cerebral Visual Impairment and Intellectual Disability (ortholog); genetic disease (ortholog); hereditary spastic paraplegia (ortholog); FOUND IN endoplasmic reticulum (ortholog) NW_004955403 3527398 3582004 + 9068941;7240710 102025426 A0A8C2VL39 MODEL AGCD01001769;AGCD01001770;GBCE01082448;GBDI01167905;XM_013512108 XP_013367562 GPI inositol-deacylase;post-GPI attachment to proteins 1 APPROVED protein-coding ENSCLAG00000011838 NW_004955403 3527138 3582004 + 8706978 Sfrp4 secreted frizzled related protein 4 ENCODES a protein that exhibits Wnt-protein binding (ortholog); INVOLVED IN bone morphogenesis (ortholog); decidualization (ortholog); female pregnancy (ortholog); PARTICIPATES IN Wnt signaling, canonical pathway; ASSOCIATED WITH Colorectal Neoplasms (ortholog); Experimental Arthritis (ortholog); genetic disease (ortholog); FOUND IN cell surface (ortholog); cytoplasm (ortholog); extracellular space (ortholog) NW_004955460 5654187 5666475 + 9068941 102026611 A0A8C2V5Q3 MODEL AGCD01048456;GBDJ01005445;XM_005397748 XP_005397805 secreted frizzled-related protein 4 APPROVED protein-coding ENSCLAG00000007024 NW_004955460 5654288 5664219 + 8706988 Pten phosphatase and tensin homolog ENCODES a protein that exhibits anaphase-promoting complex binding (ortholog); enzyme binding (ortholog); identical protein binding (ortholog); INVOLVED IN adult behavior (ortholog); angiogenesis (ortholog); B cell proliferation (ortholog); PARTICIPATES IN altered phosphatidylinositol 3-kinase signaling pathway; altered phosphatidylinositol 3-kinase-Akt signaling pathway; endometrial cancer pathway; ASSOCIATED WITH acute lymphoblastic leukemia (ortholog); acute megakaryocytic leukemia (ortholog); acute myocardial infarction (ortholog); FOUND IN apical plasma membrane (ortholog); cell projection (ortholog); cytoplasm (ortholog) NW_004955425 5007811 5091829 - 9068941;7240710 102026655 A0A8C2W3G4 MODEL AGCD01025329;AGCD01025330;AGCD01025331;AGCD01025332;GBDJ01081006;XM_013514767 XP_013370221 phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN protein-coding ENSCLAG00000014815 NW_004955425 5014147 5091829 - 8707008 Nfix nuclear factor I X ENCODES a protein that exhibits chromatin binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); RNA polymerase II cis-regulatory region sequence-specific DNA binding (ortholog); INVOLVED IN astrocyte differentiation (ortholog); atrioventricular canal morphogenesis (ortholog); bone mineralization (ortholog); ASSOCIATED WITH alpha-mannosidosis (ortholog); Charcot-Marie-Tooth disease dominant intermediate B (ortholog); developmental and epileptic encephalopathy 11 (ortholog); FOUND IN nucleoplasm (ortholog); nucleus (ortholog) NW_004955415 32055926 32121611 + 9068941;7240710 102027295 A0A8C2VRY5;A0A8C2VU04;A0A8C2VVZ7;A0A8C2VZ80 MODEL AGCD01016709;AGCD01016710;GBBH01062548;GBCB01005540;XM_005381046 XP_005381103 nuclear factor 1 X-type;nuclear factor I/X (CCAAT-binding transcription factor) APPROVED protein-coding ENSCLAG00000013479 NW_004955415 32055375 32117833 + 8707038 Dyrk2 dual specificity tyrosine phosphorylation regulated kinase 2 ENCODES a protein that exhibits ATP binding (ortholog); magnesium ion binding (ortholog); manganese ion binding (ortholog); INVOLVED IN DNA damage response (ortholog); intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator (ortholog); negative regulation of calcineurin-NFAT signaling cascade (ortholog); PARTICIPATES IN p53 signaling pathway; ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955458 14199912 14201712 + 9068941 102027496 A0A8C2VSS1 MODEL AGCD01047829;GBDF01187898;GBDJ01087414;XM_013520977 XP_013376431 dual specificity tyrosine-phosphorylation-regulated kinase 2;dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 2 APPROVED protein-coding ENSCLAG00000013694 NW_004955458 14193303 14218957 + 8707053 LOC102028733 putative uncharacterized protein FLJ38447 NW_004955467 9024888 9027668 + 102028733 A0A8C2VA70 MODEL AGCD01051481;GBDI01045379;XM_005399449 XP_005399506 APPROVED protein-coding ENSCLAG00000008516 NW_004955467 9025497 9026170 + 8707059 B3galt6 beta-1,3-galactosyltransferase 6 ENCODES a protein that exhibits galactosylxylosylprotein 3-beta-galactosyltransferase activity (ortholog); UDP-galactosyltransferase activity (ortholog); INVOLVED IN glycosaminoglycan biosynthetic process (ortholog); proteoglycan biosynthetic process (ortholog); ASSOCIATED WITH Al-Gazali Syndrome (ortholog); chromosome 1p36 deletion syndrome (ortholog); congenital myasthenic syndrome 8 (ortholog); FOUND IN Golgi apparatus (ortholog); Golgi medial cisterna (ortholog) NW_004955486 9553765 9555675 - 9068941;7240710 102029184 A0A8C2VF61 MODEL AGCD01059190;AGCD01059191;GBDF01304798;XM_013504220 XP_013359674 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6 APPROVED protein-coding ENSCLAG00000010125 NW_004955486 9554435 9555459 - 8707065 LOC102029253 nuclear RNA export factor 2-like NW_004956896 2063 2522 - 102029253 MODEL AGCD01080291;GBDK01180905;GBDK01180907;XM_013510237 XP_013365691 APPROVED protein-coding 8707069 LOC102030370 olfactory receptor 4F3/4F16/4F29-like NW_004955614 202113 222828 + 102030370 MODEL AGCD01077235;AGCD01077236 pseudo 8707070 Nop14 NOP14 nucleolar protein ENCODES a protein that exhibits enzyme binding (ortholog); ASSOCIATED WITH cherubism (ortholog); Ellis-Van Creveld syndrome (ortholog); genetic disease (ortholog); FOUND IN nucleolus (ortholog); nucleoplasm (ortholog) NW_004955514 1817645 1837011 - 9068941 102030559 A0A8C2VGS9 MODEL AGCD01067065;GBCQ01068048;XM_005408757 XP_005408814 nucleolar protein 14 protein-coding ENSCLAG00000008622 NW_004955514 1817980 1836984 - 8707092 Trnai-gau transfer RNA isoleucine (anticodon GAU) This record serves to anchor the annotations of this class of tRNAs at multiple locations on the chinchilla, long-tailed genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMe NW_004955500 8293826 8293897 + 101978795 MODEL AGCD01063986 trna 8707093 LOC102003597 uncharacterized LOC102003597 NW_004955447 15301309 15312329 + 102003597 MODEL AGCD01041045;GBDF01277712;XR_262434 ncrna 8707099 Znf512 zinc finger protein 512 ASSOCIATED WITH genetic disease (ortholog); Tatton-Brown-Rahman syndrome (ortholog) NW_004955469 9525501 9571050 + 9068941 102004374 A0A8C2V5E3;A0A8C2V7X6 MODEL AGCD01052505;AGCD01052506;AGCD01052507;AGCD01052508;AGCD01052509;AGCD01052510;GBBH01164970;GBDF01085710;XM_013522661;XM_013522662 XP_013378115;XP_013378116 protein-coding ENSCLAG00000006325 NW_004955469 9525637 9569412 + 8707116 Bpifb6 BPI fold containing family B member 6 ASSOCIATED WITH genetic disease (ortholog) NW_004955422 28214188 28224604 - 9068941 102004396 A0A8C2W8J7 MODEL AGCD01023345;GBDF01181601;XM_005384854 XP_005384911 BPI fold containing family B, member 6;BPI fold-containing family B member 6 APPROVED protein-coding ENSCLAG00000016956 NW_004955422 28214350 28224604 - 8707134 Clic4 chloride intracellular channel 4 ENCODES a protein that exhibits chloride channel activity (ortholog); protein-containing complex binding (ortholog); INVOLVED IN angiogenesis (ortholog); branching morphogenesis of an epithelial tube (ortholog); cellular response to calcium ion (ortholog); ASSOCIATED WITH Dwarfism (ortholog); genetic disease (ortholog); osteoarthritis (ortholog); FOUND IN apical part of cell (ortholog); cell surface (ortholog); cell-cell junction (ortholog) NW_004955452 4479783 4534115 + 9068941 102005101 A0A8C2VEC2 MODEL AGCD01043983;AGCD01043984;GBCB01039631;XM_005394817 XP_005394874 chloride intracellular channel protein 4 protein-coding ENSCLAG00000007919 NW_004955452 4479783 4534115 + 8707149 LOC102005329 uncharacterized LOC102005329 NW_004955602 418672 420204 - 102005329 MODEL AGCD01076784;GBDF01158942;XR_265157 ncrna 8707153 Slitrk1 SLIT and NTRK like family member 1 INVOLVED IN adult behavior (ortholog); axonogenesis (ortholog); homeostatic process (ortholog); ASSOCIATED WITH chromosome 13q14 deletion syndrome (ortholog); genetic disease (ortholog); Gilles de la Tourette syndrome (ortholog); FOUND IN GABA-ergic synapse (ortholog); glutamatergic synapse (ortholog); postsynaptic density membrane (ortholog) NW_004955404 24436394 24439749 + 9068941;7240710 102005990 A0A8C2YV31 MODEL AGCD01003820;XM_005374122 XP_005374179 SLIT and NTRK-like family, member 1;SLIT and NTRK-like protein 1 APPROVED protein-coding ENSCLAG00000017541 NW_004955404 24437299 24439389 + 8707158 LOC102006623 uncharacterized LOC102006623 NW_004955563 2035807 2036366 + 102006623 MODEL AGCD01074168;GBDF01050491;XR_265019 ncrna 8707162 Thap4 THAP domain containing 4 ENCODES a protein that exhibits heme binding (ortholog); identical protein binding (ortholog); nitric oxide binding (ortholog); INVOLVED IN nitrate metabolic process (ortholog); tyrosine metabolic process (ortholog); ASSOCIATED WITH Bethlem Myopathy 1 (ortholog); chromosome 2q37 deletion syndrome (ortholog); D-2-hydroxyglutaric aciduria 1 (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog) NW_004955542 192888 217985 + 9068941 102006957 A0A8C2UNS2;A0A8C2URL8 MODEL AGCD01071461;AGCD01071462;AGCD01071463;AGCD01071464;GBBH01061509;GBDF01047758;XM_013508087 XP_013363541 THAP domain-containing protein 4 protein-coding ENSCLAG00000002361 NW_004955542 195088 217831 + 8707171 LOC102007137 glucose-6-phosphatase 3 pseudogene NW_004955503 444692 461910 + 102007137 MODEL AGCD01064504 APPROVED pseudo 8707172 LOC102007219 tRNA methyltransferase 10 homolog B pseudogene NW_004955472 2140534 2143118 - 102007219 MODEL AGCD01053437 APPROVED pseudo 8707173 LOC102007528 histone H2B type 1 NW_004955465 13392728 13393418 + 102007528 A0A8C2WA51 MODEL AGCD01050607;XM_005398952 XP_005399009 APPROVED protein-coding ENSCLAG00000001916;ENSCLAG00000017473;ENSCLAG00000017500;ENSCLAG00000017549 8707178 Slc16a1 solute carrier family 16 member 1 ENCODES a protein that exhibits carboxylic acid transmembrane transporter activity (ortholog); identical protein binding (ortholog); lactate transmembrane transporter activity (ortholog); INVOLVED IN behavioral response to nutrient (ortholog); carboxylic acid transmembrane transport (ortholog); cellular response to organic cyclic compound (ortholog); ASSOCIATED WITH amenorrhea (ortholog); autism spectrum disorder (ortholog); Colonic Neoplasms (ortholog); FOUND IN apical plasma membrane (ortholog); basal plasma membrane (ortholog); basolateral plasma membrane (ortholog) NW_004955435 16334382 16361737 - 7240710;9068941 102007930 A0A8C2V4M0 MODEL AGCD01033319;GBDF01006604;XM_005388972;XM_005388973;XM_005388975 XP_005389029;XP_005389030;XP_005389032 monocarboxylate transporter 1;solute carrier family 16 (monocarboxylate transporter), member 1 APPROVED protein-coding ENSCLAG00000006864 NW_004955435 16334793 16342552 - 8707196 LOC102008404 RNA-binding protein with serine-rich domain 1 pseudogene NW_004955415 22507523 22528364 - 102008404 MODEL AGCD01016538;AGCD01016539 APPROVED pseudo 8707197 LOC102008559 olfactory receptor 1440-like NW_004955511 3846306 3866765 - 102008559 MODEL AGCD01066478;AGCD01066479;XM_013506388 XP_013361842 APPROVED protein-coding 8707198 Alcam activated leukocyte cell adhesion molecule ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN axon guidance (ortholog); heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules (ortholog); motor neuron axon guidance (ortholog); ASSOCIATED WITH Animal Mammary Neoplasms (ortholog); carcinoma (ortholog); COVID-19 (ortholog); FOUND IN axon (ortholog); external side of plasma membrane (ortholog); immunological synapse (ortholog) NW_004955427 6494657 6544668 + 9068941 102009083 A0A8C2YR62;A0A8C2YR67 MODEL AGCD01027030;GBBH01035028;GBCC01001133;XM_005386343 XP_005386400 CD166 antigen protein-coding ENSCLAG00000011855 NW_004955427 6494124 6545963 + 8707218 LOC102011469 60S ribosomal protein L36a-like NW_004955431 5509247 5509567 - 102011469 MODEL AGCD01030034 pseudo 8707225 LOC102012902 E3 ubiquitin-protein ligase RNF13-like NW_004955550 44557 45787 + 102012902 MODEL AGCD01072481 pseudo 8707232 Asic5 acid sensing ion channel subunit family member 5 ENCODES a protein that exhibits ligand-gated sodium channel activity (ortholog); proton channel activity (ortholog); sodium channel activity (ortholog); INVOLVED IN sodium ion transmembrane transport (ortholog); ASSOCIATED WITH genetic disease (ortholog); Habitual Abortions (ortholog) NW_004955471 11262213 11287720 + 9068941 102014131 A0A8C2V7F3 MODEL AGCD01053251;XM_005400949 XP_005401006 acid sensing (proton gated) ion channel family member 5;acid-sensing (proton-gated) ion channel family member 5;acid-sensing ion channel 5 APPROVED protein-coding ENSCLAG00000007474 NW_004955471 11262216 11287709 + 8707244 Gigyf1 GRB10 interacting GYF protein 1 INVOLVED IN insulin-like growth factor receptor signaling pathway (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN protein-containing complex (ortholog) NW_004955573 228926 240425 + 9068941 102014624 A0A8C2YIZ7 MODEL AGCD01074969;GBDF01192387;XM_005413696;XM_005413697;XM_005413698 XP_005413753;XP_005413754;XP_005413755 PERQ amino acid-rich with GYF domain-containing protein 1 protein-coding ENSCLAG00000001568 NW_004955573 233219 243084 + 8707293 LOC102014805 male-specific submandibular salivary gland protein-like NW_004955499 3197990 3217211 - 102014805 A0A8C2UM26 MODEL AGCD01063457;AGCD01063458;GBCC01016299;XM_005406529;XM_005406530;XM_005406531 XP_005406586;XP_005406587;XP_005406588 APPROVED protein-coding ENSCLAG00000000341 8707315 LOC102014876 AN1-type zinc finger protein 1 pseudogene NW_004955411 9595102 9617042 + 102014876 MODEL AGCD01011760;AGCD01011761 APPROVED pseudo 8707316 Apom apolipoprotein M ENCODES a protein that exhibits antioxidant activity (ortholog); lipid transporter activity (ortholog); phospholipid binding (ortholog); INVOLVED IN cholesterol efflux (ortholog); high-density lipoprotein particle assembly (ortholog); high-density lipoprotein particle clearance (ortholog); ASSOCIATED WITH coronary artery disease (ortholog); Experimental Diabetes Mellitus (ortholog); genetic disease (ortholog); FOUND IN discoidal high-density lipoprotein particle (ortholog); extracellular region (ortholog); extracellular space (ortholog) NW_004955437 190609 192781 + 9068941 102014943 A0A8C2VPD1 MODEL AGCD01034108;GBDF01004738;XM_005389332;XM_005389333 XP_005389389;XP_005389390 protein-coding ENSCLAG00000012748 NW_004955437 190609 197342 + 8707331 Bcas1 brain enriched myelin associated protein 1 INVOLVED IN myelination (ortholog); ASSOCIATED WITH Familial Prostate Cancer (ortholog); genetic disease (ortholog); Prostatic Neoplasms (ortholog); FOUND IN cytoplasm (ortholog); synapse (ortholog) NW_004955445 4951645 5049925 + 9068941 102015058 A0A8C2V407;A0A8C2V6U3;A0A8C2V7T3 MODEL AGCD01039434;AGCD01039435;AGCD01039436;AGCD01039437;GBDJ01021202;XM_005392286;XM_013518334;XM_013518335 XP_005392343;XP_013373788;XP_013373789 breast carcinoma amplified sequence 1;breast carcinoma-amplified sequence 1 APPROVED protein-coding ENSCLAG00000006299 NW_004955445 4951433 5055238 + 8707347 LOC102015660 uncharacterized LOC102015660 NW_004955434 17409506 17447739 + 102015660 MODEL AGCD01032535;AGCD01032536;AGCD01032537;GBDJ01404981;XR_001234793;XR_001234794;XR_001234795;XR_001234796;XR_261625 LOC102015140;LOC102015438 uncharacterized LOC102015140;uncharacterized LOC102015438 PROVISIONAL ncrna 8707357 Tmem39a transmembrane protein 39A INVOLVED IN negative regulation of autophagosome assembly (ortholog); negative regulation of autophagosome maturation (ortholog); positive regulation of viral genome replication (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN endoplasmic reticulum membrane (ortholog) NW_004955427 19118631 19184315 - 9068941 102016937 A0A8C2VV06;A0A8C2VV09 MODEL AGCD01027359;GBDF01050777;XM_005386440;XM_013515085;XM_013515086;XM_013515087;XM_013515088 XP_005386497;XP_013370539;XP_013370540;XP_013370541;XP_013370542 protein-coding ENSCLAG00000014429 NW_004955427 19133434 19184344 - 8707374 Gss glutathione synthetase ENCODES a protein that exhibits ATP binding (ortholog); glutathione binding (ortholog); glutathione synthase activity (ortholog); INVOLVED IN glutathione biosynthetic process (ortholog); response to amino acid (ortholog); response to cadmium ion (ortholog); PARTICIPATES IN 2-hydroxyglutaric aciduria pathway; glutamic acid/glutamate metabolic pathway; glutathione metabolic pathway; ASSOCIATED WITH Acute Experimental Pancreatitis (ortholog); Alzheimer's disease (ortholog); Animal Mammary Neoplasms (ortholog) NW_004955422 26427581 26483380 + 9068941;7240710 102017250 A0A8C2W518;A0A8C2YUV6 MODEL AGCD01023288;GBCQ01006900;XM_005384810;XM_013514053;XM_013514054 XP_005384867;XP_013369507;XP_013369508 protein-coding ENSCLAG00000017163 NW_004955422 26427581 26463781 + 8707394 LOC102017496 protein SCAF11-like NW_004955529 791404 796397 + 102017496 MODEL AGCD01069657;AGCD01069658 pseudo 8707395 Metrn meteorin, glial cell differentiation regulator INVOLVED IN axonogenesis (ortholog); positive regulation of axonogenesis (ortholog); radial glial cell differentiation (ortholog); ASSOCIATED WITH epilepsy (ortholog); genetic disease (ortholog); idiopathic generalized epilepsy (ortholog); FOUND IN extracellular space (ortholog) NW_004955442 16485482 16488949 - 9068941 102017512 A0A8C2VUL9 MODEL AGCD01037901;GBDF01192895;XM_013517755 XP_013373209 meteorin protein-coding ENSCLAG00000014251 NW_004955442 16485482 16488949 - 8707404 LOC102019550 uncharacterized LOC102019550 NW_004955402 26587384 26638965 + 102019550 MODEL AGCD01000682;GBDF01306098;XR_001236745;XR_259068 ncrna 8707413 LOC102020011 uncharacterized LOC102020011 NW_004955483 8366749 8377144 - 102020011 MODEL AGCD01057833;GBDF01162005;XR_001231025;XR_263868 ncrna 8707420 LOC102020950 uncharacterized LOC102020950 NW_004955436 4306094 4347032 - 102020950 MODEL AGCD01033661;GBDF01043200;XR_001234965 ncrna 8707425 LOC102021052 olfactory receptor 4K5-like NW_004955550 475406 483319 - 9068941 102021052 A0A8C2UH29 MODEL AGCD01072506;AGCD01072507;XM_013508546 XP_013364000 protein-coding ENSCLAG00000000657 NW_004955550 475406 476370 - 8707426 LOC102021248 nucleolar GTP-binding protein 1 pseudogene NW_004955420 8696925 8699253 + 102021248 MODEL AGCD01020731 APPROVED pseudo 8707427 Ep400 E1A binding protein p400 ENCODES a protein that exhibits chromatin binding (ortholog); protein antigen binding (ortholog); INVOLVED IN histone H2A acetylation (ortholog); histone H4 acetylation (ortholog); positive regulation of double-strand break repair via homologous recombination (ortholog); PARTICIPATES IN INO80 family mediated chromatin remodeling pathway; ASSOCIATED WITH colorectal cancer (ortholog); genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN NuA4 histone acetyltransferase complex (ortholog); nuclear speck (ortholog); nucleosome (ortholog) NW_004955482 639316 746331 - 9068941 102022599 A0A8C2V907;A0A8C2V9Y4;A0A8C2VBB2;A0A8C2VDW6;A0A8C2VEE3 MODEL AGCD01057180;AGCD01057181;AGCD01057182;AGCD01057183;AGCD01057184;AGCD01057185;AGCD01057186;GBCQ01006240;XM_005402961;XM_013503598;XM_013503599;XM_013503600;XM_013503601;XM_013503602;XM_013503603;XM_013503604;XM_013503605;XM_013503606;XM_013503607;XM_013503608 XP_005403018;XP_013359052;XP_013359053;XP_013359054;XP_013359055;XP_013359056;XP_013359057;XP_013359058;XP_013359059;XP_013359060;XP_013359061;XP_013359062 E1A-binding protein p400 protein-coding ENSCLAG00000007936 NW_004955482 641214 746331 - 8707504 C8a complement C8 alpha chain ENCODES a protein that exhibits complement binding (ortholog); protein-containing complex binding (ortholog); INVOLVED IN complement activation (ortholog); ASSOCIATED WITH genetic disease (ortholog); meningitis (ortholog); myocardial infarction (ortholog); FOUND IN extracellular region (ortholog); extracellular space (ortholog); membrane attack complex (ortholog) NW_004955464 2806859 2874444 - 9068941;7240710 102023240 MODEL AGCD01049965;AGCD01049966;XM_005398770 XP_005398827 complement component 8 alpha subunit;complement component 8, alpha polypeptide APPROVED protein-coding 8707533 LOC102027026 putative olfactory receptor 14L1 NW_004955581 860614 863806 + 102027026 MODEL AGCD01075699;XM_005414272 XP_005414329 APPROVED protein-coding 8707537 Bspry B-box and SPRY domain containing INVOLVED IN cellular response to leukemia inhibitory factor (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cell leading edge (ortholog); perinuclear region of cytoplasm (ortholog) NW_004955419 14124167 14139181 - 9068941 102027074 A0A8C2VLH6 MODEL AGCD01020012;GBCE01170004;GBDI01012219;XM_013513135 XP_013368589 protein-coding ENSCLAG00000010059 NW_004955419 14124980 14136199 - 8707548 LOC102027172 tripartite motif-containing protein 52-like NW_004955473 7795328 7799661 - 102027172 MODEL AGCD01054040 pseudo 8707549 Timm17b translocase of inner mitochondrial membrane 17B ASSOCIATED WITH autistic disorder (ortholog); congenital disorder of glycosylation type IIm (ortholog); genetic disease (ortholog); FOUND IN mitochondrial inner membrane (ortholog); TIM23 mitochondrial import inner membrane translocase complex (ortholog) NW_004955543 425076 430767 - 9068941 102027342 A0A8C2UST5;A0A8C2UYI6 MODEL AGCD01071585;GBCE01032810;XM_005411288 XP_005411345 mitochondrial import inner membrane translocase subunit Tim17-B;translocase of inner mitochondrial membrane 17 homolog B;translocase of inner mitochondrial membrane 17 homolog B (yeast) APPROVED protein-coding ENSCLAG00000003552 NW_004955543 425076 430767 - 8707558 Rimoc1 RAB7A interacting MON1-CCZ1 complex subunit 1 INVOLVED IN mitophagy (ortholog); ASSOCIATED WITH Neurodevelopmental Disorders (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog) NW_004955426 26026284 26040311 + 102027428 A0A8C2VD89 MODEL AGCD01026735;GBCE01122894;XM_005386249;XM_005386250;XM_005386251;XM_013514996;XM_013514997 XP_005386306;XP_005386307;XP_005386308;XP_013370450;XP_013370451 CUNH5orf51;LOC102027428 UPF0600 protein C5orf51 homolog;chromosome unknown C5orf51 homolog;chromosome unknown open reading frame, human C5orf51 APPROVED protein-coding ENSCLAG00000009605 NW_004955426 26026290 26040311 + 8707577 Ddx18 DEAD-box helicase 18 INVOLVED IN cellular response to estradiol stimulus (ortholog); PARTICIPATES IN ribosome biogenesis pathway; ASSOCIATED WITH genetic disease (ortholog); FOUND IN chromosome (ortholog); nucleolus (ortholog) NW_004955459 11799435 11810973 - 9068941 102027723 A0A8C2UYF0 MODEL AGCD01048237;GBCB01076894;XM_005397693 XP_005397750 ATP-dependent RNA helicase DDX18;DEAD (Asp-Glu-Ala-Asp) box polypeptide 18 APPROVED protein-coding ENSCLAG00000004684 NW_004955459 11800684 11810876 - 8707596 Map4k2 mitogen-activated protein kinase kinase kinase kinase 2 ENCODES a protein that exhibits ATP binding (ortholog); mitogen-activated protein kinase kinase kinase binding (ortholog); protein serine/threonine kinase activity (ortholog); INVOLVED IN intracellular signal transduction (ortholog); positive regulation of JNK cascade (ortholog); positive regulation of JUN kinase activity (ortholog); PARTICIPATES IN tumor necrosis factor mediated signaling pathway; ASSOCIATED WITH Bardet-Biedl syndrome (ortholog); genetic disease (ortholog); glycogen storage disease V (ortholog) NW_004955422 20363778 20375699 + 9068941 102027992 A0A8C2W1V3;A0A8C2W4B4 MODEL AGCD01023075;GBDI01126901;GBDK01141597;XM_005384555;XM_005384556 XP_005384612;XP_005384613 protein-coding ENSCLAG00000015778 NW_004955422 20363778 20379527 + 8707634 LOC102028488 AT-hook-containing transcription factor NW_004955934 1287 9868 + 102028488 MODEL AGCD01078694;GBDJ01180201;GBDK01128523;XM_005415151 XP_005415208 Akna AT-hook transcription factor APPROVED protein-coding 8707642 LOC102028705 olfactory receptor 4F3/4F16/4F29-like NW_004955614 117232 118170 + 102028705 A0A8C2UFA7 MODEL AGCD01077227;XM_005414974 XP_005415031 APPROVED protein-coding ENSCLAG00000000100 8707656 Mcrs1 microspherule protein 1 ENCODES a protein that exhibits G-quadruplex RNA binding (ortholog); poly(G) binding (ortholog); poly(U) RNA binding (ortholog); INVOLVED IN chromatin remodeling (ortholog); histone H4-K16 acetylation (ortholog); histone H4-K5 acetylation (ortholog); PARTICIPATES IN INO80 family mediated chromatin remodeling pathway; ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); dendrite (ortholog); histone acetyltransferase complex (ortholog) NW_004955547 180783 189980 - 9068941 102029798 A0A8C2YIX4 MODEL AGCD01072136;GBDF01083324;XM_005411829 XP_005411886 protein-coding ENSCLAG00000001468 NW_004955547 178301 189980 - 8707675 LOC102003635 uncharacterized LOC102003635 NW_004955412 994166 1000278 + 102003635 MODEL AGCD01012505;GBDF01113084;XR_259960 ncrna 8707681 Hdgfl3 HDGF like 3 ENCODES a protein that exhibits microtubule binding (ortholog); tubulin binding (ortholog); INVOLVED IN microtubule polymerization (ortholog); negative regulation of microtubule depolymerization (ortholog); neuron projection development (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955416 13501132 13561095 + 9068941 102003763 A0A8C2V8A8 MODEL AGCD01017225;AGCD01017226;GBDF01050153;XM_005381466;XM_013512568 XP_005381523;XP_013368022 LOC102003763 hepatoma-derived growth factor-related protein 3 APPROVED protein-coding ENSCLAG00000007952 NW_004955416 13538387 13561095 + 8707690 LOC102004996 uncharacterized LOC102004996 NW_004955451 5008763 5013506 + 102004996 MODEL AGCD01043159;GBDF01208277;XR_001235984;XR_262579 ncrna 8707694 Kat2b lysine acetyltransferase 2B ENCODES a protein that exhibits acetyltransferase activity (ortholog); chromatin binding (ortholog); cyclin-dependent protein serine/threonine kinase inhibitor activity (ortholog); INVOLVED IN cellular response to insulin stimulus (ortholog); cellular response to oxidative stress (ortholog); cellular response to parathyroid hormone stimulus (ortholog); PARTICIPATES IN cortisol signaling pathway; histone modification pathway; p53 signaling pathway; ASSOCIATED WITH 3p deletion syndrome (ortholog); breast cancer (ortholog); Coronary Disease (ortholog); FOUND IN A band (ortholog); actomyosin (ortholog); ATAC complex (ortholog) NW_004955430 12109493 12196102 + 9068941 102005162 A0A8C2V7P3 MODEL AGCD01029488;AGCD01029489;GBDF01081550;XM_005387463;XM_005387464;XM_013515665;XM_013515666 XP_005387520;XP_005387521;XP_013371119;XP_013371120 K(lysine) acetyltransferase 2B;histone acetyltransferase KAT2B APPROVED protein-coding ENSCLAG00000006506 NW_004955430 12128069 12198117 + 8707725 LOC102005318 BRISC complex subunit Abro1 pseudogene NW_004955446 7660056 7661294 - 102005318 MODEL AGCD01040126 APPROVED pseudo 8707726 Rnf175 ring finger protein 175 ASSOCIATED WITH genetic disease (ortholog) NW_004955471 8019842 8079565 - 9068941 102006022 A0A8C2UWX6 MODEL AGCD01053174;AGCD01053175;AGCD01053176;GBDF01194289;XM_005400926 XP_005400983 protein-coding ENSCLAG00000004608 NW_004955471 8021443 8079571 - 8707739 LOC102006300 60S ribosomal protein L30-like NW_004955402 43644927 43645275 + 102006300 MODEL AGCD01001075 pseudo 8707748 Chd1 chromodomain helicase DNA binding protein 1 ENCODES a protein that exhibits methylated histone binding (ortholog); INVOLVED IN chromatin remodeling (ortholog); positive regulation by host of viral transcription (ortholog); PARTICIPATES IN histone modification pathway; ASSOCIATED WITH autistic disorder (ortholog); castration-resistant prostate carcinoma (ortholog); Colorectal Neoplasms (ortholog); FOUND IN cytoplasm (ortholog); nuclear chromosome (ortholog); nucleus (ortholog) NW_004955418 14200618 14268361 + 9068941 102007339 A0A8C2YNZ7 MODEL AGCD01019069;GBBH01162092;GBCQ01088613;XM_005382216 XP_005382273 chromodomain-helicase-DNA-binding protein 1 protein-coding ENSCLAG00000008757 NW_004955418 14200617 14268361 + 8707787 LOC102007358 olfactory receptor 5W2-like NW_004955511 700104 706604 - 102007358 A0A8C2WCR7 MODEL AGCD01066338;AGCD01066339;XM_005408208 pseudo ENSCLAG00000017600 8707790 Hax1 HCLS1 associated protein X-1 ENCODES a protein that exhibits interleukin-1 binding (ortholog); protein domain specific binding (ortholog); INVOLVED IN cellular response to cytokine stimulus (ortholog); mitochondrion organization (ortholog); negative regulation of apoptotic process (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease type 2 (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN actin cytoskeleton (ortholog); apical plasma membrane (ortholog); clathrin-coated vesicle (ortholog) NW_004955545 816789 819667 + 9068941;7240710 102009107 A0A8C2UYW8 MODEL AGCD01071817;GBBH01119014;XM_005411511;XM_005411512;XM_005411513;XM_005411514 XP_005411568;XP_005411569;XP_005411570;XP_005411571 HCLS1-associated protein X-1 protein-coding ENSCLAG00000004829 8707822 Asmt acetylserotonin O-methyltransferase ENCODES a protein that exhibits acetylserotonin O-methyltransferase activity (ortholog); identical protein binding (ortholog); protein homodimerization activity (ortholog); INVOLVED IN male gonad development (ortholog); melatonin biosynthetic process (ortholog); negative regulation of male gonad development (ortholog); PARTICIPATES IN methionine cycle/metabolic pathway; tryptophan metabolic pathway; ASSOCIATED WITH autistic disorder (ortholog); Wilson disease (ortholog) NW_004955499 1131637 1151861 + 9068941 102009198 A0A8C2UHZ9 MODEL AGCD01063323;AGCD01063324;AGCD01063325;XM_005406516 XP_005406573 protein-coding ENSCLAG00000000340 NW_004955499 1131588 1152802 + 8707836 Slc51a solute carrier family 51 subunit alpha ENCODES a protein that exhibits bile acid transmembrane transporter activity (ortholog); protein heterodimerization activity (ortholog); protein homodimerization activity (ortholog); INVOLVED IN bile acid and bile salt transport (ortholog); bile acid secretion (ortholog); organic substance transport (ortholog); ASSOCIATED WITH autistic disorder (ortholog); cholestasis (ortholog); chromosome 3q29 microdeletion syndrome (ortholog); FOUND IN basolateral plasma membrane (ortholog); endoplasmic reticulum membrane (ortholog); membrane (ortholog) NW_004955420 12452562 12463369 + 9068941 102009507 A0A8C2VL02 MODEL AGCD01020865;GBDF01222832;XM_005383122;XM_005383123;XM_013513396;XM_013513397 XP_005383179;XP_005383180;XP_013368850;XP_013368851 organic solute transporter subunit alpha;solute carrier family 51 alpha subunit;solute carrier family 51, alpha subunit APPROVED protein-coding ENSCLAG00000011171 NW_004955420 12453554 12463150 + 8707854 Fkbp9 FKBP prolyl isomerase 9 ENCODES a protein that exhibits calcium ion binding (ortholog); INVOLVED IN protein folding (ortholog); ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN endoplasmic reticulum (ortholog) NW_004955617 196845 234431 + 9068941 102010012 A0A8C2YIH1 MODEL AGCD01077274;AGCD01077275;GBDF01081147;XM_005414998;XM_013510142 XP_005415055;XP_013365596 FK506 binding protein 9;FK506 binding protein 9, 63 kDa;peptidyl-prolyl cis-trans isomerase FKBP9 APPROVED protein-coding ENSCLAG00000000839 NW_004955617 201944 237048 + 8707874 LOC102010301 uncharacterized LOC102010301 NW_004955524 791217 792333 + 102010301 MODEL AGCD01068708;GBDF01013580;XR_001231946 ncrna 8707882 LOC102011087 olfactory receptor 9K2-like NW_004955458 2223510 2224451 + 9068941 102011087 A0A8C2YV53 MODEL AGCD01047218;XM_005397237 XP_005397294 protein-coding ENSCLAG00000017693 8707885 Syt16 synaptotagmin 16 ENCODES a protein that exhibits calcium-dependent phospholipid binding (ortholog); identical protein binding (ortholog); phospholipid binding (ortholog); ASSOCIATED WITH genetic disease (ortholog) NW_004955466 7600990 7927710 - 9068941 102011187 A0A8C2V9J1 MODEL AGCD01050959;AGCD01050960;AGCD01050961;AGCD01050962;AGCD01050963;AGCD01050964;AGCD01050965;AGCD01050966;AGCD01050967;AGCD01050968;AGCD01050969;AGCD01050970;AGCD01050971;AGCD01050972;AGCD01050973;GBDJ01218054;XM_013522016 XP_013377470 synaptotagmin XVI;synaptotagmin-16 APPROVED protein-coding ENSCLAG00000007034 NW_004955466 7601796 7797793 - 8707896 R3hcc1l R3H domain and coiled-coil containing 1 like ASSOCIATED WITH genetic disease (ortholog); FOUND IN exon-exon junction complex (ortholog) NW_004955507 4150389 4228412 + 9068941 102011345 A0A8C2URU6;A0A8C2UUA7 MODEL AGCD01065640;AGCD01065641;AGCD01065642;GBDF01123772;XM_005407656;XM_005407657;XM_005407659;XM_005407660 XP_005407713;XP_005407714;XP_005407716;XP_005407717 R3H domain and coiled-coil containing 1-like;coiled-coil domain-containing protein R3HCC1L APPROVED protein-coding ENSCLAG00000002695 NW_004955507 4150451 4227640 + 8707916 LOC102011579 pancreatic alpha-amylase NW_004955435 7974418 8023066 + 9068941 102011579 A0A8C2YLN1 MODEL AGCD01032983;AGCD01032984;AGCD01032985;AGCD01032986;AGCD01032987;AGCD01032988;AGCD01032989;GBDK01013521;XM_005388812;XM_013516505;XM_013516506 XP_005388869;XP_013371959;XP_013371960 Amy2a amylase, alpha 2A (pancreatic) APPROVED protein-coding ENSCLAG00000005447 8707931 Med22 mediator complex subunit 22 PARTICIPATES IN RNA polymerase II transcription pathway; ASSOCIATED WITH developmental and epileptic encephalopathy 14 (ortholog); Ehlers-Danlos syndrome classic type 1 (ortholog); genetic disease (ortholog); FOUND IN core mediator complex (ortholog); mediator complex (ortholog); nucleus (ortholog) NW_004955513 2697812 2704748 - 9068941 102012229 A0A8C2UW86 MODEL AGCD01066886;GBDI01137425;XM_005408427 XP_005408484 mediator of RNA polymerase II transcription subunit 22 protein-coding ENSCLAG00000004487 NW_004955513 2697585 2704748 - 8707940 LOC102013488 disintegrin and metalloproteinase domain-containing protein 29-like NW_004955466 20379 80896 + 102013488 MODEL AGCD01050641;AGCD01050642;AGCD01050643;AGCD01050644;AGCD01050645;AGCD01050646;AGCD01050647;AGCD01050648;AGCD01050649;XM_005399240 XP_005399297 protein-coding 8707944 Lingo4 leucine rich repeat and Ig domain containing 4 INVOLVED IN positive regulation of synapse assembly (ortholog); ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); immunodeficiency 42 (ortholog) NW_004955589 618959 623915 + 9068941 102013567 A0A8C2UIC0 MODEL AGCD01076179;GBDF01150351;XM_005414547 XP_005414604 leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 4 APPROVED protein-coding ENSCLAG00000000770 NW_004955589 618998 623239 + 8707950 LOC102013619 uncharacterized LOC102013619 NW_004955421 18803353 18811236 - 102013619 MODEL AGCD01022056;GBDF01014486;XR_001233862;XR_260797 ncrna 8707955 Flt3lg fms related receptor tyrosine kinase 3 ligand ENCODES a protein that exhibits identical protein binding (ortholog); receptor tyrosine kinase binding (ortholog); INVOLVED IN embryonic hemopoiesis (ortholog); homeostasis of number of cells within a tissue (ortholog); lymphocyte differentiation (ortholog); ASSOCIATED WITH aplastic anemia (ortholog); colon carcinoma (ortholog); developmental and epileptic encephalopathy 12 (ortholog); FOUND IN cell surface (ortholog); external side of plasma membrane (ortholog); extracellular space (ortholog) NW_004955559 1364056 1371245 - 9068941 102014503 A0A8C2UUC6;A0A8C2YKH6;A0A8C2YKI9 MODEL AGCD01073641;GBBH01091697;XM_013509008;XM_013509009;XM_013509010;XM_013509011;XM_013509012;XM_013509013;XM_013509014;XM_013509015;XM_013509016;XM_013509017 XP_013364462;XP_013364463;XP_013364464;XP_013364465;XP_013364466;XP_013364467;XP_013364468;XP_013364469;XP_013364470;XP_013364471 fms related tyrosine kinase 3 ligand;fms-related tyrosine kinase 3 ligand APPROVED protein-coding ENSCLAG00000003815 NW_004955559 1365938 1370002 - 8707975 Casq1 calsequestrin 1 ENCODES a protein that exhibits calcium ion binding (ortholog); identical protein binding (ortholog); INVOLVED IN endoplasmic reticulum organization (ortholog); positive regulation of release of sequestered calcium ion into cytosol (ortholog); positive regulation of store-operated calcium channel activity (ortholog); PARTICIPATES IN calcium/calcium-mediated signaling pathway; ASSOCIATED WITH autoimmune interstitial lung, joint, and kidney disease (ortholog); Experimental Diabetes Mellitus (ortholog); familial hemiplegic migraine (ortholog); FOUND IN endoplasmic reticulum (ortholog); I band (ortholog); mitochondrial matrix (ortholog) NW_004955468 11967678 11978836 + 9068941 102014657 A0A8C2W1B6;A0A8C2W998 MODEL AGCD01052140;GBDF01026889;XM_005400195 XP_005400252 calsequestrin 1 (fast-twitch, skeletal muscle);calsequestrin-1 APPROVED protein-coding ENSCLAG00000016275 NW_004955468 11967678 11978836 + 8707990 LOC102018022 uncharacterized LOC102018022 NW_004955533 900860 904030 - 102018022 MODEL AGCD01070334;GBDF01261009;XR_264740 ncrna 8707995 LOC102018173 protein SPT2 homolog NW_004955412 18553976 18555107 + 102018173 MODEL AGCD01012944;AGCD01012945;GBDF01021744;XM_013510975 XP_013366429 APPROVED protein-coding 8708001 LOC102018366 uncharacterized LOC102018366 NW_004955409 33777180 33840794 - 102018366 MODEL AGCD01010400;GBDF01249318;XR_259801 ncrna ENSCLAG00000024068 8708006 LOC102018938 olfactory receptor 7D4-like NW_004955495 581689 582633 + 102018938 MODEL AGCD01061640;XM_005405557 XP_005405614 protein-coding 8708009 LOC102019505 AP-3 complex subunit sigma-1 pseudogene NW_004955419 14065813 14066477 + 102019505 MODEL AGCD01020010 APPROVED pseudo 8708010 Foxk2 forkhead box K2 ENCODES a protein that exhibits DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); DNA-binding transcription factor activity (ortholog); DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); INVOLVED IN canonical glycolysis (ortholog); intracellular glucose homeostasis (ortholog); negative regulation of autophagy (ortholog); ASSOCIATED WITH genetic disease (ortholog); male infertility (ortholog); primary ovarian insufficiency (ortholog); FOUND IN cytoplasm (ortholog); intracellular membrane-bounded organelle (ortholog); mitochondrion (ortholog) NW_004955506 567770 614505 - 9068941 102020270 A0A8C2YSI7 MODEL AGCD01065232;GBCB01044212;GBDF01003155;XM_005407499 XP_005407556 forkhead box protein K2 protein-coding ENSCLAG00000013784 NW_004955506 569143 614503 - 8708022 Parvg parvin gamma PARTICIPATES IN integrin mediated signaling pathway; ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); Phelan-McDermid syndrome (ortholog) NW_004955413 29028573 29046745 + 9068941 102021958 A0A8C2W468 MODEL AGCD01014573;AGCD01014574;GBDI01080132;XM_005379457;XM_005379458;XM_005379459 XP_005379514;XP_005379515;XP_005379516 gamma-parvin;parvin, gamma APPROVED protein-coding ENSCLAG00000017133 NW_004955413 29028461 29047288 + 8708046 Cldn4 claudin 4 ENCODES a protein that exhibits chloride channel activity (ortholog); INVOLVED IN circadian rhythm (ortholog); establishment of skin barrier (ortholog); female pregnancy (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); Breast Neoplasms (ortholog); FOUND IN apical plasma membrane (ortholog); apicolateral plasma membrane (ortholog); basal plasma membrane (ortholog) NW_004955456 13961743 13965498 - 9068941 102022359 A0A8C2W6K4 MODEL AGCD01046629;GBDJ01020810;XM_005396763 XP_005396820 claudin-4 protein-coding ENSCLAG00000017992 NW_004955456 13962497 13963126 - 8708051 LOC102022541 uncharacterized LOC102022541 NW_004955538 1159133 1176031 - 102022541 MODEL AGCD01071047;AGCD01071048;AGCD01071049;AGCD01071050;GBDF01044132;XR_001232085;XR_001232086;XR_264795 ncrna 8708057 LOC102022658 conserved oligomeric Golgi complex subunit 1-like NW_004955716 2740 4643 - 102022658 MODEL AGCD01078165;GBDJ01020819;XM_005415076 XP_005415133 protein-coding 8708063 Paqr6 progestin and adipoQ receptor family member 6 ASSOCIATED WITH calcium oxalate nephrolithiasis (ortholog); Charcot-Marie-Tooth disease type 2 (ortholog); gastrointestinal stromal tumor (ortholog) NW_004955545 2382214 2386406 - 9068941 102023397 A0A8C2UTZ6;A0A8C2UZP1 MODEL AGCD01071898;GBDJ01188717;XM_005411662;XM_013508270;XM_013508271;XM_013508272;XM_013508273 XP_005411719;XP_013363724;XP_013363725;XP_013363726;XP_013363727 progestin and adipoQ receptor family member VI APPROVED protein-coding ENSCLAG00000003899 NW_004955545 2382818 2385325 - 8708085 Nr5a1 nuclear receptor subfamily 5 group A member 1 ENCODES a protein that exhibits chromatin binding (ortholog); DNA binding (ortholog); DNA-binding transcription factor activity (ortholog); INVOLVED IN adrenal gland development (ortholog); calcineurin-mediated signaling (ortholog); female gonad development (ortholog); ASSOCIATED WITH 46 XX gonadal dysgenesis (ortholog); 46, XY Disorders of Sex Development (ortholog); 46,XX sex reversal 4 (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955419 3632248 3654367 + 9068941;7240710 102023700 A0A8C2VTX3 MODEL AGCD01019730;AGCD01019731;AGCD01019732;GBDF01156391;XM_005382492;XM_005382493 XP_005382549;XP_005382550 nuclear receptor subfamily 5, group A, member 1;steroidogenic factor 1 APPROVED protein-coding ENSCLAG00000012090 NW_004955419 3632220 3654375 + 8708100 Aldh3a2 aldehyde dehydrogenase 3 family member A2 ENCODES a protein that exhibits 3-chloroallyl aldehyde dehydrogenase activity (ortholog); aldehyde dehydrogenase (NAD+) activity (ortholog); long-chain-alcohol oxidase activity (ortholog); INVOLVED IN cellular aldehyde metabolic process (ortholog); central nervous system development (ortholog); epidermis development (ortholog); PARTICIPATES IN phytanic acid degradation pathway; Refsum disease pathway; ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); common variable immunodeficiency 2 (ortholog); FOUND IN endoplasmic reticulum (ortholog); endoplasmic reticulum membrane (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955467 141592 162376 - 9068941;7240710 102024986 A0A8C2VT52;A0A8C2VTG8 MODEL AGCD01051211;GBCB01005261;XM_005399257;XM_005399258 XP_005399314;XP_005399315 aldehyde dehydrogenase 3 family, member A2;fatty aldehyde dehydrogenase APPROVED protein-coding ENSCLAG00000013890 NW_004955467 140760 162742 - 8708121 LOC102025302 zinc finger protein 791 pseudogene NW_004955448 14214649 14216042 - 102025302 MODEL AGCD01041628 APPROVED pseudo 8708122 Efna1 ephrin A1 ENCODES a protein that exhibits ephrin receptor binding (ortholog); INVOLVED IN aortic valve morphogenesis (ortholog); cell migration (ortholog); endocardial cushion to mesenchymal transition involved in heart valve formation (ortholog); PARTICIPATES IN E-cadherin signaling pathway; ephrin - ephrin receptor bidirectional signaling axis; hypoxia inducible factor pathway; ASSOCIATED WITH Breast Neoplasms (ortholog); Charcot-Marie-Tooth disease type 2 (ortholog); gastrointestinal stromal tumor (ortholog); FOUND IN plasma membrane (ortholog) NW_004955545 1610929 1617217 + 9068941 102025845 A0A8C2UT78;A0A8C2UUD4 MODEL AGCD01071863;GBBH01228706;XM_005411571 XP_005411628 ephrin-A1 APPROVED protein-coding ENSCLAG00000003890 NW_004955545 1610929 1617460 + 8708132 Tnfaip8l2 TNF alpha induced protein 8 like 2 INVOLVED IN negative regulation of inflammatory response (ortholog); negative regulation of T cell activation (ortholog); T cell activation (ortholog); ASSOCIATED WITH COVID-19 (ortholog); Dravet syndrome (ortholog); gastrointestinal stromal tumor (ortholog); FOUND IN cytoplasm (ortholog) NW_004955588 514567 517314 + 9068941 102026059 A0A8C2YI16 MODEL AGCD01076115;GBDF01159306;XM_005414498 XP_005414555 tumor necrosis factor alpha-induced protein 8-like protein 2;tumor necrosis factor, alpha-induced protein 8-like 2 APPROVED protein-coding ENSCLAG00000000171 NW_004955588 514567 517314 + 8708144 Tgfb3 transforming growth factor beta 3 ENCODES a protein that exhibits identical protein binding (ortholog); protein-containing complex binding (ortholog); transforming growth factor beta binding (ortholog); INVOLVED IN animal organ morphogenesis (ortholog); cell population proliferation (ortholog); cell-cell junction organization (ortholog); PARTICIPATES IN glypican signaling pathway; transforming growth factor-beta Smad dependent signaling pathway; ASSOCIATED WITH arrhythmogenic right ventricular cardiomyopathy (ortholog); arrhythmogenic right ventricular dysplasia 1 (ortholog); Brugada syndrome (ortholog); FOUND IN cell surface (ortholog); collagen-containing extracellular matrix (ortholog); extracellular matrix (ortholog) NW_004955438 33129 55180 - 9068941;7240710 102026475 A0A8C2VEL2 MODEL AGCD01034940;GBCE01098971;XM_005390146 XP_005390203 transforming growth factor beta-3;transforming growth factor, beta 3 APPROVED protein-coding ENSCLAG00000008424 NW_004955438 29415 55180 - 8708155 Rragb Ras related GTP binding B ENCODES a protein that exhibits GTP binding (ortholog); GTPase activity (ortholog); GTPase binding (ortholog); INVOLVED IN cellular response to amino acid starvation (ortholog); cellular response to amino acid stimulus (ortholog); cellular response to leucine starvation (ortholog); PARTICIPATES IN mTOR signaling pathway; ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); syndromic X-linked intellectual disability Lubs type (ortholog); FOUND IN cytoplasm (ortholog); lysosome (ortholog) NW_004955475 2662969 2692253 + 9068941 102026858 A0A8C2UUM9;A0A8C2UZQ9;A0A8C2YKL2 MODEL AGCD01054817;GBBH01019101;XM_005401539;XM_005401540;XM_013502883 XP_005401596;XP_005401597;XP_013358337 Ras-related GTP binding B;ras-related GTP-binding protein B APPROVED protein-coding ENSCLAG00000003913 NW_004955475 2662868 2696364 + 8708171 LOC102027381 uncharacterized LOC102027381 NW_004955456 14118331 14119176 + 102027381 MODEL AGCD01046633;GBDJ01068818;XR_262900 ncrna 8708176 Mpv17 mitochondrial inner membrane protein MPV17 ENCODES a protein that exhibits channel activity (ortholog); INVOLVED IN cellular response to reactive oxygen species (ortholog); glomerular basement membrane development (ortholog); homeostatic process (ortholog); ASSOCIATED WITH autosomal recessive Alport syndrome (ortholog); Charcot-Marie-Tooth disease type 2EE (ortholog); cochlear disease (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrion (ortholog); peroxisome (ortholog) NW_004955469 9279540 9292012 - 9068941;7240710 102027398 A0A8C2VA95;A0A8C2VBN2;A0A8C2VD51;A0A8C2VE77 MODEL AGCD01052498;GBDF01124910;XM_005400482;XM_005400483;XM_005400484;XM_005400485;XM_005400486;XM_013522599;XM_013522600;XM_013522601;XM_013522602;XM_013522603;XM_013522604 XP_005400539;XP_005400540;XP_005400541;XP_005400542;XP_005400543;XP_013378053;XP_013378054;XP_013378055;XP_013378056;XP_013378057;XP_013378058 APPROVED protein-coding ENSCLAG00000008028 NW_004955469 9279540 9291954 - 8708204 Rpgr retinitis pigmentosa GTPase regulator INVOLVED IN cellular response to light stimulus (ortholog); cilium assembly (ortholog); eye photoreceptor cell development (ortholog); PARTICIPATES IN retinitis pigmentosa pathway; ASSOCIATED WITH autistic disorder (ortholog); Ciliary Motility Disorders (ortholog); cone dystrophy (ortholog); FOUND IN cell projection (ortholog); centrosome (ortholog); ciliary basal body (ortholog) NW_004955601 398772 453271 - 9068941;7240710 102028252 A0A8C2UGL8;A0A8C2UHM2;A0A8C2ULM0 MODEL AGCD01076755;AGCD01076756;AGCD01076757;GBDJ01114355;XM_005414820;XM_005414821;XM_013510073;XM_013510074 XP_005414877;XP_005414878;XP_013365527;XP_013365528 X-linked retinitis pigmentosa GTPase regulator protein-coding ENSCLAG00000000216 8708231 Psph phosphoserine phosphatase ENCODES a protein that exhibits identical protein binding (ortholog); L-phosphoserine phosphatase activity (ortholog); magnesium ion binding (ortholog); INVOLVED IN in utero embryonic development (ortholog); L-serine biosynthetic process (ortholog); L-serine metabolic process (ortholog); PARTICIPATES IN dihydropyrimidine dehydrogenase deficiency pathway; dimethylglycine dehydrogenase deficiency pathway; nonketotic hyperglycinemia pathway; ASSOCIATED WITH amelogenesis imperfecta (ortholog); amino acid metabolic disorder (ortholog); autistic disorder (ortholog) NW_004955456 8198739 8212111 - 9068941;7240710 102029365 A0A8C2VAM5;A0A8C2YP10 MODEL AGCD01046460;AGCD01046461;GBDF01278340;XM_005396697;XM_013520546 XP_005396754;XP_013376000 protein-coding ENSCLAG00000008790 NW_004955456 8198739 8212025 - 8708242 LOC102029368 uncharacterized LOC102029368 NW_004955408 3840809 3844015 + 102029368 MODEL AGCD01008079;GBDF01078381;XR_001232189 ncrna 8708247 Rgl3 ral guanine nucleotide dissociation stimulator like 3 ENCODES a protein that exhibits guanyl-nucleotide exchange factor activity (ortholog); small GTPase binding (ortholog); ASSOCIATED WITH alpha-mannosidosis (ortholog); Charcot-Marie-Tooth disease dominant intermediate B (ortholog); episodic ataxia type 2 (ortholog) NW_004955495 2304820 2319171 - 9068941 102029874 A0A8C2YNX4 MODEL AGCD01061764;AGCD01061765;AGCD01061766;GBCE01074618;XM_013505110 XP_013360564 ral guanine nucleotide dissociation stimulator-like 3 APPROVED protein-coding ENSCLAG00000008655 NW_004955495 2305053 2316841 - 8708268 LOC102030372 prolactin-like NW_004955632 63921 71559 - 102030372 MODEL AGCD01077572;XM_005415040 XP_005415097 protein-coding 8708275 Ubr7 ubiquitin protein ligase E3 component n-recognin 7 ASSOCIATED WITH achondrogenesis type IA (ortholog); Developmental Disabilities (ortholog); DICER1 syndrome (ortholog) NW_004955438 15321605 15341902 + 9068941 102003805 A0A8C2VPJ0 MODEL AGCD01035365;GBBH01126778;XM_005390342;XM_013517242 XP_005390399;XP_013372696 putative E3 ubiquitin-protein ligase UBR7;ubiquitin protein ligase E3 component n-recognin 7 (putative) APPROVED protein-coding ENSCLAG00000012180 NW_004955438 15321719 15342116 + 8708291 Dpp7 dipeptidyl peptidase 7 ENCODES a protein that exhibits dipeptidyl-peptidase activity (ortholog); INVOLVED IN lysosomal protein catabolic process (ortholog); protein catabolic process (ortholog); ASSOCIATED WITH Adams-Oliver Syndrome 5 (ortholog); autosomal dominant intellectual developmental disorder 8 (ortholog); autosomal dominant nocturnal frontal lobe epilepsy 5 (ortholog); FOUND IN Golgi apparatus (ortholog); intracellular membrane-bounded organelle (ortholog); lysosome (ortholog) NW_004955513 5105833 5109676 + 9068941 102004102 A0A8C2VEP0 MODEL AGCD01066956;GBDI01001030;XM_005408580;XM_013506709 XP_005408637;XP_013362163 dipeptidyl peptidase 2;dipeptidyl-peptidase 7 APPROVED protein-coding ENSCLAG00000008918 NW_004955513 5106430 5109483 + 8708307 Barhl2 BarH like homeobox 2 ENCODES a protein that exhibits DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); DNA-binding transcription factor activity (ortholog); sequence-specific double-stranded DNA binding (ortholog); INVOLVED IN amacrine cell differentiation (ortholog); cell fate commitment (ortholog); cell fate determination (ortholog); ASSOCIATED WITH colorectal cancer (ortholog); genetic disease (ortholog); Lymphatic Metastasis (ortholog); FOUND IN nucleus (ortholog) NW_004955423 3516973 3522459 + 9068941 102005484 A0A8C2UVZ6 MODEL AGCD01023515;GBDF01014640;GBDF01014641;XM_013514374 XP_013369828 BarH-like homeobox 2 APPROVED protein-coding ENSCLAG00000004382 NW_004955423 3516660 3522536 + 8708315 LOC102006058 olfactory receptor 5D16-like NW_004955511 662118 663074 + 9068941 102006058 MODEL AGCD01066337;XM_005408204 XP_005408261 protein-coding 8708318 Hnrnpdl heterogeneous nuclear ribonucleoprotein D like ENCODES a protein that exhibits double-stranded DNA binding (ortholog); poly(A) binding (ortholog); poly(G) binding (ortholog); INVOLVED IN regulation of gene expression (ortholog); ASSOCIATED WITH autosomal dominant limb-girdle muscular dystrophy type 3 (ortholog); chromosome 4q21 deletion syndrome (ortholog); genetic disease (ortholog); FOUND IN nucleoplasm (ortholog); nucleus (ortholog); synapse (ortholog) NW_004955433 6515509 6522081 - 9068941;7240710 102006156 A0A8C2V9Y5;A0A8C2YNS1 MODEL AGCD01031539;GBBH01000726;XM_005388241 XP_005388298 heterogeneous nuclear ribonucleoprotein D-like APPROVED protein-coding ENSCLAG00000008428 NW_004955433 6512399 6522377 - 8708333 LOC102008854 uncharacterized LOC102008854 NW_004955418 25551560 25572621 - 102008854 MODEL AGCD01019367;GBDF01180351;XR_260584 ncrna 8708340 Pcca propionyl-CoA carboxylase subunit alpha ENCODES a protein that exhibits enzyme binding (ortholog); propionyl-CoA carboxylase activity (ortholog); PARTICIPATES IN 3-hydroxy-3-methylglutaryl-CoA lyase deficiency pathway; 3-hydroxyisobutyric aciduria pathway; 3-methylcrotonyl CoA carboxylase 1 deficiency pathway; ASSOCIATED WITH amino acid metabolic disorder (ortholog); Anal Atresia, Hypospadias, and Penoscrotal Inversion (ortholog); genetic disease (ortholog); FOUND IN catalytic complex (ortholog); mitochondrial matrix (ortholog); mitochondrion (ortholog) NW_004955404 10317640 10719148 - 9068941;7240710 102009676 A0A8C2UWZ0 MODEL AGCD01003378;AGCD01003379;AGCD01003380;AGCD01003381;AGCD01003382;AGCD01003383;AGCD01003384;AGCD01003385;AGCD01003386;AGCD01003387;AGCD01003388;AGCD01003389;AGCD01003390;AGCD01003391;GBCE01030421;XM_005374053;XM_005374054;XM_005374058;XM_013516015 XP_005374110;XP_005374111;XP_005374115;XP_013371469 propionyl CoA carboxylase, alpha polypeptide;propionyl-CoA carboxylase alpha chain, mitochondrial;propionyl-CoA carboxylase alpha subunit APPROVED protein-coding ENSCLAG00000003205 NW_004955404 10317640 10661496 - 8708380 LOC102010232 suppressor of cytokine signaling 5-like NW_004955458 3896343 3898873 + 102010232 MODEL AGCD01047353 pseudo 8708381 LOC102010762 RNA-binding protein 3 pseudogene NW_004955403 33567014 33567530 + 102010762 MODEL AGCD01002457 APPROVED pseudo 8708382 Thap1 THAP domain containing 1 ENCODES a protein that exhibits DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); identical protein binding (ortholog); protein homodimerization activity (ortholog); INVOLVED IN DNA-templated transcription (ortholog); endothelial cell proliferation (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH congenital muscular dystrophy-dystroglycanopathy type A12 (ortholog); dystonia (ortholog); genetic disease (ortholog); FOUND IN fibrillar center (ortholog); intracellular membrane-bounded organelle (ortholog); nucleoplasm (ortholog) NW_004955457 13077015 13088406 - 9068941;7240710 102011739 A0A8C2UUL3 MODEL AGCD01047037;GBCB01074927;XM_005397068;XM_013520673;XR_001236385;XR_001236386;XR_001236387;XR_001236388;XR_001236389;XR_001236390;XR_001236391;XR_001236392 XP_005397125;XP_013376127 THAP domain containing, apoptosis associated protein 1;THAP domain-containing protein 1 APPROVED protein-coding ENSCLAG00000003969 NW_004955457 13072697 13088406 - 8708389 Slc35g6 solute carrier family 35 member G6 ASSOCIATED WITH common variable immunodeficiency (ortholog); congenital myasthenic syndrome 2A (ortholog); dyskeratosis congenita (ortholog) NW_004955467 9447756 9450653 - 9068941 102012080 MODEL AGCD01051511;GBDF01001619;XM_013522195 XP_013377649 solute carrier family 35, member G6 APPROVED protein-coding 8708397 Coil coilin ENCODES a protein that exhibits disulfide oxidoreductase activity (ortholog); identical protein binding (ortholog); ASSOCIATED WITH genetic disease (ortholog); Joubert syndrome (ortholog); FOUND IN Cajal body (ortholog); cytosol (ortholog); female germ cell nucleus (ortholog) NW_004955451 5884233 5898525 + 9068941 102012267 A0A8C2W2C4 MODEL AGCD01043185;AGCD01043186;GBDF01007401;XM_005394065;XM_005394066 XP_005394122;XP_005394123 protein-coding ENSCLAG00000014496 8708410 LOC102012439 uncharacterized LOC102012439 NW_004955421 24954942 25002542 - 102012439 MODEL AGCD01022225;AGCD01022226;AGCD01022227;GBCQ01157706;XR_001233829;XR_260827 ncrna 8708415 Pmvk phosphomevalonate kinase ENCODES a protein that exhibits ATP binding (ortholog); phosphomevalonate kinase activity (ortholog); INVOLVED IN cholesterol biosynthetic process (ortholog); isopentenyl diphosphate biosynthetic process, mevalonate pathway (ortholog); response to cholesterol (ortholog); PARTICIPATES IN alendronate pharmacodynamics pathway; cholesterol biosynthetic pathway; cholesterol ester storage disease pathway; ASSOCIATED WITH Charcot-Marie-Tooth disease type 2 (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); peroxisome (ortholog) NW_004955545 1421562 1440038 - 9068941 102015153 A0A8C2YL69 MODEL AGCD01071854;AGCD01071855;GBCB01025659;XM_005411529;XM_013508335 XP_005411586;XP_013363789 protein-coding ENSCLAG00000004787 NW_004955545 1421562 1440038 - 8708424 Wdr76 WD repeat domain 76 ENCODES a protein that exhibits enzyme binding (ortholog); INVOLVED IN DNA damage response (ortholog); ASSOCIATED WITH Bloom syndrome (ortholog); colorectal cancer (ortholog); genetic disease (ortholog); FOUND IN heterochromatin (ortholog); nucleus (ortholog); site of DNA damage (ortholog) NW_004955416 10280112 10337963 + 9068941 102015196 A0A8C2YQ19 MODEL AGCD01017129;AGCD01017130;AGCD01017131;AGCD01017132;AGCD01017133;AGCD01017134;AGCD01017135;GBDF01163138;XM_005381415;XM_013512615;XM_013512616;XM_013512617 XP_005381472;XP_013368069;XP_013368070;XP_013368071 WD repeat-containing protein 76 protein-coding ENSCLAG00000010272 NW_004955416 10279835 10335521 + 8708441 Ccdc33 coiled-coil domain containing 33 ASSOCIATED WITH Bardet-Biedl syndrome (ortholog); Bloom syndrome (ortholog); colorectal cancer (ortholog); FOUND IN peroxisome (ortholog) NW_004955450 3485789 3576768 - 9068941 102015260 A0A8C2UXI9;A0A8C2V326 MODEL AGCD01042436;GBDK01395390;XM_005393560;XM_005393569;XM_005393570;XM_013519027;XM_013519028;XM_013519029;XM_013519030;XM_013519031;XM_013519032;XM_013519033;XM_013519034;XM_013519035 XP_005393617;XP_005393626;XP_005393627;XP_013374481;XP_013374482;XP_013374483;XP_013374484;XP_013374485;XP_013374486;XP_013374487;XP_013374488;XP_013374489 coiled-coil domain-containing protein 33 protein-coding ENSCLAG00000004853 NW_004955450 3481232 3576771 - 8708504 LOC102015474 CSC1-like protein 1 NW_004956265 355 5982 - 102015474 MODEL AGCD01079347;GBBH01033680;GBDK01145453;XM_005415187 XP_005415244 APPROVED protein-coding 8708515 LOC102015521 histone H3.1 NW_004955483 786482 786943 + 102015521 A0A8C2USV1 MODEL AGCD01057630;XM_005403292 XP_005403349 APPROVED protein-coding ENSCLAG00000002704;ENSCLAG00000017470;ENSCLAG00000017522 8708520 Slain1 SLAIN motif family member 1 ASSOCIATED WITH chromosome 13q14 deletion syndrome (ortholog); genetic disease (ortholog); neuronal ceroid lipofuscinosis (ortholog) NW_004955404 29537497 29594617 - 9068941 102015594 A0A8C2UVH5;A0A8C2UYC0;A0A8C2V118 MODEL AGCD01003978;AGCD01003979;GBBH01069566;GBDF01054223;XM_005374150;XM_005374151 XP_005374207;XP_005374208 SLAIN motif family, member 1;SLAIN motif-containing protein 1 APPROVED protein-coding ENSCLAG00000004290 NW_004955404 29535923 29595141 - 8708539 Tex13b testis expressed 13B ASSOCIATED WITH autistic disorder (ortholog); Charcot-Marie-Tooth disease type X (ortholog); genetic disease (ortholog) NW_004955490 7943444 7944995 + 102015732 MODEL AGCD01060269;GBDF01087099;XM_005404683 XP_005404740 APPROVED protein-coding 8708546 Catsperg cation channel sperm associated auxiliary subunit gamma ASSOCIATED WITH genetic disease (ortholog) NW_004955468 1056197 1099804 - 9068941 102016464 MODEL AGCD01051749;AGCD01051750;AGCD01051751;AGCD01051752;AGCD01051753;AGCD01051754;AGCD01051755;AGCD01051756;GBDF01008471;GBDI01315833;XM_013522464 XP_013377918 cation channel sperm-associated protein subunit gamma;catsper channel auxiliary subunit gamma APPROVED protein-coding 8708577 Triqk triple QxxK/R motif containing ASSOCIATED WITH genetic disease (ortholog) NW_004955417 9397726 9450794 - 9068941 102017014 A0A8C2V1P1 MODEL AGCD01018052;GBDK01025200;XM_005381781;XM_005381782;XM_005381783;XM_013512847;XM_013512848 XP_005381838;XP_005381839;XP_005381840;XP_013368301;XP_013368302 protein-coding ENSCLAG00000004830 NW_004955417 9397750 9450794 - 8708601 Jade2 jade family PHD finger 2 ENCODES a protein that exhibits histone H3K14 acetyltransferase activity (ortholog); histone H4K12 acetyltransferase activity (ortholog); histone H4K16 acetyltransferase activity (ortholog); INVOLVED IN histone H4-K12 acetylation (ortholog); histone H4-K5 acetylation (ortholog); histone H4-K8 acetylation (ortholog); ASSOCIATED WITH familial adenomatous polyposis 1 (ortholog); genetic disease (ortholog); Hereditary Neoplastic Syndromes (ortholog); FOUND IN histone acetyltransferase complex (ortholog); nucleoplasm (ortholog) NW_004955408 5676590 5722726 + 9068941 102017198 A0A8C2W2S1 MODEL AGCD01008148;AGCD01008149;AGCD01008150;GBCQ01121630;XM_005376152;XM_005376153;XM_005376155;XM_005376156;XM_005376157 XP_005376209;XP_005376210;XP_005376212;XP_005376213;XP_005376214 Phf15 PHD finger protein 15 APPROVED protein-coding ENSCLAG00000014619 NW_004955408 5687544 5723122 + 8708630 LOC102017628 uncharacterized LOC102017628 NW_004955454 3267669 3273574 - 102017628 MODEL AGCD01045061;GBDF01144321;XR_262778 ncrna 8708635 LOC102017857 40S ribosomal protein S15a pseudogene NW_004955412 16023672 16024171 - 102017857 A0A8C2WED2 MODEL AGCD01012891;XM_005378627 APPROVED pseudo ENSCLAG00000017767 8708639 Tubb1 tubulin beta 1 class VI ENCODES a protein that exhibits structural constituent of cytoskeleton (ortholog); INVOLVED IN microtubule polymerization (ortholog); microtubule-based process (ortholog); platelet aggregation (ortholog); PARTICIPATES IN docetaxel pharmacodynamics pathway; tyrosinemia type III pathway; vinblastine pharmacodynamics pathway; ASSOCIATED WITH Acute Coronary Syndrome (ortholog); autosomal dominant macrothrombocytopenia TUBB1-related (ortholog); congenital hypothyroidism (ortholog); FOUND IN cytoplasm (ortholog); intercellular bridge (ortholog); microtubule (ortholog) NW_004955445 569504 576129 - 9068941;7240710 102019117 A0A8C2UY68 MODEL AGCD01039320;GBDJ01340647;XM_005392213 XP_005392270 tubulin beta-1 chain;tubulin, beta 1 class VI APPROVED protein-coding ENSCLAG00000004602 NW_004955445 569504 576345 - 8708647 Gda guanine deaminase ENCODES a protein that exhibits guanine deaminase activity (ortholog); INVOLVED IN allantoin metabolic process (ortholog); amide catabolic process (ortholog); deoxyguanosine catabolic process (ortholog); PARTICIPATES IN adenine phoshoribosyltransferase deficiency pathway; adenosine monophosphate deaminase deficiency pathway; adenylosuccinate lyase deficiency pathway; ASSOCIATED WITH Animal Mammary Neoplasms (ortholog); carcinoma (ortholog); Chemical and Drug Induced Liver Injury (ortholog); FOUND IN cytosol (ortholog) NW_004955434 983388 1050413 - 9068941 102019310 A0A8C2V6D2 MODEL AGCD01032047;AGCD01032048;AGCD01032049;AGCD01032050;GBBH01187473;GBCB01101187;XM_005388518 XP_005388575 protein-coding ENSCLAG00000006160 NW_004955434 983388 1049948 - 8708668 LOC102019617 serine-rich coiled-coil domain-containing protein 2 pseudogene NW_004955424 3832086 3840893 + 102019617 MODEL AGCD01024331 APPROVED pseudo 8708669 LOC102020158 uncharacterized LOC102020158 NW_004955527 937906 940168 + 102020158 MODEL AGCD01069387;GBDF01019742;XR_264665 ncrna 8708675 Ttc6 tetratricopeptide repeat domain 6 ASSOCIATED WITH Brain-Lung-Thyroid Syndrome (ortholog); Meckel syndrome (ortholog) NW_004955409 23349294 23580993 - 102020218 A0A8C2VL38;A0A8C2VNV7 MODEL AGCD01010059;AGCD01010060;AGCD01010061;AGCD01010062;AGCD01010063;AGCD01010064;AGCD01010065;AGCD01010066;AGCD01010067;AGCD01010068;GBBH01162846;GBDI01355143;XM_013510165 XP_013365619 tetratricopeptide repeat protein 6 APPROVED protein-coding ENSCLAG00000010689 NW_004955409 23348460 23568749 - 8708707 Ears2 glutamyl-tRNA synthetase 2, mitochondrial ENCODES a protein that exhibits glutamate-tRNA ligase activity (ortholog); glutamate-tRNA(Gln) ligase activity (ortholog); INVOLVED IN glutamyl-tRNA aminoacylation (ortholog); tRNA aminoacylation for mitochondrial protein translation (ortholog); PARTICIPATES IN 2-hydroxyglutaric aciduria pathway; glutamic acid/glutamate metabolic pathway; homocarnosinosis pathway; ASSOCIATED WITH combined oxidative phosphorylation deficiency (ortholog); combined oxidative phosphorylation deficiency 12 (ortholog); congenital disorder of glycosylation type IIe (ortholog); FOUND IN mitochondrion (ortholog) NW_004955493 2083272 2113403 - 9068941;7240710 102021021 A0A8C2VPQ1 MODEL AGCD01060925;AGCD01060926;GBCQ01035758;XM_005405096;XM_013504806;XM_013504807;XM_013504808 XP_005405153;XP_013360260;XP_013360261;XP_013360262 probable glutamate--tRNA ligase, mitochondrial protein-coding ENSCLAG00000010779 NW_004955493 2090940 2113843 - 8708720 LOC102021634 granzyme B(G,H)-like NW_004955409 35533853 35535909 + 102021634 MODEL AGCD01010425 APPROVED pseudo 8708721 LOC102021711 disintegrin and metalloproteinase domain-containing protein 10 pseudogene NW_004955550 500606 504358 - 102021711 MODEL AGCD01072509 APPROVED pseudo 8708722 LOC102022153 uncharacterized LOC102022153 NW_004955403 379285 396291 - 9068941;7240710 102022153 MODEL AGCD01001691;GBDI01039089;XM_013511757 XP_013367211 Casp10 caspase 10, apoptosis-related cysteine peptidase APPROVED protein-coding 8708731 LOC102022481 uncharacterized LOC102022481 NW_004955465 10453747 10455158 + 102022481 MODEL AGCD01050510;GBCQ01164306;XR_263266 ncrna 8708735 Cep63 centrosomal protein 63 ENCODES a protein that exhibits molecular adaptor activity (ortholog); INVOLVED IN centriole replication (ortholog); centrosome duplication (ortholog); intrinsic apoptotic signaling pathway by p53 class mediator (ortholog); ASSOCIATED WITH genetic disease (ortholog); hereditary spastic paraplegia (ortholog); microcephaly (ortholog); FOUND IN centriolar satellite (ortholog); centriole (ortholog); centrosome (ortholog) NW_004955501 4032281 4095990 - 9068941;7240710 102022721 A0A8C2YJB5;A0A8C2YJC2 MODEL AGCD01064106;AGCD01064107;AGCD01064108;AGCD01064109;AGCD01064110;AGCD01064111;GBCE01065764;XM_005406794;XM_005406795;XM_005406798;XM_013505782;XM_013505783;XM_013505785;XM_013505786;XM_013505787 XP_005406851;XP_005406852;XP_005406855;XP_013361236;XP_013361237;XP_013361239;XP_013361240;XP_013361241 centrosomal protein 63kDa;centrosomal protein of 63 kDa APPROVED protein-coding ENSCLAG00000002080 NW_004955501 4032223 4095970 - 8708767 LOC102023750 uncharacterized LOC102023750 NW_004955562 409617 461561 - 102023750 MODEL AGCD01073925;GBDK01125417;XR_001232360;XR_001232361;XR_001232362;XR_001232363;XR_001232364;XR_001232365 ncrna 8708772 Amotl1 angiomotin like 1 ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN blood vessel endothelial cell migration (ortholog); establishment of cell polarity involved in ameboidal cell migration (ortholog); establishment of epithelial cell polarity (ortholog); ASSOCIATED WITH ataxia telangiectasia (ortholog); Disease Progression (ortholog); genetic disease (ortholog); FOUND IN apical plasma membrane (ortholog); bicellular tight junction (ortholog); COP9 signalosome (ortholog) NW_004955605 113570 275921 - 9068941 102024076 A0A8C2UIG2;A0A8C2UJ81;A0A8C2ULD5 MODEL AGCD01076930;AGCD01076931;AGCD01076932;AGCD01076933;AGCD01076934;AGCD01076935;AGCD01076936;AGCD01076937;AGCD01076938;GBCE01000888;XM_005414888;XM_005414889;XM_005414890;XM_005414891;XM_005414892;XM_013510098 XP_005414945;XP_005414946;XP_005414947;XP_005414948;XP_005414949;XP_013365552 angiomotin-like protein 1 protein-coding ENSCLAG00000000175 NW_004955605 113570 245932 - 8708805 LOC102024125 uncharacterized LOC102024125 NW_004955422 26926363 26963457 - 102024125 MODEL AGCD01023305;AGCD01023306;AGCD01023307;GBDF01036002;XR_260925 ncrna 8708810 LOC102024553 olfactory receptor 52E1-like NW_004955414 20797441 20798379 + 102024553 MODEL AGCD01015389;XM_005380068 XP_005380125 protein-coding 8708813 Gml glycosylphosphatidylinositol anchored molecule like ASSOCIATED WITH epidermolysis bullosa simplex with muscular dystrophy (ortholog); genetic disease (ortholog); holoprosencephaly (ortholog) NW_004955454 1724929 1735380 + 9068941 102025079 A0A8C2VN78 MODEL AGCD01044979;AGCD01044980;AGCD01044981;GBDF01052200;XM_005395752 XP_005395809 APPROVED protein-coding ENSCLAG00000010524 NW_004955454 1724859 1735424 + 8708820 LOC102025137 melanoma-associated antigen 10-like NW_004955498 4797137 4797895 + 102025137 MODEL AGCD01063020;GBDF01246816;XM_005406487 XP_005406544 protein-coding 8708823 LOC102025361 coiled-coil domain-containing protein 152 pseudogene NW_004955418 6274363 6275849 + 102025361 MODEL AGCD01018870;AGCD01018871 APPROVED pseudo 8708824 Itm2c integral membrane protein 2C ENCODES a protein that exhibits amyloid-beta binding (ortholog); ATP binding (ortholog); INVOLVED IN negative regulation of neuron projection development (ortholog); neuron differentiation (ortholog); positive regulation of extrinsic apoptotic signaling pathway (ortholog); ASSOCIATED WITH genetic disease (ortholog); Joubert syndrome 22 (ortholog); Perlman syndrome (ortholog); FOUND IN Golgi apparatus (ortholog); lysosome (ortholog); perinuclear region of cytoplasm (ortholog) NW_004955453 4546736 4557649 - 9068941 102025537 A0A8C2V2X3;A0A8C2V2Y8 MODEL AGCD01044692;GBCQ01010113;XM_005395408;XM_005395409 XP_005395465;XP_005395466 protein-coding ENSCLAG00000006596 NW_004955453 4543476 4557757 - 8708841 LOC102025596 RNA-binding protein 6 pseudogene NW_004955495 807714 809120 + 102025596 MODEL AGCD01061654 APPROVED pseudo 8708842 Pecr peroxisomal trans-2-enoyl-CoA reductase ENCODES a protein that exhibits 2,4-dienoyl-CoA reductase (NADPH) activity (ortholog); signaling receptor binding (ortholog); trans-2-enoyl-CoA reductase (NADPH) activity (ortholog); INVOLVED IN phytol metabolic process (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN mitochondrion (ortholog); peroxisome (ortholog) NW_004955453 17059779 17109531 + 9068941 102025651 A0A8C2VVY7 MODEL AGCD01044917;AGCD01044918;GBDF01081665;XM_005395692;XM_013519993 XP_005395749;XP_013375447 protein-coding ENSCLAG00000013472 NW_004955453 17076115 17108957 + 8708855 Actl10 actin like 10 ASSOCIATED WITH genetic disease (ortholog); long QT syndrome (ortholog) NW_004955422 27650166 27651452 - 102026990 A0A8C2WBP5 MODEL AGCD01023331;GBDF01090365;XM_005384923 XP_005384980 actin-like 10;actin-like protein 10 APPROVED protein-coding ENSCLAG00000018112 NW_004955422 27650277 27651317 - 8708859 Emid1 EMI domain containing 1 ASSOCIATED WITH Breast Cancer, Familial (ortholog); genetic disease (ortholog); neurofibromatosis 2 (ortholog); FOUND IN endoplasmic reticulum (ortholog); extracellular matrix (ortholog); Golgi apparatus (ortholog) NW_004955455 3514350 3564584 + 9068941 102027713 A0A8C2VIG1;A0A8C2VL31 MODEL AGCD01045632;AGCD01045633;AGCD01045634;AGCD01045635;AGCD01045636;GBBH01172676;GBDI01170247;XM_005396178;XM_005396179;XM_005396180;XM_005396181;XM_005396182;XM_005396188 XP_005396235;XP_005396236;XP_005396237;XP_005396238;XP_005396239;XP_005396245 EMI domain-containing protein 1 protein-coding ENSCLAG00000009945 NW_004955455 3514397 3563904 + 8708902 LOC102027838 olfactory receptor 51V1-like NW_004955414 21106478 21108278 - 102027838 MODEL AGCD01015407 pseudo 8708903 Ndst4 N-deacetylase and N-sulfotransferase 4 ENCODES a protein that exhibits [heparan sulfate]-glucosamine N-sulfotransferase activity (ortholog); deacetylase activity (ortholog); N-acetylglucosamine deacetylase activity (ortholog); ASSOCIATED WITH genetic disease (ortholog); Prostatic Neoplasms (ortholog) NW_004955428 24376587 24636555 + 9068941 102028318 A0A8C2VJY4;A0A8C2VMP2 MODEL AGCD01028255;AGCD01028256;AGCD01028257;AGCD01028258;AGCD01028259;AGCD01028260;AGCD01028261;AGCD01028262;AGCD01028263;AGCD01028264;AGCD01028265;GBDF01226340;XM_013515257;XM_013515258;XM_013515259;XM_013515260;XM_013515261 XP_013370711;XP_013370712;XP_013370713;XP_013370714;XP_013370715 LOC102028114 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 4;bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 4;uncharacterized LOC102028114 PROVISIONAL protein-coding ENSCLAG00000010385 NW_004955428 24346191 24637737 + 8708921 Polq DNA polymerase theta ENCODES a protein that exhibits 5'-deoxyribose-5-phosphate lyase activity (ortholog); chromatin binding (ortholog); DNA-directed DNA polymerase activity (ortholog); INVOLVED IN base-excision repair (ortholog); DNA damage response (ortholog); DNA repair (ortholog); ASSOCIATED WITH alkaptonuria (ortholog); COVID-19 (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); Golgi apparatus (ortholog); nucleoplasm (ortholog) NW_004955427 20779332 20895094 - 9068941 102029881 A0A8C2V9C1;A0A8C2V9C8 MODEL AGCD01027416;AGCD01027417;AGCD01027418;AGCD01027419;AGCD01027420;AGCD01027421;AGCD01027422;AGCD01027423;GBDJ01300677;XM_005386484;XM_013515227;XM_013515228 XP_005386541;XP_013370681;XP_013370682 polymerase (DNA directed), theta APPROVED protein-coding ENSCLAG00000008388 NW_004955427 20778952 20894989 - 8708958 CYTB cytochrome b MT 14163 15302 + 15822234 A0A172JU28;M9NW54;Q8HH85;Q8HH86;Q8HH87;Q94QI2;Q94QI3;Q94QI4;Q9B595;Q9B596;Q9B597;Q9B598;Q9B599;Q9B5A0 REVIEWED JX312692 AFQ55789;YP_008080757 APPROVED protein-coding ENSCLAG00000000035 MT 14163 15302 + 8708959 LOC102004256 archaemetzincin-2-like NW_004955463 752523 753108 + 102004256 MODEL AGCD01049497 pseudo 8708960 Atm ATM serine/threonine kinase ENCODES a protein that exhibits 1-phosphatidylinositol-3-kinase activity (ortholog); DNA-dependent protein kinase activity (ortholog); identical protein binding (ortholog); INVOLVED IN brain development (ortholog); cellular response to gamma radiation (ortholog); cellular response to ionizing radiation (ortholog); PARTICIPATES IN ataxia telangiectasia-mutated (ATM) signaling pathway; nuclear factor kappa B signaling pathway; p38 MAPK signaling pathway; ASSOCIATED WITH Acute Liver Failure (ortholog); adenocarcinoma (ortholog); adenoid cystic carcinoma (ortholog); FOUND IN centrosome (ortholog); chromosome, telomeric region (ortholog); cytoplasm (ortholog) NW_004955412 10422753 10531406 + 9068941;7240710 102005238 A0A8C2VT21 MODEL AGCD01012767;AGCD01012768;AGCD01012769;GBDF01279272;XM_005378035;XM_013510995;XM_013510996;XR_001232882 XP_005378092;XP_013366449;XP_013366450 ataxia telangiectasia mutated;serine-protein kinase ATM APPROVED protein-coding ENSCLAG00000011868 NW_004955412 10426135 10530545 + 8709027 Smox spermine oxidase ENCODES a protein that exhibits polyamine oxidase activity (ortholog); INVOLVED IN polyamine catabolic process (ortholog); spermine catabolic process (ortholog); PARTICIPATES IN polyamine metabolic pathway; ASSOCIATED WITH genetic disease (ortholog); Huntington's disease-like 1 (ortholog); middle cerebral artery infarction (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955415 14937438 14971874 + 9068941 102005704 A0A8C2VM02;A0A8C2VM12;A0A8C2VM71;A0A8C2VP74;A0A8C2VUC4;A0A8C2YRC1;A0A8C2YRC8 MODEL AGCD01016319;AGCD01016320;GBDF01089694;XM_005380812;XM_005380813;XM_005380814;XM_005380815;XM_005380816;XM_013512389;XM_013512390 XP_005380869;XP_005380870;XP_005380871;XP_005380872;XP_005380873;XP_013367843;XP_013367844 protein-coding ENSCLAG00000012093 NW_004955415 14937131 14989972 + 8709056 Pheta1 PH domain containing endocytic trafficking adaptor 1 ENCODES a protein that exhibits protein homodimerization activity (ortholog); INVOLVED IN endosome organization (ortholog); receptor recycling (ortholog); retrograde transport, endosome to Golgi (ortholog); ASSOCIATED WITH Colorectal Neoplasms (ortholog); genetic disease (ortholog); FOUND IN clathrin-coated vesicle (ortholog); early endosome (ortholog); recycling endosome (ortholog) NW_004955482 8052534 8058004 - 9068941 102005711 MODEL AGCD01057499;AGCD01057500;GBBH01207880;GBCE01030281;XM_013503647 XP_013359101 Fam109a family with sequence similarity 109 member A;family with sequence similarity 109, member A;sesquipedalian-1 APPROVED protein-coding 8709063 Hdac11 histone deacetylase 11 ENCODES a protein that exhibits histone deacetylase activity (ortholog); INVOLVED IN oligodendrocyte development (ortholog); PARTICIPATES IN histone modification pathway; ASSOCIATED WITH 3p deletion syndrome (ortholog); genetic disease (ortholog); FOUND IN histone deacetylase complex (ortholog); nucleus (ortholog); plasma membrane (ortholog) NW_004955429 12890939 12907749 - 9068941 102005736 A0A8C2VFE5;A0A8C2VHJ9 MODEL AGCD01028733;GBBH01209100;XM_005386979;XM_005386981 XP_005387036;XP_005387038 protein-coding ENSCLAG00000009712 NW_004955429 12890879 12907749 - 8709084 S100a9 S100 calcium binding protein A9 INVOLVED IN actin cytoskeleton organization (ortholog); activation of cysteine-type endopeptidase activity involved in apoptotic process (ortholog); astrocyte development (ortholog); ASSOCIATED WITH Acute Otitis Media; adult respiratory distress syndrome (ortholog); celiac disease (ortholog); FOUND IN cornified envelope (ortholog); cytoplasm (ortholog); extracellular space (ortholog) NW_004955592 90647 93842 - 9068941;11553828 26711468 102006189 MODEL AGCD01076300;GBCC01036093;XM_005414603;XM_013509984 XP_005414660;XP_013365438 protein-coding 8709091 LOC102006234 apolipoprotein L2-like NW_004955413 22477358 22499340 - 102006234 MODEL AGCD01014302;GBDK01079420;XM_005379648 XP_005379705 APPROVED protein-coding 8709099 LOC102006596 3-ketoacyl-CoA thiolase B, peroxisomal NW_004955427 25541841 25552096 - 102006596 A0A8C2VMG8;A0A8C2VQK6 MODEL AGCD01027545;GBDK01085734;XM_013515208 XP_013370662 APPROVED protein-coding ENSCLAG00000011568 8709119 LOC102007286 prolactin-like NW_004955576 959769 969369 + 102007286 A0A8C2UIL5 MODEL AGCD01075349;GBDK01091111;XM_005413940 XP_005413997 protein-coding ENSCLAG00000001106 8709129 Wdr89 WD repeat domain 89 INVOLVED IN corpus callosum development (ortholog); ventricular system development (ortholog); ASSOCIATED WITH genetic disease (ortholog) NW_004955466 6171553 6204818 + 102007319 A0A8C2W7Z8 MODEL AGCD01050912;AGCD01050913;AGCD01050914;GBDF01276584;XM_005399148;XM_005399149;XM_005399150;XM_005399151;XM_013522006;XM_013522007 XP_005399205;XP_005399206;XP_005399207;XP_005399208;XP_013377460;XP_013377461 WD repeat-containing protein 89 protein-coding ENSCLAG00000017740 NW_004955466 6203391 6204548 + 8709149 LOC102007512 keratin-associated protein 10-7-like NW_004955407 41555800 41557892 - 102007512 A0A8C2UVF0 MODEL AGCD01007870;XM_005375893 XP_005375950 protein-coding ENSCLAG00000004501 8709157 Asxl2 ASXL transcriptional regulator 2 ENCODES a protein that exhibits chromatin binding (ortholog); peroxisome proliferator activated receptor binding (ortholog); INVOLVED IN adult heart development (ortholog); bone mineralization involved in bone maturation (ortholog); embryonic skeletal system morphogenesis (ortholog); ASSOCIATED WITH acute myeloid leukemia (ortholog); autism spectrum disorder (ortholog); Developmental Disease (ortholog); FOUND IN nucleoplasm (ortholog); nucleus (ortholog) NW_004955469 7786030 7923739 - 9068941 102007881 A0A8C2VJI7;A0A8C2VJN9 MODEL AGCD01052432;AGCD01052433;AGCD01052434;AGCD01052435;AGCD01052436;AGCD01052437;AGCD01052438;GBDJ01018939;XM_005400412;XM_005400413;XM_005400414;XM_013522575 XP_005400469;XP_005400470;XP_005400471;XP_013378029 additional sex combs like 2;additional sex combs like 2, transcriptional regulator;additional sex combs like transcriptional regulator 2;putative Polycomb group protein ASXL2 APPROVED protein-coding ENSCLAG00000011428 NW_004955469 7786154 7923500 - 8709179 Plcg2 phospholipase C gamma 2 ENCODES a protein that exhibits phosphatidylinositol phospholipase C activity (ortholog); phosphorylation-dependent protein binding (ortholog); phosphotyrosine residue binding (ortholog); INVOLVED IN activation of store-operated calcium channel activity (ortholog); antifungal innate immune response (ortholog); B cell differentiation (ortholog); PARTICIPATES IN erythropoietin signaling pathway; phosphatidylinositol 3-kinase class I signaling pathway; ASSOCIATED WITH Alzheimer's disease (ortholog); Autoinflammation, Antibody Deficiency, and Immune Dysregulation, PLCG2-Associated (ortholog); B-Cell Chronic Lymphocytic Leukemia (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); intracellular vesicle (ortholog) NW_004955522 4352890 4480735 + 9068941;7240710 102007928 A0A8C2UJ26 MODEL AGCD01068416;AGCD01068417;AGCD01068418;AGCD01068419;AGCD01068420;AGCD01068421;AGCD01068422;GBCE01092331;GBDJ01422643;XM_013507097 XP_013362551 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-2;phospholipase C, gamma 2 (phosphatidylinositol-specific) APPROVED protein-coding ENSCLAG00000000592 NW_004955522 4358233 4468986 + 8709213 LOC102008177 uncharacterized LOC102008177 NW_004955404 49258791 49264921 - 102008177 MODEL AGCD01004518;GBCQ01074933;XR_259344 ncrna 8709218 Mcm10 minichromosome maintenance 10 replication initiation factor ENCODES a protein that exhibits enzyme binding (ortholog); identical protein binding (ortholog); INVOLVED IN cell population proliferation (ortholog); DNA damage response (ortholog); DNA replication initiation (ortholog); ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog); hepatocellular carcinoma (ortholog); FOUND IN nucleolus (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955462 1151163 1186601 + 9068941 102008508 A0A8C2VSB4 MODEL AGCD01049103;GBBH01038474;XM_005398088;XM_013521441 XP_005398145;XP_013376895 minichromosome maintenance complex component 10 APPROVED protein-coding ENSCLAG00000012085 NW_004955462 1153058 1188799 + 8709250 LOC102009395 uncharacterized LOC102009395 NW_004955422 28736276 28739914 + 102009395 MODEL AGCD01023368;GBDF01220110;XR_260928 ncrna 8709255 Trim65 tripartite motif containing 65 ENCODES a protein that exhibits ubiquitin protein ligase activity (ortholog); ubiquitin-protein transferase activity (ortholog); INVOLVED IN antiviral innate immune response (ortholog); negative regulation of inflammatory response (ortholog); positive regulation of autophagy (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955506 6362360 6366743 + 9068941 102010076 A0A8C2VBB3 MODEL AGCD01065413;AGCD01065414;GBCE01065169;GBDI01290894;XM_013506003 XP_013361457 tripartite motif-containing protein 65 protein-coding ENSCLAG00000007508 NW_004955506 6362396 6366591 + 8709267 Capzb capping actin protein of muscle Z-line subunit beta ENCODES a protein that exhibits actin binding (ortholog); actin filament binding (ortholog); beta-tubulin binding (ortholog); INVOLVED IN actin polymerization or depolymerization (ortholog); barbed-end actin filament capping (ortholog); cell projection organization (ortholog); ASSOCIATED WITH 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (ortholog); Acute Coronary Syndrome (ortholog); Animal Mammary Neoplasms (ortholog); FOUND IN asymmetric synapse (ortholog); brush border (ortholog); cortical cytoskeleton (ortholog) NW_004955452 34454 168514 - 9068941 102011618 A0A8C2V6N4;A0A8C2V6P0 MODEL AGCD01043797;AGCD01043798;AGCD01043799;AGCD01043800;AGCD01043801;AGCD01043802;GBCE01000866;XM_005394657;XM_005394658 XP_005394714;XP_005394715 F-actin-capping protein subunit beta;capping actin protein of muscle Z-line beta subunit;capping protein (actin filament) muscle Z-line, beta APPROVED protein-coding ENSCLAG00000007637 NW_004955452 30589 169693 - 8709291 Pola2 DNA polymerase alpha 2, accessory subunit ENCODES a protein that exhibits DNA-directed DNA polymerase activity (ortholog); INVOLVED IN DNA replication (ortholog); DNA replication initiation (ortholog); DNA replication, synthesis of RNA primer (ortholog); ASSOCIATED WITH Aicardi-Goutieres Syndrome 3 (ortholog); Bardet-Biedl syndrome (ortholog); genetic disease (ortholog); FOUND IN alpha DNA polymerase:primase complex (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955422 19939971 19963753 - 9068941 102012445 A0A8C2W4T3;A0A8C2W7K0 MODEL AGCD01023049;AGCD01023050;GBDF01279643;XM_005384504;XM_005384505;XM_005384506 XP_005384561;XP_005384562;XP_005384563 DNA polymerase alpha subunit B;polymerase (DNA directed), alpha 2, accessory subunit APPROVED protein-coding ENSCLAG00000016655 NW_004955422 19939933 19963753 - 8709322 Kitlg KIT ligand ENCODES a protein that exhibits cytokine activity (ortholog); stem cell factor receptor binding (ortholog); INVOLVED IN apoptotic process (ortholog); cell population proliferation (ortholog); ectopic germ cell programmed cell death (ortholog); ASSOCIATED WITH Animal Mammary Neoplasms (ortholog); autosomal dominant nonsyndromic deafness 69 (ortholog); carcinoma (ortholog); FOUND IN cytoplasm (ortholog); extracellular space (ortholog); filopodium (ortholog) NW_004955405 25816137 25969006 - 9068941;7240710 102012494 A0A8C2V181;A0A8C2V182 MODEL AGCD01005186;AGCD01005187;AGCD01005188;AGCD01005189;AGCD01005190;AGCD01005191;AGCD01005192;GBDJ01354458;XM_005374430;XM_005374432;XM_013518150;XM_013518152;XR_001235502 XP_005374487;XP_005374489;XP_013373604;XP_013373606 protein-coding ENSCLAG00000006139 NW_004955405 25886447 25969395 - 8709348 LOC102014190 E3 ubiquitin-protein ligase TRIM39 NW_004955583 454579 466005 + 9068941 102014190 A0A8C2URF0 MODEL AGCD01075825;GBBH01186352;GBCE01008619;XM_005414304;XM_013509782;XM_013509783 XP_005414361;XP_013365236;XP_013365237 Trim39 tripartite motif containing 39 APPROVED protein-coding ENSCLAG00000003141 NW_004955583 454579 466005 + 8709359 LOC102015072 hematopoietic prostaglandin D synthase NW_004955405 4958128 4976383 - 9068941 102015072 MODEL AGCD01004669;AGCD01004670;GBDI01323199;XM_013519363 XP_013374817 Hpgds APPROVED protein-coding 8709367 Alx3 ALX homeobox 3 ENCODES a protein that exhibits sequence-specific double-stranded DNA binding (ortholog); INVOLVED IN embryonic forelimb morphogenesis (ortholog); embryonic hindlimb morphogenesis (ortholog); embryonic skeletal system morphogenesis (ortholog); ASSOCIATED WITH autistic disorder (ortholog); developmental and epileptic encephalopathy 32 (ortholog); frontonasal dysplasia (ortholog) NW_004955435 13584129 13594316 - 9068941;7240710 102015236 A0A8C2VI79 MODEL AGCD01033205;GBDF01222447;XM_005388911 XP_005388968 homeobox protein aristaless-like 3 protein-coding ENSCLAG00000009014 NW_004955435 13583611 13594316 - 8709375 Mbd1 methyl-CpG binding domain protein 1 ENCODES a protein that exhibits chromatin binding (ortholog); DNA binding (ortholog); double-stranded methylated DNA binding (ortholog); INVOLVED IN heart development (ortholog); negative regulation of astrocyte differentiation (ortholog); negative regulation of gene expression (ortholog); PARTICIPATES IN DNA modification pathway; ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN chromatin (ortholog); cytoplasm (ortholog); heterochromatin (ortholog) NW_004955402 35320755 35334751 - 9068941 102016004 A0A8C2V8C9;A0A8C2VB53 MODEL AGCD01000878;GBDI01171831;XM_013510642;XM_013510643;XM_013510646;XM_013510648;XM_013510651;XM_013510655;XM_013510661;XM_013510667;XM_013510672;XM_013510676;XM_013510682;XM_013510687 XP_013366096;XP_013366097;XP_013366100;XP_013366102;XP_013366105;XP_013366109;XP_013366115;XP_013366121;XP_013366126;XP_013366130;XP_013366136;XP_013366141 methyl-CpG-binding domain protein 1 protein-coding ENSCLAG00000007457 NW_004955402 35319810 35334678 - 8709419 LOC102016036 gamma-secretase subunit APH-1A pseudogene NW_004955465 10446172 10447450 - 102016036 MODEL AGCD01050510 APPROVED pseudo 8709420 LOC102016575 uncharacterized LOC102016575 NW_004955467 1729810 1730372 + 102016575 MODEL AGCD01051282;GBCE01002421;XR_263330 ncrna 8709424 Crct1 cysteine rich C-terminal 1 ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); immunodeficiency 42 (ortholog) NW_004955592 895325 896939 - 9068941 102016768 A0A8C2UVT6 MODEL AGCD01076334;GBDI01182859;XM_005414629;XM_013509979 XP_005414686;XP_013365433 cysteine-rich C-terminal 1;cysteine-rich C-terminal protein 1 APPROVED protein-coding ENSCLAG00000002891 8709430 LOC102017705 uncharacterized LOC102017705 NW_004955439 13711628 13716911 + 102017705 MODEL AGCD01035964;GBDF01041651;XR_261989 ncrna ENSCLAG00000025550 8709435 Pole DNA polymerase epsilon, catalytic subunit ENCODES a protein that exhibits chromatin binding (ortholog); DNA binding (ortholog); DNA-directed DNA polymerase activity (ortholog); INVOLVED IN base-excision repair, gap-filling (ortholog); DNA biosynthetic process (ortholog); DNA replication (ortholog); PARTICIPATES IN nucleotide excision repair pathway; ASSOCIATED WITH ascending colon cancer (ortholog); breast cancer (ortholog); Breast Neoplasms (ortholog); FOUND IN epsilon DNA polymerase complex (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955482 373467 418000 + 9068941 102019698 A0A8C2VAL1;A0A8C2VFU2 MODEL AGCD01057171;AGCD01057172;GBDF01088484;XM_005402950;XM_005402952;XM_013503642;XM_013503643 XP_005403007;XP_005403009;XP_013359096;XP_013359097 DNA polymerase epsilon catalytic subunit A;polymerase (DNA directed), epsilon, catalytic subunit APPROVED protein-coding ENSCLAG00000008788 NW_004955482 373555 417266 + 8709496 LOC102020311 proton-coupled amino acid transporter 1 NW_004955408 5895042 5933710 + 9068941 102020311 A0A8C2VZW9 MODEL AGCD01008159;GBDK01305420;XM_005376161;XM_005376162 XP_005376218;XP_005376219 Slc36a1 solute carrier family 36 (proton/amino acid symporter), member 1 APPROVED protein-coding ENSCLAG00000013787 NW_004955408 5894988 5936232 + 8709512 LOC102020870 magnesium transporter MRS2 homolog, mitochondrial-like NW_004955694 5431 7611 + 102020870 MODEL AGCD01078077;GBBH01208983;GBDI01228450;XM_005415072 XP_005415129 protein-coding 8709530 Tnp1 transition protein 1 ENCODES a protein that exhibits DNA binding (ortholog); INVOLVED IN chromatin remodeling (ortholog); flagellated sperm motility (ortholog); heterochromatin formation (ortholog); ASSOCIATED WITH genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN male germ cell nucleus (ortholog); nucleosome (ortholog); nucleus (ortholog) NW_004955453 16387897 16388513 + 9068941 102021623 A0A8C2VF77 MODEL AGCD01044902;GBDF01007631;XM_005395680 XP_005395737 spermatid nuclear transition protein 1;transition protein 1 (during histone to protamine replacement) APPROVED protein-coding ENSCLAG00000009510 NW_004955453 16387527 16388890 + 8709536 LOC102022469 uncharacterized LOC102022469 NW_004955408 24472374 24475060 - 102022469 MODEL AGCD01008610;GBCE01106540;XR_001231905;XR_001231907 ncrna 8709544 LOC102022557 serine protease 55 NW_004955403 52130187 52140797 + 9068941 102022557 A0A8C2W2M2 MODEL AGCD01003002;AGCD01003003;GBDF01031608;XM_005373804 XP_005373861 Prss55 protease, serine, 55 APPROVED protein-coding ENSCLAG00000015325 NW_004955403 52130253 52140938 + 8709553 LOC102024170 uncharacterized LOC102024170 NW_004955445 701392 713169 + 102024170 MODEL AGCD01039323;GBDK01292464;XR_001235572;XR_001235573;XR_262289 ncrna 8709558 Cd86 CD86 molecule ENCODES a protein that exhibits receptor ligand activity (ortholog); signaling receptor binding (ortholog); INVOLVED IN activation of phospholipase C activity (ortholog); activation of protein kinase C activity (ortholog); B cell activation (ortholog); ASSOCIATED WITH acute lymphoblastic leukemia (ortholog); acute myeloid leukemia (ortholog); adult T-cell leukemia/lymphoma (ortholog); FOUND IN cell surface (ortholog); centriolar satellite (ortholog); external side of plasma membrane (ortholog) NW_004955427 21375820 21436767 + 9068941 102024258 A0A8C2VJE6;A0A8C2YQU9;A0A8C2YQV2 MODEL AGCD01027444;AGCD01027445;GBDK01357791;XM_013515233;XM_013515234;XM_013515236;XM_013515237 XP_013370687;XP_013370688;XP_013370690;XP_013370691 T-lymphocyte activation antigen CD86 protein-coding ENSCLAG00000011396 NW_004955427 21375794 21435874 + 8709564 LOC102024488 olfactory receptor 1020-like NW_004955511 1747705 1751671 + 102024488 MODEL AGCD01066378;XM_005408242 XP_005408299 protein-coding 8709568 C4bpb complement component 4 binding protein beta INVOLVED IN negative regulation of complement activation, classical pathway (ortholog); positive regulation of protein catabolic process (ortholog); regulation of opsonization (ortholog); PARTICIPATES IN forkhead class A signaling pathway; ASSOCIATED WITH autistic disorder (ortholog); common variable immunodeficiency 7 (ortholog); COVID-19 (ortholog); FOUND IN extracellular space (ortholog) NW_004955406 42601164 42608912 + 9068941 102024876 MODEL AGCD01006712;GBDF01118429;XM_005375411 XP_005375468 complement component 4 binding protein, beta APPROVED protein-coding 8709578 LOC102025832 vomeronasal type-2 receptor 116-like NW_004955432 4760218 4786103 + 102025832 MODEL AGCD01030744;XM_013515917 XP_013371371 APPROVED protein-coding 8709587 LOC102026025 elongation factor 1-alpha 1 pseudogene NW_004955425 22371390 22372772 + 102026025 MODEL AGCD01025819 APPROVED pseudo 8709588 Rabep1 rabaptin, RAB GTPase binding effector protein 1 ENCODES a protein that exhibits protein domain specific binding (ortholog); protein homodimerization activity (ortholog); INVOLVED IN Golgi to plasma membrane transport (ortholog); protein localization to ciliary membrane (ortholog); vesicle-mediated transport (ortholog); ASSOCIATED WITH fetal akinesia deformation sequence syndrome 4 (ortholog); genetic disease (ortholog); teratoma (ortholog); FOUND IN endocytic vesicle (ortholog); endosome (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955467 10613671 10748122 + 9068941 102026623 A0A8C2W1J2;A0A8C2W1L6;A0A8C2W234;A0A8C2YUA4;A0A8C2YUA9 MODEL AGCD01051578;AGCD01051579;AGCD01051580;AGCD01051581;AGCD01051582;AGCD01051583;GBDF01156135;XM_005399641;XM_005399642 XP_005399698;XP_005399699 rab GTPase-binding effector protein 1 protein-coding ENSCLAG00000016358 NW_004955467 10613861 10747255 + 8709611 LOC102027019 uncharacterized LOC102027019 NW_004955445 7961948 7972321 - 102027019 MODEL AGCD01039557;GBDK01005281;XR_001235604;XR_001235605;XR_001235606;XR_262314;XR_262316;XR_262317 ncrna 8709626 Nup88 nucleoporin 88 PARTICIPATES IN ribosome biogenesis pathway; ASSOCIATED WITH developmental and epileptic encephalopathy 25 (ortholog); fetal akinesia deformation sequence syndrome 4 (ortholog); genetic disease (ortholog); FOUND IN nuclear envelope (ortholog); nuclear pore (ortholog); nucleoplasm (ortholog) NW_004955467 10749910 10780423 - 9068941 102028070 A0A8C2VQ10;A0A8C2YRX3 MODEL AGCD01051583;GBDI01220761;XM_005399646 XP_005399703 nuclear pore complex protein Nup88;nucleoporin 88kDa APPROVED protein-coding ENSCLAG00000012899 NW_004955467 10749910 10780423 - 8709647 Cdc16 cell division cycle 16 INVOLVED IN protein K11-linked ubiquitination (ortholog); ASSOCIATED WITH factor X deficiency (ortholog); genetic disease (ortholog); FOUND IN anaphase-promoting complex (ortholog); centrosome (ortholog); cytoplasm (ortholog) NW_004955404 47126 71602 - 9068941 102028259 A0A8C2YM72 MODEL AGCD01003194;GBBH01228480;GBDJ01129351;XM_013515461;XM_013515464;XM_013515469;XM_013515473;XM_013515476 XP_013370915;XP_013370918;XP_013370923;XP_013370927;XP_013370930 cell division cycle protein 16 homolog protein-coding ENSCLAG00000006234 NW_004955404 45383 71466 - 8709668 Ighmbp2 immunoglobulin mu DNA binding protein 2 ENCODES a protein that exhibits 5'-3' DNA helicase activity (ortholog); 5'-3' RNA helicase activity (ortholog); ATP binding (ortholog); INVOLVED IN DNA duplex unwinding (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); neuromuscular process (ortholog); ASSOCIATED WITH Abnormal Reflexes (ortholog); Aicardi-Goutieres Syndrome 3 (ortholog); autosomal dominant distal hereditary motor neuronopathy (ortholog); FOUND IN axon (ortholog); cytoplasm (ortholog); growth cone (ortholog) NW_004955422 17017855 17047724 - 9068941;7240710 102028646 A0A8C2W3B2 MODEL AGCD01022906;AGCD01022907;AGCD01022908;GBDF01154386;XM_005384263 XP_005384320 DNA-binding protein SMUBP-2;immunoglobulin mu binding protein 2 APPROVED protein-coding ENSCLAG00000015500 NW_004955422 17017358 17048650 - 8709690 Kdm5b lysine demethylase 5B ENCODES a protein that exhibits DNA binding (ortholog); histone binding (ortholog); histone H3K4 demethylase activity (ortholog); INVOLVED IN branching involved in mammary gland duct morphogenesis (ortholog); cellular response to fibroblast growth factor stimulus (ortholog); cellular response to leukemia inhibitory factor (ortholog); PARTICIPATES IN histone modification pathway; ASSOCIATED WITH autism spectrum disorder (ortholog); autosomal recessive intellectual developmental disorder 65 (ortholog); breast cancer (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955406 38755220 38823094 - 9068941 102028822 A0A8C2VYY6 MODEL AGCD01006609;AGCD01006610;GBDK01322713;XM_005375227 XP_005375284 lysine (K)-specific demethylase 5B;lysine-specific demethylase 5B APPROVED protein-coding ENSCLAG00000014743 NW_004955406 38755220 38823088 - 8709724 Gpr12 G protein-coupled receptor 12 ENCODES a protein that exhibits phosphatidylcholine binding (ortholog); INVOLVED IN G protein-coupled receptor signaling pathway (ortholog); intracellular calcium ion homeostasis (ortholog); ASSOCIATED WITH genetic disease (ortholog); obesity (ortholog) NW_004955497 6248096 6251106 - 9068941 102029530 A0A8C2URL0 MODEL AGCD01062628;GBDK01402621;XM_005406351 XP_005406408 G-protein coupled receptor 12 protein-coding ENSCLAG00000003409 NW_004955497 6248096 6251106 - 8709730 Icam1 intercellular adhesion molecule 1 ENCODES a protein that exhibits integrin binding (ortholog); protein-containing complex binding (ortholog); INVOLVED IN acute inflammatory response to antigenic stimulus (ortholog); cell adhesion (ortholog); cell adhesion mediated by integrin (ortholog); PARTICIPATES IN eicosanoid signaling pathway; pro-inflammatory cytokine mediated pathway; ASSOCIATED WITH Acute Experimental Pancreatitis (ortholog); acute kidney failure (ortholog); Acute Lung Injury (ortholog); FOUND IN cell surface (ortholog); external side of plasma membrane (ortholog); extracellular exosome (ortholog) NW_004955495 1561464 1573282 + 9068941;7240710 102029873 A0A8C2UYH7 MODEL AGCD01061701;AGCD01061702;AGCD01061703;GBDK01022433;XM_005405586;XM_005405587 XP_005405643;XP_005405644 protein-coding ENSCLAG00000005350 NW_004955495 1561714 1574755 + 8709743 Trnak-cuu transfer RNA lysine (anticodon CUU) This record serves to anchor the annotations of this class of tRNAs at multiple locations on the chinchilla, long-tailed genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMe MT 1 1 101978827 MODEL AGCD01037806;AGCD01051106;AGCD01057606;AGCD01069830;AGCD01074502 trna 8709744 Nme5 NME/NM23 family member 5 INVOLVED IN cilium assembly (ortholog); epithelial cilium movement involved in extracellular fluid movement (ortholog); establishment of localization in cell (ortholog); ASSOCIATED WITH autosomal dominant intellectual developmental disorder 31 (ortholog); familial adenomatous polyposis 1 (ortholog); genetic disease (ortholog); FOUND IN cilium (ortholog); extracellular region (ortholog); sperm flagellum (ortholog) NW_004955418 2282721 2301997 + 9068941 102006913 A0A8C2VQK4 MODEL AGCD01018755;AGCD01018756;AGCD01018757;GBDF01044025;XM_005382131;XM_005382132 XP_005382188;XP_005382189 nucleoside diphosphate kinase homolog 5 protein-coding ENSCLAG00000013063 NW_004955418 2282574 2302106 + 8709757 Arfgef1 ADP ribosylation factor guanine nucleotide exchange factor 1 ENCODES a protein that exhibits GTPase activator activity (ortholog); guanyl-nucleotide exchange factor activity (ortholog); myosin binding (ortholog); INVOLVED IN endomembrane system organization (ortholog); Golgi organization (ortholog); negative regulation of actin filament polymerization (ortholog); ASSOCIATED WITH DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES (ortholog); DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES, WITH OR WITHOUT SEIZURES (ortholog); Developmental Disabilities (ortholog); FOUND IN cytosol (ortholog); Golgi apparatus (ortholog); Golgi membrane (ortholog) NW_004955444 11986595 12110172 + 9068941 102008357 A0A8C2UVF3;A0A8C2UY33 MODEL AGCD01039059;AGCD01039060;GBCQ01064317;GBDF01053271;XM_005392122 XP_005392179 ADP-ribosylation factor guanine nucleotide-exchange factor 1 (brefeldin A-inhibited);brefeldin A-inhibited guanine nucleotide-exchange protein 1 APPROVED protein-coding ENSCLAG00000003828 NW_004955444 11986595 12110172 + 8709800 LOC102008454 uncharacterized LOC102008454 NW_004955436 22240028 22281455 + 102008454 MODEL AGCD01034088;AGCD01034089 pseudo 8709801 LOC102008469 protein FAM209B NW_004955445 2725178 2727984 - 9068941 102008469 A0A8C2V0C1 MODEL AGCD01039364;GBDJ01263846;XM_005392264 XP_005392321 Fam209b family with sequence similarity 209, member B APPROVED protein-coding ENSCLAG00000005877 8709807 LOC102008830 ATP synthase F(0) complex subunit C3, mitochondrial pseudogene NW_004955464 13405011 13405720 + 102008830 MODEL AGCD01050275 APPROVED pseudo 8709808 Usp19 ubiquitin specific peptidase 19 ENCODES a protein that exhibits cysteine-type deubiquitinase activity (ortholog); Hsp90 protein binding (ortholog); K48-linked deubiquitinase activity (ortholog); INVOLVED IN negative regulation of proteasomal protein catabolic process (ortholog); negative regulation of skeletal muscle tissue development (ortholog); positive regulation of cell cycle process (ortholog); ASSOCIATED WITH Aicardi-Goutieres Syndrome 1 (ortholog); Generalized Epilepsy (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); endoplasmic reticulum membrane (ortholog) NW_004955532 1104212 1115267 - 9068941 102009214 A0A8C2VCT9;A0A8C2VCW6;A0A8C2YPH1 MODEL AGCD01070165;GBDJ01091689;XM_005410189;XM_005410190;XM_005410191;XM_013507630 XP_005410246;XP_005410247;XP_005410248;XP_013363084 ubiquitin carboxyl-terminal hydrolase 19 protein-coding ENSCLAG00000009469 NW_004955532 1104591 1113567 - 8709846 Nudt16 nudix hydrolase 16 ENCODES a protein that exhibits 5'-(N(7)-methylguanosine 5'-triphospho)-[mRNA] hydrolase activity (ortholog); chloride ion binding (ortholog); cobalt ion binding (ortholog); INVOLVED IN chromosome organization (ortholog); dITP catabolic process (ortholog); mRNA catabolic process (ortholog); ASSOCIATED WITH alkaptonuria (ortholog); COVID-19 (ortholog); Experimental Liver Cirrhosis (ortholog); FOUND IN cytoplasm (ortholog); nucleolus (ortholog); nucleoplasm (ortholog) NW_004955501 7083068 7085505 - 9068941 102009297 A0A8C2US59 MODEL AGCD01064204;GBDF01144639;XM_005406842 XP_005406899 U8 snoRNA-decapping enzyme;nudix (nucleoside diphosphate linked moiety X)-type motif 16 APPROVED protein-coding ENSCLAG00000003557 8709853 LOC102009550 olfactory receptor 5AU1 ASSOCIATED WITH Brain-Lung-Thyroid Syndrome (ortholog); genetic disease (ortholog); purine nucleoside phosphorylase deficiency (ortholog) NW_004955550 1921231 1923589 - 9068941 102009550 A0A8C2UHH9 MODEL AGCD01072598;XM_013508583 XP_013364037 APPROVED protein-coding ENSCLAG00000000791 NW_004955550 1921231 1923223 - 8709854 Ptk6 protein tyrosine kinase 6 ENCODES a protein that exhibits identical protein binding (ortholog); non-membrane spanning protein tyrosine kinase activity (ortholog); protein tyrosine kinase activity (ortholog); INVOLVED IN cell migration (ortholog); cellular response to retinoic acid (ortholog); intestinal epithelial cell differentiation (ortholog); ASSOCIATED WITH autosomal dominant nocturnal frontal lobe epilepsy (ortholog); autosomal recessive dyskeratosis congenita 5 (ortholog); benign familial infantile seizures 6 (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nuclear body (ortholog) NW_004955528 687996 695596 + 9068941 102009754 A0A8C2V5F5 MODEL AGCD01069542;GBCQ01083858;XM_005409962 XP_005410019 protein-tyrosine kinase 6 protein-coding ENSCLAG00000005884 NW_004955528 687996 695596 + 8709873 Borcs7 BLOC-1 related complex subunit 7 ASSOCIATED WITH genetic disease (ortholog); hereditary spastic paraplegia (ortholog); neuroaxonal dystrophy (ortholog); FOUND IN BORC complex (ortholog) NW_004955485 7605277 7615924 - 102010267 A0A8C2URL5 MODEL AGCD01058665;GBCB01024707;XM_005403820 XP_005403877 UPF0693 protein C10orf32 homolog APPROVED protein-coding ENSCLAG00000001557 NW_004955485 7605277 7615924 - 8709888 LOC102010349 uncharacterized LOC102010349 NW_004955465 9065822 9075222 + 102010349 MODEL AGCD01050484;GBDK01032471;XR_001236720;XR_263253 ncrna 8709893 Fxyd5 FXYD domain containing ion transport regulator 5 ENCODES a protein that exhibits actin binding (ortholog); cadherin binding (ortholog); ASSOCIATED WITH Brugada syndrome 5 (ortholog); dystonia (ortholog); Experimental Liver Cirrhosis (ortholog); FOUND IN membrane (ortholog) NW_004955468 4470148 4480386 + 9068941 102010790 MODEL AGCD01051911;GBDK01083415;XM_005400021;XM_013522441 XP_005400078;XP_013377895 FXYD domain-containing ion transport regulator 5 protein-coding 8709907 Ccdc50 coiled-coil domain containing 50 ENCODES a protein that exhibits ubiquitin protein ligase binding (ortholog); INVOLVED IN sensory perception of sound (ortholog); ASSOCIATED WITH autosomal dominant nonsyndromic deafness 44 (ortholog); B-Cell Chronic Lymphocytic Leukemia (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); microtubule cytoskeleton (ortholog) NW_004955420 16884985 16948038 - 9068941;7240710 102013510 A0A8C2VTZ6;A0A8C2VTZ8;A0A8C2VZ46 MODEL AGCD01021008;AGCD01021009;AGCD01021010;AGCD01021011;GBCE01117027;XM_005383218 XP_005383275 coiled-coil domain-containing protein 50 protein-coding ENSCLAG00000014114 NW_004955420 16891217 16948008 - 8709926 LOC102014160 zinc finger protein 709-like NW_004955432 4036003 4057987 - 102014160 MODEL AGCD01030688;AGCD01030689;GBDI01208211;XM_013515926 XP_013371380 APPROVED protein-coding 8709927 LOC102014337 uncharacterized LOC102014337 NW_004955412 25816755 25817421 - 102014337 MODEL AGCD01013174;GBDK01223923;XR_260023 ncrna 8709932 LOC102014811 uncharacterized LOC102014811 NW_004955429 21319251 21321579 + 102014811 MODEL AGCD01029000;GBDF01176350;XR_261372 ncrna 8709936 Ube2d2 ubiquitin conjugating enzyme E2 D2 ENCODES a protein that exhibits ubiquitin conjugating enzyme activity (ortholog); ubiquitin protein ligase activity (ortholog); ubiquitin-protein transferase activity (ortholog); INVOLVED IN protein autoubiquitination (ortholog); protein K48-linked ubiquitination (ortholog); protein polyubiquitination (ortholog); PARTICIPATES IN ubiquitin/proteasome degradation pathway; ASSOCIATED WITH autosomal dominant intellectual developmental disorder 31 (ortholog); familial adenomatous polyposis 1 (ortholog); genetic disease (ortholog); FOUND IN protein-containing complex (ortholog); ubiquitin ligase complex (ortholog) NW_004955418 990124 1043544 - 9068941 102014898 A0A8C2UWT3 MODEL AGCD01018699;AGCD01018700;AGCD01018701;AGCD01018702;AGCD01018703;GBDI01019168;XM_005382059;XM_005382060;XM_013512968;XM_013512969;XM_013512970 XP_005382116;XP_005382117;XP_013368422;XP_013368423;XP_013368424 ubiquitin-conjugating enzyme E2 D2;ubiquitin-conjugating enzyme E2D 2 APPROVED protein-coding ENSCLAG00000004214 NW_004955418 989802 1006262 - 8709960 Smim6 small integral membrane protein 6 INVOLVED IN negative regulation of ATPase-coupled calcium transmembrane transporter activity (ortholog); negative regulation of calcium ion binding (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN endoplasmic reticulum membrane (ortholog) NW_004955506 6590028 6592474 - 9068941 102014927 MODEL AGCD01065432;GBDF01040884;XM_005407489 XP_005407546 protein-coding 8709971 Itm2b integral membrane protein 2B ENCODES a protein that exhibits amyloid-beta binding (ortholog); ATP binding (ortholog); INVOLVED IN extrinsic apoptotic signaling pathway in absence of ligand (ortholog); negative regulation of amyloid precursor protein biosynthetic process (ortholog); ASSOCIATED WITH cerebral amyloid angiopathy (ortholog); chromosome 13q14 deletion syndrome (ortholog); familial adenomatous polyposis 2 (ortholog); FOUND IN extracellular space (ortholog); Golgi apparatus (ortholog); Golgi-associated vesicle membrane (ortholog) NW_004955431 1928706 1935010 + 9068941;7240710 102015136 A0A8C2V2R6 MODEL AGCD01029919;GBCC01001251;XM_005387555 XP_005387612 protein-coding ENSCLAG00000006439 NW_004955431 1928706 1937238 + 8709980 Tmem269 transmembrane protein 269 NW_004955537 2312276 2327745 + 102015763 A0A8C2UPR7 MODEL AGCD01070923;AGCD01070924;GBBH01078218;XM_005410619;XM_005410620;XM_005410621 XP_005410676;XP_005410677;XP_005410678 LOC102015763 uncharacterized LOC102015763;uncharacterized protein LOC102015763 APPROVED protein-coding ENSCLAG00000002885 NW_004955537 2312984 2324917 + 8709998 Prkrip1 PRKR interacting protein 1 ENCODES a protein that exhibits double-stranded RNA binding (ortholog); protein kinase binding (ortholog); protein kinase inhibitor activity (ortholog); INVOLVED IN negative regulation of phosphorylation (ortholog); negative regulation of protein kinase activity (ortholog); renal system process (ortholog); ASSOCIATED WITH genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN nucleolus (ortholog) NW_004955456 15188211 15216267 - 9068941 102016022 A0A8C2UXW6 MODEL AGCD01046663;AGCD01046664;GBDF01085713;XM_005396837 XP_005396894 PRKR interacting protein 1 (IL11 inducible);PRKR-interacting protein 1 APPROVED protein-coding ENSCLAG00000004919 NW_004955456 15186059 15216267 - 8710011 LOC102016171 olfactory receptor 7A17-like NW_004955495 8434964 8435920 + 102016171 MODEL AGCD01062208;XM_005406108 XP_005406165 protein-coding 8710014 LOC102016612 uncharacterized LOC102016612 NW_004955423 5447517 5458475 - 102016612 MODEL AGCD01023560;GBCQ01074215;XR_260954 ncrna 8710019 LOC102017257 60S acidic ribosomal protein P2 pseudogene NW_004955501 1411347 1416378 - 102017257 MODEL AGCD01064052 APPROVED pseudo 8710020 LOC102017826 uncharacterized LOC102017826 NW_004955447 224885 228738 - 102017826 MODEL AGCD01040449;GBDI01039983;XR_262402 ncrna 8710025 LOC102017953 uncharacterized LOC102017953 NW_004955455 12326192 12375978 + 102017953 MODEL AGCD01046033;AGCD01046034;AGCD01046035;AGCD01046036;GBCB01036113;XR_262857 ncrna 8710031 Mob3c MOB kinase activator 3C ASSOCIATED WITH genetic disease (ortholog) NW_004955464 11697952 11705495 + 9068941 102018170 A0A8C2V5L0;A0A8C2V9C4 MODEL AGCD01050161;GBDJ01385749;XM_005398672 XP_005398729 protein-coding ENSCLAG00000006684 NW_004955464 11662566 11705495 + 8710039 Smyd5 SMYD family member 5 ENCODES a protein that exhibits histone H4K20 methyltransferase activity (ortholog); INVOLVED IN negative regulation of gene expression, epigenetic (ortholog); regulation of stem cell differentiation (ortholog); regulation of stem cell division (ortholog); ASSOCIATED WITH Alstrom syndrome (ortholog); congenital disorder of glycosylation type IIb (ortholog); dystonia (ortholog) NW_004955424 12408059 12422424 - 9068941 102018619 A0A8C2V1F6 MODEL AGCD01024604;GBCQ01129452;XM_005385571;XM_013514725;XM_013514726 XP_005385628;XP_013370179;XP_013370180 SET and MYND domain-containing protein 5 protein-coding ENSCLAG00000006061 NW_004955424 12408059 12423164 - 8710056 LOC102018675 uncharacterized LOC102018675 NW_004955622 83258 210783 - 102018675 MODEL AGCD01077384;AGCD01077385;AGCD01077386;AGCD01077387;AGCD01077388;AGCD01077389;AGCD01077390;AGCD01077391;AGCD01077392;AGCD01077393;AGCD01077394;AGCD01077395;XM_013510157 XP_013365611 LOC102019010;LOC102019346 uncharacterized protein LOC102018675;vomeronasal type-2 receptor 26-like PROVISIONAL protein-coding 8710064 Arc activity regulated cytoskeleton associated protein ENCODES a protein that exhibits mRNA binding (ortholog); INVOLVED IN anterior/posterior pattern specification (ortholog); cell migration (ortholog); cytoskeleton organization (ortholog); ASSOCIATED WITH Alzheimer's disease (ortholog); Cocaine-Related Disorders (ortholog); genetic disease (ortholog); FOUND IN actin cytoskeleton (ortholog); cytoplasm (ortholog); dendrite (ortholog) NW_004955454 1379998 1383414 - 9068941;7240710 102018684 A0A8C2YRS6 MODEL AGCD01044968;GBDJ01389179;XM_005395731 XP_005395788 APPROVED protein-coding ENSCLAG00000012732 NW_004955454 1379998 1383414 - 8710071 Ces3 carboxylesterase 3 ASSOCIATED WITH adult respiratory distress syndrome (ortholog); autism spectrum disorder (ortholog); autosomal dominant dyskeratosis congenita 6 (ortholog) NW_004955484 9602861 9620025 - 9068941 102018731 A0A8C2YKM5 MODEL AGCD01058422;AGCD01058423;AGCD01058424;GBCQ01152279;XM_005403709 XP_005403766 protein-coding ENSCLAG00000003979 NW_004955484 9603912 9620102 - 8710090 Znf236 zinc finger protein 236 INVOLVED IN cellular response to glucose stimulus (ortholog); ASSOCIATED WITH Burn-McKeown syndrome (ortholog); cerebellar ataxia (ortholog); chromosome 18q deletion syndrome (ortholog) NW_004955402 60185687 60315589 + 9068941 102019005 A0A8C2VAS1;A0A8C2VDD4 MODEL AGCD01001583;AGCD01001584;AGCD01001585;AGCD01001586;AGCD01001587;GBCE01027117;XM_005373095;XM_005373097;XM_013511517;XM_013511523;XR_001232999 XP_005373152;XP_005373154;XP_013366971;XP_013366977 protein-coding ENSCLAG00000007793 NW_004955402 60185646 60315584 + 8710139 Jrk Jrk helix-turn-helix protein ENCODES a protein that exhibits mRNA binding (ortholog); INVOLVED IN positive regulation of canonical Wnt signaling pathway (ortholog); ASSOCIATED WITH childhood absence epilepsy (ortholog); Generalized Epilepsy (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog); ribonucleoprotein complex (ortholog) NW_004955454 1415811 1423705 - 9068941 102019566 A0A8C2VBX6 MODEL AGCD01044968;GBDI01323657;XM_005395734;XM_013520234;XM_013520235 XP_005395791;XP_013375688;XP_013375689 jerky homolog;jerky protein homolog APPROVED protein-coding ENSCLAG00000008108 NW_004955454 1415811 1423705 - 8710151 LOC102019985 uncharacterized LOC102019985 NW_004955409 34993912 35001323 - 102019985 MODEL AGCD01010413;GBDF01176152;XR_259802 ncrna 8710156 LOC102021679 zinc finger CCHC domain-containing protein 7-like NW_004955492 3567660 3571346 + 102021679 MODEL AGCD01060698 pseudo 8710157 Crk CRK proto-oncogene, adaptor protein ENCODES a protein that exhibits cytoskeletal protein binding (ortholog); enzyme binding (ortholog); ephrin receptor binding (ortholog); INVOLVED IN actin cytoskeleton organization (ortholog); activation of GTPase activity (ortholog); cell chemotaxis (ortholog); PARTICIPATES IN E-cadherin signaling pathway; endothelin signaling pathway; ephrin - ephrin receptor bidirectional signaling axis; ASSOCIATED WITH chromosome 17p13.3 duplication syndrome (ortholog); degenerative disc disease (ortholog); genetic disease (ortholog); FOUND IN actin cytoskeleton (ortholog); membrane (ortholog); neuromuscular junction (ortholog) NW_004955481 1705595 1748363 + 9068941 102022192 A0A8C2V0P2;A0A8C2V157 MODEL AGCD01056843;AGCD01056844;AGCD01056845;AGCD01056846;AGCD01056847;GBDI01185611;XM_005402628;XM_005402629;XM_005402630 XP_005402685;XP_005402686;XP_005402687 adapter molecule crk;v-crk avian sarcoma virus CT10 oncogene homolog APPROVED protein-coding ENSCLAG00000005975 NW_004955481 1705520 1734859 + 8710174 LOC102024440 elongation factor 1-alpha 1 pseudogene NW_004955466 13847858 13849554 + 102024440 MODEL AGCD01051188;XR_263320 APPROVED pseudo 8710178 Dlk1 delta like non-canonical Notch ligand 1 INVOLVED IN bone mineralization (ortholog); cell differentiation (ortholog); embryonic skeletal system development (ortholog); PARTICIPATES IN forkhead class A signaling pathway; Notch signaling pathway; p38 MAPK signaling pathway; ASSOCIATED WITH biliary atresia (ortholog); Experimental Autoimmune Encephalomyelitis (ortholog); Fetal Growth Retardation (ortholog); FOUND IN external side of plasma membrane (ortholog); extracellular space (ortholog) NW_004955627 37886 43730 - 9068941 102024746 A0A8C2ULN7 MODEL AGCD01077479;GBDF01049151;GBDK01224500;XM_005415026 XP_005415083 delta-like 1 homolog (Drosophila) APPROVED protein-coding ENSCLAG00000000232 NW_004955627 38128 43728 - 8710200 LOC102025187 zinc finger protein 709-like NW_004955569 27899 63427 + 102025187 MODEL AGCD01074557;AGCD01074558;GBCE01006195;XM_005413488 XP_005413545 protein-coding 8710208 LOC102025756 uncharacterized LOC102025756 NW_004955405 36781488 36788485 - 102025756 MODEL AGCD01005428;GBCQ01032855;XR_001235799 ncrna 8710213 Pcyox1l prenylcysteine oxidase 1 like ASSOCIATED WITH familial adenomatous polyposis 1 (ortholog); genetic disease (ortholog); Hereditary Neoplastic Syndromes (ortholog) NW_004955415 5052782 5059939 - 9068941 102026102 A0A8C2VIB1 MODEL AGCD01015989;GBBH01177322;GBDF01075424;XM_005380613 XP_005380670 prenylcysteine oxidase-like protein-coding ENSCLAG00000010474 NW_004955415 5052726 5059958 - 8710221 Cnga1 cyclic nucleotide gated channel subunit alpha 1 ENCODES a protein that exhibits cGMP binding (ortholog); intracellular cGMP-activated cation channel activity (ortholog); INVOLVED IN membrane depolarization (ortholog); regulation of cytosolic calcium ion concentration (ortholog); spermatogenesis (ortholog); PARTICIPATES IN altered visual phototransduction pathway; calcium transport pathway; calcium/calcium-mediated signaling pathway; ASSOCIATED WITH cone-rod dystrophy (ortholog); fundus dystrophy (ortholog); genetic disease (ortholog); FOUND IN intracellular cyclic nucleotide activated cation channel complex (ortholog); membrane (ortholog); photoreceptor outer segment (ortholog) NW_004955443 615061 649693 + 9068941;7240710 102026484 A0A8C2UR09 MODEL AGCD01038117;XM_005391887 XP_005391944 cGMP-gated cation channel alpha-1;cyclic nucleotide gated channel alpha 1 APPROVED protein-coding ENSCLAG00000001415 NW_004955443 639096 649606 + 8710234 LOC102026615 poly(rC)-binding protein 2 pseudogene NW_004955462 2702918 2704104 + 102026615 MODEL AGCD01049179;XR_263137 APPROVED pseudo 8710237 Twf2 twinfilin actin binding protein 2 ENCODES a protein that exhibits actin monomer binding (ortholog); ATP binding (ortholog); phosphatidylinositol-4,5-bisphosphate binding (ortholog); INVOLVED IN barbed-end actin filament capping (ortholog); cellular response to growth factor stimulus (ortholog); cellular response to retinoic acid (ortholog); ASSOCIATED WITH congenital disorder of glycosylation In (ortholog); COVID-19 (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); filopodium (ortholog); growth cone (ortholog) NW_004955532 3835620 3844760 - 9068941 102027109 A0A8C2YRL2 MODEL AGCD01070299;GBBH01064145;XM_013507654;XM_013507655 XP_013363108;XP_013363109 twinfilin actin-binding protein 2;twinfilin-2 APPROVED protein-coding ENSCLAG00000012465 NW_004955532 3834579 3844760 - 8710259 Prkra protein activator of interferon induced protein kinase EIF2AK2 ENCODES a protein that exhibits double-stranded RNA binding (ortholog); enzyme binding (ortholog); identical protein binding (ortholog); INVOLVED IN cellular response to oxidative stress (ortholog); ear development (ortholog); middle ear morphogenesis (ortholog); PARTICIPATES IN ceramide signaling pathway; ASSOCIATED WITH autosomal recessive nonsyndromic deafness 59 (ortholog); Congenital Microtia (ortholog); Craniofacial Abnormalities (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955403 18394609 18410381 + 9068941;7240710 102027598 A0A8C2VFW7 MODEL AGCD01002099;GBDF01113358;GBDK01432396;XM_013512630 XP_013368084 interferon-inducible double-stranded RNA-dependent protein kinase activator A APPROVED protein-coding ENSCLAG00000010338 NW_004955403 18373375 18410627 + 8710271 LOC102028300 eukaryotic translation initiation factor 1A, X-chromosomal-like NW_004955482 8142443 8144293 + 102028300 MODEL AGCD01057506 pseudo 8710272 Ifrd2 interferon related developmental regulator 2 ENCODES a protein that exhibits ribosome binding (ortholog); translation repressor activity (ortholog); INVOLVED IN negative regulation of translation (ortholog); ASSOCIATED WITH Aicardi-Goutieres Syndrome 1 (ortholog); developmental and epileptic encephalopathy (ortholog); early infantile epileptic encephalopathy (ortholog) NW_004955532 2101202 2106779 - 9068941 102028796 A0A8C2VS15 MODEL AGCD01070216;AGCD01070217;GBCB01001546;XM_005410255 XP_005410312 LOC102008888 interferon-related developmental regulator 2;skin secretory protein xP2-like PROVISIONAL protein-coding ENSCLAG00000013489 NW_004955532 2101202 2104104 - 8710288 LOC102028843 uncharacterized LOC102028843 NW_004955466 11746935 11749866 - 102028843 MODEL AGCD01051100;GBDF01160432;XR_263313 ncrna ENSCLAG00000026537 8710293 Creg2 cellular repressor of E1A stimulated genes 2 ASSOCIATED WITH genetic disease (ortholog); FOUND IN endoplasmic reticulum (ortholog); Golgi apparatus (ortholog) NW_004955470 7094483 7115792 - 9068941 102029500 MODEL AGCD01052791;GBBH01023857;GBDJ01041433;XM_013522681 XP_013378135 cellular repressor of E1A-stimulated genes 2 APPROVED protein-coding 8710300 Vti1a vesicle transport through interaction with t-SNAREs 1A ENCODES a protein that exhibits SNAP receptor activity (ortholog); INVOLVED IN autophagy (ortholog); endocytic recycling (ortholog); endoplasmic reticulum to Golgi vesicle-mediated transport (ortholog); ASSOCIATED WITH adenocarcinoma (ortholog); Colorectal Neoplasms (ortholog); genetic disease (ortholog); FOUND IN autophagosome (ortholog); clathrin-coated vesicle (ortholog); Golgi apparatus (ortholog) NW_004955431 17542605 17910809 + 9068941;7240710 102029547 A0A8C2VL11 MODEL AGCD01030409;AGCD01030410;AGCD01030411;AGCD01030412;AGCD01030413;AGCD01030414;AGCD01030415;AGCD01030416;AGCD01030417;AGCD01030418;GBDF01220882;XM_005387765;XM_005387768;XM_013515814;XM_013515815;XM_013515816;XM_013515818;XM_013515819 XP_005387822;XP_005387825;XP_013371268;XP_013371269;XP_013371270;XP_013371272;XP_013371273 vesicle transport through interaction with t-SNAREs homolog 1A protein-coding ENSCLAG00000009927 NW_004955431 17542979 17919191 + 8710322 LOC102003411 nuclease-sensitive element-binding protein 1 pseudogene NW_004955454 11898396 11903297 + 102003411 MODEL AGCD01045401;AGCD01045402;XR_262803 APPROVED pseudo 8710326 LOC102003998 uncharacterized LOC102003998 NW_004955433 12835847 12849596 + 102003998 MODEL AGCD01031671;GBDF01156740;XR_261588 ncrna 8710333 Klhl38 kelch like family member 38 ASSOCIATED WITH genetic disease (ortholog); trichorhinophalangeal syndrome type I (ortholog) NW_004955540 2443230 2452037 - 9068941 102004118 A0A8C2ULD6 MODEL AGCD01071321;GBCB01021997;XM_005410931 XP_005410988 kelch-like family member 38;kelch-like protein 38 APPROVED protein-coding ENSCLAG00000000484 NW_004955540 2443230 2452037 - 8710348 Plce1 phospholipase C epsilon 1 ENCODES a protein that exhibits enzyme binding (ortholog); phosphatidylinositol phospholipase C activity (ortholog); phospholipase C activity (ortholog); INVOLVED IN diacylglycerol biosynthetic process (ortholog); epidermal growth factor receptor signaling pathway (ortholog); G protein-coupled receptor signaling pathway (ortholog); ASSOCIATED WITH adenocarcinoma (ortholog); benign familial hematuria (ortholog); dengue hemorrhagic fever (ortholog); FOUND IN cytosol (ortholog); lamellipodium (ortholog); plasma membrane (ortholog) NW_004955507 555570 825568 + 9068941;7240710 102004404 A0A8C2V0T8 MODEL AGCD01065477;AGCD01065478;AGCD01065479;AGCD01065480;AGCD01065481;AGCD01065482;AGCD01065483;AGCD01065484;AGCD01065485;AGCD01065486;AGCD01065487;AGCD01065488;GBDK01321403;XM_005407528;XM_013506159;XM_013506160 XP_005407585;XP_013361613;XP_013361614 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase epsilon-1;phospholipase C, epsilon 1 APPROVED protein-coding ENSCLAG00000005878 NW_004955507 555499 825568 + 8710384 Fam177a1 family with sequence similarity 177 member A1 ASSOCIATED WITH genetic disease (ortholog); Myoectodermal Gonadal Dysgenesis Syndrome (ortholog); spermatogenic failure 36 (ortholog) NW_004955409 25946694 25969387 - 9068941 102004572 A0A8C2W0G4 MODEL AGCD01010143;AGCD01010144;GBDI01011683;XM_005376932 XP_005376989 family with sequence similarity 177, member A1 APPROVED protein-coding ENSCLAG00000015226 NW_004955409 25946694 25969387 - 8710393 LOC102005126 olfactory receptor 149-like NW_004955412 25061204 25062136 + 102005126 A0A8C2W7A4 MODEL AGCD01013133;XM_005378414 XP_005378471 protein-coding ENSCLAG00000018057 8710396 LOC102005447 rho-associated protein kinase 1-like NW_004955459 1724049 1732649 + 102005447 MODEL AGCD01047977 pseudo 8710397 Chrdl2 chordin like 2 INVOLVED IN chondrocyte differentiation (ortholog); negative regulation of BMP signaling pathway (ortholog); ASSOCIATED WITH 3-methylglutaconic aciduria type 7b (ortholog); genetic disease (ortholog); intellectual disability (ortholog) NW_004955414 16986199 17018166 + 9068941 102005586 A0A8C2W875 MODEL AGCD01015232;AGCD01015233;GBDJ01311671;XM_005379912;XM_005379913 XP_005379969;XP_005379970 chordin-like 2;chordin-like protein 2 APPROVED protein-coding ENSCLAG00000016930 NW_004955414 16986233 17018225 + 8710415 Ica1l islet cell autoantigen 1 like INVOLVED IN spermatid development (ortholog); ASSOCIATED WITH autoimmune lymphoproliferative syndrome type 2B (ortholog); Autoimmune Lymphoproliferative Syndrome, Type V (ortholog); common variable immunodeficiency 1 (ortholog); FOUND IN acrosomal vesicle (ortholog) NW_004955457 11983201 12085870 + 9068941 102005670 A0A8C2UY86;A0A8C2YLC5 MODEL AGCD01046997;AGCD01046998;AGCD01046999;GBDF01125399;XM_005397050;XM_005397051;XM_005397052;XM_005397053;XM_005397054 XP_005397107;XP_005397108;XP_005397109;XP_005397110;XP_005397111 islet cell autoantigen 1,69kDa-like APPROVED protein-coding ENSCLAG00000005015 NW_004955457 12006306 12085799 + 8710451 Skic2 SKI2 subunit of superkiller complex ENCODES a protein that exhibits 3'-5' RNA helicase activity (ortholog); INVOLVED IN nuclear-transcribed mRNA catabolic process, 3'-5' exonucleolytic nonsense-mediated decay (ortholog); rescue of stalled ribosome (ortholog); ASSOCIATED WITH genetic disease (ortholog); JMP syndrome (ortholog); trichohepatoenteric syndrome (ortholog); FOUND IN Ski complex (ortholog) NW_004955437 473192 482811 + 9068941;7240710 102005746 A0A8C2VDG8 MODEL AGCD01034137;GBDF01120948;XM_005389400 XP_005389457 Skiv2l SKI2 homolog, superkiller viralicidic activity 2-like;Ski2 like RNA helicase;helicase SKI2W;superkiller viralicidic activity 2-like APPROVED protein-coding ENSCLAG00000007678 NW_004955437 473192 482811 + 8710483 LOC102006745 chromosome unknown open reading frame, human C5orf24 ASSOCIATED WITH familial adenomatous polyposis 1 (ortholog); Hereditary Neoplastic Syndromes (ortholog); Neurodevelopmental Disorders (ortholog) NW_004955408 30043402 30054015 + 9068941 102006745 A0A8C2W4Y8 MODEL AGCD01008792;AGCD01008793;GBDI01171520;XM_005376466;XM_005376467;XM_005376468 XP_005376523;XP_005376524;XP_005376525 UPF0461 protein C5orf24 homolog protein-coding ENSCLAG00000017309 NW_004955408 30044031 30054015 + 8710498 LOC102007044 nucleolar GTP-binding protein 2 pseudogene NW_004955430 12703634 12705804 - 102007044 MODEL AGCD01029509 APPROVED pseudo 8710499 LOC102007232 uncharacterized LOC102007232 NW_004955484 9389101 9390143 - 102007232 MODEL AGCD01058415;GBDF01039018;XR_001231046 ncrna 8710505 LOC102008855 S-formylglutathione hydrolase pseudogene NW_004955483 8647789 8648240 - 102008855 MODEL AGCD01057841 APPROVED pseudo 8710511 Znf322 zinc finger protein 322 ENCODES a protein that exhibits cis-regulatory region sequence-specific DNA binding (ortholog); DNA-binding transcription factor activity (ortholog); INVOLVED IN positive regulation of stem cell population maintenance (ortholog); regulation of DNA-templated transcription (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN centrosome (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955483 243819 262593 + 9068941 102009841 MODEL AGCD01057604;AGCD01057605;GBBH01197926;XM_005403273 XP_005403330 protein-coding 8710522 Tfam transcription factor A, mitochondrial ENCODES a protein that exhibits chromatin binding (ortholog); heat shock protein binding (ortholog); mitochondrial promoter sequence-specific DNA binding (ortholog); INVOLVED IN mitochondrial respiratory chain complex assembly (ortholog); mitochondrial transcription (ortholog); positive regulation of DNA-templated transcription (ortholog); ASSOCIATED WITH Alzheimer's disease (ortholog); amyotrophic lateral sclerosis (ortholog); Animal Disease Models (ortholog); FOUND IN mitochondrial matrix (ortholog); mitochondrial nucleoid (ortholog); mitochondrion (ortholog) NW_004955425 12106506 12121625 + 9068941 102009855 A0A8C2VEP7 MODEL AGCD01025499;GBDF01004784;XM_005385914 XP_005385971 protein-coding ENSCLAG00000009976 NW_004955425 12106877 12120782 + 8710536 Rrp7a ribosomal RNA processing 7 homolog A INVOLVED IN blastocyst formation (ortholog); cilium disassembly (ortholog); protein localization to nucleolus (ortholog); ASSOCIATED WITH common variable immunodeficiency 4 (ortholog); Developmental Delay with Variable Intellectual Impairment and Behavioral Abnormalities (ortholog); genetic disease (ortholog); FOUND IN centrosome (ortholog); cilium (ortholog); cytoplasm (ortholog) NW_004955413 27936427 27941311 - 9068941 102011428 A0A8C2W2S9 MODEL AGCD01014538;GBCE01004837;XM_005379418 XP_005379475 ribosomal RNA-processing protein 7 homolog A APPROVED protein-coding ENSCLAG00000016715 NW_004955413 27933775 27941334 - 8710547 LOC102012427 uncharacterized LOC102012427 NW_004955479 4854411 4862694 - 102012427 MODEL AGCD01056335;AGCD01056336;GBDF01305284;XR_001230876 ncrna 8710554 Phlpp2 PH domain and leucine rich repeat protein phosphatase 2 ENCODES a protein that exhibits protein serine/threonine phosphatase activity (ortholog); INVOLVED IN hippocampus development (ortholog); protein dephosphorylation (ortholog); PARTICIPATES IN phosphatidylinositol 3-kinase-Akt signaling pathway; protein kinase C (PKC) signaling pathway; ASSOCIATED WITH autosomal dominant dyskeratosis congenita 6 (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); intercellular bridge (ortholog) NW_004955484 4353950 4419891 - 9068941 102012539 A0A8C2USU5 MODEL AGCD01058210;AGCD01058211;AGCD01058212;GBCE01149912;GBDF01195815;XM_013503948 XP_013359402 PH domain leucine-rich repeat-containing protein phosphatase 2 protein-coding ENSCLAG00000003562 NW_004955484 4353950 4420873 - 8710588 Sez6l seizure related 6 homolog like INVOLVED IN adult locomotory behavior (ortholog); cerebellar Purkinje cell layer development (ortholog); regulation of protein kinase C signaling (ortholog); ASSOCIATED WITH cataract 23 (ortholog); genetic disease (ortholog); prostate cancer (ortholog); FOUND IN endoplasmic reticulum (ortholog); neuronal cell body (ortholog) NW_004955455 816129 992776 + 9068941 102013250 A0A8C2VDJ1;A0A8C2VDL2;A0A8C2YPM0 MODEL AGCD01045565;AGCD01045566;AGCD01045567;GBDF01112713;XM_005396140;XM_013520286 XP_005396197;XP_013375740 seizure related 6 homolog (mouse)-like APPROVED protein-coding ENSCLAG00000009675 NW_004955455 927521 989502 + 8710613 Lrrc59 leucine rich repeat containing 59 ASSOCIATED WITH genetic disease (ortholog); glioblastoma (ortholog); hepatocellular carcinoma (ortholog); FOUND IN endoplasmic reticulum (ortholog); mitochondrial nucleoid (ortholog) NW_004955451 11316139 11328107 + 9068941 102013896 A0A8C2VR38 MODEL AGCD01043349;GBDF01007688;XM_005394173 XP_005394230 leucine-rich repeat-containing protein 59 protein-coding ENSCLAG00000012618 NW_004955451 11315725 11332394 + 8710624 Ttc19 tetratricopeptide repeat domain 19 INVOLVED IN mitochondrial respiratory chain complex III assembly (ortholog); ASSOCIATED WITH genetic disease (ortholog); infertility (ortholog); mitochondrial complex III deficiency nuclear type 1 (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrion (ortholog) NW_004955467 1381105 1405509 + 9068941;7240710 102014124 A0A8C2YMK4;A0A8C2YMK9 MODEL AGCD01051262;AGCD01051263;AGCD01051264;GBCE01045510;GBCQ01125396;XM_005399316 XP_005399373 tetratricopeptide repeat protein 19, mitochondrial protein-coding ENSCLAG00000006736 NW_004955467 1381625 1405014 + 8710654 LOC102015000 chromatin modification-related protein eaf-1-like NW_004955413 33532336 33534770 + 102015000 MODEL AGCD01014676;AGCD01014677;GBDK01189129;XM_013511308 XP_013366762 APPROVED protein-coding 8710659 Cnnm1 cyclin and CBS domain divalent metal cation transport mediator 1 ASSOCIATED WITH breast ductal carcinoma (ortholog); genetic disease (ortholog); melanoma (ortholog); FOUND IN dendrite (ortholog); neuronal cell body (ortholog); plasma membrane (ortholog) NW_004955507 5283948 5342860 + 9068941 102015134 A0A8C2UMM9;A0A8C2UT82 MODEL AGCD01065668;AGCD01065669;AGCD01065670;GBDF01172174;XM_005407668;XM_005407669 XP_005407725;XP_005407726 cyclin M1;metal transporter CNNM1 APPROVED protein-coding ENSCLAG00000002026 NW_004955507 5283460 5345219 + 8710676 Cisd2 CDGSH iron sulfur domain 2 ENCODES a protein that exhibits 2 iron, 2 sulfur cluster binding (ortholog); protein homodimerization activity (ortholog); INVOLVED IN autophagy of mitochondrion (ortholog); regulation of autophagy (ortholog); ASSOCIATED WITH beta-mannosidosis (ortholog); genetic disease (ortholog); type 2 diabetes mellitus (ortholog); FOUND IN endoplasmic reticulum (ortholog); endoplasmic reticulum membrane (ortholog); mitochondrial outer membrane (ortholog) NW_004955496 5656686 5672888 - 9068941;7240710 102015646 A0A8C2UM95 MODEL AGCD01062355;AGCD01062356;GBCE01053957;XM_005406245 XP_005406302 CDGSH iron-sulfur domain-containing protein 2 protein-coding ENSCLAG00000001906 NW_004955496 5656686 5673529 - 8710683 LOC102016894 retinol dehydrogenase 16-like NW_004955458 4576846 4594189 - 102016894 MODEL AGCD01047419;AGCD01047420;AGCD01047421;AGCD01047422;GBCQ01014167;XM_013520791 XP_013376245 protein-coding 8710684 Fermt1 FERM domain containing kindlin 1 ENCODES a protein that exhibits actin filament binding (ortholog); INVOLVED IN basement membrane organization (ortholog); cell adhesion (ortholog); establishment of epithelial cell polarity (ortholog); PARTICIPATES IN integrin mediated signaling pathway; ASSOCIATED WITH Atrophy (ortholog); Erythema (ortholog); genetic disease (ortholog); FOUND IN cell junction (ortholog); cell periphery (ortholog); cytoplasm (ortholog) NW_004955415 16447921 16483221 - 9068941 102017978 A0A8C2VT56 MODEL AGCD01016382;AGCD01016383;AGCD01016384;AGCD01016385;AGCD01016386;AGCD01016387;GBBH01008568;GBDK01181773;XM_013512377 XP_013367831 fermitin family homolog 1;fermitin family member 1 APPROVED protein-coding ENSCLAG00000012675 NW_004955415 16446934 16483369 - 8710706 LOC102018352 PEST proteolytic signal-containing nuclear protein pseudogene NW_004955597 71046 72218 - 102018352 MODEL AGCD01076536;XR_265145 APPROVED pseudo 8710709 LOC102019841 melanoma-associated antigen B3-like NW_004955531 802330 814697 - 102019841 MODEL AGCD01070013;GBDF01304372;XM_005410137;XM_005410138;XM_013507560 XP_005410194;XP_005410195;XP_013363014 protein-coding 8710719 Fndc7 fibronectin type III domain containing 7 ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); hereditary spastic paraplegia 63 (ortholog) NW_004955435 12185187 12213242 + 9068941 102020045 A0A8C2V314 MODEL AGCD01033135;AGCD01033136;XM_005388833 XP_005388890 fibronectin type III domain-containing protein 7 protein-coding ENSCLAG00000006340 NW_004955435 12185187 12208334 + 8710741 LOC102020972 uncharacterized LOC102020972 NW_004955403 32363451 32367762 - 102020972 MODEL AGCD01002433;GBDK01040815;XR_259218 ncrna 8710746 LOC102021642 serpin B9-like NW_004955465 10392685 10403396 - 102021642 MODEL AGCD01050508;XM_005398915 XP_005398972 protein-coding 8710758 LOC102023385 olfactory receptor 4A47-like NW_004955511 106509 107426 - 102023385 A0A8C2W896 MODEL AGCD01066320;XM_005407936 XP_005407993 APPROVED protein-coding ENSCLAG00000017601 8710761 LOC102023675 uncharacterized LOC102023675 NW_004955465 5504102 5599648 - 102023675 MODEL AGCD01050430;AGCD01050431;GBDF01277920;XR_263237 ncrna 8710766 LOC102023912 uncharacterized LOC102023912 NW_004955482 5728073 5735532 - 102023912 MODEL AGCD01057346;GBDF01111631;XM_005403059;XR_001230978;XR_001230979 XP_005403116 uncharacterized protein LOC102023912 protein-coding 8710773 LOC102024077 olfactory receptor-like protein OLF4 NW_004955626 120729 121640 + 102024077 MODEL AGCD01077468 APPROVED pseudo 8710774 Asb13 ankyrin repeat and SOCS box containing 13 ASSOCIATED WITH genetic disease (ortholog); hypoparathyroidism-deafness-renal disease syndrome (ortholog); schizophrenia (ortholog) NW_004955421 22328393 22380656 - 9068941 102024917 A0A8C2V6X7 MODEL AGCD01022132;AGCD01022133;AGCD01022134;GBDF01088974;XM_005383841;XM_013513669 XP_005383898;XP_013369123 LOC102024689 ankyrin repeat and SOCS box protein 13;uncharacterized LOC102024689 PROVISIONAL protein-coding ENSCLAG00000006056 NW_004955421 22327523 22349641 - 8710784 Itm2a integral membrane protein 2A INVOLVED IN plasma cell differentiation (ortholog); ASSOCIATED WITH autistic disorder (ortholog); COVID-19 (ortholog); genetic disease (ortholog) NW_004955557 2235223 2243911 - 9068941 102025950 A0A8C2UHR3;A0A8C2UKF9 MODEL AGCD01073326;AGCD01073327;GBCQ01150407;XM_005412649;XM_013508828;XM_013508829;XM_013508830;XM_013508831 XP_005412706;XP_013364282;XP_013364283;XP_013364284;XP_013364285 protein-coding ENSCLAG00000000574 NW_004955557 2235223 2243927 - 8710803 Fam83a family with sequence similarity 83 member A ENCODES a protein that exhibits identical protein binding (ortholog); phosphatidylinositol 3-kinase regulatory subunit binding (ortholog); protein kinase binding (ortholog); INVOLVED IN cell population proliferation (ortholog); epidermal growth factor receptor signaling pathway (ortholog); ASSOCIATED WITH Disease Progression (ortholog); genetic disease (ortholog); Neoplasm Invasiveness (ortholog) NW_004955540 2070396 2095341 + 9068941 102028131 A0A8C2UH00 MODEL AGCD01071312;GBDK01170278;XM_005410920;XM_005410921 XP_005410977;XP_005410978 family with sequence similarity 83, member A APPROVED protein-coding ENSCLAG00000000631 NW_004955540 2070396 2089665 + 8710812 Hspbp1 HSPA (Hsp70) binding protein 1 ENCODES a protein that exhibits molecular function inhibitor activity (ortholog); molecular sequestering activity (ortholog); ubiquitin protein ligase binding (ortholog); INVOLVED IN positive regulation of proteasomal ubiquitin-dependent protein catabolic process (ortholog); positive regulation of protein ubiquitination (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN extracellular space (ortholog) NW_004955567 948040 960621 + 9068941 102028243 A0A8C2UHJ8;A0A8C2UML7 MODEL AGCD01074448;AGCD01074449;GBDF01051098;XM_005413338;XM_005413345;XM_013509270 XP_005413395;XP_005413402;XP_013364724 HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1;hsp70-binding protein 1 APPROVED protein-coding ENSCLAG00000000510 NW_004955567 947798 960678 + 8710847 LOC102028388 zinc finger protein 263 pseudogene NW_004955461 1215351 1218656 + 102028388 MODEL AGCD01048804 APPROVED pseudo 8710848 C4bpa complement component 4 binding protein alpha INVOLVED IN binding of sperm to zona pellucida (ortholog); negative regulation of complement activation, classical pathway (ortholog); positive regulation of protein catabolic process (ortholog); ASSOCIATED WITH autistic disorder (ortholog); common variable immunodeficiency 7 (ortholog); COVID-19 (ortholog); FOUND IN acrosomal matrix (ortholog); acrosomal vesicle (ortholog); cell body (ortholog) NW_004955406 42613659 42641918 + 9068941 102028495 A0A8C2W798 MODEL AGCD01006712;AGCD01006713;GBDI01193239;XM_005375423;XM_013502872;XM_013502874 XP_005375480;XP_013358326;XP_013358328 C4b-binding protein alpha chain;complement component 4 binding protein, alpha APPROVED protein-coding ENSCLAG00000016607 NW_004955406 42613607 42641670 + 8710866 Ddx20 DEAD-box helicase 20 ENCODES a protein that exhibits DNA-binding transcription factor binding (ortholog); histone deacetylase binding (ortholog); protein domain specific binding (ortholog); INVOLVED IN negative regulation of cell population proliferation (ortholog); negative regulation of DNA-templated transcription (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH amyotrophic lateral sclerosis (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); nuclear body (ortholog); nucleoplasm (ortholog) NW_004955435 15209640 15219698 + 9068941 102028792 A0A8C2YP29 MODEL AGCD01033264;GBDF01003762;XM_005388953 XP_005389010 DEAD (Asp-Glu-Ala-Asp) box polypeptide 20;probable ATP-dependent RNA helicase DDX20 APPROVED protein-coding ENSCLAG00000008874 NW_004955435 15209640 15220378 + 8710882 Tpm1 tropomyosin 1 ENCODES a protein that exhibits actin binding (ortholog); actin filament binding (ortholog); cytoskeletal protein binding (ortholog); INVOLVED IN actin filament capping (ortholog); cardiac muscle contraction (ortholog); cellular response to reactive oxygen species (ortholog); PARTICIPATES IN acebutolol pharmacodynamics pathway; adrenergic beta receptor agonist and beta-blocker pharmacodynamics pathway; amiodarone pharmacodynamics pathway; ASSOCIATED WITH atrial heart septal defect 1 (ortholog); Bloom syndrome (ortholog); cardiomyopathy (ortholog); FOUND IN actin cytoskeleton (ortholog); bleb (ortholog); cytoplasm (ortholog) NW_004955450 12197241 12223372 - 9068941;7240710 102029136 A0A8C2VB15;A0A8C2VB18;A0A8C2VB21;A0A8C2VGB5;A0A8C2YP40;A0A8C2YP41 MODEL AGCD01042694;AGCD01042695;GBDI01010272;XM_005393795;XM_005393797;XM_005393799;XM_005393800;XM_005393801;XM_013518944;XM_013518945 XP_005393852;XP_005393854;XP_005393856;XP_005393857;XP_005393858;XP_013374398;XP_013374399 tropomyosin 1 (alpha);tropomyosin alpha-1 chain APPROVED protein-coding ENSCLAG00000008921 NW_004955450 12194755 12224011 - 8710924 Schip1 schwannomin interacting protein 1 ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN estrogen metabolic process (ortholog); face morphogenesis (ortholog); female gonad development (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cell junction (ortholog); cytosol (ortholog); nuclear body (ortholog) NW_004955448 10364261 10502799 + 9068941 102029245 A0A8C2URP4;A0A8C2UTG4;A0A8C2UUN7;A0A8C2UX25;A0A8C2UXC3 MODEL AGCD01041490;AGCD01041491;AGCD01041492;AGCD01041493;GBDK01070603;XM_005393115;XM_005393116;XM_005393117 XP_005393172;XP_005393173;XP_005393174 schwannomin-interacting protein 1 protein-coding ENSCLAG00000003229 NW_004955448 9980467 10504308 + 8710956 LOC102029510 39S ribosomal protein L33, mitochondrial-like NW_004955478 10474275 10474974 + 102029510 MODEL AGCD01056134 pseudo 8710965 Spata2 spermatogenesis associated 2 ENCODES a protein that exhibits protein-containing complex binding (ortholog); signaling receptor complex adaptor activity (ortholog); ubiquitin-specific protease binding (ortholog); INVOLVED IN necroptotic process (ortholog); protein K63-linked deubiquitination (ortholog); protein linear deubiquitination (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); fibrillar center (ortholog); nucleoplasm (ortholog) NW_004955445 8281280 8292951 + 9068941 102003595 A0A8C2W7Q5;A0A8C2W9P7 MODEL AGCD01039573;AGCD01039574;GBCB01074585;GBDF01180673;XM_013518262 XP_013373716 spermatogenesis-associated protein 2 protein-coding ENSCLAG00000017362 NW_004955445 8281545 8292951 + 8710978 Myo15a myosin XVA INVOLVED IN inner ear morphogenesis (ortholog); locomotory behavior (ortholog); response to light stimulus (ortholog); PARTICIPATES IN auditory mechanotransduction pathway; ASSOCIATED WITH Alport syndrome (ortholog); autistic disorder (ortholog); autosomal recessive nonsyndromic deafness (ortholog); FOUND IN stereocilium (ortholog); stereocilium bundle (ortholog) NW_004955478 11131908 11186465 - 9068941;7240710 102004068 A0A8C2YKT1;A0A8C2YKT7 MODEL AGCD01056161;AGCD01056162;GBBH01115108;XM_013503134 XP_013358588 unconventional myosin-XV protein-coding ENSCLAG00000004240 NW_004955478 11132719 11186378 - 8711048 Tollip toll interacting protein ENCODES a protein that exhibits interleukin-1, type I receptor binding (ortholog); kinase binding (ortholog); molecular adaptor activity (ortholog); INVOLVED IN epithelial cell differentiation (ortholog); interleukin-1-mediated signaling pathway (ortholog); phosphorylation (ortholog); PARTICIPATES IN interleukin-1 signaling pathway; ASSOCIATED WITH chronic obstructive pulmonary disease (ortholog); delta beta-thalassemia (ortholog); developmental and epileptic encephalopathy (ortholog); FOUND IN nuclear body (ortholog); perinuclear region of cytoplasm (ortholog); protein-containing complex (ortholog) NW_004955476 10987223 11009134 + 9068941 102004475 A0A8C2UMN2;A0A8C2UQS4 MODEL AGCD01055434;AGCD01055435;GBDF01003680;XM_005401793 XP_005401850 protein-coding ENSCLAG00000001459 NW_004955476 10987223 11010808 + 8711058 LOC102007057 uncharacterized LOC102007057 NW_004955439 18083547 18090067 + 102007057 MODEL AGCD01036049;GBDK01269094;XR_001235223;XR_001235224 ncrna 8711063 Slc4a1ap solute carrier family 4 member 1 adaptor protein ASSOCIATED WITH genetic disease (ortholog); Tatton-Brown-Rahman syndrome (ortholog); FOUND IN intracellular membrane-bounded organelle (ortholog); nucleoplasm (ortholog); plasma membrane (ortholog) NW_004955469 9617238 9654972 + 9068941 102007215 A0A8C2VIK7 MODEL AGCD01052510;AGCD01052511;GBDF01089096;XM_005400510;XM_005400511 XP_005400567;XP_005400568 kanadaptin APPROVED protein-coding ENSCLAG00000009564 NW_004955469 9617269 9654458 + 8711088 LOC102009319 HLA class II histocompatibility antigen, DRB1-1 beta chain-like NW_004955437 1228243 1262090 - 102009319 MODEL AGCD01034197;AGCD01034198;GBDK01061271;XM_013517040;XM_013517041 XP_013372494;XP_013372495 protein-coding 8711089 Angpt2 angiopoietin 2 ENCODES a protein that exhibits receptor tyrosine kinase binding (ortholog); INVOLVED IN angiogenesis (ortholog); animal organ regeneration (ortholog); blood vessel morphogenesis (ortholog); ASSOCIATED WITH adenocarcinoma (ortholog); Alcoholic Liver Diseases (ortholog); angiosarcoma (ortholog); FOUND IN cell projection (ortholog); extracellular space (ortholog) NW_004955403 54139823 54193740 + 9068941 102009568 A0A8C2YSE1 MODEL AGCD01003089;GBCQ01175373;XM_005373846 XP_005373903 angiopoietin-2 protein-coding ENSCLAG00000013588 NW_004955403 54139823 54195032 + 8711111 CUNH6orf201 chromosome unknown C6orf201 homolog ASSOCIATED WITH genetic disease (ortholog) NW_004955465 9303368 9339691 - 102011518 A0A8C2UUH5 MODEL AGCD01050489;AGCD01050490;GBDF01006952;XM_005398888 XP_005398945 LOC102011518 chromosome unknown open reading frame, human C6orf201;uncharacterized protein C6orf201 homolog APPROVED protein-coding ENSCLAG00000003863 8711121 Aste1 asteroid homolog 1 ASSOCIATED WITH alkaptonuria (ortholog); genetic disease (ortholog); Lynch syndrome (ortholog) NW_004955501 7373713 7383092 + 9068941 102011561 MODEL AGCD01064214;GBDF01225117;XM_013505735;XR_001231517;XR_001231518 XP_013361189 asteroid homolog 1 (Drosophila) APPROVED protein-coding 8711142 Nek9 NIMA related kinase 9 ENCODES a protein that exhibits protein kinase activator activity (ortholog); protein kinase binding (ortholog); protein serine/threonine kinase activity (ortholog); INVOLVED IN mitotic cell cycle (ortholog); regulation of mitotic cell cycle (ortholog); ASSOCIATED WITH ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY (ortholog); cleft palate (ortholog); genetic disease (ortholog); FOUND IN centrosome (ortholog) NW_004955523 443832 483397 + 9068941 102011901 A0A8C2UPS5 MODEL AGCD01068457;AGCD01068458;GBDF01189505;GBDJ01229358;XM_013507146 XP_013362600 NIMA-related kinase 9;serine/threonine-protein kinase Nek9 APPROVED protein-coding ENSCLAG00000002894 NW_004955523 446748 482246 + 8711176 LOC102012100 target of rapamycin complex 2 subunit MAPKAP1-like NW_004955421 30163102 30165459 + 102012100 MODEL AGCD01022382 pseudo 8711177 LOC102012383 zinc finger protein 132-like NW_004955584 1075427 1081804 - 102012383 MODEL AGCD01075978;XR_265112;XR_265113 APPROVED pseudo 8711184 Hectd1 HECT domain E3 ubiquitin protein ligase 1 ENCODES a protein that exhibits ubiquitin protein ligase activity (ortholog); INVOLVED IN aorta development (ortholog); embryonic placenta development (ortholog); heart valve development (ortholog); ASSOCIATED WITH Brain-Lung-Thyroid Syndrome (ortholog); genetic disease (ortholog); mitochondrial complex I deficiency (ortholog) NW_004955409 29373572 29470623 + 9068941 102012510 A0A8C2VMI6 MODEL AGCD01010267;GBDJ01141199;XM_005376961 XP_005377018 E3 ubiquitin-protein ligase HECTD1;HECT domain containing E3 ubiquitin protein ligase 1 APPROVED protein-coding ENSCLAG00000011096 NW_004955409 29373572 29470623 + 8711236 Tulp1 TUB like protein 1 ENCODES a protein that exhibits actin filament binding (ortholog); phosphatidylinositol-4,5-bisphosphate binding (ortholog); INVOLVED IN dendrite development (ortholog); detection of light stimulus involved in visual perception (ortholog); eye photoreceptor cell development (ortholog); PARTICIPATES IN retinitis pigmentosa pathway; ASSOCIATED WITH brachydactyly (ortholog); Eye Abnormalities (ortholog); fundus dystrophy (ortholog); FOUND IN axon terminus (ortholog); cell projection (ortholog); cytosol (ortholog) NW_004955437 3405218 3417079 - 9068941;7240710 102012897 MODEL AGCD01034311;AGCD01034312;GBDF01075341;XM_013516916 XP_013372370 tubby like protein 1;tubby-related protein 1 APPROVED protein-coding 8711253 LOC102014055 40S ribosomal protein S29 pseudogene NW_004955421 41674 43155 + 102014055 MODEL AGCD01021542 APPROVED pseudo 8711254 St7 suppression of tumorigenicity 7 ASSOCIATED WITH Developmental Disabilities (ortholog); genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog) NW_004955432 22665745 22937163 + 9068941 102014077 A0A8C2V1X5;A0A8C2V295;A0A8C2V2L4;A0A8C2V814;A0A8C2YM66;A0A8C2YM71 MODEL AGCD01031264;AGCD01031265;AGCD01031266;AGCD01031267;AGCD01031268;AGCD01031269;GBCB01040963;XM_005388126;XM_013515981;XM_013515983;XM_013515984;XM_013515985;XM_013515986;XM_013515987;XM_013515988 XP_005388183;XP_013371435;XP_013371437;XP_013371438;XP_013371439;XP_013371440;XP_013371441;XP_013371442 protein-coding ENSCLAG00000006207 NW_004955432 22665284 22937873 + 8711299 Ubl4b ubiquitin like 4B INVOLVED IN positive regulation of protein targeting to mitochondrion (ortholog); ASSOCIATED WITH autistic disorder (ortholog); developmental and epileptic encephalopathy 32 (ortholog); genetic disease (ortholog) NW_004955435 13637910 13638635 + 9068941 102015561 MODEL AGCD01033207;GBDF01008282;XM_005388912 XP_005388969 ubiquitin-like 4B;ubiquitin-like protein 4B APPROVED protein-coding 8711305 Ryr1 ryanodine receptor 1 ENCODES a protein that exhibits calcium channel activity (ortholog); calcium-induced calcium release activity (ortholog); enzyme binding (ortholog); INVOLVED IN calcium ion transport (ortholog); cellular response to ATP (ortholog); cellular response to caffeine (ortholog); PARTICIPATES IN calcium transport pathway; calcium/calcium-mediated signaling pathway; ASSOCIATED WITH ankyloglossia (ortholog); Aortic Coarctation (ortholog); arthrogryposis multiplex congenita (ortholog); FOUND IN cell cortex (ortholog); cytoplasm (ortholog); extrinsic component of cytoplasmic side of plasma membrane (ortholog) NW_004955468 879807 1000118 - 9068941;7240710 102016148 A0A8C2W4T9;A0A8C2W5I7;A0A8C2YUY0;A0A8C2YUY5 MODEL AGCD01051742;AGCD01051743;AGCD01051744;AGCD01051745;AGCD01051746;AGCD01051747;AGCD01051748;GBCB01005975;GBDI01002716;XM_013522408 XP_013377862 ryanodine receptor 1 (skeletal) APPROVED protein-coding ENSCLAG00000017292 NW_004955468 879951 1000036 - 8711416 Ppp1r10 protein phosphatase 1 regulatory subunit 10 ENCODES a protein that exhibits protein phosphatase 1 binding (ortholog); protein phosphatase inhibitor activity (ortholog); INVOLVED IN negative regulation of cardiac muscle cell apoptotic process (ortholog); negative regulation of mitotic DNA damage checkpoint (ortholog); positive regulation of telomere maintenance (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); megacolon (ortholog); FOUND IN chromatin (ortholog); chromosome, telomeric region (ortholog); nuclear body (ortholog) NW_004955583 621380 635595 - 9068941 102016764 A0A8C2UN18;A0A8C2UN21 MODEL AGCD01075842;AGCD01075843;GBBH01092539;XM_005414310;XM_005414312;XM_005414313;XM_013509798 XP_005414367;XP_005414369;XP_005414370;XP_013365252 serine/threonine-protein phosphatase 1 regulatory subunit 10 APPROVED protein-coding ENSCLAG00000002371 NW_004955583 621092 634929 - 8711447 Rab1b RAB1B, member RAS oncogene family ENCODES a protein that exhibits GTP binding (ortholog); INVOLVED IN endoplasmic reticulum to Golgi vesicle-mediated transport (ortholog); establishment of endothelial intestinal barrier (ortholog); Golgi organization (ortholog); ASSOCIATED WITH Aicardi-Goutieres Syndrome 3 (ortholog); autosomal recessive cutis laxa type IB (ortholog); Bardet-Biedl syndrome (ortholog); FOUND IN endoplasmic reticulum-Golgi intermediate compartment (ortholog); Golgi apparatus (ortholog); phagophore assembly site membrane (ortholog) NW_004955422 19039741 19047088 - 9068941 102017133 A0A8C2YTW4 MODEL AGCD01022973;GBDJ01003487;XM_005384425 XP_005384482 ras-related protein Rab-1B protein-coding ENSCLAG00000015776 NW_004955422 19039632 19047088 - 8711463 LOC102017351 olfactory receptor 7D4-like NW_004955495 294354 343997 + 102017351 A0A8C2VWE7;A0A8C2W1H0 MODEL AGCD01061618;AGCD01061619;AGCD01061620;AGCD01061621;AGCD01061622;AGCD01061623;AGCD01061624;XM_005405554 XP_005405611 protein-coding ENSCLAG00000014801 8711469 Adgrb1 adhesion G protein-coupled receptor B1 ENCODES a protein that exhibits G protein-coupled receptor activity (ortholog); lipopolysaccharide binding (ortholog); PDZ domain binding (ortholog); INVOLVED IN apoptotic cell clearance (ortholog); defense response to Gram-negative bacterium (ortholog); engulfment of apoptotic cell (ortholog); ASSOCIATED WITH colorectal cancer (ortholog); genetic disease (ortholog); glioblastoma (ortholog); FOUND IN dendrite (ortholog); extracellular space (ortholog); focal adhesion (ortholog) NW_004955454 1250261 1313547 + 9068941 102017627 A0A8C2VU12;A0A8C2VWS0 MODEL AGCD01044967;AGCD01044968;GBBH01028741;XM_013520249 XP_013375703 Bai1 brain-specific angiogenesis inhibitor 1 APPROVED protein-coding ENSCLAG00000013421 NW_004955454 1237363 1314127 + 8711509 Syn2 synapsin II ENCODES a protein that exhibits calcium-dependent protein binding (ortholog); identical protein binding (ortholog); INVOLVED IN calcium-ion regulated exocytosis (ortholog); neurotransmitter secretion (ortholog); synaptic vesicle clustering (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); COVID-19 (ortholog); epilepsy (ortholog); FOUND IN extrinsic component of synaptic vesicle membrane (ortholog); glutamatergic synapse (ortholog); plasma membrane (ortholog) NW_004955429 14676286 14724625 + 9068941;7240710 102017687 A0A8C2UYN6 MODEL AGCD01028784;GBDF01094658;XM_013515353 XP_013370807 synapsin-2 protein-coding ENSCLAG00000005221 8711525 Kcnab1 potassium voltage-gated channel subfamily A regulatory beta subunit 1 ENCODES a protein that exhibits aldo-keto reductase (NADP) activity (ortholog); molecular function inhibitor activity (ortholog); NADPH binding (ortholog); INVOLVED IN diaphragm development (ortholog); heart development (ortholog); learning or memory (ortholog); ASSOCIATED WITH genetic disease (ortholog); hypertension (ortholog); Hypoxia (ortholog); FOUND IN axon (ortholog); cytosol (ortholog); dendrite cytoplasm (ortholog) NW_004955448 7145471 7553090 + 9068941 102018545 A0A8C2VUB2 MODEL AGCD01041401;AGCD01041402;AGCD01041403;AGCD01041404;AGCD01041405;AGCD01041406;AGCD01041407;AGCD01041408;AGCD01041409;AGCD01041410;AGCD01041411;AGCD01041412;AGCD01041413;AGCD01041414;GBDI01387048;XM_005393077;XM_005393078 XP_005393134;XP_005393135 potassium channel, voltage gated subfamily A regulatory beta subunit 1;potassium voltage-gated channel subfamily A member regulatory beta subunit 1;potassium voltage-gated channel, shaker-related subfamily, beta member 1;voltage-gated potassium channel subunit beta-1 APPROVED protein-coding ENSCLAG00000012692 NW_004955448 7309717 7551432 + 8711549 Izumo1r IZUMO1 receptor, JUNO ENCODES a protein that exhibits folic acid binding (ortholog); signaling receptor activity (ortholog); signaling receptor binding (ortholog); INVOLVED IN cell adhesion (ortholog); fusion of sperm to egg plasma membrane involved in single fertilization (ortholog); single fertilization (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog) NW_004955414 283646 287422 - 9068941 102018589 A0A8C2W4F0 MODEL AGCD01014715;GBDI01316974;XM_005379681;XM_013511756;XM_013511758 XP_005379738;XP_013367210;XP_013367212 Folr4 folate receptor 4, delta (putative);sperm-egg fusion protein Juno APPROVED protein-coding ENSCLAG00000015110 NW_004955414 283630 287433 - 8711559 LOC102018904 uncharacterized LOC102018904 NW_004955411 12608628 12618065 + 102018904 MODEL AGCD01011851;GBDF01241604;XR_259934 ncrna 8711564 Aco2 aconitase 2 ENCODES a protein that exhibits 3 iron, 4 sulfur cluster binding (ortholog); 4 iron, 4 sulfur cluster binding (ortholog); aconitate hydratase activity (ortholog); INVOLVED IN citrate metabolic process (ortholog); isocitrate metabolic process (ortholog); liver development (ortholog); PARTICIPATES IN citric acid cycle pathway; fumaric aciduria pathway; mitochondrial complex II deficiency pathway; ASSOCIATED WITH adenylosuccinase lyase deficiency (ortholog); adult respiratory distress syndrome (ortholog); common variable immunodeficiency 4 (ortholog); FOUND IN mitochondrial matrix (ortholog); mitochondrion (ortholog) NW_004955413 27027341 27065227 + 9068941;7240710 102019378 A0A8C2W4H0 MODEL AGCD01014491;GBDF01000245;XM_005379352 XP_005379409 aconitase 2, mitochondrial;aconitate hydratase, mitochondrial APPROVED protein-coding ENSCLAG00000016998 NW_004955413 27027341 27065227 + 8711586 Mindy1 MINDY lysine 48 deubiquitinase 1 ENCODES a protein that exhibits cysteine-type carboxypeptidase activity (ortholog); K48-linked deubiquitinase activity (ortholog); K48-linked polyubiquitin modification-dependent protein binding (ortholog); ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); immunodeficiency 42 (ortholog); FOUND IN nuclear body (ortholog); nucleoplasm (ortholog) NW_004955588 371325 382167 - 9068941 102019453 A0A8C2UJ25 MODEL AGCD01076108;GBCQ01086431;XM_005414472;XM_005414473;XM_005414474;XM_005414477;XM_005414478;XM_013509912;XM_013509913 XP_005414529;XP_005414530;XP_005414531;XP_005414534;XP_005414535;XP_013365366;XP_013365367 Fam63a family with sequence similarity 63 member A;family with sequence similarity 63, member A APPROVED protein-coding ENSCLAG00000000123 NW_004955588 371739 377004 - 8711622 LOC102020690 L-lactate dehydrogenase A chain pseudogene NW_004955428 23400275 23400773 - 102020690 MODEL AGCD01028222 APPROVED pseudo 8711623 Apoa5 apolipoprotein A5 ENCODES a protein that exhibits enzyme activator activity (ortholog); enzyme binding (ortholog); heparin binding (ortholog); INVOLVED IN acylglycerol homeostasis (ortholog); animal organ regeneration (ortholog); cholesterol homeostasis (ortholog); PARTICIPATES IN lipoprotein metabolic pathway; ASSOCIATED WITH cerebral infarction (ortholog); Chromosome 11, Partial Trisomy 11q (ortholog); coronary artery disease (ortholog); FOUND IN chylomicron (ortholog); extracellular region (ortholog); extracellular space (ortholog) NW_004955412 18128861 18131752 - 9068941;7240710 102021108 A0A8C2VUE4 MODEL AGCD01012926;XM_005378185;XM_005378186;XM_013511206 XP_005378242;XP_005378243;XP_013366660 apolipoprotein A-V APPROVED protein-coding ENSCLAG00000013015 NW_004955412 18129603 18131115 - 8711635 LOC102021193 C-terminal-binding protein 2 pseudogene NW_004955450 17232209 17233685 + 102021193 MODEL AGCD01042865 APPROVED pseudo 8711636 Tcte1 t-complex-associated-testis-expressed 1 INVOLVED IN flagellated sperm motility (ortholog); ASSOCIATED WITH genetic disease (ortholog); male infertility (ortholog); FOUND IN sperm flagellum (ortholog) NW_004955437 9900295 9913955 - 102021594 A0A8C2VXL4 MODEL AGCD01034549;GBDF01120599;XM_005389817 XP_005389874 T-complex-associated testis-expressed protein 1 protein-coding ENSCLAG00000013096 NW_004955437 9900301 9908379 - 8711659 Exoc6b exocyst complex component 6B ASSOCIATED WITH congenital disorder of glycosylation type IIb (ortholog); dystonia (ortholog); genetic disease (ortholog) NW_004955424 12777638 13308358 + 9068941 102021892 A0A8C2VTX6;A0A8C2VTX9 MODEL AGCD01024619;AGCD01024620;AGCD01024621;AGCD01024622;AGCD01024623;AGCD01024624;AGCD01024625;AGCD01024626;AGCD01024627;AGCD01024628;AGCD01024629;AGCD01024630;GBDF01252038;XM_005385581;XM_005385582;XM_005385583;XM_013514675;XM_013514676;XM_013514677 XP_005385638;XP_005385639;XP_005385640;XP_013370129;XP_013370130;XP_013370131 protein-coding ENSCLAG00000014097 NW_004955424 12777595 13305056 + 8711688 Tbx6 T-box transcription factor 6 ENCODES a protein that exhibits RNA polymerase II cis-regulatory region sequence-specific DNA binding (ortholog); RNA polymerase II-specific DNA-binding transcription factor binding (ortholog); sequence-specific double-stranded DNA binding (ortholog); INVOLVED IN mesoderm formation (ortholog); mesodermal cell fate specification (ortholog); negative regulation of DNA-binding transcription factor activity (ortholog); ASSOCIATED WITH 16p11.2 Deletion Syndrome (ortholog); atrial heart septal defect (ortholog); autism spectrum disorder (ortholog); FOUND IN chromatin (ortholog); nucleus (ortholog) NW_004955493 6888832 6894840 + 9068941;7240710 102022612 A0A8C2VMF1;A0A8C2VMF9 MODEL AGCD01061147;GBDK01329897;XM_005405189 XP_005405246 T-box 6;T-box transcription factor TBX6 APPROVED protein-coding ENSCLAG00000012212 NW_004955493 6888832 6894831 + 8711700 LOC102023200 transcription elongation factor A protein-like 5 NW_004955548 416862 420750 - 9068941 102023200 A0A8C2UIH6 MODEL AGCD01072331;GBCE01005297;XM_005411979;XM_005411980 XP_005412036;XP_005412037 Tceal5 transcription elongation factor A (SII)-like 5 APPROVED protein-coding ENSCLAG00000000409 8711710 Mypop Myb related transcription factor, partner of profilin ENCODES a protein that exhibits DNA binding (ortholog); DNA-binding transcription factor activity (ortholog); DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); INVOLVED IN negative regulation of transcription by RNA polymerase II (ortholog); regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN nucleus (ortholog) NW_004955574 316188 325288 - 9068941;7240710 102023541 A0A8C2US36 MODEL AGCD01075098;GBDF01125819;XM_005413821;XM_013509574;XM_013509575 XP_005413878;XP_013365028;XP_013365029 Myb-related transcription factor, partner of profilin APPROVED protein-coding ENSCLAG00000001704 NW_004955574 312744 325288 - 8711720 LOC102023612 uncharacterized LOC102023612 NW_004955493 7795315 7798040 - 102023612 MODEL AGCD01061227;GBDF01039121;XR_001231264 ncrna 8711726 LOC102023825 thyroid hormone receptor-associated protein 3 pseudogene NW_004955506 3169804 3172644 + 102023825 MODEL AGCD01065313 APPROVED pseudo 8711727 Klhl21 kelch like family member 21 ENCODES a protein that exhibits cullin family protein binding (ortholog); ubiquitin-protein transferase activity (ortholog); INVOLVED IN chromosome passenger complex localization to spindle midzone (ortholog); protein ubiquitination (ortholog); regulation of cytokinesis (ortholog); ASSOCIATED WITH chromosome 1p36 deletion syndrome (ortholog); genetic disease (ortholog); high grade glioma (ortholog); FOUND IN Cul3-RING ubiquitin ligase complex (ortholog); polar microtubule (ortholog) NW_004955486 6038291 6047814 + 9068941 102024915 A0A8C2V027 MODEL AGCD01059105;GBCB01002232;GBCE01134534;XM_005404316 XP_005404373 kelch-like family member 21;kelch-like protein 21 APPROVED protein-coding ENSCLAG00000004379 8711734 LOC102025231 60S ribosomal protein L36 pseudogene NW_004955469 290871 292912 + 102025231 MODEL AGCD01052216 APPROVED pseudo 8711742 Pltp phospholipid transfer protein ENCODES a protein that exhibits ceramide binding (ortholog); cerebroside transfer activity (ortholog); cholesterol transfer activity (ortholog); INVOLVED IN ceramide transport (ortholog); flagellated sperm motility (ortholog); glycolipid transport (ortholog); PARTICIPATES IN reverse cholesterol transport pathway; ASSOCIATED WITH atherosclerosis (ortholog); Coronary Disease (ortholog); dry eye syndrome (ortholog); FOUND IN extracellular region (ortholog); extracellular space (ortholog); high-density lipoprotein particle (ortholog) NW_004955445 11384723 11399217 + 9068941 102026050 A0A8C2V6Z1 MODEL AGCD01039689;AGCD01039690;GBCE01006971;XM_005392402 XP_005392459 protein-coding ENSCLAG00000005928 NW_004955445 11384723 11399217 + 8711762 Ttc4 tetratricopeptide repeat domain 4 INVOLVED IN defense response to virus (ortholog); innate immune response (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog) NW_004955464 4629061 4669054 - 102027156 A0A8C2W4V3 MODEL AGCD01049992;GBDF01123002;XM_005398518;XM_005398519;XR_001236700 XP_005398575;XP_005398576 tetratricopeptide repeat protein 4 protein-coding ENSCLAG00000017302 NW_004955464 4629932 4669333 - 8711780 Grhl1 grainyhead like transcription factor 1 ENCODES a protein that exhibits chromatin DNA binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); protein homodimerization activity (ortholog); INVOLVED IN desmosome organization (ortholog); epidermis development (ortholog); establishment of skin barrier (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN intracellular membrane-bounded organelle (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955487 5407187 5432828 + 9068941 102027193 A0A8C2UW07 MODEL AGCD01059332;GBDF01305732;GBDF01305734;XM_005404405 XP_005404462 grainyhead-like 1;grainyhead-like protein 1 homolog;grainyhead-like transcription factor 1 APPROVED protein-coding ENSCLAG00000004000 NW_004955487 5407128 5433113 + 8711803 Corin corin, serine peptidase ENCODES a protein that exhibits endopeptidase activity (ortholog); serine-type endopeptidase activity (ortholog); INVOLVED IN female pregnancy (ortholog); peptide hormone processing (ortholog); regulation of blood pressure (ortholog); PARTICIPATES IN atrial natriuretic peptide signaling pathway; ASSOCIATED WITH Cardiomegaly (ortholog); congestive heart failure (ortholog); genetic disease (ortholog); FOUND IN actin cytoskeleton (ortholog); cell surface (ortholog); cytoplasmic vesicle (ortholog) NW_004955443 721655 970600 + 9068941;7240710 102027350 A0A8C2UKH8;A0A8C2UKK4 MODEL AGCD01038119;AGCD01038120;AGCD01038121;AGCD01038122;AGCD01038123;AGCD01038124;AGCD01038125;AGCD01038126;AGCD01038127;GBDJ01377729;XM_005391890;XM_013518121;XM_013518122 XP_005391947;XP_013373575;XP_013373576 atrial natriuretic peptide-converting enzyme protein-coding ENSCLAG00000001635 NW_004955443 722201 969014 + 8711829 Crebrf CREB3 regulatory factor ENCODES a protein that exhibits DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); RNA polymerase II transcription regulatory region sequence-specific DNA binding (ortholog); INVOLVED IN maternal behavior (ortholog); negative regulation of endoplasmic reticulum unfolded protein response (ortholog); negative regulation of glucocorticoid mediated signaling pathway (ortholog); ASSOCIATED WITH atrial heart septal defect 7 (ortholog); Atrial Septal Defect with Atrioventricular Conduction Defects (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); nuclear body (ortholog); nucleoplasm (ortholog) NW_004955408 25718523 25769551 + 9068941 102028501 A0A8C2VVP8;A0A8C2VXT8;A0A8C2W392 MODEL AGCD01008651;GBDF01224359;XM_005376346;XM_005376347;XM_005376348 XP_005376403;XP_005376404;XP_005376405 protein-coding ENSCLAG00000014588 NW_004955408 25719187 25774555 + 8711849 LOC102003870 eotaxin NW_004955481 9017930 9020436 + 9068941;7240710 102003870 A0A8C2YL61 MODEL AGCD01057092;GBDF01030595;XM_005402838 XP_005402895 Ccl11 chemokine (C-C motif) ligand 11 APPROVED protein-coding ENSCLAG00000004752 NW_004955481 9017946 9020509 + 8711858 LOC102004024 KATNB1-like protein 1 NW_004955402 52891404 52893054 - 102004024 MODEL AGCD01001350 APPROVED pseudo 8711859 LOC102004093 uncharacterized LOC102004093 NW_004955506 3778930 3780204 - 102004093 MODEL AGCD01065319;GBDF01208779;XR_264347 ncrna 8711863 Mgst3 microsomal glutathione S-transferase 3 ENCODES a protein that exhibits glutathione peroxidase activity (ortholog); glutathione transferase activity (ortholog); identical protein binding (ortholog); INVOLVED IN leukotriene biosynthetic process (ortholog); lipid metabolic process (ortholog); response to organonitrogen compound (ortholog); ASSOCIATED WITH chronic obstructive pulmonary disease (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN intracellular membrane-bounded organelle (ortholog); membrane (ortholog) NW_004955462 11024678 11041851 - 9068941 102004577 A0A8C2VCZ9 MODEL AGCD01049383;GBDK01018760;XM_005398246 XP_005398303 protein-coding ENSCLAG00000007690 NW_004955462 11024789 11031282 - 8711873 LOC102006247 uncharacterized LOC102006247 NW_004955418 22849622 22877924 - 102006247 MODEL AGCD01019292;GBDF01144012;XR_260583 ncrna 8711878 LOC102006795 nuclear receptor subfamily 5 group A member 2 pseudogene NW_004955503 337968 338545 + 102006795 MODEL AGCD01064497 APPROVED pseudo 8711879 Slc49a3 solute carrier family 49 member 3 ASSOCIATED WITH cherubism (ortholog); genetic disease (ortholog); Mental Retardation, Autosomal Recessive 53 (ortholog) NW_004955514 289301 295443 - 9068941 102007146 A0A8C2VFM6 MODEL AGCD01067006;GBDJ01187158;XM_005408673;XM_013506845;XM_013506846;XR_001231781 XP_005408730;XP_013362299;XP_013362300 Mfsd7 major facilitator superfamily domain containing 7;major facilitator superfamily domain-containing protein 7 APPROVED protein-coding ENSCLAG00000010259 NW_004955514 289874 295127 - 8711893 Spats2l spermatogenesis associated serine rich 2 like ASSOCIATED WITH atrial fibrillation (ortholog); COVID-19 (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); nucleolus (ortholog); nucleoplasm (ortholog) NW_004955403 930622 1085906 - 9068941 102007171 A0A8C2VQK7;A0A8C2VQM9;A0A8C2VQZ8 MODEL AGCD01001712;AGCD01001713;AGCD01001714;AGCD01001715;GBCC01017701;XM_005373252;XM_005373253 XP_005373309;XP_005373310 spermatogenesis associated, serine-rich 2-like APPROVED protein-coding ENSCLAG00000013167 NW_004955403 930622 1013777 - 8711921 LOC102008850 centromere protein Q-like NW_004955481 3368425 3369339 + 102008850 MODEL AGCD01056902;XM_013503357 XP_013358811 protein-coding 8711922 LOC102010104 olfactory receptor 7G2-like NW_004955563 273849 274787 + 102010104 MODEL AGCD01074059;XM_005413199 XP_005413256 protein-coding 8711925 LOC102010533 olfactory receptor 2B6-like NW_004955576 1225109 1226068 - 102010533 A0A8C2WDN5 MODEL AGCD01075364;XM_005413950 APPROVED pseudo ENSCLAG00000017429 8711928 Nap1l1 nucleosome assembly protein 1 like 1 ENCODES a protein that exhibits histone chaperone activity (ortholog); kinase binding (ortholog); INVOLVED IN cellular response to peptide hormone stimulus (ortholog); positive regulation of neural precursor cell proliferation (ortholog); positive regulation of neurogenesis (ortholog); PARTICIPATES IN histone modification pathway; ASSOCIATED WITH appendiceal neoplasm (ortholog); Colorectal Neoplasms (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog) NW_004955405 15332696 15365181 - 9068941 102010541 A0A8C2UZA9;A0A8C2V4T9;A0A8C2YLK3 MODEL AGCD01004943;AGCD01004944;GBCE01030847;XM_005374339;XM_005374340;XM_013517718;XM_013517723;XM_013517725 XP_005374396;XP_005374397;XP_013373172;XP_013373177;XP_013373179 nucleosome assembly protein 1-like 1 APPROVED protein-coding ENSCLAG00000005333 NW_004955405 15330328 15365208 - 8711974 Wwc2 WW and C2 domain containing 2 ENCODES a protein that exhibits kinase binding (ortholog); molecular adaptor activity (ortholog); INVOLVED IN negative regulation of hippo signaling (ortholog); negative regulation of organ growth (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH genetic disease (ortholog); long QT syndrome (ortholog); FOUND IN cytosol (ortholog) NW_004955403 25482601 25602412 - 9068941 102011268 A0A8C2VM35;A0A8C2YRB3 MODEL AGCD01002289;AGCD01002290;AGCD01002291;GBDK01018936;XM_013513141 XP_013368595 protein-coding ENSCLAG00000012066 NW_004955403 25482601 25627580 - 8712001 Emp3 epithelial membrane protein 3 INVOLVED IN apoptotic process (ortholog); bleb assembly (ortholog); ASSOCIATED WITH genetic disease (ortholog); Prostatic Neoplasms (ortholog); FOUND IN plasma membrane (ortholog) NW_004955559 2117200 2121366 - 9068941 102012480 A0A8C2UWK8 MODEL AGCD01073691;GBDJ01005369;XM_005412959;XM_013509045 XP_005413016;XP_013364499 protein-coding ENSCLAG00000004840 NW_004955559 2117200 2121366 - 8712010 LOC102013001 putative spermatogenesis-associated protein 31D3 NW_004955530 1751228 1756912 - 102013001 MODEL AGCD01069899;GBDF01052090;XM_013507542;XM_013507543;XM_013507544 XP_013362996;XP_013362997;XP_013362998 APPROVED protein-coding 8712019 Ift57 intraflagellar transport 57 INVOLVED IN activation of cysteine-type endopeptidase activity involved in apoptotic process (ortholog); apoptotic process (ortholog); heart looping (ortholog); ASSOCIATED WITH genetic disease (ortholog); Huntington's disease (ortholog); Orofaciodigital Syndrome XVIII (ortholog); FOUND IN axoneme (ortholog); centrosome (ortholog); ciliary basal body (ortholog) NW_004955427 8814298 8871671 - 9068941 102013524 A0A8C2VE94 MODEL AGCD01027078;AGCD01027079;GBBH01033666;XM_005386354 XP_005386411 intraflagellar transport 57 homolog;intraflagellar transport protein 57 homolog APPROVED protein-coding ENSCLAG00000009845 NW_004955427 8814298 8871720 - 8712034 Cul5 cullin 5 ENCODES a protein that exhibits ubiquitin protein ligase binding (ortholog); INVOLVED IN cerebral cortex radially oriented cell migration (ortholog); protein ubiquitination (ortholog); radial glia guided migration of Purkinje cell (ortholog); PARTICIPATES IN neddylation pathway; proteasome degradation pathway involving cullin-dependent ubiquitin ligases; ASSOCIATED WITH ataxia telangiectasia (ortholog); Brain Injuries (ortholog); Breast Neoplasms (ortholog); FOUND IN Cul5-RING ubiquitin ligase complex (ortholog); site of DNA damage (ortholog) NW_004955412 10266072 10336156 + 9068941 102014031 A0A8C2VRB6;A0A8C2VWF8 MODEL AGCD01012764;AGCD01012765;AGCD01012766;GBDF01053200;XM_013510972 XP_013366426 cullin-5 protein-coding ENSCLAG00000012699 NW_004955412 10256381 10336156 + 8712066 Stard7 StAR related lipid transfer domain containing 7 INVOLVED IN establishment of skin barrier (ortholog); inflammatory response (ortholog); mucociliary clearance (ortholog); ASSOCIATED WITH familial adult myoclonic epilepsy 2 (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN cytoplasm (ortholog) NW_004955470 3771410 3790667 - 9068941 102015002 A0A8C2VE89 MODEL AGCD01052711;GBDJ01087829;XM_005400653 XP_005400710 StAR-related lipid transfer (START) domain containing 7;stAR-related lipid transfer protein 7, mitochondrial APPROVED protein-coding ENSCLAG00000009844 NW_004955470 3770817 3790667 - 8712078 Ccm2 CCM2 scaffold protein INVOLVED IN blood vessel development (ortholog); blood vessel endothelial cell differentiation (ortholog); cell-cell junction organization (ortholog); PARTICIPATES IN p38 MAPK signaling pathway; ASSOCIATED WITH cavernous hemangioma (ortholog); Central Nervous System Vascular Malformations (ortholog); cerebral cavernous malformation (ortholog); FOUND IN cytoplasm (ortholog); mitochondrion (ortholog); protein-containing complex (ortholog) NW_004955456 7232224 7251012 - 9068941;7240710 102015078 A0A8C2V321;A0A8C2V5X1 MODEL AGCD01046401;GBDJ01137048;GBDJ01137052;XM_013520603 XP_013376057 cerebral cavernous malformation 2 APPROVED protein-coding ENSCLAG00000006017 NW_004955456 7227667 7256206 - 8712092 LOC102015875 uncharacterized LOC102015875 NW_004955429 21522975 21526531 + 102015875 MODEL AGCD01029005;GBDF01223359;XR_261378 ncrna 8712098 LOC102016629 uncharacterized LOC102016629 NW_004955517 1599049 1602884 - 102016629 MODEL AGCD01067601;XR_264544 ncrna 8712105 Ikbke inhibitor of nuclear factor kappa B kinase subunit epsilon ENCODES a protein that exhibits identical protein binding (ortholog); IkappaB kinase activity (ortholog); K48-linked polyubiquitin modification-dependent protein binding (ortholog); INVOLVED IN cellular response to virus (ortholog); gene expression (ortholog); I-kappaB phosphorylation (ortholog); ASSOCIATED WITH autistic disorder (ortholog); familial adult myoclonic epilepsy 5 (ortholog); gastrointestinal stromal tumor (ortholog); FOUND IN cytoplasm (ortholog); mitochondrial membrane (ortholog); nucleus (ortholog) NW_004955406 42056014 42077701 + 9068941 102017949 A0A8C2VT69 MODEL AGCD01006696;GBDK01143454;XM_005375388;XM_005375389;XM_005375390;XM_005375392;XM_005375393 XP_005375445;XP_005375446;XP_005375447;XP_005375449;XP_005375450 inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase epsilon;inhibitor of nuclear factor kappa-B kinase subunit epsilon APPROVED protein-coding ENSCLAG00000013208 NW_004955406 42056014 42077701 + 8712147 LOC102018014 endothelial differentiation-related factor 1 pseudogene NW_004955518 3788942 3789430 - 102018014 MODEL AGCD01067809 APPROVED pseudo 8712148 Tmem232 transmembrane protein 232 ASSOCIATED WITH familial adenomatous polyposis 1 (ortholog); genetic disease (ortholog); Hereditary Neoplastic Syndromes (ortholog) NW_004955418 4342019 4566967 + 9068941 102018186 A0A8C2V735 MODEL AGCD01018821;AGCD01018822;AGCD01018823;AGCD01018824;AGCD01018825;AGCD01018826;GBDF01082890;XM_005382169;XM_005382170;XM_005382171;XM_005382172;XM_013513023;XM_013513024 XP_005382226;XP_005382227;XP_005382228;XP_005382229;XP_013368477;XP_013368478 protein-coding ENSCLAG00000005961 NW_004955418 4352789 4569658 + 8712175 Cibar1 CBY1 interacting BAR domain containing 1 ENCODES a protein that exhibits phospholipid binding (ortholog); INVOLVED IN cilium assembly (ortholog); inner mitochondrial membrane organization (ortholog); limb morphogenesis (ortholog); ASSOCIATED WITH ciliopathy (ortholog); genetic disease (ortholog); polydactyly (ortholog); FOUND IN centriole (ortholog); ciliary basal body (ortholog); ciliary base (ortholog) NW_004955417 10060500 10080119 + 9068941 102018928 A0A8C2UX89 MODEL AGCD01018065;GBDF01009145;XM_005381785 XP_005381842 Fam92a;Fam92a1 family with sequence similarity 92 member A;family with sequence similarity 92 member A1;family with sequence similarity 92, member A1 APPROVED protein-coding ENSCLAG00000005013 NW_004955417 10059844 10079192 + 8712202 LOC102020201 uncharacterized LOC102020201 NW_004955406 40111451 40112653 + 102020201 MODEL AGCD01006654;GBDF01027492;XR_259530 ncrna 8712207 LOC102020548 putative monooxygenase p33MONOX pseudogene NW_004955466 8052265 8053164 + 102020548 MODEL AGCD01050977 APPROVED pseudo 8712208 Nsd2 nuclear receptor binding SET domain protein 2 ENCODES a protein that exhibits chromatin binding (ortholog); histone H3K36 methyltransferase activity (ortholog); histone H3K36 trimethyltransferase activity (ortholog); INVOLVED IN atrial septum primum morphogenesis (ortholog); atrial septum secundum morphogenesis (ortholog); bone development (ortholog); ASSOCIATED WITH acute lymphoblastic leukemia (ortholog); anemia (ortholog); Breast Neoplasms (ortholog); FOUND IN nucleoplasm (ortholog); nucleus (ortholog) NW_004955514 1084522 1162624 + 9068941 102020695 A0A8C2VV90;A0A8C2VXB1;A0A8C2W2Q6 MODEL AGCD01067037;GBDF01040595;XM_005408719;XM_005408720 XP_005408776;XP_005408777 Whsc1 Wolf-Hirschhorn syndrome candidate 1;histone-lysine N-methyltransferase NSD2 APPROVED protein-coding ENSCLAG00000014450 NW_004955514 1069085 1162624 + 8712239 Cd59 CD59 molecule (CD59 blood group) ENCODES a protein that exhibits complement binding (ortholog); INVOLVED IN innate immune response (ortholog); negative regulation of activation of membrane attack complex (ortholog); negative regulation of apoptotic process (ortholog); ASSOCIATED WITH acute necrotizing pancreatitis (ortholog); Alcoholic Liver Diseases (ortholog); anterior uveitis (ortholog); FOUND IN cell surface (ortholog); compact myelin (ortholog); external side of plasma membrane (ortholog) NW_004955422 12500572 12528738 + 9068941;7240710 102020811 A0A8C2VY68 MODEL AGCD01022796;GBDF01046537;XM_005384156 XP_005384213 CD59 glycoprotein;CD59 molecule APPROVED protein-coding ENSCLAG00000014692 8712247 LOC102021172 SLA class II histocompatibility antigen, DQ haplotype D alpha chain-like NW_004955437 1350477 1355574 + 102021172 A0A8C2VJZ5 MODEL AGCD01034204;GBDJ01016936;XM_005389453 XP_005389510 protein-coding ENSCLAG00000009507 8712256 LOC102022609 putative MAGE domain-containing protein MAGEA13P NW_004955489 6761364 6855797 - 102022609 MODEL AGCD01059965;AGCD01059966;AGCD01059967;GBDF01303343;XM_013504466;XM_013504467 XP_013359920;XP_013359921 APPROVED protein-coding 8712262 LOC102023128 cytochrome c oxidase assembly protein COX16 homolog, mitochondrial INVOLVED IN mitochondrial cytochrome c oxidase assembly (ortholog); ASSOCIATED WITH genetic disease (ortholog); Mitochondrial Complex IV Deficiency, Nuclear Type 22 (ortholog); FOUND IN mitochondrial inner membrane (ortholog) NW_004955466 130341 142969 + 9068941 102023128 A0A8C2V8T9 MODEL AGCD01050650;AGCD01050651;GBCQ01038746;XM_005399020 XP_005399077 APPROVED protein-coding ENSCLAG00000006541 NW_004955466 130341 142969 + 8712270 LOC102023395 uncharacterized LOC102023395 NW_004955437 3132934 3153018 - 102023395 MODEL AGCD01034298;AGCD01034299;GBDI01326354;XR_001235053 ncrna 8712275 Ehd3 EH domain containing 3 INVOLVED IN cilium assembly (ortholog); early endosome to Golgi transport (ortholog); endocytic recycling (ortholog); ASSOCIATED WITH acute myeloid leukemia (ortholog); genetic disease (ortholog); hepatocellular carcinoma (ortholog); FOUND IN ciliary pocket membrane (ortholog); cytoplasm (ortholog); endocytic vesicle (ortholog) NW_004955469 12953800 12984296 + 9068941 102023575 A0A8C2VI54 MODEL AGCD01052589;AGCD01052590;GBDK01084893;XM_005400561 XP_005400618 EH domain-containing protein 3;EH-domain containing 3 APPROVED protein-coding ENSCLAG00000010983 NW_004955469 12953645 12984430 + 8712285 LOC102023845 chromosome unknown open reading frame, human C14orf180 ASSOCIATED WITH Charcot-Marie-Tooth disease axonal type 2O (ortholog); genetic disease (ortholog); hepatocellular carcinoma (ortholog); FOUND IN plasma membrane (ortholog) NW_004955538 3076578 3083867 + 9068941 102023845 A0A8C2YNS2 MODEL AGCD01071145;GBDJ01239820;XM_005410829;XM_005410830;XM_005410831;XM_005410832;XM_005410833;XM_005410835;XM_013507905 XP_005410886;XP_005410887;XP_005410888;XP_005410889;XP_005410890;XP_005410892;XP_013363359 nutritionally-regulated adipose and cardiac enriched protein homolog;nutritionally-regulated adipose and cardiac-enriched protein homolog protein-coding ENSCLAG00000008417 NW_004955538 3080112 3082282 + 8712309 Ccdc134 coiled-coil domain containing 134 INVOLVED IN angiogenesis (ortholog); embryonic hemopoiesis (ortholog); embryonic liver development (ortholog); ASSOCIATED WITH adenylosuccinase lyase deficiency (ortholog); Bone Fractures (ortholog); common variable immunodeficiency 4 (ortholog); FOUND IN cytosol (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955413 27248879 27265635 + 9068941 102023998 A0A8C2W910 MODEL AGCD01014500;GBDK01039791;XM_005379367;XM_005379369 XP_005379424;XP_005379426 coiled-coil domain-containing protein 134 protein-coding ENSCLAG00000017160 NW_004955413 27249272 27265635 + 8712326 Psmd1 proteasome 26S subunit, non-ATPase 1 ENCODES a protein that exhibits ubiquitin protein ligase binding (ortholog); ASSOCIATED WITH Bardet-Biedl syndrome (ortholog); genetic disease (ortholog); Joubert syndrome 22 (ortholog); FOUND IN proteasome accessory complex (ortholog); proteasome complex (ortholog) NW_004955453 4314177 4397972 - 9068941 102024421 A0A8C2VK92 MODEL AGCD01044686;AGCD01044687;GBCQ01003438;GBDI01005709;XM_013519960 XP_013375414 26S proteasome non-ATPase regulatory subunit 1;proteasome (prosome, macropain) 26S subunit, non-ATPase, 1 APPROVED protein-coding ENSCLAG00000009721 NW_004955453 4314177 4397975 - 8712354 Ece2 endothelin converting enzyme 2 ENCODES a protein that exhibits metalloendopeptidase activity (ortholog); INVOLVED IN peptide hormone processing (ortholog); ASSOCIATED WITH 3-Methylcrotonyl-CoA carboxylase 1 deficiency (ortholog); congenital disorder of glycosylation Id (ortholog); Currarino syndrome (ortholog); FOUND IN cytoplasmic vesicle membrane (ortholog) NW_004955420 23199627 23217078 - 9068941 102024685 A0A8C2VLQ3;A0A8C2VP19;A0A8C2VS44;A0A8C2VTM3 MODEL AGCD01021233;GBDF01270605;XM_005383341;XM_013513360 XP_005383398;XP_013368814 endothelin-converting enzyme 2 protein-coding ENSCLAG00000012028 NW_004955420 23202668 23235977 - 8712392 LOC102025910 olfactory receptor-like protein DTMT NW_004955481 29339 30283 - 102025910 A0A8C2WAS1 MODEL AGCD01056777;XM_005402548 XP_005402605 APPROVED protein-coding ENSCLAG00000017700 8712395 Fam135a family with sequence similarity 135 member A ASSOCIATED WITH genetic disease (ortholog); infantile histiocytoid cardiomyopathy (ortholog) NW_004955488 5529579 5616188 + 9068941 102026646 A0A8C2UGI3;A0A8C2ULE6 MODEL AGCD01059625;GBCQ01100199;XM_005404471;XM_005404473 XP_005404528;XP_005404530 family with sequence similarity 135, member A APPROVED protein-coding ENSCLAG00000000497 NW_004955488 5529505 5617396 + 8712427 LOC102026824 uncharacterized LOC102026824 NW_004955451 16663500 16672386 - 102026824 MODEL AGCD01043697;GBCQ01187617;XM_013519259;XR_262619;XR_262620 XP_013374713 uncharacterized protein LOC102026824 protein-coding 8712436 LOC102026978 uncharacterized LOC102026978 NW_004955484 3031441 3043406 + 102026978 MODEL AGCD01058149;AGCD01058150;GBDK01273591;XR_263879 ncrna 8712441 Kmt5a lysine methyltransferase 5A ENCODES a protein that exhibits histone H4K20 methyltransferase activity (ortholog); histone methyltransferase activity (ortholog); protein-lysine N-methyltransferase activity (ortholog); INVOLVED IN negative regulation of DNA-templated transcription (ortholog); negative regulation of double-strand break repair via homologous recombination (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); PARTICIPATES IN histone modification pathway; methionine cycle/metabolic pathway; p53 signaling pathway; ASSOCIATED WITH genetic disease (ortholog); prostate cancer (ortholog); FOUND IN chromatin (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955482 5488151 5500764 - 9068941 102027186 A0A8C2VXP6 MODEL AGCD01057337;AGCD01057338;AGCD01057339;GBCQ01093635;GBDI01180644;XM_013503555 XP_013359009 Setd8 N-lysine methyltransferase SETD8;SET domain containing (lysine methyltransferase) 8 APPROVED protein-coding ENSCLAG00000015060 NW_004955482 5485649 5501636 - 8712453 Prxl2a peroxiredoxin like 2A ENCODES a protein that exhibits antioxidant activity (ortholog); INVOLVED IN regulation of osteoclast differentiation (ortholog); FOUND IN cytoplasm (ortholog) NW_004955510 400454 420900 + 9068941 102027556 A0A8C2YI36 MODEL AGCD01066147;AGCD01066148;GBDJ01064130;XM_005407871;XM_005407872;XM_005407873;XM_013506334;XM_013506335 XP_005407928;XP_005407929;XP_005407930;XP_013361788;XP_013361789 Fam213a family with sequence similarity 213 member A;family with sequence similarity 213, member A;redox-regulatory protein FAM213A APPROVED protein-coding ENSCLAG00000000254 NW_004955510 400469 423056 + 8712471 LOC102028239 ribonuclease pancreatic-like NW_004955550 1701601 1702672 + 102028239 A0A8C2UN59 MODEL AGCD01072584;XM_013508544 XP_013363998 protein-coding ENSCLAG00000000721 8712476 LOC102028258 uncharacterized LOC102028258 NW_004956812 12 2877 + 102028258 MODEL AGCD01080189;GBDK01070408;XR_265213 ncrna 8712482 LOC102029753 uncharacterized LOC102029753 NW_004955421 15677291 15677895 + 102029753 MODEL AGCD01021987;GBCQ01116030;XR_260796 ncrna 8712486 LOC102030405 uncharacterized LOC102030405 NW_004955413 20449750 20450775 + 102030405 MODEL AGCD01014216;GBDF01209169;XR_260089 ncrna 8712490 LOC102004357 transcription elongation factor SPT4-A-like NW_004955457 12370358 12370718 + 102004357 MODEL AGCD01047009 APPROVED pseudo 8712491 Rabac1 Rab acceptor 1 ENCODES a protein that exhibits GTPase binding (ortholog); identical protein binding (ortholog); proline-rich region binding (ortholog); ASSOCIATED WITH Carpenter Syndrome 2 (ortholog); congenital hypoplastic anemia (ortholog); craniosynostosis (ortholog); FOUND IN Golgi apparatus (ortholog); membrane (ortholog); synapse (ortholog) NW_004955555 897927 900406 + 9068941 102005848 A0A8C2ULE9;A0A8C2UP86 MODEL AGCD01073051;GBDF01002277;XM_005412402 XP_005412459 Rab acceptor 1 (prenylated);prenylated Rab acceptor protein 1 APPROVED protein-coding ENSCLAG00000001671 NW_004955555 897846 902636 + 8712499 LOC102005902 uncharacterized LOC102005902 NW_004955409 9536684 9555161 + 102005902 MODEL AGCD01009443;AGCD01009444;GBDF01156061;XR_259761 ncrna ENSCLAG00000027513 8712506 LOC102007099 uncharacterized LOC102007099 NW_004955413 26714 54739 + 102007099 MODEL AGCD01013432;AGCD01013433;AGCD01013434;AGCD01013435;GBDF01192955;XR_001232930;XR_260037 ncrna 8712514 Fzd2 frizzled class receptor 2 ENCODES a protein that exhibits identical protein binding (ortholog); PDZ domain binding (ortholog); protein heterodimerization activity (ortholog); INVOLVED IN canonical Wnt signaling pathway (ortholog); cell-cell signaling (ortholog); cellular response to growth factor stimulus (ortholog); PARTICIPATES IN Wnt signaling pathway; Wnt signaling, non-canonical pathway; ASSOCIATED WITH autosomal dominant Robinow syndrome 1 (ortholog); autosomal dominant Robinow syndrome 2 (ortholog); autosomal dominant Robinow syndrome 3 (ortholog); FOUND IN cytoplasm (ortholog); plasma membrane (ortholog) NW_004955451 17501410 17503726 + 9068941 102007727 MODEL AGCD01043754;GBBH01225132;XM_005394650 XP_005394707 frizzled family receptor 2;frizzled-2 APPROVED protein-coding 8712518 LOC102007913 uncharacterized LOC102007913 NW_004955423 26618752 26622551 + 102007913 MODEL AGCD01024102;AGCD01024103;GBDF01148474;XM_005385372 XP_005385429 uncharacterized protein LOC102007913 protein-coding ENSCLAG00000023034 8712526 Clptm1l CLPTM1 like ENCODES a protein that exhibits phospholipid scramblase activity (ortholog); ASSOCIATED WITH autosomal dominant dyskeratosis congenita 2 (ortholog); basal cell carcinoma (ortholog); esophagus squamous cell carcinoma (ortholog); FOUND IN endoplasmic reticulum membrane (ortholog) NW_004955504 677824 695660 - 9068941 102007920 A0A8C2V851 MODEL AGCD01064826;GBBH01064845;XM_005407055;XM_005407056 XP_005407112;XP_005407113 CLPTM1-like APPROVED protein-coding ENSCLAG00000006371 NW_004955504 677772 695660 - 8712549 Med21 mediator complex subunit 21 ENCODES a protein that exhibits transcription coactivator activity (ortholog); ubiquitin protein ligase activity (ortholog); INVOLVED IN blastocyst development (ortholog); positive regulation of transcription by RNA polymerase II (ortholog); protein ubiquitination (ortholog); PARTICIPATES IN RNA polymerase II transcription pathway; FOUND IN core mediator complex (ortholog); mediator complex (ortholog); nucleus (ortholog) NW_004955413 21898579 21904759 + 9068941 102008081 A0A8C2W4M0;A0A8C2W7D8 MODEL AGCD01014274;AGCD01014275;GBDJ01138309;XM_005379118 XP_005379175 mediator of RNA polymerase II transcription subunit 21 protein-coding ENSCLAG00000016595 NW_004955413 21898514 21908167 + 8712557 Tube1 tubulin epsilon 1 ASSOCIATED WITH genetic disease (ortholog) NW_004955526 4484867 4519603 + 9068941 102008142 A0A8C2YHZ2 MODEL AGCD01069368;GBDF01193580;XM_005409771;XM_005409772;XR_264663 XP_005409828;XP_005409829 tubulin epsilon chain;tubulin, epsilon 1 APPROVED protein-coding ENSCLAG00000000067 NW_004955526 4484128 4501709 + 8712595 LOC102008356 kinetochore-associated protein DSN1 homolog pseudogene NW_004955444 350531 351610 - 102008356 MODEL AGCD01038664;XM_005392056 APPROVED pseudo 8712598 Lrrc7 leucine rich repeat containing 7 ENCODES a protein that exhibits protein kinase binding (ortholog); INVOLVED IN positive regulation of neuron projection development (ortholog); response to organic cyclic compound (ortholog); PARTICIPATES IN calcium/calmodulin dependent kinase 2 signaling pathway; ASSOCIATED WITH Cocaine-Related Disorders (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN actin cytoskeleton (ortholog); axon initial segment (ortholog); centrosome (ortholog) NW_004955423 21764046 22269590 - 9068941 102009075 A0A8C2VCR2;A0A8C2VDC8;A0A8C2VES7;A0A8C2VHI7 MODEL AGCD01023948;AGCD01023949;AGCD01023950;AGCD01023951;AGCD01023952;AGCD01023953;AGCD01023954;AGCD01023955;AGCD01023956;AGCD01023957;AGCD01023958;AGCD01023959;AGCD01023960;AGCD01023961;GBCE01048900;XM_013514395;XM_013514396;XM_013514397 XP_013369849;XP_013369850;XP_013369851 leucine-rich repeat-containing protein 7 protein-coding ENSCLAG00000008949 NW_004955423 21769366 22269781 - 8712631 LOC102009219 uncharacterized LOC102009219 NW_004955438 11481547 11499549 - 102009219 MODEL AGCD01035239;AGCD01035240;GBDF01306429;XR_261927 ncrna 8712636 Krr1 KRR1 small subunit processome component homolog INVOLVED IN ribosomal small subunit biogenesis (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN chromosome (ortholog); intercellular bridge (ortholog); nucleolus (ortholog) NW_004955405 14851602 14864838 - 9068941 102009909 A0A8C2UYA8;A0A8C2YLE7 MODEL AGCD01004933;GBDK01195874;XM_005374336 XP_005374393 KRR1, small subunit (SSU) processome component, homolog (yeast);KRR1, small subunit processome component homolog APPROVED protein-coding ENSCLAG00000005111 NW_004955405 14851602 14864985 - 8712650 Hmox2 heme oxygenase 2 ENCODES a protein that exhibits heme oxygenase (decyclizing) activity (ortholog); INVOLVED IN response to hypoxia (ortholog); response to oxidative stress (ortholog); ASSOCIATED WITH Cerebral Hemorrhage (ortholog); epilepsy (ortholog); genetic disease (ortholog); FOUND IN plasma membrane (ortholog) NW_004955442 12913983 12947412 - 9068941 102010418 A0A8C2VM46 MODEL AGCD01037748;AGCD01037749;AGCD01037750;GBBH01007410;XM_005391291;XM_013517724 XP_005391348;XP_013373178 heme oxygenase (decycling) 2 APPROVED protein-coding ENSCLAG00000011474 NW_004955442 12913983 12920152 - 8712673 LOC102010643 leukocyte immunoglobulin-like receptor subfamily A member 3 NW_004955567 1316802 1426452 - 102010643 MODEL AGCD01074467;AGCD01074468;AGCD01074469;AGCD01074470;AGCD01074471;AGCD01074472;AGCD01074473;AGCD01074474;AGCD01074475;AGCD01074476;XM_013509260 XP_013364714 APPROVED protein-coding 8712674 LOC102012144 cytochrome b5 ENCODES a protein that exhibits enzyme binding (ortholog); INVOLVED IN response to cadmium ion (ortholog); ASSOCIATED WITH adult respiratory distress syndrome (ortholog); chromosome 18q deletion syndrome (ortholog); Congenital Methemoglobinemia (ortholog); FOUND IN cytosol (ortholog); endoplasmic reticulum (ortholog); endoplasmic reticulum membrane (ortholog) NW_004955402 57701931 57739163 - 9068941;7240710 102012144 A0A8C2YP88;A0A8C2YP89 MODEL AGCD01001508;AGCD01001509;GBDK01022341;XM_005373076 XP_005373133 APPROVED protein-coding ENSCLAG00000009123 NW_004955402 57701931 57739163 - 8712693 Exoc3l1 exocyst complex component 3 like 1 INVOLVED IN exocytosis (ortholog); peptide hormone secretion (ortholog); ASSOCIATED WITH autosomal dominant dyskeratosis congenita 6 (ortholog); genetic disease (ortholog); FOUND IN exocyst (ortholog); secretory granule (ortholog) NW_004955484 9429578 9434982 + 9068941 102013087 A0A8C2YNU4 MODEL AGCD01058415;GBDJ01264398;XM_005403687;XM_013503982;XM_013503983;XM_013503984 XP_005403744;XP_013359436;XP_013359437;XP_013359438 exocyst complex component 3-like 1 APPROVED protein-coding ENSCLAG00000008542 NW_004955484 9429683 9434982 + 8712714 Scube1 signal peptide, CUB domain and EGF like domain containing 1 ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN positive regulation of smoothened signaling pathway (ortholog); ASSOCIATED WITH Developmental Delay with Variable Intellectual Impairment and Behavioral Abnormalities (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN cell surface (ortholog); external side of plasma membrane (ortholog); extracellular space (ortholog) NW_004955413 28339212 28461626 - 9068941 102013711 A0A8C2W3I3;A0A8C2W3J0;A0A8C2W478 MODEL AGCD01014556;AGCD01014557;GBDF01285768;XM_005379668 XP_005379725 signal peptide, CUB and EGF-like domain-containing protein 1;signal peptide, CUB domain, EGF-like 1 APPROVED protein-coding ENSCLAG00000016931 NW_004955413 28338254 28461626 - 8712742 CUNH1orf122 chromosome unknown C1orf122 homolog ASSOCIATED WITH Charcot-Marie-Tooth disease dominant intermediate C (ortholog); Galloway-Mowat Syndrome 10 (ortholog); genetic disease (ortholog) NW_004955452 15579225 15580362 + 102014638 A0A8C2V846;A0A8C2VE93 MODEL AGCD01044488;GBDF01049582;XM_005395219 XP_005395276 LOC102014638 chromosome unknown open reading frame, human C1orf122;uncharacterized protein C1orf122 homolog APPROVED protein-coding ENSCLAG00000007899 NW_004955452 15579035 15580362 + 8712749 Got1l1 glutamic-oxaloacetic transaminase 1 like 1 ASSOCIATED WITH genetic disease (ortholog); hereditary spastic paraplegia 54 (ortholog); hypogonadotropic hypogonadism 2 with or without anosmia (ortholog) NW_004955463 13622781 13627165 - 9068941 102014990 A0A8C2V0A8 MODEL AGCD01049876;GBDF01088565;XM_005398420;XM_005398421 XP_005398477;XP_005398478 glutamic-oxaloacetic transaminase 1-like 1;putative aspartate aminotransferase, cytoplasmic 2 APPROVED protein-coding ENSCLAG00000004452 NW_004955463 13622717 13627241 - 8712764 LOC102015165 prostaglandin E synthase 3-like NW_004955450 17741936 17745554 - 102015165 MODEL AGCD01042884 pseudo 8712765 Cfap53 cilia and flagella associated protein 53 INVOLVED IN cerebrospinal fluid circulation (ortholog); determination of left/right symmetry (ortholog); epithelial cilium movement involved in determination of left/right asymmetry (ortholog); ASSOCIATED WITH dextrocardia (ortholog); genetic disease (ortholog); hypoplastic left heart syndrome (ortholog); FOUND IN 9+0 motile cilium (ortholog); 9+2 motile cilium (ortholog); axoneme (ortholog) NW_004955402 35295007 35318800 - 9068941 102015679 A0A8C2V9G4 MODEL AGCD01000878;GBDJ01272671;XM_005372915;XM_013510706 XP_005372972;XP_013366160 Ccdc11 cilia- and flagella-associated protein 53;coiled-coil domain containing 11 APPROVED protein-coding ENSCLAG00000008426 NW_004955402 35295007 35318799 - 8712782 Senp5 SUMO specific peptidase 5 ENCODES a protein that exhibits SUMO-specific endopeptidase activity (ortholog); ASSOCIATED WITH autistic disorder (ortholog); chromosome 3q29 microdeletion syndrome (ortholog); genetic disease (ortholog) NW_004955420 12943783 12975239 + 9068941 102016274 A0A8C2VQH2 MODEL AGCD01020907;AGCD01020908;GBBH01137461;XM_005383146;XM_005383147;XM_005383149;XM_005383150 XP_005383203;XP_005383204;XP_005383206;XP_005383207 SUMO1/sentrin specific peptidase 5;sentrin-specific protease 5 APPROVED protein-coding ENSCLAG00000013120 NW_004955420 12943447 12975085 + 8712812 LOC102017330 uncharacterized LOC102017330 NW_004955475 519946 550542 + 102017330 MODEL AGCD01054697;AGCD01054698;AGCD01054699;AGCD01054700;GBDK01432758;XR_001230750;XR_001230751;XR_001230752 ncrna 8712820 Papln papilin, proteoglycan like sulfated glycoprotein ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); FOUND IN basement membrane (ortholog) NW_004955523 2077496 2104826 - 9068941 102017377 A0A8C2UWD1;A0A8C2UYQ2;A0A8C2V1G2 MODEL AGCD01068556;AGCD01068557;GBBH01004337;XM_013507154;XM_013507155;XM_013507156;XM_013507157;XM_013507158 XP_013362608;XP_013362609;XP_013362610;XP_013362611;XP_013362612 papilin;papilin, proteoglycan-like sulfated glycoprotein APPROVED protein-coding ENSCLAG00000004775 NW_004955523 2077856 2104134 - 8712852 Adat1 adenosine deaminase tRNA specific 1 ENCODES a protein that exhibits RNA binding (ortholog); tRNA-specific adenosine deaminase activity (ortholog); INVOLVED IN tRNA processing (ortholog); ASSOCIATED WITH genetic disease (ortholog); Joubert syndrome 20 (ortholog); prostate cancer (ortholog) NW_004955484 1942868 1964901 + 9068941 102017878 A0A8C2V754 MODEL AGCD01058073;GBDI01263685;XM_013504003;XM_013504004;XM_013504005;XM_013504006;XM_013504007;XM_013504008 XP_013359457;XP_013359458;XP_013359459;XP_013359460;XP_013359461;XP_013359462 adenosine deaminase, tRNA specific 1;adenosine deaminase, tRNA-specific 1;tRNA-specific adenosine deaminase 1 APPROVED protein-coding ENSCLAG00000006384 NW_004955484 1942529 1967830 + 8712869 LOC102018362 U2 snRNP-associated SURP motif-containing protein pseudogene NW_004955406 30253163 30256294 - 102018362 MODEL AGCD01006363 APPROVED pseudo 8712870 Fcrl1 Fc receptor like 1 ENCODES a protein that exhibits coreceptor activity (ortholog); INVOLVED IN B cell activation (ortholog); ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); parathyroid carcinoma (ortholog); FOUND IN cell surface (ortholog) NW_004955468 9641739 9660743 - 9068941 102018819 A0A8C2YT31 MODEL AGCD01052052;GBDK01419337;XM_005400129;XM_005400130;XM_005400131;XM_005400132 XP_005400186;XP_005400187;XP_005400188;XP_005400189 Fc receptor-like 1;Fc receptor-like protein 1 APPROVED protein-coding ENSCLAG00000014567 NW_004955468 9645106 9660644 - 8712895 Pmfbp1 polyamine modulated factor 1 binding protein 1 INVOLVED IN spermatogenesis (ortholog); ASSOCIATED WITH genetic disease (ortholog); male infertility (ortholog); spermatogenic failure 31 (ortholog); FOUND IN cytoplasm (ortholog); sperm connecting piece (ortholog) NW_004955484 4776358 4822312 - 9068941 102018933 A0A8C2YPF2 MODEL AGCD01058232;GBDF01043820;XM_005403532;XM_013503846;XM_013503847 XP_005403589;XP_013359300;XP_013359301 polyamine-modulated factor 1-binding protein 1 protein-coding ENSCLAG00000009396 NW_004955484 4775706 4821146 - 8712920 Awat2 acyl-CoA wax alcohol acyltransferase 2 ENCODES a protein that exhibits long-chain-alcohol O-fatty-acyltransferase activity (ortholog); retinol O-fatty-acyltransferase activity (ortholog); INVOLVED IN monoacylglycerol biosynthetic process (ortholog); wax biosynthetic process (ortholog); ASSOCIATED WITH autistic disorder (ortholog); dry eye syndrome (ortholog); genetic disease (ortholog); FOUND IN endoplasmic reticulum membrane (ortholog) NW_004955475 9594157 9634596 - 9068941 102019267 A0A8C2VFR7 MODEL AGCD01055068;GBCC01013125;XM_005401606;XM_005401607;XM_005401608 XP_005401663;XP_005401664;XP_005401665 protein-coding ENSCLAG00000009802 NW_004955475 9592984 9634811 - 8712939 Ssr3 signal sequence receptor subunit 3 ASSOCIATED WITH congenital disorder of glycosylation (ortholog); genetic disease (ortholog) NW_004955448 7554303 7569022 - 9068941 102019340 A0A8C2UMR7;A0A8C2UPE9 MODEL AGCD01041414;AGCD01041415;AGCD01041416;GBCE01031602;XM_005393079 XP_005393136 signal sequence receptor, gamma (translocon-associated protein gamma);translocon-associated protein subunit gamma APPROVED protein-coding ENSCLAG00000002284 NW_004955448 7554303 7569602 - 8712953 Lipn lipase family member N ASSOCIATED WITH autoimmune lymphoproliferative syndrome (ortholog); autosomal recessive congenital ichthyosis 8 (ortholog); genetic disease (ortholog) NW_004955425 4187537 4205066 - 9068941;7240710 102020818 A0A8C2YRV3 MODEL AGCD01025310;GBDK01267087;XM_005385863;XM_013514915 XP_005385920;XP_013370369 lipase member N;lipase, family member N APPROVED protein-coding ENSCLAG00000012833 NW_004955425 4187537 4205066 - 8712968 Ube2m ubiquitin conjugating enzyme E2 M ENCODES a protein that exhibits NEDD8 transferase activity (ortholog); ubiquitin-protein transferase activity (ortholog); INVOLVED IN positive regulation of neuron apoptotic process (ortholog); protein modification process (ortholog); protein neddylation (ortholog); PARTICIPATES IN neddylation pathway; proteasome degradation pathway involving cullin-dependent ubiquitin ligases; ASSOCIATED WITH genetic disease (ortholog) NW_004955584 1160155 1163441 - 9068941 102020859 A0A8C2UIA5;A0A8C2YI78 MODEL AGCD01075982;AGCD01075983;GBBH01001454;GBDF01004154;XM_005414400 XP_005414457 NEDD8-conjugating enzyme Ubc12;ubiquitin-conjugating enzyme E2M APPROVED protein-coding ENSCLAG00000000436 NW_004955584 1160155 1162756 - 8712981 Ndufa11 NADH:ubiquinone oxidoreductase subunit A11 INVOLVED IN mitochondrial respiratory chain complex I assembly (ortholog); ASSOCIATED WITH genetic disease (ortholog); nuclear type mitochondrial complex I deficiency 1 (ortholog); nuclear type mitochondrial complex I deficiency 14 (ortholog); FOUND IN mitochondrial respiratory chain complex I (ortholog); mitochondrion (ortholog) NW_004955495 3557016 3564999 + 9068941;7240710 102022306 A0A8C2YNI1 MODEL AGCD01061862;GBDK01308518;XM_005405752 XP_005405809 NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 11, 14.7kDa;NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 11 APPROVED protein-coding ENSCLAG00000008043 NW_004955495 3557016 3564999 + 8712989 Cnrip1 cannabinoid receptor interacting protein 1 ENCODES a protein that exhibits type 1 cannabinoid receptor binding (ortholog); INVOLVED IN negative regulation of signaling receptor activity (ortholog); regulation of signaling receptor activity (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); plasma membrane (ortholog) NW_004955424 16563499 16588711 + 9068941 102022406 A0A8C2VLR2 MODEL AGCD01024745;GBBH01102483;GBCQ01177682;XM_005385669 XP_005385726 CB1 cannabinoid receptor-interacting protein 1 protein-coding ENSCLAG00000012035 NW_004955424 16563499 16588711 + 8712997 Ramp2 receptor activity modifying protein 2 ENCODES a protein that exhibits adrenomedullin binding (ortholog); adrenomedullin receptor activity (ortholog); amylin receptor activity (ortholog); INVOLVED IN adenylate cyclase-activating G protein-coupled receptor signaling pathway (ortholog); adherens junction assembly (ortholog); adrenomedullin receptor signaling pathway (ortholog); ASSOCIATED WITH adenocarcinoma (ortholog); adult respiratory distress syndrome (ortholog); Cardiomegaly (ortholog); FOUND IN adrenomedullin receptor complex (ortholog); amylin receptor complex 2 (ortholog); cell surface (ortholog) NW_004955451 16584742 16586093 + 9068941 102022993 MODEL AGCD01043695;GBCB01022684;GBDJ01020216;XM_005394475 XP_005394532 receptor (G protein-coupled) activity modifying protein 2;receptor activity-modifying protein 2 APPROVED protein-coding 8713005 Nmnat3 nicotinamide nucleotide adenylyltransferase 3 ENCODES a protein that exhibits nicotinamide-nucleotide adenylyltransferase activity (ortholog); nicotinate-nucleotide adenylyltransferase activity (ortholog); INVOLVED IN NAD biosynthetic process (ortholog); response to tumor necrosis factor (ortholog); response to wounding (ortholog); PARTICIPATES IN de novo nicotinamide adenine dinucleotide biosynthetic pathway; nicotinamide adenine dinucleotide biosynthesis, the salvage pathway; ASSOCIATED WITH genetic disease (ortholog); glaucoma (ortholog); polycystic ovary syndrome (ortholog); FOUND IN axon (ortholog); mitochondrion (ortholog); neuronal cell body (ortholog) NW_004955508 5909808 6024301 + 9068941 102024146 A0A8C2UM28 MODEL AGCD01065911;AGCD01065912;GBDF01089477;XM_005407781;XM_013506279;XM_013506280;XM_013506281;XM_013506282;XM_013506283;XM_013506284 XP_005407838;XP_013361733;XP_013361734;XP_013361735;XP_013361736;XP_013361737;XP_013361738 nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3 protein-coding ENSCLAG00000001306 NW_004955508 5913898 6022128 + 8713018 LOC102024562 uncharacterized LOC102024562 NW_004955416 31688788 31730228 + 102024562 MODEL AGCD01017769;GBDF01307972;XR_001233366;XR_001233367;XR_001233368;XR_260450 ncrna 8713032 Hsd11b1l hydroxysteroid 11-beta dehydrogenase 1 like ASSOCIATED WITH genetic disease (ortholog); FOUND IN intracellular membrane-bounded organelle (ortholog); nucleoplasm (ortholog) NW_004955495 3732550 3733625 - 9068941 102025022 MODEL AGCD01061879;GBDF01061504;XM_013505053 XP_013360507 hydroxysteroid (11-beta) dehydrogenase 1-like APPROVED protein-coding 8713038 C2cd4c C2 calcium dependent domain containing 4C ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog) NW_004955495 7236627 7243099 + 9068941 102025260 A0A8C2VHR2 MODEL AGCD01062125;GBDF01192259;XM_005406041 XP_005406098 C2 calcium-dependent domain containing 4C;C2 calcium-dependent domain-containing protein 4C APPROVED protein-coding ENSCLAG00000010846 NW_004955495 7236627 7243099 + 8713044 Bcas4 breast carcinoma amplified sequence 4 ASSOCIATED WITH genetic disease (ortholog) NW_004955445 7542545 7603896 - 9068941 102026052 A0A8C2VBJ0 MODEL AGCD01039544;AGCD01039545;AGCD01039546;GBCE01013075;GBDI01222160;XM_013518344;XM_013518345;XM_013518346 XP_013373798;XP_013373799;XP_013373800 breast carcinoma-amplified sequence 4 protein-coding ENSCLAG00000009069 NW_004955445 7544829 7603887 - 8713054 Adss1 adenylosuccinate synthase 1 ENCODES a protein that exhibits actin filament binding (ortholog); adenylosuccinate synthase activity (ortholog); GTPase activity (ortholog); INVOLVED IN AMP biosynthetic process (ortholog); AMP salvage (ortholog); aspartate metabolic process (ortholog); PARTICIPATES IN Canavan disease pathway; de novo purine biosynthetic pathway; ASSOCIATED WITH Charcot-Marie-Tooth disease axonal type 2O (ortholog); Distal Myopathy 5 (ortholog); Experimental Diabetes Mellitus (ortholog); FOUND IN cytoplasm (ortholog) NW_004955538 3179299 3196251 + 9068941 102026474 A0A8C2UXM2;A0A8C2V305 MODEL AGCD01071153;GBCB01005620;GBDJ01133679;XM_005410839;XM_013507879 XP_005410896;XP_013363333 Adssl1 adenylosuccinate synthase like 1;adenylosuccinate synthetase isozyme 1 APPROVED protein-coding ENSCLAG00000004836 NW_004955538 3179299 3196251 + 8713073 Zbtb49 zinc finger and BTB domain containing 49 ENCODES a protein that exhibits DNA-binding transcription factor binding (ortholog); sequence-specific DNA binding (ortholog); transcription coactivator binding (ortholog); INVOLVED IN negative regulation of cell population proliferation (ortholog); positive regulation of transcription by RNA polymerase II (ortholog); regulation of cell cycle (ortholog); ASSOCIATED WITH Ellis-Van Creveld syndrome (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); microtubule cytoskeleton (ortholog) NW_004955514 5335216 5358791 - 9068941 102027003 A0A8C2W139 MODEL AGCD01067151;AGCD01067152;AGCD01067153;GBDJ01064291;XM_005408833;XM_005408834;XM_005408835;XM_005408837;XM_013506837;XM_013506838 XP_005408890;XP_005408891;XP_005408892;XP_005408894;XP_013362291;XP_013362292 zinc finger and BTB domain-containing protein 49 protein-coding ENSCLAG00000014857 NW_004955514 5335525 5351587 - 8713097 CUNH19orf18 chromosome unknown C19orf18 homolog ASSOCIATED WITH substance-related disorder (ortholog) NW_004955584 682191 690357 - 9068941 102027474 MODEL AGCD01075955;GBDF01260757;XM_013509846 XP_013365300 LOC102027474 chromosome unknown open reading frame, human C19orf18;uncharacterized protein C19orf18 homolog APPROVED protein-coding 8713105 LOC102028907 histone acetyltransferase KAT2B-like NW_004955557 683826 708841 + 102028907 MODEL AGCD01073256;AGCD01073257;AGCD01073258 pseudo 8713106 LOC102030187 tyrosine-protein kinase Fer-like NW_004955473 11140402 11146666 - 102030187 MODEL AGCD01054130 pseudo 8713107 Toe1 target of EGR1, exonuclease ENCODES a protein that exhibits 3'-5'-RNA exonuclease activity (ortholog); poly(A)-specific ribonuclease activity (ortholog); snRNA binding (ortholog); INVOLVED IN RNA phosphodiester bond hydrolysis, exonucleolytic (ortholog); snRNA 3'-end processing (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease dominant intermediate C (ortholog); colon carcinoma (ortholog); developmental and epileptic encephalopathy (ortholog); FOUND IN Cajal body (ortholog); cytoplasm (ortholog); nuclear body (ortholog) NW_004955464 12924185 12927567 - 9068941 102003324 A0A8C2UX20 MODEL AGCD01050240;GBDK01239343;XM_005398712;XM_013521661 XP_005398769;XP_013377115 target of EGR1 protein 1;target of EGR1, member 1 (nuclear) APPROVED protein-coding ENSCLAG00000003906 NW_004955464 12924191 12927567 - 8713119 LOC102003369 uncharacterized LOC102003369 NW_004955518 211147 307647 + 102003369 MODEL AGCD01067721;AGCD01067722;AGCD01067723;AGCD01067724;AGCD01067725;AGCD01067726;AGCD01067727;GBDF01095069;XR_001231851;XR_001231852 ncrna 8713124 Mbd6 methyl-CpG binding domain protein 6 ENCODES a protein that exhibits chromatin binding (ortholog); DNA binding (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); Charcot-Marie-Tooth disease axonal type 2U (ortholog); familial melanoma (ortholog); FOUND IN chromocenter (ortholog); fibrillar center (ortholog); nucleoplasm (ortholog) NW_004955458 5238570 5247711 + 9068941 102003735 A0A8C2VFG2;A0A8C2YPX0 MODEL AGCD01047470;GBDI01017619;XM_005397387;XM_005397394;XM_013520884;XM_013520885;XM_013520886;XM_013520887;XM_013520888;XM_013520889;XM_013520890;XM_013520891;XM_013520893;XR_001236449;XR_001236450 XP_005397444;XP_005397451;XP_013376338;XP_013376339;XP_013376340;XP_013376341;XP_013376342;XP_013376343;XP_013376344;XP_013376345;XP_013376347 methyl-CpG-binding domain protein 6 protein-coding ENSCLAG00000010083 NW_004955458 5238570 5247711 + 8713163 LOC102004318 vomeronasal type-2 receptor 116-like NW_004955532 320637 360886 - 102004318 MODEL AGCD01070114;AGCD01070115;AGCD01070116;XM_013507576 XP_013363030 APPROVED protein-coding 8713164 Prss56 serine protease 56 ENCODES a protein that exhibits serine-type endopeptidase activity (ortholog); INVOLVED IN camera-type eye development (ortholog); proteolysis (ortholog); ASSOCIATED WITH angle-closure glaucoma (ortholog); cholangiocarcinoma (ortholog); genetic disease (ortholog); FOUND IN endoplasmic reticulum (ortholog) NW_004955453 3440871 3446090 - 9068941;7240710 102005105 A0A8C2V7V6 MODEL AGCD01044658;AGCD01044659;GBBH01030283;GBBH01042828;XM_013519998 XP_013375452 protease, serine 56;protease, serine, 56 APPROVED protein-coding ENSCLAG00000007988 NW_004955453 3441109 3446090 - 8713180 LOC102005852 60S ribosomal protein L21 pseudogene NW_004955565 1247877 1249322 - 102005852 MODEL AGCD01074307 APPROVED pseudo 8713181 Mafb MAF bZIP transcription factor B ENCODES a protein that exhibits DNA binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); DNA-binding transcription factor activity, RNA polymerase II-specific (ortholog); INVOLVED IN abducens nerve formation (ortholog); brain segmentation (ortholog); cornified envelope assembly (ortholog); ASSOCIATED WITH cleft lip (ortholog); COVID-19 (ortholog); Duane retraction syndrome (ortholog); FOUND IN nucleus (ortholog); RNA polymerase II transcription regulator complex (ortholog); transcription regulator complex (ortholog) NW_004955445 16219675 16222913 + 9068941;7240710 102005853 MODEL AGCD01039866;GBCQ01176924;XM_005392522 XP_005392579 transcription factor MafB;v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B APPROVED protein-coding 8713186 LOC102006677 uncharacterized LOC102006677 NW_004955422 22593229 22599979 + 102006677 MODEL AGCD01023163;GBDF01074983;XR_260905 ncrna 8713191 Prex2 phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2 ENCODES a protein that exhibits GTPase activator activity (ortholog); guanyl-nucleotide exchange factor activity (ortholog); INVOLVED IN adult locomotory behavior (ortholog); dendrite morphogenesis (ortholog); G protein-coupled receptor signaling pathway (ortholog); ASSOCIATED WITH arteriovenous malformations of the brain (ortholog); cholangiocarcinoma (ortholog); genetic disease (ortholog); FOUND IN plasma membrane (ortholog) NW_004955444 11154318 11414680 - 9068941 102007377 A0A8C2UQI0;A0A8C2UTD8 MODEL AGCD01039035;AGCD01039036;AGCD01039037;AGCD01039038;AGCD01039039;AGCD01039040;AGCD01039041;GBCQ01125181;GBDK01093613;XM_005392120 XP_005392177 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2 APPROVED protein-coding ENSCLAG00000002871 NW_004955444 11154318 11414075 - 8713235 Nckap1l NCK associated protein 1 like ENCODES a protein that exhibits GTPase activator activity (ortholog); protein kinase activator activity (ortholog); protein-containing complex binding (ortholog); INVOLVED IN actin polymerization-dependent cell motility (ortholog); B cell homeostasis (ortholog); B cell receptor signaling pathway (ortholog); ASSOCIATED WITH Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog); immunodeficiency 72 (ortholog); FOUND IN cytosol (ortholog); plasma membrane (ortholog); SCAR complex (ortholog) NW_004955458 1733799 1785591 + 9068941 102008293 A0A8C2VPB2 MODEL AGCD01047202;AGCD01047203;AGCD01047204;GBDF01307320;XM_005397228 XP_005397285 NCK-associated protein 1-like APPROVED protein-coding ENSCLAG00000012783 NW_004955458 1733883 1784182 + 8713287 Krt18 keratin 18 ENCODES a protein that exhibits scaffold protein binding (ortholog); INVOLVED IN cholangiocyte apoptotic process (ortholog); extrinsic apoptotic signaling pathway (ortholog); Golgi to plasma membrane protein transport (ortholog); ASSOCIATED WITH Acute Liver Failure (ortholog); Breast Neoplasms (ortholog); Chemical and Drug Induced Liver Injury (ortholog); FOUND IN cell periphery (ortholog); centriolar satellite (ortholog); cytoplasm (ortholog) NW_004955458 227017 230752 + 9068941;7240710 102008919 A0A8C2YUA2 MODEL AGCD01047113;GBCE01028708;XM_005397132;XM_005397133 XP_005397189;XP_005397190 keratin 18, type I;keratin, type I cytoskeletal 18 APPROVED protein-coding ENSCLAG00000016350 NW_004955458 226805 232728 + 8713303 Map3k15 mitogen-activated protein kinase kinase kinase 15 ASSOCIATED WITH autistic disorder (ortholog); Coffin-Lowry syndrome (ortholog); developmental and epileptic encephalopathy 2 (ortholog) NW_004955586 5856 99662 + 9068941 102009442 A0A8C2UK45 MODEL AGCD01076017;AGCD01076018;AGCD01076019;AGCD01076020;GBDF01122059;XM_013509902 XP_013365356 protein-coding ENSCLAG00000000098 NW_004955586 5345 99534 + 8713337 LOC102011101 HAUS augmin-like complex subunit 6 pseudogene NW_004955467 12349080 12357812 + 102011101 MODEL AGCD01051631;XR_263364 LOC102013811 HAUS augmin-like complex subunit 6-like PROVISIONAL pseudo 8713342 LOC102012041 uncharacterized LOC102012041 NW_004955402 6962055 6984367 - 102012041 MODEL AGCD01000163;GBDF01177670;XR_001235410;XR_001235416;XR_001235420;XR_001235423;XR_259036 ncrna 8713347 Eef1akmt1 EEF1A lysine methyltransferase 1 ENCODES a protein that exhibits methyltransferase activity (ortholog); protein-lysine N-methyltransferase activity (ortholog); INVOLVED IN peptidyl-lysine methylation (ortholog); ASSOCIATED WITH autosomal dominant nonsyndromic deafness 3B (ortholog); autosomal recessive nonsyndromic deafness 1A (ortholog); autosomal recessive nonsyndromic deafness 1B (ortholog) NW_004955497 1509855 1540786 - 9068941 102012103 A0A8C2UX69 MODEL AGCD01062464;AGCD01062465;GBDK01144753;XM_005406311;XM_013505465 XP_005406368;XP_013360919 N6amt2 N-6 adenine-specific DNA methyltransferase 2 (putative);eukaryotic translation elongation factor 1 alpha lysine methyltransferase 1;protein-lysine N-methyltransferase N6AMT2 APPROVED protein-coding ENSCLAG00000003951 NW_004955497 1506742 1521850 - 8713356 Unk unk zinc finger ENCODES a protein that exhibits mRNA CDS binding (ortholog); polysome binding (ortholog); INVOLVED IN cell morphogenesis involved in neuron differentiation (ortholog); in utero embryonic development (ortholog); negative regulation of cytoplasmic translation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN polysome (ortholog) NW_004955506 6424638 6470406 - 9068941 102012224 A0A8C2VF01 MODEL AGCD01065420;AGCD01065421;AGCD01065422;AGCD01065423;AGCD01065424;AGCD01065425;AGCD01065426;GBDK01004322;XM_005407478 XP_005407535 RING finger protein unkempt homolog;unkempt family zinc finger;unkempt homolog APPROVED protein-coding ENSCLAG00000008106 NW_004955506 6424638 6470874 - 8713381 LOC102012343 uncharacterized LOC102012343 NW_004955427 8525675 8532142 - 102012343 MODEL AGCD01027075;GBDF01226078;XR_261241 ncrna 8713386 Eif3k eukaryotic translation initiation factor 3 subunit K ENCODES a protein that exhibits translation initiation factor activity (ortholog); INVOLVED IN translational initiation (ortholog); PARTICIPATES IN translation initiation pathway; ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); eukaryotic translation initiation factor 3 complex (ortholog) NW_004955468 849149 858239 - 9068941 102012521 A0A8C2VNQ0;A0A8C2VVW6 MODEL AGCD01051741;GBBH01000032;XM_005399841 XP_005399898 eukaryotic translation initiation factor 3, subunit K APPROVED protein-coding ENSCLAG00000012529 NW_004955468 848406 858239 - 8713398 LOC102013185 uncharacterized LOC102013185 NW_004955495 5765435 5770369 - 102013185 MODEL AGCD01062026;AGCD01062027;GBDF01083739;XR_264157 ncrna 8713405 Iqce IQ motif containing E INVOLVED IN limb morphogenesis (ortholog); positive regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH brachydactyly (ortholog); genetic disease (ortholog); immunodeficiency 11A (ortholog); FOUND IN ciliary membrane (ortholog); extrinsic component of membrane (ortholog); plasma membrane protein complex (ortholog) NW_004955460 12676649 12724613 + 9068941 102013257 A0A8C2VAX3;A0A8C2VAX6;A0A8C2VG59 MODEL AGCD01048661;AGCD01048662;GBBH01003129;GBDF01005523;XM_013521153 XP_013376607 LOC102012931 IQ domain-containing protein E;IQ domain-containing protein E-like PROVISIONAL protein-coding ENSCLAG00000008881 8713441 LOC102013793 DNA-directed RNA polymerase III subunit RPC7 pseudogene NW_004955405 1278334 1278982 + 102013793 MODEL AGCD01004601 APPROVED pseudo 8713442 LOC102014505 uncharacterized LOC102014505 NW_004955568 879303 891710 + 102014505 MODEL AGCD01074526;GBDF01226190;XR_265039 ncrna 8713447 Eif2b2 eukaryotic translation initiation factor 2B subunit beta ENCODES a protein that exhibits ATP binding (ortholog); GTP binding (ortholog); guanyl-nucleotide exchange factor activity (ortholog); INVOLVED IN central nervous system development (ortholog); hippocampus development (ortholog); myelination (ortholog); PARTICIPATES IN translation initiation pathway; ASSOCIATED WITH genetic disease (ortholog); hereditary nonpolyposis colorectal cancer type 7 (ortholog); intellectual disability (ortholog); FOUND IN axon (ortholog); cytoplasm (ortholog); endoplasmic reticulum (ortholog) NW_004955523 553356 559376 - 9068941;7240710 102014819 A0A8C2YK89 MODEL AGCD01068464;GBDF01154329;XM_005409380 XP_005409437 eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa;translation initiation factor eIF-2B subunit beta APPROVED protein-coding ENSCLAG00000003404 NW_004955523 553356 559376 - 8713459 Rab20 RAB20, member RAS oncogene family INVOLVED IN cellular response to type II interferon (ortholog); phagosome acidification (ortholog); phagosome-lysosome fusion (ortholog); ASSOCIATED WITH Anal Atresia, Hypospadias, and Penoscrotal Inversion (ortholog); COVID-19 (ortholog); factor X deficiency (ortholog); FOUND IN Golgi apparatus (ortholog); intracellular membrane-bounded organelle (ortholog); phagocytic vesicle (ortholog) NW_004955404 2087580 2088545 + 9068941 102014972 MODEL AGCD01003250;GBCQ01098101;GBDK01193260;XM_013515757 XP_013371211 ras-related protein Rab-20 protein-coding 8713466 Dmtf1 cyclin D binding myb like transcription factor 1 ENCODES a protein that exhibits DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); RNA polymerase II cis-regulatory region sequence-specific DNA binding (ortholog); INVOLVED IN positive regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH epilepsy (ortholog); genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog) NW_004955621 50457 95460 - 9068941 102016546 A0A8C2UGQ6;A0A8C2UJF0;A0A8C2ULQ7 MODEL AGCD01077372;AGCD01077373;GBDI01173819;XM_005415012;XM_013510153;XM_013510154;XM_013510155 XP_005415069;XP_013365607;XP_013365608;XP_013365609 cyclin D binding myb-like transcription factor 1;cyclin-D-binding Myb-like transcription factor 1 APPROVED protein-coding ENSCLAG00000000245 NW_004955621 50457 95460 - 8713491 Galnt5 polypeptide N-acetylgalactosaminyltransferase 5 ENCODES a protein that exhibits polypeptide N-acetylgalactosaminyltransferase activity (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); genetic disease (ortholog) NW_004955449 16051293 16113069 - 9068941 102017616 A0A8C2UU60 MODEL AGCD01042208;GBDF01039827;XM_005393412;XR_001235826 XP_005393469 LOC102017403 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 5 (GalNAc-T5);uncharacterized LOC102017403 PROVISIONAL protein-coding ENSCLAG00000003428 NW_004955449 16070476 16113161 - 8713505 Gpr37 G protein-coupled receptor 37 ENCODES a protein that exhibits G protein-coupled peptide receptor activity (ortholog); heat shock protein binding (ortholog); Hsp70 protein binding (ortholog); INVOLVED IN adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway (ortholog); dendrite development (ortholog); dopamine biosynthetic process (ortholog); ASSOCIATED WITH genetic disease (ortholog); Lewy body dementia (ortholog); malignant mesothelioma (ortholog); FOUND IN cell surface (ortholog); cytoplasm (ortholog); endoplasmic reticulum (ortholog) NW_004955479 6061424 6080129 - 9068941 102017872 A0A8C2V0R3 MODEL AGCD01056375;GBDF01251628;XM_005402343 XP_005402400 G protein-coupled receptor 37 (endothelin receptor type B-like);prosaposin receptor GPR37 APPROVED protein-coding ENSCLAG00000004210 NW_004955479 6057276 6080994 - 8713511 Greb1l GREB1 like retinoic acid receptor coactivator INVOLVED IN branching involved in ureteric bud morphogenesis (ortholog); cardiac ventricle development (ortholog); epithelial tube morphogenesis (ortholog); ASSOCIATED WITH autosomal dominant nonsyndromic deafness (ortholog); Autosomal Dominant Nonsyndromic Deafness 80 (ortholog); branchiootic syndrome (ortholog) NW_004955402 9865934 10204990 + 9068941 102018548 A0A8C2VJI2 MODEL AGCD01000233;AGCD01000234;AGCD01000235;AGCD01000236;AGCD01000237;AGCD01000238;AGCD01000239;AGCD01000240;AGCD01000241;AGCD01000242;AGCD01000243;AGCD01000244;AGCD01000245;AGCD01000246;AGCD01000247;AGCD01000248;AGCD01000249;AGCD01000250;AGCD01000251;AGCD01000252;GBDF01250435;XM_013503842 XP_013359296 growth regulation by estrogen in breast cancer 1 like;growth regulation by estrogen in breast cancer-like APPROVED protein-coding ENSCLAG00000009372 NW_004955402 10104225 10201479 + 8713550 Gpx3 glutathione peroxidase 3 ENCODES a protein that exhibits glutathione peroxidase activity (ortholog); identical protein binding (ortholog); selenium binding (ortholog); INVOLVED IN glutathione metabolic process (ortholog); hydrogen peroxide catabolic process (ortholog); response to corticosterone (ortholog); ASSOCIATED WITH adenocarcinoma (ortholog); Barrett's adenocarcinoma (ortholog); Barrett's esophagus (ortholog); FOUND IN extracellular space (ortholog) NW_004955408 2622162 2629088 - 9068941 102019030 A0A8C2VS33 MODEL AGCD01008015;GBCQ01000317;XM_005376065 XP_005376122 glutathione peroxidase 3 (plasma) APPROVED protein-coding ENSCLAG00000012373 NW_004955408 2622741 2629032 - 8713559 Ttc36 tetratricopeptide repeat domain 36 INVOLVED IN central nervous system neuron development (ortholog); memory (ortholog); negative regulation of peptidyl-threonine phosphorylation (ortholog); ASSOCIATED WITH CD3epsilon deficiency (ortholog); Chromosome 11, Partial Trisomy 11q (ortholog); Dwarfism (ortholog) NW_004955412 19670590 19672495 + 102019157 MODEL AGCD01012968;GBCQ01033714;XM_013511203 XP_013366657 tetratricopeptide repeat protein 36 APPROVED protein-coding 8713571 Filip1l filamin A interacting protein 1 like ASSOCIATED WITH genetic disease (ortholog) NW_004955427 1386163 1641985 - 9068941 102019187 A0A8C2YQZ7 MODEL AGCD01026873;AGCD01026874;AGCD01026875;AGCD01026876;AGCD01026877;AGCD01026878;AGCD01026879;GBDK01232581;XM_005386289;XM_013515090 XP_005386346;XP_013370544 filamin A interacting protein 1-like;filamin A-interacting protein 1-like APPROVED protein-coding ENSCLAG00000011562 NW_004955427 1365112 1471901 - 8713593 Cmas cytidine monophosphate N-acetylneuraminic acid synthetase PARTICIPATES IN amino sugar metabolic pathway; french type sialuria pathway; sialic acid storage disease pathway; ASSOCIATED WITH focal segmental glomerulosclerosis (ortholog); genetic disease (ortholog) NW_004955413 17575469 17596379 + 9068941 102020789 A0A8C2W3C8 MODEL AGCD01014159;GBDJ01176956;XM_005379071 XP_005379128 N-acylneuraminate cytidylyltransferase protein-coding ENSCLAG00000016228 NW_004955413 17575469 17599859 + 8713605 Ebna1bp2 EBNA1 binding protein 2 ASSOCIATED WITH Charcot-Marie-Tooth disease dominant intermediate C (ortholog); genetic disease (ortholog); GLUT1 Deficiency Syndrome (ortholog); FOUND IN chromosome (ortholog); nucleolus (ortholog) NW_004955537 2792295 2800249 - 9068941 102020955 A0A8C2URA6 MODEL AGCD01070938;GBCE01095072;XM_005410632 XP_005410689 LOC102018645 uncharacterized LOC102018645 PROVISIONAL protein-coding ENSCLAG00000002547 NW_004955537 2791502 2800249 - 8713618 Mtfr1 mitochondrial fission regulator 1 INVOLVED IN aerobic respiration (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); mitochondrion (ortholog); plasma membrane (ortholog) NW_004955444 13481270 13520673 - 9068941 102021182 A0A8C2UU03 MODEL AGCD01039101;AGCD01039102;AGCD01039103;GBCC01008320;XM_013518201 XP_013373655 protein-coding ENSCLAG00000002242 8713631 Tspan15 tetraspanin 15 ENCODES a protein that exhibits enzyme binding (ortholog); INVOLVED IN negative regulation of Notch signaling pathway (ortholog); protein localization to plasma membrane (ortholog); protein maturation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cell junction (ortholog); cell surface (ortholog); cytosol (ortholog) NW_004955437 21643018 21687355 - 9068941 102022633 A0A8C2VSQ0 MODEL AGCD01034919;GBDI01066539;XM_005390084;XM_013517075;XM_013517076 XP_005390141;XP_013372529;XP_013372530 tetraspanin-15 protein-coding ENSCLAG00000011763 NW_004955437 21641377 21688007 - 8713647 LOC102022991 opioid growth factor receptor-like protein 1 pseudogene NW_004955897 13719 14864 - 102022991 MODEL AGCD01078610 APPROVED pseudo 8713648 Plk1 polo like kinase 1 ENCODES a protein that exhibits anaphase-promoting complex binding (ortholog); ATP binding (ortholog); identical protein binding (ortholog); INVOLVED IN centrosome cycle (ortholog); establishment of mitotic spindle orientation (ortholog); establishment of protein localization (ortholog); ASSOCIATED WITH breast carcinoma (ortholog); COVID-19 (ortholog); endometriosis (ortholog); FOUND IN centriolar satellite (ortholog); centriole (ortholog); centrosome (ortholog) NW_004955493 2206353 2217231 + 9068941 102023160 A0A8C2YU47 MODEL AGCD01060935;GBCQ01178810;XM_005405103 XP_005405160 polo-like kinase 1;serine/threonine-protein kinase PLK1 APPROVED protein-coding ENSCLAG00000016113 NW_004955493 2206353 2217231 + 8713662 LOC102023454 ferritin heavy chain-like NW_004955466 10676155 10735470 - 102023454 MODEL AGCD01051071;AGCD01051072;AGCD01051073;XR_263303 pseudo 8713666 Gjb7 gap junction protein beta 7 ENCODES a protein that exhibits gap junction channel activity (ortholog); INVOLVED IN transmembrane transport (ortholog); ASSOCIATED WITH genetic disease (ortholog) NW_004955411 14285142 14303036 - 9068941 102024320 MODEL AGCD01011913;AGCD01011914;GBBH01089738;XM_005377716;XM_005377717;XM_005377718 XP_005377773;XP_005377774;XP_005377775 gap junction protein, beta 7, 25kDa APPROVED protein-coding 8713676 Apex2 apurinic/apyrimidinic endodeoxyribonuclease 2 ASSOCIATED WITH autistic disorder (ortholog); Cornelia de Lange syndrome 2 (ortholog); genetic disease (ortholog); FOUND IN fibrillar center (ortholog); intracellular membrane-bounded organelle (ortholog); mitochondrial inner membrane (ortholog) NW_004955475 2343992 2359492 + 9068941 102024790 A0A8C2W709 MODEL AGCD01054801;GBCB01086482;XM_005401531 XP_005401588 APEX nuclease (apurinic/apyrimidinic endonuclease) 2;DNA-(apurinic or apyrimidinic site) lyase 2 APPROVED protein-coding ENSCLAG00000017315 NW_004955475 2344087 2359906 + 8713689 LOC102024925 cilia- and flagella-associated protein 45-like NW_004955422 23895002 23902521 - 102024925 MODEL AGCD01023210 APPROVED pseudo 8713690 LOC102024990 T-cell surface glycoprotein CD1e, membrane-associated-like NW_004955468 10236378 10239755 + 102024990 MODEL AGCD01052075;GBDI01361288;XM_013522341 XP_013377795 protein-coding 8713691 Mybl2 MYB proto-oncogene like 2 ENCODES a protein that exhibits DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); RNA polymerase II cis-regulatory region sequence-specific DNA binding (ortholog); sequence-specific double-stranded DNA binding (ortholog); INVOLVED IN cellular response to leukemia inhibitory factor (ortholog); mitotic spindle assembly (ortholog); positive regulation of neuron apoptotic process (ortholog); ASSOCIATED WITH acute myeloid leukemia (ortholog); COVID-19 (ortholog); focal epilepsy (ortholog); FOUND IN Myb complex (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955445 13496919 13530689 - 9068941 102025300 A0A8C2VN03 MODEL AGCD01039785;AGCD01039786;GBDF01120059;XM_005392496 XP_005392553 myb-related protein B;v-myb avian myeloblastosis viral oncogene homolog-like 2 APPROVED protein-coding ENSCLAG00000010803 NW_004955445 13496919 13530689 - 8713710 LOC102025579 uncharacterized LOC102025579 NW_004955418 20819141 20822115 + 102025579 MODEL AGCD01019242;GBCQ01000651;XR_260576 ncrna 8713714 LOC102026743 uncharacterized LOC102026743 NW_004955414 33712969 33718861 + 102026743 MODEL AGCD01015821;GBDF01045373;XR_260234 ncrna 8713719 LOC102027143 uncharacterized LOC102027143 NW_004955455 4911109 4927967 - 102027143 MODEL AGCD01045705;AGCD01045706;AGCD01045707;GBDF01157410;XM_013520308 XP_013375762 LOC102026602 uncharacterized LOC102026602;uncharacterized protein LOC102027143 PROVISIONAL protein-coding 8713732 Calu calumenin ENCODES a protein that exhibits calcium ion binding (ortholog); enzyme binding (ortholog); enzyme inhibitor activity (ortholog); INVOLVED IN peripheral nervous system axon regeneration (ortholog); response to organic cyclic compound (ortholog); ASSOCIATED WITH atrial fibrillation (ortholog); colorectal carcinoma (ortholog); Developmental Disease (ortholog); FOUND IN endoplasmic reticulum (ortholog); endoplasmic reticulum lumen (ortholog); endoplasmic reticulum membrane (ortholog) NW_004955479 9541574 9572189 + 9068941 102028748 A0A8C2V0U0;A0A8C2V131;A0A8C2V6G1 MODEL AGCD01056480;AGCD01056481;AGCD01056482;GBCE01001921;XM_005402382;XM_013503287 XP_005402439;XP_013358741 protein-coding ENSCLAG00000005800 NW_004955479 9541568 9572266 + 8713747 Clptm1 CLPTM1 regulator of GABA type A receptor forward trafficking ENCODES a protein that exhibits GABA receptor binding (ortholog); INVOLVED IN regulation of postsynaptic membrane neurotransmitter receptor levels (ortholog); regulation of T cell differentiation in thymus (ortholog); ASSOCIATED WITH genetic disease (ortholog); pancreatic cancer (ortholog); FOUND IN external side of plasma membrane (ortholog); GABA-ergic synapse (ortholog) NW_004955555 2029591 2056321 + 9068941 102029671 A0A8C2YIR4 MODEL AGCD01073126;GBDF01005692;XM_005412483 XP_005412540 cleft lip and palate associated transmembrane protein 1;cleft lip and palate transmembrane protein 1;cleft lip and palate transmembrane protein 1 homolog APPROVED protein-coding ENSCLAG00000001254 NW_004955555 2029546 2058497 + 8713765 Nt5dc1 5'-nucleotidase domain containing 1 ASSOCIATED WITH body dysmorphic disorder (ortholog); congenital disorder of glycosylation Iaa (ortholog); genetic disease (ortholog) NW_004955526 568307 604941 - 9068941 102029785 MODEL AGCD01069242;AGCD01069243;AGCD01069244;GBCC01048928;XM_013507352 XP_013362806 5'-nucleotidase domain-containing protein 1 protein-coding 8713781 Irx3 iroquois homeobox 3 ENCODES a protein that exhibits DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); RNA polymerase II cis-regulatory region sequence-specific DNA binding (ortholog); INVOLVED IN atrioventricular bundle cell differentiation (ortholog); energy homeostasis (ortholog); His-Purkinje system cell differentiation (ortholog); ASSOCIATED WITH genetic disease (ortholog); Joubert syndrome (ortholog); lung disease (ortholog); FOUND IN axon (ortholog); cytoplasm (ortholog); nucleus (ortholog) NW_004955433 11944890 11948372 - 9068941 102003053 A0A8C2YSF7 MODEL AGCD01031656;GBCQ01004638;XM_005388313;XM_013516268 XP_005388370;XP_013371722 iroquois-class homeodomain protein IRX-3 protein-coding ENSCLAG00000013650 NW_004955433 11944890 11948369 - 8713794 LOC102003513 UDP-glucuronosyltransferase 1-8-like NW_004955453 2600059 2624326 - 102003513 MODEL AGCD01044634 APPROVED pseudo 8713802 Prdx1 peroxiredoxin 1 ENCODES a protein that exhibits heme binding (ortholog); identical protein binding (ortholog); peroxidase activity (ortholog); INVOLVED IN erythrocyte homeostasis (ortholog); fibroblast proliferation (ortholog); hydrogen peroxide catabolic process (ortholog); ASSOCIATED WITH asbestosis (ortholog); Charcot-Marie-Tooth disease dominant intermediate C (ortholog); COVID-19 (ortholog); FOUND IN cytoplasm (ortholog); euchromatin (ortholog); mitochondrial matrix (ortholog) NW_004955464 12761390 12773413 + 9068941 102004364 A0A8C2VKZ4;A0A8C2VNR7 MODEL AGCD01050224;AGCD01050225;AGCD01050226;AGCD01050227;AGCD01050228;GBCC01001560;GBCE01002844;XM_013521663 XP_013377117 peroxiredoxin-1 protein-coding ENSCLAG00000010656 NW_004955464 12761401 12773146 + 8713810 Dcx doublecortin ENCODES a protein that exhibits microtubule binding (ortholog); protein kinase binding (ortholog); INVOLVED IN axon extension (ortholog); brain development (ortholog); central nervous system projection neuron axonogenesis (ortholog); ASSOCIATED WITH Abnormal Cortical Gyration (ortholog); autistic disorder (ortholog); brain infarction (ortholog); FOUND IN axon (ortholog); cytoplasm (ortholog); dendrite (ortholog) NW_004955490 4354307 4469055 + 9068941;7240710 102004827 A0A8C2YIE6 MODEL AGCD01060187;AGCD01060188;XM_005404644;XM_005404645 XP_005404701;XP_005404702 neuronal migration protein doublecortin protein-coding ENSCLAG00000000751 NW_004955490 4354307 4469055 + 8713835 Mamstr MEF2 activating motif and SAP domain containing transcriptional regulator INVOLVED IN positive regulation of myotube differentiation (ortholog); positive regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN nucleus (ortholog) NW_004955559 1844488 1850301 + 9068941 102005518 A0A8C2V0L3;A0A8C2YLX1 MODEL AGCD01073675;AGCD01073676;GBCB01002515;XM_005412936 XP_005412993 MEF2-activating motif and SAP domain-containing transcriptional regulator protein-coding ENSCLAG00000005822 NW_004955559 1845514 1850021 + 8713851 Atp6ap2 ATPase H+ transporting accessory protein 2 INVOLVED IN angiotensin maturation (ortholog); central nervous system maturation (ortholog); eye pigmentation (ortholog); PARTICIPATES IN renin-angiotensin cascade pathway; ASSOCIATED WITH autistic disorder (ortholog); Congenital Disorder of Glycosylation Type IIr (ortholog); Craniofacial Abnormalities (ortholog); FOUND IN apical plasma membrane (ortholog); cell body (ortholog); endoplasmic reticulum membrane (ortholog) NW_004955565 2006154 2029921 - 9068941;7240710 102005522 A0A8C2YI87 MODEL AGCD01074337;AGCD01074338;AGCD01074339;GBCQ01011649;XM_005413271 XP_005413328 ATPase, H+ transporting, lysosomal accessory protein 2;renin receptor APPROVED protein-coding ENSCLAG00000000487 8713864 Zfp62 ZFP62 zinc finger protein ASSOCIATED WITH genetic disease (ortholog) NW_004955530 379499 394098 + 9068941 102006070 A0A8C2YKD2 MODEL AGCD01069848;GBCE01034223;XM_005410106;XM_013507546 XP_005410163;XP_013363000 zinc finger protein 62 homolog protein-coding ENSCLAG00000003627 NW_004955530 390287 393031 + 8713878 LOC102006829 uncharacterized LOC102006829 NW_004955554 382953 396502 + 102006829 MODEL AGCD01072948;GBDF01112731;XR_264945 ncrna 8713883 Tnpo3 transportin 3 ENCODES a protein that exhibits identical protein binding (ortholog); small GTPase binding (ortholog); INVOLVED IN protein import into nucleus (ortholog); ASSOCIATED WITH autosomal dominant limb-girdle muscular dystrophy type 2 (ortholog); genetic disease (ortholog); myofibrillar myopathy 5 (ortholog); FOUND IN annulate lamellae (ortholog); intracellular membrane-bounded organelle (ortholog); nuclear envelope (ortholog) NW_004955479 9739927 9831276 - 9068941;7240710 102007011 A0A8C2W1D5;A0A8C2W1G1 MODEL AGCD01056494;AGCD01056495;AGCD01056496;AGCD01056497;GBDK01146655;XM_005402403;XM_005402405 XP_005402460;XP_005402462 transportin-3 protein-coding ENSCLAG00000016298 NW_004955479 9740805 9831339 - 8713916 Trafd1 TRAF-type zinc finger domain containing 1 INVOLVED IN negative regulation of innate immune response (ortholog); response to cytokine (ortholog); ASSOCIATED WITH Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog) NW_004955482 8693323 8710226 + 9068941 102007771 A0A8C2VIV2 MODEL AGCD01057549;AGCD01057550;GBCB01077429;GBDF01048404;XM_005403189 XP_005403246 TRAF-type zinc finger domain-containing protein 1 protein-coding ENSCLAG00000009321 8713930 Ulk3 unc-51 like kinase 3 ENCODES a protein that exhibits protein serine/threonine kinase activity (ortholog); INVOLVED IN fibroblast activation (ortholog); negative regulation of smoothened signaling pathway (ortholog); positive regulation of smoothened signaling pathway (ortholog); ASSOCIATED WITH Bardet-Biedl syndrome (ortholog); Bloom syndrome (ortholog); colorectal cancer (ortholog); FOUND IN cytoplasm (ortholog) NW_004955450 3095604 3101774 + 9068941 102007958 A0A8C2V8J1 MODEL AGCD01042422;GBDI01220634;XM_005393538;XM_005393539;XM_013518858;XM_013518859 XP_005393595;XP_005393596;XP_013374312;XP_013374313 serine/threonine-protein kinase ULK3 protein-coding ENSCLAG00000007175 NW_004955450 3095607 3101832 + 8713968 Draxin dorsal inhibitory axon guidance protein INVOLVED IN anterior commissure morphogenesis (ortholog); axon guidance (ortholog); commissural neuron differentiation in spinal cord (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease type 2 (ortholog); chromosome 1p36 deletion syndrome (ortholog); COVID-19 (ortholog); FOUND IN extracellular region (ortholog) NW_004955486 2161927 2185230 - 9068941 102008420 A0A8C2V122 MODEL AGCD01058992;AGCD01058993;GBDF01260547;XM_013504311;XM_013504312 XP_013359765;XP_013359766 protein-coding ENSCLAG00000005857 NW_004955486 2161913 2174013 - 8713977 Tmem97 transmembrane protein 97 INVOLVED IN cholesterol homeostasis (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN endoplasmic reticulum (ortholog); lysosome (ortholog); nuclear membrane (ortholog) NW_004955481 4807850 4817006 - 9068941 102009178 A0A8C2VN71 MODEL AGCD01056953;GBDI01175765;XM_005402770 XP_005402827 protein-coding ENSCLAG00000012393 NW_004955481 4807850 4817006 - 8713984 Med6 mediator complex subunit 6 ENCODES a protein that exhibits DNA binding (ortholog); transcription coactivator activity (ortholog); transcription coactivator binding (ortholog); INVOLVED IN positive regulation of transcription by RNA polymerase II (ortholog); protein ubiquitination (ortholog); somatic stem cell population maintenance (ortholog); PARTICIPATES IN RNA polymerase II transcription pathway; ASSOCIATED WITH genetic disease (ortholog); FOUND IN core mediator complex (ortholog); mediator complex (ortholog); nucleoplasm (ortholog) NW_004955523 4550348 4558806 + 9068941 102009313 A0A8C2YME7 MODEL AGCD01068654;GBDF01080520;XM_005409458 XP_005409515 mediator of RNA polymerase II transcription subunit 6 protein-coding ENSCLAG00000006511 8713993 LOC102009385 olfactory receptor 2T27-like NW_004955418 29991095 30001887 - 102009385 MODEL AGCD01019496;XM_005382363 XP_005382420 APPROVED protein-coding 8713997 Slc1a2 solute carrier family 1 member 2 ENCODES a protein that exhibits cysteine transmembrane transporter activity (ortholog); glutamate:sodium symporter activity (ortholog); high-affinity L-glutamate transmembrane transporter activity (ortholog); INVOLVED IN adult behavior (ortholog); cellular response to cocaine (ortholog); cellular response to extracellular stimulus (ortholog); PARTICIPATES IN amyotrophic lateral sclerosis pathway; ASSOCIATED WITH amyotrophic lateral sclerosis (ortholog); Cocaine-Related Disorders (ortholog); developmental and epileptic encephalopathy 41 (ortholog); FOUND IN astrocyte projection (ortholog); axolemma (ortholog); axon (ortholog) NW_004955422 10929987 11082220 + 9068941 102009619 A0A8C2VWM3;A0A8C2VYR7;A0A8C2W1F9 MODEL AGCD01022749;GBDK01332009;XM_005384124;XM_005384125;XM_013514335 XP_005384181;XP_005384182;XP_013369789 excitatory amino acid transporter 2;solute carrier family 1 (glial high affinity glutamate transporter), member 2 APPROVED protein-coding ENSCLAG00000014237 NW_004955422 10930296 11073032 + 8714015 LOC102009633 chromosome unknown open reading frame, human C17orf62 INVOLVED IN innate immune response (ortholog); respiratory burst after phagocytosis (ortholog); ASSOCIATED WITH autosomal recessive chronic granulomatous disease 5 (ortholog); FOUND IN endoplasmic reticulum (ortholog) NW_004955506 697091 702900 + 9068941 102009633 A0A8C2V4C4 MODEL AGCD01065234;GBCQ01009071;XM_005407199;XM_005407201;XM_005407202;XM_013506085;XM_013506086 XP_005407256;XP_005407258;XP_005407259;XP_013361539;XP_013361540 uncharacterized protein C17orf62 homolog protein-coding ENSCLAG00000005191 NW_004955506 697599 702900 + 8714037 Ncoa3 nuclear receptor coactivator 3 ENCODES a protein that exhibits chromatin binding (ortholog); disordered domain specific binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); INVOLVED IN cell dedifferentiation (ortholog); cellular response to estradiol stimulus (ortholog); cerebellum development (ortholog); PARTICIPATES IN androgen signaling pathway; cortisol signaling pathway; estrogen signaling pathway; ASSOCIATED WITH adenocarcinoma (ortholog); Bone Neoplasms (ortholog); breast cancer (ortholog); FOUND IN chromatin (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955445 10020916 10085318 - 9068941 102010000 A0A8C2VEN1 MODEL AGCD01039639;AGCD01039640;AGCD01039641;AGCD01039642;AGCD01039643;GBDF01157839;GBDI01127910;XM_005392342 XP_005392399 protein-coding ENSCLAG00000008442 NW_004955445 10024308 10052472 - 8714068 LOC102011483 tryptase-like NW_004955442 16039127 16040641 + 102011483 A0A8C2VTK8 MODEL AGCD01037891;GBCE01068870;XM_005391590 XP_005391647 protein-coding ENSCLAG00000014024 8714078 LOC102011654 uncharacterized LOC102011654 NW_004955476 4365503 4385423 - 102011654 MODEL AGCD01055280;GBDI01309143;XR_001230807;XR_001230808;XR_001230809;XR_001230810 ncrna 8714095 Ebpl EBP like ASSOCIATED WITH chromosome 13q14 deletion syndrome (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN endoplasmic reticulum (ortholog) NW_004955431 3114160 3122448 - 9068941 102012014 A0A8C2UTK7 MODEL AGCD01029949;GBDK01284622;XM_005387891 XP_005387948 emopamil binding protein like;emopamil binding protein-like;emopamil-binding protein-like APPROVED protein-coding ENSCLAG00000003551 NW_004955431 3112134 3121780 - 8714102 Spata33 spermatogenesis associated 33 ENCODES a protein that exhibits protein-containing complex binding (ortholog); INVOLVED IN fertilization (ortholog); flagellated sperm motility (ortholog); mitophagy (ortholog); ASSOCIATED WITH autosomal recessive chronic granulomatous disease 4 (ortholog); Fanconi anemia (ortholog); Fanconi anemia complementation group A (ortholog); FOUND IN cytoplasm (ortholog); male germ cell nucleus (ortholog); mitochondrion (ortholog) NW_004955541 3223552 3232837 + 9068941 102012026 MODEL AGCD01071440;GBDI01027080;XM_005411046;XM_005411047;XM_013507946 XP_005411103;XP_005411104;XP_013363400 spermatogenesis-associated protein 33 protein-coding 8714112 Mosmo modulator of smoothened INVOLVED IN negative regulation of smoothened signaling pathway (ortholog); regulation of neuron differentiation (ortholog); regulation of protein stability (ortholog); ASSOCIATED WITH autistic disorder (ortholog); mitochondrial complex III deficiency nuclear type 5 (ortholog); schizophrenia (ortholog); FOUND IN ciliary membrane (ortholog); Golgi apparatus (ortholog); plasma membrane (ortholog) NW_004955493 760729 771996 + 9068941 102012447 MODEL AGCD01060864;GBDK01169588;XM_013504743 XP_013360197 LOC102012447 chromosome unknown open reading frame, human C16orf52;uncharacterized protein C16orf52 homolog APPROVED protein-coding 8714119 LOC102012709 40S ribosomal protein S29 pseudogene NW_004955587 108587 108779 - 102012709 MODEL AGCD01076058 APPROVED pseudo 8714120 LOC102013953 uncharacterized LOC102013953 NW_004955504 3387462 3397789 + 102013953 MODEL AGCD01064868;GBCB01085852;XR_264292 ncrna 8714125 LOC102014885 olfactory receptor 56A3 NW_004955414 21818642 21819592 + 9068941 102014885 A0A8C2W6L2 MODEL AGCD01015433;XM_005380115 XP_005380172 APPROVED protein-coding ENSCLAG00000018004 NW_004955414 21818642 21819589 + 8714128 LOC102015852 small ubiquitin-related modifier 1 pseudogene NW_004955486 515925 528616 + 102015852 MODEL AGCD01058860;XM_005404296 APPROVED pseudo 8714133 LOC102015927 olfactory receptor 6C68 NW_004955458 2895155 2896093 + 9068941 102015927 A0A8C2WEB1 MODEL AGCD01047255;XM_005397246 XP_005397303 APPROVED protein-coding ENSCLAG00000017739 NW_004955458 2895155 2896093 + 8714138 LOC102016684 tyrosine-protein kinase Fyn pseudogene NW_004955465 730076 731579 + 102016684 MODEL AGCD01050314 APPROVED pseudo 8714139 LOC102017650 Fc receptor-like protein 3 NW_004955468 9539939 9611259 - 9068941 102017650 A0A8C2VNP1 MODEL AGCD01052049;AGCD01052050;GBDI01278495;XM_005400124;XM_005400128;XM_013522495;XM_013522496;XM_013522497 XP_005400181;XP_005400185;XP_013377949;XP_013377950;XP_013377951 Fcrl3 Fc receptor-like 3 APPROVED protein-coding ENSCLAG00000012604 NW_004955468 9541384 9598899 - 8714168 Kbtbd4 kelch repeat and BTB domain containing 4 ASSOCIATED WITH congenital disorder of glycosylation type IIc (ortholog); genetic disease (ortholog); intellectual disability (ortholog) NW_004955422 717977 722918 + 102017673 A0A8C2W184 MODEL AGCD01022432;GBDF01043941;XM_005383955;XM_005383957 XP_005384012;XP_005384014 kelch repeat and BTB (POZ) domain containing 4;kelch repeat and BTB domain-containing protein 4 APPROVED protein-coding ENSCLAG00000016255 NW_004955422 718065 726324 + 8714189 Dtd1 D-aminoacyl-tRNA deacylase 1 ENCODES a protein that exhibits DNA binding (ortholog); INVOLVED IN DNA duplex unwinding (ortholog); ASSOCIATED WITH genetic disease (ortholog) NW_004955415 27089117 27195034 + 9068941 102018386 A0A8C2VY11 MODEL AGCD01016622;AGCD01016623;GBDF01081467;XM_005380934;XM_005380935 XP_005380991;XP_005380992 D-tyrosyl-tRNA deacylase 1;D-tyrosyl-tRNA(Tyr) deacylase 1 APPROVED protein-coding ENSCLAG00000015302 NW_004955415 27089044 27195040 + 8714201 Myrfl myelin regulatory factor like NW_004955405 10107312 10218739 + 9068941 102018559 A0A8C2V4K7 MODEL AGCD01004808;GBDI01321645;XM_013519404 XP_013374858 myelin regulatory factor-like APPROVED protein-coding ENSCLAG00000006967 NW_004955405 10107312 10218545 + 8714229 LOC102018637 dnaJ homolog subfamily B member 11-like NW_004955524 100914 102457 - 102018637 MODEL AGCD01068664 pseudo 8714236 LOC102019614 olfactory receptor 10T2-like NW_004955495 8054019 8062946 - 102019614 MODEL AGCD01062177;XM_005406177 XP_005406234 protein-coding 8714239 Kcna2 potassium voltage-gated channel subfamily A member 2 ENCODES a protein that exhibits delayed rectifier potassium channel activity (ortholog); kinesin binding (ortholog); outward rectifier potassium channel activity (ortholog); INVOLVED IN cerebral cortex development (ortholog); corpus callosum development (ortholog); neuronal action potential (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); developmental and epileptic encephalopathy 1 (ortholog); FOUND IN axon (ortholog); axon initial segment (ortholog); axon terminus (ortholog) NW_004955435 14074346 14080026 - 9068941 102019634 A0A8C2VAU8 MODEL AGCD01033215;AGCD01033216;GBDI01208819;XM_005388926;XM_005388927;XM_005388929;XM_005388930;XM_013516559 XP_005388983;XP_005388984;XP_005388986;XP_005388987;XP_013372013 potassium channel, voltage gated shaker related subfamily A, member 2;potassium voltage-gated channel, shaker-related subfamily, member 2 APPROVED protein-coding ENSCLAG00000006952 NW_004955435 14074346 14078806 - 8714257 LOC102020778 low affinity immunoglobulin gamma Fc region receptor III-B-like NW_004955462 14705877 14711037 + 102020778 A0A8C2V8U6 MODEL AGCD01049456;GBDF01001028;XM_005398304;XM_013521431 XP_005398361;XP_013376885 APPROVED protein-coding ENSCLAG00000007260 8714280 Ids iduronate 2-sulfatase ENCODES a protein that exhibits calcium ion binding (ortholog); iduronate-2-sulfatase activity (ortholog); sulfuric ester hydrolase activity (ortholog); INVOLVED IN dermatan sulfate catabolic process (ortholog); glycosaminoglycan catabolic process (ortholog); heparan sulfate proteoglycan catabolic process (ortholog); ASSOCIATED WITH autistic disorder (ortholog); Developmental Disabilities (ortholog); Epidermolysis Bullosa Simplex 5D with Nail Dystrophy (ortholog); FOUND IN lysosomal lumen (ortholog); lysosome (ortholog) NW_004955498 1863002 1886720 - 9068941;7240710 102021366 A0A8C2UK87 MODEL AGCD01062752;GBCE01115350;XM_005406397 XP_005406454 protein-coding ENSCLAG00000001342 NW_004955498 1860628 1886867 - 8714296 Ecd ecdysoneless cell cycle regulator ENCODES a protein that exhibits histone acetyltransferase binding (ortholog); INVOLVED IN fibroblast proliferation (ortholog); positive regulation of transcription by RNA polymerase II (ortholog); regulation of G1/S transition of mitotic cell cycle (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955437 18537726 18566870 + 9068941 102021706 A0A8C2W334 MODEL AGCD01034800;AGCD01034801;AGCD01034802;AGCD01034803;GBDF01044847;XM_005389989 XP_005390046 ecdysoneless homolog (Drosophila) APPROVED protein-coding ENSCLAG00000016794 NW_004955437 18539584 18566810 + 8714317 Tfcp2 transcription factor CP2 ENCODES a protein that exhibits cis-regulatory region sequence-specific DNA binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); RNA polymerase II cis-regulatory region sequence-specific DNA binding (ortholog); INVOLVED IN mRNA transcription by RNA polymerase II (ortholog); positive regulation of transcription by RNA polymerase II (ortholog); regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955547 1608631 1675331 - 9068941 102021920 A0A8C2UHQ0 MODEL AGCD01072234;AGCD01072235;AGCD01072236;AGCD01072237;AGCD01072238;AGCD01072239;GBDI01324425;GBDJ01132761;XM_005411895 XP_005411952 alpha-globin transcription factor CP2 protein-coding ENSCLAG00000000852 NW_004955547 1604461 1675856 - 8714356 LOC102022699 60S ribosomal protein L39 NW_004955416 31552058 31553403 + 102022699 A0A8C2VUY6 MODEL AGCD01017761;AGCD01017762;XM_005381677 XP_005381734 APPROVED protein-coding ENSCLAG00000006877;ENSCLAG00000012264 8714362 LOC102023232 transcription termination factor 1, mitochondrial-like NW_004955458 5088372 5089612 + 102023232 MODEL AGCD01047452 APPROVED pseudo 8714363 Mybpc3 myosin binding protein C3 ENCODES a protein that exhibits identical protein binding (ortholog); myosin binding (ortholog); myosin heavy chain binding (ortholog); INVOLVED IN cardiac muscle contraction (ortholog); heart morphogenesis (ortholog); myosin filament assembly (ortholog); ASSOCIATED WITH Animal Disease Models (ortholog); arrhythmogenic right ventricular dysplasia 1 (ortholog); Brugada syndrome (ortholog); FOUND IN A band (ortholog); cardiac myofibril (ortholog); myofibril (ortholog) NW_004955422 888529 902074 + 9068941;7240710 102023370 A0A8C2W0K0;A0A8C2W2Z2;A0A8C2W5B2 MODEL AGCD01022442;GBDJ01045183;XM_005383977;XM_013514330 XP_005384034;XP_013369784 myosin binding protein C, cardiac;myosin-binding protein C, cardiac-type APPROVED protein-coding ENSCLAG00000015418 NW_004955422 888589 901725 + 8714405 LOC102025233 olfactory receptor 52B2-like NW_004955414 20838501 20839444 - 102025233 MODEL AGCD01015390 pseudo 8714406 LOC102025274 olfactory receptor 9I1-like NW_004955511 2929294 2930226 + 102025274 MODEL AGCD01066436;XM_005408021 XP_005408078 protein-coding 8714409 LOC102028496 uncharacterized LOC102028496 NW_004955455 5114049 5163486 + 102028496 MODEL AGCD01045718;AGCD01045719;GBDF01044531;XR_001236287;XR_001236288;XR_001236289 ncrna 8714420 Sypl2 synaptophysin like 2 INVOLVED IN heart development (ortholog); intracellular calcium ion homeostasis (ortholog); substantia nigra development (ortholog); ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); hereditary spastic paraplegia 63 (ortholog) NW_004955435 12889266 12901455 + 9068941 102029221 A0A8C2V6Q6 MODEL AGCD01033172;AGCD01033173;GBDI01297200;GBDI01297201;XM_005388862 XP_005388919 synaptophysin-like 2;synaptophysin-like protein 2 APPROVED protein-coding ENSCLAG00000005995 NW_004955435 12888895 12904634 + 8714430 LOC102029843 C-type lectin domain family 4 member A-like NW_004955413 6845798 6858340 + 102029843 A0A8C2VVR9 MODEL AGCD01013780;AGCD01013781;GBDK01343126;XM_005378918;XM_005378919 XP_005378975;XP_005378976 protein-coding ENSCLAG00000014536 8714450 Trnat-agu transfer RNA threonine (anticodon AGU) This record serves to anchor the annotations of this class of tRNAs at multiple locations on the chinchilla, long-tailed genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMe MT 1 1 101978810 MODEL AGCD01035275;AGCD01037196;AGCD01050588;AGCD01050597;AGCD01051466;AGCD01051472;AGCD01051842;AGCD01057606;AGCD01071886 trna 8714451 LOC102003947 cytochrome c oxidase subunit 7A2, mitochondrial pseudogene NW_004955408 862783 863268 + 102003947 MODEL AGCD01007937 APPROVED pseudo 8714452 Faap100 FA core complex associated protein 100 INVOLVED IN protein monoubiquitination (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN chromatin (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955506 1515908 1525660 + 9068941 102004187 A0A8C2VT58 MODEL AGCD01065269;GBDK01145858;XM_005407273;XR_264322 XP_005407330 Fanconi anemia core complex associated protein 100;Fanconi anemia-associated protein of 100 kDa APPROVED protein-coding ENSCLAG00000012330 NW_004955506 1515998 1527668 + 8714476 Slc6a6 solute carrier family 6 member 6 ENCODES a protein that exhibits alanine transmembrane transporter activity (ortholog); amino acid transmembrane transporter activity (ortholog); amino acid:sodium symporter activity (ortholog); INVOLVED IN alanine transport (ortholog); amino acid import across plasma membrane (ortholog); beta-alanine transport (ortholog); ASSOCIATED WITH 3p deletion syndrome (ortholog); genetic disease (ortholog); Hypertaurinuric Cardiomyopathy (ortholog); FOUND IN apical plasma membrane (ortholog); basolateral plasma membrane (ortholog); dendrite (ortholog) NW_004955429 17097753 17130079 + 9068941 102004955 A0A8C2VMH2 MODEL AGCD01028845;AGCD01028846;GBBH01032840;XM_005387062;XM_005387064 XP_005387119;XP_005387121 sodium- and chloride-dependent taurine transporter;solute carrier family 6 (neurotransmitter transporter), member 6 APPROVED protein-coding ENSCLAG00000010187 NW_004955429 17098268 17130433 + 8714502 LOC102005387 uncharacterized LOC102005387 NW_004955493 5235633 5241231 + 102005387 MODEL AGCD01061061;GBDF01080114;XR_001231263 ncrna 8714507 Ing3 inhibitor of growth family member 3 ENCODES a protein that exhibits histone H2A acetyltransferase activity (ortholog); histone H4 acetyltransferase activity (ortholog); histone H4K12 acetyltransferase activity (ortholog); INVOLVED IN histone acetylation (ortholog); histone H2A acetylation (ortholog); histone H4 acetylation (ortholog); PARTICIPATES IN INO80 family mediated chromatin remodeling pathway; ASSOCIATED WITH genetic disease (ortholog); hepatocellular carcinoma (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN NuA4 histone acetyltransferase complex (ortholog); nucleoplasm (ortholog); nucleosome (ortholog) NW_004955479 2741554 2771524 + 9068941 102006242 A0A8C2UWQ6 MODEL AGCD01056281;GBDF01158853;XM_005402308;XM_005402309;XM_005402310;XM_013503291;XM_013503292 XP_005402365;XP_005402366;XP_005402367;XP_013358745;XP_013358746 inhibitor of growth family, member 3;inhibitor of growth protein 3 APPROVED protein-coding ENSCLAG00000004878 NW_004955479 2743655 2774247 + 8714527 LOC102007111 uncharacterized LOC102007111 NW_004955415 1538810 1543595 + 102007111 MODEL AGCD01015868;GBDF01258856;XR_260258 ncrna 8714532 Dxo decapping exoribonuclease ENCODES a protein that exhibits 5'-3' exonuclease activity (ortholog); magnesium ion binding (ortholog); mRNA 5'-diphosphatase activity (ortholog); INVOLVED IN mRNA catabolic process (ortholog); NAD-cap decapping (ortholog); nuclear mRNA surveillance (ortholog); PARTICIPATES IN 3'-end pre-mRNA processing pathway; RNA polymerase II transcription termination pathway; ASSOCIATED WITH genetic disease (ortholog); JMP syndrome (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955437 482866 484989 - 9068941 102007366 A0A8C2V4G9;A0A8C2V9V8 MODEL AGCD01034137;GBBH01005656;XM_005389406 XP_005389463 Dom3z dom-3 homolog Z APPROVED protein-coding ENSCLAG00000006682 NW_004955437 481554 484989 - 8714543 LOC102007462 vesicle-associated membrane protein 8 pseudogene NW_004955434 10962508 10964570 + 102007462 MODEL AGCD01032368 APPROVED pseudo 8714545 LOC102008336 60S ribosomal protein L13 pseudogene NW_004955508 1222169 1222822 + 102008336 MODEL AGCD01065759 APPROVED pseudo 8714546 Cst7 cystatin F ENCODES a protein that exhibits cysteine-type endopeptidase inhibitor activity (ortholog); peptidase inhibitor activity (ortholog); protein homodimerization activity (ortholog); INVOLVED IN inhibition of cysteine-type endopeptidase activity (ortholog); negative regulation of microglial cell activation (ortholog); negative regulation of peptidase activity (ortholog); ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog); Stomach Neoplasms (ortholog); FOUND IN cytoplasm (ortholog); cytoplasmic vesicle (ortholog); endoplasmic reticulum (ortholog) NW_004955415 31082978 31086379 + 9068941 102008720 A0A8C2YTN6 MODEL AGCD01016669;GBBH01155183;XM_005380981 XP_005381038 cystatin F (leukocystatin);cystatin-F APPROVED protein-coding ENSCLAG00000015428 NW_004955415 31082978 31086379 + 8714554 Coq5 coenzyme Q5, methyltransferase ENCODES a protein that exhibits 2-octaprenyl-6-methoxy-1,4-benzoquinone methylase activity (ortholog); INVOLVED IN methylation (ortholog); ubiquinone biosynthetic process (ortholog); PARTICIPATES IN ubiquinone biosynthetic pathway; ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrial matrix (ortholog); protein-containing complex (ortholog) NW_004955455 11124009 11142665 + 9068941 102008820 A0A8C2VKD7 MODEL AGCD01045984;GBDF01251415;XM_005396500;XM_005396501 XP_005396557;XP_005396558 2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial;coenzyme Q5 homolog, methyltransferase APPROVED protein-coding ENSCLAG00000011645 NW_004955455 11124009 11142665 + 8714568 Stap2 signal transducing adaptor family member 2 ASSOCIATED WITH amenorrhea (ortholog); genetic disease (ortholog); FOUND IN plasma membrane (ortholog) NW_004955495 4540867 4548769 + 9068941 102009074 A0A8C2VBB6;A0A8C2VHL7 MODEL AGCD01061928;AGCD01061929;GBCB01054733;GBDI01225013;XM_005405797;XM_005405798 XP_005405854;XP_005405855 signal-transducing adaptor protein 2 protein-coding ENSCLAG00000008850 NW_004955495 4541131 4553458 + 8714588 Timm21 translocase of inner mitochondrial membrane 21 INVOLVED IN mitochondrial cytochrome c oxidase assembly (ortholog); mitochondrial respiratory chain complex I assembly (ortholog); protein import into mitochondrial matrix (ortholog); PARTICIPATES IN presequence pathway of mitochondrial protein import; ASSOCIATED WITH chromosome 18q deletion syndrome (ortholog); genetic disease (ortholog); intestinal volvulus (ortholog); FOUND IN TIM23 mitochondrial import inner membrane translocase complex (ortholog) NW_004955402 57586651 57598817 + 9068941 102009241 A0A8C2VIW3 MODEL AGCD01001501;GBDF01305105;XM_005373066;XR_259107;XR_259108 XP_005373123 mitochondrial import inner membrane translocase subunit Tim21;translocase of inner mitochondrial membrane 21 homolog (yeast) APPROVED protein-coding ENSCLAG00000010578 NW_004955402 57586998 57599869 + 8714607 Dennd1c DENN domain containing 1C ENCODES a protein that exhibits guanyl-nucleotide exchange factor activity (ortholog); PARTICIPATES IN insulin responsive facilitative sugar transporter mediated glucose transport pathway; Rab family mediated signaling pathway; ASSOCIATED WITH genetic disease (ortholog); mucolipidosis type IV (ortholog); FOUND IN centrosome (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955495 3139411 3148389 + 9068941 102010278 A0A8C2VMW0;A0A8C2VV37;A0A8C2YRH0 MODEL AGCD01061828;GBBH01150256;XM_005405710;XM_005405711;XM_013505301;XM_013505302;XM_013505303;XM_013505304;XM_013505305 XP_005405767;XP_005405768;XP_013360755;XP_013360756;XP_013360757;XP_013360758;XP_013360759 DENN domain-containing protein 1C;DENN/MADD domain containing 1C APPROVED protein-coding ENSCLAG00000012303 NW_004955495 3140480 3148334 + 8714643 Znf394 zinc finger protein 394 ASSOCIATED WITH genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog) NW_004955460 15159737 15167439 - 9068941 102011414 A0A8C2UYI0 MODEL AGCD01048769;GBDJ01019048;XM_005397951 XP_005398008 protein-coding ENSCLAG00000005098 NW_004955460 15159620 15168188 - 8714655 LOC102011437 phospholipid-transporting ATPase FetA-like NW_004955472 770636 868645 - 102011437 A0A8C2UN72 MODEL AGCD01053355;AGCD01053356;AGCD01053357;AGCD01053358;AGCD01053359;AGCD01053360;AGCD01053361;AGCD01053362;AGCD01053363;GBDK01126213;XM_005401014;XM_005401015;XM_013523039;XM_013523040;XM_013523041;XM_013523042;XM_013523043 XP_005401071;XP_005401072;XP_013378493;XP_013378494;XP_013378495;XP_013378496;XP_013378497 APPROVED protein-coding ENSCLAG00000001958 8714690 Ttc29 tetratricopeptide repeat domain 29 INVOLVED IN cilium movement (ortholog); cilium organization (ortholog); ASSOCIATED WITH genetic disease (ortholog); methylmalonic acidemia cblA type (ortholog); spermatogenic failure 42 (ortholog); FOUND IN sperm flagellum (ortholog) NW_004955428 2378498 2571246 - 102011464 A0A8C2V1J7 MODEL AGCD01027633;AGCD01027634;AGCD01027635;GBBH01076528;XM_005386666;XM_013515339;XM_013515340 XP_005386723;XP_013370793;XP_013370794 tetratricopeptide repeat protein 29 protein-coding ENSCLAG00000004530 NW_004955428 2378631 2571259 - 8714706 Map4k1 mitogen-activated protein kinase kinase kinase kinase 1 ENCODES a protein that exhibits ATP binding (ortholog); MAP kinase kinase kinase kinase activity (ortholog); protein serine/threonine kinase activity (ortholog); INVOLVED IN cell population proliferation (ortholog); cellular response to phorbol 13-acetate 12-myristate (ortholog); intracellular signal transduction (ortholog); ASSOCIATED WITH genetic disease (ortholog); transient cerebral ischemia (ortholog) NW_004955468 859123 879727 + 9068941 102012846 A0A8C2VRF8;A0A8C2VW52 MODEL AGCD01051741;AGCD01051742;GBDF01026345;XM_005399842;XM_013522409 XP_005399899;XP_013377863 protein-coding ENSCLAG00000012702 NW_004955468 859126 879727 + 8714741 Stoml2 stomatin like 2 ENCODES a protein that exhibits cardiolipin binding (ortholog); GTPase binding (ortholog); T cell receptor binding (ortholog); INVOLVED IN CD4-positive, alpha-beta T cell activation (ortholog); intracellular calcium ion homeostasis (ortholog); lipid localization (ortholog); PARTICIPATES IN mitochondria fusion pathway; ASSOCIATED WITH acromesomelic dysplasia, Maroteaux type (ortholog); anauxetic dysplasia (ortholog); contact dermatitis (ortholog); FOUND IN actin cytoskeleton (ortholog); immunological synapse (ortholog); membrane raft (ortholog) NW_004955472 1079261 1082632 + 9068941 102013819 A0A8C2UNR0 MODEL AGCD01053372;AGCD01053373;GBBH01062970;XM_005401022;XM_013523046 XP_005401079;XP_013378500 stomatin (EPB72)-like 2;stomatin-like protein 2, mitochondrial APPROVED protein-coding ENSCLAG00000001785 NW_004955472 1079578 1082486 + 8714761 LOC102014157 olfactory receptor 8H1-like NW_004955511 1057094 1058032 + 102014157 MODEL AGCD01066354;XM_013506419 XP_013361873 protein-coding 8714766 LOC102014759 coiled-coil domain-containing protein 177 NW_004955466 820834 821991 + 102014759 MODEL AGCD01050678;XM_005399242 XP_005399299 Ccdc177 coiled-coil domain containing 177 APPROVED protein-coding 8714770 Ggn gametogenetin ENCODES a protein that exhibits identical protein binding (ortholog); ubiquitin protein ligase binding (ortholog); INVOLVED IN double-strand break repair (ortholog); embryo implantation (ortholog); gamete generation (ortholog); ASSOCIATED WITH genetic disease (ortholog); Spermatogenic Failure 69 (ortholog); FOUND IN cytoplasm (ortholog); nucleolus (ortholog); perinuclear region of cytoplasm (ortholog) NW_004955468 1039531 1044513 + 9068941 102015708 A0A8C2VT94;A0A8C2VXY1 MODEL AGCD01051748;AGCD01051749;GBDF01007916;XM_013522470 XP_013377924 protein-coding ENSCLAG00000013190 NW_004955468 1040453 1044441 + 8714779 Ccdc116 coiled-coil domain containing 116 ASSOCIATED WITH chromosome 22q11.2 deletion syndrome, distal (ortholog); DiGeorge syndrome (ortholog); genetic disease (ortholog); FOUND IN centrosome (ortholog) NW_004955442 17474743 17482389 - 9068941 102016317 MODEL AGCD01037955;GBDF01021116;XM_005391705;XM_005391707;XM_005391708;XM_013518019 XP_005391762;XP_005391764;XP_005391765;XP_013373473 coiled-coil domain-containing protein 116 protein-coding ENSCLAG00000029167 8714798 LOC102016593 uncharacterized LOC102016593 NW_004955417 8741394 8742945 + 102016593 MODEL AGCD01018033;GBDJ01122966;XR_260466 ncrna 8714803 LOC102016668 ras-related protein Rab-5A pseudogene NW_004955406 8075906 8076761 + 102016668 MODEL AGCD01005791 APPROVED pseudo 8714804 Mob3a MOB kinase activator 3A ASSOCIATED WITH cyclic hematopoiesis (ortholog); Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog) NW_004955495 6018368 6033399 + 9068941 102019077 A0A8C2VUS7 MODEL AGCD01062046;GBDF01005380;XM_005405922;XM_005405923;XM_005405924;XM_013505261 XP_005405979;XP_005405980;XP_005405981;XP_013360715 protein-coding ENSCLAG00000014306 NW_004955495 6018368 6035489 + 8714818 LOC102019251 uncharacterized LOC102019251 NW_004955409 23260141 23267863 - 102019251 MODEL AGCD01010059;GBBH01137462;XR_259787 ncrna 8714822 Pxmp2 peroxisomal membrane protein 2 ASSOCIATED WITH colorectal cancer (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); peroxisomal membrane (ortholog); peroxisome (ortholog) NW_004955482 366613 373339 - 9068941 102019391 A0A8C2VBE7 MODEL AGCD01057171;GBCB01058833;XM_005402949 XP_005403006 peroxisomal membrane protein 2, 22kDa APPROVED protein-coding ENSCLAG00000007105 NW_004955482 366874 373125 - 8714831 LOC102019845 uncharacterized LOC102019845 NW_004955538 147301 158216 + 102019845 MODEL AGCD01070990;GBBH01172789;XR_264783 ncrna 8714835 LOC102019856 uncharacterized LOC102019856 NW_004955442 15495092 15496400 + 102019856 MODEL AGCD01037875;GBBH01200853;XR_001235363 ncrna 8714840 Timm50 translocase of inner mitochondrial membrane 50 ENCODES a protein that exhibits interleukin-2 receptor binding (ortholog); phosphoprotein phosphatase activity (ortholog); protein serine/threonine phosphatase activity (ortholog); INVOLVED IN mitochondrial membrane organization (ortholog); protein dephosphorylation (ortholog); release of cytochrome c from mitochondria (ortholog); PARTICIPATES IN presequence pathway of mitochondrial protein import; ASSOCIATED WITH 3-methylglutaconic aciduria type 9 (ortholog); Carpenter Syndrome 2 (ortholog); congenital hypoplastic anemia (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrion (ortholog); nuclear speck (ortholog) NW_004955468 85681 94300 - 9068941 102020644 A0A8C2VX78 MODEL AGCD01051681;GBDF01010510;XM_005399767 XP_005399824 mitochondrial import inner membrane translocase subunit TIM50;translocase of inner mitochondrial membrane 50 homolog (S. cerevisiae) APPROVED protein-coding ENSCLAG00000013556 NW_004955468 83679 95113 - 8714855 Stx7 syntaxin 7 ENCODES a protein that exhibits chloride channel inhibitor activity (ortholog); protein-containing complex binding (ortholog); SNAP receptor activity (ortholog); INVOLVED IN endosome to lysosome transport (ortholog); organelle assembly (ortholog); organelle localization (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN azurophil granule (ortholog); early endosome (ortholog); endocytic vesicle (ortholog) NW_004955436 12928274 12975745 - 9068941 102021385 A0A8C2VKG8 MODEL AGCD01033846;AGCD01033847;GBDF01102992;XM_005389208;XM_005389209;XM_005389210 XP_005389265;XP_005389266;XP_005389267 syntaxin-7 protein-coding ENSCLAG00000011580 8714882 Pdcd6ip programmed cell death 6 interacting protein ENCODES a protein that exhibits calcium-dependent protein binding (ortholog); identical protein binding (ortholog); protein dimerization activity (ortholog); INVOLVED IN actomyosin contractile ring assembly (ortholog); bicellular tight junction assembly (ortholog); maintenance of epithelial cell apical/basal polarity (ortholog); ASSOCIATED WITH genetic disease (ortholog); osteoarthritis (ortholog); Primary Autosomal Recessive Microcephaly 29 (ortholog); FOUND IN actomyosin (ortholog); cytosol (ortholog); endoplasmic reticulum exit site (ortholog) NW_004955421 1034843 1109637 + 9068941 102022707 A0A8C2YKP2 MODEL AGCD01021587;AGCD01021588;GBDI01120341;XM_005383657;XM_005383658 XP_005383714;XP_005383715 protein-coding ENSCLAG00000004047 NW_004955421 1034843 1110438 + 8714909 Pdlim3 PDZ and LIM domain 3 ENCODES a protein that exhibits actinin binding (ortholog); cytoskeletal protein binding (ortholog); structural constituent of muscle (ortholog); INVOLVED IN actin filament organization (ortholog); heart development (ortholog); skeletal muscle tissue development (ortholog); ASSOCIATED WITH arrhythmogenic right ventricular cardiomyopathy (ortholog); autistic disorder (ortholog); cardiomyopathy (ortholog); FOUND IN actin cytoskeleton (ortholog); cytosol (ortholog); Z disc (ortholog) NW_004955403 23546291 23579975 + 9068941 102023423 A0A8C2VP91;A0A8C2VWE8;A0A8C2YRR5 MODEL AGCD01002248;GBCB01003860;XM_005373451;XM_005373453;XM_005373455 XP_005373508;XP_005373510;XP_005373512 PDZ and LIM domain protein 3 protein-coding ENSCLAG00000012689 NW_004955403 23546291 23579975 + 8714944 LOC102023797 uncharacterized LOC102023797 NW_004955471 5896019 5897182 + 102023797 MODEL AGCD01053115;GBDF01054811;XR_263526 ncrna 8714948 Npr3 natriuretic peptide receptor 3 ENCODES a protein that exhibits chloride ion binding (ortholog); G protein-coupled peptide receptor activity (ortholog); hormone binding (ortholog); INVOLVED IN adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway (ortholog); angiogenesis (ortholog); blood vessel remodeling (ortholog); PARTICIPATES IN C-type natriuretic peptide signaling pathway; ASSOCIATED WITH bone disease (ortholog); BOUDIN-MORTIER SYNDROME (ortholog); diabetic retinopathy (ortholog); FOUND IN protein-containing complex (ortholog) NW_004955426 18491350 18559299 + 9068941 102024479 A0A8C2VFM4 MODEL AGCD01026524;AGCD01026525;GBCE01056173;XM_005386161;XM_005386162 XP_005386218;XP_005386219 atrial natriuretic peptide receptor 3;natriuretic peptide receptor C/guanylate cyclase C (atrionatriuretic peptide receptor C) APPROVED protein-coding ENSCLAG00000008283 NW_004955426 18491350 18553743 + 8714964 Dgka diacylglycerol kinase alpha ENCODES a protein that exhibits ATP-dependent diacylglycerol kinase activity (ortholog); kinase activity (ortholog); lipid binding (ortholog); INVOLVED IN diacylglycerol metabolic process (ortholog); glycerolipid metabolic process (ortholog); lipid phosphorylation (ortholog); PARTICIPATES IN D-glycericacidemia pathway; familial lipoprotein lipase deficiency pathway; glycerol kinase deficiency pathway; ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); plasma membrane (ortholog) NW_004955458 3517519 3544651 + 9068941 102024532 A0A8C2YNT0 MODEL AGCD01047314;AGCD01047315;AGCD01047316;AGCD01047317;GBCE01166881;XM_005397269;XM_013520902;XM_013520903;XM_013520904;XM_013520905 XP_005397326;XP_013376356;XP_013376357;XP_013376358;XP_013376359 diacylglycerol kinase, alpha 80kDa APPROVED protein-coding ENSCLAG00000008477 NW_004955458 3524542 3544374 + 8714992 LOC102026589 vomeronasal type-2 receptor 116-like NW_004955600 608288 614453 - 102026589 MODEL AGCD01076740;AGCD01076741;XM_005414814 XP_005414871 APPROVED protein-coding 8714998 LOC102026661 acyl-protein thioesterase 1-like NW_004955430 8305298 8308149 - 102026661 MODEL AGCD01029385 pseudo 8714999 Dtna dystrobrevin alpha ENCODES a protein that exhibits PDZ domain binding (ortholog); phosphatase binding (ortholog); ASSOCIATED WITH Cardiac Arrhythmias (ortholog); cardiomyopathy (ortholog); dilated cardiomyopathy (ortholog); FOUND IN axon (ortholog); cell junction (ortholog); cell projection (ortholog) NW_004955402 21414122 21676389 + 9068941;7240710 102026692 A0A8C2VAE5;A0A8C2VAW5;A0A8C2YNY9;A0A8C2YNZ2 MODEL AGCD01000590;AGCD01000591;AGCD01000592;GBDJ01229810;XM_005372772;XM_005372773;XM_005372775;XM_005372778;XM_005372779;XM_005372780;XM_005372782;XM_005372783;XM_005372786;XM_005372788;XM_005372790;XM_013508451;XM_013508483;XM_013508554;XM_013508773;XM_013508872 XP_005372829;XP_005372830;XP_005372832;XP_005372835;XP_005372836;XP_005372837;XP_005372839;XP_005372840;XP_005372843;XP_005372845;XP_005372847;XP_013363905;XP_013363937;XP_013364008;XP_013364227;XP_013364326 dystrobrevin, alpha APPROVED protein-coding ENSCLAG00000008729 NW_004955402 21315889 21673044 + 8715082 Znf282 zinc finger protein 282 ENCODES a protein that exhibits sequence-specific double-stranded DNA binding (ortholog); ASSOCIATED WITH genetic disease (ortholog) NW_004955491 4457963 4480732 + 9068941 102027864 A0A8C2UMT6 MODEL AGCD01060435;AGCD01060436;AGCD01060437;AGCD01060438;AGCD01060439;GBCE01095666;GBDK01022328;XM_013504590 XP_013360044 APPROVED protein-coding ENSCLAG00000001502 NW_004955491 4458051 4479143 + 8715103 Oxnad1 oxidoreductase NAD binding domain containing 1 ASSOCIATED WITH 3p deletion syndrome (ortholog); genetic disease (ortholog) NW_004955430 8550370 8586863 + 9068941 102027888 A0A8C2VC48 MODEL AGCD01029389;GBDF01193697;XM_005387452;XM_013515697;XM_013515698 XP_005387509;XP_013371151;XP_013371152 oxidoreductase NAD-binding domain containing 1;oxidoreductase NAD-binding domain-containing protein 1 APPROVED protein-coding ENSCLAG00000009252 NW_004955430 8550372 8586863 + 8715118 Abi1 abl interactor 1 ENCODES a protein that exhibits protein tyrosine kinase activator activity (ortholog); SH3 domain binding (ortholog); signaling adaptor activity (ortholog); INVOLVED IN dendrite morphogenesis (ortholog); lamellipodium morphogenesis (ortholog); megakaryocyte development (ortholog); PARTICIPATES IN E-cadherin signaling pathway; platelet-derived growth factor signaling pathway; ASSOCIATED WITH Chemical and Drug Induced Liver Injury (ortholog); genetic disease (ortholog); primary coenzyme Q10 deficiency 2 (ortholog); FOUND IN cell leading edge (ortholog); filopodium tip (ortholog); glutamatergic synapse (ortholog) NW_004955429 2682341 2783752 + 9068941 102028665 A0A8C2VGY6;A0A8C2VH17;A0A8C2VH20;A0A8C2YQB6;A0A8C2YQC1 MODEL AGCD01028435;AGCD01028436;AGCD01028437;AGCD01028438;GBDF01119577;XM_005386876;XM_005386878;XM_005386879;XM_005386881;XM_005386882;XM_005386884;XM_005386885;XM_005386886;XM_005386888;XM_005386890;XM_005386891;XM_013515431;XM_013515432 XP_005386933;XP_005386935;XP_005386936;XP_005386938;XP_005386939;XP_005386941;XP_005386942;XP_005386943;XP_005386945;XP_005386947;XP_005386948;XP_013370885;XP_013370886 abl-interactor 1 APPROVED protein-coding ENSCLAG00000010653 NW_004955429 2682343 2783752 + 8715171 LOC102028807 hematological and neurological expressed 1 protein pseudogene NW_004955444 9014695 9015132 + 102028807 MODEL AGCD01038953 APPROVED pseudo 8715172 Rhobtb3 Rho related BTB domain containing 3 ENCODES a protein that exhibits ATP binding (ortholog); ATP hydrolysis activity (ortholog); small GTPase binding (ortholog); INVOLVED IN male gonad development (ortholog); retrograde transport, endosome to Golgi (ortholog); ASSOCIATED WITH COVID-19 (ortholog); familial adenomatous polyposis 1 (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog) NW_004955418 16772363 16839347 - 9068941 102028966 MODEL AGCD01019128;AGCD01019129;GBCE01159877;GBDK01193526;XM_013512974 XP_013368428 Rho-related BTB domain containing 3;rho-related BTB domain-containing protein 3 APPROVED protein-coding 8715189 Pde6c phosphodiesterase 6C INVOLVED IN phototransduction, visible light (ortholog); retinal cone cell development (ortholog); sensory perception of light stimulus (ortholog); PARTICIPATES IN visual phototransduction pathway; ASSOCIATED WITH achromatopsia (ortholog); Achromatopsia 5 (ortholog); amphetamine abuse (ortholog) NW_004955507 129678 179586 + 9068941;7240710 102029539 A0A8C2UX87;A0A8C2V2T3 MODEL AGCD01065463;AGCD01065464;GBDF01128897;XM_005407518;XM_005407519 XP_005407575;XP_005407576 cone cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha';phosphodiesterase 6C, cGMP-specific, cone, alpha prime APPROVED protein-coding ENSCLAG00000004779 NW_004955507 129678 179305 + 8715217 LOC102029656 methionine aminopeptidase 2 pseudogene NW_004955433 11147410 11149598 + 102029656 MODEL AGCD01031649 APPROVED pseudo 8715218 Rmnd1 required for meiotic nuclear division 1 homolog INVOLVED IN positive regulation of mitochondrial translation (ortholog); ASSOCIATED WITH Breast Neoplasms (ortholog); combined oxidative phosphorylation deficiency 11 (ortholog); genetic disease (ortholog); FOUND IN mitochondrion (ortholog) NW_004955439 10151357 10193765 + 9068941;7240710 102029902 A0A8C2UTI4 MODEL AGCD01035858;GBDF01252199;XM_005390579;XM_005390581 XP_005390636;XP_005390638 required for meiotic nuclear division protein 1 homolog APPROVED protein-coding ENSCLAG00000003248 8715244 trnL1(tag) MT 11681 11750 + 15822232 trna 8715245 Zfc3h1 zinc finger C3H1-type containing ASSOCIATED WITH Dwarfism (ortholog); genetic disease (ortholog); juvenile rheumatoid arthritis (ortholog); FOUND IN exosome (RNase complex) (ortholog); nucleolus (ortholog); nucleus (ortholog) NW_004955405 11598802 11647135 - 9068941 102004348 A0A8C2V6P2 MODEL AGCD01004835;GBDK01229431;XM_005374321 XP_005374378 zinc finger, C3H1-type containing APPROVED protein-coding ENSCLAG00000007646 NW_004955405 11596399 11647135 - 8715284 LOC102004542 zinc finger protein 14-like NW_004955607 5112 93169 + 102004542 MODEL AGCD01076967;AGCD01076968;AGCD01076969;AGCD01076970;AGCD01076971;AGCD01076972;AGCD01076973;AGCD01076974;XM_005414908 pseudo 8715297 LOC102004631 quinone oxidoreductase-like protein 2 NW_004955432 19214738 19226859 - 102004631 MODEL AGCD01031171;AGCD01031172;AGCD01031173;AGCD01031174 APPROVED pseudo 8715298 Ptpro protein tyrosine phosphatase receptor type O ENCODES a protein that exhibits cadherin binding (ortholog); protein homodimerization activity (ortholog); protein tyrosine phosphatase activity (ortholog); INVOLVED IN axon guidance (ortholog); cell morphogenesis (ortholog); glomerulus development (ortholog); ASSOCIATED WITH autosomal dominant intellectual developmental disorder 6 (ortholog); COVID-19 (ortholog); developmental and epileptic encephalopathy 27 (ortholog); FOUND IN apical plasma membrane (ortholog); dendritic spine (ortholog); GABA-ergic synapse (ortholog) NW_004955413 12019026 12248026 + 9068941;7240710 102005022 A0A8C2W2T8;A0A8C2W2V3 MODEL AGCD01013977;AGCD01013978;AGCD01013979;AGCD01013980;AGCD01013981;AGCD01013982;AGCD01013983;AGCD01013984;AGCD01013985;GBDJ01377144;XM_005379017;XM_013511680;XM_013511681 XP_005379074;XP_013367134;XP_013367135 receptor-type tyrosine-protein phosphatase O APPROVED protein-coding ENSCLAG00000016725 NW_004955413 12018888 12248807 + 8715336 Perp p53 apoptosis effector related to PMP22 INVOLVED IN activation of cysteine-type endopeptidase activity (ortholog); amelogenesis (ortholog); desmosome organization (ortholog); ASSOCIATED WITH Erythrokeratodermia Variabilis et Progressiva 7 (ortholog); familial Behcet-like autoinflammatory syndrome (ortholog); genetic disease (ortholog); FOUND IN Golgi apparatus (ortholog); mitochondrion (ortholog); plasma membrane (ortholog) NW_004955436 21425321 21430780 + 9068941 102007150 A0A8C2VBE5 MODEL AGCD01034054;GBCC01000076;GBDI01001313;XM_013516698 XP_013372152 PERP, TP53 apoptosis effector;p53 apoptosis effector related to PMP-22 APPROVED protein-coding ENSCLAG00000009030 NW_004955436 21417332 21431312 + 8715346 Znf275 zinc finger protein 275 ASSOCIATED WITH autistic disorder (ortholog); syndromic X-linked intellectual disability Lubs type (ortholog) NW_004955580 83091 99862 + 9068941 102007383 A0A8C2UUT5 MODEL AGCD01075585;GBDF01224114;XM_005414108;XM_005414109;XM_005414111;XM_005414112;XM_013509714 XP_005414165;XP_005414166;XP_005414168;XP_005414169;XP_013365168 protein-coding ENSCLAG00000002477 8715372 Aass aminoadipate-semialdehyde synthase ENCODES a protein that exhibits saccharopine dehydrogenase (NAD+, L-glutamate-forming) activity (ortholog); saccharopine dehydrogenase (NADP+, L-lysine-forming) activity (ortholog); INVOLVED IN L-lysine catabolic process (ortholog); lysine catabolic process (ortholog); PARTICIPATES IN 2-aminoadipic 2-oxoadipic aciduria pathway; glutaric aciduria type I pathway; hyperlysinemia pathway; ASSOCIATED WITH Chemical and Drug Induced Liver Injury (ortholog); genetic disease (ortholog); hyperlysinemia (ortholog); FOUND IN intracellular membrane-bounded organelle (ortholog); mitochondrion (ortholog) NW_004955479 3746003 3805835 - 9068941;7240710 102008622 A0A8C2VBG2 MODEL AGCD01056301;AGCD01056302;AGCD01056303;GBDJ01423946;GBDK01279764;XM_013503294 XP_013358748 alpha-aminoadipic semialdehyde synthase, mitochondrial protein-coding ENSCLAG00000008604 NW_004955479 3742757 3814338 - 8715403 Cdk18 cyclin dependent kinase 18 ASSOCIATED WITH autistic disorder (ortholog); familial adult myoclonic epilepsy 5 (ortholog); gastrointestinal stromal tumor (ortholog) NW_004955406 41228802 41256413 + 9068941 102009249 A0A8C2VN56 MODEL AGCD01006674;AGCD01006675;GBBH01188253;XM_005375359 XP_005375416 cyclin-dependent kinase 18 APPROVED protein-coding ENSCLAG00000010383 NW_004955406 41228678 41252543 + 8715429 LOC102009800 uncharacterized LOC102009800 NW_004955407 17251314 17300456 + 102009800 MODEL AGCD01007243;AGCD01007244;AGCD01007245;AGCD01007246;GBDF01192314;XR_001231024 ncrna 8715438 Peli3 pellino E3 ubiquitin protein ligase family member 3 ENCODES a protein that exhibits ubiquitin protein ligase activity (ortholog); ubiquitin-protein transferase activity (ortholog); INVOLVED IN defense response to Gram-negative bacterium (ortholog); negative regulation of extrinsic apoptotic signaling pathway (ortholog); negative regulation of protein ubiquitination (ortholog); PARTICIPATES IN interleukin-1 signaling pathway; ASSOCIATED WITH Aicardi-Goutieres Syndrome 3 (ortholog); Bardet-Biedl syndrome (ortholog); congenital muscular dystrophy-dystroglycanopathy type A13 (ortholog) NW_004955422 18868696 18877826 - 9068941 102010594 A0A8C2W161;A0A8C2W605 MODEL AGCD01022964;GBDF01002198;XM_005384400;XM_005384401;XM_005384402 XP_005384457;XP_005384458;XP_005384459 E3 ubiquitin-protein ligase pellino homolog 3 protein-coding ENSCLAG00000016239 NW_004955422 18868696 18877438 - 8715454 Akap1 A-kinase anchoring protein 1 ENCODES a protein that exhibits beta-tubulin binding (ortholog); microtubule binding (ortholog); molecular adaptor activity (ortholog); INVOLVED IN antiviral innate immune response (ortholog); apoptotic process (ortholog); cellular response to cAMP (ortholog); PARTICIPATES IN protein kinase A (PKA) signaling pathway; vascular endothelial growth factor signaling pathway; ASSOCIATED WITH brain ischemia (ortholog); genetic disease (ortholog); Joubert syndrome (ortholog); FOUND IN cytoplasm (ortholog); lipid droplet (ortholog); mitochondrial crista (ortholog) NW_004955451 5756648 5787617 - 9068941 102010655 A0A8C2VXV9;A0A8C2YTJ4 MODEL AGCD01043175;AGCD01043176;GBCE01114894;XM_005394060;XM_013519400;XM_013519401;XM_013519402 XP_005394117;XP_013374854;XP_013374855;XP_013374856 A kinase (PRKA) anchor protein 1;A-kinase anchor protein 1, mitochondrial APPROVED protein-coding ENSCLAG00000015261 NW_004955451 5756835 5770238 - 8715479 Itgb2 integrin subunit beta 2 ENCODES a protein that exhibits amyloid-beta binding (ortholog); cargo receptor activity (ortholog); cell adhesion molecule binding (ortholog); INVOLVED IN activated T cell proliferation (ortholog); amyloid-beta clearance (ortholog); cell adhesion (ortholog); PARTICIPATES IN hypoxia inducible factor pathway; integrin mediated signaling pathway; ASSOCIATED WITH Acute Lung Injury (ortholog); acute promyelocytic leukemia (ortholog); allergic disease (ortholog); FOUND IN cell surface (ortholog); external side of plasma membrane (ortholog); integrin alphaL-beta2 complex (ortholog) NW_004955407 41779849 41805637 - 9068941;7240710 102010671 A0A8C2VKA8 MODEL AGCD01007882;GBBH01033820;XM_005375904;XM_005375905;XM_005375906;XM_013505502;XM_013505508;XM_013505517;XM_013505519;XM_013505523 XP_005375961;XP_005375962;XP_005375963;XP_013360956;XP_013360962;XP_013360971;XP_013360973;XP_013360977 integrin beta-2;integrin, beta 2 (complement component 3 receptor 3 and 4 subunit) APPROVED protein-coding ENSCLAG00000011530 NW_004955407 41777777 41800201 - 8715506 LOC102010697 olfactory receptor 2L3-like NW_004955418 30109107 30110042 + 102010697 MODEL AGCD01019503;XM_005382366 XP_005382423 protein-coding 8715509 CUNH22orf23 chromosome unknown C22orf23 homolog ASSOCIATED WITH adenylosuccinase lyase deficiency (ortholog); Emery-Dreifuss muscular dystrophy (ortholog); genetic disease (ortholog) NW_004955413 24291712 24300294 - 9068941 102012847 MODEL AGCD01014360;GBDF01011259;XM_005379234;XM_013511473 XP_005379291;XP_013366927 LOC102012847 UPF0193 protein EVG1;UPF0193 protein EVG1 homolog;chromosome unknown open reading frame, human C22orf23 APPROVED protein-coding 8715523 LOC102012988 uncharacterized LOC102012988 NW_004955429 20903019 20922730 - 102012988 MODEL AGCD01028992;GBDF01263063;XR_261369 ncrna 8715528 Otoa otoancorin INVOLVED IN cell-matrix adhesion (ortholog); sensory perception of sound (ortholog); transmission of nerve impulse (ortholog); ASSOCIATED WITH autosomal recessive nonsyndromic deafness (ortholog); autosomal recessive nonsyndromic deafness 22 (ortholog); autosomal recessive nonsyndromic deafness 7 (ortholog); FOUND IN apical plasma membrane (ortholog) NW_004955493 1154695 1228997 + 9068941;7240710 102013425 A0A8C2VNK4;A0A8C2VNQ5;A0A8C2YRN3;A0A8C2YRP0 MODEL AGCD01060882;AGCD01060883;AGCD01060884;AGCD01060885;AGCD01060886;AGCD01060887;GBBH01195751;XM_013504888 XP_013360342 protein-coding ENSCLAG00000012547 NW_004955493 1154751 1224962 + 8715561 LOC102014142 uncharacterized LOC102014142 NW_004955422 14683499 14685264 + 102014142 MODEL AGCD01022863;GBDF01252177;XR_001233942 ncrna 8715568 LOC102014473 olfactory receptor 8H1-like NW_004955511 1088261 1089199 + 102014473 MODEL AGCD01066356;XM_013506423 XP_013361877 APPROVED protein-coding 8715569 LOC102014488 eukaryotic initiation factor 4A-I-like NW_004955537 31525 32199 + 102014488 MODEL AGCD01070847;GBDF01010973;XM_013507746 XP_013363200 protein-coding 8715575 LOC102015055 lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog NW_004955442 9360262 9366950 - 102015055 MODEL AGCD01037678;GBDF01277879;XM_005391208;XM_005391210;XM_013517832;XM_013517833;XM_013517834 XP_005391265;XP_005391267;XP_013373286;XP_013373287;XP_013373288 uncharacterized protein C6orf132 homolog;uncharacterized protein LOC102015055 protein-coding 8715598 LOC102015088 eukaryotic translation initiation factor 5 pseudogene NW_004955411 11502058 11504279 + 102015088 MODEL AGCD01011822 APPROVED pseudo 8715599 B3gat3 beta-1,3-glucuronyltransferase 3 ENCODES a protein that exhibits glucuronosyltransferase activity (ortholog); protein phosphatase activator activity (ortholog); INVOLVED IN chondroitin sulfate proteoglycan biosynthetic process (ortholog); dermatan sulfate proteoglycan biosynthetic process (ortholog); glycosaminoglycan biosynthetic process (ortholog); ASSOCIATED WITH Craniofacial Abnormalities (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN cis-Golgi network (ortholog); Golgi apparatus (ortholog) NW_004955599 573982 578032 + 9068941;7240710 102015263 A0A8C2URW4 MODEL AGCD01076660;GBDK01069802;XM_005414790 XP_005414847 beta-1,3-glucuronyltransferase 3 (glucuronosyltransferase I);galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 APPROVED protein-coding ENSCLAG00000001628 NW_004955599 573426 578032 + 8715608 Olig2 oligodendrocyte transcription factor 2 ENCODES a protein that exhibits DNA-binding transcription factor activity (ortholog); DNA-binding transcription factor activity, RNA polymerase II-specific (ortholog); HMG box domain binding (ortholog); INVOLVED IN myelination (ortholog); negative regulation of neuron differentiation (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH amyotrophic lateral sclerosis type 1 (ortholog); autosomal dominant intellectual developmental disorder 7 (ortholog); Experimental Autoimmune Encephalomyelitis (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog) NW_004955407 32432888 32436209 + 9068941 102015606 A0A8C2YPU7 MODEL AGCD01007675;AGCD01007676;GBDJ01093209;XM_005375974 XP_005376031 oligodendrocyte lineage transcription factor 2 APPROVED protein-coding ENSCLAG00000009979 NW_004955407 32433849 32434923 + 8715614 Ap3b1 adaptor related protein complex 3 subunit beta 1 ENCODES a protein that exhibits GTP-dependent protein binding (ortholog); protein phosphatase binding (ortholog); INVOLVED IN anterograde axonal transport (ortholog); anterograde synaptic vesicle transport (ortholog); antigen processing and presentation (ortholog); ASSOCIATED WITH Chediak-Higashi syndrome (ortholog); cyclic hematopoiesis (ortholog); genetic disease (ortholog) NW_004955425 22792616 23051509 + 9068941;7240710 102015649 A0A8C2YUZ8 MODEL AGCD01025833;AGCD01025834;AGCD01025835;AGCD01025836;AGCD01025837;AGCD01025838;GBDF01157461;XM_005386022 XP_005386079 AP-3 complex subunit beta-1;adaptor related protein complex 3 beta 1 subunit;adaptor-related protein complex 3, beta 1 subunit APPROVED protein-coding ENSCLAG00000017374 NW_004955425 22792616 23051737 + 8715651 Mmp27 matrix metallopeptidase 27 ASSOCIATED WITH asphyxiating thoracic dystrophy (ortholog); ataxia telangiectasia (ortholog); genetic disease (ortholog); FOUND IN extrinsic component of endoplasmic reticulum membrane (ortholog) NW_004955412 5912877 5922463 - 9068941 102016143 A0A8C2YQF2 MODEL AGCD01012660;GBDF01130176;XM_005377983 XP_005378040 matrix metalloproteinase-27 protein-coding ENSCLAG00000010798 NW_004955412 5912877 5922463 - 8715664 LOC102016624 oxidative stress-responsive serine-rich protein 1 pseudogene NW_004955430 7526938 7528180 - 102016624 MODEL AGCD01029355 APPROVED pseudo 8715665 Dcp2 decapping mRNA 2 ENCODES a protein that exhibits 5'-(N(7)-methylguanosine 5'-triphospho)-[mRNA] hydrolase activity (ortholog); 5'-3' RNA exonuclease activity (ortholog); INVOLVED IN histone mRNA catabolic process (ortholog); mRNA catabolic process (ortholog); negative regulation of telomere maintenance via telomerase (ortholog); PARTICIPATES IN microRNA pathway; ASSOCIATED WITH familial adenomatous polyposis 1 (ortholog); genetic disease (ortholog); Hereditary Neoplastic Syndromes (ortholog); FOUND IN cell junction (ortholog); cytoplasmic ribonucleoprotein granule (ortholog); nucleoplasm (ortholog) NW_004955408 32868184 32923788 + 9068941 102018473 A0A8C2VYZ5;A0A8C2W391 MODEL AGCD01008857;AGCD01008858;GBDF01250860;XM_005376510;XM_013506864 XP_005376567;XP_013362318 m7GpppN-mRNA hydrolase protein-coding ENSCLAG00000014751 NW_004955408 32868184 32916807 + 8715687 Rap1gds1 Rap1 GTPase-GDP dissociation stimulator 1 ENCODES a protein that exhibits GTPase regulator activity (ortholog); guanyl-nucleotide exchange factor activity (ortholog); INVOLVED IN angiotensin-activated signaling pathway involved in heart process (ortholog); CAAX-box protein maturation (ortholog); cardiac muscle hypertrophy (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); endoplasmic reticulum (ortholog); extracellular space (ortholog) NW_004955405 8555117 8708604 + 9068941 102019351 A0A8C2UWP1;A0A8C2YL08;A0A8C2YL09 MODEL AGCD01004747;AGCD01004748;AGCD01004749;AGCD01004750;GBDF01002792;GBDF01002797;XM_013517446;XM_013517447 XP_013372900;XP_013372901 RAP1, GTP-GDP dissociation stimulator 1 APPROVED protein-coding ENSCLAG00000004545 NW_004955405 8573932 8709990 + 8715714 LOC102019411 probable global transcription activator SNF2L2 NW_004955500 1745320 1748206 + 102019411 MODEL AGCD01063681 APPROVED pseudo 8715715 Fbxl3 F-box and leucine rich repeat protein 3 ENCODES a protein that exhibits ubiquitin-protein transferase activity (ortholog); INVOLVED IN entrainment of circadian clock by photoperiod (ortholog); proteasome-mediated ubiquitin-dependent protein catabolic process (ortholog); protein destabilization (ortholog); ASSOCIATED WITH chromosome 13q14 deletion syndrome (ortholog); genetic disease (ortholog); INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE, FACIAL ANOMALIES, AND SPEECH DEFECTS (ortholog); FOUND IN cytosol (ortholog); nuclear body (ortholog); nucleus (ortholog) NW_004955404 30215140 30229798 + 9068941 102019461 A0A8C2UNK4;A0A8C2UNL0 MODEL AGCD01004001;GBCE01095386;GBDK01093958;XM_005374164 XP_005374221 F-box and leucine-rich repeat protein 3;F-box/LRR-repeat protein 3 APPROVED protein-coding ENSCLAG00000002524 NW_004955404 30215108 30229798 + 8715723 LOC102020057 T-complex protein 1 subunit gamma pseudogene NW_004955442 5409499 5411146 + 102020057 MODEL AGCD01037559;XR_262116 APPROVED pseudo 8715726 Sdhaf3 succinate dehydrogenase complex assembly factor 3 ASSOCIATED WITH genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog) NW_004955432 13512594 13586984 + 9068941 102021790 A0A8C2YJY8 MODEL AGCD01031019;AGCD01031020;AGCD01031021;AGCD01031022;AGCD01031023;AGCD01031024;AGCD01031025;GBDF01176739;XM_005388076 XP_005388133 Acn9 ACN9 homolog;succinate dehydrogenase assembly factor 3, mitochondrial APPROVED protein-coding ENSCLAG00000003011 NW_004955432 13512594 13586978 + 8715733 Yes1 YES proto-oncogene 1, Src family tyrosine kinase ENCODES a protein that exhibits enzyme binding (ortholog); epidermal growth factor receptor binding (ortholog); phosphotyrosine residue binding (ortholog); INVOLVED IN cellular response to platelet-derived growth factor stimulus (ortholog); cellular response to retinoic acid (ortholog); cellular response to transforming growth factor beta stimulus (ortholog); PARTICIPATES IN eicosanoid signaling pathway; ephrin - ephrin receptor bidirectional signaling axis; glypican signaling pathway; ASSOCIATED WITH autistic disorder (ortholog); COVID-19 (ortholog); double outlet right ventricle (ortholog); FOUND IN actin filament (ortholog); cytosol (ortholog); glutamatergic synapse (ortholog) NW_004955402 9199704 9255183 + 9068941 102021819 A0A8C2V712 MODEL AGCD01000209;AGCD01000210;AGCD01000211;GBDF01249763;XM_005372669 XP_005372726 tyrosine-protein kinase Yes;v-yes-1 Yamaguchi sarcoma viral oncogene homolog 1 APPROVED protein-coding ENSCLAG00000007748 NW_004955402 9226295 9256044 + 8715752 Rspo2 R-spondin 2 ENCODES a protein that exhibits heparin binding (ortholog); signaling receptor binding (ortholog); INVOLVED IN bone mineralization (ortholog); canonical Wnt signaling pathway (ortholog); dopaminergic neuron differentiation (ortholog); PARTICIPATES IN Wnt signaling, canonical pathway; ASSOCIATED WITH genetic disease (ortholog); Humerofemoral Hypoplasia with Radiotibial Ray Deficiency (ortholog); tetraamelia syndrome 2 (ortholog); FOUND IN cell surface (ortholog); extracellular region (ortholog) NW_004955417 30643554 30704497 - 9068941 102023033 A0A8C2VXC4 MODEL AGCD01018628;GBDK01061470;XM_005382000 XP_005382057 R-spondin-2 protein-coding ENSCLAG00000013840 NW_004955417 30643554 30704497 - 8715762 Higd1a HIG1 hypoxia inducible domain family member 1A INVOLVED IN cellular response to glucose starvation (ortholog); cellular response to hypoxia (ortholog); negative regulation of apoptotic process (ortholog); ASSOCIATED WITH congenital muscular dystrophy-dystroglycanopathy type A8 (ortholog); genetic disease (ortholog); FOUND IN membrane (ortholog); mitochondrial inner membrane (ortholog); mitochondrion (ortholog) NW_004955420 28040320 28050723 + 9068941 102024120 A0A8C2W6G1 MODEL AGCD01021468;AGCD01021469;GBDF01086654;XM_005383528;XM_005383529;XM_005383530;XM_013513604 XP_005383585;XP_005383586;XP_005383587;XP_013369058 HIG1 domain family member 1A, mitochondrial;HIG1 hypoxia inducible domain family, member 1A APPROVED protein-coding ENSCLAG00000015507 NW_004955420 28045410 28049758 + 8715778 LOC102024328 uncharacterized LOC102024328 NW_004955471 6006346 6008801 - 102024328 MODEL AGCD01053116;GBDF01188582;XR_001237053 ncrna 8715783 LOC102024636 keratin-associated protein 4-3-like NW_004955451 15571355 15602825 - 102024636 MODEL AGCD01043618;AGCD01043619;AGCD01043620;AGCD01043621;XM_013519179 XP_013374633 APPROVED protein-coding 8715785 Sap30 Sin3A associated protein 30 ENCODES a protein that exhibits transcription corepressor activity (ortholog); INVOLVED IN modulation by host of symbiont transcription (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); skeletal muscle cell differentiation (ortholog); PARTICIPATES IN Hedgehog signaling pathway; ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN histone deacetylase complex (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955403 33633028 33639271 - 9068941 102026062 A0A8C2VTA0 MODEL AGCD01002457;AGCD01002458;GBBH01076242;GBDF01154171;XM_013513303 XP_013368757 Sin3A-associated protein, 30kDa;histone deacetylase complex subunit SAP30 APPROVED protein-coding ENSCLAG00000013849 NW_004955403 33633236 33638983 - 8715794 Slc10a1 solute carrier family 10 member 1 ENCODES a protein that exhibits bile acid transmembrane transporter activity (ortholog); bile acid:sodium symporter activity (ortholog); INVOLVED IN bile acid and bile salt transport (ortholog); bile acid signaling pathway (ortholog); cellular response to xenobiotic stimulus (ortholog); PARTICIPATES IN bile acid signaling pathway; ASSOCIATED WITH alcoholic hepatitis (ortholog); Chemical and Drug Induced Liver Injury (ortholog); cholestasis (ortholog); FOUND IN basolateral plasma membrane (ortholog); membrane (ortholog) NW_004955466 597081 609254 + 9068941 102026303 A0A8C2UYI5 MODEL AGCD01050667;GBCB01029096;XM_005399028 XP_005399085 sodium/bile acid cotransporter;solute carrier family 10 (sodium/bile acid cotransporter), member 1 APPROVED protein-coding ENSCLAG00000004713 NW_004955466 597204 608756 + 8715803 Ccrl2 C-C motif chemokine receptor like 2 ENCODES a protein that exhibits CCR chemokine receptor binding (ortholog); chemokine receptor binding (ortholog); INVOLVED IN inflammatory response (ortholog); ASSOCIATED WITH Arsenic Poisoning (ortholog); COVID-19 (ortholog); genetic disease (ortholog); FOUND IN plasma membrane (ortholog) NW_004955420 25613632 25616770 - 9068941 102026644 A0A8C2YV75 MODEL AGCD01021367;GBDK01185255;XM_005383444;XM_013513477;XM_013513478;XM_013513479 XP_005383501;XP_013368931;XP_013368932;XP_013368933 C-C chemokine receptor-like 2;chemokine (C-C motif) receptor-like 2 APPROVED protein-coding ENSCLAG00000017845 8715819 LOC102027001 uncharacterized LOC102027001 NW_004955432 1618245 1628231 - 102027001 MODEL AGCD01030600;AGCD01030601;GBCB01009360;XR_261501;XR_261502 ncrna 8715826 LOC102028082 MORC family CW-type zinc finger protein 2 pseudogene NW_004955474 6210799 6214924 + 102028082 MODEL AGCD01054460;XM_005401381 APPROVED pseudo 8715831 LOC102028224 60S ribosomal protein L30-like NW_004955434 2063707 2064055 - 102028224 MODEL AGCD01032086 pseudo 8715832 LOC102028511 protein FAM134B pseudogene NW_004955464 7935764 7936955 + 102028511 MODEL AGCD01050073;XR_263225 APPROVED pseudo 8715835 LOC102029043 apolipoprotein R-like NW_004955406 42682040 42688031 + 102029043 A0A8C2VTP7 MODEL AGCD01006714;GBDJ01064610;XM_005375425 XP_005375482 protein-coding ENSCLAG00000013380 8715843 F2rl3 F2R like thrombin or trypsin receptor 3 ENCODES a protein that exhibits protease binding (ortholog); INVOLVED IN platelet activation (ortholog); platelet aggregation (ortholog); positive regulation of release of sequestered calcium ion into cytosol (ortholog); PARTICIPATES IN protease mediated signaling via protease-activated receptor 4; ASSOCIATED WITH Chemical and Drug Induced Liver Injury (ortholog); cholestasis (ortholog); genetic disease (ortholog); FOUND IN plasma membrane (ortholog) NW_004955524 1045493 1047924 - 9068941 102029220 A0A8C2V759 MODEL AGCD01068733;GBDF01142310;XM_005409505;XM_005409506 XP_005409562;XP_005409563 F2R like thrombin/trypsin receptor 3;coagulation factor II (thrombin) receptor-like 3;proteinase-activated receptor 4 APPROVED protein-coding ENSCLAG00000006791 NW_004955524 1044792 1047819 - 8715851 Stk26 serine/threonine kinase 26 ENCODES a protein that exhibits ATP binding (ortholog); identical protein binding (ortholog); magnesium ion binding (ortholog); INVOLVED IN cellular response to starvation (ortholog); microvillus assembly (ortholog); negative regulation of cell migration (ortholog); ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); syndromic X-linked intellectual disability Lubs type (ortholog); FOUND IN apical plasma membrane (ortholog); cell periphery (ortholog); cytoplasm (ortholog) NW_004955473 2819644 2878561 - 9068941 102029284 A0A8C2ULT3;A0A8C2YIY9;A0A8C2YIZ2 MODEL AGCD01053907;AGCD01053908;GBDJ01061871;XM_005401218 XP_005401275 serine/threonine protein kinase 26;serine/threonine-protein kinase 26 APPROVED protein-coding ENSCLAG00000001539 NW_004955473 2819585 2878561 - 8715867 Znf644 zinc finger protein 644 ENCODES a protein that exhibits DNA-binding transcription factor activity, RNA polymerase II-specific (ortholog); RNA polymerase II cis-regulatory region sequence-specific DNA binding (ortholog); transcription corepressor binding (ortholog); ASSOCIATED WITH genetic disease (ortholog); Myopia 21, Autosomal Dominant (ortholog) NW_004955423 3251726 3346023 + 9068941;7240710 102029306 A0A8C2V4X2;A0A8C2V769;A0A8C2V9T3;A0A8C2VAB4 MODEL AGCD01023509;AGCD01023510;AGCD01023511;GBCQ01175826;XM_005385070;XM_005385071;XM_005385072;XM_005385073;XM_005385074;XM_005385075;XM_005385076;XM_005385078;XM_005385079;XM_013514496;XM_013514497;XM_013514498;XM_013514499;XM_013514500;XM_013514501;XM_013514502;XR_260944;XR_260945 XP_005385127;XP_005385128;XP_005385129;XP_005385130;XP_005385131;XP_005385132;XP_005385133;XP_005385135;XP_005385136;XP_013369950;XP_013369951;XP_013369952;XP_013369953;XP_013369954;XP_013369955;XP_013369956 protein-coding ENSCLAG00000006797 NW_004955423 3251119 3348039 + 8715918 Frrs1 ferric chelate reductase 1 ENCODES a protein that exhibits oxidoreductase activity, acting on metal ions (ortholog); INVOLVED IN intracellular iron ion homeostasis (ortholog); ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog) NW_004955435 4531279 4578146 - 9068941 102029896 A0A8C2UZP9 MODEL AGCD01032832;AGCD01032833;GBDF01159747;XM_005388788 XP_005388845 ferric-chelate reductase 1 APPROVED protein-coding ENSCLAG00000005704 NW_004955435 4527309 4578147 - 8715938 LOC102003293 exportin-6 pseudogene NW_004955445 11816035 11825133 + 102003293 MODEL AGCD01039717 APPROVED pseudo 8715939 St8sia5 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5 ENCODES a protein that exhibits alpha-N-acetylneuraminate alpha-2,8-sialyltransferase activity (ortholog); sialyltransferase activity (ortholog); INVOLVED IN glycosphingolipid biosynthetic process (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); Microcephaly, Epilepsy, and Diabetes Syndrome (ortholog); FOUND IN Golgi membrane (ortholog) NW_004955402 32165912 32232683 - 9068941 102003602 A0A8C2VR90;A0A8C2VVY9 MODEL AGCD01000814;GBCB01129792;XM_005372876;XM_005372877;XM_005372878;XM_013510464;XM_013510476;XR_259076 XP_005372933;XP_005372934;XP_005372935;XP_013365918;XP_013365930 alpha-2,8-sialyltransferase 8E protein-coding ENSCLAG00000012639 NW_004955402 32165912 32232674 - 8715958 Tmub1 transmembrane and ubiquitin like domain containing 1 INVOLVED IN ubiquitin-dependent ERAD pathway (ortholog); ASSOCIATED WITH genetic disease (ortholog); lethal congenital glycogen storage disease of heart (ortholog); long QT syndrome (ortholog) NW_004955491 5518199 5520743 - 9068941 102004076 A0A8C2V8X8 MODEL AGCD01060486;GBDJ01125606;XM_005404815;XM_005404816 XP_005404872;XP_005404873 transmembrane and ubiquitin-like domain containing 1;transmembrane and ubiquitin-like domain-containing protein 1 APPROVED protein-coding ENSCLAG00000008132 NW_004955491 5518193 5520521 - 8715969 LOC102004144 palladin-like NW_004955408 32788476 32810588 + 102004144 MODEL AGCD01008854;AGCD01008855;GBDF01234212;XM_005376593 XP_005376650 protein-coding 8715985 LOC102004351 NADH-cytochrome b5 reductase 1 ASSOCIATED WITH familial adult myoclonic epilepsy 5 (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); mitochondrion (ortholog) NW_004955406 38958766 38964597 - 9068941 102004351 A0A8C2VLA5 MODEL AGCD01006614;GBDK01276274;XM_005375237 XP_005375294 APPROVED protein-coding ENSCLAG00000010011 NW_004955406 38955997 38965127 - 8715999 Foxred1 FAD dependent oxidoreductase domain containing 1 INVOLVED IN mitochondrial respiratory chain complex I assembly (ortholog); ASSOCIATED WITH Chromosome 11, Partial Trisomy 11q (ortholog); Developmental Disabilities (ortholog); Dwarfism (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrial respiratory chain complex I (ortholog); mitochondrion (ortholog) NW_004955412 27293467 27300522 + 9068941;7240710 102004367 MODEL AGCD01013233;GBBH01209105;XM_005378501;XM_013511027 XP_005378558;XP_013366481 FAD-dependent oxidoreductase domain containing 1;FAD-dependent oxidoreductase domain-containing protein 1 APPROVED protein-coding 8716014 Cabp7 calcium binding protein 7 ASSOCIATED WITH Breast Cancer, Familial (ortholog); genetic disease (ortholog); neurofibromatosis 2 (ortholog); FOUND IN trans-Golgi network membrane (ortholog) NW_004955455 3977977 3981646 + 9068941 102004561 A0A8C2YTP2 MODEL AGCD01045662;GBDI01161267;XM_005396566 XP_005396623 calcium-binding protein 7 protein-coding ENSCLAG00000015456 NW_004955455 3977593 3981646 + 8716021 Ttll4 tubulin tyrosine ligase like 4 ENCODES a protein that exhibits protein-glutamic acid ligase activity (ortholog); tubulin binding (ortholog); tubulin-glutamic acid ligase activity (ortholog); INVOLVED IN peptidyl-glutamic acid modification (ortholog); protein polyglutamylation (ortholog); regulation of blastocyst development (ortholog); ASSOCIATED WITH alacrima, achalasia, and impaired intellectual development syndrome (ortholog); cerebrotendinous xanthomatosis (ortholog); genetic disease (ortholog); FOUND IN 9+0 non-motile cilium (ortholog); ciliary basal body (ortholog) NW_004955453 14679945 14720025 - 9068941 102005219 A0A8C2V8E8;A0A8C2V9C2;A0A8C2VAM1;A0A8C2VD88;A0A8C2VDR8 MODEL AGCD01044871;AGCD01044872;AGCD01044873;GBDK01078009;XM_013519796;XM_013519797;XM_013519798;XM_013519799;XM_013519800;XM_013519801 XP_013375250;XP_013375251;XP_013375252;XP_013375253;XP_013375254;XP_013375255 tubulin polyglutamylase TTLL4;tubulin tyrosine ligase-like family member 4;tubulin tyrosine ligase-like family, member 4 APPROVED protein-coding ENSCLAG00000007759 8716046 Npc1 NPC intracellular cholesterol transporter 1 ENCODES a protein that exhibits cholesterol binding (ortholog); INVOLVED IN adult walking behavior (ortholog); autophagy (ortholog); cellular response to low-density lipoprotein particle stimulus (ortholog); ASSOCIATED WITH Ataxia (ortholog); atherosclerosis (ortholog); brucellosis (ortholog); FOUND IN endoplasmic reticulum (ortholog); endosome (ortholog); extracellular region (ortholog) NW_004955402 11699434 11742899 - 9068941;7240710 102006185 A0A8C2V9R0 MODEL AGCD01000305;AGCD01000306;GBDK01075626;XM_005372706 XP_005372763 Niemann-Pick disease, type C1 APPROVED protein-coding ENSCLAG00000008539 NW_004955402 11699434 11742899 - 8716075 B3galnt1 beta-1,3-N-acetylgalactosaminyltransferase 1 (globoside blood group) ENCODES a protein that exhibits UDP-galactose:beta-N-acetylglucosamine beta-1,3-galactosyltransferase activity (ortholog); INVOLVED IN oligosaccharide biosynthetic process (ortholog); ASSOCIATED WITH genetic disease (ortholog); polyagglutination (ortholog) NW_004955448 11556179 11583556 - 9068941 102006843 A0A8C2UQW4 MODEL AGCD01041528;GBCB01129821;GBCE01169869;XM_005393126;XM_005393128;XM_013518678;XM_013518679;XM_013518680 XP_005393183;XP_005393185;XP_013374132;XP_013374133;XP_013374134 UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 1 protein-coding ENSCLAG00000002991 NW_004955448 11556179 11583556 - 8716099 L3hypdh trans-L-3-hydroxyproline dehydratase ENCODES a protein that exhibits hydro-lyase activity (ortholog); proline racemase activity (ortholog); ASSOCIATED WITH Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog) NW_004955466 13196223 13205339 - 9068941 102008078 A0A8C2UTP9 MODEL AGCD01051152;GBCQ01072766;XM_005399227;XR_001236806 XP_005399284 L-3-hydroxyproline dehydratase (trans-);trans-3-hydroxy-L-proline dehydratase APPROVED protein-coding ENSCLAG00000003825 NW_004955466 13196223 13205158 - 8716108 LOC102008096 60S ribosomal protein L6-like NW_004955477 11186663 11187511 - 102008096 MODEL AGCD01055719 pseudo 8716117 LOC102008549 nuclear ubiquitous casein and cyclin-dependent kinase substrate 1 pseudogene NW_004955495 3015938 3016703 + 102008549 MODEL AGCD01061815 APPROVED pseudo 8716118 LOC102008692 olfactory receptor 5P3-like NW_004955453 4970345 4985354 - 102008692 A0A8C2VKN5 MODEL AGCD01044701;XM_013519758 XP_013375212 APPROVED protein-coding ENSCLAG00000011634 8716119 Trim44 tripartite motif containing 44 INVOLVED IN negative regulation of protein K48-linked ubiquitination (ortholog); positive regulation of cytokine-mediated signaling pathway (ortholog); positive regulation of defense response to virus by host (ortholog); ASSOCIATED WITH aniridia (ortholog); Aniridia 3 (ortholog); genetic disease (ortholog) NW_004955422 10580002 10690349 - 9068941 102008739 A0A8C2YSU0 MODEL AGCD01022741;AGCD01022742;AGCD01022743;GBCB01005350;XM_005384121 XP_005384178 tripartite motif-containing protein 44 protein-coding ENSCLAG00000014212 NW_004955422 10580002 10690349 - 8716128 LOC102008990 uncharacterized LOC102008990 NW_004955549 117973 173721 + 102008990 MODEL AGCD01072419;GBDF01076042;XR_001232252;XR_264912 ncrna 8716137 LOC102009565 phosphoinositide-3-kinase-interacting protein 1-like NW_004957624 10 1097 - 102009565 MODEL AGCD01081020;GBDJ01181150;GBDK01091793;XM_005415233 XP_005415290 protein-coding 8716142 Nkx2-8 NK2 homeobox 8 ENCODES a protein that exhibits DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); DNA-binding transcription factor activity (ortholog); double-stranded DNA binding (ortholog); INVOLVED IN axonogenesis (ortholog); DNA-templated transcription (ortholog); epithelial cell proliferation (ortholog); ASSOCIATED WITH Brain-Lung-Thyroid Syndrome (ortholog); choreatic disease (ortholog); genetic disease (ortholog) NW_004955409 24529414 24531293 + 9068941 102009807 A0A8C2VGN8 MODEL AGCD01010086;AGCD01010087;GBDI01245180;XM_013510168 XP_013365622 homeobox protein Nkx-2.8 protein-coding ENSCLAG00000010559 NW_004955409 24529594 24530998 + 8716148 LOC102009929 uncharacterized LOC102009929 NW_004955468 11697494 11712294 + 102009929 MODEL AGCD01052137;GBBH01041129;XR_001236933;XR_263414;XR_263415 ncrna 8716155 LOC102010019 phospholipase A2, membrane associated-like NW_004955452 597005 599899 - 102010019 MODEL AGCD01043819;XM_005395284 XP_005395341 protein-coding 8716160 Trim47 tripartite motif containing 47 ENCODES a protein that exhibits molecular function inhibitor activity (ortholog); ubiquitin protein ligase activity (ortholog); ubiquitin-protein transferase activity (ortholog); INVOLVED IN protein ubiquitination (ortholog); ASSOCIATED WITH Breast Neoplasms (ortholog); Experimental Neoplasms (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog) NW_004955506 6379088 6383671 + 9068941 102010607 A0A8C2YNK6 MODEL AGCD01065416;GBDK01285018;XM_005407473 XP_005407530 tripartite motif-containing protein 47 protein-coding ENSCLAG00000008148 NW_004955506 6379088 6385446 + 8716170 LOC102011138 mitochondrial calcium uniporter regulator 1 pseudogene NW_004955430 1898687 1900786 - 102011138 MODEL AGCD01029142 APPROVED pseudo 8716171 Iqck IQ motif containing K ASSOCIATED WITH Alzheimer's disease (ortholog); genetic disease (ortholog) NW_004955442 3428245 3548718 + 102011363 A0A8C2YTV2 MODEL AGCD01037506;AGCD01037507;GBDF01043787;XM_005391117 XP_005391174 IQ domain-containing protein K protein-coding ENSCLAG00000015720 NW_004955442 3428259 3519014 + 8716185 Polr2a RNA polymerase II subunit A ENCODES a protein that exhibits core promoter sequence-specific DNA binding (ortholog); DNA binding (ortholog); kinase binding (ortholog); INVOLVED IN cellular response to oxygen levels (ortholog); DNA-templated transcription termination (ortholog); positive regulation of RNA splicing (ortholog); PARTICIPATES IN RNA polymerase II transcription pathway; ASSOCIATED WITH Bainbridge-Ropers syndrome (ortholog); common variable immunodeficiency (ortholog); congenital myasthenic syndrome 2A (ortholog); FOUND IN euchromatin (ortholog); nucleolus (ortholog); nucleus (ortholog) NW_004955467 9423540 9447530 - 9068941 102011523 A0A8C2VMD6;A0A8C2YRE5;A0A8C2YRF2 MODEL AGCD01051511;GBCQ01005514;XM_005399484 XP_005399541 DNA-directed RNA polymerase II subunit RPB1;polymerase (RNA) II (DNA directed) polypeptide A, 220kDa APPROVED protein-coding ENSCLAG00000012196 NW_004955467 9421256 9447530 - 8716221 LOC102012259 uncharacterized LOC102012259 NW_004955402 6847522 6850356 - 102012259 MODEL AGCD01000162;GBDF01162294;XR_001235451 ncrna 8716228 LOC102012773 fatty acid-binding protein, liver NW_004955424 624397 629958 + 9068941 102012773 A0A8C2VIS4 MODEL AGCD01024188;GBCQ01000092;XM_005385381 XP_005385438 Fabp1 fatty acid binding protein 1, liver APPROVED protein-coding ENSCLAG00000009296 NW_004955424 624397 629949 + 8716236 Tmem216 transmembrane protein 216 INVOLVED IN cilium assembly (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); Joubert syndrome (ortholog); FOUND IN ciliary transition zone (ortholog); cilium (ortholog); MKS complex (ortholog) NW_004955511 6164143 6167887 - 9068941;7240710 102013856 A0A8C2URX2;A0A8C2UUX1 MODEL AGCD01066598;GBDI01182797;XM_005408153;XM_005408154;XM_005408155 XP_005408210;XP_005408211;XP_005408212 protein-coding ENSCLAG00000003298 NW_004955511 6164143 6167887 - 8716258 Nsun7 NOP2/Sun RNA methyltransferase family member 7 INVOLVED IN flagellated sperm motility (ortholog); sperm mitochondrion organization (ortholog); ASSOCIATED WITH genetic disease (ortholog); Hyperglycinemia, Lactic Acidosis, and Seizures (ortholog); male infertility (ortholog) NW_004955443 6788155 6830659 - 9068941 102016109 A0A8C2UR28 MODEL AGCD01038263;AGCD01038264;GBBH01061569;XM_005391949;XM_013518051 XP_005392006;XP_013373505 NOP2/Sun domain family, member 7;putative methyltransferase NSUN7 APPROVED protein-coding ENSCLAG00000001525 NW_004955443 6789224 6830813 - 8716274 LOC102016964 vomeronasal type-2 receptor 26-like NW_004955584 764198 810131 + 102016964 A0A8C2YIC4 MODEL AGCD01075958;AGCD01075959;AGCD01075960;AGCD01075961;GBDJ01214238;XM_013509866;XM_013509867 XP_013365320;XP_013365321 extracellular calcium-sensing receptor-like APPROVED protein-coding ENSCLAG00000000652 8716284 Camk2a calcium/calmodulin dependent protein kinase II alpha ENCODES a protein that exhibits calcium-dependent protein serine/threonine kinase activity (ortholog); calmodulin binding (ortholog); calmodulin-dependent protein kinase activity (ortholog); INVOLVED IN angiotensin-activated signaling pathway (ortholog); calcium ion transport (ortholog); calmodulin dependent kinase signaling pathway (ortholog); PARTICIPATES IN calcium/calmodulin dependent kinase 2 signaling pathway; fibroblast growth factor signaling pathway; transforming growth factor-beta Smad dependent signaling pathway; ASSOCIATED WITH Alzheimer's disease (ortholog); autism spectrum disorder (ortholog); autosomal dominant intellectual developmental disorder 53 (ortholog); FOUND IN axon (ortholog); calcium- and calmodulin-dependent protein kinase complex (ortholog); dendrite (ortholog) NW_004955415 4247307 4307402 + 9068941 102017328 A0A8C2VLM7;A0A8C2VLP3;A0A8C2VS14 MODEL AGCD01015968;GBDF01299177;XM_005380581;XM_005380582 XP_005380638;XP_005380639 calcium/calmodulin-dependent protein kinase II alpha;calcium/calmodulin-dependent protein kinase type II subunit alpha APPROVED protein-coding ENSCLAG00000012010 NW_004955415 4247014 4307458 + 8716314 Klkb1 kallikrein B1 INVOLVED IN blood coagulation, intrinsic pathway (ortholog); liver regeneration (ortholog); plasminogen activation (ortholog); PARTICIPATES IN acenocoumarol pharmacodynamics pathway; alteplase pharmacodynamics pathway; aminocaproic acid pharmacodynamics pathway; ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); Bietti crystalline corneoretinal dystrophy (ortholog); FOUND IN extracellular space (ortholog) NW_004955403 22835544 22856355 - 9068941;7240710 102017618 A0A8C2YUM1 MODEL AGCD01002231;GBDK01227470;XM_005373431 XP_005373488 kallikrein B, plasma (Fletcher factor) 1;plasma kallikrein APPROVED protein-coding ENSCLAG00000016848 NW_004955403 22833982 22856389 - 8716337 LOC102017682 deoxynucleotidyltransferase terminal-interacting protein 2 pseudogene NW_004955498 2146251 2152131 + 102017682 MODEL AGCD01062766;AGCD01062767 APPROVED pseudo 8716338 Slc41a3 solute carrier family 41 member 3 ENCODES a protein that exhibits magnesium:sodium antiporter activity (ortholog); INVOLVED IN mitochondrial magnesium ion transmembrane transport (ortholog); ASSOCIATED WITH alkaptonuria (ortholog); genetic disease (ortholog); Primary Lymphedema with Myelodysplasia (ortholog); FOUND IN mitochondrial inner membrane (ortholog); plasma membrane (ortholog) NW_004955421 21349484 21407171 - 9068941 102017779 A0A8C2UW19;A0A8C2UWX0 MODEL AGCD01022107;AGCD01022108;GBCQ01151305;XM_005383826;XM_005383827;XM_005383828;XM_005383829;XM_013513732 XP_005383883;XP_005383884;XP_005383885;XP_005383886;XP_013369186 solute carrier family 41, member 3 APPROVED protein-coding ENSCLAG00000004678 NW_004955421 21349484 21407171 - 8716362 Tac4 tachykinin precursor 4 ENCODES a protein that exhibits receptor ligand activity (ortholog); signaling receptor binding (ortholog); substance K receptor binding (ortholog); INVOLVED IN detection of temperature stimulus involved in sensory perception of pain (ortholog); negative regulation of sensory perception of pain (ortholog); negative regulation of systemic arterial blood pressure (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN extracellular space (ortholog) NW_004955451 11755645 11763281 + 9068941 102018879 MODEL AGCD01043364;GBBH01091448;XM_005394188 XP_005394245 tachykinin 4;tachykinin 4 (hemokinin);tachykinin-4 APPROVED protein-coding 8716371 LOC102019238 uncharacterized LOC102019238 NW_004955453 3959312 3961658 - 102019238 MODEL AGCD01044670;GBDJ01054424;XR_262710 ncrna 8716376 LOC102019721 uncharacterized LOC102019721 NW_004955429 21904557 21908894 - 102019721 MODEL AGCD01029013;GBDF01264646;XR_261379 ncrna 8716381 Emc8 ER membrane protein complex subunit 8 ENCODES a protein that exhibits membrane insertase activity (ortholog); INVOLVED IN protein insertion into ER membrane by stop-transfer membrane-anchor sequence (ortholog); tail-anchored membrane protein insertion into ER membrane (ortholog); ASSOCIATED WITH genetic disease (ortholog); persistent fetal circulation syndrome (ortholog); FOUND IN cytoplasm (ortholog); EMC complex (ortholog); endoplasmic reticulum (ortholog) NW_004955541 873354 884247 - 9068941 102020052 A0A8C2UM37;A0A8C2UQ84 MODEL AGCD01071363;GBDI01066673;GBDJ01075485;XM_005410981;XM_013507992 XP_005411038;XP_013363446 protein-coding ENSCLAG00000001317 NW_004955541 871657 884247 - 8716390 Kif17 kinesin family member 17 ENCODES a protein that exhibits microtubule motor activity (ortholog); INVOLVED IN anterograde dendritic transport of neurotransmitter receptor complex (ortholog); microtubule-based process (ortholog); protein-containing complex localization (ortholog); ASSOCIATED WITH 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (ortholog); autism spectrum disorder (ortholog); congenital disorder of glycosylation Ir (ortholog); FOUND IN axoneme (ortholog); ciliary basal body (ortholog); cilium (ortholog) NW_004955452 1197839 1239209 - 9068941 102021077 MODEL AGCD01043836;GBDK01380952;XM_005394685;XM_005394686;XM_013519654;XM_013519655;XM_013519656;XM_013519657;XM_013519658;XM_013519659 XP_005394742;XP_005394743;XP_013375108;XP_013375109;XP_013375110;XP_013375111;XP_013375112;XP_013375113 kinesin-like protein KIF17 protein-coding 8716418 CUNH3orf38 chromosome unknown C3orf38 homolog INVOLVED IN positive regulation of apoptotic process (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN nucleus (ortholog) NW_004955407 5339389 5348894 - 9068941 102022463 A0A8C2VHT7 MODEL AGCD01006912;AGCD01006913;GBDK01359287;XM_005375526;XM_005375527 XP_005375583;XP_005375584 LOC102022463 chromosome unknown open reading frame, human C3orf38;uncharacterized protein C3orf38 homolog APPROVED protein-coding ENSCLAG00000008911 NW_004955407 5343010 5348508 - 8716427 LOC102022779 U6 snRNA-associated Sm-like protein LSm6 pseudogene NW_004955405 17212899 17223254 + 102022779 MODEL AGCD01004987 APPROVED pseudo 8716428 LOC102025767 cytochrome c-like NW_004955460 9853014 9853345 - 102025767 A0A8C2W649 MODEL AGCD01048556;XM_005397827 XP_005397884 protein-coding ENSCLAG00000017774 8716432 Gdf11 growth differentiation factor 11 INVOLVED IN amacrine cell differentiation (ortholog); animal organ morphogenesis (ortholog); anterior/posterior pattern specification (ortholog); ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog); orofacial cleft (ortholog); FOUND IN extracellular space (ortholog); intracellular membrane-bounded organelle (ortholog); nucleoplasm (ortholog) NW_004955458 3388402 3398040 + 9068941 102026079 A0A8C2VJT4 MODEL AGCD01047301;GBBH01160450;GBDJ01213704;XM_005397510 XP_005397567 growth/differentiation factor 11 protein-coding ENSCLAG00000011406 NW_004955458 3388402 3398040 + 8716438 Dnmt1 DNA methyltransferase 1 ENCODES a protein that exhibits chromatin binding (ortholog); DNA (cytosine-5-)-methyltransferase activity (ortholog); DNA binding (ortholog); INVOLVED IN cellular response to amino acid stimulus (ortholog); cellular response to bisphenol A (ortholog); cellular response to lead ion (ortholog); PARTICIPATES IN DNA modification pathway; glycine N-methyltransferase deficiency pathway; homocysteine metabolic pathway; ASSOCIATED WITH acute myeloid leukemia (ortholog); adenocarcinoma (ortholog); Alcoholic Fatty Liver (ortholog); FOUND IN female germ cell nucleus (ortholog); germ cell nucleus (ortholog); heterochromatin (ortholog) NW_004955495 1465529 1505379 - 9068941;7240710 102028310 A0A8C2VD84;A0A8C2VIL5 MODEL AGCD01061693;AGCD01061694;AGCD01061695;GBDF01053790;XM_005405582;XM_005405583;XM_013505316;XM_013505317 XP_005405639;XP_005405640;XP_013360770;XP_013360771 DNA (cytosine-5)-methyltransferase 1;DNA (cytosine-5-)-methyltransferase 1 APPROVED protein-coding ENSCLAG00000009575 NW_004955495 1465480 1505462 - 8716485 Ifi16 interferon gamma inducible protein 16 ENCODES a protein that exhibits double-stranded DNA binding (ortholog); identical protein binding (ortholog); transcription coregulator activity (ortholog); INVOLVED IN activation of cysteine-type endopeptidase activity (ortholog); activation of innate immune response (ortholog); cellular response to glucose starvation (ortholog); ASSOCIATED WITH autoimmune interstitial lung, joint, and kidney disease (ortholog); Experimental Liver Cirrhosis (ortholog); gastrointestinal stromal tumor (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nuclear inclusion body (ortholog) NW_004955468 10828726 10845853 + 9068941 102029846 MODEL AGCD01052105;GBDI01294199;XM_013522456;XM_013522457;XR_001236915 XP_013377910;XP_013377911 gamma-interferon-inducible protein 16;interferon, gamma-inducible protein 16 PROVISIONAL protein-coding 8716486 Laptm5 lysosomal protein transmembrane 5 ENCODES a protein that exhibits enzyme binding (ortholog); protein sequestering activity (ortholog); ubiquitin protein ligase binding (ortholog); INVOLVED IN activation of cysteine-type endopeptidase activity involved in apoptotic process (ortholog); cellular response to leukemia inhibitory factor (ortholog); defense response to tumor cell (ortholog); ASSOCIATED WITH Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog); IgA glomerulonephritis (ortholog); FOUND IN cytoplasmic vesicle (ortholog); lysosomal membrane (ortholog); lysosome (ortholog) NW_004955452 9335481 9358177 - 9068941 102030146 A0A8C2VJP3 MODEL AGCD01044236;GBDJ01075689;XM_005394999 XP_005395056 lysosomal-associated transmembrane protein 5 protein-coding ENSCLAG00000009573 NW_004955452 9334587 9358444 - 8716498 LOC102030315 ATP-dependent RNA helicase DDX19A NW_004955484 3142544 3169853 + 9068941 102030315 A0A8C2YLC0 MODEL AGCD01058156;AGCD01058157;AGCD01058158;GBDJ01191109;XM_005403476 XP_005403533 Ddx19a DEAD (Asp-Glu-Ala-Asp) box polypeptide 19A APPROVED protein-coding ENSCLAG00000004996 NW_004955484 3142544 3169853 + 8716519 LOC102002984 60S ribosomal protein L8 pseudogene NW_004955403 16745732 16746501 + 102002984 MODEL AGCD01002067 APPROVED pseudo 8716520 LOC102003601 EKC/KEOPS complex subunit LAGE3-like NW_004955585 4764 6040 + 102003601 MODEL AGCD01075987;XM_005414426 XP_005414483 APPROVED protein-coding 8716527 Figla folliculogenesis specific bHLH transcription factor ENCODES a protein that exhibits bHLH transcription factor binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); E-box binding (ortholog); INVOLVED IN positive regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH dystonia (ortholog); genetic disease (ortholog); hereditary breast ovarian cancer syndrome (ortholog); FOUND IN transcription regulator complex (ortholog) NW_004955424 14393566 14402971 + 9068941;7240710 102003889 MODEL AGCD01024654;GBDF01007679;XM_013514581;XM_013514582 XP_013370035;XP_013370036 factor in the germline alpha;folliculogenesis specific basic helix-loop-helix APPROVED protein-coding 8716536 LOC102004137 uncharacterized LOC102004137 NW_004955404 19087590 19138303 + 102004137 MODEL AGCD01003636;AGCD01003637;AGCD01003638;AGCD01003639;GBCE01122216;XR_259319 ncrna ENSCLAG00000022395 8716542 LOC102004903 uncharacterized LOC102004903 NW_004955409 9055420 9070182 + 102004903 MODEL AGCD01009428;AGCD01009429;AGCD01009430;GBDF01194507;XR_259760 ncrna ENSCLAG00000027497 8716548 LOC102005449 ubiquitin carboxyl-terminal hydrolase 42-like NW_004955460 10831510 10832892 + 102005449 MODEL AGCD01048617;XM_013521142 XP_013376596 APPROVED protein-coding 8716554 Cst8 cystatin 8 ASSOCIATED WITH genetic disease (ortholog); male infertility (ortholog); FOUND IN cell surface (ortholog); cytoplasm (ortholog); extracellular region (ortholog) NW_004955415 30459008 30466128 + 9068941 102005461 A0A8C2YTI3 MODEL AGCD01016664;GBDF01008792;XM_005380971;XM_005380972 XP_005381028;XP_005381029 cystatin 8 (cystatin-related epididymal specific);cystatin-8 APPROVED protein-coding ENSCLAG00000015212 8716564 LOC102005912 uncharacterized LOC102005912 NW_004955412 3097642 3103353 - 102005912 MODEL AGCD01012565;GBDF01016512;XR_001232865;XR_001232866;XR_001232867 ncrna 8716572 LOC102006974 40S ribosomal protein S10 pseudogene NW_004955404 27148218 27148697 + 102006974 MODEL AGCD01003909 APPROVED pseudo 8716577 Gfral GDNF family receptor alpha like ENCODES a protein that exhibits glial cell-derived neurotrophic factor receptor activity (ortholog); receptor tyrosine kinase binding (ortholog); INVOLVED IN glial cell-derived neurotrophic factor receptor signaling pathway (ortholog); negative regulation of extrinsic apoptotic signaling pathway in absence of ligand (ortholog); negative regulation of neuron apoptotic process (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN actin cytoskeleton (ortholog); external side of plasma membrane (ortholog); focal adhesion (ortholog) NW_004955411 903001 952750 - 9068941 102007749 A0A8C2W5S6 MODEL AGCD01011468;AGCD01011469;GBDF01165025;XM_005377916 XP_005377973 GDNF family receptor alpha-like protein-coding ENSCLAG00000015534 NW_004955411 903061 952750 - 8716588 LOC102009036 60S ribosomal protein L5 NW_004955469 9922760 9923788 - 102009036 A0A8C2V9F8 MODEL AGCD01052521;XM_005400516 XP_005400573 APPROVED protein-coding ENSCLAG00000008425;ENSCLAG00000017712 8716593 Hdgf heparin binding growth factor ENCODES a protein that exhibits actin binding (ortholog); DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); heparin binding (ortholog); INVOLVED IN cellular response to interleukin-7 (ortholog); negative regulation of neuron apoptotic process (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease type 2 (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); extracellular space (ortholog); nucleoplasm (ortholog) NW_004955545 2819960 2831197 - 9068941 102009108 A0A8C2UTD6 MODEL AGCD01071923;AGCD01071924;GBDI01008805;XM_005411700;XM_005411701 XP_005411757;XP_005411758 hepatoma derived growth factor;hepatoma-derived growth factor APPROVED protein-coding ENSCLAG00000003548 NW_004955545 2819960 2830047 - 8716606 Card9 caspase recruitment domain family member 9 ENCODES a protein that exhibits CARD domain binding (ortholog); identical protein binding (ortholog); protein domain specific binding (ortholog); INVOLVED IN antifungal innate immune response (ortholog); defense response to Gram-positive bacterium (ortholog); defense response to virus (ortholog); ASSOCIATED WITH Adams-Oliver Syndrome 5 (ortholog); ankylosing spondylitis (ortholog); autosomal dominant intellectual developmental disorder 8 (ortholog); FOUND IN CBM complex (ortholog); cytoplasm (ortholog); protein-containing complex (ortholog) NW_004955513 4350873 4359345 + 7240710;9068941 102010082 A0A8C2V3M9 MODEL AGCD01066927;GBBH01090040;XM_005408509;XM_013506614;XM_013506615;XM_013506616 XP_005408566;XP_013362068;XP_013362069;XP_013362070 caspase recruitment domain family, member 9;caspase recruitment domain-containing protein 9 APPROVED protein-coding ENSCLAG00000006761 NW_004955513 4350147 4359345 + 8716639 Rph3a rabphilin 3A ENCODES a protein that exhibits calcium ion binding (ortholog); calcium-dependent phospholipid binding (ortholog); inositol 1,4,5 trisphosphate binding (ortholog); INVOLVED IN dendritic spine organization (ortholog); regulation of NMDA receptor activity (ortholog); spontaneous neurotransmitter secretion (ortholog); ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog); FOUND IN cholinergic synapse (ortholog); dendritic spine (ortholog); extrinsic component of membrane (ortholog) NW_004955482 9190137 9312596 + 9068941 102010485 A0A8C2VG22 MODEL AGCD01057563;AGCD01057564;GBDI01143739;XM_005403200;XM_005403201;XM_005403202;XM_005403203;XM_005403204;XM_005403205;XM_005403206;XM_005403207;XM_013503738 XP_005403257;XP_005403258;XP_005403259;XP_005403260;XP_005403261;XP_005403262;XP_005403263;XP_005403264;XP_013359192 rabphilin 3A homolog;rabphilin-3A APPROVED protein-coding ENSCLAG00000009863 NW_004955482 9225845 9312695 + 8716687 LOC102010566 olfactory receptor 151-like NW_004955412 25630768 25631700 + 9068941 102010566 A0A8C2WAV8 MODEL AGCD01013166;XM_005378428 XP_005378485 APPROVED protein-coding ENSCLAG00000017942 8716690 LOC102011313 uncharacterized LOC102011313 NW_004955417 26374063 26401589 - 102011313 MODEL AGCD01018507;AGCD01018508;AGCD01018509;GBBH01003039;XM_005381923;XM_013512715;XM_013512716;XM_013512717;XM_013512718;XM_013512719;XM_013512720;XM_013512721;XM_013512722;XM_013512723;XM_013512724;XM_013512725;XM_013512726;XM_013512727;XM_013512728;XM_013512729;XM_013512730;XM_013512731;XM_013512732;XM_013512734;XR_001233417;XR_001233418 XP_005381980;XP_013368169;XP_013368170;XP_013368171;XP_013368172;XP_013368173;XP_013368174;XP_013368175;XP_013368176;XP_013368177;XP_013368178;XP_013368179;XP_013368180;XP_013368181;XP_013368182;XP_013368183;XP_013368184;XP_013368185;XP_013368186;XP_013368188 uncharacterized protein LOC102011313 protein-coding 8716732 Pigf phosphatidylinositol glycan anchor biosynthesis class F INVOLVED IN GPI anchor biosynthetic process (ortholog); ASSOCIATED WITH genetic disease (ortholog); Lynch syndrome (ortholog); ONYCHODYSTROPHY, OSTEODYSTROPHY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES SYNDROME (ortholog); FOUND IN endoplasmic reticulum membrane (ortholog) NW_004955441 13492334 13525581 - 9068941 102012131 A0A8C2VIP6 MODEL AGCD01037151;GBDF01043189;XM_005390976;XM_005390977;XR_262076 XP_005391033;XP_005391034 phosphatidylinositol glycan anchor biosynthesis, class F APPROVED protein-coding ENSCLAG00000009602 8716753 LOC102012411 uncharacterized LOC102012411 NW_004955411 2942448 2946613 + 102012411 MODEL AGCD01011526;GBCQ01140642;XR_259913 ncrna 8716765 Cd47 CD47 molecule ENCODES a protein that exhibits cell-cell adhesion mediator activity (ortholog); protein binding involved in heterotypic cell-cell adhesion (ortholog); thrombospondin receptor activity (ortholog); INVOLVED IN ATP export (ortholog); cell migration (ortholog); cellular response to interleukin-1 (ortholog); ASSOCIATED WITH bipolar disorder (ortholog); genetic disease (ortholog); FOUND IN cell surface (ortholog); extracellular exosome (ortholog); plasma membrane (ortholog) NW_004955427 8704519 8740962 - 9068941 102012780 A0A8C2VC18 MODEL AGCD01027076;GBDJ01079526;XM_013515051 XP_013370505 leukocyte surface antigen CD47 protein-coding ENSCLAG00000009218 8716779 Kctd4 potassium channel tetramerization domain containing 4 ASSOCIATED WITH genetic disease (ortholog) NW_004955518 2977055 2987676 - 9068941 102013203 A0A8C2UIV8 MODEL AGCD01067789;GBCC01038644;XM_005409082;XM_005409083 XP_005409139;XP_005409140 BTB/POZ domain-containing protein KCTD4 protein-coding ENSCLAG00000000309 NW_004955518 2977055 2987676 - 8716787 LOC102013743 olfactory receptor 4C6-like NW_004955511 4928189 4955200 + 102013743 A0A8C2V2W4 MODEL AGCD01066539;GBCE01171519;XM_005408279;XM_013506517;XM_013506518 XP_005408336;XP_013361971;XP_013361972 protein-coding ENSCLAG00000005602 8716793 LOC102014327 uncharacterized LOC102014327 NW_004955408 3419831 3442678 - 102014327 MODEL AGCD01008056;GBDF01039360;XM_005376570 XP_005376627 uncharacterized protein LOC102014327 protein-coding 8716803 Tmem104 transmembrane protein 104 ASSOCIATED WITH genetic disease (ortholog) NW_004955553 1664464 1726965 + 9068941 102014614 A0A8C2VCS3 MODEL AGCD01072893;AGCD01072894;AGCD01072895;AGCD01072896;AGCD01072897;GBDF01039977;XM_005412255;XM_005412256;XM_013508654;XM_013508655 XP_005412312;XP_005412313;XP_013364108;XP_013364109 protein-coding ENSCLAG00000008787 NW_004955553 1664457 1729088 + 8716819 Prpf3 pre-mRNA processing factor 3 ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN mRNA splicing, via spliceosome (ortholog); spliceosomal tri-snRNP complex assembly (ortholog); PARTICIPATES IN spliceosome pathway; ASSOCIATED WITH fundus dystrophy (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN Cajal body (ortholog); cytosol (ortholog); nuclear speck (ortholog) NW_004955413 429259 455449 - 9068941;7240710 102015301 A0A8C2VX22;A0A8C2YTD6 MODEL AGCD01013465;AGCD01013466;AGCD01013467;AGCD01013468;GBDK01133619;XM_005378686;XM_005378687;XR_001232982 XP_005378743;XP_005378744 U4/U6 small nuclear ribonucleoprotein Prp3 protein-coding ENSCLAG00000015009 NW_004955413 429259 455463 - 8716845 LOC102015667 olfactory receptor 4N2 NW_004955550 562632 566690 - 9068941 102015667 A0A8C2UPG7 MODEL AGCD01072510;XM_005412033 XP_005412090 APPROVED protein-coding ENSCLAG00000001004 NW_004955550 562632 566690 - 8716851 Usp54 ubiquitin specific peptidase 54 ASSOCIATED WITH genetic disease (ortholog) NW_004955437 18240303 18322197 + 9068941 102015888 A0A8C2VJT9 MODEL AGCD01034787;AGCD01034788;AGCD01034789;GBDF01086628;XM_013516768 XP_013372222 protein-coding ENSCLAG00000010343 NW_004955437 18258024 18321481 + 8716878 LOC102016215 60S ribosomal protein L39 pseudogene NW_004955402 44397823 44398005 - 102016215 A0A8C2W6J8 MODEL AGCD01001113;XM_005373008 APPROVED pseudo ENSCLAG00000017707 8716882 LOC102017276 uncharacterized LOC102017276 NW_004955441 14023333 14027820 + 102017276 MODEL AGCD01037169;GBDJ01298866;XR_262078 ncrna 8716887 Lsm8 LSM8 homolog, U6 small nuclear RNA associated INVOLVED IN mRNA splicing, via spliceosome (ortholog); PARTICIPATES IN spliceosome pathway; ASSOCIATED WITH pleomorphic xanthoastrocytoma (ortholog); FOUND IN Lsm2-8 complex (ortholog); nucleus (ortholog); U2-type precatalytic spliceosome (ortholog) NW_004955432 23818036 23823550 + 9068941 102017691 A0A8C2UTC9 MODEL AGCD01031298;GBCE01029815;XM_005388137 XP_005388194 protein-coding ENSCLAG00000003726 NW_004955432 23818227 23823382 + 8716895 LOC102017731 arylamine N-acetyltransferase 2-like NW_004955403 42305517 42311914 + 102017731 A0A8C2YTJ8 MODEL AGCD01002751;GBDJ01116357;XM_005373603 XP_005373660 protein-coding ENSCLAG00000015279 8716901 H1-4 H1.4 linker histone, cluster member ENCODES a protein that exhibits ADP binding (ortholog); AMP binding (ortholog); ATP binding (ortholog); INVOLVED IN chromatin organization (ortholog); histone H3-K27 trimethylation (ortholog); histone H3-K4 trimethylation (ortholog); ASSOCIATED WITH adenoid cystic carcinoma (ortholog); Developmental Disease (ortholog); genetic disease (ortholog); FOUND IN heterochromatin (ortholog); nucleolus (ortholog); nucleosome (ortholog) NW_004955483 870957 871724 - 9068941 102018601 MODEL AGCD01057634;GBDJ01046421;XM_005403302 XP_005403359 LOC102018601 histone H1.4 APPROVED protein-coding 8716906 LOC102018740 uncharacterized LOC102018740 NW_004955423 15350156 15352340 + 102018740 MODEL AGCD01023805;GBCB01061780;XR_260970 ncrna 8716913 LOC102018968 ubiquitin-conjugating enzyme E2 D2-like NW_004955525 1602357 1603209 - 102018968 MODEL AGCD01069046;GBDF01048294;XM_005409726;XR_001231960 XP_005409783 protein-coding 8716919 LOC102019119 zinc finger protein 501-like NW_004955569 1687711 1702017 + 102019119 MODEL AGCD01074676;AGCD01074677;XM_013509378 XP_013364832 APPROVED protein-coding 8716920 Mapk6 mitogen-activated protein kinase 6 ENCODES a protein that exhibits MAP kinase activity (ortholog); protein heterodimerization activity (ortholog); protein kinase activity (ortholog); INVOLVED IN positive regulation of dendritic spine development (ortholog); protein phosphorylation (ortholog); ASSOCIATED WITH Bloom syndrome (ortholog); colorectal cancer (ortholog); COVID-19 (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleus (ortholog) NW_004955409 2664017 2676538 - 9068941 102019890 A0A8C2YQV7 MODEL AGCD01009210;GBCE01085622;GBDF01052518;XM_005376633 XP_005376690 protein-coding ENSCLAG00000011430 NW_004955409 2663569 2676544 - 8716929 LOC102019954 DLA class II histocompatibility antigen, DR-1 beta chain-like NW_004955437 1153576 1167424 - 102019954 A0A8C2W0H7;A0A8C2W3E5;A0A8C2W580;A0A8C2W5D7;A0A8C2W7G6 MODEL AGCD01034190;GBDI01262878;XM_005389451;XM_013517127;XM_013517128 XP_005389508;XP_013372581;XP_013372582 H-2 class II histocompatibility antigen, E-S beta chain-like;HLA class II histocompatibility antigen, DRB1-13 beta chain-like APPROVED protein-coding ENSCLAG00000016042 8716939 Ly6g6f lymphocyte antigen 6 family member G6F ASSOCIATED WITH genetic disease (ortholog); JMP syndrome (ortholog); megacolon (ortholog) NW_004955437 247408 250877 + 9068941 102021797 A0A8C2VIN3 MODEL AGCD01034115;GBDF01270679;XM_005389359;XM_005389360;XM_013516851 XP_005389416;XP_005389417;XP_013372305 lymphocyte antigen 6 complex locus protein G6f;lymphocyte antigen 6 complex, locus G6F APPROVED protein-coding ENSCLAG00000011200 NW_004955437 247094 250695 + 8716957 Hpgd 15-hydroxyprostaglandin dehydrogenase ENCODES a protein that exhibits 15-hydroxyprostaglandin dehydrogenase (NAD+) activity (ortholog); identical protein binding (ortholog); NAD binding (ortholog); INVOLVED IN ductus arteriosus closure (ortholog); female pregnancy (ortholog); kidney development (ortholog); ASSOCIATED WITH carcinoma (ortholog); colon carcinoma (ortholog); Fever (ortholog); FOUND IN basolateral plasma membrane (ortholog); cytosol (ortholog); extracellular space (ortholog) NW_004955403 32569841 32614860 + 9068941;7240710 102021932 A0A8C2YTP1 MODEL AGCD01002436;AGCD01002437;AGCD01002438;GBCQ01010378;XM_005373533 XP_005373590 15-hydroxyprostaglandin dehydrogenase [NAD(+)];hydroxyprostaglandin dehydrogenase 15-(NAD) APPROVED protein-coding ENSCLAG00000015466 NW_004955403 32569841 32613763 + 8716974 Vamp2 vesicle associated membrane protein 2 ENCODES a protein that exhibits calcium-dependent protein binding (ortholog); calmodulin binding (ortholog); identical protein binding (ortholog); INVOLVED IN calcium-ion regulated exocytosis (ortholog); cellular response to insulin stimulus (ortholog); eosinophil degranulation (ortholog); PARTICIPATES IN insulin responsive facilitative sugar transporter mediated glucose transport pathway; insulin secretion pathway; vasopressin signaling pathway; ASSOCIATED WITH common variable immunodeficiency (ortholog); Diamond-Blackfan anemia (ortholog); dyskeratosis congenita (ortholog); FOUND IN clathrin-coated vesicle (ortholog); cytoplasm (ortholog); cytoplasmic vesicle (ortholog) NW_004955467 8793296 8796771 + 9068941 102023680 A0A8C2VRT0;A0A8C2VUP8 MODEL AGCD01051472;GBCE01120199;GBDF01080447;XM_005399431 XP_005399488 vesicle-associated membrane protein 2;vesicle-associated membrane protein 2 (synaptobrevin 2) APPROVED protein-coding ENSCLAG00000012796 NW_004955467 8793296 8796771 + 8716983 LOC102023895 cytochrome c oxidase subunit 6C-like NW_004955469 7454142 7456205 + 102023895 MODEL AGCD01052416 pseudo 8716984 Dhcr24 24-dehydrocholesterol reductase ENCODES a protein that exhibits delta24(24-1) sterol reductase activity (ortholog); delta24-sterol reductase activity (ortholog); enzyme binding (ortholog); INVOLVED IN amyloid precursor protein catabolic process (ortholog); cholesterol biosynthetic process (ortholog); cholesterol biosynthetic process via desmosterol (ortholog); PARTICIPATES IN alendronate pharmacodynamics pathway; cholesterol biosynthetic pathway; cholesterol ester storage disease pathway; ASSOCIATED WITH Alzheimer's disease (ortholog); autism spectrum disorder (ortholog); COVID-19 (ortholog); FOUND IN endoplasmic reticulum (ortholog); nucleus (ortholog) NW_004955464 4533928 4557893 + 9068941;7240710 102024198 A0A8C2VJ74 MODEL AGCD01049992;GBCE01031278;XM_005398508 XP_005398565 delta(24)-sterol reductase protein-coding ENSCLAG00000010157 NW_004955464 4533928 4558133 + 8717000 Tmem86a transmembrane protein 86A ASSOCIATED WITH genetic disease (ortholog); hypertrophic cardiomyopathy 12 (ortholog); intellectual disability (ortholog) NW_004955414 33357432 33361478 + 9068941 102024787 A0A8C2WCR1 MODEL AGCD01015805;GBCE01065788;XM_005380425 XP_005380482 lysoplasmalogenase-like protein TMEM86A protein-coding ENSCLAG00000017173 NW_004955414 33357383 33361478 + 8717012 LOC102025486 taste receptor type 2 member 1-like NW_004955504 6894085 6897218 - 102025486 MODEL AGCD01064930;XM_005407093 XP_005407150 protein-coding 8717015 LOC102025955 NXPE family member 3-like NW_004955573 723592 744642 + 102025955 A0A8C2UM12 MODEL AGCD01075003;AGCD01075004;GBCE01055284;XM_005413736 XP_005413793 protein-coding ENSCLAG00000001293 8717033 LOC102026920 NXPE family member 3-like NW_004955573 684923 715573 + 102026920 A0A8C2UQK2 MODEL AGCD01075002;AGCD01075003;GBDF01217033;XM_005413739 XP_005413796 protein-coding ENSCLAG00000002337 8717042 LOC102027184 olfactory receptor 3A1 NW_004955481 180252 181211 + 102027184 A0A8C2WEK7 MODEL AGCD01056783;XM_013503360 XP_013358814 APPROVED protein-coding ENSCLAG00000017862 NW_004955481 180264 181211 + 8717046 Eif3g eukaryotic translation initiation factor 3 subunit G ENCODES a protein that exhibits RNA binding (ortholog); translation initiation factor activity (ortholog); INVOLVED IN translational initiation (ortholog); viral translational termination-reinitiation (ortholog); PARTICIPATES IN translation initiation pathway; ASSOCIATED WITH Cataplexy and Narcolepsy (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); eukaryotic translation initiation factor 3 complex (ortholog) NW_004955495 1452806 1456834 - 9068941 102027654 A0A8C2V993 MODEL AGCD01061693;GBDF01000179;XM_005405580 XP_005405637 eukaryotic translation initiation factor 3, subunit G APPROVED protein-coding ENSCLAG00000007381 NW_004955495 1451454 1457216 - 8717066 Kif23 kinesin family member 23 ENCODES a protein that exhibits microtubule binding (ortholog); INVOLVED IN mitotic cytokinesis (ortholog); mitotic spindle midzone assembly (ortholog); positive regulation of cytokinesis (ortholog); ASSOCIATED WITH Bloom syndrome (ortholog); colorectal cancer (ortholog); congenital dyserythropoietic anemia (ortholog); FOUND IN centralspindlin complex (ortholog); centrosome (ortholog); Flemming body (ortholog) NW_004955450 7060240 7083818 - 9068941 102004769 A0A8C2YPF8 MODEL AGCD01042531;AGCD01042532;GBDF01086111;XM_005393877;XM_013519019;XM_013519020;XM_013519021 XP_005393934;XP_013374473;XP_013374474;XP_013374475 kinesin-like protein KIF23 protein-coding ENSCLAG00000009415 NW_004955450 7060823 7082169 - 8717092 Prkd3 protein kinase D3 ENCODES a protein that exhibits kinase activity (ortholog); ASSOCIATED WITH genetic disease (ortholog); RASopathy (ortholog); Weight Gain (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog) NW_004955441 5051079 5112791 - 9068941 102004976 A0A8C2V227 MODEL AGCD01036867;AGCD01036868;AGCD01036869;GBBH01149583;GBDJ01031250;XM_005390869 XP_005390926 serine/threonine-protein kinase D3 protein-coding ENSCLAG00000004573 NW_004955441 5051079 5112799 - 8717128 LOC102005214 uncharacterized LOC102005214 NW_004955451 1877295 1878130 - 102005214 MODEL AGCD01042992;GBDF01085621;XR_001235999 ncrna 8717136 LOC102006243 calsyntenin-1 NW_004955479 9732376 9734653 + 9068941;7240710 102006243 A0A8C2VG28;A0A8C2VHK6;A0A8C2VMU3 MODEL AGCD01056494;GBCE01076233;GBDI01068209;XM_013503286 XP_013358740 Irf5 interferon regulatory factor 5 APPROVED protein-coding ENSCLAG00000010292 NW_004955479 9729557 9740893 + 8717155 LOC102007084 signal transducer CD24 pseudogene NW_004955406 23812162 23812599 - 102007084 MODEL AGCD01006185 APPROVED pseudo 8717156 LOC102007397 uncharacterized LOC102007397 NW_004955403 53982569 53983635 + 102007397 MODEL AGCD01003083;GBDK01203485;XM_005373841 XP_005373898 uncharacterized protein LOC102007397 protein-coding 8717162 LOC102007693 uncharacterized LOC102007693 NW_004955437 532416 541946 + 102007693 MODEL AGCD01034142;AGCD01034143;AGCD01034144;GBDJ01142993;XR_261816 ncrna 8717167 LOC102007929 uncharacterized LOC102007929 NW_004955435 5612861 5627141 + 102007929 MODEL AGCD01032892;AGCD01032893;GBDF01113740;XR_261663 ncrna 8717172 LOC102008034 MAP3K12-binding inhibitory protein 1 pseudogene NW_004955441 160336 161394 + 102008034 MODEL AGCD01036685 APPROVED pseudo 8717173 LOC102008165 filaggrin-2 NW_004955589 115942 127045 + 102008165 MODEL AGCD01076155;AGCD01076156;GBCC01029912;XM_005414527;XM_013509950;XM_013509951 XP_005414584;XP_013365404;XP_013365405 Flg2 filaggrin family member 2 APPROVED protein-coding 8717181 LOC102008487 actin cytoskeleton-regulatory complex protein pan1-like NW_004955451 2446558 2456251 - 102008487 MODEL AGCD01043009;GBBH01184630;XM_013519305 XP_013374759 APPROVED protein-coding 8717189 LOC102008682 plakophilin-2-like NW_004956130 12 5617 + 102008682 MODEL AGCD01079104;GBDK01128349;GBDK01128352;XM_005415169 XP_005415226 protein-coding 8717195 LOC102008881 uncharacterized LOC102008881 NW_004955520 1038221 1056799 - 102008881 MODEL AGCD01068041;AGCD01068042;GBDF01278076;XR_264581 ncrna 8717200 LOC102009434 zinc finger protein 709-like NW_004955569 187430 209724 + 102009434 MODEL AGCD01074566;GBDF01011185;XM_013509367 XP_013364821 protein-coding 8717204 Cdk15 cyclin dependent kinase 15 ENCODES a protein that exhibits protein serine/threonine kinase activity (ortholog); PARTICIPATES IN Wnt signaling pathway; ASSOCIATED WITH autoimmune lymphoproliferative syndrome type 2B (ortholog); Autoimmune Lymphoproliferative Syndrome, Type V (ortholog); common variable immunodeficiency 1 (ortholog) NW_004955457 12878736 12966434 - 9068941 102010553 A0A8C2URJ9 MODEL AGCD01047031;AGCD01047032;AGCD01047033;GBDI01384668;XM_005397066 XP_005397123 cyclin-dependent kinase 15 APPROVED protein-coding ENSCLAG00000003400 NW_004955457 12880959 12966410 - 8717228 Psmf1 proteasome inhibitor subunit 1 ENCODES a protein that exhibits proteasome binding (ortholog); protein heterodimerization activity (ortholog); protein homodimerization activity (ortholog); INVOLVED IN negative regulation of proteasomal protein catabolic process (ortholog); ubiquitin-dependent protein catabolic process (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); endoplasmic reticulum (ortholog); perinuclear region of cytoplasm (ortholog) NW_004955596 381080 414307 + 9068941 102011068 A0A8C2UI75;A0A8C2UL48 MODEL AGCD01076517;GBDF01007515;XM_005414689 XP_005414746 proteasome (prosome, macropain) inhibitor subunit 1 (PI31);proteasome inhibitor PI31 subunit APPROVED protein-coding ENSCLAG00000000097 NW_004955596 381068 416055 + 8717240 Iqank1 IQ motif and ankyrin repeat containing 1 NW_004955454 2427621 2461556 + 102011174 A0A8C2VVK5 MODEL AGCD01045020;AGCD01045021;GBCE01142105;XM_005395804;XM_005395805;XM_005395806;XM_013520055;XM_013520056;XM_013520057 XP_005395861;XP_005395862;XP_005395863;XP_013375509;XP_013375510;XP_013375511 LOC102011174 putative IQ motif and ankyrin repeat domain-containing protein LOC642574 homolog APPROVED protein-coding ENSCLAG00000013041 NW_004955454 2432299 2461364 + 8717272 Adora2b adenosine A2b receptor ENCODES a protein that exhibits G protein-coupled receptor activity (ortholog); INVOLVED IN adenylate cyclase-activating G protein-coupled receptor signaling pathway (ortholog); cellular response to extracellular stimulus (ortholog); cGMP-mediated signaling (ortholog); PARTICIPATES IN adenosine signaling pathway; ASSOCIATED WITH Chemical and Drug Induced Liver Injury (ortholog); genetic disease (ortholog); Neoplasm Metastasis (ortholog); FOUND IN cell surface (ortholog); glutamatergic synapse (ortholog); plasma membrane (ortholog) NW_004955467 1342271 1363149 + 9068941 102011637 A0A8C2V289 MODEL AGCD01051262;GBDJ01175337;XM_005399305 XP_005399362 adenosine receptor A2b protein-coding ENSCLAG00000006111 NW_004955467 1342271 1363138 + 8717278 LOC102011922 protein kinase C iota type pseudogene NW_004955446 1525926 1528371 + 102011922 MODEL AGCD01039967;XM_005392599 APPROVED pseudo 8717283 LOC102013146 gametocyte-specific factor 1-like NW_004955458 1718253 1730596 - 102013146 A0A8C2VG64 MODEL AGCD01047201;AGCD01047202;GBBH01224139;XM_013520795 XP_013376249 protein-coding ENSCLAG00000008579 8717294 LOC102013421 uncharacterized LOC102013421 NW_004955487 9461547 9465656 - 102013421 MODEL AGCD01059459;XR_263994 ncrna 8717299 LOC102013922 uncharacterized LOC102013922 NW_004955470 5868613 5875570 + 102013922 MODEL AGCD01052761;GBDF01111358;XM_005400752;XM_005400753;XR_263472 XP_005400809;XP_005400810 uncharacterized protein LOC102013922 protein-coding 8717310 LOC102014069 high mobility group protein B3 pseudogene NW_004955505 5110525 5111126 + 102014069 MODEL AGCD01065145 APPROVED pseudo 8717311 Tns4 tensin 4 INVOLVED IN protein localization (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN focal adhesion (ortholog) NW_004955451 15036773 15053199 - 9068941 102014200 A0A8C2VT11;A0A8C2YSI6 MODEL AGCD01043593;GBBH01062587;XM_005394360;XM_013519361;XM_013519362;XR_001235981 XP_005394417;XP_013374815;XP_013374816 tensin-4 protein-coding ENSCLAG00000013766 NW_004955451 15034977 15053253 - 8717328 Spred3 sprouty related EVH1 domain containing 3 ENCODES a protein that exhibits stem cell factor receptor binding (ortholog); INVOLVED IN negative regulation of epithelial to mesenchymal transition (ortholog); negative regulation of ERK1 and ERK2 cascade (ortholog); negative regulation of lens fiber cell differentiation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN plasma membrane (ortholog) NW_004955468 1030964 1039495 - 9068941 102014764 A0A8C2VRH6 MODEL AGCD01051748;GBDF01220614;XM_005399849;XM_005399850;XM_005399851;XM_005399852;XM_013522465;XM_013522466;XM_013522467 XP_005399906;XP_005399907;XP_005399908;XP_005399909;XP_013377919;XP_013377920;XP_013377921 sprouty-related, EVH1 domain containing 3;sprouty-related, EVH1 domain-containing protein 3 APPROVED protein-coding ENSCLAG00000013431 NW_004955468 1028470 1039495 - 8717346 Apeh acylaminoacyl-peptide hydrolase ENCODES a protein that exhibits identical protein binding (ortholog); omega peptidase activity (ortholog); serine-type endopeptidase activity (ortholog); INVOLVED IN amyloid-beta metabolic process (ortholog); proteolysis (ortholog); ASSOCIATED WITH Aicardi-Goutieres Syndrome 1 (ortholog); developmental and epileptic encephalopathy (ortholog); early infantile epileptic encephalopathy (ortholog); FOUND IN cytosol (ortholog); nuclear membrane (ortholog) NW_004955532 1580473 1590274 + 9068941 102015239 A0A8C2V504 MODEL AGCD01070195;GBDF01119664;XM_005410206 XP_005410263 acylamino-acid-releasing enzyme protein-coding ENSCLAG00000006987 NW_004955532 1580553 1590138 + 8717372 LOC102015355 heat shock cognate 71 kDa protein pseudogene NW_004955444 12513405 12515314 - 102015355 MODEL AGCD01039075 APPROVED pseudo 8717373 LOC102015630 uncharacterized LOC102015630 NW_004955476 6348897 6368660 - 102015630 MODEL AGCD01055328;AGCD01055329;AGCD01055330;GBBH01045751;XR_001230802;XR_263624 ncrna 8717379 Clec4e C-type lectin domain family 4 member E ENCODES a protein that exhibits calcium ion binding (ortholog); glycolipid binding (ortholog); pattern recognition receptor activity (ortholog); INVOLVED IN antifungal innate immune response (ortholog); defense response to bacterium (ortholog); Fc-gamma receptor signaling pathway (ortholog); ASSOCIATED WITH Brain Injuries (ortholog); developmental and epileptic encephalopathy 21 (ortholog); genetic disease (ortholog); FOUND IN membrane (ortholog); phagocytic vesicle membrane (ortholog); plasma membrane (ortholog) NW_004955413 5256523 5261385 + 9068941 102015706 A0A8C2VWD4 MODEL AGCD01013659;GBDF01076579;XM_005378867;XM_005378868;XR_001233008 XP_005378924;XP_005378925 C-type lectin domain family 4, member E APPROVED protein-coding ENSCLAG00000014802 NW_004955413 5256440 5262938 + 8717395 Larp1b La ribonucleoprotein 1B ASSOCIATED WITH genetic disease (ortholog); neuronal ceroid lipofuscinosis 7 (ortholog); prostate cancer (ortholog) NW_004955428 13319322 13427932 - 9068941 102015871 MODEL AGCD01027948;AGCD01027949;AGCD01027950;AGCD01027951;GBDK01309285;XM_013515251 XP_013370705 La ribonucleoprotein domain family member 1B;La ribonucleoprotein domain family, member 1B APPROVED protein-coding 8717418 Gnb2 G protein subunit beta 2 ENCODES a protein that exhibits calcium channel regulator activity (ortholog); GTPase binding (ortholog); protein-containing complex binding (ortholog); INVOLVED IN regulation of potassium ion transmembrane transport (ortholog); ASSOCIATED WITH Developmental Delay with or without Dysmorphic Facies and Autism (ortholog); Developmental Disabilities (ortholog); genetic disease (ortholog); FOUND IN cell body (ortholog); perinuclear region of cytoplasm (ortholog); plasma membrane (ortholog) NW_004955573 242815 247740 - 9068941 102016209 A0A8C2YJ55 MODEL AGCD01074969;GBDK01018772;XM_005413702 XP_005413759 guanine nucleotide binding protein (G protein), beta polypeptide 2;guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-2 APPROVED protein-coding ENSCLAG00000001809 NW_004955573 241854 247849 - 8717435 G2e3 G2/M-phase specific E3 ubiquitin protein ligase ENCODES a protein that exhibits ubiquitin protein ligase activity (ortholog); INVOLVED IN blastocyst development (ortholog); negative regulation of intrinsic apoptotic signaling pathway (ortholog); protein polyubiquitination (ortholog); ASSOCIATED WITH Brain-Lung-Thyroid Syndrome (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); Golgi apparatus (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955409 29908075 29965331 - 9068941 102016897 A0A8C2VAB0;A0A8C2VFI5 MODEL AGCD01010283;GBDJ01348371;XM_013510386 XP_013365840 G2/M phase-specific E3 ubiquitin-protein ligase protein-coding ENSCLAG00000008721 NW_004955409 29908148 29945497 - 8717453 Unc5a unc-5 netrin receptor A ENCODES a protein that exhibits netrin receptor activity (ortholog); INVOLVED IN anterior/posterior axon guidance (ortholog); axon guidance (ortholog); netrin-activated signaling pathway (ortholog); ASSOCIATED WITH Chromosome 5, Trisomy 5q (ortholog); Ehlers-Danlos syndrome dermatosparaxis type (ortholog); Ehlers-Danlos syndrome spondylodysplastic type 2 (ortholog); FOUND IN neuron projection membrane (ortholog); neuronal cell body membrane (ortholog); plasma membrane (ortholog) NW_004955408 29071812 29132744 + 9068941 102017746 A0A8C2VT64;A0A8C2YSJ3;A0A8C2YSJ6 MODEL AGCD01008738;GBBH01004842;XM_005376402;XM_005376404;XM_005376405 XP_005376459;XP_005376461;XP_005376462 netrin receptor UNC5A;unc-5 homolog A APPROVED protein-coding ENSCLAG00000013808 NW_004955408 29071792 29132037 + 8717483 Gpr161 G protein-coupled receptor 161 ENCODES a protein that exhibits G protein-coupled receptor activity (ortholog); INVOLVED IN adenylate cyclase-activating G protein-coupled receptor signaling pathway (ortholog); negative regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning (ortholog); ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); immunodeficiency 25 (ortholog); FOUND IN cilium (ortholog); glial cell projection (ortholog); neuron projection (ortholog) NW_004955462 8981729 9034009 + 9068941 102019895 A0A8C2V1Z2 MODEL AGCD01049331;AGCD01049332;GBDF01156462;XM_005398214;XM_005398215;XM_005398216;XM_005398217;XM_005398218;XM_005398219;XM_013521419;XM_013521420 XP_005398271;XP_005398272;XP_005398273;XP_005398274;XP_005398275;XP_005398276;XP_013376873;XP_013376874 G-protein coupled receptor 161 protein-coding ENSCLAG00000005310 NW_004955462 8981157 9028946 + 8717510 LOC102020633 uncharacterized LOC102020633 NW_004955453 16423553 16456778 - 102020633 MODEL AGCD01044903;AGCD01044904;GBDI01378176;XR_001236202;XR_001236203;XR_001236204 ncrna 8717521 Capn3 calpain 3 ENCODES a protein that exhibits calcium ion binding (ortholog); calcium-dependent cysteine-type endopeptidase activity (ortholog); catalytic activity (ortholog); INVOLVED IN calcium-dependent self proteolysis (ortholog); cellular response to calcium ion (ortholog); cellular response to salt stress (ortholog); ASSOCIATED WITH Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 4 (ortholog); autosomal recessive limb-girdle muscular dystrophy (ortholog); autosomal recessive limb-girdle muscular dystrophy type 2A (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); myofibril (ortholog) NW_004955416 9070479 9121099 + 9068941;7240710 102021120 A0A8C2VBG4;A0A8C2VBG8;A0A8C2YP70;A0A8C2YP71 MODEL AGCD01017075;AGCD01017076;AGCD01017077;GBCB01004371;XM_005381335;XM_005381338;XM_005381339;XM_005381340;XM_005381342;XM_013512462;XM_013512463;XM_013512464;XM_013512466 XP_005381392;XP_005381395;XP_005381396;XP_005381397;XP_005381399;XP_013367916;XP_013367917;XP_013367918;XP_013367920 calpain 3, (p94);calpain-3 APPROVED protein-coding ENSCLAG00000009048 NW_004955416 9070399 9117794 + 8717564 Sirt7 sirtuin 7 ENCODES a protein that exhibits chromatin binding (ortholog); NAD-dependent histone H3K18 deacetylase activity (ortholog); NAD-dependent protein deacetylase activity (ortholog); INVOLVED IN DNA damage response (ortholog); DNA repair-dependent chromatin remodeling (ortholog); homologous chromosome pairing at meiosis (ortholog); PARTICIPATES IN histone modification pathway; RNA polymerase I transcription pathway; Sirtuin mediated pathway; ASSOCIATED WITH fatty liver disease (ortholog); genetic disease (ortholog); Reperfusion Injury (ortholog); FOUND IN chromatin (ortholog); nuclear speck (ortholog); nucleolus (ortholog) NW_004955506 1252271 1258728 + 9068941 102021374 A0A8C2UY45;A0A8C2YLB6;A0A8C2YLB7 MODEL AGCD01065252;GBDF01192905;XM_005407236;XM_005407237;XM_005407238;XM_005407239;XM_005407240;XM_013506059;XM_013506060 XP_005407293;XP_005407294;XP_005407295;XP_005407296;XP_005407297;XP_013361513;XP_013361514 NAD-dependent protein deacetylase sirtuin-7 protein-coding ENSCLAG00000004980 NW_004955506 1252274 1258728 + 8717588 LOC102021394 uncharacterized LOC102021394 NW_004955547 1572431 1574209 - 102021394 MODEL AGCD01072233;GBBH01184529;XR_264902 ncrna 8717592 Slc30a6 solute carrier family 30 member 6 ENCODES a protein that exhibits zinc ion transmembrane transporter activity (ortholog); zinc:proton antiporter activity (ortholog); INVOLVED IN Golgi to endosome transport (ortholog); regulation of zinc ion transport (ortholog); zinc ion import into Golgi lumen (ortholog); ASSOCIATED WITH Alzheimer's disease (ortholog); Autoinflammation with Infantile Enterocolitis (ortholog); familial cold autoinflammatory syndrome 4 (ortholog); FOUND IN Golgi apparatus (ortholog); trans-Golgi network membrane (ortholog) NW_004955441 528256 567382 + 9068941 102021600 A0A8C2YLM8 MODEL AGCD01036710;AGCD01036711;AGCD01036712;GBDF01128354;XM_005390837;XM_013517595 XP_005390894;XP_013373049 solute carrier family 30 (zinc transporter), member 6;zinc transporter 6 APPROVED protein-coding ENSCLAG00000005442 NW_004955441 528234 567382 + 8717611 Znf410 zinc finger protein 410 ENCODES a protein that exhibits DNA-binding transcription factor activity (ortholog); RNA polymerase II cis-regulatory region sequence-specific DNA binding (ortholog); sequence-specific double-stranded DNA binding (ortholog); INVOLVED IN negative regulation of gene expression (ortholog); positive regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); primary ciliary dyskinesia 16 (ortholog) NW_004955523 1479042 1509889 - 9068941 102023066 A0A8C2UUV6 MODEL AGCD01068522;GBBH01060511;XM_013507138;XM_013507139 XP_013362592;XP_013362593 protein-coding ENSCLAG00000003640 NW_004955523 1475908 1514465 - 8717636 Syce1l synaptonemal complex central element protein 1 like ASSOCIATED WITH genetic disease (ortholog); spermatogenic failure 3 (ortholog); FOUND IN intermediate filament cytoskeleton (ortholog) NW_004955522 469418 480090 + 9068941 102023628 A0A8C2YI21;A0A8C2YI24 MODEL AGCD01068345;AGCD01068346;GBDF01083831;GBDF01083833;XM_013507106 XP_013362560 synaptonemal complex central element protein 1-like APPROVED protein-coding ENSCLAG00000000207 8717640 LOC102025226 olfactory receptor 1468-like NW_004955467 13332532 13333473 + 102025226 A0A8C2W5U0 MODEL AGCD01051671;XM_005399734 XP_005399791 APPROVED protein-coding ENSCLAG00000017734 8717643 Ergic1 endoplasmic reticulum-golgi intermediate compartment 1 INVOLVED IN endoplasmic reticulum to Golgi vesicle-mediated transport (ortholog); ASSOCIATED WITH arthrogryposis multiplex congenita (ortholog); atrial heart septal defect 7 (ortholog); Atrial Septal Defect with Atrioventricular Conduction Defects (ortholog); FOUND IN endoplasmic reticulum-Golgi intermediate compartment (ortholog); intracellular membrane-bounded organelle (ortholog); nucleoplasm (ortholog) NW_004955408 25540149 25644108 + 9068941 102027272 A0A8C2VUK5;A0A8C2VUW7 MODEL AGCD01008647;GBCB01057939;XM_005376342;XM_013509355;XM_013509357;XM_013509359 XP_005376399;XP_013364809;XP_013364811;XP_013364813 endoplasmic reticulum-Golgi intermediate compartment protein 1;endoplasmic reticulum-golgi intermediate compartment (ERGIC) 1 APPROVED protein-coding ENSCLAG00000014304 NW_004955408 25540013 25645503 + 8717660 LOC102028800 uncharacterized LOC102028800 NW_004955438 8518357 8529062 - 102028800 MODEL AGCD01035161;GBDF01251003;XR_261921 ncrna 8717665 Wbp11 WW domain binding protein 11 ENCODES a protein that exhibits protein phosphatase regulator activity (ortholog); WW domain binding (ortholog); INVOLVED IN RNA splicing (ortholog); ASSOCIATED WITH autosomal dominant intellectual developmental disorder 6 (ortholog); developmental and epileptic encephalopathy 27 (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955413 11533303 11549067 - 9068941 102028846 A0A8C2W297 MODEL AGCD01013964;GBCQ01067517;XM_005379004;XM_005379005;XM_013511645 XP_005379061;XP_005379062;XP_013367099 WW domain-binding protein 11 protein-coding ENSCLAG00000016400 8717684 LOC102029223 uncharacterized LOC102029223 NW_004955538 3291100 3295111 - 102029223 MODEL AGCD01071157;XR_264808 ncrna ENSCLAG00000029018 8717689 Pld4 phospholipase D family member 4 ENCODES a protein that exhibits phospholipase D activity (ortholog); single-stranded DNA 5'-3' DNA exonuclease activity (ortholog); INVOLVED IN establishment of localization in cell (ortholog); hematopoietic progenitor cell differentiation (ortholog); phagocytosis (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease axonal type 2O (ortholog); Experimental Liver Cirrhosis (ortholog); focal segmental glomerulosclerosis 5 (ortholog); FOUND IN early endosome (ortholog); endoplasmic reticulum (ortholog); endoplasmic reticulum membrane (ortholog) NW_004955538 3296581 3303187 + 9068941 102029444 A0A8C2V066 MODEL AGCD01071157;GBDJ01237040;XM_005410848 XP_005410905 phospholipase D family, member 4;phospholipase D4 APPROVED protein-coding ENSCLAG00000004150 NW_004955538 3295937 3303802 + 8717709 LOC102030021 arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1-like NW_004955402 35443964 35454925 - 102030021 MODEL AGCD01000887 pseudo 8717710 Gpr3 G protein-coupled receptor 3 INVOLVED IN adenylate cyclase-activating G protein-coupled receptor signaling pathway (ortholog); G protein-coupled receptor signaling pathway coupled to cGMP nucleotide second messenger (ortholog); negative regulation of cell cycle (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); nuclear membrane (ortholog); plasma membrane (ortholog) NW_004955452 6648470 6651938 + 9068941 102004233 A0A8C2VPY2 MODEL AGCD01044118;GBDF01030401;XM_005394907;XM_005394908 XP_005394964;XP_005394965 G-protein coupled receptor 3 protein-coding ENSCLAG00000012893 NW_004955452 6648470 6651389 + 8717722 Calhm2 calcium homeostasis modulator family member 2 INVOLVED IN positive regulation of apoptotic process (ortholog); ASSOCIATED WITH genetic disease (ortholog) NW_004955485 7106926 7111745 + 9068941 102004935 A0A8C2UNZ5 MODEL AGCD01058635;GBBH01186775;XM_005403804 XP_005403861 calcium homeostasis modulator 2;calcium homeostasis modulator protein 2 APPROVED protein-coding ENSCLAG00000001846 NW_004955485 7106926 7113249 + 8717729 Rnf25 ring finger protein 25 ENCODES a protein that exhibits molecular function inhibitor activity (ortholog); NF-kappaB binding (ortholog); ubiquitin protein ligase activity (ortholog); INVOLVED IN positive regulation of NF-kappaB transcription factor activity (ortholog); protein K6-linked ubiquitination (ortholog); protein ubiquitination (ortholog); ASSOCIATED WITH alacrima, achalasia, and impaired intellectual development syndrome (ortholog); cerebrotendinous xanthomatosis (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); cytosolic ribosome (ortholog); nucleus (ortholog) NW_004955453 14753575 14761617 + 9068941 102005555 A0A8C2YRW6 MODEL AGCD01044873;GBDF01084559;XM_005395628 XP_005395685 E3 ubiquitin-protein ligase RNF25 protein-coding ENSCLAG00000012866 NW_004955453 14753575 14761617 + 8717743 Gprc5c G protein-coupled receptor class C group 5 member C ASSOCIATED WITH genetic disease (ortholog); FOUND IN receptor complex (ortholog) NW_004955553 1303176 1315482 + 9068941 102007816 A0A8C2YJU9 MODEL AGCD01072878;GBCB01003226;XM_005412233;XM_013508636 XP_005412290;XP_013364090 G protein-coupled receptor, class C, group 5, member C;G protein-coupled receptor, family C, group 5, member C;G-protein coupled receptor family C group 5 member C APPROVED protein-coding ENSCLAG00000002852 NW_004955553 1297560 1321373 + 8717760 LOC102008303 zinc finger protein 419-like NW_004955468 4251476 4270784 + 102008303 A0A8C2YRL0;A0A8C2YRL6 MODEL AGCD01051903;AGCD01051904;GBCE01148167;XM_005400012;XM_013522366 XP_005400069;XP_013377820 zinc finger protein 883-like APPROVED protein-coding ENSCLAG00000012457 8717769 Tomm40l translocase of outer mitochondrial membrane 40 like ENCODES a protein that exhibits mitochondrion targeting sequence binding (ortholog); preprotein binding (ortholog); ASSOCIATED WITH autoimmune interstitial lung, joint, and kidney disease (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN mitochondrial outer membrane translocase complex (ortholog); protein-containing complex (ortholog) NW_004955468 12981023 12984999 + 9068941 102008304 A0A8C2VU66;A0A8C2VWW5 MODEL AGCD01052194;GBCE01159608;XM_005400273;XM_013522479 XP_005400330;XP_013377933 mitochondrial import receptor subunit TOM40B;translocase of outer mitochondrial membrane 40 homolog (yeast)-like APPROVED protein-coding ENSCLAG00000013465 NW_004955468 12981024 12984999 + 8717791 LOC102008333 thrombospondin type-1 domain-containing protein 1-like NW_004955426 16226528 16227149 - 102008333 MODEL AGCD01026464 pseudo 8717792 Dipk2a divergent protein kinase domain 2A INVOLVED IN cardiac muscle cell proliferation (ortholog); negative regulation of smooth muscle cell apoptotic process (ortholog); positive regulation of protein kinase C activity (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); Experimental Liver Cirrhosis (ortholog); FOUND IN COPI vesicle coat (ortholog); COPI-coated vesicle (ortholog); extracellular region (ortholog) NW_004955508 1954600 1975842 - 9068941 102008647 A0A8C2YIM7 MODEL AGCD01065777;GBCE01030452;XM_005407727 XP_005407784 LOC102008647 chromosome unknown open reading frame, human C3orf58;deleted in autism protein 1 APPROVED protein-coding ENSCLAG00000001078 NW_004955508 1953923 1975842 - 8717799 Spc24 SPC24 component of NDC80 kinetochore complex INVOLVED IN attachment of spindle microtubules to kinetochore (ortholog); ASSOCIATED WITH alpha-mannosidosis (ortholog); Charcot-Marie-Tooth disease dominant intermediate B (ortholog); episodic ataxia type 2 (ortholog); FOUND IN kinetochore (ortholog); Ndc80 complex (ortholog); nucleolus (ortholog) NW_004955774 5456 9810 - 9068941 102008681 A0A8C2UMU5 MODEL AGCD01078321;GBDF01226288;XM_005415107 XP_005415164 SPC24, NDC80 kinetochore complex component;kinetochore protein Spc24 APPROVED protein-coding ENSCLAG00000000916 NW_004955774 5658 9769 - 8717808 LOC102008974 DNA primase small subunit pseudogene NW_004955434 12000624 12001975 + 102008974 MODEL AGCD01032382 APPROVED pseudo 8717809 LOC102009512 aldehyde dehydrogenase family 3 member B2-like NW_004955422 17841051 17848453 + 102009512 A0A8C2W7I4 MODEL AGCD01022932;GBDK01152699;XM_005384296 XP_005384353 APPROVED protein-coding ENSCLAG00000017296 NW_004955422 17840780 17849174 + 8717825 Ccdc58 coiled-coil domain containing 58 ASSOCIATED WITH alkaptonuria (ortholog); familial hypocalciuric hypercalcemia (ortholog); Primary Lymphedema with Myelodysplasia (ortholog) NW_004955427 21639392 21667642 - 9068941 102009860 A0A8C2VMM2;A0A8C2VQQ6 MODEL AGCD01027453;GBCQ01066280;XM_005386509;XM_005386510 XP_005386566;XP_005386567 coiled-coil domain-containing protein 58 protein-coding ENSCLAG00000011614 NW_004955427 21639392 21667696 - 8717837 LOC102010136 uncharacterized LOC102010136 NW_004955411 9963098 9981570 - 102010136 MODEL AGCD01011768;GBDF01305717;XR_259928 ncrna 8717841 LOC102010841 Ig lambda-2 chain C regions-like NW_004955442 17155684 17169023 - 102010841 A0A8C2YUH2 MODEL AGCD01037943;AGCD01037944;XM_005391686;XM_005391687 immunoglobulin lambda-like polypeptide 5-like APPROVED gene ENSCLAG00000016611 NW_004955442 17155808 17169237 - 8717850 Fgl2 fibrinogen like 2 ENCODES a protein that exhibits peptidase activator activity (ortholog); INVOLVED IN negative regulation of defense response to virus (ortholog); negative regulation of dendritic cell antigen processing and presentation (ortholog); negative regulation of macrophage antigen processing and presentation (ortholog); ASSOCIATED WITH allergic contact dermatitis (ortholog); autoimmune glomerulonephritis (ortholog); Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB (ortholog); FOUND IN cell surface (ortholog) NW_004955410 7899263 7903499 + 9068941 102010979 A0A8C2V2N4 MODEL AGCD01010726;GBCE01075859;GBDF01281505;XM_005377557 XP_005377614 fibrinogen-like 2;fibroleukin APPROVED protein-coding ENSCLAG00000004828 NW_004955410 7899309 7902722 + 8717855 Npw neuropeptide W ENCODES a protein that exhibits G protein-coupled receptor binding (ortholog); INVOLVED IN feeding behavior (ortholog); G protein-coupled receptor signaling pathway (ortholog); ASSOCIATED WITH epilepsy (ortholog); genetic disease (ortholog); idiopathic generalized epilepsy (ortholog) NW_004955442 15241140 15244387 - 9068941 102012031 A0A8C2W119 MODEL AGCD01037860;AGCD01037861;GBDK01264615;XM_013517652 XP_013373106 protein-coding ENSCLAG00000014103 NW_004955442 15241231 15242064 - 8717861 LOC102012280 uncharacterized LOC102012280 NW_004955455 541374 542760 - 102012280 MODEL AGCD01045560;GBDF01021764;XR_262806 ncrna 8717866 LOC102012658 uncharacterized LOC102012658 NW_004955421 25068843 25105800 + 102012658 MODEL AGCD01022227;AGCD01022228;GBCQ01032486;XR_260828 ncrna 8717872 LOC102012953 olfactory receptor 491-like NW_004955414 23663348 23664286 - 102012953 MODEL AGCD01015514;XM_013511761 XP_013367215 protein-coding 8717873 Nfil3 nuclear factor, interleukin 3 regulated ENCODES a protein that exhibits DNA-binding transcription factor activity (ortholog); DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); identical protein binding (ortholog); INVOLVED IN cellular response to interleukin-4 (ortholog); natural killer cell differentiation (ortholog); negative regulation of DNA-templated transcription (ortholog); ASSOCIATED WITH 3-methylglutaconic aciduria type 1 (ortholog); advanced sleep phase syndrome (ortholog); genetic disease (ortholog); FOUND IN RNA polymerase II transcription regulator complex (ortholog) NW_004955515 908313 910159 + 9068941 102012994 A0A8C2YV20 MODEL AGCD01067214;GBDJ01272876;XM_013506902 XP_013362356 protein-coding ENSCLAG00000017505 NW_004955515 908477 909868 + 8717879 Mcee methylmalonyl-CoA epimerase ENCODES a protein that exhibits methylmalonyl-CoA epimerase activity (ortholog); INVOLVED IN L-methylmalonyl-CoA metabolic process (ortholog); PARTICIPATES IN 3-hydroxy-3-methylglutaryl-CoA lyase deficiency pathway; 3-hydroxyisobutyric aciduria pathway; 3-methylcrotonyl CoA carboxylase 1 deficiency pathway; ASSOCIATED WITH dystonia (ortholog); genetic disease (ortholog); methylmalonic acidemia (ortholog) NW_004955416 29684557 29703495 - 9068941;7240710 102015515 A0A8C2YQQ4 MODEL AGCD01017663;AGCD01017664;GBCB01089267;GBDK01147232;XM_013512610 XP_013368064 methylmalonyl CoA epimerase;methylmalonyl-CoA epimerase, mitochondrial APPROVED protein-coding ENSCLAG00000011216 NW_004955416 29685385 29698557 - 8717885 LOC102016449 mucin-17 NW_004955456 16203150 16214796 - 9068941 102016449 A0A8C2VM39 MODEL AGCD01046694;GBDF01024236;XM_005396900 XP_005396957 Muc17 mucin 17, cell surface associated APPROVED protein-coding ENSCLAG00000010067 8717899 LOC102016704 40S ribosomal protein S10 pseudogene NW_004955416 8818949 8819438 + 102016704 A0A8C2WAK0 MODEL AGCD01017070 APPROVED pseudo ENSCLAG00000017787 8717900 Ccdc69 coiled-coil domain containing 69 INVOLVED IN spindle midzone assembly (ortholog); ASSOCIATED WITH familial adenomatous polyposis 1 (ortholog); genetic disease (ortholog); Hereditary Neoplastic Syndromes (ortholog); FOUND IN spindle midzone (ortholog) NW_004955408 2471157 2498611 + 102016979 MODEL AGCD01008007;GBCB01038685;XM_005376057 XP_005376114 coiled-coil domain-containing protein 69 protein-coding 8717913 Tecr trans-2,3-enoyl-CoA reductase ENCODES a protein that exhibits very-long-chain enoyl-CoA reductase activity (ortholog); INVOLVED IN fatty acid elongation (ortholog); sphingolipid metabolic process (ortholog); very long-chain fatty acid biosynthetic process (ortholog); ASSOCIATED WITH autosomal recessive intellectual developmental disorder 14 (ortholog); genetic disease (ortholog); FOUND IN endoplasmic reticulum (ortholog); endoplasmic reticulum membrane (ortholog) NW_004955415 33112098 33138810 + 9068941;7240710 102017231 A0A8C2VZJ3;A0A8C2W1S0;A0A8C2W7C6;A0A8C2YTV8;A0A8C2YTW3 MODEL AGCD01016751;AGCD01016752;GBDF01043421;XM_005381105 XP_005381162 very-long-chain enoyl-CoA reductase protein-coding ENSCLAG00000015751 NW_004955415 33135646 33143145 + 8717930 Mib2 MIB E3 ubiquitin protein ligase 2 ENCODES a protein that exhibits ubiquitin protein ligase activity (ortholog); ubiquitin-protein transferase activity (ortholog); INVOLVED IN positive regulation of I-kappaB kinase/NF-kappaB signaling (ortholog); protein ubiquitination (ortholog); ASSOCIATED WITH chromosome 1p36 deletion syndrome (ortholog); congenital myasthenic syndrome 8 (ortholog); COVID-19 (ortholog); FOUND IN early endosome (ortholog); plasma membrane (ortholog); ubiquitin ligase complex (ortholog) NW_004955486 9273580 9285682 - 9068941 102017345 A0A8C2VZ65;A0A8C2W4M2 MODEL AGCD01059172;GBBH01119864;GBDI01179221;XM_013504154;XM_013504155;XM_013504156;XM_013504157;XM_013504158 XP_013359608;XP_013359609;XP_013359610;XP_013359611;XP_013359612 E3 ubiquitin-protein ligase MIB2;mindbomb E3 ubiquitin protein ligase 2 APPROVED protein-coding ENSCLAG00000014976 NW_004955486 9271099 9285682 - 8717962 LOC102017591 uncharacterized LOC102017591 NW_004955510 6375997 6377249 - 102017591 MODEL AGCD01066306;GBDF01087880;XR_264412 ncrna 8717966 Ppif peptidylprolyl isomerase F ENCODES a protein that exhibits cyclosporin A binding (ortholog); peptide binding (ortholog); peptidyl-prolyl cis-trans isomerase activity (ortholog); INVOLVED IN apoptotic mitochondrial changes (ortholog); cellular response to arsenic-containing substance (ortholog); cellular response to calcium ion (ortholog); ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog); intestinal disease (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrial matrix (ortholog); mitochondrial permeability transition pore complex (ortholog) NW_004955437 13295766 13301918 - 9068941 102018024 A0A8C2VWK0 MODEL AGCD01034655;GBCQ01093166;XM_005389888 XP_005389945 peptidyl-prolyl cis-trans isomerase F, mitochondrial protein-coding ENSCLAG00000014222 NW_004955437 13295663 13302175 - 8717976 Mpv17l2 MPV17 mitochondrial inner membrane protein like 2 INVOLVED IN mitochondrial ribosome assembly (ortholog); positive regulation of mitochondrial translation (ortholog); ASSOCIATED WITH genetic disease (ortholog); Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrial large ribosomal subunit (ortholog) NW_004955524 3224356 3226373 - 9068941 102019633 A0A8C2W544 MODEL AGCD01068868;GBBH01060228;XM_005409561 XP_005409618 MPV17 mitochondrial membrane protein-like 2;mpv17-like protein 2 APPROVED protein-coding ENSCLAG00000015953 NW_004955524 3224992 3226373 - 8717985 Dohh deoxyhypusine hydroxylase ENCODES a protein that exhibits deoxyhypusine monooxygenase activity (ortholog); iron ion binding (ortholog); INVOLVED IN peptidyl-lysine modification to peptidyl-hypusine (ortholog); ASSOCIATED WITH genetic disease (ortholog); Neurodevelopmental Disorder with Microcephaly, Cerebral Atrophy, and Visual Impairment (ortholog); Neurodevelopmental Disorders (ortholog) NW_004955495 5073794 5080298 + 9068941 102020024 A0A8C2V8M1;A0A8C2VDZ0 MODEL AGCD01061973;GBDF01193806;XM_005405836;XM_013505247;XM_013505248 XP_005405893;XP_013360701;XP_013360702 deoxyhypusine hydroxylase/monooxygenase APPROVED protein-coding ENSCLAG00000007817 NW_004955495 5076705 5079798 + 8717993 Rtl1 retrotransposon Gag like 1 INVOLVED IN angiogenesis (ortholog); embryonic placenta development (ortholog); gene expression (ortholog); ASSOCIATED WITH genetic disease (ortholog); Kagami-Ogata syndrome (ortholog); FOUND IN Z disc (ortholog) NW_004955538 177078 181557 - 9068941 102020050 A0A8C2W8C1 MODEL AGCD01070991;XM_005410721 XP_005410778 retrotransposon-like 1;retrotransposon-like protein 1 APPROVED protein-coding ENSCLAG00000017642 NW_004955538 176998 181184 - 8717997 Flnb filamin B ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN actin cytoskeleton organization (ortholog); cellular response to type II interferon (ortholog); epithelial cell morphogenesis (ortholog); PARTICIPATES IN integrin mediated signaling pathway; ASSOCIATED WITH Atelosteogenesis Type 1 (ortholog); Atelosteogenesis Type 3 (ortholog); bone development disease (ortholog); FOUND IN brush border (ortholog); cytosol (ortholog); focal adhesion (ortholog) NW_004955430 7680394 7832124 + 9068941;7240710 102020827 A0A8C2V6B0 MODEL AGCD01029367;AGCD01029368;AGCD01029369;AGCD01029370;AGCD01029371;GBDF01196019;XM_005387431;XM_005387432;XM_005387433;XM_013515640 XP_005387488;XP_005387489;XP_005387490;XP_013371094 filamin B, beta;filamin-B APPROVED protein-coding ENSCLAG00000007353 NW_004955430 7680394 7832124 + 8718050 Awat1 acyl-CoA wax alcohol acyltransferase 1 ENCODES a protein that exhibits long-chain-alcohol O-fatty-acyltransferase activity (ortholog); PARTICIPATES IN retinol metabolic pathway; vitamin A deficiency pathway; ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); syndromic X-linked intellectual disability Lubs type (ortholog) NW_004955475 9780080 9785675 + 9068941 102021337 A0A8C2VJ92 MODEL AGCD01055075;GBCE01147851;XM_005401614 XP_005401671 protein-coding ENSCLAG00000010172 NW_004955475 9780080 9789448 + 8718061 LOC102021471 secretoglobin family 1D member-like NW_004955511 6342089 6346015 + 102021471 MODEL AGCD01066602;GBCB01129881;XM_013506417 XP_013361871 APPROVED protein-coding 8718067 Nyap1 neuronal tyrosine phosphorylated phosphoinositide-3-kinase adaptor 1 INVOLVED IN neuron projection morphogenesis (ortholog); phosphatidylinositol 3-kinase signaling (ortholog); ASSOCIATED WITH genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog) NW_004955573 402180 410729 - 9068941 102022551 A0A8C2UP49 MODEL AGCD01074976;GBDJ01403614;XM_005413725;XM_005413726;XM_013509491;XM_013509492 XP_005413782;XP_005413783;XP_013364945;XP_013364946 neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1;neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 1 APPROVED protein-coding ENSCLAG00000002252 NW_004955573 400969 410729 - 8718085 Ubl5 ubiquitin like 5 INVOLVED IN positive regulation of protein targeting to mitochondrion (ortholog); ASSOCIATED WITH autistic disorder (ortholog); FOUND IN cytoplasm (ortholog) NW_004955495 1242733 1244238 + 9068941 102024583 A0A8C2VBT7 MODEL AGCD01061677;GBDF01010519;XM_005405572 XP_005405629 ubiquitin-like 5;ubiquitin-like protein 5 APPROVED protein-coding ENSCLAG00000009157 NW_004955495 1242733 1244238 + 8718094 Slc4a11 solute carrier family 4 member 11 ENCODES a protein that exhibits active borate transmembrane transporter activity (ortholog); bicarbonate transmembrane transporter activity (ortholog); protein dimerization activity (ortholog); INVOLVED IN bicarbonate transport (ortholog); borate transport (ortholog); cellular hypotonic response (ortholog); ASSOCIATED WITH congenital hereditary endothelial dystrophy of cornea (ortholog); corneal dystrophy (ortholog); Corneal Dystrophy, Fuchs Endothelial, 4 (ortholog); FOUND IN apical plasma membrane (ortholog); basolateral plasma membrane (ortholog); plasma membrane (ortholog) NW_004955415 14123021 14133437 - 9068941;7240710 102025571 A0A8C2VU27 MODEL AGCD01016288;GBCE01153106;GBDK01418034;XM_013512257 XP_013367711 sodium bicarbonate transporter-like protein 11;solute carrier family 4, sodium borate transporter, member 11 APPROVED protein-coding ENSCLAG00000012612 NW_004955415 14120301 14131989 - 8718124 Cx3cl1 C-X3-C motif chemokine ligand 1 ENCODES a protein that exhibits chemoattractant activity (ortholog); chemokine activity (ortholog); CX3C chemokine receptor binding (ortholog); INVOLVED IN angiogenesis involved in wound healing (ortholog); autocrine signaling (ortholog); cell adhesion (ortholog); ASSOCIATED WITH acute pancreatitis (ortholog); allergic disease (ortholog); anti-basement membrane glomerulonephritis (ortholog); FOUND IN cell body (ortholog); cell projection (ortholog); cell surface (ortholog) NW_004955433 15023272 15034650 + 9068941 102025717 A0A8C2V871 MODEL AGCD01031744;AGCD01031745;GBBH01091020;XM_005388386;XM_005388387 XP_005388443;XP_005388444 chemokine (C-X3-C motif) ligand 1;fractalkine APPROVED protein-coding ENSCLAG00000006390 NW_004955433 15023050 15034711 + 8718142 LOC102025817 taste receptor type 2 member 1-like NW_004955504 6903932 6904825 - 102025817 MODEL AGCD01064930;XM_005407094 XP_005407151 protein-coding 8718145 LOC102025841 60S ribosomal protein L26-like 1 pseudogene NW_004955437 18774210 18776027 + 102025841 MODEL AGCD01034814 APPROVED pseudo 8718146 LOC102026379 inositol polyphosphate multikinase pseudogene NW_004955613 60321 81299 - 102026379 MODEL AGCD01077193;AGCD01077194;AGCD01077195 APPROVED pseudo 8718147 Ak3 adenylate kinase 3 ENCODES a protein that exhibits adenylate kinase activity (ortholog); identical protein binding (ortholog); nucleoside triphosphate adenylate kinase activity (ortholog); INVOLVED IN ADP biosynthetic process (ortholog); AMP metabolic process (ortholog); AMP phosphorylation (ortholog); PARTICIPATES IN beta-ureidopropionase deficiency pathway; de novo purine biosynthetic pathway; dihydropyrimidinase deficiency pathway; ASSOCIATED WITH chromosome 9p deletion syndrome (ortholog); chronic lymphocytic leukemia (ortholog); genetic disease (ortholog); FOUND IN mitochondrial matrix (ortholog); mitochondrion (ortholog) NW_004955434 8998357 9010468 - 9068941 102027332 A0A8C2V1V6;A0A8C2V2B9 MODEL AGCD01032282;GBBH01062690;GBCE01029526;XM_013516310 XP_013371764 GTP:AMP phosphotransferase AK3, mitochondrial protein-coding ENSCLAG00000006329 NW_004955434 9000158 9011250 - 8718165 LOC102027745 uncharacterized LOC102027745 NW_004955477 10389637 10391254 + 102027745 MODEL AGCD01055695;GBDK01035566;XR_263669;XR_263670 ncrna 8718174 Xkr9 XK related 9 ENCODES a protein that exhibits phospholipid scramblase activity (ortholog); INVOLVED IN phosphatidylserine exposure on apoptotic cell surface (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN plasma membrane (ortholog) NW_004955444 9027662 9059911 - 9068941 102029130 A0A8C2UUC1 MODEL AGCD01038953;AGCD01038954;AGCD01038955;AGCD01038956;GBCQ01014012;XM_005392101;XM_005392102;XM_013518143;XM_013518144;XM_013518145 XP_005392158;XP_005392159;XP_013373597;XP_013373598;XP_013373599 XK, Kell blood group complex subunit-related family, member 9;XK-related protein 9 APPROVED protein-coding ENSCLAG00000004198 NW_004955444 9025635 9053775 - 8718189 LOC102029763 heterochromatin protein 1-binding protein 3 pseudogene NW_004955424 22152445 22160546 + 102029763 MODEL AGCD01024934;XR_261113 APPROVED pseudo 8718195 LOC102030179 zinc finger BED domain-containing protein 1-like NW_004955469 8357587 8369632 - 102030179 MODEL AGCD01052465 pseudo 8718196 Nck2 NCK adaptor protein 2 ENCODES a protein that exhibits phosphotyrosine residue binding (ortholog); protein-containing complex binding (ortholog); scaffold protein binding (ortholog); INVOLVED IN actin filament organization (ortholog); cell migration (ortholog); dendritic spine development (ortholog); PARTICIPATES IN ephrin - ephrin receptor bidirectional signaling axis; epidermal growth factor/neuregulin signaling pathway; insulin signaling pathway; ASSOCIATED WITH Albuminuria (ortholog); Alzheimer's disease (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); endoplasmic reticulum (ortholog); postsynaptic density (ortholog) NW_004955470 10487962 10593046 + 9068941 102030183 A0A8C2VAI2 MODEL AGCD01052871;AGCD01052872;GBDF01223303;XM_005400789 XP_005400846 cytoplasmic protein NCK2 protein-coding ENSCLAG00000008756 NW_004955470 10487481 10593046 + 8718208 Cd55 CD55 molecule (Cromer blood group) ENCODES a protein that exhibits enzyme inhibitor activity (ortholog); lipid binding (ortholog); virus receptor activity (ortholog); INVOLVED IN maternal process involved in parturition (ortholog); negative regulation of complement activation (ortholog); positive regulation of CD4-positive, alpha-beta T cell activation (ortholog); PARTICIPATES IN complement system pathway; ASSOCIATED WITH amphetamine abuse (ortholog); autistic disorder (ortholog); breast cancer (ortholog); FOUND IN apical plasma membrane (ortholog); cell surface (ortholog); external side of plasma membrane (ortholog) NW_004955406 42773368 42796205 + 9068941 102030273 MODEL AGCD01006718;AGCD01006719;GBCE01002757;GBCQ01070157;XM_013502893;XM_013502896;XM_013502897;XM_013502899;XM_013502901;XM_013502903 XP_013358347;XP_013358350;XP_013358351;XP_013358353;XP_013358355;XP_013358357 CD55 molecule, decay accelerating factor for complement (Cromer blood group);complement decay-accelerating factor APPROVED protein-coding 8718235 Pa2g4 proliferation-associated 2G4 ENCODES a protein that exhibits nucleic acid binding (ortholog); transcription corepressor activity (ortholog); ubiquitin protein ligase binding (ortholog); INVOLVED IN negative regulation of apoptotic process (ortholog); negative regulation of DNA-templated transcription (ortholog); positive regulation of cell differentiation (ortholog); ASSOCIATED WITH Disease Progression (ortholog); genetic disease (ortholog); Stomach Neoplasms (ortholog); FOUND IN cytoplasm (ortholog); nucleolus (ortholog); nucleus (ortholog) NW_004955458 3705704 3715782 + 9068941 102030282 A0A8C2VCD5 MODEL AGCD01047338;AGCD01047339;GBDF01001985;XM_005397287 XP_005397344 proliferation-associated 2G4, 38kDa;proliferation-associated protein 2G4 APPROVED protein-coding ENSCLAG00000008851 NW_004955458 3705704 3717403 + 8718252 Arhgef9 Cdc42 guanine nucleotide exchange factor 9 INVOLVED IN receptor clustering (ortholog); regulation of postsynaptic specialization assembly (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); developmental and epileptic encephalopathy 1 (ortholog); FOUND IN cell cortex (ortholog); cytosol (ortholog); GABA-ergic synapse (ortholog) NW_004955475 4020922 4214464 - 9068941;7240710 102030524 A0A8C2UVY1;A0A8C2UW91;A0A8C2UXH7;A0A8C2UYR8;A0A8C2V154;A0A8C2V1G6 MODEL AGCD01054863;AGCD01054864;AGCD01054865;AGCD01054866;AGCD01054867;GBBH01172150;XM_005401551;XM_005401552;XM_005401553;XM_013502875;XM_013502876;XM_013502877;XM_013502878;XM_013502879 XP_005401608;XP_005401609;XP_005401610;XP_013358329;XP_013358330;XP_013358331;XP_013358332;XP_013358333 Cdc42 guanine nucleotide exchange factor (GEF) 9;rho guanine nucleotide exchange factor 9 APPROVED protein-coding ENSCLAG00000004407 NW_004955475 4017632 4214563 - 8718278 Galc galactosylceramidase ENCODES a protein that exhibits galactosylceramidase activity (ortholog); INVOLVED IN galactosylceramide catabolic process (ortholog); myelination (ortholog); PARTICIPATES IN Fabry disease pathway; Gaucher's disease pathway; Krabbe disease pathway; ASSOCIATED WITH Creutzfeldt-Jakob disease (ortholog); Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog) NW_004955438 10667807 10704386 - 9068941;7240710 102003695 A0A8C2VMJ0 MODEL AGCD01035214;GBBH01007063;XM_005390247;XM_013517230;XM_013517231 XP_005390304;XP_013372684;XP_013372685 galactocerebrosidase protein-coding ENSCLAG00000011636 NW_004955438 10667807 10704384 - 8718303 Lratd2 LRAT domain containing 2 ASSOCIATED WITH genetic disease (ortholog); trichorhinophalangeal syndrome type I (ortholog); FOUND IN cytoplasm (ortholog); plasma membrane (ortholog) NW_004955461 1623114 1627515 - 9068941 102003740 A0A8C2WA26 MODEL AGCD01048818;GBBH01142184;XM_013521345 XP_013376799 Fam84b family with sequence similarity 84 member B;family with sequence similarity 84, member B APPROVED protein-coding ENSCLAG00000017512 NW_004955461 1626560 1627495 - 8718309 Hoxb2 homeobox B2 ENCODES a protein that exhibits DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); sequence-specific DNA binding (ortholog); sequence-specific double-stranded DNA binding (ortholog); INVOLVED IN anterior/posterior pattern specification (ortholog); dorsal/ventral pattern formation (ortholog); embryonic skeletal system morphogenesis (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN nucleoplasm (ortholog) NW_004955451 12693764 12697825 + 9068941 102004227 A0A8C2W5J6 MODEL AGCD01043420;GBCQ01100488;XM_005394234;XM_005394235 XP_005394291;XP_005394292 homeobox protein Hox-B2 protein-coding ENSCLAG00000015271 NW_004955451 12694868 12697846 + 8718317 LOC102004518 microfibrillar-associated protein 1 pseudogene NW_004955437 7042525 7045014 + 102004518 MODEL AGCD01034448 APPROVED pseudo 8718318 Dynap dynactin associated protein INVOLVED IN activation of protein kinase B activity (ortholog); cellular response to ergosterol (ortholog); positive regulation of cell population proliferation (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); FOUND IN Golgi apparatus (ortholog); plasma membrane (ortholog) NW_004955402 39097723 39142938 + 9068941 102004539 MODEL AGCD01000976;AGCD01000977;XM_013510770 XP_013366224 LOC102004539 dynactin associated protein-like APPROVED protein-coding 8718319 St3gal3 ST3 beta-galactoside alpha-2,3-sialyltransferase 3 ENCODES a protein that exhibits beta-galactoside (CMP) alpha-2,3-sialyltransferase activity (ortholog); INVOLVED IN ganglioside biosynthetic process via lactosylceramide (ortholog); protein glycosylation (ortholog); ASSOCIATED WITH autosomal recessive intellectual developmental disorder 12 (ortholog); Charcot-Marie-Tooth disease dominant intermediate C (ortholog); developmental and epileptic encephalopathy (ortholog) NW_004955537 3258076 3458742 + 9068941;7240710 102005081 A0A8C2UT97;A0A8C2YKA4 MODEL AGCD01070953;AGCD01070954;AGCD01070955;AGCD01070956;AGCD01070957;AGCD01070958;AGCD01070959;GBBH01076952;XM_005410678;XM_005410679 XP_005410735;XP_005410736 CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-sialyltransferase protein-coding ENSCLAG00000003460 NW_004955537 3258076 3458742 + 8718368 Tinag tubulointerstitial nephritis antigen INVOLVED IN cell adhesion (ortholog); ASSOCIATED WITH Diabetic Nephropathies (ortholog); genetic disease (ortholog); FOUND IN basement membrane (ortholog) NW_004955411 1718969 1809370 - 9068941 102006107 A0A8C2VMR7 MODEL AGCD01011487;AGCD01011488;AGCD01011489;AGCD01011490;GBCQ01040782;XM_005377590;XM_013510703 XP_005377647;XP_013366157 protein-coding ENSCLAG00000012331 NW_004955411 1717026 1810055 - 8718383 Nrip1 nuclear receptor interacting protein 1 ENCODES a protein that exhibits histone deacetylase binding (ortholog); nuclear estrogen receptor binding (ortholog); nuclear glucocorticoid receptor binding (ortholog); INVOLVED IN cellular response to estradiol stimulus (ortholog); circadian regulation of gene expression (ortholog); circadian rhythm (ortholog); PARTICIPATES IN estrogen signaling pathway; forkhead class A signaling pathway; retinoic acid signaling pathway; ASSOCIATED WITH Alzheimer's disease (ortholog); Breast Neoplasms (ortholog); CAKUT (ortholog); FOUND IN chromatin (ortholog); cytosol (ortholog); fibrillar center (ortholog) NW_004955407 16740253 16820297 - 9068941 102008061 A0A8C2UX09 MODEL AGCD01007226;AGCD01007227;AGCD01007228;GBDJ01419988;XM_005375568;XM_005375569;XM_005375570 XP_005375625;XP_005375626;XP_005375627 nuclear receptor-interacting protein 1 protein-coding ENSCLAG00000004956 NW_004955407 16740253 16820297 - 8718403 LOC102008436 uncharacterized LOC102008436 NW_004955501 720309 731808 + 102008436 MODEL AGCD01064038;GBDF01158739;XR_001231521 ncrna 8718409 LOC102008515 uncharacterized LOC102008515 NW_004955412 14935574 14945274 - 102008515 MODEL AGCD01012863;GBCQ01079249;XR_259995 ncrna 8718414 Thsd4 thrombospondin type 1 domain containing 4 INVOLVED IN elastic fiber assembly (ortholog); microfibril assembly (ortholog); ASSOCIATED WITH Bloom syndrome (ortholog); colorectal cancer (ortholog); Familial Thoracic Aortic Aneurysm 12 (ortholog); FOUND IN extracellular matrix (ortholog); microfibril (ortholog) NW_004955450 5296670 5827252 - 9068941 102009131 A0A8C2W9E8 MODEL AGCD01042499;AGCD01042500;AGCD01042501;AGCD01042502;AGCD01042503;AGCD01042504;AGCD01042505;AGCD01042506;AGCD01042507;AGCD01042508;AGCD01042509;AGCD01042510;GBBH01142626;GBCQ01066873;XM_013518949 XP_013374403 LOC102003507;LOC102007835 thrombospondin type-1 domain-containing protein 4;thrombospondin type-1 domain-containing protein 4-like;thrombospondin, type I, domain containing 4 PROVISIONAL protein-coding ENSCLAG00000017203 NW_004955450 5301765 5479638 - 8718430 Entpd1 ectonucleoside triphosphate diphosphohydrolase 1 ENCODES a protein that exhibits ADP phosphatase activity (ortholog); ATP hydrolysis activity (ortholog); identical protein binding (ortholog); INVOLVED IN ADP catabolic process (ortholog); cellular response to aluminum ion (ortholog); cellular response to interferon-alpha (ortholog); ASSOCIATED WITH agammaglobulinemia 4 (ortholog); demyelinating disease (ortholog); Developmental Disabilities (ortholog); FOUND IN basement membrane (ortholog); basolateral plasma membrane (ortholog); cell surface (ortholog) NW_004955507 2035918 2141327 + 9068941;7240710 102010183 A0A8C2USU2 MODEL AGCD01065577;AGCD01065578;AGCD01065579;AGCD01065580;GBDF01127217;XM_005407549;XM_005407551;XM_005407553;XM_013506151;XM_013506153 XP_005407606;XP_005407608;XP_005407610;XP_013361605;XP_013361607 protein-coding ENSCLAG00000002693 NW_004955507 2036050 2137377 + 8718456 Usp47 ubiquitin specific peptidase 47 ENCODES a protein that exhibits cysteine-type deubiquitinase activity (ortholog); deubiquitinase activity (ortholog); WD40-repeat domain binding (ortholog); INVOLVED IN base-excision repair (ortholog); cellular response to UV (ortholog); DNA damage response (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog); SCF ubiquitin ligase complex (ortholog) NW_004955414 27357602 27462481 + 9068941 102010360 A0A8C2W8C3;A0A8C2WAG3 MODEL AGCD01015663;GBDK01139174;XM_005380290;XM_005380291;XM_005380292;XM_013511963 XP_005380347;XP_005380348;XP_005380349;XP_013367417 ubiquitin carboxyl-terminal hydrolase 47 protein-coding ENSCLAG00000016904 NW_004955414 27357602 27462731 + 8718496 Hoxd3 homeobox D3 ENCODES a protein that exhibits DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); RNA polymerase II transcription regulatory region sequence-specific DNA binding (ortholog); sequence-specific double-stranded DNA binding (ortholog); INVOLVED IN anterior/posterior pattern specification (ortholog); cartilage development (ortholog); cell-matrix adhesion (ortholog); ASSOCIATED WITH genetic disease (ortholog); Prostatic Neoplasms (ortholog); split hand-foot malformation 5 (ortholog); FOUND IN aggresome (ortholog); nuclear body (ortholog); nucleoplasm (ortholog) NW_004955403 20489663 20496021 - 9068941 102010855 A0A8C2YSE0 MODEL AGCD01002160;XM_005373413;XR_001233436;XR_259190 XP_005373470 homeobox protein Hox-D3 protein-coding ENSCLAG00000000379;ENSCLAG00000013605 8718506 LOC102010880 methylcrotonoyl-CoA carboxylase beta chain, mitochondrial pseudogene NW_004955410 29866734 29868389 - 102010880 MODEL AGCD01011297 APPROVED pseudo 8718507 Cetn2 centrin 2 ENCODES a protein that exhibits G-protein beta/gamma-subunit complex binding (ortholog); heterotrimeric G-protein binding (ortholog); microtubule binding (ortholog); INVOLVED IN centriole replication (ortholog); nucleotide-excision repair (ortholog); regulation of cytokinesis (ortholog); PARTICIPATES IN nucleotide excision repair pathway; ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); syndromic X-linked intellectual disability Lubs type (ortholog); FOUND IN 9+2 motile cilium (ortholog); apical part of cell (ortholog); centriole (ortholog) NW_004955498 8131356 8135751 - 9068941 102012104 A0A8C2ULD4;A0A8C2UR32 MODEL AGCD01063167;GBCQ01000744;XM_005406455 XP_005406512 centrin, EF-hand protein, 2;centrin-2 APPROVED protein-coding ENSCLAG00000001433 NW_004955498 8131295 8135751 - 8718522 LOC102012794 uncharacterized LOC102012794 NW_004955515 468692 476022 + 102012794 MODEL AGCD01067199;GBDF01281122;XR_264518 ncrna 8718527 Magi3 membrane associated guanylate kinase, WW and PDZ domain containing 3 ENCODES a protein that exhibits frizzled binding (ortholog); protein phosphatase binding (ortholog); INVOLVED IN positive regulation of JUN kinase activity (ortholog); ASSOCIATED WITH fetal akinesia deformation sequence syndrome 1 (ortholog); genetic disease (ortholog); hereditary spastic paraplegia 47 (ortholog); FOUND IN cell junction (ortholog); cell-cell junction (ortholog) NW_004955435 16735598 16974005 + 9068941 102012797 A0A8C2UZB9;A0A8C2YLK5 MODEL AGCD01033338;AGCD01033339;AGCD01033340;AGCD01033341;AGCD01033342;AGCD01033343;GBDF01155172;GBDI01255703;XM_005388980 XP_005389037 membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3 protein-coding ENSCLAG00000005341 NW_004955435 16735598 16972204 + 8718562 LOC102013560 uncharacterized LOC102013560 NW_004955443 13036898 13044656 - 102013560 MODEL AGCD01038459;GBDF01022385;XR_262205 ncrna 8718567 Ankrd34c ankyrin repeat domain 34C ASSOCIATED WITH Bloom syndrome (ortholog); colorectal cancer (ortholog); genetic disease (ortholog) NW_004955533 311863 320185 + 102014083 A0A8C2UKU5 MODEL AGCD01070314;XM_005410382;XM_005410383 XP_005410439;XP_005410440 ankyrin repeat domain-containing protein 34C protein-coding ENSCLAG00000001500 8718576 Amer2 APC membrane recruitment protein 2 ENCODES a protein that exhibits phosphatidylinositol-4,5-bisphosphate binding (ortholog); INVOLVED IN negative regulation of canonical Wnt signaling pathway (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN plasma membrane (ortholog) NW_004955497 4640343 4645314 - 9068941 102014466 MODEL AGCD01062583;AGCD01062584;GBDF01074697;XM_013505515 XP_013360969 protein-coding 8718582 Zzef1 zinc finger ZZ-type and EF-hand domain containing 1 ENCODES a protein that exhibits histone reader activity (ortholog); lysine-acetylated histone binding (ortholog); methylated histone binding (ortholog); INVOLVED IN neuroblast proliferation (ortholog); protein ubiquitination (ortholog); regulation of peptidyl-tyrosine phosphorylation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cell surface (ortholog); postsynapse (ortholog); presynaptic active zone (ortholog) NW_004955467 12760334 12882049 + 9068941 102014547 A0A8C2VQ77 MODEL AGCD01051658;GBDF01221149;XM_005399693;XM_005399694 XP_005399750;XP_005399751 zinc finger ZZ-type and EF-hand domain-containing protein 1;zinc finger, ZZ-type with EF-hand domain 1 APPROVED protein-coding ENSCLAG00000011468 NW_004955467 12760483 12879636 + 8718651 LOC102015656 zinc finger protein 709-like NW_004955432 4541720 4566319 + 102015656 MODEL AGCD01030725;AGCD01030726;GBDF01013752;XM_013515929;XM_013515931 XP_013371383;XP_013371385 protein-coding 8718652 LOC102016316 isocitrate dehydrogenase [NADP] cytoplasmic-like NW_004955442 13154777 13160551 - 102016316 MODEL AGCD01037762;AGCD01037763 pseudo 8718653 Mboat1 membrane bound O-acyltransferase domain containing 1 ENCODES a protein that exhibits 1-acylglycerophosphoethanolamine O-acyltransferase activity (ortholog); 1-acylglycerophosphoserine O-acyltransferase activity (ortholog); INVOLVED IN phosphatidylethanolamine acyl-chain remodeling (ortholog); phosphatidylserine acyl-chain remodeling (ortholog); phospholipid biosynthetic process (ortholog); ASSOCIATED WITH cholestasis (ortholog); genetic disease (ortholog); FOUND IN endoplasmic reticulum membrane (ortholog) NW_004955483 6273729 6379844 + 9068941 102016812 A0A8C2ULX4 MODEL AGCD01057775;GBDK01192821;XM_013503839 XP_013359293 lysophospholipid acyltransferase 1 protein-coding ENSCLAG00000001819 NW_004955483 6273729 6381559 + 8718667 Lenep lens epithelial protein ASSOCIATED WITH Charcot-Marie-Tooth disease type 2 (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog) NW_004955545 1495877 1497014 + 9068941 102017062 MODEL AGCD01071857;GBDF01240724;XM_005411536 XP_005411593 lens epithelial cell protein LEP503 protein-coding 8718679 Kiss1r KISS1 receptor ENCODES a protein that exhibits G protein-coupled peptide receptor activity (ortholog); neuropeptide binding (ortholog); neuropeptide receptor activity (ortholog); INVOLVED IN arachidonic acid secretion (ortholog); calcium-mediated signaling (ortholog); G protein-coupled receptor signaling pathway (ortholog); ASSOCIATED WITH breast cancer (ortholog); central precocious puberty 1 (ortholog); cerebral creatine deficiency syndrome (ortholog); FOUND IN cell surface (ortholog); cilium (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955495 6918632 6921891 - 9068941;7240710 102017471 A0A8C2VAC9 MODEL AGCD01062100;GBDI01039469;XM_005406013;XM_013505106 XP_005406070;XP_013360560 kiSS-1 receptor protein-coding ENSCLAG00000007689 8718688 Fah fumarylacetoacetate hydrolase ENCODES a protein that exhibits fumarylacetoacetase activity (ortholog); INVOLVED IN arginine catabolic process (ortholog); PARTICIPATES IN alkaptonuria pathway; disulfiram pharmacodynamics pathway; dopamine beta-hydroxylase deficiency pathway; ASSOCIATED WITH Bloom syndrome (ortholog); colorectal cancer (ortholog); COVID-19 (ortholog) NW_004955533 904294 921730 + 9068941;7240710 102018221 A0A8C2UPZ3 MODEL AGCD01070334;AGCD01070335;GBBH01229682;XM_005410393;XM_005410394 XP_005410450;XP_005410451 fumarylacetoacetase;fumarylacetoacetate hydrolase (fumarylacetoacetase) APPROVED protein-coding ENSCLAG00000002458 NW_004955533 904295 921730 + 8718710 Cpeb2 cytoplasmic polyadenylation element binding protein 2 ENCODES a protein that exhibits GTPase inhibitor activity (ortholog); mRNA 3'-UTR AU-rich region binding (ortholog); mRNA regulatory element binding translation repressor activity (ortholog); INVOLVED IN cellular response to arsenic-containing substance (ortholog); cellular response to hypoxia (ortholog); cellular response to insulin stimulus (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); glutamatergic synapse (ortholog); messenger ribonucleoprotein complex (ortholog) NW_004955480 8853449 8906859 - 9068941 102019499 A0A8C2YIJ2 MODEL AGCD01056733;GBCQ01006152;GBDK01277233;XM_013503330 XP_013358784 cytoplasmic polyadenylation element-binding protein 2 protein-coding ENSCLAG00000000949 8718744 Adcyap1 adenylate cyclase activating polypeptide 1 ENCODES a protein that exhibits neuropeptide hormone activity (ortholog); peptide hormone receptor binding (ortholog); pituitary adenylate cyclase activating polypeptide activity (ortholog); INVOLVED IN adenylate cyclase-activating G protein-coupled receptor signaling pathway (ortholog); behavioral fear response (ortholog); cAMP-mediated signaling (ortholog); ASSOCIATED WITH acute necrotizing pancreatitis (ortholog); autistic disorder (ortholog); Brain Injuries (ortholog); FOUND IN extracellular space (ortholog); terminal bouton (ortholog) NW_004955402 9091927 9099803 - 9068941 102021292 A0A8C2V8M8 MODEL AGCD01000205;XM_005372667;XM_005372668 XP_005372724;XP_005372725 adenylate cyclase activating polypeptide 1 (pituitary);pituitary adenylate cyclase-activating polypeptide APPROVED protein-coding ENSCLAG00000007209 NW_004955402 9091725 9099803 - 8718756 Fgd2 FYVE, RhoGEF and PH domain containing 2 ENCODES a protein that exhibits guanyl-nucleotide exchange factor activity (ortholog); phosphatidylinositol phosphate binding (ortholog); INVOLVED IN positive regulation of JUN kinase activity (ortholog); ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog); ovarian cyst (ortholog); FOUND IN cytoplasm (ortholog); early endosome (ortholog); nucleus (ortholog) NW_004955437 6026087 6038740 - 9068941;7240710 102021388 A0A8C2YQQ8 MODEL AGCD01034413;AGCD01034414;GBDK01184372;XM_005389626;XM_005389627;XM_005389628;XM_013516942;XM_013516943 XP_005389683;XP_005389684;XP_005389685;XP_013372396;XP_013372397 FYVE, RhoGEF and PH domain-containing protein 2 protein-coding ENSCLAG00000011231 NW_004955437 6024301 6038349 - 8718794 LOC102021859 uncharacterized LOC102021859 NW_004955463 6152064 6152789 - 102021859 MODEL AGCD01049657;GBDF01145117;XR_001236626 ncrna 8718814 Eea1 early endosome antigen 1 ENCODES a protein that exhibits 1-phosphatidylinositol binding (ortholog); GTP-dependent protein binding (ortholog); protein homodimerization activity (ortholog); INVOLVED IN chemical synaptic transmission, postsynaptic (ortholog); endocytosis (ortholog); vesicle fusion (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN axonal spine (ortholog); cytoplasmic vesicle (ortholog); cytosol (ortholog) NW_004955405 29760332 29959553 - 9068941 102022251 A0A8C2V3E0;A0A8C2V740 MODEL AGCD01005256;AGCD01005257;AGCD01005258;AGCD01005259;AGCD01005260;AGCD01005261;AGCD01005262;AGCD01005263;GBDJ01165087;XM_013518252 XP_013373706 protein-coding ENSCLAG00000006113 NW_004955405 29760332 29868755 - 8718847 Tap2 transporter 2, ATP binding cassette subfamily B member ENCODES a protein that exhibits ABC-type peptide antigen transporter activity (ortholog); ADP binding (ortholog); ATP binding (ortholog); INVOLVED IN antigen processing and presentation of endogenous peptide antigen via MHC class I (ortholog); antigen processing and presentation of endogenous peptide antigen via MHC class I via ER pathway, TAP-dependent (ortholog); antigen processing and presentation of endogenous peptide antigen via MHC class Ib via ER pathway, TAP-dependent (ortholog); ASSOCIATED WITH allergic contact dermatitis (ortholog); Alzheimer's disease (ortholog); ankylosing spondylitis (ortholog); FOUND IN endoplasmic reticulum (ortholog); endoplasmic reticulum membrane (ortholog); membrane (ortholog) NW_004955437 1480217 1499032 - 9068941;7240710 102022851 A0A8C2VP24;A0A8C2YRR4 MODEL AGCD01034211;AGCD01034212;GBDK01022859;XM_013516933;XM_013516934 XP_013372387;XP_013372388 antigen peptide transporter 2;transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) APPROVED protein-coding ENSCLAG00000012654 NW_004955437 1477341 1498575 - 8718863 LOC102023358 uncharacterized LOC102023358 NW_004955481 7044388 7067422 - 102023358 MODEL AGCD01057048;AGCD01057049;AGCD01057050;AGCD01057051;GBBH01013120;XR_263788 ncrna 8718868 Ttc22 tetratricopeptide repeat domain 22 ASSOCIATED WITH genetic disease (ortholog) NW_004955464 4592667 4609148 + 102024775 A0A8C2VIW6 MODEL AGCD01049992;GBDI01128402;XM_005398510;XM_013521666 XP_005398567;XP_013377120 tetratricopeptide repeat protein 22 protein-coding ENSCLAG00000011140 NW_004955464 4592667 4610376 + 8718879 Stx18 syntaxin 18 ENCODES a protein that exhibits protein domain specific binding (ortholog); INVOLVED IN endoplasmic reticulum membrane organization (ortholog); positive regulation of ER to Golgi vesicle-mediated transport (ortholog); positive regulation of organelle assembly (ortholog); ASSOCIATED WITH Ellis-Van Creveld syndrome (ortholog); genetic disease (ortholog); FOUND IN endoplasmic reticulum (ortholog) NW_004955514 5168143 5272655 + 9068941 102025830 A0A8C2VZ88;A0A8C2W1J7 MODEL AGCD01067149;AGCD01067150;GBDI01254691;XM_005408831 XP_005408888 syntaxin-18 protein-coding ENSCLAG00000014826 NW_004955514 5168143 5272649 + 8718908 Rnf181 ring finger protein 181 ENCODES a protein that exhibits ubiquitin protein ligase activity (ortholog); ubiquitin-protein transferase activity (ortholog); INVOLVED IN protein autoubiquitination (ortholog); ASSOCIATED WITH genetic disease (ortholog); hereditary spastic paraplegia 31 (ortholog) NW_004955424 1907745 1910037 - 9068941 102027657 A0A8C2V104 MODEL AGCD01024250;GBCQ01010722;XM_005385422 XP_005385479 E3 ubiquitin-protein ligase RNF181 protein-coding ENSCLAG00000006082 NW_004955424 1907745 1910037 - 8718917 Lims2 LIM zinc finger domain containing 2 INVOLVED IN cell-cell adhesion (ortholog); cell-cell junction organization (ortholog); cholangiocyte proliferation (ortholog); PARTICIPATES IN integrin mediated signaling pathway; ASSOCIATED WITH autosomal dominant thrombophilia due to protein C deficiency (ortholog); autosomal recessive limb-girdle muscular dystrophy type 2W (ortholog); centronuclear myopathy 2 (ortholog); FOUND IN focal adhesion (ortholog) NW_004955459 2874282 2913956 + 9068941 102027722 A0A8C2UY69;A0A8C2UYS6 MODEL AGCD01048004;GBCB01111199;XM_005397601;XM_005397602;XM_005397604;XM_013521048 XP_005397658;XP_005397659;XP_005397661;XP_013376502 LIM and senescent cell antigen-like domains 2;LIM and senescent cell antigen-like-containing domain protein 2 APPROVED protein-coding ENSCLAG00000005260 NW_004955459 2864580 2914263 + 8718955 Dao D-amino acid oxidase ENCODES a protein that exhibits D-amino-acid oxidase activity (ortholog); FAD binding (ortholog); identical protein binding (ortholog); INVOLVED IN D-alanine catabolic process (ortholog); D-amino acid catabolic process (ortholog); D-serine catabolic process (ortholog); PARTICIPATES IN AGAT deficiency pathway; arginine and proline metabolic pathway; guanidinoacetate methyltransferase deficiency pathway; ASSOCIATED WITH amyotrophic lateral sclerosis (ortholog); autistic disorder (ortholog); Experimental Liver Cirrhosis (ortholog); FOUND IN cytosol (ortholog); mitochondrial outer membrane (ortholog); peroxisomal membrane (ortholog) NW_004955455 10095597 10127244 + 9068941;7240710 102028267 A0A8C2YSA0 MODEL AGCD01045938;AGCD01045939;AGCD01045940;AGCD01045941;AGCD01045942;AGCD01045943;AGCD01045944;AGCD01045945;GBDF01299326;XM_005396478 XP_005396535 D-amino-acid oxidase APPROVED protein-coding ENSCLAG00000013453 NW_004955455 10095300 10127666 + 8718973 LOC102028633 olfactory receptor 1E5-like NW_004955481 7646 8650 + 102028633 MODEL AGCD01056774 APPROVED pseudo 8718974 LOC102029360 uncharacterized LOC102029360 NW_004955406 35445518 35583778 - 102029360 MODEL AGCD01006525;AGCD01006526;AGCD01006527;AGCD01006528;GBDK01170412;XR_001236810 ncrna 8718979 Edem1 ER degradation enhancing alpha-mannosidase like protein 1 ENCODES a protein that exhibits alpha-mannosidase activity (ortholog); mannosyl-oligosaccharide 1,2-alpha-mannosidase activity (ortholog); misfolded protein binding (ortholog); INVOLVED IN mannose trimming involved in glycoprotein ERAD pathway (ortholog); positive regulation of retrograde protein transport, ER to cytosol (ortholog); protein targeting to ER (ortholog); ASSOCIATED WITH Chemical and Drug Induced Liver Injury (ortholog); genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN aggresome (ortholog); endoplasmic reticulum (ortholog); endoplasmic reticulum membrane (ortholog) NW_004955421 8196631 8225561 - 9068941 102029754 A0A8C2V2Y9 MODEL AGCD01021799;AGCD01021800;GBDI01139845;GBDK01133751;XM_005383919;XM_013513728 XP_005383976;XP_013369182 ER degradation enhancer, mannosidase alpha-like 1;ER degradation-enhancing alpha-mannosidase-like protein 1 APPROVED protein-coding ENSCLAG00000004922 NW_004955421 8196557 8225561 - 8718994 Fra10ac1 fragile site, folic acid type, rare, fra(10)(q23.3) or fra(10)(q24.2) candidate 1 INVOLVED IN mRNA splicing, via spliceosome (ortholog); ASSOCIATED WITH familial temporal lobe epilepsy 1 (ortholog); genetic disease (ortholog); Neurodevelopmental Disorder with Growth Retardation, Dysmorphic Facies, and Corpus Callosum Abnormalities (ortholog); FOUND IN nucleus (ortholog) NW_004955507 182212 242313 - 9068941 102030101 A0A8C2V774 MODEL AGCD01065464;AGCD01065465;GBBH01006628;XM_005407520;XM_005407521;XM_005407522 XP_005407577;XP_005407578;XP_005407579 protein-coding ENSCLAG00000006397 8719018 LOC102030362 transmembrane protease serine 11B-like protein NW_004955447 4696572 4715733 + 102030362 A0A8C2YKL7 MODEL AGCD01040730;XM_013518484;XM_013518485 XP_013373938;XP_013373939 APPROVED protein-coding ENSCLAG00000003989 8719038 LOC102030522 nuclear receptor-binding factor 2 pseudogene NW_004955473 11156099 11161630 - 102030522 MODEL AGCD01054130;AGCD01054131 APPROVED pseudo 8719040 Gpr22 G protein-coupled receptor 22 ENCODES a protein that exhibits G protein-coupled receptor activity (ortholog); ASSOCIATED WITH congenital disorder of glycosylation type IIi (ortholog); genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN plasma membrane (ortholog) NW_004955410 11841813 11849441 + 9068941 102004576 A0A8C2YN08 MODEL AGCD01010835;XM_013510539;XM_013510540 XP_013365993;XP_013365994 probable G-protein coupled receptor 22 protein-coding ENSCLAG00000007346 NW_004955410 11841850 11849441 + 8719051 Ca3 carbonic anhydrase 3 ENCODES a protein that exhibits carbonate dehydratase activity (ortholog); nickel cation binding (ortholog); phosphatase activity (ortholog); INVOLVED IN response to bacterium (ortholog); response to ethanol (ortholog); response to oxidative stress (ortholog); ASSOCIATED WITH Chemical and Drug Induced Liver Injury (ortholog); Experimental Liver Cirrhosis (ortholog); Experimental Liver Neoplasms (ortholog); FOUND IN cytosol (ortholog) NW_004955417 3362091 3372270 + 9068941 102004705 A0A8C2VL10 MODEL AGCD01017912;GBDF01125791;XM_005381744;XM_013512802;XM_013512803;XM_013512804 XP_005381801;XP_013368256;XP_013368257;XP_013368258 carbonic anhydrase III;carbonic anhydrase III, muscle specific APPROVED protein-coding ENSCLAG00000009786 NW_004955417 3362492 3372932 + 8719062 Slc66a3 solute carrier family 66 member 3 ASSOCIATED WITH Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog); Liver Neoplasms (ortholog) NW_004955487 5848723 5855425 + 9068941 102005382 A0A8C2VAF0;A0A8C2YNV5 MODEL AGCD01059348;GBCE01054645;XM_005404424 XP_005404481 Pqlc3 PQ loop repeat containing 3;PQ-loop repeat-containing protein 3 APPROVED protein-coding ENSCLAG00000008584 NW_004955487 5848501 5855425 + 8719073 Alkal2 ALK and LTK ligand 2 ENCODES a protein that exhibits cytokine activity (ortholog); receptor signaling protein tyrosine kinase activator activity (ortholog); receptor tyrosine kinase binding (ortholog); INVOLVED IN positive regulation of ERK1 and ERK2 cascade (ortholog); positive regulation of ERK5 cascade (ortholog); positive regulation of neuron projection development (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN extracellular region (ortholog); extracellular space (ortholog) NW_004955487 304019 312577 - 9068941 102005811 A0A8C2UQH9 MODEL AGCD01059216;AGCD01059217;GBCB01076160;XM_005404337 XP_005404394 Fam150b family with sequence similarity 150 member B;family with sequence similarity 150, member B APPROVED protein-coding ENSCLAG00000001643 NW_004955487 307055 311990 - 8719081 C3 complement C3 ENCODES a protein that exhibits C5L2 anaphylatoxin chemotactic receptor binding (ortholog); lipid binding (ortholog); INVOLVED IN amyloid-beta clearance (ortholog); cell surface receptor signaling pathway involved in cell-cell signaling (ortholog); complement activation (ortholog); PARTICIPATES IN classical complement pathway; ASSOCIATED WITH otitis media; acute kidney failure (ortholog); Acute Lung Injury (ortholog); FOUND IN cell surface (ortholog); extracellular region (ortholog); extracellular space (ortholog) NW_004955495 2796601 2824233 + 9068941;7240710;11554035 19139190 102006475 A0A8C2YNS8 MODEL AGCD01061799;AGCD01061800;AGCD01061801;AGCD01061802;GBDJ01009718;XM_005405700 XP_005405757 complement component 3 APPROVED protein-coding ENSCLAG00000008464 NW_004955495 2796663 2824697 + 8719129 LOC102006846 peptidoglycan recognition protein 3 NW_004955592 116878 131316 + 9068941 102006846 A0A8C2UW04 MODEL AGCD01076300;GBCQ01082261;XM_005414605;XM_013509976;XM_013509977 XP_005414662;XP_013365430;XP_013365431 Pglyrp3 APPROVED protein-coding ENSCLAG00000003607 NW_004955592 116878 131316 + 8719140 LOC102007118 casein kinase I isoform alpha pseudogene NW_004955416 10129649 10130798 + 102007118 MODEL AGCD01017109 APPROVED pseudo 8719141 LOC102009339 netrin receptor UNC5D-like NW_004955775 2794 4739 - 102009339 MODEL AGCD01078325;GBBH01098166;XM_005415109 XP_005415166 protein-coding 8719146 Map4 microtubule associated protein 4 ENCODES a protein that exhibits microtubule binding (ortholog); microtubule stabilizing activity (ortholog); INVOLVED IN cell division (ortholog); cilium disassembly (ortholog); establishment of spindle orientation (ortholog); ASSOCIATED WITH genetic disease (ortholog); Kleine-Levin syndrome (ortholog); Progressive Microcephaly with Seizures and Cerebral and Cerebellar Atrophy (ortholog); FOUND IN axon (ortholog); axoneme (ortholog); microtubule (ortholog) NW_004955420 24437492 24537410 + 9068941 102009613 A0A8C2W4E6 MODEL AGCD01021311;AGCD01021312;AGCD01021313;AGCD01021314;AGCD01021315;GBBH01061287;XM_005383381;XM_005383382;XM_005383384;XM_005383385;XM_005383386;XM_005383387;XM_005383388;XM_005383389;XM_005383390;XM_005383391;XM_005383392;XM_013513377 XP_005383438;XP_005383439;XP_005383441;XP_005383442;XP_005383443;XP_005383444;XP_005383445;XP_005383446;XP_005383447;XP_005383448;XP_005383449;XP_013368831 microtubule-associated protein 4 APPROVED protein-coding ENSCLAG00000014892 8719190 Lacc1 laccase domain containing 1 ENCODES a protein that exhibits adenosine deaminase activity (ortholog); guanosine phosphorylase activity (ortholog); oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor (ortholog); INVOLVED IN nucleotide-binding oligomerization domain containing 2 signaling pathway (ortholog); pattern recognition receptor signaling pathway (ortholog); positive regulation of cytokine production involved in immune response (ortholog); ASSOCIATED WITH genetic disease (ortholog); juvenile rheumatoid arthritis (ortholog); leprosy (ortholog); FOUND IN cytoplasm (ortholog); endoplasmic reticulum (ortholog); nucleus (ortholog) NW_004955518 1794067 1809150 + 102009748 A0A8C2UKL4 MODEL AGCD01067765;AGCD01067766;GBDF01277558;GBDF01277559;XM_005409073 XP_005409130 laccase (multicopper oxidoreductase) domain containing 1;laccase domain-containing protein 1 APPROVED protein-coding ENSCLAG00000001645 NW_004955518 1793352 1805808 + 8719200 Inpp4b inositol polyphosphate-4-phosphatase type II B ENCODES a protein that exhibits lipid binding (ortholog); phosphatidylinositol bisphosphate phosphatase activity (ortholog); phosphatidylinositol trisphosphate phosphatase activity (ortholog); INVOLVED IN intracellular calcium ion homeostasis (ortholog); negative regulation of osteoclast differentiation (ortholog); phosphatidylinositol dephosphorylation (ortholog); PARTICIPATES IN inositol phosphate metabolic pathway; phosphoinositide metabolic pathway; ASSOCIATED WITH acute myeloid leukemia (ortholog); genetic disease (ortholog); hepatocellular carcinoma (ortholog); FOUND IN cytoplasm (ortholog); Golgi apparatus (ortholog) NW_004955471 938005 1291695 + 9068941 102010359 A0A8C2V5T1;A0A8C2V6F9;A0A8C2V8P1;A0A8C2VBT3 MODEL AGCD01052969;AGCD01052970;AGCD01052971;AGCD01052972;AGCD01052973;AGCD01052974;GBDF01155666;XM_005400855;XM_005400857;XM_005400858 XP_005400912;XP_005400914;XP_005400915 inositol polyphosphate-4-phosphatase, type II, 105kDa;type II inositol 3,4-bisphosphate 4-phosphatase APPROVED protein-coding ENSCLAG00000007216 NW_004955471 938005 1291695 + 8719237 Paaf1 proteasomal ATPase associated factor 1 ASSOCIATED WITH 3-methylglutaconic aciduria type 7b (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN proteasome complex (ortholog) NW_004955414 17625117 17658183 - 9068941 102011528 A0A8C2VW25 MODEL AGCD01015246;AGCD01015247;GBCE01097154;XM_005379933 XP_005379990 proteasomal ATPase-associated factor 1 APPROVED protein-coding ENSCLAG00000013956 NW_004955414 17625440 17658980 - 8719271 Ngef neuronal guanine nucleotide exchange factor ENCODES a protein that exhibits ephrin receptor binding (ortholog); guanyl-nucleotide exchange factor activity (ortholog); INVOLVED IN ephrin receptor signaling pathway (ortholog); negative regulation of dendritic spine morphogenesis (ortholog); regulation of GTPase activity (ortholog); PARTICIPATES IN ephrin - ephrin receptor bidirectional signaling axis; ASSOCIATED WITH genetic disease (ortholog); Joubert syndrome 22 (ortholog); Perlman syndrome (ortholog); FOUND IN glutamatergic synapse (ortholog); postsynapse (ortholog) NW_004955453 3082826 3186039 + 9068941 102012604 A0A8C2W457 MODEL AGCD01044648;AGCD01044649;AGCD01044650;AGCD01044651;AGCD01044652;AGCD01044653;GBBH01146161;XM_005395362;XM_013519899 XP_005395419;XP_013375353 ephexin-1 protein-coding ENSCLAG00000016466 NW_004955453 3082628 3186039 + 8719291 LOC102013084 cyclic AMP-dependent transcription factor ATF-4 pseudogene NW_004955417 10565016 10567924 - 102013084 MODEL AGCD01018079 APPROVED pseudo 8719292 LOC102013368 disintegrin and metalloproteinase domain-containing protein 20-like NW_004955656 248 2205 - 102013368 MODEL AGCD01077844;GBDF01010724;GBDF01010725;XM_005415057 XP_005415114 protein-coding 8719296 Unc45b unc-45 myosin chaperone B ENCODES a protein that exhibits Hsp90 protein binding (ortholog); INVOLVED IN chaperone-mediated protein folding (ortholog); ASSOCIATED WITH cataract 43 (ortholog); Craniofacial Abnormalities (ortholog); dilated cardiomyopathy 1A (ortholog); FOUND IN cytosol (ortholog) NW_004955481 9833918 9860202 + 9068941 102013415 A0A8C2VW55 MODEL AGCD01057119;GBCB01006042;XM_005402873;XM_013503334 XP_005402930;XP_013358788 unc-45 homolog B APPROVED protein-coding ENSCLAG00000013212 NW_004955481 9833905 9860697 + 8719320 LOC102013746 uncharacterized LOC102013746 NW_004955513 5355935 5367253 + 102013746 MODEL AGCD01066968;GBCB01130230;XR_001231758;XR_264483;XR_264484 ncrna 8719330 LOC102013995 disintegrin and metalloproteinase domain-containing protein 21 NW_004955656 37920 44620 - 102013995 MODEL AGCD01077846;GBDF01082523;XM_005415059 XP_005415116 Adam21 ADAM metallopeptidase domain 21 APPROVED protein-coding 8719339 LOC102014084 uncharacterized LOC102014084 NW_004955437 20958744 20959376 - 102014084 MODEL AGCD01034893;GBDF01307365;XR_261899 ncrna 8719343 Grid2 glutamate ionotropic receptor delta type subunit 2 ENCODES a protein that exhibits identical protein binding (ortholog); PDZ domain binding (ortholog); scaffold protein binding (ortholog); INVOLVED IN cerebellar granule cell differentiation (ortholog); excitatory postsynaptic potential (ortholog); excitatory synapse assembly (ortholog); ASSOCIATED WITH autosomal recessive spinocerebellar ataxia 18 (ortholog); genetic disease (ortholog); schizophrenia (ortholog); FOUND IN dendritic spine (ortholog); glutamatergic synapse (ortholog); ionotropic glutamate receptor complex (ortholog) NW_004955405 3291793 4411249 + 9068941 102014411 A0A8C2V3W7;A0A8C2V480 MODEL AGCD01004634;AGCD01004635;AGCD01004636;AGCD01004637;AGCD01004638;AGCD01004639;AGCD01004640;AGCD01004641;AGCD01004642;AGCD01004643;AGCD01004644;AGCD01004645;AGCD01004646;GBCE01036544;XM_005374673 XP_005374730 glutamate receptor ionotropic, delta-2;glutamate receptor, ionotropic, delta 2 APPROVED protein-coding ENSCLAG00000006838 NW_004955405 3344763 4443836 + 8719364 LOC102014497 uncharacterized LOC102014497 NW_004955440 5842469 5909890 - 102014497 MODEL AGCD01036283;AGCD01036284;AGCD01036285;GBDF01120225;XR_001235242;XR_001235243;XR_001235244;XR_001235245;XR_262007;XR_262008 ncrna ENSCLAG00000028795 8719373 Tbx21 T-box transcription factor 21 ENCODES a protein that exhibits DNA binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); INVOLVED IN cellular response to organic substance (ortholog); lymphocyte migration (ortholog); negative regulation of DNA-templated transcription (ortholog); PARTICIPATES IN interleukin-12 signaling pathway; interleukin-27 signaling pathway; ASSOCIATED WITH aspirin-induced respiratory disease (ortholog); asthma (ortholog); Asthma and Nasal Polyps (ortholog); FOUND IN neuronal cell body (ortholog); nucleus (ortholog) NW_004955451 13315237 13317888 - 7240710;9068941 102014732 A0A8C2W2S2 MODEL AGCD01043467;GBCB01014995;GBDI01106988;XM_013519056 XP_013374510 T-box 21;T-box transcription factor TBX21 APPROVED protein-coding ENSCLAG00000015235 NW_004955451 13315859 13325937 - 8719386 LOC102014955 protein SET-like NW_004955444 17766981 17772556 + 102014955 MODEL AGCD01039223 pseudo 8719387 Eif2s3 eukaryotic translation initiation factor 2 subunit gamma ENCODES a protein that exhibits translation factor activity, RNA binding (ortholog); translation initiation factor activity (ortholog); INVOLVED IN translational initiation (ortholog); PARTICIPATES IN translation initiation pathway; ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); MEHMO syndrome (ortholog); FOUND IN cytoplasm (ortholog); eukaryotic translation initiation factor 2 complex (ortholog); nucleus (ortholog) NW_004955509 4437044 4457819 + 9068941 102016732 A0A8C2URY1 MODEL AGCD01066065;AGCD01066066;AGCD01066067;GBCQ01034165;XM_005407839 XP_005407896 eukaryotic translation initiation factor 2 subunit 3;eukaryotic translation initiation factor 2, subunit 3 gamma, 52kDa APPROVED protein-coding ENSCLAG00000001649 NW_004955509 4436750 4457819 + 8719403 Adtrp androgen dependent TFPI regulating protein ENCODES a protein that exhibits hydrolase activity (ortholog); INVOLVED IN cell migration involved in sprouting angiogenesis (ortholog); cellular response to oxidised low-density lipoprotein particle stimulus (ortholog); cellular response to steroid hormone stimulus (ortholog); ASSOCIATED WITH coronary artery disease (ortholog); genetic disease (ortholog); FOUND IN caveola (ortholog); cell surface (ortholog); membrane (ortholog) NW_004955465 2721171 2823368 + 9068941 102017207 A0A8C2UZS0 MODEL AGCD01050361;AGCD01050362;GBDK01307017;XM_005398822;XM_005398823;XM_013521868;XM_013521869;XM_013521870 XP_005398879;XP_005398880;XP_013377322;XP_013377323;XP_013377324 APPROVED protein-coding ENSCLAG00000005720 NW_004955465 2742169 2809790 + 8719421 Slc2a1 solute carrier family 2 member 1 ENCODES a protein that exhibits D-glucose transmembrane transporter activity (ortholog); dehydroascorbic acid transmembrane transporter activity (ortholog); glucose transmembrane transporter activity (ortholog); INVOLVED IN cellular hyperosmotic response (ortholog); cellular response to glucose starvation (ortholog); cellular response to mechanical stimulus (ortholog); PARTICIPATES IN facilitative sugar transporter mediated glucose transport pathway; Glut1 deficiency syndrome pathway; hypoxia inducible factor pathway; ASSOCIATED WITH Alzheimer's disease (ortholog); Ataxia (ortholog); benign epilepsy with centrotemporal spikes (ortholog); FOUND IN apical plasma membrane (ortholog); basolateral plasma membrane (ortholog); caveola (ortholog) NW_004955537 2408042 2438788 - 9068941;7240710 102017914 A0A8C2UNX0;A0A8C2YJC3 MODEL AGCD01070929;AGCD01070930;GBCQ01066583;XM_005410625 XP_005410682 solute carrier family 2 (facilitated glucose transporter), member 1;solute carrier family 2, facilitated glucose transporter member 1 APPROVED protein-coding ENSCLAG00000002106 NW_004955537 2408042 2439511 - 8719435 LOC102018242 vomeronasal type-2 receptor 1-like NW_004955448 7059300 7085760 + 102018242 A0A8C2VR47 MODEL AGCD01041399;AGCD01041400;XM_005393075 XP_005393132 protein-coding ENSCLAG00000012602 8719443 LOC102018418 putative ATP-dependent RNA helicase Pl10 NW_004955427 10783970 10784631 + 102018418 MODEL AGCD01027157 APPROVED pseudo 8719444 Skida1 SKI/DACH domain containing 1 ASSOCIATED WITH genetic disease (ortholog) NW_004955429 7181234 7187309 + 9068941 102018422 A0A8C2V2B3 MODEL AGCD01028583;AGCD01028584;GBDJ01303835;XM_013515352 XP_013370806 SKI/DACH domain-containing protein 1 protein-coding ENSCLAG00000006225 NW_004955429 7184430 7187146 + 8719450 Ly6g5b lymphocyte antigen 6 family member G5B ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN phosphorylation (ortholog); ASSOCIATED WITH genetic disease (ortholog); JMP syndrome (ortholog); megacolon (ortholog); FOUND IN external side of plasma membrane (ortholog); protein-containing complex (ortholog) NW_004955437 215824 218262 + 9068941 102018641 A0A8C2VU30 MODEL AGCD01034111;GBDJ01125465;XM_005389348 XP_005389405 lymphocyte antigen 6 complex locus protein G5b;lymphocyte antigen 6 complex, locus G5B APPROVED protein-coding ENSCLAG00000013439 NW_004955437 216686 219694 + 8719457 LOC102018688 uncharacterized LOC102018688 NW_004955406 40043515 40046054 + 102018688 MODEL AGCD01006652;GBCQ01091085;XR_259528 ncrna 8719462 Lmna lamin A/C ENCODES a protein that exhibits identical protein binding (ortholog); protein phosphatase 1 binding (ortholog); INVOLVED IN cellular response to hypoxia (ortholog); cellular senescence (ortholog); DNA double-strand break attachment to nuclear envelope (ortholog); PARTICIPATES IN atherosclerosis pathway; ASSOCIATED WITH achalasia (ortholog); aortic valve disease 2 (ortholog); arrhythmogenic right ventricular cardiomyopathy (ortholog); FOUND IN lamin filament (ortholog); nuclear envelope (ortholog); nuclear matrix (ortholog) NW_004955545 2290076 2310982 + 9068941;7240710 102018770 A0A8C2UTB4;A0A8C2UVN4;A0A8C2UYA7 MODEL AGCD01071894;AGCD01071895;GBBH01034310;XM_005411648;XM_013508332 XP_005411705;XP_013363786 lamin protein-coding ENSCLAG00000003894 NW_004955545 2290037 2313033 + 8719493 LOC102019354 ankyrin repeat family A protein 2 pseudogene NW_004955452 7466022 7466911 - 102019354 MODEL AGCD01044161 APPROVED pseudo 8719494 LOC102019568 uncharacterized LOC102019568 NW_004955455 1787821 1789349 + 102019568 MODEL AGCD01045585;GBDF01251154;XR_001236284;XR_001236285 ncrna ENSCLAG00000024506 8719500 LOC102019978 uncharacterized LOC102019978 NW_004955454 2669191 2673784 - 102019978 MODEL AGCD01045028;GBDF01208782;XR_001236254;XR_262770 ncrna 8719505 Olfml2a olfactomedin like 2A ENCODES a protein that exhibits extracellular matrix binding (ortholog); identical protein binding (ortholog); INVOLVED IN extracellular matrix organization (ortholog); ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog); hepatocellular carcinoma (ortholog); FOUND IN extracellular matrix (ortholog) NW_004955419 3397543 3420118 - 9068941 102021349 A0A8C2VWQ2 MODEL AGCD01019721;AGCD01019722;GBDI01325705;GBDI01325706;XM_005382483 XP_005382540 olfactomedin-like 2A;olfactomedin-like protein 2A APPROVED protein-coding ENSCLAG00000014121 NW_004955419 3393024 3414359 - 8719517 LOC102023061 uncharacterized LOC102023061 NW_004955513 3164898 3174163 + 102023061 MODEL AGCD01066896;GBDF01158696;XM_005408461 XP_005408518 uncharacterized protein LOC102023061 protein-coding 8719523 Rab24 RAB24, member RAS oncogene family ASSOCIATED WITH cerebellar ataxia (ortholog); Chromosome 5, Trisomy 5q (ortholog); colorectal adenocarcinoma (ortholog); FOUND IN autophagosome (ortholog); cytosol (ortholog) NW_004955408 29548839 29551184 - 9068941 102023117 A0A8C2VZL4 MODEL AGCD01008762;GBCB01023942;XM_005376424 XP_005376481 ras-related protein Rab-24 protein-coding ENSCLAG00000015766 NW_004955408 29548839 29551184 - 8719535 Erich2 glutamate rich 2 ASSOCIATED WITH split hand-foot malformation 5 (ortholog) NW_004955449 4013473 4040524 - 9068941 102023213 A0A8C2V6S7;A0A8C2VCU2 MODEL AGCD01041872;GBBH01000968;XM_005393243;XM_013518737;XM_013518738;XM_013518739;XM_013518740;XM_013518741;XM_013518742;XM_013518743 XP_005393300;XP_013374191;XP_013374192;XP_013374193;XP_013374194;XP_013374195;XP_013374196;XP_013374197 glutamate-rich 2;glutamate-rich protein 2 APPROVED protein-coding ENSCLAG00000007491;ENSCLAG00000028111 NW_004955449 4013693 4027539 - 8719548 Twist2 twist family bHLH transcription factor 2 ENCODES a protein that exhibits chromatin binding (ortholog); DNA-binding transcription factor activity (ortholog); protein domain specific binding (ortholog); INVOLVED IN cell population proliferation (ortholog); cornea development in camera-type eye (ortholog); embryonic cranial skeleton morphogenesis (ortholog); ASSOCIATED WITH ablepharon macrostomia syndrome (ortholog); Barber-Say syndrome (ortholog); Bethlem Myopathy 1 (ortholog); FOUND IN cytoplasm (ortholog); nucleolus (ortholog); nucleoplasm (ortholog) NW_004955542 1959765 2000665 - 9068941;7240710 102023744 A0A8C2YK97 MODEL AGCD01071509;GBBH01091431;GBCE01029840;XM_005411181 XP_005411238 twist basic helix-loop-helix transcription factor 2;twist-related protein 2 APPROVED protein-coding ENSCLAG00000003476 NW_004955542 1959765 2000665 - 8719554 LOC102024938 olfactory receptor 6Q1 ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog) NW_004955511 2822493 2823456 + 9068941 102024938 A0A8C2WAE4 MODEL AGCD01066428;XM_005408020 XP_005408077 APPROVED protein-coding ENSCLAG00000017704 NW_004955511 2822503 2823456 + 8719559 LOC102025857 tyrosine-protein phosphatase non-receptor type 9 pseudogene NW_004955578 378235 383809 + 102025857 MODEL AGCD01075479 APPROVED pseudo 8719560 Tgfbrap1 transforming growth factor beta receptor associated protein 1 ENCODES a protein that exhibits SMAD binding (ortholog); transforming growth factor beta receptor binding (ortholog); INVOLVED IN endosomal vesicle fusion (ortholog); endosome to lysosome transport (ortholog); regulation of DNA-templated transcription (ortholog); PARTICIPATES IN transforming growth factor-beta Smad dependent signaling pathway; ASSOCIATED WITH genetic disease (ortholog); long QT syndrome (ortholog); FOUND IN CORVET complex (ortholog); early endosome (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955470 10178936 10223234 - 9068941 102027290 A0A8C2V2L0 MODEL AGCD01052858;AGCD01052859;GBDI01294775;XM_005400783;XM_005400784;XM_005400785;XM_013522763 XP_005400840;XP_005400841;XP_005400842;XP_013378217 transforming growth factor, beta receptor associated protein 1;transforming growth factor-beta receptor-associated protein 1 APPROVED protein-coding ENSCLAG00000005507 NW_004955470 10176607 10223234 - 8719582 LOC102027360 sulfotransferase 1 family member D1 NW_004955447 2990990 3016299 + 102027360 A0A8C2YK88 MODEL AGCD01040570;AGCD01040571;GBBH01215647;XM_005392791 XP_005392848 APPROVED protein-coding ENSCLAG00000003433 8719593 Sypl1 synaptophysin like 1 ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN membrane (ortholog); secretory granule (ortholog); synaptic vesicle membrane (ortholog) NW_004955410 10571888 10590978 - 9068941 102027951 A0A8C2YPM8 MODEL AGCD01010795;AGCD01010796;GBDF01047643;XM_005377266 XP_005377323 synaptophysin-like 1;synaptophysin-like protein 1 APPROVED protein-coding ENSCLAG00000009703 NW_004955410 10568594 10591040 - 8719603 Cdc7 cell division cycle 7 ENCODES a protein that exhibits kinase activity (ortholog); protein kinase activity (ortholog); INVOLVED IN cell cycle phase transition (ortholog); positive regulation of cell population proliferation (ortholog); positive regulation of G2/M transition of mitotic cell cycle (ortholog); ASSOCIATED WITH genetic disease (ortholog); primary ovarian insufficiency (ortholog); FOUND IN cytoplasm (ortholog); intercellular bridge (ortholog); mitotic spindle (ortholog) NW_004955423 2902352 2923743 - 9068941 102027995 A0A8C2V638;A0A8C2V641 MODEL AGCD01023492;AGCD01023493;GBCE01072842;XM_005385064;XM_005385065 XP_005385121;XP_005385122 cell division cycle 7-related protein kinase protein-coding ENSCLAG00000007469 NW_004955423 2902048 2924573 - 8719625 Ap5b1 adaptor related protein complex 5 subunit beta 1 INVOLVED IN endosomal transport (ortholog); ASSOCIATED WITH Aicardi-Goutieres Syndrome 3 (ortholog); Bardet-Biedl syndrome (ortholog); genetic disease (ortholog); FOUND IN AP-type membrane coat adaptor complex (ortholog) NW_004955422 19544255 19547212 + 9068941 102028981 A0A8C2WA33 MODEL AGCD01023018;GBCE01085788;GBDK01317435;XM_005384462 XP_005384519 AP-5 complex subunit beta-1;adaptor related protein complex 5 beta 1 subunit;adaptor-related protein complex 5, beta 1 subunit APPROVED protein-coding ENSCLAG00000016777 NW_004955422 19544344 19547429 + 8719631 Mks1 MKS transition zone complex subunit 1 INVOLVED IN branching morphogenesis of an epithelial tube (ortholog); cardiac septum morphogenesis (ortholog); cilium assembly (ortholog); ASSOCIATED WITH atrioventricular septal defect (ortholog); Bardet-Biedl syndrome (ortholog); Bardet-Biedl syndrome 13 (ortholog); FOUND IN centriole (ortholog); centrosome (ortholog); ciliary basal body (ortholog) NW_004955451 4805542 4818233 + 9068941;7240710 102029139 A0A8C2YUB1 MODEL AGCD01043142;GBDF01248745;XM_005394033 XP_005394090 Meckel syndrome, type 1 APPROVED protein-coding ENSCLAG00000016366 NW_004955451 4804838 4821556 + 8719652 Fam114a2 family with sequence similarity 114 member A2 ASSOCIATED WITH familial adenomatous polyposis 1 (ortholog); genetic disease (ortholog); Hereditary Neoplastic Syndromes (ortholog) NW_004955408 8396185 8434656 - 9068941 102029266 A0A8C2VZE1 MODEL AGCD01008218;GBCE01152740;XM_005376191;XM_013508608;XM_013508610;XM_013508613 XP_005376248;XP_013364062;XP_013364064;XP_013364067 family with sequence similarity 114, member A2 APPROVED protein-coding ENSCLAG00000013645 NW_004955408 8397281 8429502 - 8719672 LOC102030408 actin-like NW_004955413 12934722 12936356 - 102030408 MODEL AGCD01014004 APPROVED pseudo 8719673 Slc4a2 solute carrier family 4 member 2 ENCODES a protein that exhibits chloride transmembrane transporter activity (ortholog); chloride:bicarbonate antiporter activity (ortholog); enzyme binding (ortholog); INVOLVED IN amelogenesis (ortholog); chloride transport (ortholog); digestive tract development (ortholog); ASSOCIATED WITH Alkalosis (ortholog); Autosomal Recessive Osteopetrosis 9 (ortholog); autosomal recessive polycystic kidney disease (ortholog); FOUND IN apical plasma membrane (ortholog); basolateral plasma membrane (ortholog); membrane (ortholog) NW_004955491 5498472 5513389 + 9068941 102030539 A0A8C2USY3;A0A8C2UTP6;A0A8C2UYN1;A0A8C2YKD7 MODEL AGCD01060485;GBDJ01004266;XM_005404810;XM_005404811;XM_013504586 XP_005404867;XP_005404868;XP_013360040 anion exchange protein 2;solute carrier family 4 (anion exchanger), member 2 APPROVED protein-coding ENSCLAG00000003594 NW_004955491 5499033 5517319 + 8719709 Clps colipase ENCODES a protein that exhibits enzyme activator activity (ortholog); INVOLVED IN positive regulation of catalytic activity (ortholog); post-embryonic development (ortholog); response to bacterium (ortholog); ASSOCIATED WITH Experimental Diabetes Mellitus (ortholog); genetic disease (ortholog); JMP syndrome (ortholog) NW_004955437 3624676 3626529 - 9068941 102003063 A0A8C2VRP1 MODEL AGCD01034327;XM_005389567 XP_005389624 colipase, pancreatic APPROVED protein-coding ENSCLAG00000013482 8719720 Ppp2r1a protein phosphatase 2 scaffold subunit Aalpha ENCODES a protein that exhibits protein antigen binding (ortholog); protein heterodimerization activity (ortholog); protein serine/threonine phosphatase activity (ortholog); INVOLVED IN chromosome segregation (ortholog); female meiotic nuclear division (ortholog); meiotic sister chromatid cohesion, centromeric (ortholog); PARTICIPATES IN phosphatidylinositol 3-kinase-Akt signaling pathway; platelet-derived growth factor signaling pathway; ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); autosomal dominant intellectual developmental disorder 36 (ortholog); FOUND IN chromosome, centromeric region (ortholog); cytosol (ortholog); glutamatergic synapse (ortholog) NW_004955558 381794 410485 + 9068941 102004524 A0A8C2YJ41 MODEL AGCD01073369;GBBH01030900;XM_005412660 XP_005412717 serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform APPROVED protein-coding ENSCLAG00000001749 NW_004955558 381794 410485 + 8719739 LOC102005152 olfactory receptor 2A2-like NW_004955491 447741 450169 + 9068941 102005152 MODEL AGCD01060335;XM_005404725 XP_005404782 protein-coding 8719744 Crip3 cysteine rich protein 3 INVOLVED IN T cell proliferation (ortholog); ASSOCIATED WITH genetic disease (ortholog); infantile Refsum disease (ortholog); Zellweger syndrome (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog) NW_004955437 9210901 9215471 - 9068941 102006163 A0A8C2VGF7;A0A8C2VGG3;A0A8C2VLX2 MODEL AGCD01034522;GBDJ01337171;XM_005389761;XM_013516979;XM_013516980 XP_005389818;XP_013372433;XP_013372434 LOC102006953 cysteine-rich protein 2-like;cysteine-rich protein 3 PROVISIONAL protein-coding ENSCLAG00000010491 NW_004955437 9210901 9215471 - 8719759 LOC102007390 EKC/KEOPS complex subunit LAGE3-like NW_004955595 891199 900679 + 102007390 MODEL AGCD01076488;AGCD01076489;AGCD01076490;GBDK01408734;XM_005414678 XP_005414735 APPROVED protein-coding 8719766 Commd7 COMM domain containing 7 ENCODES a protein that exhibits NF-kappaB binding (ortholog); INVOLVED IN negative regulation of DNA-templated transcription (ortholog); negative regulation of NF-kappaB transcription factor activity (ortholog); tumor necrosis factor-mediated signaling pathway (ortholog); ASSOCIATED WITH genetic disease (ortholog); immunodeficiency-centromeric instability-facial anomalies syndrome 1 (ortholog) NW_004955422 28454984 28464885 + 9068941 102007443 A0A8C2W4H5 MODEL AGCD01023354;AGCD01023355;AGCD01023356;GBCB01020579;GBCQ01006048;XM_013514154 XP_013369608 COMM domain-containing protein 7 protein-coding ENSCLAG00000017227 NW_004955422 28442274 28467057 + 8719785 LOC102008440 high mobility group protein B1-like NW_004955427 3052920 3061332 - 102008440 MODEL AGCD01026912 pseudo 8719786 Ttc8 tetratricopeptide repeat domain 8 ENCODES a protein that exhibits RNA polymerase II-specific DNA-binding transcription factor binding (ortholog); INVOLVED IN axon guidance (ortholog); camera-type eye photoreceptor cell differentiation (ortholog); cilium assembly (ortholog); ASSOCIATED WITH Bardet-Biedl syndrome (ortholog); Bardet-Biedl syndrome 8 (ortholog); fundus dystrophy (ortholog); FOUND IN BBSome (ortholog); centrosome (ortholog); ciliary basal body (ortholog) NW_004955438 11410196 11466044 + 9068941;7240710 102008459 A0A8C2VBV3;A0A8C2VFX3 MODEL AGCD01035237;AGCD01035238;AGCD01035239;GBDF01187164;XM_005390265 XP_005390322 tetratricopeptide repeat protein 8 protein-coding ENSCLAG00000008510 NW_004955438 11409982 11466523 + 8719809 Prrt2 proline rich transmembrane protein 2 ENCODES a protein that exhibits SH3 domain binding (ortholog); syntaxin-1 binding (ortholog); INVOLVED IN negative regulation of short-term synaptic potentiation (ortholog); negative regulation of SNARE complex assembly (ortholog); neuromuscular process controlling posture (ortholog); ASSOCIATED WITH 16p11.2 Deletion Syndrome (ortholog); atrial heart septal defect (ortholog); autism spectrum disorder (ortholog); FOUND IN axon terminus (ortholog); glutamatergic synapse (ortholog); membrane (ortholog) NW_004955493 7144389 7148613 - 7240710;9068941 102008740 A0A8C2VF42 MODEL AGCD01061156;GBCC01002602;XM_013504775;XM_013504776;XM_013504777;XM_013504778 XP_013360229;XP_013360230;XP_013360231;XP_013360232 proline-rich transmembrane protein 2 APPROVED protein-coding ENSCLAG00000010098 8719840 LOC102009525 sperm motility kinase 2B-like NW_004955429 13400335 13403083 + 102009525 MODEL AGCD01028747;GBDK01097126;XM_005386993 XP_005387050 APPROVED protein-coding 8719849 LOC102009819 splicing factor, arginine/serine-rich 19-like NW_004955413 3207197 3209122 - 102009819 MODEL AGCD01013568;GBDI01085078;XM_005378751;XM_005378752;XM_013511272;XR_001232932 XP_005378808;XP_005378809;XP_013366726 transcription initiation factor TFIID subunit 3-like;uncharacterized protein LOC102009819 APPROVED protein-coding 8719858 Vil1 villin 1 ENCODES a protein that exhibits actin filament binding (ortholog); calcium ion binding (ortholog); cysteine-type endopeptidase inhibitor activity involved in apoptotic process (ortholog); INVOLVED IN actin filament capping (ortholog); actin filament depolymerization (ortholog); actin filament polymerization (ortholog); ASSOCIATED WITH alacrima, achalasia, and impaired intellectual development syndrome (ortholog); cerebrotendinous xanthomatosis (ortholog); cholestasis (ortholog); FOUND IN actin filament bundle (ortholog); brush border (ortholog); filopodium (ortholog) NW_004955453 14935450 14961011 - 9068941 102010225 A0A8C2V9L6 MODEL AGCD01044877;GBCQ01002955;XM_005395646 XP_005395703 villin-1 protein-coding ENSCLAG00000008436 NW_004955453 14935456 14961011 - 8719892 Tll1 tolloid like 1 ENCODES a protein that exhibits collagen binding (ortholog); ASSOCIATED WITH atrial heart septal defect 6 (ortholog); congenital heart disease (ortholog); coronary artery disease (ortholog) NW_004955403 39299461 39491638 - 9068941;7240710 102011072 A0A8C2VSG4 MODEL AGCD01002627;AGCD01002628;AGCD01002629;AGCD01002630;GBCE01123233;GBCQ01016540;XM_005373585 XP_005373642 tolloid-like 1;tolloid-like protein 1 APPROVED protein-coding ENSCLAG00000011556 NW_004955403 39299461 39491638 - 8719921 LOC102012800 uncharacterized LOC102012800 NW_004955436 20441094 20445316 - 102012800 MODEL AGCD01034024;GBCB01036539;XR_261802 ncrna 8719926 LOC102012938 60S ribosomal protein L37a-like NW_004955464 13764223 13764774 + 102012938 MODEL AGCD01050293 pseudo 8719927 Tenm3 teneurin transmembrane protein 3 ENCODES a protein that exhibits identical protein binding (ortholog); protein heterodimerization activity (ortholog); protein homodimerization activity (ortholog); INVOLVED IN camera-type eye morphogenesis (ortholog); homophilic cell adhesion via plasma membrane adhesion molecules (ortholog); positive regulation of neuron projection development (ortholog); ASSOCIATED WITH Cocaine-Related Disorders (ortholog); genetic disease (ortholog); Isolated Microphthalmia with Coloboma 9 (ortholog); FOUND IN membrane (ortholog); plasma membrane (ortholog) NW_004955403 25920919 26534817 - 7240710;9068941 102013237 A0A8C2VSW3;A0A8C2VUZ2;A0A8C2W075 MODEL AGCD01002295;AGCD01002296;AGCD01002297;AGCD01002298;AGCD01002299;AGCD01002300;AGCD01002301;AGCD01002302;AGCD01002303;AGCD01002304;AGCD01002305;AGCD01002306;AGCD01002307;AGCD01002308;GBCB01121667;XM_013513152;XM_013513154 XP_013368606;XP_013368608 teneurin-3 protein-coding ENSCLAG00000013736 NW_004955403 25923750 26365894 - 8719963 Slc24a5 solute carrier family 24 member 5 ENCODES a protein that exhibits calcium ion transmembrane transporter activity (ortholog); calcium, potassium:sodium antiporter activity (ortholog); INVOLVED IN calcium ion import (ortholog); melanin biosynthetic process (ortholog); monoatomic ion transmembrane transport (ortholog); PARTICIPATES IN calcium transport pathway; calcium/calcium-mediated signaling pathway; ASSOCIATED WITH Bloom syndrome (ortholog); colorectal cancer (ortholog); genetic disease (ortholog); FOUND IN trans-Golgi network (ortholog) NW_004955409 5747624 5768122 - 9068941;7240710 102013803 A0A8C2VD47 MODEL AGCD01009322;AGCD01009323;GBDI01093137;XM_005376708 XP_005376765 sodium/potassium/calcium exchanger 5;solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 APPROVED protein-coding ENSCLAG00000009536 NW_004955409 5747624 5768122 - 8719979 Srp14 signal recognition particle 14 INVOLVED IN protein targeting to ER (ortholog); ASSOCIATED WITH Bloom syndrome (ortholog); colorectal cancer (ortholog); genetic disease (ortholog); FOUND IN nucleus (ortholog); signal recognition particle, endoplasmic reticulum targeting (ortholog) NW_004955416 7006240 7009569 - 9068941 102013931 A0A8C2VZV7;A0A8C2W268 MODEL AGCD01016961;GBDJ01001152;XM_005381213 XP_005381270 signal recognition particle 14kDa (homologous Alu RNA binding protein) APPROVED protein-coding ENSCLAG00000015031 NW_004955416 7006240 7009965 - 8719988 LOC102013999 protein mago nashi homolog 2 pseudogene NW_004955403 41539551 41539998 + 102013999 MODEL AGCD01002723 APPROVED pseudo 8719989 Ganab glucosidase II alpha subunit ENCODES a protein that exhibits alpha-glucosidase activity (ortholog); glucan 1,3-alpha-glucosidase activity (ortholog); INVOLVED IN N-glycan processing (ortholog); ASSOCIATED WITH autosomal dominant polycystic kidney disease (ortholog); Chemical and Drug Induced Liver Injury (ortholog); chronic kidney disease (ortholog); FOUND IN glucosidase II complex (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955599 556510 569891 + 9068941 102014306 A0A8C2UKX5 MODEL AGCD01076659;AGCD01076660;GBCE01030836;XM_005414786;XM_005414787 XP_005414843;XP_005414844 glucosidase, alpha;neutral AB;neutral alpha-glucosidase AB APPROVED protein-coding ENSCLAG00000000345 NW_004955599 556362 573353 + 8720025 Puf60 poly(U) binding splicing factor 60 ENCODES a protein that exhibits identical protein binding (ortholog); ASSOCIATED WITH Brown-Vialetto-Van Laere syndrome 2 (ortholog); CHARGE syndrome (ortholog); epidermolysis bullosa simplex with muscular dystrophy (ortholog); FOUND IN cell junction (ortholog); nucleoplasm (ortholog) NW_004955454 2482968 2497339 - 9068941;7240710 102014866 A0A8C2VE28;A0A8C2VH65 MODEL AGCD01045022;GBDK01022705;XM_005395816;XM_005395817;XM_005395818;XM_013520058;XM_013520059;XM_013520060 XP_005395873;XP_005395874;XP_005395875;XP_013375512;XP_013375513;XP_013375514 poly(U)-binding-splicing factor PUF60;poly-U binding splicing factor 60KDa APPROVED protein-coding ENSCLAG00000009154 NW_004955454 2482968 2497339 - 8720045 Slc22a4 solute carrier family 22 member 4 ENCODES a protein that exhibits amino acid transmembrane transporter activity (ortholog); carnitine transmembrane transporter activity (ortholog); organic cation transmembrane transporter activity (ortholog); INVOLVED IN amino acid import across plasma membrane (ortholog); carnitine metabolic process (ortholog); carnitine transport (ortholog); PARTICIPATES IN cisplatin response pathway; ASSOCIATED WITH Coxsackievirus Infections (ortholog); Enterovirus Infections (ortholog); familial adenomatous polyposis 1 (ortholog); FOUND IN apical plasma membrane (ortholog); basal plasma membrane (ortholog); mitochondrion (ortholog) NW_004955408 3671772 3737946 + 9068941;7240710 102014984 A0A8C2VIA7 MODEL AGCD01008071;AGCD01008072;AGCD01008073;GBDI01289956;XM_013508300 XP_013363754 solute carrier family 22 (organic cation/zwitterion transporter), member 4 APPROVED protein-coding ENSCLAG00000011046 NW_004955408 3671772 3737612 + 8720060 LOC102015215 olfactory receptor 7C2 ASSOCIATED WITH genetic disease (ortholog) NW_004955495 8328332 8329291 - 9068941 102015215 MODEL AGCD01062198;XM_005406105 XP_005406162 APPROVED protein-coding 8720063 Gpr35 G protein-coupled receptor 35 ENCODES a protein that exhibits C-X-C chemokine receptor activity (ortholog); G protein-coupled receptor activity (ortholog); INVOLVED IN chemokine-mediated signaling pathway (ortholog); cytoskeleton organization (ortholog); G protein-coupled receptor signaling pathway (ortholog); ASSOCIATED WITH Bethlem Myopathy 1 (ortholog); chromosome 2q37 deletion syndrome (ortholog); D-2-hydroxyglutaric aciduria 1 (ortholog); FOUND IN plasma membrane (ortholog) NW_004955542 851895 856688 - 9068941 102015450 A0A8C2UMY1 MODEL AGCD01071481;GBCE01072681;XM_005411154 XP_005411211 G-protein coupled receptor 35 protein-coding ENSCLAG00000001799 NW_004955542 851895 856688 - 8720069 LOC102016205 chondroitin sulfate N-acetylgalactosaminyltransferase 2-like NW_004955442 17178781 17201854 - 102016205 MODEL AGCD01037944;AGCD01037945;AGCD01037946 pseudo 8720070 LOC102016255 S-phase kinase-associated protein 1 pseudogene NW_004955413 32899725 32900339 - 102016255 MODEL AGCD01014649;XM_005379524 APPROVED pseudo ENSCLAG00000018059 8720074 Nod2 nucleotide binding oligomerization domain containing 2 ENCODES a protein that exhibits actin binding (ortholog); CARD domain binding (ortholog); enzyme binding (ortholog); INVOLVED IN activation of immune response (ortholog); biosynthetic process of antibacterial peptides active against Gram-positive bacteria (ortholog); cellular response to lipopolysaccharide (ortholog); PARTICIPATES IN NOD-like receptor signaling pathway; nuclear factor kappa B signaling pathway; ASSOCIATED WITH acne (ortholog); Acute Lung Injury (ortholog); allergic rhinitis (ortholog); FOUND IN basolateral plasma membrane (ortholog); cell surface (ortholog); cytoplasm (ortholog) NW_004955433 8746213 8780119 + 9068941;7240710 102016837 A0A8C2VBW8 MODEL AGCD01031603;GBCQ01045878;XM_005388272;XM_005388273 XP_005388329;XP_005388330 nucleotide-binding oligomerization domain containing 2;nucleotide-binding oligomerization domain-containing protein 2 APPROVED protein-coding ENSCLAG00000009024 NW_004955433 8746004 8782710 + 8720094 LOC102017188 60S acidic ribosomal protein P0-like NW_004955404 6462391 6489586 - 102017188 MODEL AGCD01003320;AGCD01003321;AGCD01003322 pseudo 8720095 Bpgm bisphosphoglycerate mutase ENCODES a protein that exhibits bisphosphoglycerate mutase activity (ortholog); INVOLVED IN defense response to protozoan (ortholog); erythrocyte development (ortholog); establishment of blood-brain barrier (ortholog); PARTICIPATES IN Fanconi syndrome pathway; fructose-1,6-bisphosphatase deficiency pathway; gluconeogenesis pathway; ASSOCIATED WITH familial erythrocytosis 8 (ortholog); genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog) NW_004955494 7867295 7889440 - 9068941;7240710 102019610 A0A8C2UQ71 MODEL AGCD01061558;GBBH01208829;XM_005405507;XM_005405508;XM_013505024 XP_005405564;XP_005405565;XP_013360478 2,3-bisphosphoglycerate mutase APPROVED protein-coding ENSCLAG00000001189 NW_004955494 7866693 7883641 - 8720105 LOC102020031 uncharacterized LOC102020031 NW_004955501 3463765 3466302 + 102020031 MODEL AGCD01064105;GBDF01189492;XR_264251 ncrna 8720110 Rdh5 retinol dehydrogenase 5 ENCODES a protein that exhibits androstan-3-alpha,17-beta-diol dehydrogenase activity (ortholog); androsterone dehydrogenase activity (ortholog); NAD-retinol dehydrogenase activity (ortholog); INVOLVED IN retinoid metabolic process (ortholog); steroid metabolic process (ortholog); PARTICIPATES IN retinoid cycle metabolic pathway; ASSOCIATED WITH Congenital Abnormalities (ortholog); fundus albipunctatus (ortholog); fundus dystrophy (ortholog); FOUND IN cell body (ortholog); endoplasmic reticulum lumen (ortholog); endoplasmic reticulum membrane (ortholog) NW_004955458 3356324 3361701 + 9068941;7240710 102020090 A0A8C2VHB2;A0A8C2VHN0;A0A8C2VM20 MODEL AGCD01047296;GBDI01078451;XM_005397255;XM_005397256;XM_005397257 XP_005397312;XP_005397313;XP_005397314 11-cis retinol dehydrogenase;retinol dehydrogenase 5 (11-cis/9-cis) APPROVED protein-coding ENSCLAG00000010216 NW_004955458 3352012 3365080 + 8720125 Sh2d4a SH2 domain containing 4A ENCODES a protein that exhibits phosphatase binding (ortholog); ASSOCIATED WITH COVID-19 (ortholog); genetic disease (ortholog); hereditary spastic paraplegia 53 (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog) NW_004955403 43111804 43170344 + 9068941 102020738 A0A8C2VVV3;A0A8C2YT47 MODEL AGCD01002767;GBDK01136635;GBDK01136639;XM_005373614;XM_005373615 XP_005373671;XP_005373672 SH2 domain-containing protein 4A protein-coding ENSCLAG00000014633 NW_004955403 43111804 43170397 + 8720145 LOC102021945 granzyme H-like NW_004955409 35505067 35515345 + 102021945 A0A8C2VJT2 MODEL AGCD01010424;AGCD01010425;GBDK01074391;XM_005376986;XM_005376989;XM_005376990;XM_013510455 XP_005377043;XP_005377046;XP_005377047;XP_013365909 LOC102016244 granzyme B-like PROVISIONAL protein-coding ENSCLAG00000010860 NW_004955409 35505045 35515391 + 8720163 Traf1 TNF receptor associated factor 1 ENCODES a protein that exhibits identical protein binding (ortholog); thioesterase binding (ortholog); tumor necrosis factor receptor binding (ortholog); INVOLVED IN positive regulation of NF-kappaB transcription factor activity (ortholog); regulation of extrinsic apoptotic signaling pathway (ortholog); PARTICIPATES IN tumor necrosis factor mediated signaling pathway; ASSOCIATED WITH genetic disease (ortholog); multiple sclerosis (ortholog); patent ductus arteriosus (ortholog) NW_004955419 7117869 7145274 + 9068941 102021974 A0A8C2VN72 MODEL AGCD01019874;GBDK01090336;XM_013513240;XM_013513241;XM_013513242;XR_001233625;XR_001233626 XP_013368694;XP_013368695;XP_013368696 TNF receptor-associated factor 1 APPROVED protein-coding ENSCLAG00000010515 NW_004955419 7121382 7137763 + 8720188 Tmem11 transmembrane protein 11 INVOLVED IN mitochondrion organization (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrion (ortholog) NW_004955577 1126353 1140145 - 9068941 102022980 A0A8C2UJY5;A0A8C2UM71 MODEL AGCD01075436;AGCD01075437;AGCD01075438;GBCB01025567;XM_005413988;XM_005413989 XP_005414045;XP_005414046 transmembrane protein 11, mitochondrial protein-coding ENSCLAG00000000422 NW_004955577 1126353 1140682 - 8720197 Psme3ip1 proteasome activator subunit 3 interacting protein 1 INVOLVED IN negative regulation of proteasomal protein catabolic process (ortholog); negative regulation of protein binding (ortholog); ASSOCIATED WITH Bardet-Biedl syndrome (ortholog); developmental and epileptic encephalopathy (ortholog); early infantile epileptic encephalopathy (ortholog); FOUND IN intracellular membrane-bounded organelle (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955433 14813688 14843446 - 9068941 102023627 A0A8C2V0K1 MODEL AGCD01031729;AGCD01031730;GBCB01023782;XM_005388378;XM_005388379;XM_005388380;XM_005388381;XM_005388383;XM_013516131 XP_005388435;XP_005388436;XP_005388437;XP_005388438;XP_005388440;XP_013371585 Fam192a family with sequence similarity 192 member A;family with sequence similarity 192, member A APPROVED protein-coding ENSCLAG00000004156 NW_004955433 14813688 14843223 - 8720223 Cdc34 cell division cycle 34, ubiqiutin conjugating enzyme ENCODES a protein that exhibits ubiquitin conjugating enzyme activity (ortholog); ubiquitin-protein transferase activity (ortholog); INVOLVED IN cellular response to interferon-beta (ortholog); negative regulation of cAMP-mediated signaling (ortholog); positive regulation of inclusion body assembly (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); nuclear speck (ortholog) NW_004955495 7170419 7178093 - 9068941 102024252 A0A8C2VBB7 MODEL AGCD01062123;GBDF01155493;GBDJ01006834;XM_005406038 XP_005406095 cell division cycle 34;ubiquitin-conjugating enzyme E2 R1 APPROVED protein-coding ENSCLAG00000009001 NW_004955495 7170419 7178093 - 8720232 Ngfr nerve growth factor receptor ENCODES a protein that exhibits amyloid-beta binding (ortholog); calmodulin binding (ortholog); coreceptor activity (ortholog); INVOLVED IN activation of cysteine-type endopeptidase activity involved in apoptotic process (ortholog); axon guidance (ortholog); cellular response to amyloid-beta (ortholog); ASSOCIATED WITH Alzheimer's disease (ortholog); asthma (ortholog); atherosclerosis (ortholog); FOUND IN cell surface (ortholog); cell-cell junction (ortholog); clathrin-coated endocytic vesicle (ortholog) NW_004955451 12030303 12047305 - 9068941 102025073 A0A8C2W0B6 MODEL AGCD01043372;GBCE01123716;GBDI01176680;XM_005394210 XP_005394267 tumor necrosis factor receptor superfamily member 16 protein-coding ENSCLAG00000015829 NW_004955451 12030252 12047305 - 8720242 Hgd homogentisate 1,2-dioxygenase ENCODES a protein that exhibits homogentisate 1,2-dioxygenase activity (ortholog); identical protein binding (ortholog); INVOLVED IN amino acid metabolic process (ortholog); PARTICIPATES IN alkaptonuria pathway; disulfiram pharmacodynamics pathway; dopamine beta-hydroxylase deficiency pathway; ASSOCIATED WITH alkaptonuria (ortholog); Alkaptonuric Ochronosis (ortholog); genetic disease (ortholog) NW_004955427 20141522 20188700 - 9068941;7240710 102025268 A0A8C2YPB6 MODEL AGCD01027394;GBDJ01267025;XM_005386468 XP_005386525 protein-coding ENSCLAG00000009244 NW_004955427 20137861 20188700 - 8720262 LOC102025786 uncharacterized protein C12orf45 pseudogene NW_004955475 6151506 6152080 - 102025786 MODEL AGCD01054952 APPROVED pseudo 8720263 LOC102025925 stathmin pseudogene NW_004955500 7348048 7348466 + 102025925 MODEL AGCD01063916 APPROVED pseudo 8720264 LOC102026044 A-kinase anchor protein 17A-like NW_004955439 8813335 8830470 - 102026044 A0A8C2USZ7 MODEL AGCD01035813;GBDF01082647;XM_005390568;XM_013517409 XP_005390625;XP_013372863 protein-coding ENSCLAG00000003820 NW_004955439 8813824 8817788 - 8720270 Mier2 MIER family member 2 ENCODES a protein that exhibits histone deacetylase activity (ortholog); histone deacetylase binding (ortholog); ASSOCIATED WITH adenoid cystic carcinoma (ortholog); genetic disease (ortholog); Salivary Gland Neoplasms (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog); protein-containing complex (ortholog) NW_004955495 7279507 7300202 + 9068941 102026543 A0A8C2V836;A0A8C2VE85 MODEL AGCD01062129;GBCQ01153851;XM_005406046;XM_005406047;XM_005406048;XM_005406049;XM_005406051;XM_013505349;XM_013505350 XP_005406103;XP_005406104;XP_005406105;XP_005406106;XP_005406108;XP_013360803;XP_013360804 mesoderm induction early response 1, family member 2;mesoderm induction early response protein 2 APPROVED protein-coding ENSCLAG00000007889 NW_004955495 7279451 7302123 + 8720300 Fam43a family with sequence similarity 43 member A ASSOCIATED WITH Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog) NW_004955420 14202955 14206087 - 102027191 A0A8C2VK70 MODEL AGCD01020933;GBDJ01138402;XM_005383185 XP_005383242 family with sequence similarity 43, member A APPROVED protein-coding ENSCLAG00000011597 NW_004955420 14203879 14205165 - 8720305 LOC102027512 b(0,+)-type amino acid transporter 1-like NW_004955469 2887053 2935439 + 102027512 A0A8C2V0V8;A0A8C2YLW8 MODEL AGCD01052288;GBDF01278413;XM_013522632;XM_013522633;XM_013522635;XM_013522636 XP_013378086;XP_013378087;XP_013378089;XP_013378090 LOC102027166 uncharacterized LOC102027166 PROVISIONAL protein-coding ENSCLAG00000005814 8720314 Gtf3c4 general transcription factor IIIC subunit 4 ENCODES a protein that exhibits RNA polymerase III general transcription initiation factor activity (ortholog); PARTICIPATES IN RNA polymerase III transcription pathway; ASSOCIATED WITH developmental and epileptic encephalopathy 14 (ortholog); Ehlers-Danlos syndrome classic type 1 (ortholog); genetic disease (ortholog); FOUND IN mitochondrion (ortholog); nucleoplasm (ortholog); transcription factor TFIIIC complex (ortholog) NW_004955513 2037312 2054451 + 9068941 102027560 A0A8C2VEJ4 MODEL AGCD01066868;GBDI01019040;GBDI01019069;XM_005408381 XP_005408438 general transcription factor 3C polypeptide 4;general transcription factor IIIC, polypeptide 4, 90kDa APPROVED protein-coding ENSCLAG00000009930 NW_004955513 2037312 2054451 + 8720329 Grik1 glutamate ionotropic receptor kainate type subunit 1 ENCODES a protein that exhibits extracellularly glutamate-gated ion channel activity (ortholog); glutamate binding (ortholog); heterocyclic compound binding (ortholog); INVOLVED IN adult behavior (ortholog); behavioral response to pain (ortholog); establishment of localization in cell (ortholog); PARTICIPATES IN long term potentiation; ASSOCIATED WITH childhood absence epilepsy (ortholog); genetic disease (ortholog); status epilepticus (ortholog); FOUND IN dendrite (ortholog); glutamatergic synapse (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955407 28899643 29308936 - 9068941 102027813 A0A8C2V2H6;A0A8C2V2I7;A0A8C2V2X1;A0A8C2YME2 MODEL AGCD01007596;AGCD01007597;AGCD01007598;AGCD01007599;AGCD01007600;AGCD01007601;AGCD01007602;AGCD01007603;AGCD01007604;AGCD01007605;AGCD01007606;XM_005375621;XM_005375622 XP_005375678;XP_005375679 glutamate receptor ionotropic, kainate 1;glutamate receptor, ionotropic, kainate 1 APPROVED protein-coding ENSCLAG00000006476 NW_004955407 28899899 29308470 - 8720353 LOC102028097 cyclin-dependent kinase 4 pseudogene NW_004955421 3868940 3869860 - 102028097 MODEL AGCD01021671 APPROVED pseudo 8720354 LOC102028430 prolactin-inducible protein homolog NW_004955494 506278 511778 - 102028430 MODEL AGCD01061380;GBDF01274186;XM_013504916 XP_013360370 protein-coding 8720362 Etfrf1 electron transfer flavoprotein regulatory factor 1 INVOLVED IN respiratory electron transport chain (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN mitochondrion (ortholog) NW_004955413 20287287 20294430 + 9068941 102029279 A0A8C2W412 MODEL AGCD01014212;GBDF01080150;XM_005379098;XM_013511449 XP_005379155;XP_013366903 Lyrm5 LYR motif containing 5;LYR motif-containing protein 5 APPROVED protein-coding ENSCLAG00000016238 NW_004955413 20293398 20293738 + 8720369 LOC102003284 uncharacterized LOC102003284 NW_004955438 10342037 10345901 + 102003284 MODEL AGCD01035203;GBDF01305498;XR_261924 ncrna 8720374 LOC102004352 tomoregulin-1-like NW_004955454 12413700 12441760 + 102004352 MODEL AGCD01045411;AGCD01045412;XM_013520017 XP_013375471 protein-coding 8720375 LOC102005916 COMM domain-containing protein 8 pseudogene NW_004955466 2360352 2361351 - 102005916 MODEL AGCD01050734 APPROVED pseudo 8720376 LOC102005953 olfactory receptor 5B2-like NW_004955511 3211089 3212036 - 102005953 A0A8C2UXD6 MODEL AGCD01066450;XM_013506385 XP_013361839 APPROVED protein-coding ENSCLAG00000004811 8720377 LOC102006553 CAP-Gly domain-containing linker protein 1 pseudogene NW_004955463 5125915 5126991 - 102006553 MODEL AGCD01049632 APPROVED pseudo 8720378 LOC102006569 olfactory receptor 51L1-like NW_004955414 21331309 21332259 - 102006569 A0A8C2W6B1 MODEL AGCD01015415;XM_005380496 XP_005380553 protein-coding ENSCLAG00000017960 8720381 LOC102006698 olfactory receptor 1020-like NW_004955511 682056 682990 + 102006698 MODEL AGCD01066337;XM_013506361 XP_013361815 protein-coding 8720386 LOC102007426 GMP synthase [glutamine-hydrolyzing] pseudogene NW_004955476 3481522 3489789 + 102007426 MODEL AGCD01055252 APPROVED pseudo 8720387 Fgf7 fibroblast growth factor 7 ENCODES a protein that exhibits chemoattractant activity (ortholog); growth factor activity (ortholog); heparin binding (ortholog); INVOLVED IN actin cytoskeleton reorganization (ortholog); branching involved in salivary gland morphogenesis (ortholog); endothelial cell proliferation (ortholog); PARTICIPATES IN glypican signaling pathway; ASSOCIATED WITH Bloom syndrome (ortholog); cervical squamous cell carcinoma (ortholog); cleft lip (ortholog); FOUND IN extracellular region (ortholog); extracellular space (ortholog); Golgi apparatus (ortholog) NW_004955409 4633542 4686768 - 9068941 102007739 A0A8C2V9E2 MODEL AGCD01009294;AGCD01009295;GBDI01327012;XM_005376685;XM_005376686;XM_013510298 XP_005376742;XP_005376743;XP_013365752 protein-coding ENSCLAG00000008404 NW_004955409 4632858 4686860 - 8720398 LOC102007896 olfactory receptor 1J1-like NW_004955419 5455988 5456929 + 102007896 A0A8C2W8I6 MODEL AGCD01019810;XM_005382528 XP_005382585 protein-coding ENSCLAG00000017743 NW_004955419 5455988 5456929 + 8720402 Stk25 serine/threonine kinase 25 ENCODES a protein that exhibits protein homodimerization activity (ortholog); INVOLVED IN axonogenesis (ortholog); establishment of Golgi localization (ortholog); establishment or maintenance of cell polarity (ortholog); ASSOCIATED WITH Bethlem Myopathy 1 (ortholog); chromosome 2q37 deletion syndrome (ortholog); D-2-hydroxyglutaric aciduria 1 (ortholog); FOUND IN cytoplasm (ortholog); Golgi apparatus (ortholog); Golgi membrane (ortholog) NW_004955542 268406 279323 + 9068941 102008148 A0A8C2UNG0;A0A8C2UT99 MODEL AGCD01071465;AGCD01071466;GBCE01001429;XM_005411127 XP_005411184 serine/threonine-protein kinase 25 protein-coding ENSCLAG00000002040 NW_004955542 272715 280110 + 8720420 LOC102008179 uncharacterized LOC102008179 NW_004955405 32467481 32489401 + 102008179 MODEL AGCD01005333;GBDF01013620;XR_001235728 ncrna 8720435 LOC102010374 uncharacterized LOC102010374 NW_004955487 1473174 1486730 + 102010374 MODEL AGCD01059246;GBDF01209774;XR_263982 ncrna ENSCLAG00000023426 8720440 LOC102012491 kinesin-like protein KIF13B NW_004955802 3103 18233 - 102012491 MODEL AGCD01078376;GBDK01191507;GBDK01191509;XM_005415115 XP_005415172 APPROVED protein-coding 8720449 LOC102012517 60S ribosomal protein L38 pseudogene NW_004955412 19711838 19712048 + 102012517 MODEL AGCD01012971 APPROVED pseudo 8720450 Bhmt betaine--homocysteine S-methyltransferase ENCODES a protein that exhibits betaine-homocysteine S-methyltransferase activity (ortholog); identical protein binding (ortholog); methyltransferase activity (ortholog); INVOLVED IN 'de novo' L-methionine biosynthetic process (ortholog); amino-acid betaine metabolic process (ortholog); L-methionine salvage (ortholog); PARTICIPATES IN choline metabolic pathway; dihydropyrimidine dehydrogenase deficiency pathway; dimethylglycine dehydrogenase deficiency pathway; ASSOCIATED WITH genetic disease (ortholog); hepatocellular carcinoma (ortholog); neural tube defect (ortholog); FOUND IN cytosol (ortholog); extracellular exosome (ortholog); nucleus (ortholog) NW_004955425 21992219 22009389 - 9068941 102013102 A0A8C2VFL7 MODEL AGCD01025810;AGCD01025811;AGCD01025812;GBCQ01010786;XM_005386012 XP_005386069 betaine--homocysteine S-methyltransferase 1 protein-coding ENSCLAG00000010253 NW_004955425 21991665 22009855 - 8720467 Il17rd interleukin 17 receptor D INVOLVED IN negative regulation of epithelial to mesenchymal transition (ortholog); negative regulation of transforming growth factor beta receptor signaling pathway (ortholog); PARTICIPATES IN fibroblast growth factor signaling pathway; ASSOCIATED WITH adenoid cystic carcinoma (ortholog); arteriovenous malformations of the brain (ortholog); Brain Injuries (ortholog); FOUND IN Golgi apparatus (ortholog); nucleoplasm (ortholog) NW_004955430 6842756 6873195 - 9068941;7240710 102013322 A0A8C2UU33;A0A8C2UU39;A0A8C2UZ66 MODEL AGCD01029316;GBDK01095576;GBDK01353156;XM_013515704 XP_013371158 interleukin-17 receptor D protein-coding ENSCLAG00000004131 NW_004955430 6848820 6898704 - 8720484 Spdl1 spindle apparatus coiled-coil protein 1 ENCODES a protein that exhibits enzyme binding (ortholog); kinetochore binding (ortholog); INVOLVED IN cell migration (ortholog); establishment of mitotic spindle orientation (ortholog); mitotic metaphase plate congression (ortholog); ASSOCIATED WITH genetic disease (ortholog); immunodeficiency 40 (ortholog); Perinatal Death (ortholog); FOUND IN nucleus (ortholog); outer kinetochore (ortholog); spindle pole (ortholog) NW_004955408 22590474 22619168 + 9068941 102013477 A0A8C2VZJ1;A0A8C2W3T7 MODEL AGCD01008578;GBDF01223309;XM_005376306;XM_005376307;XM_005376308 XP_005376363;XP_005376364;XP_005376365 protein-coding ENSCLAG00000014912 NW_004955408 22594776 22628429 + 8720505 LOC102014332 thyroid hormone receptor-associated protein 3 pseudogene NW_004955409 28045982 28056875 - 102014332 MODEL AGCD01010226 APPROVED pseudo 8720506 LOC102014334 uncharacterized LOC102014334 NW_004955463 13600074 13616315 + 102014334 MODEL AGCD01049875;GBDF01049402;XR_001236642;XR_001236643;XR_001236644;XR_001236645;XR_001236646;XR_263174 ncrna 8720519 Gip gastric inhibitory polypeptide ENCODES a protein that exhibits gastric inhibitory polypeptide receptor binding (ortholog); receptor ligand activity (ortholog); signaling receptor binding (ortholog); INVOLVED IN adenylate cyclase-activating G protein-coupled receptor signaling pathway (ortholog); adult locomotory behavior (ortholog); digestive system development (ortholog); ASSOCIATED WITH Anorexia (ortholog); autonomic nervous system disease (ortholog); Experimental Diabetes Mellitus (ortholog); FOUND IN extracellular space (ortholog); neuronal cell body (ortholog) NW_004955451 12390938 12396599 + 9068941;7240710 102014635 MODEL AGCD01043392;GBDF01099659;XM_005394598 XP_005394655 protein-coding 8720526 Nfkb2 nuclear factor kappa B subunit 2 ENCODES a protein that exhibits DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); RNA polymerase II cis-regulatory region sequence-specific DNA binding (ortholog); sequence-specific double-stranded DNA binding (ortholog); INVOLVED IN extracellular matrix organization (ortholog); follicular dendritic cell differentiation (ortholog); germinal center formation (ortholog); PARTICIPATES IN adenosine signaling pathway; interleukin-12 signaling pathway; nuclear factor kappa B signaling pathway; ASSOCIATED WITH atrophic gastritis (ortholog); Cerebral Hemorrhage (ortholog); common variable immunodeficiency (ortholog); FOUND IN Bcl3/NF-kappaB2 complex (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955485 7994730 8001776 - 9068941;7240710 102015728 A0A8C2UZ28 MODEL AGCD01058686;AGCD01058687;AGCD01058688;GBBH01092140;GBDK01090755;XM_013504082 XP_013359536 nuclear factor NF-kappa-B p100 subunit;nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100) APPROVED protein-coding ENSCLAG00000004104 NW_004955485 7994874 8000444 - 8720553 LOC102016720 uncharacterized LOC102016720 NW_004955495 3352618 3356536 + 102016720 MODEL AGCD01061849;AGCD01061850;GBCQ01113516;XR_001231390;XR_001231391;XR_264142 ncrna 8720560 Exosc2 exosome component 2 ENCODES a protein that exhibits RNA exonuclease activity (ortholog); INVOLVED IN positive regulation of cell growth (ortholog); RNA catabolic process (ortholog); RNA processing (ortholog); ASSOCIATED WITH autosomal recessive limb-girdle muscular dystrophy type 2K (ortholog); citrullinemia (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); exosome (RNase complex) (ortholog) NW_004955513 639798 648360 + 9068941 102017042 A0A8C2YM62;A0A8C2YM67 MODEL AGCD01066829;GBCE01033210;XM_005408346 XP_005408403 exosome complex component RRP4 protein-coding ENSCLAG00000006195 NW_004955513 639731 651418 + 8720573 Alg12 ALG12 alpha-1,6-mannosyltransferase INVOLVED IN dolichol-linked oligosaccharide biosynthetic process (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); chromosome 22q13 duplication syndrome (ortholog); congenital disorder of glycosylation (ortholog) NW_004955413 33030994 33039622 - 9068941;7240710 102017860 A0A8C2YUP8 MODEL AGCD01014655;GBCB01058939;XM_005379529 XP_005379586 ALG12, alpha-1,6-mannosyltransferase;dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase APPROVED protein-coding ENSCLAG00000016932 NW_004955413 33029116 33039700 - 8720593 Ppp1r18 protein phosphatase 1 regulatory subunit 18 ASSOCIATED WITH Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog); megacolon (ortholog) NW_004955583 673634 681439 - 9068941 102018043 A0A8C2UP78 MODEL AGCD01075848;AGCD01075849;AGCD01075850;GBDI01067824;GBDK01075378;XM_005414315 XP_005414372 phostensin APPROVED protein-coding ENSCLAG00000002490 NW_004955583 673393 680836 - 8720600 LOC102018700 receptor-type tyrosine-protein phosphatase alpha pseudogene NW_004955411 21173967 21176388 - 102018700 MODEL AGCD01012069 APPROVED pseudo 8720601 LOC102018945 LIM domain only protein 3 pseudogene NW_004955498 2522907 2523749 + 102018945 MODEL AGCD01062802 APPROVED pseudo 8720602 Dmbx1 diencephalon/mesencephalon homeobox 1 ENCODES a protein that exhibits DNA binding (ortholog); DNA-binding transcription factor activity (ortholog); DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); INVOLVED IN adult feeding behavior (ortholog); adult locomotory behavior (ortholog); brain development (ortholog); ASSOCIATED WITH Developmental Disabilities (ortholog); genetic disease (ortholog); FOUND IN transcription regulator complex (ortholog) NW_004955464 11788526 11811885 - 9068941 102019153 A0A8C2UXE6 MODEL AGCD01050161;GBDF01264890;XM_005398674 XP_005398731 diencephalon/mesencephalon homeobox protein 1 protein-coding ENSCLAG00000004842 NW_004955464 11788494 11811890 - 8720611 LOC102019496 60S ribosomal protein L7a pseudogene NW_004955414 25104299 25108383 + 102019496 MODEL AGCD01015573;AGCD01015574 APPROVED pseudo 8720612 LOC102019823 dual specificity protein kinase TTK pseudogene NW_004955425 15961112 15962176 + 102019823 MODEL AGCD01025594 APPROVED pseudo 8720613 LOC102019891 olfactory receptor 6C2-like NW_004955458 2686793 2687737 - 102019891 MODEL AGCD01047240;XM_013520844 XP_013376298 protein-coding 8720614 Prdm13 PR/SET domain 13 ENCODES a protein that exhibits chromatin binding (ortholog); histone methyltransferase activity (ortholog); RNA polymerase II-specific DNA-binding transcription factor binding (ortholog); INVOLVED IN GABAergic neuron differentiation (ortholog); hypothalamus cell differentiation (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH CEREBELLAR DYSFUNCTION, IMPAIRED INTELLECTUAL DEVELOPMENT, AND HYPOGONADOTROPIC HYPOGONADISM (ortholog); fundus dystrophy (ortholog); genetic disease (ortholog); FOUND IN nucleus (ortholog) NW_004955411 25481601 25489049 + 9068941 102020641 A0A8C2VI23 MODEL AGCD01012160;AGCD01012161;GBDF01198351;XM_005377940 XP_005377997 PR domain containing 13 APPROVED protein-coding ENSCLAG00000010966 NW_004955411 25481741 25489049 + 8720621 LOC102020731 uncharacterized LOC102020731 NW_004955447 18643804 18688153 + 102020731 MODEL AGCD01041182;AGCD01041183;AGCD01041184;GBCE01132641;XR_001235746;XR_001235747;XR_001235748 ncrna 8720634 Avpr2 arginine vasopressin receptor 2 ENCODES a protein that exhibits vasopressin receptor activity (ortholog); INVOLVED IN I-kappaB kinase/NF-kappaB signaling (ortholog); negative regulation of cell population proliferation (ortholog); negative regulation of urine volume (ortholog); PARTICIPATES IN G protein mediated signaling pathway via Galphas family; vasopressin signaling pathway; vasopressin signaling pathway via receptor type 2; ASSOCIATED WITH adrenoleukodystrophy (ortholog); autistic disorder (ortholog); Barth syndrome (ortholog); FOUND IN endocytic vesicle (ortholog); endosome (ortholog); perinuclear region of cytoplasm (ortholog) NW_004955580 583827 586739 + 9068941;7240710 102021498 A0A8C2UP17 MODEL AGCD01075613;GBCQ01038848;XM_005414164;XM_005414165;XM_005414166;XM_005414167;XM_013509695;XM_013509696;XM_013509697;XM_013509698;XM_013509699;XM_013509700 XP_005414221;XP_005414222;XP_005414223;XP_005414224;XP_013365149;XP_013365150;XP_013365151;XP_013365152;XP_013365153;XP_013365154 vasopressin V2 receptor protein-coding ENSCLAG00000002650 NW_004955580 583480 586456 + 8720662 Yipf5 Yip1 domain family member 5 INVOLVED IN insulin processing (ortholog); regulation of ER to Golgi vesicle-mediated transport (ortholog); ASSOCIATED WITH familial adenomatous polyposis 1 (ortholog); genetic disease (ortholog); Hereditary Neoplastic Syndromes (ortholog); FOUND IN COPII-coated ER to Golgi transport vesicle (ortholog); endoplasmic reticulum (ortholog); endoplasmic reticulum exit site (ortholog) NW_004955415 9795214 9809871 + 9068941 102021548 A0A8C2VN48 MODEL AGCD01016110;GBDF01085610;XM_005380690 XP_005380747 Yip1 domain family, member 5 APPROVED protein-coding ENSCLAG00000011264 NW_004955415 9795214 9812405 + 8720677 LOC102022767 cytochrome P450 2U1-like NW_004955402 17306760 17461686 + 102022767 MODEL AGCD01000502;AGCD01000503;AGCD01000504;AGCD01000505;AGCD01000506 pseudo 8720678 LOC102022790 cytohesin-3 NW_004955460 13486286 13490486 + 9068941 102022790 A0A8C2VBI3 MODEL AGCD01048690;GBCE01032925;XM_005397893 XP_005397950 Cyth3 cytohesin 3 APPROVED protein-coding ENSCLAG00000007268 8720686 N6amt1 N-6 adenine-specific DNA methyltransferase 1 ENCODES a protein that exhibits histone H4K12 methyltransferase activity (ortholog); methylarsonite methyltransferase activity (ortholog); protein methyltransferase activity (ortholog); INVOLVED IN arsonoacetate metabolic process (ortholog); DNA methylation on adenine (ortholog); methylation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN nucleus (ortholog); protein-containing complex (ortholog) NW_004955407 28256654 28277514 + 9068941 102023329 A0A8C2VDX3 MODEL AGCD01007579;AGCD01007580;GBCB01099656;XM_005375604;XM_005375607;XR_259592 XP_005375661;XP_005375664 N-6 adenine-specific DNA methyltransferase 1 (putative);hemK methyltransferase family member 2 APPROVED protein-coding ENSCLAG00000009758 NW_004955407 28256649 28276460 + 8720706 LOC102023949 uncharacterized LOC102023949 NW_004955435 18533431 18550571 + 102023949 MODEL AGCD01033406;GBDJ01257305;XR_261721 ncrna 8720711 LOC102026166 T-complex protein 1 subunit alpha-like NW_004955443 18350075 18354651 + 102026166 MODEL AGCD01038597 pseudo 8720712 Uba52 ubiquitin A-52 residue ribosomal protein fusion product 1 ENCODES a protein that exhibits structural constituent of ribosome (ortholog); INVOLVED IN response to insecticide (ortholog); PARTICIPATES IN ribosome biogenesis pathway; translation pathway; ASSOCIATED WITH Brain Injuries (ortholog); colon carcinoma (ortholog); Diabetic Nephropathies (ortholog); FOUND IN cytoplasmic side of rough endoplasmic reticulum membrane (ortholog); cytosol (ortholog); cytosolic large ribosomal subunit (ortholog) NW_004955524 3007074 3009886 - 9068941 102027224 A0A8C2V067;A0A8C2YLT8;A0A8C2YLT9 MODEL AGCD01068849;GBDK01005256;XM_005409587;XM_005409588 XP_005409644;XP_005409645 ubiquitin-60S ribosomal protein L40 protein-coding ENSCLAG00000005686 NW_004955524 3006147 3018772 - 8720731 LOC102027835 protein S100-A10 pseudogene NW_004955414 9467734 9468058 - 102027835 A0A8C2W8U1 MODEL AGCD01015026;XM_005379803 APPROVED pseudo ENSCLAG00000017890 8720735 Ccdc80 coiled-coil domain containing 80 ENCODES a protein that exhibits fibronectin binding (ortholog); glycosaminoglycan binding (ortholog); heparin binding (ortholog); INVOLVED IN extracellular matrix organization (ortholog); positive regulation of cell-substrate adhesion (ortholog); response to bacterium (ortholog); ASSOCIATED WITH atopic dermatitis (ortholog); Chemical and Drug Induced Liver Injury (ortholog); COVID-19 (ortholog); FOUND IN basement membrane (ortholog); extracellular matrix (ortholog); interstitial matrix (ortholog) NW_004955427 12945230 12975020 - 9068941 102028661 A0A8C2V7Z2 MODEL AGCD01027230;GBCE01076690;XM_005386391 XP_005386448 coiled-coil domain-containing protein 80 protein-coding ENSCLAG00000007848 NW_004955427 12945230 12975114 - 8720751 LOC102028739 uncharacterized LOC102028739 NW_004955472 9866964 9882559 - 102028739 MODEL AGCD01053697;GBDF01254458;XR_001237075 ncrna 8720757 Amacr alpha-methylacyl-CoA racemase ENCODES a protein that exhibits alpha-methylacyl-CoA racemase activity (ortholog); signaling receptor binding (ortholog); INVOLVED IN bile acid biosynthetic process (ortholog); bile acid metabolic process (ortholog); PARTICIPATES IN bile acid biosynthetic pathway; cerebrotendinous xanthomatosis pathway; congenital bile acid synthesis defect pathway; ASSOCIATED WITH adenoma (ortholog); alpha-methylacyl-CoA racemase deficiency (ortholog); breast carcinoma (ortholog); FOUND IN cytoplasm (ortholog); intracellular membrane-bounded organelle (ortholog); mitochondrion (ortholog) NW_004955426 19570179 19580920 - 9068941;7240710 102028990 A0A8C2V7D3 MODEL AGCD01026549;GBCB01061062;XM_005386170;XM_005386171 XP_005386227;XP_005386228 protein-coding ENSCLAG00000007664 NW_004955426 19570070 19580818 - 8720768 LOC102029356 keratin, type I cuticular Ha3-I-like NW_004955451 15752134 15756262 - 102029356 MODEL AGCD01043636;AGCD01043637;XM_005394580 XP_005394637 protein-coding 8720789 LOC102030641 chromobox protein homolog 3 pseudogene NW_004955422 7000285 7000848 - 102030641 MODEL AGCD01022613 APPROVED pseudo 8720790 Nckipsd NCK interacting protein with SH3 domain INVOLVED IN positive regulation of neuron projection development (ortholog); ASSOCIATED WITH Aicardi-Goutieres Syndrome 1 (ortholog); genetic disease (ortholog); Progressive Microcephaly with Seizures and Cerebral and Cerebellar Atrophy (ortholog); FOUND IN COP9 signalosome (ortholog) NW_004955532 755997 766202 - 9068941 102030664 A0A8C2VPH7 MODEL AGCD01070151;AGCD01070152;GBDI01323136;XM_005410166;XM_013507637;XM_013507638 XP_005410223;XP_013363091;XP_013363092 NCK-interacting protein with SH3 domain protein-coding ENSCLAG00000010729 NW_004955532 755997 764855 - 8720813 Pros1 protein S ENCODES a protein that exhibits protein-containing complex binding (ortholog); INVOLVED IN liver development (ortholog); negative regulation of coagulation (ortholog); positive regulation of phagocytosis (ortholog); PARTICIPATES IN protein C anticoagulant pathway; ASSOCIATED WITH adult respiratory distress syndrome (ortholog); autosomal dominant thrombophilia due to protein S deficiency (ortholog); autosomal recessive thrombophilia due to protein S deficiency (ortholog); FOUND IN extracellular space (ortholog); protein-containing complex (ortholog) NW_004955407 3514900 3566165 + 9068941;7240710 102002997 A0A8C2V354 MODEL AGCD01006863;GBCQ01040731;GBDF01157496;XM_013503591 XP_013359045 vitamin K-dependent protein S APPROVED protein-coding ENSCLAG00000006656 NW_004955407 3535388 3565058 + 8720833 Armcx3 armadillo repeat containing X-linked 3 INVOLVED IN axonal transport of mitochondrion (ortholog); mitochondrion organization (ortholog); positive regulation of transcription by RNA polymerase II (ortholog); ASSOCIATED WITH autistic disorder (ortholog); developmental and epileptic encephalopathy 9 (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); mitochondrial outer membrane (ortholog); mitochondrion (ortholog) NW_004955503 7705821 7709169 + 9068941 102003468 A0A8C2UP73 MODEL AGCD01064799;GBCE01005020;XM_005406971;XM_005406972 XP_005407028;XP_005407029 armadillo repeat containing, X-linked 3;armadillo repeat-containing X-linked protein 3 APPROVED protein-coding ENSCLAG00000002213 NW_004955503 7705821 7709142 + 8720848 Cdca3 cell division cycle associated 3 ASSOCIATED WITH congenital stationary night blindness 1H (ortholog); COVID-19 (ortholog); developmental and epileptic encephalopathy 21 (ortholog); FOUND IN adherens junction (ortholog) NW_004955413 4448711 4450917 - 9068941 102004048 A0A8C2VSH3 MODEL AGCD01013615;GBDI01105802;XM_013511344 XP_013366798 cell division cycle-associated protein 3 protein-coding ENSCLAG00000013619 NW_004955413 4448917 4450553 - 8720862 Tnfrsf14 TNF receptor superfamily member 14 ENCODES a protein that exhibits cytokine binding (ortholog); ubiquitin protein ligase binding (ortholog); INVOLVED IN CD4-positive, alpha-beta T cell proliferation (ortholog); defense response to Gram-negative bacterium (ortholog); defense response to Gram-positive bacterium (ortholog); ASSOCIATED WITH arteriosclerosis (ortholog); Brain Injuries (ortholog); celiac disease (ortholog); FOUND IN external side of plasma membrane (ortholog); plasma membrane (ortholog) NW_004955486 8670182 8684677 - 9068941 102005150 A0A8C2V2R8 MODEL AGCD01059153;GBCE01053037;XM_005404162;XM_005404163;XM_013504242;XM_013504243;XM_013504244;XM_013504245;XM_013504246 XP_005404219;XP_005404220;XP_013359696;XP_013359697;XP_013359698;XP_013359699;XP_013359700 tumor necrosis factor receptor superfamily member 14;tumor necrosis factor receptor superfamily, member 14 APPROVED protein-coding ENSCLAG00000005555 8720878 Pex1 peroxisomal biogenesis factor 1 ENCODES a protein that exhibits ATP binding (ortholog); ATP hydrolysis activity (ortholog); protein transporter activity (ortholog); INVOLVED IN microtubule-based peroxisome localization (ortholog); peroxisome organization (ortholog); protein import into peroxisome matrix (ortholog); ASSOCIATED WITH autosomal recessive nonsyndromic deafness 111 (ortholog); Developmental Disabilities (ortholog); epilepsy (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); peroxisomal membrane (ortholog) NW_004955432 9418480 9461507 - 9068941;7240710 102005290 A0A8C2USR1 MODEL AGCD01030906;GBDI01218587;XM_005388022;XM_005388023;XM_013515937 XP_005388079;XP_005388080;XP_013371391 peroxisome biogenesis factor 1 protein-coding ENSCLAG00000003719 NW_004955432 9418678 9461419 - 8720912 Tnc tenascin C ENCODES a protein that exhibits syndecan binding (ortholog); INVOLVED IN bud outgrowth involved in lung branching (ortholog); cellular response to prostaglandin D stimulus (ortholog); cellular response to retinoic acid (ortholog); PARTICIPATES IN syndecan signaling pathway; ASSOCIATED WITH allergic conjunctivitis (ortholog); asbestosis (ortholog); asthma (ortholog); FOUND IN basement membrane (ortholog); collagen-containing extracellular matrix (ortholog); extracellular region (ortholog) NW_004955419 12569620 12662897 + 9068941;7240710;11556225;11553836 10190750;10320102 102005935 A0A8C2VHI4;A0A8C2VKU1;A0A8C2VLX3 MODEL AGCD01019976;AGCD01019977;AGCD01019978;GBCE01000789;GBCQ01126227;XM_013513252;XM_013513253 XP_013368706;XP_013368707 tenascin protein-coding ENSCLAG00000010182 NW_004955419 12569547 12662958 + 8720941 LOC102005963 uncharacterized LOC102005963 NW_004955526 3269899 3285554 + 102005963 MODEL AGCD01069333;AGCD01069334;GBDI01352716;XR_001231967;XR_001231968;XR_264661 ncrna 8720946 Swt1 SWT1 RNA endoribonuclease homolog ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); megacolon (ortholog) NW_004955406 23772192 23861365 + 102007406 A0A8C2VTE5 MODEL AGCD01006184;AGCD01006185;AGCD01006186;GBDF01080351;XM_005375066;XM_005375067;XM_005375068;XM_005375069;XM_005375070;XM_005375071;XM_013521667 XP_005375123;XP_005375124;XP_005375125;XP_005375126;XP_005375127;XP_005375128;XP_013377121 SWT1 RNA endoribonuclease homolog (S. cerevisiae);SWT1, RNA endoribonuclease homolog;transcriptional protein SWT1 APPROVED protein-coding ENSCLAG00000013959 NW_004955406 23772095 23860360 + 8720989 LOC102008445 proteasome assembly chaperone 1-like NW_004955431 13381828 13382937 - 102008445 MODEL AGCD01030304 pseudo 8720990 LOC102008519 mitochondrial import inner membrane translocase subunit TIM14-like NW_004955412 23530210 23530974 + 102008519 MODEL AGCD01013090 pseudo 8720991 Igf2bp2 insulin like growth factor 2 mRNA binding protein 2 ENCODES a protein that exhibits mRNA 3'-UTR binding (ortholog); mRNA 5'-UTR binding (ortholog); N6-methyladenosine-containing RNA binding (ortholog); INVOLVED IN cold-induced thermogenesis (ortholog); CRD-mediated mRNA stabilization (ortholog); energy homeostasis (ortholog); ASSOCIATED WITH Arsenic Poisoning (ortholog); Currarino syndrome (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytoplasmic stress granule (ortholog); cytoskeleton (ortholog) NW_004955420 21818970 21957295 + 9068941;7240710 102009390 A0A8C2W1H9 MODEL AGCD01021171;AGCD01021172;AGCD01021173;AGCD01021174;AGCD01021175;GBBH01160648;GBDJ01356061;XM_013513485 XP_013368939 insulin-like growth factor 2 mRNA binding protein 2;insulin-like growth factor 2 mRNA-binding protein 2 APPROVED protein-coding ENSCLAG00000014808 NW_004955420 21818972 21958440 + 8721022 LOC102009438 nucleobindin-2 pseudogene NW_004955580 212934 215509 + 102009438 MODEL AGCD01075591 APPROVED pseudo 8721023 LOC102009464 chromosome unknown open reading frame, human C5orf15 ASSOCIATED WITH familial adenomatous polyposis 1 (ortholog); genetic disease (ortholog); Hereditary Neoplastic Syndromes (ortholog) NW_004955408 5245336 5256655 - 9068941 102009464 A0A8C2VXI5 MODEL AGCD01008129;GBCQ01005179;XM_005376124;XM_005376125 XP_005376181;XP_005376182 keratinocyte-associated transmembrane protein 2 protein-coding ENSCLAG00000015163 NW_004955408 5246667 5256604 - 8721033 LOC102009735 uncharacterized LOC102009735 NW_004955500 4775193 4791358 - 102009735 MODEL AGCD01063811;GBDF01219713;XR_001231484;XR_001231485;XR_001231486 ncrna 8721043 LOC102009858 uncharacterized LOC102009858 NW_004955426 4649998 4654801 + 102009858 MODEL AGCD01026105;GBDF01248724;XR_261189 ncrna 8721050 LOC102009927 centrin-3 pseudogene NW_004955467 10028525 10029023 + 102009927 MODEL AGCD01051543 APPROVED pseudo 8721051 Tnpo1 transportin 1 INVOLVED IN protein import into nucleus (ortholog); ASSOCIATED WITH genetic disease (ortholog); Neurodevelopmental Disorders (ortholog) NW_004955425 27666091 27748920 - 9068941 102009966 A0A8C2W3W2;A0A8C2W808 MODEL AGCD01025978;AGCD01025979;AGCD01025980;AGCD01025981;AGCD01025982;GBCB01061676;XM_005386079;XM_005386080;XM_005386081;XM_005386082;XM_013514849 XP_005386136;XP_005386137;XP_005386138;XP_005386139;XP_013370303 transportin-1 protein-coding ENSCLAG00000016191 NW_004955425 27666091 27748920 - 8721089 LOC102010412 uncharacterized LOC102010412 NW_004955545 2843891 2852564 - 102010412 MODEL AGCD01071925;GBDI01188014;XR_264882 ncrna 8721093 LOC102010512 uncharacterized LOC102010512 NW_004955432 10654891 10664188 - 102010512 MODEL AGCD01030936;GBCE01078510;XR_001234668;XR_261522 ncrna 8721098 Pla2g4c phospholipase A2 group IVC ENCODES a protein that exhibits calcium-independent phospholipase A2 activity (ortholog); lysophospholipase activity (ortholog); O-acyltransferase activity (ortholog); INVOLVED IN glycerophospholipid catabolic process (ortholog); lipid droplet formation (ortholog); phosphatidylcholine acyl-chain remodeling (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cell cortex (ortholog); endoplasmic reticulum membrane (ortholog); lipid droplet (ortholog) NW_004955609 182706 212102 + 9068941 102010967 A0A8C2ULB4 MODEL AGCD01077053;AGCD01077054;GBDJ01028499;XM_013510120 XP_013365574 cytosolic phospholipase A2 gamma;phospholipase A2, group IVC (cytosolic, calcium-independent) APPROVED protein-coding ENSCLAG00000000156 8721119 LOC102012428 uncharacterized LOC102012428 NW_004955417 7483800 7490830 + 102012428 MODEL AGCD01018005;AGCD01018006;GBDF01137161;XR_260463 ncrna 8721124 Dnm2 dynamin 2 ENCODES a protein that exhibits D2 dopamine receptor binding (ortholog); GTPase activity (ortholog); nitric-oxide synthase binding (ortholog); INVOLVED IN aorta development (ortholog); cellular response to carbon monoxide (ortholog); cellular response to dopamine (ortholog); PARTICIPATES IN platelet-derived growth factor signaling pathway; syndecan signaling pathway; vascular endothelial growth factor signaling pathway; ASSOCIATED WITH alpha-mannosidosis (ortholog); autosomal dominant centronuclear myopathy (ortholog); centronuclear myopathy (ortholog); FOUND IN cell cortex (ortholog); cell junction (ortholog); centrosome (ortholog) NW_004955495 1860644 1934589 + 9068941;7240710 102012552 A0A8C2V908;A0A8C2VF75;A0A8C2YNK8 MODEL AGCD01061736;AGCD01061737;AGCD01061738;AGCD01061739;GBDF01010591;XM_005405625;XM_005405626;XM_005405627;XM_005405628;XM_005405629;XM_005405630 XP_005405682;XP_005405683;XP_005405684;XP_005405685;XP_005405686;XP_005405687 dynamin-2 protein-coding ENSCLAG00000008156 NW_004955495 1860644 1934818 + 8721160 LOC102013213 uncharacterized LOC102013213 NW_004955538 373207 647107 + 102013213 MODEL AGCD01070995;AGCD01070996;AGCD01070997;AGCD01070998;AGCD01070999;AGCD01071000;AGCD01071001;AGCD01071002;AGCD01071003;AGCD01071004;AGCD01071005;AGCD01071006;AGCD01071007;AGCD01071008;AGCD01071009;AGCD01071010;AGCD01071011;AGCD01071012;AGCD01071013;AGCD01071014;AGCD01071015;AGCD01071016;AGCD01071017;AGCD01071018;AGCD01071019;AGCD01071020;AGCD01071021;AGCD01071022;AGCD01071023;AGCD01071024;AGCD01071025;AGCD01071026;AGCD01071027;AGCD01071028;AGCD01071029;AGCD01071030;AGCD01071031;AGCD01071032;GBDF01017551;XM_005410885 XP_005410942 uncharacterized protein LOC102013213 protein-coding 8721167 LOC102014474 RNA polymerase II subunit A C-terminal domain phosphatase pseudogene NW_004955431 1777431 1784253 - 102014474 MODEL AGCD01029918;XM_005387553 APPROVED pseudo 8721172 LOC102014682 uncharacterized LOC102014682 NW_004955422 20057801 20067907 - 102014682 MODEL AGCD01023063;AGCD01023064;GBBH01003567;XR_260899 ncrna 8721176 Mansc1 MANSC domain containing 1 ASSOCIATED WITH autosomal dominant intellectual developmental disorder 6 (ortholog); developmental and epileptic encephalopathy 27 (ortholog); genetic disease (ortholog) NW_004955413 9288565 9309762 - 9068941 102015186 A0A8C2W068 MODEL AGCD01013902;GBDK01091298;XM_005378959;XM_013511426;XM_013511427;XM_013511428;XM_013511429 XP_005379016;XP_013366880;XP_013366881;XP_013366882;XP_013366883 MANSC domain-containing protein 1 protein-coding ENSCLAG00000015944 NW_004955413 9286500 9309549 - 8721183 Phldb3 pleckstrin homology like domain family B member 3 ENCODES a protein that exhibits enzyme binding (ortholog); ASSOCIATED WITH genetic disease (ortholog); schizophrenia (ortholog) NW_004955555 1241728 1261531 - 9068941 102015777 A0A8C2UNT7 MODEL AGCD01073067;AGCD01073068;GBDI01004272;XM_005412439;XM_013508778;XM_013508779 XP_005412496;XP_013364232;XP_013364233 pleckstrin homology-like domain family B member 3;pleckstrin homology-like domain, family B, member 3 APPROVED protein-coding ENSCLAG00000001550 NW_004955555 1241202 1260935 - 8721203 Itgb7 integrin subunit beta 7 ENCODES a protein that exhibits cell adhesion molecule binding (ortholog); INVOLVED IN cell-matrix adhesion (ortholog); cell-matrix adhesion involved in ameboidal cell migration (ortholog); heterotypic cell-cell adhesion (ortholog); PARTICIPATES IN E-cadherin signaling pathway; integrin mediated signaling pathway; ASSOCIATED WITH genetic disease (ortholog); FOUND IN cell surface (ortholog); integrin alpha4-beta7 complex (ortholog); receptor complex (ortholog) NW_004955458 460619 478361 - 9068941 102016026 A0A8C2YPD2 MODEL AGCD01047127;AGCD01047128;AGCD01047129;GBCE01104733;XM_005397161;XM_013520946 XP_005397218;XP_013376400 integrin beta-7;integrin, beta 7 APPROVED protein-coding ENSCLAG00000009316 NW_004955458 460651 470145 - 8721223 Smagp small cell adhesion glycoprotein ASSOCIATED WITH genetic disease (ortholog); FOUND IN cell junction (ortholog); nucleoplasm (ortholog); plasma membrane (ortholog) NW_004955547 1742597 1766460 - 9068941 102016202 A0A8C2UKN6 MODEL AGCD01072245;GBBH01031858;GBDF01305508;XM_005411960 XP_005412017 APPROVED protein-coding ENSCLAG00000000875 NW_004955547 1742597 1766487 - 8721235 Mtrex Mtr4 exosome RNA helicase ENCODES a protein that exhibits ATP binding (ortholog); RNA helicase activity (ortholog); INVOLVED IN DNA damage response (ortholog); maturation of 5.8S rRNA (ortholog); RNA catabolic process (ortholog); PARTICIPATES IN ribosome biogenesis pathway; ASSOCIATED WITH amyotrophic lateral sclerosis (ortholog); genetic disease (ortholog); Marfanoid Mental Retardation Syndrome, Autosomal (ortholog); FOUND IN catalytic step 2 spliceosome (ortholog); exosome (RNase complex) (ortholog); nuclear exosome (RNase complex) (ortholog) NW_004955446 12270338 12362064 - 9068941 102017719 A0A8C2V847 MODEL AGCD01040228;AGCD01040229;AGCD01040230;GBBH01026395;XM_005392698;XM_005392699;XM_005392700 XP_005392755;XP_005392756;XP_005392757 Skiv2l2 Ski2 like RNA helicase 2;superkiller viralicidic activity 2-like 2;superkiller viralicidic activity 2-like 2 (S. cerevisiae) APPROVED protein-coding ENSCLAG00000006622 NW_004955446 12270344 12362882 - 8721272 LOC102017894 protein FAM69B-like NW_004955425 7507821 7533856 + 102017894 MODEL AGCD01025387 pseudo 8721273 Dpp4 dipeptidyl peptidase 4 ENCODES a protein that exhibits chemorepellent activity (ortholog); collagen binding (ortholog); dipeptidyl-peptidase activity (ortholog); INVOLVED IN B-1a B cell differentiation (ortholog); behavioral fear response (ortholog); endothelial cell migration (ortholog); ASSOCIATED WITH autistic disorder (ortholog); Coronavirus infectious disease (ortholog); esophagus squamous cell carcinoma (ortholog); FOUND IN apical plasma membrane (ortholog); cell surface (ortholog); endocytic vesicle (ortholog) NW_004955449 11795994 11873408 + 9068941 102019124 A0A8C2UQ08 MODEL AGCD01042093;AGCD01042094;GBDJ01180000;XM_005393318;XM_005393319 XP_005393375;XP_005393376 dipeptidyl-peptidase 4 APPROVED protein-coding ENSCLAG00000002709 NW_004955449 11795536 11875412 + 8721309 LOC102019406 uncharacterized LOC102019406 NW_004955422 17689447 17710741 - 102019406 MODEL AGCD01022932;GBDF01207243;XR_001233931;XR_001233932 ncrna 8721316 Hmgn1 high mobility group nucleosome binding domain 1 ENCODES a protein that exhibits chromatin binding (ortholog); INVOLVED IN chromatin organization (ortholog); positive regulation of NAD+ ADP-ribosyltransferase activity (ortholog); post-embryonic camera-type eye morphogenesis (ortholog); PARTICIPATES IN nucleotide excision repair pathway; ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); Neoplastic Cell Transformation (ortholog); FOUND IN female germ cell nucleus (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955407 38136386 38142587 - 9068941 102019775 A0A8C2V4X0 MODEL AGCD01007796;GBDF01047791;XM_005375983 XP_005376040 non-histone chromosomal protein HMG-14 protein-coding ENSCLAG00000005744 NW_004955407 38136386 38143479 - 8721324 Upk2 uroplakin 2 INVOLVED IN epithelial cell differentiation (ortholog); ASSOCIATED WITH CD3epsilon deficiency (ortholog); Chromosome 11, Partial Trisomy 11q (ortholog); Dwarfism (ortholog); FOUND IN apical plasma membrane (ortholog); apical plasma membrane urothelial plaque (ortholog) NW_004955412 20086991 20089062 + 9068941 102020642 A0A8C2YTB4 MODEL AGCD01012992;GBDF01144032;XM_005378283;XM_005378284 XP_005378340;XP_005378341 uroplakin-2 protein-coding ENSCLAG00000014907 NW_004955412 20084801 20089289 + 8721335 Actl8 actin like 8 INVOLVED IN epithelial cell differentiation (ortholog); ASSOCIATED WITH chromosome 1p36 deletion syndrome (ortholog); genetic disease (ortholog) NW_004955527 1217950 1274453 - 9068941 102020702 A0A8C2VNB8 MODEL AGCD01069392;AGCD01069393;AGCD01069394;AGCD01069395;AGCD01069396;GBDF01193552;XM_005409807;XM_005409808 XP_005409864;XP_005409865 actin-like 8;actin-like protein 8 APPROVED protein-coding ENSCLAG00000012471 NW_004955527 1217943 1274466 - 8721345 Ndufa10 NADH:ubiquinone oxidoreductase subunit A10 ENCODES a protein that exhibits NADH dehydrogenase (ubiquinone) activity (ortholog); INVOLVED IN electron transport chain (ortholog); mitochondrial electron transport, NADH to ubiquinone (ortholog); mitochondrial respiratory chain complex I assembly (ortholog); ASSOCIATED WITH Bethlem Myopathy 1 (ortholog); chromosome 2q37 deletion syndrome (ortholog); D-2-hydroxyglutaric aciduria 1 (ortholog); FOUND IN mitochondrial respiratory chain complex I (ortholog); mitochondrion (ortholog) NW_004955542 1329802 1370109 + 9068941;7240710 102020716 A0A8C2UMM4 MODEL AGCD01071502;GBCB01005748;XM_005411173 XP_005411230 NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 10, 42kDa;NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial APPROVED protein-coding ENSCLAG00000002249 NW_004955542 1329212 1370695 + 8721359 Pcm1 pericentriolar material 1 ENCODES a protein that exhibits molecular adaptor activity (ortholog); molecular function activator activity (ortholog); INVOLVED IN centrosome cycle (ortholog); cilium assembly (ortholog); cytoplasmic microtubule organization (ortholog); ASSOCIATED WITH genetic disease (ortholog); hereditary spastic paraplegia 53 (ortholog); schizophrenia (ortholog); FOUND IN apical part of cell (ortholog); centriolar satellite (ortholog); centriole (ortholog) NW_004955552 1675477 1768902 - 9068941;7240710 102020848 A0A8C2UJ17;A0A8C2UKZ2;A0A8C2ULZ9 MODEL AGCD01072784;AGCD01072785;AGCD01072786;AGCD01072787;GBDF01001895;XM_005412193;XM_005412194;XM_005412195;XM_005412196;XM_005412197;XM_005412198;XM_013508598;XM_013508599;XM_013508600;XM_013508601 XP_005412250;XP_005412251;XP_005412252;XP_005412253;XP_005412254;XP_005412255;XP_013364052;XP_013364053;XP_013364054;XP_013364055 protein-coding ENSCLAG00000000363 NW_004955552 1675477 1768900 - 8721413 LOC102020910 uncharacterized LOC102020910 NW_004955416 21877127 21881463 - 102020910 MODEL AGCD01017517;AGCD01017518;GBDF01253505;XR_260409 ncrna 8721420 Sec14l3 SEC14 like lipid binding 3 ASSOCIATED WITH genetic disease (ortholog) NW_004955455 4681026 4692277 - 9068941 102021729 A0A8C2VRS9 MODEL AGCD01045684;GBCE01005166;XM_005396263;XM_005396267 XP_005396320;XP_005396324 SEC14-like 3;SEC14-like lipid binding 3;SEC14-like protein 3 APPROVED protein-coding ENSCLAG00000012290 NW_004955455 4681026 4692490 - 8721452 LOC102022450 uncharacterized LOC102022450 NW_004955403 48110321 48128265 - 102022450 MODEL AGCD01002914;GBDK01024559;XR_001234474;XR_259248 ncrna 8721457 LOC102022684 serpin B9-like NW_004955465 10437606 10476747 - 102022684 A0A8C2UNH4;A0A8C2UNI3;A0A8C2UQ47;A0A8C2US24;A0A8C2UTJ0;A0A8C2UUI0;A0A8C2YJL6 MODEL AGCD01050510;GBCB01089957;XM_005398917;XM_005398918;XM_005398928;XM_013521824;XM_013521825;XM_013521826;XM_013521827 XP_005398974;XP_005398975;XP_005398985;XP_013377278;XP_013377279;XP_013377280;XP_013377281 Serpinb9 serpin peptidase inhibitor, clade B (ovalbumin), member 9 PROVISIONAL protein-coding ENSCLAG00000002501 8721471 LOC102023176 O(6)-methylguanine-induced apoptosis 2-like NW_004955506 1972894 1985977 - 102023176 MODEL AGCD01065284;AGCD01065285;AGCD01065286 pseudo 8721472 LOC102024400 olfactory receptor 15-like NW_004955581 637852 638793 - 102024400 MODEL AGCD01075684;XM_013509726 XP_013365180 APPROVED protein-coding ENSCLAG00000000782 8721481 Stac2 SH3 and cysteine rich domain 2 INVOLVED IN positive regulation of protein localization to plasma membrane (ortholog); positive regulation of voltage-gated calcium channel activity (ortholog); ASSOCIATED WITH Childhood Schizophrenia (ortholog); genetic disease (ortholog); High Myopia (ortholog); FOUND IN extrinsic component of cytoplasmic side of plasma membrane (ortholog) NW_004955451 14070422 14079781 - 9068941 102024749 A0A8C2W4I9 MODEL AGCD01043529;GBCQ01095616;GBDF01225870;XM_005394300 XP_005394357 SH3 and cysteine-rich domain-containing protein 2 protein-coding ENSCLAG00000015772 NW_004955451 14068900 14079781 - 8721499 Fbxw7 F-box and WD repeat domain containing 7 ENCODES a protein that exhibits cyclin binding (ortholog); identical protein binding (ortholog); phosphothreonine residue binding (ortholog); INVOLVED IN cellular response to UV (ortholog); DNA damage response (ortholog); lung development (ortholog); PARTICIPATES IN Notch signaling pathway; ASSOCIATED WITH adenoid cystic carcinoma (ortholog); B-Cell Chronic Lymphocytic Leukemia (ortholog); basal cell carcinoma (ortholog); FOUND IN cytoplasm (ortholog); endoplasmic reticulum (ortholog); Golgi apparatus (ortholog) NW_004955471 6852459 7026590 - 9068941 102025567 A0A8C2V5Y5;A0A8C2V8P6;A0A8C2V9Q6 MODEL AGCD01053132;AGCD01053133;GBDF01249324;XM_005400897;XM_005400898;XM_005400900;XM_005400901 XP_005400954;XP_005400955;XP_005400957;XP_005400958 F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase;F-box/WD repeat-containing protein 7 APPROVED protein-coding ENSCLAG00000006777 NW_004955471 6848101 6955881 - 8721530 LOC102027097 olfactory receptor 5G3-like NW_004955511 1927117 1927701 - 102027097 MODEL AGCD01066385;XM_005408249 XP_005408306 protein-coding 8721533 LOC102029185 uncharacterized LOC102029185 NW_004955487 5622794 5639560 - 102029185 MODEL AGCD01059343;GBBH01053577;XM_005404411;XM_013504363;XM_013504364;XM_013504365;XM_013504366;XR_001231158 XP_005404468;XP_013359817;XP_013359818;XP_013359819;XP_013359820 uncharacterized protein LOC102029185 protein-coding 8721541 Cpt1a carnitine palmitoyltransferase 1A ENCODES a protein that exhibits carnitine O-palmitoyltransferase activity (ortholog); identical protein binding (ortholog); palmitoleoyltransferase activity (ortholog); INVOLVED IN carnitine metabolic process (ortholog); cellular response to fatty acid (ortholog); eating behavior (ortholog); PARTICIPATES IN adenosine monophosphate-activated protein kinase (AMPK) signaling pathway; carnitine palmitoyltransferase I deficiency pathway; ethylmalonic encephalopathy pathway; ASSOCIATED WITH Aicardi-Goutieres Syndrome 3 (ortholog); alcoholic hepatitis (ortholog); Breast Neoplasms (ortholog); FOUND IN mitochondrial outer membrane (ortholog); mitochondrion (ortholog) NW_004955422 17105887 17159696 + 9068941;7240710 102029191 A0A8C2WAI4 MODEL AGCD01022912;AGCD01022913;GBDF01249181;XM_005384264;XM_005384265 XP_005384321;XP_005384322 carnitine O-palmitoyltransferase 1, liver isoform;carnitine palmitoyltransferase 1A (liver) APPROVED protein-coding ENSCLAG00000016594 NW_004955422 17109256 17159838 + 8721567 Chpf chondroitin polymerizing factor ENCODES a protein that exhibits glucuronosyl-N-acetylgalactosaminyl-proteoglycan 4-beta-N-acetylgalactosaminyltransferase activity (ortholog); glycosyltransferase activity (ortholog); N-acetylgalactosaminyl-proteoglycan 3-beta-glucuronosyltransferase activity (ortholog); INVOLVED IN chondroitin sulfate biosynthetic process (ortholog); ASSOCIATED WITH alacrima, achalasia, and impaired intellectual development syndrome (ortholog); cerebrotendinous xanthomatosis (ortholog); genetic disease (ortholog); FOUND IN Golgi apparatus (ortholog) NW_004955453 13932822 13937587 + 9068941 102029261 A0A8C2VB78 MODEL AGCD01044855;GBCQ01040789;XM_005395509 XP_005395566 chondroitin sulfate synthase 2 protein-coding ENSCLAG00000007193 NW_004955453 13932822 13939350 + 8721581 Ptov1 PTOV1 extended AT-hook containing adaptor protein ASSOCIATED WITH developmental and epileptic encephalopathy 12 (ortholog); Disease Progression (ortholog); genetic disease (ortholog); FOUND IN nucleoplasm (ortholog) NW_004955559 1070856 1079052 - 9068941 102029454 A0A8C2V9E0;A0A8C2VC80 MODEL AGCD01073628;AGCD01073629;GBDK01007823;GBDK01196056;XM_013508969 XP_013364423 prostate tumor overexpressed 1 APPROVED protein-coding ENSCLAG00000007773 NW_004955559 1069481 1078735 - 8721598 LOC102030491 piezo-type mechanosensitive ion channel component 1-like NW_004955964 4 4333 + 102030491 MODEL AGCD01078759;GBCC01019104;XM_005415156 XP_005415213 protein-coding 8721613 LOC102003450 uncharacterized LOC102003450 NW_004955485 6812985 6814556 - 102003450 MODEL AGCD01058629;GBDF01041975;XR_263914 ncrna 8721617 LOC102003523 dimethylaniline monooxygenase [N-oxide-forming] 5-like NW_004955462 10251055 10272845 - 102003523 MODEL AGCD01049359;AGCD01049360 pseudo 8721618 Rce1 Ras converting CAAX endopeptidase 1 ENCODES a protein that exhibits endopeptidase activity (ortholog); exopeptidase activity (ortholog); INVOLVED IN CAAX-box protein processing (ortholog); protein prenylation (ortholog); ASSOCIATED WITH Aicardi-Goutieres Syndrome 3 (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN endoplasmic reticulum membrane (ortholog) NW_004955422 18538251 18541322 - 9068941 102004171 A0A8C2W004 MODEL AGCD01022951;GBCQ01101305;XM_005384377;XM_013513907;XM_013513908 XP_005384434;XP_013369361;XP_013369362 CAAX prenyl protease 2;RCE1 homolog, prenyl protein protease APPROVED protein-coding ENSCLAG00000015888 NW_004955422 18538251 18541863 - 8721634 Selenom selenoprotein M INVOLVED IN adipose tissue development (ortholog); corticosterone secretion (ortholog); hormone metabolic process (ortholog); ASSOCIATED WITH Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog); FOUND IN endoplasmic reticulum (ortholog); Golgi apparatus (ortholog) NW_004955455 5294317 5303621 - 9068941 102004353 A0A8C2VHS2 MODEL AGCD01045720;GBDF01089321;XM_005396296;XM_013520299 XP_005396353;XP_013375753 LOC102004353 APPROVED protein-coding ENSCLAG00000010856 NW_004955455 5294503 5296748 - 8721643 Rgs6 regulator of G protein signaling 6 ENCODES a protein that exhibits GTPase activator activity (ortholog); protein domain specific binding (ortholog); INVOLVED IN positive regulation of GTPase activity (ortholog); positive regulation of neuron differentiation (ortholog); PARTICIPATES IN acetylcholine signaling pathway via muscarinic acetylcholine receptor; ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); extrinsic component of membrane (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955523 2763143 3366851 - 9068941 102004846 A0A8C2UXK4;A0A8C2UXQ3;A0A8C2V338;A0A8C2YL86;A0A8C2YL87 MODEL AGCD01068588;AGCD01068589;AGCD01068590;AGCD01068591;AGCD01068592;AGCD01068593;AGCD01068594;AGCD01068595;AGCD01068596;AGCD01068597;AGCD01068598;AGCD01068599;AGCD01068600;AGCD01068601;AGCD01068602;AGCD01068603;AGCD01068604;AGCD01068605;GBDJ01403741;XM_005409440;XM_005409442;XM_005409443;XM_013507178 XP_005409497;XP_005409499;XP_005409500;XP_013362632 regulator of G-protein signaling 6 APPROVED protein-coding ENSCLAG00000004860 NW_004955523 2762987 3335474 - 8721672 Ap2a2 adaptor related protein complex 2 subunit alpha 2 ENCODES a protein that exhibits disordered domain specific binding (ortholog); kinase binding (ortholog); phosphatidylinositol binding (ortholog); INVOLVED IN clathrin-dependent endocytosis (ortholog); PARTICIPATES IN clathrin-dependent synaptic vesicle endocytosis; ASSOCIATED WITH delta beta-thalassemia (ortholog); developmental and epileptic encephalopathy (ortholog); early infantile epileptic encephalopathy (ortholog); FOUND IN AP-2 adaptor complex (ortholog); cytoplasmic vesicle (ortholog); membrane coat (ortholog) NW_004955476 11184944 11229385 - 9068941 102005465 A0A8C2UL11 MODEL AGCD01055443;AGCD01055444;GBCQ01002043;XM_005401795 XP_005401852 AP-2 complex subunit alpha-2;adaptor related protein complex 2 alpha 2 subunit;adaptor-related protein complex 2, alpha 2 subunit APPROVED protein-coding ENSCLAG00000001787 NW_004955476 11185223 11229409 - 8721704 LOC102005589 uncharacterized LOC102005589 NW_004955415 23433810 23434272 + 102005589 MODEL AGCD01016554;GBDF01207363;XR_260313 ncrna 8721708 Znf326 zinc finger protein 326 ENCODES a protein that exhibits DNA binding (ortholog); RNA polymerase II complex binding (ortholog); zinc ion binding (ortholog); INVOLVED IN positive regulation of DNA-templated transcription (ortholog); regulation of DNA-templated transcription elongation (ortholog); regulation of RNA splicing (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN DBIRD complex (ortholog); intracellular membrane-bounded organelle (ortholog); nuclear matrix (ortholog) NW_004955423 4145169 4178409 - 9068941 102006147 A0A8C2YKY7 MODEL AGCD01023529;GBDK01281590;XM_005385083 XP_005385140 DBIRD complex subunit ZNF326 protein-coding ENSCLAG00000004446 NW_004955423 4145998 4178320 - 8721724 Grap GRB2 related adaptor protein INVOLVED IN sensory perception of sound (ortholog); ASSOCIATED WITH autistic disorder (ortholog); autosomal recessive nonsyndromic deafness 114 (ortholog); common variable immunodeficiency 2 (ortholog) NW_004955467 559411 581098 + 9068941 102006995 A0A8C2VLD3 MODEL AGCD01051226;GBDI01132002;XM_005399286 XP_005399343 APPROVED protein-coding ENSCLAG00000010753 NW_004955467 559397 581098 + 8721736 LOC102007261 uncharacterized LOC102007261 NW_004955431 18572768 18575376 - 102007261 MODEL AGCD01030431;XR_261488 ncrna 8721741 LOC102007773 BAG family molecular chaperone regulator 5-like NW_004955484 8703188 8705376 + 102007773 MODEL AGCD01058394 pseudo 8721742 Ndufs8 NADH:ubiquinone oxidoreductase core subunit S8 ENCODES a protein that exhibits NADH dehydrogenase (ubiquinone) activity (ortholog); NADH dehydrogenase activity (ortholog); INVOLVED IN mitochondrial electron transport, NADH to ubiquinone (ortholog); mitochondrial respiratory chain complex I assembly (ortholog); response to oxidative stress (ortholog); ASSOCIATED WITH Aicardi-Goutieres Syndrome 3 (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN mitochondrial respiratory chain complex I (ortholog); mitochondrion (ortholog) NW_004955422 17781374 17785395 - 9068941;7240710 102007780 A0A8C2W6I4 MODEL AGCD01022932;GBDK01002250;XM_005384289;XM_013514041 XP_005384346;XP_013369495 NADH dehydrogenase (ubiquinone) Fe-S protein 8, 23kDa (NADH-coenzyme Q reductase);NADH dehydrogenase [ubiquinone] iron-sulfur protein 8, mitochondrial APPROVED protein-coding ENSCLAG00000017156 NW_004955422 17781204 17784404 - 8721753 Fam110b family with sequence similarity 110 member B ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); mitochondrion (ortholog) NW_004955454 16677016 16678568 + 9068941 102008286 MODEL AGCD01045522;GBCQ01154757;GBDF01194712;XM_013520248 XP_013375702 family with sequence similarity 110, member B APPROVED protein-coding 8721762 LOC102008585 U6 snRNA-associated Sm-like protein LSm3 pseudogene NW_004955583 83314 85152 - 102008585 MODEL AGCD01075793 APPROVED pseudo 8721763 LOC102008589 protein FAM170A-like NW_004955644 8842 16020 + 102008589 MODEL AGCD01077727;GBDF01075273;XM_005415048;XM_005415049 XP_005415105;XP_005415106 protein-coding 8721772 Mb21d2 Mab-21 domain containing 2 ENCODES a protein that exhibits protein-containing complex binding (ortholog); ASSOCIATED WITH genetic disease (ortholog); schizophrenia (ortholog) NW_004955420 15609102 15723377 + 9068941 102009187 A0A8C2VY27;A0A8C2W3I2 MODEL AGCD01020976;AGCD01020977;AGCD01020978;AGCD01020979;GBDF01249507;XM_005383212;XM_005383213;XM_005383214;XM_013513610 XP_005383269;XP_005383270;XP_005383271;XP_013369064 protein-coding ENSCLAG00000014657 NW_004955420 15609097 15725757 + 8721786 LOC102011286 mitochondrial import inner membrane translocase subunit Tim9 pseudogene NW_004955410 11964895 11965083 - 102011286 MODEL AGCD01010838 APPROVED pseudo 8721787 Cmya5 cardiomyopathy associated 5 ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN negative regulation of calcineurin-NFAT signaling cascade (ortholog); negative regulation of phosphoprotein phosphatase activity (ortholog); regulation of skeletal muscle adaptation (ortholog); ASSOCIATED WITH genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN costamere (ortholog); cytosol (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955425 21410396 21517307 - 9068941 102011680 A0A8C2YPD6 MODEL AGCD01025790;AGCD01025791;AGCD01025792;AGCD01025793;AGCD01025794;AGCD01025795;AGCD01025796;AGCD01025797;AGCD01025798;GBCB01000768;XM_005386007;XM_005386008 XP_005386064;XP_005386065 cardiomyopathy-associated protein 5 protein-coding ENSCLAG00000009334 NW_004955425 21410112 21477638 - 8721807 LOC102012487 uncharacterized LOC102012487 NW_004955449 15407328 15451351 + 102012487 MODEL AGCD01042194;XR_262507 ncrna 8721815 LOC102013028 protein-lysine N-methyltransferase N6AMT2 pseudogene NW_004955587 123785 124367 - 102013028 MODEL AGCD01076059 APPROVED pseudo 8721816 LOC102013050 homeobox protein Hox-A4-like NW_004955407 36080940 36082388 - 102013050 MODEL AGCD01007755;GBCQ01047171;XM_013504651 XP_013360105 APPROVED protein-coding 8721822 Trim11 tripartite motif containing 11 ENCODES a protein that exhibits protein domain specific binding (ortholog); protein-macromolecule adaptor activity (ortholog); ubiquitin protein ligase activity (ortholog); INVOLVED IN innate immune response (ortholog); negative regulation of AIM2 inflammasome complex assembly (ortholog); negative regulation of DNA-templated transcription (ortholog); ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); parathyroid carcinoma (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955581 114750 123410 + 9068941 102013126 A0A8C2UKF0 MODEL AGCD01075657;GBDF01080297;XM_005414233;XM_005414234 XP_005414290;XP_005414291 E3 ubiquitin-protein ligase TRIM11 protein-coding ENSCLAG00000000197 NW_004955581 114750 125143 + 8721834 Galk1 galactokinase 1 ENCODES a protein that exhibits ATP binding (ortholog); galactokinase activity (ortholog); galactose binding (ortholog); INVOLVED IN carbohydrate phosphorylation (ortholog); galactitol metabolic process (ortholog); galactose catabolic process via UDP-galactose (ortholog); PARTICIPATES IN galactokinase deficiency pathway; galactose metabolic pathway; galactosemia pathway; ASSOCIATED WITH cataract (ortholog); COVID-19 (ortholog); galactokinase deficiency (ortholog); FOUND IN cytoplasm (ortholog); membrane (ortholog) NW_004955506 6489799 6493354 + 9068941;7240710 102013316 A0A8C2YMQ9 MODEL AGCD01065428;GBBH01065204;XM_005407482;XM_013505976 XP_005407539;XP_013361430 galactokinase protein-coding ENSCLAG00000006961 NW_004955506 6489800 6493354 + 8721846 Sdcbp2 syndecan binding protein 2 ENCODES a protein that exhibits identical protein binding (ortholog); phosphatidylinositol-4,5-bisphosphate binding (ortholog); protein heterodimerization activity (ortholog); INVOLVED IN cell population proliferation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); Golgi apparatus (ortholog) NW_004955596 531741 555710 - 9068941 102014305 A0A8C2UL43 MODEL AGCD01076521;AGCD01076522;GBBH01180478;XM_005414702 XP_005414759 syndecan binding protein (syntenin) 2;syntenin-2 APPROVED protein-coding ENSCLAG00000000407 NW_004955596 531741 555710 - 8721859 Stkld1 serine/threonine kinase like domain containing 1 ASSOCIATED WITH developmental and epileptic encephalopathy 14 (ortholog); Ehlers-Danlos syndrome classic type 1 (ortholog); genetic disease (ortholog) NW_004955513 2726339 2745099 + 9068941 102014475 A0A8C2YQL0 MODEL AGCD01066887;AGCD01066888;GBDF01001606;XM_005408434;XM_005408435;XM_005408436;XM_005408438 XP_005408491;XP_005408492;XP_005408493;XP_005408495 serine/threonine kinase-like domain containing 1;serine/threonine kinase-like domain-containing protein STKLD1 APPROVED protein-coding ENSCLAG00000011038 NW_004955513 2726339 2744998 + 8721897 LOC102015057 SIGLEC family-like protein 1 NW_004955558 1080890 1097821 - 102015057 MODEL AGCD01073414;AGCD01073415;GBDF01190928;XM_005412691;XM_005412692;XM_005412693 XP_005412748;XP_005412749;XP_005412750 APPROVED protein-coding ENSCLAG00000029259 8721913 Far2 fatty acyl-CoA reductase 2 ENCODES a protein that exhibits alcohol-forming very long-chain fatty acyl-CoA reductase activity (ortholog); INVOLVED IN long-chain fatty-acyl-CoA metabolic process (ortholog); ASSOCIATED WITH alopecia (ortholog); dry eye syndrome (ortholog); genetic disease (ortholog); FOUND IN peroxisomal membrane (ortholog); peroxisome (ortholog) NW_004955505 5585846 5724234 - 9068941 102015869 A0A8C2UJX0 MODEL AGCD01065152;AGCD01065153;AGCD01065154;GBBH01106709;GBBH01112981;XM_013505936 XP_013361390 fatty acyl CoA reductase 2 APPROVED protein-coding ENSCLAG00000000959 NW_004955505 5585846 5663895 - 8721935 Hmbox1 homeobox containing 1 ENCODES a protein that exhibits double-stranded telomeric DNA binding (ortholog); identical protein binding (ortholog); protein-containing complex binding (ortholog); INVOLVED IN negative regulation of DNA-templated transcription (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); positive regulation of chromatin binding (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN centrosome (ortholog); chromosome, telomeric region (ortholog); cytoplasm (ortholog) NW_004955403 51199547 51377249 + 9068941 102016774 A0A8C2VVS5;A0A8C2VVS7;A0A8C2VW66;A0A8C2YT52 MODEL AGCD01002988;AGCD01002989;GBDF01220457;XM_005373783;XM_005373787;XM_005373788;XM_005373789;XM_005373790;XM_013514363 XP_005373840;XP_005373844;XP_005373845;XP_005373846;XP_005373847;XP_013369817 homeobox-containing protein 1 protein-coding ENSCLAG00000014654 NW_004955403 51257472 51365835 + 8721968 Mrgprd MAS related GPR family member D ASSOCIATED WITH Aicardi-Goutieres Syndrome 3 (ortholog); dilated cardiomyopathy (ortholog); genetic disease (ortholog) NW_004955422 16980896 16981906 + 9068941 102017787 A0A8C2YUC0 MODEL AGCD01022905;XM_005384962 XP_005385019 MAS-related GPR, member D;mas-related G-protein coupled receptor member D APPROVED protein-coding ENSCLAG00000016417 NW_004955422 16980932 16981903 + 8721971 Lgals8 galectin 8 ENCODES a protein that exhibits carbohydrate binding (ortholog); integrin binding (ortholog); INVOLVED IN cellular response to virus (ortholog); lymphatic endothelial cell migration (ortholog); plasma cell differentiation (ortholog); ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); parathyroid carcinoma (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog) NW_004955492 3673233 3693777 - 9068941 102017993 A0A8C2WBY2 MODEL AGCD01060699;GBBH01093652;XM_005404932;XM_005404934;XM_005404935;XM_005404936;XM_013504707;XM_013504708;XM_013504709 XP_005404989;XP_005404991;XP_005404992;XP_005404993;XP_013360161;XP_013360162;XP_013360163 galectin-8;lectin, galactoside-binding, soluble, 8 APPROVED protein-coding ENSCLAG00000017295 NW_004955492 3673233 3693776 - 8722000 LOC102019110 natural resistance-associated macrophage protein 2-like NW_004955547 1413554 1447203 - 102019110 A0A8C2UL31 MODEL AGCD01072222;AGCD01072223;GBDJ01084229;XM_013508457 XP_013363911 protein-coding ENSCLAG00000001253 8722001 Chsy1 chondroitin sulfate synthase 1 ENCODES a protein that exhibits glucuronosyl-N-acetylgalactosaminyl-proteoglycan 4-beta-N-acetylgalactosaminyltransferase activity (ortholog); glycosyltransferase activity (ortholog); N-acetylgalactosaminyl-proteoglycan 3-beta-glucuronosyltransferase activity (ortholog); INVOLVED IN bone morphogenesis (ortholog); cartilage development (ortholog); chondrocyte development (ortholog); ASSOCIATED WITH chromosome 15q26-qter deletion syndrome (ortholog); Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog); FOUND IN extracellular region (ortholog); Golgi apparatus (ortholog) NW_004955416 28070981 28136848 - 9068941;7240710 102019389 A0A8C2VGV0 MODEL AGCD01017623;AGCD01017624;AGCD01017625;GBBH01135196;GBDJ01128858;XM_005381708 XP_005381765 protein-coding ENSCLAG00000010522 NW_004955416 28070710 28135590 - 8722007 LOC102019572 26S protease regulatory subunit 10B-like NW_004955409 2430344 2431601 - 102019572 MODEL AGCD01009199 pseudo 8722008 LOC102019611 zinc finger protein 260-like NW_004955495 925423 929850 - 102019611 A0A8C2VQX8;A0A8C2VSS2;A0A8C2VVM7 MODEL AGCD01061661;GBDJ01370795;GBDK01143905;XM_013505071 XP_013360525 APPROVED protein-coding ENSCLAG00000012556 8722030 Fam241b family with sequence similarity 241 member B NW_004955437 21526944 21529611 - 9068941 102020051 A0A8C2VN58;A0A8C2VQ72 MODEL AGCD01034908;GBDI01353327;XM_005390080;XM_013516711 XP_005390137;XP_013372165 LOC102020051 chromosome unknown open reading frame, human C10orf35;uncharacterized protein C10orf35 homolog APPROVED protein-coding ENSCLAG00000011820 NW_004955437 21526944 21578912 - 8722047 Tlx3 T cell leukemia homeobox 3 ENCODES a protein that exhibits sequence-specific double-stranded DNA binding (ortholog); INVOLVED IN central nervous system development (ortholog); GABAergic neuron differentiation (ortholog); negative regulation of neuron differentiation (ortholog); ASSOCIATED WITH congenital central hypoventilation syndrome (ortholog); genetic disease (ortholog); hereditary breast ovarian cancer syndrome (ortholog); FOUND IN nucleoplasm (ortholog); nucleus (ortholog) NW_004955408 24103123 24105292 + 9068941 102020767 A0A8C2VSR9 MODEL AGCD01008594;XM_005376328 XP_005376385 T-cell leukemia homeobox 3;T-cell leukemia homeobox protein 3 APPROVED protein-coding ENSCLAG00000013094 NW_004955408 24102996 24105292 + 8722054 Prpf38a pre-mRNA processing factor 38A INVOLVED IN mRNA splicing, via spliceosome (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN nucleoplasm (ortholog); nucleus (ortholog); precatalytic spliceosome (ortholog) NW_004955464 6742200 6761059 - 9068941 102021106 A0A8C2V155 MODEL AGCD01050038;GBDJ01016093;XM_005398588 XP_005398645 PRP38 pre-mRNA processing factor 38 (yeast) domain containing A;pre-mRNA-splicing factor 38A APPROVED protein-coding ENSCLAG00000005816 NW_004955464 6742200 6761059 - 8722068 Snrpn small nuclear ribonucleoprotein polypeptide N INVOLVED IN response to hormone (ortholog); ASSOCIATED WITH Angelman syndrome (ortholog); autism spectrum disorder (ortholog); autistic disorder (ortholog); FOUND IN nucleoplasm (ortholog); U1 snRNP (ortholog); U2 snRNP (ortholog) NW_004955416 31668789 31674144 + 7240710;9068941 102023030 A0A8C2VR70 MODEL AGCD01017768;XM_013512673 XP_013368127 small nuclear ribonucleoprotein-associated protein N APPROVED protein-coding ENSCLAG00000011376 NW_004955416 31668736 31677219 + 8722088 Ccdc178 coiled-coil domain containing 178 ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); FOUND IN ciliary basal body (ortholog) NW_004955402 20076834 20429089 - 102023311 A0A8C2VFG7;A0A8C2VFH0 MODEL AGCD01000569;AGCD01000570;AGCD01000571;AGCD01000572;AGCD01000573;AGCD01000574;GBDF01123390;XM_005372759;XM_013507772;XM_013507853;XM_013507897;XM_013507911;XM_013507942 XP_005372816;XP_013363226;XP_013363307;XP_013363351;XP_013363365;XP_013363396 coiled-coil domain-containing protein 178 protein-coding ENSCLAG00000010212 NW_004955402 20076826 20429151 - 8722126 LOC102024652 putative hydrolase RBBP9 pseudogene NW_004955408 24651679 24656006 + 102024652 MODEL AGCD01008621 APPROVED pseudo 8722127 Proca1 protein interacting with cyclin A1 ENCODES a protein that exhibits cyclin binding (ortholog); ASSOCIATED WITH genetic disease (ortholog) NW_004955481 4451649 4461296 + 9068941 102024675 A0A8C2V0M2 MODEL AGCD01056941;AGCD01056942;GBBH01155525;XM_005402725;XM_005402726;XM_005402728;XM_005402729;XM_005402730;XM_005402731;XM_005402733;XM_005402736;XM_005402737;XM_013503392;XM_013503393;XM_013503394;XM_013503395;XM_013503396;XM_013503397;XM_013503398 XP_005402782;XP_005402783;XP_005402785;XP_005402786;XP_005402787;XP_005402788;XP_005402790;XP_005402793;XP_005402794;XP_013358846;XP_013358847;XP_013358848;XP_013358849;XP_013358850;XP_013358851;XP_013358852 protein-coding ENSCLAG00000005956 NW_004955481 4451769 4460922 + 8722159 Enkd1 enkurin domain containing 1 ENCODES a protein that exhibits alpha-tubulin binding (ortholog); microtubule binding (ortholog); INVOLVED IN establishment of mitotic spindle orientation (ortholog); motile cilium assembly (ortholog); non-motile cilium assembly (ortholog); ASSOCIATED WITH autosomal dominant dyskeratosis congenita 6 (ortholog); chromosome 16q22 deletion syndrome (ortholog); genetic disease (ortholog); FOUND IN 9+0 non-motile cilium (ortholog); centriole (ortholog); centrosome (ortholog) NW_004955484 9015744 9019781 + 9068941 102025124 A0A8C2V203 MODEL AGCD01058403;GBDJ01311527;XM_005403628;XM_005403629 XP_005403685;XP_005403686 enkurin domain-containing protein 1 protein-coding ENSCLAG00000006133 NW_004955484 9016049 9019568 + 8722174 LOC102025770 myosin-16-like NW_004955460 14968287 15011219 + 102025770 MODEL AGCD01048767 APPROVED pseudo 8722175 Rab3ip RAB3A interacting protein ENCODES a protein that exhibits GTPase binding (ortholog); guanyl-nucleotide exchange factor activity (ortholog); identical protein binding (ortholog); INVOLVED IN cilium assembly (ortholog); negative regulation of filopodium assembly (ortholog); protein localization to organelle (ortholog); PARTICIPATES IN insulin responsive facilitative sugar transporter mediated glucose transport pathway; Rab family mediated signaling pathway; ASSOCIATED WITH genetic disease (ortholog); FOUND IN centrosome (ortholog); cytosol (ortholog); nucleus (ortholog) NW_004955405 10031333 10091438 + 9068941 102025971 A0A8C2V0A3 MODEL AGCD01004802;AGCD01004803;AGCD01004804;AGCD01004805;AGCD01004806;AGCD01004807;GBBH01082375;GBDF01009098;XM_013517540 XP_013372994 protein-coding ENSCLAG00000005722 NW_004955405 10031666 10090456 + 8722190 LOC102027795 vomeronasal type-1 receptor 4-like NW_004955558 429751 430847 + 102027795 MODEL AGCD01073369;XM_005412733 XP_005412790 APPROVED protein-coding 8722193 Dst dystonin ENCODES a protein that exhibits integrin binding (ortholog); microtubule binding (ortholog); microtubule plus-end binding (ortholog); INVOLVED IN axonogenesis (ortholog); cell motility (ortholog); cytoplasmic microtubule organization (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); cardiomyopathy (ortholog); Charcot-Marie-Tooth disease (ortholog); FOUND IN actin cytoskeleton (ortholog); axon (ortholog); axon cytoplasm (ortholog) NW_004955502 3175918 3610823 + 9068941;7240710 102027880 A0A8C2UJZ3;A0A8C2UK12;A0A8C2ULV8;A0A8C2UMQ8;A0A8C2UPW0 MODEL AGCD01064312;AGCD01064313;AGCD01064314;AGCD01064315;AGCD01064316;AGCD01064317;GBDF01287480;XM_005406890;XM_005406892;XM_005406893;XM_013505819;XM_013505820;XM_013505821;XM_013505822;XM_013505823 XP_005406947;XP_005406949;XP_005406950;XP_013361273;XP_013361274;XP_013361275;XP_013361276;XP_013361277 protein-coding ENSCLAG00000001478 NW_004955502 3267527 3610823 + 8722318 Slc25a10 solute carrier family 25 member 10 ENCODES a protein that exhibits antiporter activity (ortholog); dicarboxylic acid transmembrane transporter activity (ortholog); malate transmembrane transporter activity (ortholog); INVOLVED IN malate transport (ortholog); phosphate ion transport (ortholog); succinate transport (ortholog); ASSOCIATED WITH Animal Mammary Neoplasms (ortholog); carcinoma (ortholog); Experimental Mammary Neoplasms (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrion (ortholog); nucleoplasm (ortholog) NW_004955506 1389798 1396670 - 9068941 102028111 A0A8C2VZJ6 MODEL AGCD01065262;GBCQ01002900;XM_005407261 XP_005407318 mitochondrial dicarboxylate carrier;solute carrier family 25 (mitochondrial carrier, dicarboxylate transporter), member 10 APPROVED protein-coding ENSCLAG00000014262 NW_004955506 1385788 1397015 - 8722336 LOC102029208 importin subunit alpha-1 pseudogene NW_004955507 1613701 1616336 - 102029208 MODEL AGCD01065569 APPROVED pseudo 8722337 LOC102029549 E3 ubiquitin-protein ligase RNF13 pseudogene NW_004955434 3032214 3033357 + 102029549 MODEL AGCD01032121 APPROVED pseudo 8722338 LOC102030359 protein WFDC9 NW_004955445 11651479 11652659 + 9068941 102030359 MODEL AGCD01039710;GBCQ01111229;XM_005392580 XP_005392637 Wfdc9 WAP four-disulfide core domain 9 APPROVED protein-coding 8722343 Wdr12 WD repeat domain 12 INVOLVED IN maturation of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) (ortholog); maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) (ortholog); Notch signaling pathway (ortholog); ASSOCIATED WITH autoimmune lymphoproliferative syndrome type 2B (ortholog); Autoimmune Lymphoproliferative Syndrome, Type V (ortholog); common variable immunodeficiency 1 (ortholog); FOUND IN nucleolus (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955457 11947816 11970066 + 9068941 102030389 A0A8C2V0F7 MODEL AGCD01046996;AGCD01046997;GBDF01016523;XM_005397046;XM_005397047 XP_005397103;XP_005397104 ribosome biogenesis protein WDR12 protein-coding ENSCLAG00000004491 NW_004955457 11947915 11971805 + 8722367 Lrrc74a leucine rich repeat containing 74A ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog) NW_004955438 805119 834335 + 9068941 102003283 A0A8C2VG86 MODEL AGCD01034963;AGCD01034964;GBDF01210386;XM_005390160;XM_005390161;XM_013517175;XM_013517176 XP_005390217;XP_005390218;XP_013372629;XP_013372630 leucine-rich repeat-containing protein 74A APPROVED protein-coding ENSCLAG00000008596 NW_004955438 805448 831590 + 8722393 LOC102003630 uncharacterized LOC102003630 NW_004955461 9207794 9213408 + 102003630 MODEL AGCD01048943;GBDF01222087;XR_001236550;XR_001236551;XR_001236552 ncrna 8722402 Prkag3 protein kinase AMP-activated non-catalytic subunit gamma 3 ENCODES a protein that exhibits AMP-activated protein kinase activity (ortholog); protein kinase binding (ortholog); INVOLVED IN cellular response to nutrient levels (ortholog); glycogen biosynthetic process (ortholog); glycolytic process (ortholog); PARTICIPATES IN adenosine monophosphate-activated protein kinase (AMPK) signaling pathway; ASSOCIATED WITH alacrima, achalasia, and impaired intellectual development syndrome (ortholog); carbohydrate metabolic disorder (ortholog); cerebrotendinous xanthomatosis (ortholog); FOUND IN nucleotide-activated protein kinase complex (ortholog) NW_004955453 14584405 14594112 + 9068941 102003940 A0A8C2VD02;A0A8C2VI89 MODEL AGCD01044871;GBDF01176866;XM_005395623;XM_005395624;XM_005395625;XM_005395626;XM_013519792;XM_013519793;XM_013519794;XM_013519795 XP_005395680;XP_005395681;XP_005395682;XP_005395683;XP_013375246;XP_013375247;XP_013375248;XP_013375249 5'-AMP-activated protein kinase subunit gamma-3 APPROVED protein-coding ENSCLAG00000009025 NW_004955453 14584412 14595369 + 8722430 Nrg1 neuregulin 1 ENCODES a protein that exhibits chemorepellent activity (ortholog); ErbB-2 class receptor binding (ortholog); ErbB-3 class receptor binding (ortholog); INVOLVED IN activation of protein kinase B activity (ortholog); activation of transmembrane receptor protein tyrosine kinase activity (ortholog); axon ensheathment (ortholog); PARTICIPATES IN epidermal growth factor/neuregulin signaling pathway; glypican signaling pathway; ASSOCIATED WITH Alzheimer's disease (ortholog); amphetamine abuse (ortholog); bipolar disorder (ortholog); FOUND IN apical part of cell; basal part of cell; cell projection NW_004955463 8009436 9037116 + 9068941;7240710;11556218 12121740 102004046 A0A8C2UJJ0;A0A8C2UKD6;A0A8C2UMA3;A0A8C2UPX7;A0A8C2YIN0;A0A8C2YIN5 MODEL AGCD01049752;AGCD01049753;AGCD01049754;AGCD01049755;AGCD01049756;AGCD01049757;AGCD01049758;AGCD01049759;AGCD01049760;AGCD01049761;AGCD01049762;AGCD01049763;AGCD01049764;AGCD01049765;AGCD01049766;AGCD01049767;AGCD01049768;AGCD01049769;AGCD01049770;AGCD01049771;GBDK01157880;XM_005398392;XM_005398394;XM_005398395;XM_005398397;XM_005398399;XM_005398400;XM_013521518;XM_013521519;XM_013521520;XM_013521521;XM_013521522 XP_005398449;XP_005398451;XP_005398452;XP_005398454;XP_005398456;XP_005398457;XP_013376972;XP_013376973;XP_013376974;XP_013376975;XP_013376976 heregulin;pro-neuregulin-1, membrane-bound isoform;type I neuregulin protein-coding ENSCLAG00000001108 NW_004955463 8009530 9037116 + 8722473 LOC102004742 olfactory receptor 5D18-like NW_004955511 617821 618762 + 102004742 A0A8C2YV34 MODEL AGCD01066336;XM_005408202 XP_005408259 protein-coding ENSCLAG00000017595 8722476 Acad11 acyl-CoA dehydrogenase family member 11 ENCODES a protein that exhibits long-chain-acyl-CoA dehydrogenase activity (ortholog); medium-chain-acyl-CoA dehydrogenase activity (ortholog); very-long-chain-acyl-CoA dehydrogenase activity (ortholog); INVOLVED IN fatty acid beta-oxidation using acyl-CoA dehydrogenase (ortholog); ASSOCIATED WITH alkaptonuria (ortholog); developmental and epileptic encephalopathy 44 (ortholog); genetic disease (ortholog); FOUND IN mitochondrial membrane (ortholog); nucleus (ortholog); peroxisome (ortholog) NW_004955501 5871328 5952786 + 9068941 102006481 A0A8C2UZR9 MODEL AGCD01064173;AGCD01064174;AGCD01064175;GBCE01176512;GBCE01176513;XM_005406834;XM_005406835 XP_005406891;XP_005406892 acyl-CoA dehydrogenase family, member 11 APPROVED protein-coding ENSCLAG00000003923 NW_004955501 5871113 5952909 + 8722502 LOC102007365 double-stranded RNA-binding protein Staufen homolog 1 pseudogene NW_004955530 1457860 1459504 - 102007365 MODEL AGCD01069884;XR_264702 APPROVED pseudo 8722505 Cacng4 calcium voltage-gated channel auxiliary subunit gamma 4 ENCODES a protein that exhibits calcium channel regulator activity (ortholog); ionotropic glutamate receptor binding (ortholog); INVOLVED IN positive regulation of AMPA receptor activity (ortholog); regulation of AMPA receptor activity (ortholog); regulation of postsynaptic neurotransmitter receptor activity (ortholog); ASSOCIATED WITH acute myocardial infarction (ortholog); Experimental Diabetes Mellitus (ortholog); genetic disease (ortholog); FOUND IN AMPA glutamate receptor complex (ortholog); cell body (ortholog); cell surface (ortholog) NW_004955478 6219637 6278759 + 9068941 102008410 A0A8C2UWD7 MODEL AGCD01055890;AGCD01055891;GBDF01128850;XM_005402149 XP_005402206 calcium channel, voltage-dependent, gamma subunit 4;voltage-dependent calcium channel gamma-4 subunit APPROVED protein-coding ENSCLAG00000004519 NW_004955478 6219631 6280169 + 8722519 Rc3h1 ring finger and CCCH-type domains 1 ENCODES a protein that exhibits CCR4-NOT complex binding (ortholog); double-stranded RNA binding (ortholog); miRNA binding (ortholog); INVOLVED IN 3'-UTR-mediated mRNA destabilization (ortholog); B cell homeostasis (ortholog); lymph node development (ortholog); ASSOCIATED WITH 1q24 Deletion Syndrome (ortholog); antithrombin III deficiency (ortholog); autoimmune lymphoproliferative syndrome (ortholog); FOUND IN cytoplasm (ortholog); cytoplasmic stress granule (ortholog); P-body (ortholog) NW_004955406 14053122 14123023 - 9068941 102010666 A0A8C2VIW8 MODEL AGCD01005956;AGCD01005957;GBCB01000291;XM_005374881;XM_005374883 XP_005374938;XP_005374940 roquin-1 protein-coding ENSCLAG00000011267 NW_004955406 14053122 14123029 - 8722553 Tmcc1 transmembrane and coiled-coil domain family 1 ENCODES a protein that exhibits identical protein binding (ortholog); INVOLVED IN endoplasmic reticulum organization (ortholog); endosomal transport (ortholog); endosome fission (ortholog); ASSOCIATED WITH alkaptonuria (ortholog); genetic disease (ortholog); immunodeficiency 21 (ortholog); FOUND IN cytosol (ortholog); endoplasmic reticulum-endosome membrane contact site (ortholog); rough endoplasmic reticulum (ortholog) NW_004955429 17589221 17726639 + 9068941 102010930 A0A8C2VW23;A0A8C2VW31;A0A8C2VWG3;A0A8C2W169 MODEL AGCD01028863;AGCD01028864;AGCD01028865;GBDJ01298988;XM_005387083;XM_013515450;XM_013515451;XM_013515452 XP_005387140;XP_013370904;XP_013370905;XP_013370906 transmembrane and coiled-coil domains protein 1 protein-coding ENSCLAG00000014727 NW_004955429 17545534 17726977 + 8722571 Znf703 zinc finger protein 703 ENCODES a protein that exhibits DNA-binding transcription factor binding (ortholog); INVOLVED IN adherens junction assembly (ortholog); cellular response to estradiol stimulus (ortholog); mammary gland epithelial cell differentiation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); nuclear matrix (ortholog); nucleus (ortholog) NW_004955463 13407491 13411562 + 9068941 102011287 A0A8C2UJS1 MODEL AGCD01049866;GBBH01139393;XM_005398409 XP_005398466 protein-coding ENSCLAG00000000911 NW_004955463 13407491 13411562 + 8722577 Iqgap1 IQ motif containing GTPase activating protein 1 ENCODES a protein that exhibits calcium ion binding (ortholog); calmodulin binding (ortholog); MAP-kinase scaffold activity (ortholog); INVOLVED IN cell migration (ortholog); cellular response to calcium ion (ortholog); cellular response to epidermal growth factor stimulus (ortholog); PARTICIPATES IN E-cadherin signaling pathway; insulin responsive facilitative sugar transporter mediated glucose transport pathway; platelet-derived growth factor signaling pathway; ASSOCIATED WITH Bloom syndrome (ortholog); Brain Neoplasms (ortholog); colorectal cancer (ortholog); FOUND IN actin cytoskeleton (ortholog); apical plasma membrane (ortholog); axon (ortholog) NW_004955416 14558628 14652031 + 9068941 102014354 A0A8C2VXR3 MODEL AGCD01017276;AGCD01017277;AGCD01017278;AGCD01017279;GBDF01087718;XM_005381503 XP_005381560 ras GTPase-activating-like protein IQGAP1 protein-coding ENSCLAG00000013145 NW_004955416 14560292 14650036 + 8722622 LOC102014445 vomeronasal type-1 receptor 90-like NW_004955414 15126436 15130335 + 102014445 MODEL AGCD01015178;XM_005380446 XP_005380503 protein-coding 8722625 Echdc2 enoyl-CoA hydratase domain containing 2 ASSOCIATED WITH genetic disease (ortholog) NW_004955464 6284436 6300908 + 9068941 102015299 A0A8C2V3Q2;A0A8C2V6I5 MODEL AGCD01050022;AGCD01050023;GBCE01047957;XM_005398567;XM_005398570;XM_013521720 XP_005398624;XP_005398627;XP_013377174 enoyl CoA hydratase domain containing 2;enoyl-CoA hydratase domain-containing protein 2, mitochondrial APPROVED protein-coding ENSCLAG00000006204 NW_004955464 6284436 6300908 + 8722648 Ubr4 ubiquitin protein ligase E3 component n-recognin 4 ENCODES a protein that exhibits ubiquitin protein ligase activity (ortholog); INVOLVED IN negative regulation of fatty acid biosynthetic process (ortholog); ubiquitin-dependent protein catabolic process (ortholog); ASSOCIATED WITH 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (ortholog); chromosome 1p36 deletion syndrome (ortholog); congenital disorder of glycosylation Ir (ortholog); FOUND IN centrosome (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955527 57335 185727 + 9068941 102015443 A0A8C2UVI4;A0A8C2UVI6;A0A8C2UWF8;A0A8C2V0K5 MODEL AGCD01069372;AGCD01069373;GBDJ01302005;XM_005409791;XM_005409792;XM_005409793;XM_005409794;XM_005409796;XM_013507391;XM_013507392;XM_013507393 XP_005409848;XP_005409849;XP_005409850;XP_005409851;XP_005409853;XP_013362845;XP_013362846;XP_013362847 E3 ubiquitin-protein ligase UBR4 protein-coding ENSCLAG00000004532 NW_004955527 57335 185727 + 8722765 LOC102015537 polyadenylate-binding protein 4 pseudogene NW_004955422 14754359 14755652 + 102015537 MODEL AGCD01022864 APPROVED pseudo 8722766 Tcl1a TCL1 family AKT coactivator A ENCODES a protein that exhibits identical protein binding (ortholog); protein kinase binding (ortholog); protein serine/threonine kinase activator activity (ortholog); INVOLVED IN activation of protein kinase B activity (ortholog); cellular response to tumor necrosis factor (ortholog); negative regulation of apoptotic process (ortholog); ASSOCIATED WITH acute myeloid leukemia (ortholog); COVID-19 (ortholog); essential thrombocythemia (ortholog); FOUND IN cell cortex (ortholog); cytosol (ortholog); endoplasmic reticulum (ortholog) NW_004955438 16934650 16952926 + 9068941 102015770 MODEL AGCD01035425;AGCD01035426;GBDJ01309630;XM_013517147 XP_013372601 T cell leukemia/lymphoma 1A;T-cell leukemia/lymphoma 1A;T-cell leukemia/lymphoma protein 1A APPROVED protein-coding 8722772 Aldh1l2 aldehyde dehydrogenase 1 family member L2 ENCODES a protein that exhibits formyltetrahydrofolate dehydrogenase activity (ortholog); INVOLVED IN 10-formyltetrahydrofolate catabolic process (ortholog); fatty acid beta-oxidation (ortholog); folic acid metabolic process (ortholog); ASSOCIATED WITH Chemical and Drug Induced Liver Injury (ortholog); COVID-19 (ortholog); Experimental Liver Cirrhosis (ortholog); FOUND IN mitochondrion (ortholog); nucleoplasm (ortholog) NW_004955405 39387949 39437282 - 9068941 102015919 A0A8C2V983 MODEL AGCD01005499;AGCD01005500;GBDI01245189;XM_005374604 XP_005374661 aldehyde dehydrogenase 1 family, member L2;mitochondrial 10-formyltetrahydrofolate dehydrogenase APPROVED protein-coding ENSCLAG00000006653 NW_004955405 39387527 39437322 - 8722799 Hagh hydroxyacylglutathione hydrolase ENCODES a protein that exhibits hydroxyacylglutathione hydrolase activity (ortholog); INVOLVED IN glutathione biosynthetic process (ortholog); glutathione metabolic process (ortholog); PARTICIPATES IN glyoxalase metabolic pathway; Leigh disease pathway; primary hyperoxaluria type 2 pathway; ASSOCIATED WITH epilepsy (ortholog); Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); mitochondrial matrix (ortholog) NW_004955442 15451910 15465211 + 9068941 102017279 A0A8C2VSF9;A0A8C2VSR0 MODEL AGCD01037874;GBCQ01186719;XM_005391507;XM_005391508;XM_005391509 XP_005391564;XP_005391565;XP_005391566 hydroxyacylglutathione hydrolase, mitochondrial protein-coding ENSCLAG00000013689 NW_004955442 15451910 15465211 + 8722816 Shc3 SHC adaptor protein 3 ENCODES a protein that exhibits phosphotyrosine residue binding (ortholog); INVOLVED IN learning or memory (ortholog); synaptic transmission, glutamatergic (ortholog); ASSOCIATED WITH Ependymomas (ortholog); genetic disease (ortholog); FOUND IN synapse (ortholog) NW_004955515 2858971 3016467 + 9068941 102017690 A0A8C2UNW7 MODEL AGCD01067260;AGCD01067261;AGCD01067262;AGCD01067263;AGCD01067264;AGCD01067265;AGCD01067266;AGCD01067267;GBDI01163152;GBDI01244672;XM_005408881 XP_005408938 SHC (Src homology 2 domain containing) transforming protein 3;SHC-transforming protein 3 APPROVED protein-coding ENSCLAG00000000924 NW_004955515 2860230 3016467 + 8722832 Eloa elongin A INVOLVED IN regulation of transcription by RNA polymerase II (ortholog); transcription elongation by RNA polymerase II (ortholog); transcription initiation at RNA polymerase II promoter (ortholog); ASSOCIATED WITH 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (ortholog); genetic disease (ortholog); FOUND IN elongin complex (ortholog); site of DNA damage (ortholog); transcription elongation factor complex (ortholog) NW_004955452 3668868 3681506 + 9068941 102018252 A0A8C2YP92 MODEL AGCD01043934;GBDF01087483;XM_013519496 XP_013374950 Tceb3 transcription elongation factor B (SIII), polypeptide 3 (110kDa, elongin A);transcription elongation factor B polypeptide 3;transcription elongation factor B subunit 3 APPROVED protein-coding ENSCLAG00000009140 NW_004955452 3668864 3681481 + 8722851 LOC102018350 uncharacterized LOC102018350 NW_004955402 45846571 45854310 + 102018350 MODEL AGCD01001142;GBCQ01008628;XR_259093 ncrna 8722856 LOC102018423 vomeronasal type-1 receptor 90-like NW_004955429 12408891 12409616 + 102018423 MODEL AGCD01028715;XM_005387249 XP_005387306 protein-coding 8722859 LOC102018936 MLN64 N-terminal domain homolog pseudogene NW_004955420 268901 269761 + 102018936 MODEL AGCD01020539 APPROVED pseudo 8722860 Atp5mj ATP synthase membrane subunit j ASSOCIATED WITH Charcot-Marie-Tooth disease axonal type 2O (ortholog) NW_004955538 2654283 2658610 - 9068941 102018979 A0A8C2V8J3 MODEL AGCD01071134;AGCD01071135;GBCQ01008230;XM_005410814;XM_005410815;XM_005410816 XP_005410871;XP_005410872;XP_005410873 Atp5mpl;LOC102018979 6.8 kDa mitochondrial proteolipid;ATP synthase membrane subunit 6.8PL;chromosome unknown open reading frame, human C14orf2 APPROVED protein-coding ENSCLAG00000006358 8722880 Armcx5 armadillo repeat containing X-linked 5 ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); syndromic X-linked intellectual disability Lubs type (ortholog) NW_004955548 107660 113316 + 9068941 102019741 A0A8C2UG35 MODEL AGCD01072317;XM_013508519;XM_013508520 XP_013363973;XP_013363974 armadillo repeat containing, X-linked 5;armadillo repeat-containing X-linked protein 5 APPROVED protein-coding ENSCLAG00000000357 NW_004955548 108330 112490 + 8722909 Arpc3 actin related protein 2/3 complex subunit 3 ENCODES a protein that exhibits actin filament binding (ortholog); structural constituent of cytoskeleton (ortholog); INVOLVED IN Arp2/3 complex-mediated actin nucleation (ortholog); cellular response to nerve growth factor stimulus (ortholog); PARTICIPATES IN insulin responsive facilitative sugar transporter mediated glucose transport pathway; platelet-derived growth factor signaling pathway; Rab family mediated signaling pathway; ASSOCIATED WITH diabetes mellitus (ortholog); Parkinson's disease (ortholog); FOUND IN Arp2/3 protein complex (ortholog); cell leading edge (ortholog); filamentous actin (ortholog) NW_004955482 7350456 7364266 - 9068941 102021012 A0A8C2VXY9 MODEL AGCD01057459;AGCD01057460;GBCE01029082;XM_005403143 XP_005403200 actin related protein 2/3 complex, subunit 3, 21kDa;actin-related protein 2/3 complex subunit 3 APPROVED protein-coding ENSCLAG00000013105 NW_004955482 7350456 7364266 - 8722920 LOC102021062 uncharacterized LOC102021062 NW_004955447 10776188 10778367 - 102021062 MODEL AGCD01040889;GBDF01017047;XR_262418 ncrna 8722924 LOC102021242 uncharacterized LOC102021242 NW_004955419 7042095 7105331 - 102021242 MODEL AGCD01019869;AGCD01019870;AGCD01019871;AGCD01019872;AGCD01019873;GBDI01189022;XR_001233597;XR_260612 ncrna 8722929 LOC102021283 uncharacterized LOC102021283 NW_004955441 9505985 9509614 + 102021283 MODEL AGCD01037022;GBCB01131781;XR_262065 ncrna 8722933 LOC102021390 uncharacterized LOC102021390 NW_004955539 3561889 3568046 + 102021390 MODEL AGCD01071257;GBDI01058745;XR_264814 ncrna 8722938 Cntn4 contactin 4 INVOLVED IN brain development (ortholog); negative regulation of neuron differentiation (ortholog); nervous system development (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); Craniofacial Abnormalities (ortholog) NW_004955421 10267471 10928734 - 9068941 102022503 A0A8C2V5X6;A0A8C2V8G9 MODEL AGCD01021872;AGCD01021873;AGCD01021874;AGCD01021875;AGCD01021876;AGCD01021877;AGCD01021878;AGCD01021879;AGCD01021880;AGCD01021881;AGCD01021882;AGCD01021883;AGCD01021884;AGCD01021885;GBDI01025726;XM_005383751;XM_005383752;XM_005383753;XM_005383754;XM_013513798;XM_013513799 XP_005383808;XP_005383809;XP_005383810;XP_005383811;XP_013369252;XP_013369253 contactin-4 protein-coding ENSCLAG00000006463 NW_004955421 10266640 10723228 - 8722973 Plekhg7 pleckstrin homology and RhoGEF domain containing G7 ASSOCIATED WITH genetic disease (ortholog) NW_004955405 29703523 29760551 + 9068941 102022562 A0A8C2V1C2 MODEL AGCD01005256;GBDJ01353997;XM_005374457;XM_005374459;XM_005374460;XM_013518255;XM_013518257;XM_013518258;XM_013518264;XM_013518269;XM_013518275 XP_005374514;XP_005374516;XP_005374517;XP_013373709;XP_013373711;XP_013373712;XP_013373718;XP_013373723;XP_013373729 pleckstrin homology domain containing, family G (with RhoGef domain) member 7;pleckstrin homology domain-containing family G member 7 APPROVED protein-coding ENSCLAG00000005133 8723011 LOC102022763 E3 ubiquitin-protein ligase RING2 pseudogene NW_004955449 3598267 3600715 - 102022763 MODEL AGCD01041856 APPROVED pseudo 8723012 Stk32c serine/threonine kinase 32C ASSOCIATED WITH distal 10q deletion syndrome (ortholog); genetic disease (ortholog) NW_004955477 9846602 9947927 - 9068941 102024223 A0A8C2UP39;A0A8C2URY2 MODEL AGCD01055686;AGCD01055687;GBCE01145629;GBDJ01315665;XM_013503114 XP_013358568 serine/threonine-protein kinase 32C protein-coding ENSCLAG00000002454 NW_004955477 9846397 9948784 - 8723030 LOC102024714 uncharacterized LOC102024714 NW_004955432 8842134 8844999 - 102024714 MODEL AGCD01030888;GBDF01208020;XR_261515 ncrna 8723035 LOC102025119 uncharacterized LOC102025119 NW_004955416 31751765 31788345 + 102025119 MODEL AGCD01017770;AGCD01017771;AGCD01017772;AGCD01017773;GBDF01288200;XR_001233286;XR_260453;XR_260454;XR_260455;XR_260456 ncrna 8723060 Rtp3 receptor transporter protein 3 INVOLVED IN detection of chemical stimulus involved in sensory perception of bitter taste (ortholog); protein targeting to membrane (ortholog); ASSOCIATED WITH Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog); hepatocellular carcinoma (ortholog); FOUND IN cytoplasm (ortholog) NW_004955420 25545752 25550044 - 9068941 102025364 A0A8C2YU46 MODEL AGCD01021365;GBDK01129519;XM_005383440;XM_005383441;XM_005383442;XM_013513589;XM_013513590 XP_005383497;XP_005383498;XP_005383499;XP_013369043;XP_013369044 receptor (chemosensory) transporter protein 3;receptor-transporting protein 3 APPROVED protein-coding ENSCLAG00000016076 8723073 LOC102027181 uncharacterized LOC102027181 NW_004955416 25520733 25572764 - 102027181 MODEL AGCD01017588;AGCD01017589;GBDF01075796;XR_001233375;XR_001233376;XR_260422 ncrna 8723078 Tyw3 tRNA-yW synthesizing protein 3 homolog ASSOCIATED WITH genetic disease (ortholog) NW_004955423 17932008 17952681 - 9068941 102027656 A0A8C2UXC9;A0A8C2V109 MODEL AGCD01023865;AGCD01023866;GBCQ01176880;XM_005385234;XM_005385235;XM_013514508 XP_005385291;XP_005385292;XP_013369962 tRNA wybutosine-synthesizing protein 3 homolog;tRNA-yW synthesizing protein 3 homolog (S. cerevisiae) APPROVED protein-coding ENSCLAG00000004370 NW_004955423 17931947 17952669 - 8723090 LOC102027800 uncharacterized LOC102027800 NW_004955584 715563 720377 + 102027800 MODEL AGCD01075955;AGCD01075956;GBDF01076200;XM_013509847 XP_013365301 uncharacterized protein LOC102027800 protein-coding 8723097 LOC102027832 uncharacterized LOC102027832 NW_004955413 25164415 25208404 + 102027832 MODEL AGCD01014397;AGCD01014398;AGCD01014399;XR_260110 LOC102027286 uncharacterized LOC102027286 PROVISIONAL ncrna 8723102 LOC102028119 epididymal-specific lipocalin-5-like NW_004955513 4872874 4874735 - 102028119 A0A8C2V8R4 MODEL AGCD01066943;GBDI01034412;XM_013506593 XP_013362047 protein-coding ENSCLAG00000006528 8723112 Dse dermatan sulfate epimerase ENCODES a protein that exhibits chondroitin-glucuronate 5-epimerase activity (ortholog); INVOLVED IN dermatan sulfate biosynthetic process (ortholog); ASSOCIATED WITH body dysmorphic disorder (ortholog); congenital disorder of glycosylation Iaa (ortholog); Ehlers-Danlos syndrome (ortholog); FOUND IN endoplasmic reticulum (ortholog); Golgi apparatus (ortholog) NW_004955526 348673 393328 - 9068941;7240710 102028571 A0A8C2UIL0 MODEL AGCD01069226;AGCD01069227;AGCD01069228;AGCD01069229;GBDJ01028388;XM_005409751;XM_005409752 XP_005409808;XP_005409809 dermatan-sulfate epimerase protein-coding ENSCLAG00000000219 NW_004955526 348519 392507 - 8723125 Zbtb6 zinc finger and BTB domain containing 6 ASSOCIATED WITH genetic disease (ortholog); FOUND IN mitochondrion (ortholog); nucleoplasm (ortholog) NW_004955419 5031584 5052538 + 9068941 102029744 A0A8C2W4M7 MODEL AGCD01019780;AGCD01019781;GBDF01075840;XM_005382511;XM_005382512;XM_013513148 XP_005382568;XP_005382569;XP_013368602 zinc finger and BTB domain-containing protein 6 protein-coding ENSCLAG00000016422 NW_004955419 5031584 5052526 + 8723135 Garem2 GRB2 associated regulator of MAPK1 subtype 2 ASSOCIATED WITH genetic disease (ortholog); Long-Chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency (ortholog); mitochondrial trifunctional protein deficiency (ortholog) NW_004955469 8170914 8182193 + 9068941 102029848 A0A8C2VWT0 MODEL AGCD01052457;AGCD01052458;GBDF01234919;XM_013522568 XP_013378022 GRB2 associated, regulator of MAPK1-like;GRB2-associated and regulator of MAPK protein-like;Gareml APPROVED protein-coding ENSCLAG00000013430 NW_004955469 8171714 8181052 + 8723145 LOC102029853 microspherule protein 1 pseudogene NW_004955414 16007175 16008531 - 102029853 MODEL AGCD01015194 APPROVED pseudo 8723146 Vash1 vasohibin 1 ENCODES a protein that exhibits actin binding (ortholog); metallocarboxypeptidase activity (ortholog); INVOLVED IN angiogenesis (ortholog); labyrinthine layer blood vessel development (ortholog); negative regulation of angiogenesis (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); liver cirrhosis (ortholog); FOUND IN apical part of cell (ortholog); cytoplasm (ortholog); endoplasmic reticulum (ortholog) NW_004955438 753392 772937 + 9068941 102029999 A0A8C2VK69 MODEL AGCD01034962;AGCD01034963;GBDF01086610;XM_013517177;XM_013517178;XM_013517179 XP_013372631;XP_013372632;XP_013372633 vasohibin-1 protein-coding ENSCLAG00000011500 NW_004955438 752554 772937 + 8723172 LOC102030170 putative olfactory receptor 10D4 NW_004955412 24795106 24796044 + 102030170 MODEL AGCD01013126;XM_005378407 XP_005378464 APPROVED protein-coding 8723176 LOC102030238 SUMO-conjugating enzyme UBC9 pseudogene NW_004955437 9961358 9961837 - 102030238 MODEL AGCD01034554 APPROVED pseudo 8723177 LOC102003996 40S ribosomal protein S20 pseudogene NW_004955513 5462592 5467878 + 102003996 MODEL AGCD01066971 APPROVED pseudo 8723178 LOC102004029 uncharacterized LOC102004029 NW_004955451 12567051 12574581 - 102004029 MODEL AGCD01043406;AGCD01043407;AGCD01043408;GBDF01043422;XR_001235955 ncrna 8723184 LOC102004808 uncharacterized LOC102004808 NW_004955476 10982505 10987287 - 102004808 MODEL AGCD01055434;GBDF01013264;XR_263645;XR_263646 ncrna 8723191 Prr5l proline rich 5 like ENCODES a protein that exhibits ubiquitin protein ligase binding (ortholog); INVOLVED IN cellular response to oxidative stress (ortholog); negative regulation of protein phosphorylation (ortholog); phosphatidylinositol 3-kinase signaling (ortholog); PARTICIPATES IN mTOR signaling pathway; ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); FOUND IN TORC2 complex (ortholog) NW_004955422 9972588 10069411 - 9068941 102005481 A0A8C2W2T5 MODEL AGCD01022726;AGCD01022727;AGCD01022728;AGCD01022729;AGCD01022730;GBDK01140964;XM_005384107;XM_005384108;XM_005384112;XM_005384114;XM_005384115;XM_005384116;XM_013514246;XM_013514247;XM_013514248;XM_013514249 XP_005384164;XP_005384165;XP_005384169;XP_005384171;XP_005384172;XP_005384173;XP_013369700;XP_013369701;XP_013369702;XP_013369703 proline-rich protein 5-like protein-coding ENSCLAG00000015373 NW_004955422 9972588 10048669 - 8723231 LOC102005737 olfactory receptor 8J3-like NW_004955511 1491665 1492606 + 102005737 MODEL AGCD01066369;XM_005407963 XP_005408020 protein-coding 8723234 Tmem183a transmembrane protein 183A ASSOCIATED WITH familial adult myoclonic epilepsy 5 (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog) NW_004955406 39029390 39044502 + 9068941 102005892 A0A8C2VQH4;A0A8C2YS07 MODEL AGCD01006618;GBDF01003831;XM_005375243;XM_005375244 XP_005375300;XP_005375301 protein-coding ENSCLAG00000013037 NW_004955406 39029390 39046339 + 8723248 LOC102006006 uncharacterized LOC102006006 NW_004955462 11471552 11476166 - 102006006 MODEL AGCD01049391;GBDF01209715;XR_001236585 ncrna 8723254 Chrdl1 chordin like 1 ENCODES a protein that exhibits BMP binding (ortholog); transforming growth factor beta binding (ortholog); INVOLVED IN AMPA glutamate receptor clustering (ortholog); BMP signaling pathway (ortholog); cell fate determination (ortholog); PARTICIPATES IN Bone morphogenetic proteins signaling pathway; ASSOCIATED WITH autistic disorder (ortholog); developmental and epileptic encephalopathy 36 (ortholog); genetic disease (ortholog); FOUND IN extracellular region (ortholog) NW_004955490 5108308 5218679 + 9068941 102006922 A0A8C2UTK3;A0A8C2UX61 MODEL AGCD01060203;GBCE01116210;XM_005404651;XM_005404652;XM_005404653;XM_005404654;XM_013504551;XM_013504552 XP_005404708;XP_005404709;XP_005404710;XP_005404711;XP_013360005;XP_013360006 chordin-like 1;chordin-like protein 1 APPROVED protein-coding ENSCLAG00000003267 NW_004955490 5108308 5257445 + 8723280 LOC102007210 NKG2-D type II integral membrane protein NW_004955413 7623358 7639703 - 9068941 102007210 A0A8C2VX11;A0A8C2YTA4 MODEL AGCD01013827;GBDI01345487;XM_005378934 XP_005378991 Klrd1 killer cell lectin-like receptor subfamily D, member 1 APPROVED protein-coding ENSCLAG00000014861 8723303 Kdm4c lysine demethylase 4C ENCODES a protein that exhibits chromatin binding (ortholog); enzyme binding (ortholog); histone demethylase activity (ortholog); INVOLVED IN blastocyst formation (ortholog); histone H3-K9 demethylation (ortholog); positive regulation of cell population proliferation (ortholog); PARTICIPATES IN histone modification pathway; ASSOCIATED WITH alopecia areata (ortholog); autistic disorder (ortholog); breast cancer (ortholog); FOUND IN chromatin (ortholog); pericentric heterochromatin (ortholog) NW_004955434 10646524 11000589 + 9068941 102007806 A0A8C2V4Q5 MODEL AGCD01032358;AGCD01032359;AGCD01032360;AGCD01032361;AGCD01032362;AGCD01032363;AGCD01032364;AGCD01032365;AGCD01032366;AGCD01032367;AGCD01032368;AGCD01032369;GBDJ01371221;XM_005388674 XP_005388731 lysine (K)-specific demethylase 4C;lysine-specific demethylase 4C APPROVED protein-coding ENSCLAG00000006468 NW_004955434 10685704 11000644 + 8723332 Tfrc transferrin receptor ENCODES a protein that exhibits double-stranded RNA binding (ortholog); Hsp70 protein binding (ortholog); identical protein binding (ortholog); INVOLVED IN acute-phase response (ortholog); cellular response to leukemia inhibitory factor (ortholog); cellular response to xenobiotic stimulus (ortholog); PARTICIPATES IN forkhead class A signaling pathway; hypoxia inducible factor pathway; iron uptake pathway; ASSOCIATED WITH Acute-Phase Reaction (ortholog); Arenaviridae infectious disease (ortholog); autism spectrum disorder (ortholog); FOUND IN basolateral plasma membrane (ortholog); cell surface (ortholog); clathrin-coated pit (ortholog) NW_004955420 12348392 12372714 - 9068941;7240710 102008628 A0A8C2YSY3 MODEL AGCD01020861;GBCB01056114;GBCQ01039332;XM_005383119 XP_005383176 transferrin receptor (p90, CD71);transferrin receptor protein 1 APPROVED protein-coding ENSCLAG00000014371 NW_004955420 12348821 12372691 - 8723354 LOC102010324 uncharacterized LOC102010324 NW_004955403 1876109 1880828 - 102010324 MODEL AGCD01001726;GBCQ01179100;XR_259132 ncrna 8723359 LOC102011156 glutathione S-transferase alpha-3 pseudogene NW_004955446 4760282 4767429 + 102011156 MODEL AGCD01040045 APPROVED pseudo 8723360 LOC102011884 uncharacterized LOC102011884 NW_004955424 343712 352617 - 102011884 MODEL AGCD01024172;AGCD01024173;GBDF01052736;XR_261019 ncrna 8723365 LOC102011967 serine-rich single-pass membrane protein 1-like NW_004955411 5417085 5417628 - 102011967 MODEL AGCD01011638 pseudo 8723366 Znf451 zinc finger protein 451 ENCODES a protein that exhibits SUMO ligase activity (ortholog); transcription corepressor activity (ortholog); transcription regulator inhibitor activity (ortholog); INVOLVED IN negative regulation of transcription initiation by RNA polymerase II (ortholog); negative regulation of transforming growth factor beta receptor signaling pathway (ortholog); protein sumoylation (ortholog); ASSOCIATED WITH genetic disease (ortholog); schizophrenia (ortholog); FOUND IN nucleus (ortholog) NW_004955502 3003822 3087529 - 9068941 102012341 A0A8C2UJR2;A0A8C2YIG2 MODEL AGCD01064308;AGCD01064309;AGCD01064310;GBCE01142291;GBDK01357332;XM_013505835 XP_013361289 protein-coding ENSCLAG00000000819 NW_004955502 2999976 3048464 - 8723385 LOC102012742 gamma-aminobutyric acid receptor-associated protein pseudogene NW_004955409 17452914 17453267 - 102012742 MODEL AGCD01009784 APPROVED pseudo 8723386 CUNH7orf25 chromosome unknown C7orf25 homolog ASSOCIATED WITH genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog) NW_004955460 895201 897703 + 9068941 102013148 A0A8C2V7H2 MODEL AGCD01048350;GBDF01090066;XM_005397716;XM_005397717;XM_005397720;XM_013521293 XP_005397773;XP_005397774;XP_005397777;XP_013376747 LOC102013148 UPF0415 protein C7orf25 homolog;chromosome unknown open reading frame, human C7orf25 APPROVED protein-coding ENSCLAG00000006458 NW_004955460 894516 898445 + 8723404 Xpnpep2 X-prolyl aminopeptidase 2 PARTICIPATES IN kallikrein-kinin cascade pathway; ASSOCIATED WITH acquired angioedema (ortholog); angioedema (ortholog); autistic disorder (ortholog); FOUND IN extracellular exosome (ortholog) NW_004955473 5248065 5274469 - 9068941;7240710 102013166 A0A8C2UR75 MODEL AGCD01053973;GBCQ01010121;XM_005401259 XP_005401316 X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound;xaa-Pro aminopeptidase 2 APPROVED protein-coding ENSCLAG00000001456 NW_004955473 5245746 5274698 - 8723429 Hltf helicase like transcription factor ENCODES a protein that exhibits ATP-dependent activity, acting on DNA (ortholog); ubiquitin protein ligase activity (ortholog); ubiquitin protein ligase binding (ortholog); INVOLVED IN mRNA transcription by RNA polymerase II (ortholog); positive regulation of transcription by RNA polymerase II (ortholog); regulation of neurogenesis (ortholog); ASSOCIATED WITH genetic disease (ortholog); glycogen storage disease XV (ortholog); Kidney Neoplasms (ortholog); FOUND IN nucleoplasm (ortholog); RNA polymerase II transcription regulator complex (ortholog) NW_004955474 8411912 8488938 + 9068941 102013600 A0A8C2URK9;A0A8C2UU29;A0A8C2UWQ3 MODEL AGCD01054553;AGCD01054554;GBDF01004721;XM_005401415;XM_005401416;XM_005401417;XM_005401420;XM_005401421;XM_013502747 XP_005401472;XP_005401473;XP_005401474;XP_005401477;XP_005401478;XP_013358201 helicase-like transcription factor APPROVED protein-coding ENSCLAG00000003408 NW_004955474 8412136 8486752 + 8723474 Gdf10 growth differentiation factor 10 INVOLVED IN cerebellum development (ortholog); fat cell differentiation (ortholog); negative regulation of osteoblast differentiation (ortholog); ASSOCIATED WITH Breast Neoplasms (ortholog); genetic disease (ortholog); Mesothelioma (ortholog); FOUND IN extracellular space (ortholog) NW_004955556 2185121 2195150 + 9068941 102013654 A0A8C2UGV2;A0A8C2ULX0 MODEL AGCD01073208;GBCE01004420;XM_005412611 XP_005412668 growth/differentiation factor 10 protein-coding ENSCLAG00000000288 NW_004955556 2185121 2196502 + 8723480 LOC102014216 uncharacterized LOC102014216 NW_004955408 22585567 22590646 - 102014216 MODEL AGCD01008578;GBDF01208907;XR_001231743 ncrna 8723486 Ppp2r5a protein phosphatase 2 regulatory subunit B'alpha ENCODES a protein that exhibits kinase binding (ortholog); phosphoprotein phosphatase activity (ortholog); INVOLVED IN negative regulation of lipid kinase activity (ortholog); negative regulation of protein localization to plasma membrane (ortholog); positive regulation of protein dephosphorylation (ortholog); PARTICIPATES IN Wnt signaling, canonical pathway; ASSOCIATED WITH Emphysema (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN centrosome (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955406 5059826 5115312 - 9068941 102014416 A0A8C2YRV2 MODEL AGCD01005711;GBDK01003948;XM_005375450 XP_005375507 serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit alpha isoform APPROVED protein-coding ENSCLAG00000012816 NW_004955406 5059826 5115312 - 8723502 LOC102014517 uncharacterized LOC102014517 NW_004955611 131423 144766 + 102014517 MODEL AGCD01077146;AGCD01077147;GBDF01277864;XR_001232576;XR_265162;XR_265163;XR_265164 ncrna 8723520 Plpp4 phospholipid phosphatase 4 ENCODES a protein that exhibits diacylglycerol diphosphate phosphatase activity (ortholog); identical protein binding (ortholog); phosphatidate phosphatase activity (ortholog); INVOLVED IN blastocyst hatching (ortholog); phospholipid dephosphorylation (ortholog); regulation of calcium ion import (ortholog); ASSOCIATED WITH breast cancer (ortholog); genetic disease (ortholog) NW_004955551 1328652 1458714 + 9068941 102015056 A0A8C2UMU2;A0A8C2UQ53 MODEL AGCD01072692;AGCD01072693;AGCD01072694;GBDJ01262036;XM_005412174 XP_005412231 Ppapdc1a phosphatidate phosphatase PPAPDC1A;phosphatidic acid phosphatase type 2 domain containing 1A APPROVED protein-coding ENSCLAG00000001292 NW_004955551 1328652 1459077 + 8723537 Sh3bgrl3 SH3 domain binding glutamate rich protein like 3 ENCODES a protein that exhibits glutathione transferase activity (ortholog); INVOLVED IN cytoskeleton organization (ortholog); ASSOCIATED WITH autosomal recessive hypercholesterolemia (ortholog); Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); nuclear body (ortholog); ruffle membrane (ortholog) NW_004955452 5683276 5684760 + 9068941 102015367 A0A8C2V7V2;A0A8C2VCZ1 MODEL AGCD01044051;GBDF01000998;XM_005394851 XP_005394908 SH3 domain binding glutamate-rich protein like 3;SH3 domain binding glutamic acid-rich protein like 3;SH3 domain-binding glutamic acid-rich-like protein 3 APPROVED protein-coding ENSCLAG00000007979 NW_004955452 5683276 5684760 + 8723544 LOC102016269 tigger transposable element-derived protein 1-like NW_004955417 13872785 13876028 + 102016269 MODEL AGCD01018191 pseudo 8723545 LOC102016789 calcyclin-binding protein pseudogene NW_004955460 3491190 3491890 + 102016789 MODEL AGCD01048410 APPROVED pseudo 8723546 Tspan16 tetraspanin 16 ASSOCIATED WITH alpha-mannosidosis (ortholog); Charcot-Marie-Tooth disease dominant intermediate B (ortholog); episodic ataxia type 2 (ortholog) NW_004955495 2234098 2249884 + 9068941 102018409 A0A8C2VGT9 MODEL AGCD01061756;AGCD01061757;AGCD01061758;AGCD01061759;GBDF01001019;GBDF01058236;XM_005405647;XM_005405648 XP_005405704;XP_005405705 tetraspanin-16 protein-coding ENSCLAG00000008629 NW_004955495 2234516 2248513 + 8723562 Wdr83os WD repeat domain 83 opposite strand ENCODES a protein that exhibits protein folding chaperone (ortholog); INVOLVED IN multi-pass transmembrane protein insertion into ER membrane (ortholog); protein insertion into ER membrane (ortholog); ASSOCIATED WITH alpha-mannosidosis (ortholog); Charcot-Marie-Tooth disease dominant intermediate B (ortholog); episodic ataxia type 2 (ortholog); FOUND IN endoplasmic reticulum membrane (ortholog); multi-pass translocon complex (ortholog); protein folding chaperone complex (ortholog) NW_004955415 31772401 31773916 - 9068941 102018721 A0A8C2VNB9 MODEL AGCD01016697;GBCQ01011781;XM_005381018 XP_005381075 protein-coding ENSCLAG00000011821 8723570 Ccl21 C-C motif chemokine ligand 21 ENCODES a protein that exhibits CCR7 chemokine receptor binding (ortholog); chemokine activity (ortholog); chemokine receptor binding (ortholog); INVOLVED IN activation of GTPase activity (ortholog); antimicrobial humoral immune response mediated by antimicrobial peptide (ortholog); cell chemotaxis (ortholog); ASSOCIATED WITH acromesomelic dysplasia, Maroteaux type (ortholog); anauxetic dysplasia (ortholog); Cytomegalovirus Infections (ortholog) NW_004955472 1427660 1428771 + 9068941 102019495 A0A8C2UKX4 MODEL AGCD01053390;GBCE01007174;XM_005401042 XP_005401099 C-C motif chemokine 21;chemokine (C-C motif) ligand 21 APPROVED protein-coding ENSCLAG00000001747 NW_004955472 1427710 1429102 + 8723578 LOC102019723 40S ribosomal protein S2 pseudogene NW_004955430 2621172 2623152 + 102019723 MODEL AGCD01029168;XR_261413 APPROVED pseudo 8723581 Sem1 SEM1 26S proteasome subunit INVOLVED IN double-strand break repair via homologous recombination (ortholog); ASSOCIATED WITH pleomorphic xanthoastrocytoma (ortholog); squamous cell carcinoma (ortholog); FOUND IN integrator complex (ortholog); proteasome complex (ortholog); protein-containing complex (ortholog) NW_004955432 13134359 13156402 - 9068941 102019940 A0A8C2URD9 MODEL AGCD01031004;AGCD01031005;GBDF01043233;XM_005388071;XM_005388072 XP_005388128;XP_005388129 Shfm1 26S proteasome complex subunit DSS1;SEM1 26S proteasome complex subunit;SEM1, 26S proteasome complex subunit;split hand/foot malformation (ectrodactyly) type 1 APPROVED protein-coding ENSCLAG00000002949 NW_004955432 13134359 13156397 - 8723594 LOC102020878 uncharacterized LOC102020878 NW_004955453 10179788 10183274 - 102020878 MODEL AGCD01044782;GBDF01253928;XR_262725;XR_262726 ncrna 8723601 Rpl35 ribosomal protein L35 ENCODES a protein that exhibits ribonucleoprotein complex binding (ortholog); structural constituent of ribosome (ortholog); INVOLVED IN cellular response to UV-B (ortholog); PARTICIPATES IN ribosome biogenesis pathway; translation pathway; ASSOCIATED WITH Diamond-Blackfan anemia 19 (ortholog); genetic disease (ortholog); FOUND IN cytoplasmic side of rough endoplasmic reticulum membrane (ortholog); cytosolic large ribosomal subunit (ortholog); cytosolic ribosome (ortholog) NW_004955419 3371109 3374555 + 9068941 102021014 A0A8C2VY29 MODEL AGCD01019719;GBDF01006252;XM_005382482 XP_005382539 60S ribosomal protein L35 protein-coding ENSCLAG00000013142 NW_004955419 3371109 3374555 + 8723609 LOC102021990 olfactory receptor 18-like NW_004955495 512537 513481 - 102021990 MODEL AGCD01061633;XM_013505092 XP_013360546 protein-coding 8723613 C2cd5 C2 calcium dependent domain containing 5 ENCODES a protein that exhibits calcium ion binding (ortholog); calcium-dependent phospholipid binding (ortholog); INVOLVED IN cellular response to insulin stimulus (ortholog); insulin receptor signaling pathway via phosphatidylinositol 3-kinase (ortholog); intracellular protein transmembrane transport (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cell cortex (ortholog); centriolar satellite (ortholog); cytoplasmic vesicle membrane (ortholog) NW_004955413 17883411 17972865 - 9068941 102022582 A0A8C2W3K9;A0A8C2W3L7;A0A8C2W4B3;A0A8C2W8A3;A0A8C2YUQ4 MODEL AGCD01014165;AGCD01014166;GBDJ01129965;GBDJ01129976;XM_005379074 XP_005379131 C2 calcium-dependent domain containing 5;C2 domain-containing protein 5 APPROVED protein-coding ENSCLAG00000016952 NW_004955413 17884556 17972851 - 8723653 Eif5a2 eukaryotic translation initiation factor 5A2 ASSOCIATED WITH Fanconi syndrome (ortholog); genetic disease (ortholog); Premature Aging (ortholog); FOUND IN intracellular membrane-bounded organelle (ortholog) NW_004955420 1032801 1044393 - 9068941 102022604 A0A8C2VZ61 MODEL AGCD01020560;AGCD01020561;GBDI01317060;GBDJ01306217;XM_013513425 XP_013368879 eukaryotic translation initiation factor 5A-2 protein-coding ENSCLAG00000013461 8723662 LOC102023062 lipocalin-15 NW_004955513 4882042 4887684 - 9068941 102023062 MODEL AGCD01066943;GBBH01057723;XM_005408552;XM_005408553;XM_013506566 XP_005408609;XP_005408610;XP_013362020 Lcn15 lipocalin 15 APPROVED protein-coding 8723676 Slc2a5 solute carrier family 2 member 5 ENCODES a protein that exhibits fructose binding (ortholog); fructose transmembrane transporter activity (ortholog); glucose transmembrane transporter activity (ortholog); INVOLVED IN cellular response to fructose stimulus (ortholog); fructose import across plasma membrane (ortholog); fructose transmembrane transport (ortholog); ASSOCIATED WITH Breast Neoplasms (ortholog); chromosome 1p36 deletion syndrome (ortholog); genetic disease (ortholog); FOUND IN apical plasma membrane (ortholog); plasma membrane (ortholog); sarcolemma (ortholog) NW_004955486 4194568 4208568 + 9068941 102024804 A0A8C2VYD5 MODEL AGCD01059057;GBDF01002394;XM_005404044;XM_013504322 XP_005404101;XP_013359776 solute carrier family 2 (facilitated glucose/fructose transporter), member 5;solute carrier family 2, facilitated glucose transporter member 5 APPROVED protein-coding ENSCLAG00000013207 NW_004955486 4194833 4211377 + 8723692 Pus1 pseudouridine synthase 1 ENCODES a protein that exhibits chromatin binding (ortholog); nuclear receptor coactivator activity (ortholog); pseudouridine synthase activity (ortholog); INVOLVED IN mRNA pseudouridine synthesis (ortholog); positive regulation of transcription by RNA polymerase II (ortholog); tRNA pseudouridine synthesis (ortholog); ASSOCIATED WITH colorectal cancer (ortholog); Disease Progression (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); mitochondrion (ortholog); nucleolus (ortholog) NW_004955482 749265 756964 - 9068941;7240710 102024908 A0A8C2VKV2;A0A8C2VSY0 MODEL AGCD01057187;GBDF01159325;XM_005402971;XM_013503609;XM_013503610;XM_013503611;XM_013503612;XM_013503613 XP_005403028;XP_013359063;XP_013359064;XP_013359065;XP_013359066;XP_013359067 pseudouridylate synthase 1;tRNA pseudouridine synthase A, mitochondrial APPROVED protein-coding ENSCLAG00000011689 NW_004955482 748394 756747 - 8723720 LOC102026454 olfactory receptor 1009-like NW_004955511 1886579 1887529 - 102026454 MODEL AGCD01066382;XM_005408247 XP_005408304 protein-coding 8723723 LOC102026946 signal recognition particle subunit SRP72-like NW_004955408 28510159 28521759 + 102026946 MODEL AGCD01008714 pseudo 8723724 Slu7 SLU7 homolog, splicing factor ENCODES a protein that exhibits pre-mRNA 3'-splice site binding (ortholog); second spliceosomal transesterification activity (ortholog); zinc ion binding (ortholog); INVOLVED IN alternative mRNA splicing, via spliceosome (ortholog); cellular response to heat (ortholog); intracellular protein transport (ortholog); PARTICIPATES IN spliceosome pathway; ASSOCIATED WITH genetic disease (ortholog); Weight Gain (ortholog); FOUND IN catalytic step 2 spliceosome (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955408 14268958 14288114 - 9068941 102027148 A0A8C2VTM4 MODEL AGCD01008391;GBDJ01087934;XM_005376265 XP_005376322 SLU7 splicing factor homolog;pre-mRNA-splicing factor SLU7 APPROVED protein-coding ENSCLAG00000011915 NW_004955408 14267369 14288213 - 8723744 LOC102027206 splicing factor 45 pseudogene NW_004955427 2663864 2665065 + 102027206 MODEL AGCD01026900 APPROVED pseudo 8723745 LOC102027510 olfactory receptor 10X1 ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); parathyroid carcinoma (ortholog) NW_004955468 10435122 10436054 - 9068941 102027510 MODEL AGCD01052084;XM_005400315 XP_005400372 APPROVED protein-coding 8723748 Txnrd2 thioredoxin reductase 2 ENCODES a protein that exhibits protein homodimerization activity (ortholog); protein-containing complex binding (ortholog); thioredoxin-disulfide reductase activity (ortholog); INVOLVED IN cell redox homeostasis (ortholog); heart development (ortholog); hemopoiesis (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); cardiomyopathy (ortholog); FOUND IN axon (ortholog); cytosol (ortholog); dendrite (ortholog) NW_004955442 18150060 18205775 + 9068941 102028588 A0A8C2VW22;A0A8C2VYT9;A0A8C2W159;A0A8C2W339 MODEL AGCD01037998;AGCD01037999;AGCD01038000;GBBH01025755;GBDF01222267;XM_013517794;XM_013517795;XM_013517796;XM_013517797;XM_013517798;XM_013517799;XM_013517800 XP_013373248;XP_013373249;XP_013373250;XP_013373251;XP_013373252;XP_013373253;XP_013373254 thioredoxin reductase 2, mitochondrial protein-coding ENSCLAG00000014718 NW_004955442 18152152 18204327 + 8723771 Actc1 actin alpha cardiac muscle 1 ENCODES a protein that exhibits ATP binding (ortholog); microfilament motor activity (ortholog); myosin binding (ortholog); INVOLVED IN actin filament-based movement (ortholog); actin-mediated cell contraction (ortholog); actin-myosin filament sliding (ortholog); ASSOCIATED WITH atrial heart septal defect (ortholog); atrial heart septal defect 5 (ortholog); Bloom syndrome (ortholog); FOUND IN actin filament (ortholog); cytoplasm (ortholog); glutamatergic synapse (ortholog) NW_004955416 2139541 2144678 - 9068941;7240710 102028962 A0A8C2V1I2 MODEL AGCD01016849;GBDI01008524;XM_005381179 XP_005381236 actin, alpha cardiac muscle 1;actin, alpha, cardiac muscle 1 APPROVED protein-coding ENSCLAG00000006212 NW_004955416 2137101 2145416 - 8723782 Klhl5 kelch like family member 5 ASSOCIATED WITH Cocaine-Related Disorders (ortholog); genetic disease (ortholog); Hyperglycinemia, Lactic Acidosis, and Seizures (ortholog) NW_004955443 8173338 8220393 - 9068941 102029015 A0A8C2URC3;A0A8C2UWB7;A0A8C2YJX6 MODEL AGCD01038315;AGCD01038316;GBDK01185239;XM_005391987 XP_005392044 kelch-like family member 5;kelch-like protein 5 APPROVED protein-coding ENSCLAG00000002937 NW_004955443 8170497 8220393 - 8723798 Rps15a ribosomal protein S15a ENCODES a protein that exhibits structural constituent of ribosome (ortholog); INVOLVED IN positive regulation of cell cycle (ortholog); positive regulation of cell population proliferation (ortholog); response to virus (ortholog); PARTICIPATES IN ribosome biogenesis pathway; translation pathway; ASSOCIATED WITH Diamond-Blackfan anemia 20 (ortholog); FOUND IN cytoplasm (ortholog); cytosolic ribosome (ortholog); cytosolic small ribosomal subunit (ortholog) NW_004955442 2530838 2535421 - 9068941 102029668 A0A8C2W4V7 MODEL AGCD01037468;GBBH01189526;XM_005391084 XP_005391141 40S ribosomal protein S15a APPROVED protein-coding ENSCLAG00000015274 NW_004955442 2530838 2535421 - 8723813 Cerkl ceramide kinase like ENCODES a protein that exhibits ceramide kinase activity (ortholog); sphingolipid binding (ortholog); INVOLVED IN negative regulation of apoptotic process (ortholog); sphingolipid biosynthetic process (ortholog); ASSOCIATED WITH cone dystrophy (ortholog); cone-rod dystrophy (ortholog); fundus dystrophy (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); endoplasmic reticulum (ortholog) NW_004955403 15620047 15727957 + 9068941;7240710 102030029 A0A8C2W152 MODEL AGCD01002051;AGCD01002052;GBDI01208278;GBDI01208281;XM_013512521 XP_013367975 ceramide kinase-like APPROVED protein-coding ENSCLAG00000016232 8723832 Ddx3x DEAD-box helicase 3 X-linked ENCODES a protein that exhibits ATP hydrolysis activity (ortholog); CTPase activity (ortholog); DNA binding (ortholog); INVOLVED IN cellular response to arsenic-containing substance (ortholog); cellular response to osmotic stress (ortholog); cellular response to virus (ortholog); ASSOCIATED WITH autistic disorder (ortholog); breast cancer (ortholog); cerebellar hypoplasia (ortholog); FOUND IN cell leading edge (ortholog); centrosome (ortholog); cytoplasm (ortholog) NW_004955565 1387043 1403624 - 9068941;7240710 102030251 A0A8C2UPF3 MODEL AGCD01074316;AGCD01074317;GBCB01000529;XM_005413259 XP_005413316 ATP-dependent RNA helicase DDX3X;DEAD (Asp-Glu-Ala-Asp) box helicase 3, X-linked;DEAD-box helicase 3, X-linked APPROVED protein-coding ENSCLAG00000000993 NW_004955565 1386973 1404220 - 8723867 Cd207 CD207 molecule ENCODES a protein that exhibits carbohydrate binding (ortholog); INVOLVED IN defense response to virus (ortholog); ASSOCIATED WITH dystonia (ortholog); genetic disease (ortholog); Methylmalonyl-CoA Epimerase Deficiency (ortholog) NW_004955424 14355739 14361326 + 9068941 102030441 A0A8C2VDY5 MODEL AGCD01024652;GBDF01019779;XM_005385607 XP_005385664 C-type lectin domain family 4 member K;CD207 molecule, langerin APPROVED protein-coding ENSCLAG00000009303 NW_004955424 14355739 14361318 + 8723885 B9d1 B9 domain containing 1 ENCODES a protein that exhibits hedgehog receptor activity (ortholog); INVOLVED IN camera-type eye development (ortholog); cilium assembly (ortholog); embryonic digit morphogenesis (ortholog); ASSOCIATED WITH asphyxiating thoracic dystrophy (ortholog); autistic disorder (ortholog); common variable immunodeficiency 2 (ortholog); FOUND IN centrosome (ortholog); ciliary basal body (ortholog); ciliary transition zone (ortholog) NW_004955467 405487 415887 + 9068941;7240710 102003222 A0A8C2VQS7;A0A8C2YS26 MODEL AGCD01051219;GBDF01002264;XM_005399272;XM_005399273;XM_013522256 XP_005399329;XP_005399330;XP_013377710 B9 domain-containing protein 1;B9 protein domain 1 APPROVED protein-coding ENSCLAG00000013112 NW_004955467 405490 416116 + 8723900 LOC102003232 uncharacterized LOC102003232 NW_004955416 2924029 2929842 + 102003232 MODEL AGCD01016863;GBDF01042362;XR_260349;XR_260350;XR_260351 ncrna 8723910 LOC102003240 bridging integrator 2-like NW_004955418 22080594 22081909 - 102003240 MODEL AGCD01019279 pseudo 8723911 Ttc34 tetratricopeptide repeat domain 34 ASSOCIATED WITH chromosome 1p36 deletion syndrome (ortholog); dilated cardiomyopathy 1LL (ortholog); Ehlers-Danlos syndrome spondylodysplastic type 2 (ortholog) NW_004955486 8620609 8633069 + 102003451 A0A8C2UYK0 MODEL AGCD01059152;AGCD01059153;GBDJ01134032;XM_005404156 XP_005404213 tetratricopeptide repeat protein 34 protein-coding ENSCLAG00000005188 NW_004955486 8620516 8631399 + 8723925 Fbp2 fructose-bisphosphatase 2 ENCODES a protein that exhibits fructose 1,6-bisphosphate 1-phosphatase activity (ortholog); identical protein binding (ortholog); INVOLVED IN gluconeogenesis (ortholog); PARTICIPATES IN gluconeogenesis pathway; ASSOCIATED WITH Acute Liver Failure (ortholog); Childhood-Onset Remitting Leukodystrophy (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); plasma membrane (ortholog) NW_004955422 21508906 21530296 - 9068941 102003883 A0A8C2WAL8 MODEL AGCD01023124;GBDI01078846;XM_005384676 XP_005384733 fructose-1,6-bisphosphatase 2;fructose-1,6-bisphosphatase isozyme 2 APPROVED protein-coding ENSCLAG00000016623 NW_004955422 21505857 21530302 - 8723936 Ankrd33b ankyrin repeat domain 33B ASSOCIATED WITH genetic disease (ortholog) NW_004955426 363297 383013 + 102004090 A0A8C2V9D9 MODEL AGCD01026001;GBDI01359209;XM_005386256 XP_005386313 ankyrin repeat domain-containing protein 33B APPROVED protein-coding ENSCLAG00000008394 NW_004955426 363297 384415 + 8723944 LOC102005865 transcription factor BTF3 homolog 4 pseudogene NW_004955588 220604 221041 + 102005865 MODEL AGCD01076095 APPROVED pseudo 8723945 Prrx1 paired related homeobox 1 ENCODES a protein that exhibits DNA binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); INVOLVED IN artery morphogenesis (ortholog); cartilage development (ortholog); embryonic cranial skeleton morphogenesis (ortholog); ASSOCIATED WITH 1q24 Deletion Syndrome (ortholog); agnathia-otocephaly complex (ortholog); atrial fibrillation (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955462 6919905 6991733 + 9068941;7240710 102006989 A0A8C2V070;A0A8C2V595 MODEL AGCD01049292;AGCD01049293;GBCE01001518;XM_005398172;XM_005398173 XP_005398229;XP_005398230 paired mesoderm homeobox protein 1 protein-coding ENSCLAG00000005839 NW_004955462 6919899 6991733 + 8723956 LOC102007523 NEDD8-conjugating enzyme Ubc12 pseudogene NW_004955409 21637990 21714722 + 102007523 MODEL AGCD01009975;AGCD01009976;AGCD01009977;AGCD01009978;XM_005377162 APPROVED pseudo 8723968 LOC102008864 solute carrier family 25 member 36-like NW_004955421 22468586 22469764 + 102008864 MODEL AGCD01022136 pseudo 8723970 Mepce methylphosphate capping enzyme ENCODES a protein that exhibits 7SK snRNA binding (ortholog); RNA 5'-methyltransferase activity (ortholog); RNA binding (ortholog); INVOLVED IN negative regulation of chromatin binding (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); positive regulation of G1/S transition of mitotic cell cycle (ortholog); ASSOCIATED WITH genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN 7SK snRNP (ortholog); nucleus (ortholog); ribonucleoprotein complex (ortholog) NW_004955573 526083 531222 - 9068941 102010747 A0A8C2UTA7 MODEL AGCD01074989;AGCD01074990;GBBH01119041;GBCE01004510;XM_013509475 XP_013364929 7SK snRNA methylphosphate capping enzyme protein-coding ENSCLAG00000003470 NW_004955573 526613 530286 - 8723979 Afg2a AFG2 AAA ATPase homolog A ENCODES a protein that exhibits preribosome binding (ortholog); INVOLVED IN brain development (ortholog); ribosomal large subunit biogenesis (ortholog); ASSOCIATED WITH epilepsy (ortholog); genetic disease (ortholog); neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities (ortholog); FOUND IN cytoplasm (ortholog); spindle (ortholog) NW_004955428 17525388 17823478 - 9068941;7240710 102010822 A0A8C2UZ48 MODEL AGCD01028044;AGCD01028045;AGCD01028046;AGCD01028047;AGCD01028048;AGCD01028049;AGCD01028050;AGCD01028051;AGCD01028052;GBDF01224056;XM_005386754;XM_005386755 XP_005386811;XP_005386812 Spata5 spermatogenesis associated 5;spermatogenesis-associated protein 5 APPROVED protein-coding ENSCLAG00000005265 NW_004955428 17524583 17823108 - 8724001 LOC102010932 olfactory receptor 10AG1-like NW_004955511 901202 903998 - 102010932 MODEL AGCD01066346 pseudo 8724002 Btbd1 BTB domain containing 1 ENCODES a protein that exhibits cullin family protein binding (ortholog); identical protein binding (ortholog); ASSOCIATED WITH amenorrhea (ortholog); Bloom syndrome (ortholog); colorectal cancer (ortholog); FOUND IN cytoplasmic ribonucleoprotein granule (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955416 13621343 13657276 + 9068941 102011986 A0A8C2YPX2;A0A8C2YPX3 MODEL AGCD01017229;GBDF01004869;XM_013512487 XP_013367941 BTB (POZ) domain containing 1;BTB/POZ domain-containing protein 1 APPROVED protein-coding ENSCLAG00000010092 NW_004955416 13621118 13657581 + 8724016 LOC102012057 uncharacterized LOC102012057 NW_004955406 39330833 39331560 + 102012057 MODEL AGCD01006626;GBDK01343682;XR_259526 ncrna 8724020 LOC102012268 uncharacterized LOC102012268 NW_004955403 25880625 25907260 + 102012268 MODEL AGCD01002295;GBDF01251079;XR_001233582;XR_001233583;XR_259202 ncrna 8724032 Apln apelin ENCODES a protein that exhibits apelin receptor binding (ortholog); hormone activity (ortholog); identical protein binding (ortholog); INVOLVED IN apelin receptor signaling pathway (ortholog); coronary vasculature development (ortholog); drinking behavior (ortholog); PARTICIPATES IN apelin signaling pathway; ASSOCIATED WITH atrial fibrillation (ortholog); autistic disorder (ortholog); Cardiomegaly (ortholog); FOUND IN extracellular region (ortholog); extracellular space (ortholog); perinuclear region of cytoplasm (ortholog) NW_004955473 5346822 5356359 + 9068941 102013713 A0A8C2ULH0 MODEL AGCD01053974;GBDK01240998;XM_005401260;XM_005401261 XP_005401317;XP_005401318 protein-coding ENSCLAG00000001685 NW_004955473 5346747 5356359 + 8724041 LOC102014530 S-adenosylmethionine decarboxylase proenzyme-like NW_004955453 16645403 16650249 - 102014530 MODEL AGCD01044909 pseudo 8724042 LOC102014591 coiled-coil domain-containing protein 152 pseudogene NW_004955428 11405395 11408989 - 102014591 MODEL AGCD01027898 APPROVED pseudo 8724043 LOC102016208 vomeronasal type-1 receptor 4-like NW_004955569 1032355 1033407 + 102016208 MODEL AGCD01074632;XM_005413517 XP_005413574 APPROVED protein-coding 8724046 LOC102016688 60S ribosomal protein L17 pseudogene NW_004955467 10296133 10298358 - 102016688 MODEL AGCD01051558 APPROVED pseudo 8724047 Ino80d INO80 complex subunit D INVOLVED IN chromatin remodeling (ortholog); positive regulation of DNA repair (ortholog); positive regulation of DNA-templated transcription (ortholog); PARTICIPATES IN INO80 family mediated chromatin remodeling pathway; ASSOCIATED WITH genetic disease (ortholog); megacolon (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN Ino80 complex (ortholog) NW_004955457 8913625 8983859 + 9068941 102017955 A0A8C2V268 MODEL AGCD01046922;AGCD01046923;AGCD01046924;GBDK01343093;XM_005397001;XM_005397003 XP_005397058;XP_005397060 protein-coding ENSCLAG00000006191 NW_004955457 8924615 8973274 + 8724068 Crybb1 crystallin beta B1 ENCODES a protein that exhibits structural constituent of eye lens (ortholog); ASSOCIATED WITH cataract (ortholog); cataract 17 multiple types (ortholog); cataract 23 (ortholog) NW_004955455 1165048 1180826 - 9068941;7240710 102018059 A0A8C2VB35 MODEL AGCD01045570;GBBH01043266;XM_005396158 XP_005396215 beta-crystallin B1;crystallin, beta B1 APPROVED protein-coding ENSCLAG00000008489 NW_004955455 1165048 1180826 - 8724078 Dusp28 dual specificity phosphatase 28 ENCODES a protein that exhibits phosphatase activity (ortholog); INVOLVED IN dephosphorylation (ortholog); ASSOCIATED WITH Bethlem Myopathy 1 (ortholog); chromosome 2q37 deletion syndrome (ortholog); D-2-hydroxyglutaric aciduria 1 (ortholog) NW_004955542 909239 911139 - 9068941 102018333 A0A8C2ULK3 MODEL AGCD01071484;AGCD01071485;GBBH01102815;XM_005411166 XP_005411223 protein-coding ENSCLAG00000001935 NW_004955542 909917 910646 - 8724084 Siah2 siah E3 ubiquitin protein ligase 2 ENCODES a protein that exhibits ubiquitin conjugating enzyme binding (ortholog); ubiquitin protein ligase activity (ortholog); ubiquitin-protein transferase activity (ortholog); INVOLVED IN canonical Wnt signaling pathway (ortholog); negative regulation of apoptotic process (ortholog); negative regulation of canonical Wnt signaling pathway (ortholog); PARTICIPATES IN estrogen signaling pathway; nuclear factor, erythroid 2 like 2 signaling pathway; ASSOCIATED WITH genetic disease (ortholog); glycogen storage disease XV (ortholog); lens disease (ortholog); FOUND IN cytosol (ortholog); early endosome (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955448 1907478 1926445 - 9068941 102018449 A0A8C2UWD9 MODEL AGCD01041271;GBDJ01180931;GBDK01196937;XM_013518651 XP_013374105 E3 ubiquitin-protein ligase SIAH2 protein-coding ENSCLAG00000002950 NW_004955448 1907401 1926445 - 8724092 Tbc1d10a TBC1 domain family member 10A ENCODES a protein that exhibits PDZ domain binding (ortholog); INVOLVED IN activation of cysteine-type endopeptidase activity (ortholog); positive regulation of proteolysis (ortholog); regulation of cilium assembly (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN plasma membrane (ortholog) NW_004955455 4537634 4570949 - 9068941 102018564 A0A8C2VSD2 MODEL AGCD01045679;AGCD01045680;GBDF01052787;XM_005396252 XP_005396309 TBC1 domain family, member 10A APPROVED protein-coding ENSCLAG00000012935 NW_004955455 4537634 4570949 - 8724109 LOC102018853 uncharacterized LOC102018853 NW_004955433 21601809 21606853 + 102018853 MODEL AGCD01031928;GBDF01290084;XR_261604 ncrna 8724114 LOC102019745 beta-crystallin B2 NW_004955442 19887415 19891508 - 9068941;7240710 102019745 A0A8C2VYZ4 MODEL AGCD01038080;GBDK01038850;XM_013517684 XP_013373138 Crybb2 crystallin, beta B2 APPROVED protein-coding ENSCLAG00000015578 NW_004955442 19887511 19890994 - 8724121 LOC102022037 serine protease 55-like NW_004955403 52114823 52124047 - 102022037 A0A8C2W4E4 MODEL AGCD01003001;AGCD01003002;GBDF01002536;XM_013514424;XM_013514426;XM_013514430 XP_013369878;XP_013369880;XP_013369884 tryptase gamma-like protein-coding ENSCLAG00000016541 8724134 Paqr3 progestin and adipoQ receptor family member 3 INVOLVED IN negative regulation of MAP kinase activity (ortholog); negative regulation of neuron projection development (ortholog); negative regulation of peptidyl-serine phosphorylation (ortholog); ASSOCIATED WITH genetic disease (ortholog); Kabuki Syndrome 1 (ortholog); FOUND IN Golgi apparatus (ortholog) NW_004955433 3323426 3350358 - 9068941 102022216 A0A8C2YL81 MODEL AGCD01031420;GBCB01073899;XM_005388211;XM_005388212;XM_005388213;XM_013516174;XR_261551 XP_005388268;XP_005388269;XP_005388270;XP_013371628 progestin and adipoQ receptor family member III APPROVED protein-coding ENSCLAG00000004835 NW_004955433 3321625 3350588 - 8724154 LOC102022417 uncharacterized LOC102022417 NW_004955432 705758 726019 - 102022417 MODEL AGCD01030574;GBCE01049655;XR_261497 ncrna 8724161 LOC102022485 intelectin-1a-like NW_004955468 12676510 12685740 - 102022485 A0A8C2VM52;A0A8C2VPG7;A0A8C2VU42 MODEL AGCD01052176;GBCQ01163630;XM_005400223;XM_005400224;XM_013522494 XP_005400280;XP_005400281;XP_013377948 protein-coding ENSCLAG00000012147 8724176 Gadl1 glutamate decarboxylase like 1 ASSOCIATED WITH amenorrhea (ortholog); genetic disease (ortholog); Liver Neoplasms (ortholog) NW_004955430 22029481 22187807 - 9068941 102022728 A0A8C2VBJ1 MODEL AGCD01029781;GBCB01020087;XM_005387520;XM_005387521 XP_005387577;XP_005387578 acidic amino acid decarboxylase GADL1;glutamate decarboxylase-like 1 APPROVED protein-coding ENSCLAG00000008630 NW_004955430 22029450 22188133 - 8724206 Defb123 defensin beta 123 ASSOCIATED WITH genetic disease (ortholog) NW_004955422 29494221 29496697 - 9068941 102023372 A0A8C2W3W3 MODEL AGCD01023399;GBDF01049661;XM_005384919 XP_005384976 beta-defensin 123;defensin, beta 123 APPROVED protein-coding ENSCLAG00000017024 NW_004955422 29494119 29496857 - 8724212 Chd9 chromodomain helicase DNA binding protein 9 ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog) NW_004955433 10900771 11161161 + 9068941 102024041 A0A8C2V8E0;A0A8C2VB04 MODEL AGCD01031639;AGCD01031640;AGCD01031641;AGCD01031642;AGCD01031643;AGCD01031644;AGCD01031645;AGCD01031646;AGCD01031647;AGCD01031648;AGCD01031649;GBCE01009599;XM_005388286;XM_005388287;XM_005388293;XM_005388294;XM_013516196;XM_013516197;XM_013516198;XM_013516199;XM_013516200;XM_013516201 XP_005388343;XP_005388344;XP_005388350;XP_005388351;XP_013371650;XP_013371651;XP_013371652;XP_013371653;XP_013371654;XP_013371655 chromodomain-helicase-DNA-binding protein 9 protein-coding ENSCLAG00000007137 NW_004955433 10900721 11158598 + 8724276 Nr2f2 nuclear receptor subfamily 2 group F member 2 ENCODES a protein that exhibits DNA binding (ortholog); DNA-binding transcription factor activity (ortholog); nuclear receptor activity (ortholog); INVOLVED IN anterior/posterior pattern specification (ortholog); blood vessel morphogenesis (ortholog); female gonad development (ortholog); PARTICIPATES IN forkhead class A signaling pathway; ASSOCIATED WITH 46,XX sex reversal 5 (ortholog); Chemical and Drug Induced Liver Injury (ortholog); congenital diaphragmatic hernia (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955416 24148052 24154406 + 9068941 102024224 A0A8C2VI81;A0A8C2VK66;A0A8C2VMY9 MODEL AGCD01017563;GBDF01304567;GBDI01013703;XM_005381608 XP_005381665 COUP transcription factor 2;nuclear receptor subfamily 2, group F, member 2 APPROVED protein-coding ENSCLAG00000010451 NW_004955416 24141888 24168585 + 8724293 Sfn stratifin ENCODES a protein that exhibits identical protein binding (ortholog); phosphoprotein binding (ortholog); protein kinase binding (ortholog); INVOLVED IN establishment of skin barrier (ortholog); intrinsic apoptotic signaling pathway in response to DNA damage (ortholog); keratinization (ortholog); PARTICIPATES IN insulin responsive facilitative sugar transporter mediated glucose transport pathway; mTOR signaling pathway; phosphatidylinositol 3-kinase-Akt signaling pathway; ASSOCIATED WITH endometrial carcinoma (ortholog); Esophageal Neoplasms (ortholog); esophagus squamous cell carcinoma (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleus (ortholog) NW_004955452 6217519 6218481 + 9068941 102024419 A0A8C2WBM3 MODEL AGCD01044097;GBDJ01006661;XM_005394883 XP_005394940 14-3-3 protein sigma protein-coding ENSCLAG00000018088 NW_004955452 6217698 6218444 + 8724298 Ccdc51 coiled-coil domain containing 51 ENCODES a protein that exhibits mitochondrial ATP-gated potassium channel activity (ortholog); INVOLVED IN cell volume homeostasis (ortholog); mitochondrial potassium ion transmembrane transport (ortholog); potassium ion transmembrane transport (ortholog); ASSOCIATED WITH genetic disease (ortholog); Progressive Microcephaly with Seizures and Cerebral and Cerebellar Atrophy (ortholog); FOUND IN mitochondrial ATP-gated potassium channel complex (ortholog); mitochondrial inner membrane (ortholog); potassium channel complex (ortholog) NW_004955532 500963 509437 - 9068941 102025164 A0A8C2VCC9 MODEL AGCD01070127;GBDK01397852;XM_005410149;XM_005410150;XM_013507608 XP_005410206;XP_005410207;XP_013363062 coiled-coil domain-containing protein 51 protein-coding ENSCLAG00000009171 NW_004955532 500963 509325 - 8724309 Hsf5 heat shock transcription factor 5 ENCODES a protein that exhibits sequence-specific double-stranded DNA binding (ortholog); ASSOCIATED WITH Fanconi anemia complementation group O (ortholog); genetic disease (ortholog); intellectual disability (ortholog) NW_004955451 4564576 4601868 + 9068941 102025309 A0A8C2VT55 MODEL AGCD01043131;AGCD01043132;AGCD01043133;GBDF01053109;GBDF01053111;XM_013519059 XP_013374513 heat shock factor protein 5;heat shock transcription factor family member 5 APPROVED protein-coding ENSCLAG00000011761 NW_004955451 4563770 4599720 + 8724324 Ptpn5 protein tyrosine phosphatase non-receptor type 5 ENCODES a protein that exhibits identical protein binding (ortholog); phosphotyrosine residue binding (ortholog); protein tyrosine phosphatase activity (ortholog); INVOLVED IN exploration behavior (ortholog); negative regulation of MAP kinase activity (ortholog); peptidyl-tyrosine dephosphorylation (ortholog); PARTICIPATES IN dopamine signaling pathway; ASSOCIATED WITH Alzheimer's disease (ortholog); Brain Hypoxia-Ischemia (ortholog); genetic disease (ortholog); FOUND IN axon (ortholog); neuronal cell body (ortholog); perikaryon (ortholog) NW_004955414 33381783 33436974 - 9068941 102025349 A0A8C2W8T4 MODEL AGCD01015805;AGCD01015806;GBDF01076364;XM_005380426;XM_013512076 XP_005380483;XP_013367530 tyrosine-protein phosphatase non-receptor type 5 APPROVED protein-coding ENSCLAG00000016396 NW_004955414 33377322 33437118 - 8724348 Selenot selenoprotein T ENCODES a protein that exhibits thioredoxin-disulfide reductase activity (ortholog); INVOLVED IN cell redox homeostasis (ortholog); cellular oxidant detoxification (ortholog); glucose homeostasis (ortholog); ASSOCIATED WITH genetic disease (ortholog); glycogen storage disease XV (ortholog); FOUND IN endoplasmic reticulum (ortholog); endoplasmic reticulum membrane (ortholog) NW_004955448 1794959 1814282 + 9068941 102025635 A0A8C2YJZ0 MODEL AGCD01041268;AGCD01041269;AGCD01041270;GBDF01082136;XM_013518685 XP_013374139 LOC102025635 APPROVED protein-coding ENSCLAG00000003019 NW_004955448 1795043 1812930 + 8724356 LOC102026023 female-specific lacrimal gland protein-like NW_004955499 3047393 3051411 + 102026023 MODEL AGCD01063451;XM_005406560 XP_005406617 APPROVED protein-coding 8724363 Pard6a par-6 family cell polarity regulator alpha ENCODES a protein that exhibits GTP-dependent protein binding (ortholog); small GTPase binding (ortholog); INVOLVED IN cell-cell junction maintenance (ortholog); centrosome cycle (ortholog); establishment or maintenance of epithelial cell apical/basal polarity (ortholog); PARTICIPATES IN adenosine signaling pathway; insulin signaling pathway; protein kinase C (PKC) signaling pathway; ASSOCIATED WITH autosomal dominant dyskeratosis congenita 6 (ortholog); chromosome 16q22 deletion syndrome (ortholog); genetic disease (ortholog); FOUND IN apical part of cell (ortholog); axonal growth cone (ortholog); bicellular tight junction (ortholog) NW_004955484 9019929 9022561 - 9068941 102026221 A0A8C2V2J8 MODEL AGCD01058403;GBDJ01094443;XM_005403633;XM_005403634;XM_013503955 XP_005403690;XP_005403691;XP_013359409 par-6 partitioning defective 6 homolog alpha;partitioning defective 6 homolog alpha APPROVED protein-coding ENSCLAG00000006485 NW_004955484 9019929 9021995 - 8724376 LOC102026235 chromosome unknown open reading frame, human C12orf54 ASSOCIATED WITH genetic disease (ortholog) NW_004955500 7358057 7376070 + 102026235 A0A8C2UUR4 MODEL AGCD01063916;AGCD01063917;GBDF01008304;XM_013505649;XM_013505650;XM_013505651 XP_013361103;XP_013361104;XP_013361105 LOC102029764 uncharacterized LOC102029764;uncharacterized protein C12orf54 homolog PROVISIONAL protein-coding ENSCLAG00000002462 NW_004955500 7358040 7376148 + 8724386 LOC102026283 aldo-keto reductase family 1 member B10 pseudogene NW_004955404 33377343 33378282 - 102026283 MODEL AGCD01004060 APPROVED pseudo 8724387 Vangl1 VANGL planar cell polarity protein 1 INVOLVED IN pigmentation (ortholog); ASSOCIATED WITH cardiomyopathy (ortholog); catecholaminergic polymorphic ventricular tachycardia (ortholog); catecholaminergic polymorphic ventricular tachycardia 1 (ortholog); FOUND IN lateral plasma membrane (ortholog) NW_004955435 18890995 18933258 + 9068941;7240710 102026789 A0A8C2V886 MODEL AGCD01033415;GBCE01187538;GBDJ01348337;XM_013516531 XP_013371985 vang-like protein 1 protein-coding ENSCLAG00000006270 NW_004955435 18882565 18933258 + 8724412 Cubn cubilin ENCODES a protein that exhibits cargo receptor activity (ortholog); hemoglobin binding (ortholog); identical protein binding (ortholog); INVOLVED IN cobalamin catabolic process (ortholog); cobalamin metabolic process (ortholog); cobalamin transport (ortholog); ASSOCIATED WITH amphetamine abuse (ortholog); Chronic Benign Proteinuria (ortholog); Diabetic Nephropathies (ortholog); FOUND IN apical part of cell (ortholog); apical plasma membrane (ortholog); brush border (ortholog) NW_004955429 10789674 11038297 + 9068941;7240710 102028666 A0A8C2V780 MODEL AGCD01028680;AGCD01028681;AGCD01028682;AGCD01028683;AGCD01028684;AGCD01028685;GBCQ01008980;XM_005386965 XP_005387022 cubilin (intrinsic factor-cobalamin receptor) APPROVED protein-coding ENSCLAG00000007726 NW_004955429 10788959 11038845 + 8724488 Zdhhc13 zinc finger DHHC-type palmitoyltransferase 13 ENCODES a protein that exhibits magnesium ion transmembrane transporter activity (ortholog); palmitoyltransferase activity (ortholog); INVOLVED IN positive regulation of I-kappaB kinase/NF-kappaB signaling (ortholog); ASSOCIATED WITH alopecia (ortholog); amyloidosis (ortholog); Experimental Liver Cirrhosis (ortholog); FOUND IN endoplasmic reticulum (ortholog); Golgi apparatus (ortholog); Golgi membrane (ortholog) NW_004955476 105347 152415 + 9068941 102030416 A0A8C2YIR6 MODEL AGCD01055191;AGCD01055192;GBDF01081063;XM_005401710;XM_005401711;XM_013503007 XP_005401767;XP_005401768;XP_013358461 palmitoyltransferase ZDHHC13;zinc finger DHHC-type containing 13;zinc finger, DHHC-type containing 13 APPROVED protein-coding ENSCLAG00000001261 NW_004955476 105347 154615 + 8724513 Syt5 synaptotagmin 5 ENCODES a protein that exhibits calcium ion binding (ortholog); calcium-dependent phospholipid binding (ortholog); clathrin binding (ortholog); INVOLVED IN regulation of calcium ion-dependent exocytosis (ortholog); ASSOCIATED WITH genetic disease (ortholog); hypertrophic cardiomyopathy (ortholog); nemaline myopathy 5 (ortholog); FOUND IN dense core granule (ortholog); neuron projection (ortholog); neuronal cell body (ortholog) NW_004955567 1018433 1024477 + 9068941 102003705 A0A8C2UND8 MODEL AGCD01074453;GBDF01243336;XM_005413351 XP_005413408 synaptotagmin V;synaptotagmin-5 APPROVED protein-coding ENSCLAG00000000778 NW_004955567 1018433 1024477 + 8724526 Rims3 regulating synaptic membrane exocytosis 3 ENCODES a protein that exhibits transmembrane transporter binding (ortholog); INVOLVED IN calcium-ion regulated exocytosis (ortholog); regulation of membrane potential (ortholog); regulation of synapse organization (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease dominant intermediate C (ortholog); genetic disease (ortholog); FOUND IN glutamatergic synapse (ortholog); postsynaptic cytosol (ortholog) NW_004955537 483717 522053 - 9068941 102003802 A0A8C2YJ88 MODEL AGCD01070866;GBDF01220201;XM_005410577;XM_005410578;XM_005410579 XP_005410634;XP_005410635;XP_005410636 regulating synaptic membrane exocytosis protein 3 protein-coding ENSCLAG00000001965 NW_004955537 489392 522299 - 8724541 LOC102004145 cryptic protein-like NW_004955459 153874 177414 + 102004145 MODEL AGCD01047925;AGCD01047926;GBDF01016700;XM_013521086;XM_013521087;XM_013521088;XM_013521089 XP_013376540;XP_013376541;XP_013376542;XP_013376543 uncharacterized protein LOC102004145 protein-coding 8724552 LOC102004427 KATNB1-like protein 1 NW_004955553 1440942 1443862 - 102004427 MODEL AGCD01072882 APPROVED pseudo 8724553 Kif20a kinesin family member 20A ENCODES a protein that exhibits protein kinase binding (ortholog); INVOLVED IN embryonic cleavage (ortholog); meiotic cell cycle process involved in oocyte maturation (ortholog); microtubule bundle formation (ortholog); ASSOCIATED WITH autosomal dominant intellectual developmental disorder 31 (ortholog); COVID-19 (ortholog); familial adenomatous polyposis 1 (ortholog); FOUND IN chromosome, centromeric region (ortholog); intercellular bridge (ortholog); midbody (ortholog) NW_004955418 2222398 2232775 - 9068941 102004929 A0A8C2V8S8 MODEL AGCD01018753;GBDF01125758;XM_005382123 XP_005382180 kinesin-like protein KIF20A protein-coding ENSCLAG00000008096 NW_004955418 2222398 2232775 - 8724576 Dtx3 deltex E3 ubiquitin ligase 3 INVOLVED IN Notch signaling pathway (ortholog); ASSOCIATED WITH Breast Neoplasms (ortholog); familial melanoma (ortholog); genetic disease (ortholog) NW_004955458 5328723 5334092 + 9068941 102006546 A0A8C2VAB9;A0A8C2VGL3 MODEL AGCD01047476;GBDI01009417;XM_005397398;XM_005397399 XP_005397455;XP_005397456 deltex 3, E3 ubiquitin ligase;deltex homolog 3;probable E3 ubiquitin-protein ligase DTX3 APPROVED protein-coding ENSCLAG00000008560 NW_004955458 5328725 5334092 + 8724588 LOC102007016 2'-5'-oligoadenylate synthase 1-like NW_004955482 9316087 9321788 + 102007016 MODEL AGCD01057564;AGCD01057565;GBBH01096422;GBDI01244956;XM_013503740 XP_013359194 protein-coding 8724600 LOC102008498 interferon-induced GTP-binding protein Mx2-like NW_004955407 35275551 35296838 - 102008498 A0A8C2V270 MODEL AGCD01007736;GBBH01139527;XM_005375727;XM_013504510 XP_005375784;XP_013359964 protein-coding ENSCLAG00000006403 8724624 LOC102008516 epididymal secretory glutathione peroxidase NW_004955465 13787944 13795076 + 9068941 102008516 A0A8C2V9H9 MODEL AGCD01050624;AGCD01050625;XM_005399016 XP_005399073 Gpx5 glutathione peroxidase 5 (epididymal androgen-related protein) APPROVED protein-coding ENSCLAG00000008444 8724632 LOC102008614 cytochrome c oxidase subunit 7A1, mitochondrial ASSOCIATED WITH Brugada syndrome 5 (ortholog); dilated cardiomyopathy (ortholog); genetic disease (ortholog) NW_004955468 2442819 2445169 + 9068941 102008614 A0A8C2VQU6;A0A8C2VSN7 MODEL AGCD01051817;GBCQ01010676;XM_005399919 XP_005399976 APPROVED protein-coding ENSCLAG00000012530 NW_004955468 2442819 2445169 + 8724640 Cracr2b calcium release activated channel regulator 2B INVOLVED IN regulation of store-operated calcium entry (ortholog); store-operated calcium entry (ortholog); ASSOCIATED WITH delta beta-thalassemia (ortholog); developmental and epileptic encephalopathy (ortholog); early infantile epileptic encephalopathy (ortholog); FOUND IN cytoplasm (ortholog) NW_004955476 11299353 11304105 - 9068941 102008722 A0A8C2UTK0 MODEL AGCD01055448;GBCB01131476;XM_013502948;XM_013502949;XM_013502950;XM_013502951;XM_013502952;XM_013502953;XM_013502954;XM_013502955;XM_013502956;XM_013502957 XP_013358402;XP_013358403;XP_013358404;XP_013358405;XP_013358406;XP_013358407;XP_013358408;XP_013358409;XP_013358410;XP_013358411 Efcab4a EF-hand calcium binding domain 4A;EF-hand calcium-binding domain-containing protein 4A APPROVED protein-coding ENSCLAG00000002228 NW_004955476 11299614 11303657 - 8724654 LOC102008964 zinc finger CCHC-type and RNA-binding motif-containing protein 1 NW_004955426 18643581 18647670 - 102008964 MODEL AGCD01026526;AGCD01026527;GBCC01039405;XM_005386263 XP_005386320 APPROVED protein-coding 8724659 LOC102009784 small proline-rich protein 2E NW_004955592 315272 316198 + 9068941 102009784 A0A8C2URI1 MODEL AGCD01076302;XM_005414611 XP_005414668 Sprr2e APPROVED protein-coding ENSCLAG00000002946 8724662 Nmrk2 nicotinamide riboside kinase 2 ENCODES a protein that exhibits ribosylnicotinamide kinase activity (ortholog); ribosylnicotinate kinase activity (ortholog); INVOLVED IN negative regulation of myoblast differentiation (ortholog); PARTICIPATES IN nicotinamide adenine dinucleotide biosynthesis, the salvage pathway; ASSOCIATED WITH amenorrhea (ortholog); genetic disease (ortholog); FOUND IN intracellular membrane-bounded organelle (ortholog); nucleoplasm (ortholog); plasma membrane (ortholog) NW_004955495 5749303 5754889 + 9068941 102010706 A0A8C2VBK7 MODEL AGCD01062024;AGCD01062025;GBDF01182019;XM_005405892;XM_005405893;XM_005405894;XM_005405896;XM_005405897;XM_005405899;XM_005405900;XM_005405901;XM_013505253 XP_005405949;XP_005405950;XP_005405951;XP_005405953;XP_005405954;XP_005405956;XP_005405957;XP_005405958;XP_013360707 protein-coding ENSCLAG00000008930 NW_004955495 5749309 5756367 + 8724705 Nxt2 nuclear transport factor 2 like export factor 2 ASSOCIATED WITH autistic disorder (ortholog); Charcot-Marie-Tooth disease type X (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nuclear RNA export factor complex (ortholog) NW_004955490 6276791 6283768 - 9068941 102011209 A0A8C2ULN1 MODEL AGCD01060218;GBDK01117586;XM_005404666;XM_005404667;XM_005404668;XM_005404669 XP_005404723;XP_005404724;XP_005404725;XP_005404726 NTF2-related export protein 2;nuclear transport factor 2-like export factor 2 APPROVED protein-coding ENSCLAG00000001175 NW_004955490 6276756 6283808 - 8724722 LOC102011392 uncharacterized LOC102011392 NW_004955404 682584 698750 + 102011392 MODEL AGCD01003207;XR_259283 ncrna 8724731 Mtif2 mitochondrial translational initiation factor 2 ASSOCIATED WITH genetic disease (ortholog); FOUND IN mitochondrion (ortholog); nucleoplasm (ortholog) NW_004955424 27796213 27823106 + 9068941 102011679 A0A8C2V8W0 MODEL AGCD01025129;AGCD01025130;AGCD01025131;GBDF01083913;XM_005385789;XM_005385790;XM_005385792;XM_005385793;XM_005385794;XM_013514615;XM_013514616 XP_005385846;XP_005385847;XP_005385849;XP_005385850;XP_005385851;XP_013370069;XP_013370070 translation initiation factor IF-2, mitochondrial protein-coding ENSCLAG00000007900 NW_004955424 27795831 27823106 + 8724761 LOC102011964 40S ribosomal protein S3a pseudogene NW_004955410 19855730 19856950 - 102011964 MODEL AGCD01011031 APPROVED pseudo 8724762 Ddx5 DEAD-box helicase 5 ENCODES a protein that exhibits calcium-dependent protein binding (ortholog); calmodulin binding (ortholog); enzyme binding (ortholog); INVOLVED IN alternative mRNA splicing, via spliceosome (ortholog); androgen receptor signaling pathway (ortholog); BMP signaling pathway (ortholog); PARTICIPATES IN estrogen signaling pathway; ASSOCIATED WITH Developmental Disabilities (ortholog); endometriosis (ortholog); genetic disease (ortholog); FOUND IN catalytic step 2 spliceosome (ortholog); nuclear speck (ortholog); nucleolus (ortholog) NW_004955478 7367049 7375043 + 9068941 102012756 A0A8C2V4N0 MODEL AGCD01055958;AGCD01055959;GBDF01007791;XM_013503173 XP_013358627 DEAD (Asp-Glu-Ala-Asp) box helicase 5;probable ATP-dependent RNA helicase DDX5 APPROVED protein-coding ENSCLAG00000006874 NW_004955478 7366956 7376358 + 8724783 Mapt microtubule associated protein tau ENCODES a protein that exhibits apolipoprotein binding (ortholog); DNA binding (ortholog); enzyme binding (ortholog); INVOLVED IN adult walking behavior (ortholog); amyloid fibril formation (ortholog); axo-dendritic transport (ortholog); PARTICIPATES IN Reelin signaling pathway; ASSOCIATED WITH Alzheimer's disease (ortholog); Animal Disease Models (ortholog); anxiety disorder (ortholog); FOUND IN axolemma (ortholog); axon (ortholog); axonal growth cone (ortholog) NW_004955478 10222439 10271439 - 9068941;7240710 102013826 A0A8C2YLY4;A0A8C2YLY5 MODEL AGCD01056125;AGCD01056126;AGCD01056127;AGCD01056128;AGCD01056129;GBCQ01004301;XM_005402262;XM_005402263;XM_005402264;XM_005402265;XM_005402266;XM_005402267;XM_013503144;XM_013503145;XM_013503146;XM_013503147;XM_013503148;XM_013503149;XM_013503150 XP_005402319;XP_005402320;XP_005402321;XP_005402322;XP_005402323;XP_005402324;XP_013358598;XP_013358599;XP_013358600;XP_013358601;XP_013358602;XP_013358603;XP_013358604 microtubule-associated protein tau APPROVED protein-coding ENSCLAG00000005870 NW_004955478 10225823 10271442 - 8724809 Pou2af2 POU class 2 homeobox associating factor 2 ENCODES a protein that exhibits sequence-specific DNA binding (ortholog); transcription coactivator activity (ortholog); ASSOCIATED WITH ataxia telangiectasia (ortholog); Chromosome 11, Partial Trisomy 11q (ortholog); intellectual disability (ortholog); FOUND IN nucleus (ortholog) NW_004955412 13076854 13079095 + 102015300 MODEL AGCD01012827;AGCD01012828;GBCE01163326;XM_013511187 XP_013366641 CUNH11orf53;LOC102015300 chromosome unknown C11orf53 homolog;chromosome unknown open reading frame, human C11orf53;uncharacterized protein C11orf53 homolog APPROVED protein-coding 8724815 LOC102016414 uncharacterized LOC102016414 NW_004955527 3800944 3816667 - 102016414 MODEL AGCD01069485;AGCD01069486;GBDF01176376;XR_264675 ncrna 8724820 Saxo5 stabilizer of axonemal microtubules 5 ASSOCIATED WITH hereditary spastic paraplegia 39 (ortholog); mucolipidosis type IV (ortholog) NW_004955563 1723768 1729831 - 102016531 A0A8C2UQ78;A0A8C2UQ81;A0A8C2URR4 MODEL AGCD01074159;AGCD01074160;GBDF01087755;GBDF01087757;XM_013509149 XP_013364603 LOC102016531;Tex45 chromosome unknown open reading frame, human C19orf45;testis expressed 45;uncharacterized protein C19orf45 homolog APPROVED protein-coding ENSCLAG00000003025 NW_004955563 1703416 1745996 - 8724834 LOC102016779 uncharacterized LOC102016779 NW_004955455 4292626 4309360 - 102016779 MODEL AGCD01045673;GBDF01074795;XR_262828 ncrna 8724839 Cks2 CDC28 protein kinase regulatory subunit 2 ENCODES a protein that exhibits chromatin binding (ortholog); INVOLVED IN fibroblast proliferation (ortholog); meiosis I (ortholog); mitotic cell cycle phase transition (ortholog); ASSOCIATED WITH COVID-19 (ortholog); polycystic ovary syndrome (ortholog) NW_004955515 2731210 2736296 - 9068941 102017372 A0A8C2UIH9 MODEL AGCD01067260;GBDF01007976;XM_005408880 XP_005408937 cyclin-dependent kinases regulatory subunit 2 protein-coding ENSCLAG00000000823 NW_004955515 2730148 2736539 - 8724846 Flot2 flotillin 2 ENCODES a protein that exhibits ionotropic glutamate receptor binding (ortholog); protease binding (ortholog); INVOLVED IN anterograde dendritic transport (ortholog); negative regulation of amyloid precursor protein catabolic process (ortholog); negative regulation of gene expression (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN acrosomal membrane (ortholog); adherens junction (ortholog); apical plasma membrane (ortholog) NW_004955481 4276847 4298523 + 9068941 102018287 A0A8C2VY61;A0A8C2W0J7 MODEL AGCD01056933;GBBH01061429;XM_005402703;XM_005402704;XM_005402705;XM_005402707;XM_013503420 XP_005402760;XP_005402761;XP_005402762;XP_005402764;XP_013358874 flotillin-2 protein-coding ENSCLAG00000014550 NW_004955481 4276860 4298523 + 8724873 CUNH17orf50 chromosome unknown C17orf50 homolog ASSOCIATED WITH genetic disease (ortholog) NW_004955481 10202477 10206606 + 102018728 A0A8C2VM83;A0A8C2VPY8 MODEL AGCD01057138;GBDK01256624;XM_005402884 XP_005402941 LOC102018728 chromosome unknown open reading frame, human C17orf50;uncharacterized protein C17orf50 homolog APPROVED protein-coding ENSCLAG00000011018 NW_004955481 10203485 10206319 + 8724884 LOC102018973 uncharacterized LOC102018973 NW_004955533 929825 934774 + 102018973 MODEL AGCD01070335;GBDI01248267;XR_001232039;XR_001232040;XR_001232041 ncrna 8724889 Olig3 oligodendrocyte transcription factor 3 ENCODES a protein that exhibits sequence-specific double-stranded DNA binding (ortholog); INVOLVED IN negative regulation of transcription by RNA polymerase II (ortholog); regulation of gene expression (ortholog); spinal cord motor neuron cell fate specification (ortholog); ASSOCIATED WITH familial Behcet-like autoinflammatory syndrome (ortholog); genetic disease (ortholog); Nontuberculous Mycobacterium Infections (ortholog) NW_004955436 21929086 21929904 + 9068941 102019319 A0A8C2W615 MODEL AGCD01034080;XM_013516599 XP_013372053 protein-coding ENSCLAG00000017843 NW_004955436 21929086 21929904 + 8724894 Slc43a2 solute carrier family 43 member 2 ENCODES a protein that exhibits L-amino acid transmembrane transporter activity (ortholog); L-isoleucine transmembrane transporter activity (ortholog); L-leucine transmembrane transporter activity (ortholog); INVOLVED IN isoleucine transport (ortholog); L-amino acid transport (ortholog); leucine transport (ortholog); ASSOCIATED WITH Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog); FOUND IN basolateral plasma membrane (ortholog); plasma membrane (ortholog) NW_004955481 1550289 1597213 + 9068941 102019390 A0A8C2VD63;A0A8C2VHC6 MODEL AGCD01056836;AGCD01056837;AGCD01056838;GBDF01222975;XM_005402617;XM_005402618;XM_013503413 XP_005402674;XP_005402675;XP_013358867 large neutral amino acids transporter small subunit 4;solute carrier family 43 (amino acid system L transporter), member 2 APPROVED protein-coding ENSCLAG00000008904 NW_004955481 1550289 1595942 + 8724917 Nelfa negative elongation factor complex member A ENCODES a protein that exhibits chromatin binding (ortholog); molecular adaptor activity (ortholog); INVOLVED IN negative regulation of transcription elongation by RNA polymerase II (ortholog); positive regulation of histone H3-K4 methylation (ortholog); positive regulation of transcription by RNA polymerase II (ortholog); PARTICIPATES IN RNA polymerase II transcription elongation pathway; ASSOCIATED WITH cherubism (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); NELF complex (ortholog); nuclear body (ortholog) NW_004955514 1162993 1173278 - 9068941 102020367 A0A8C2VT19 MODEL AGCD01067037;GBCE01098373;XM_005408718 XP_005408775 negative elongation factor A protein-coding ENSCLAG00000012299 NW_004955514 1162993 1173278 - 8724932 LOC102021426 E3 ubiquitin-protein ligase RING2 pseudogene NW_004955409 37557200 37558907 - 102021426 MODEL AGCD01010529 APPROVED pseudo 8724933 Crnkl1 crooked neck pre-mRNA splicing factor 1 ENCODES a protein that exhibits RNA binding (ortholog); INVOLVED IN cellular response to brain-derived neurotrophic factor stimulus (ortholog); cellular response to leukemia inhibitory factor (ortholog); cerebral cortex development (ortholog); PARTICIPATES IN spliceosome pathway; ASSOCIATED WITH basal cell carcinoma (ortholog); genetic disease (ortholog); melanoma (ortholog); FOUND IN catalytic step 2 spliceosome (ortholog); nucleus (ortholog); spliceosomal complex (ortholog) NW_004955415 28158351 28171335 - 9068941 102021756 A0A8C2VXE4 MODEL AGCD01016638;GBDJ01385616;XM_005380946 XP_005381003 crooked neck pre-mRNA splicing factor-like 1;crooked neck-like protein 1 APPROVED protein-coding ENSCLAG00000013859 NW_004955415 28158351 28172055 - 8724955 Mark1 microtubule affinity regulating kinase 1 ENCODES a protein that exhibits ATP binding (ortholog); magnesium ion binding (ortholog); phosphatidic acid binding (ortholog); INVOLVED IN cytoskeleton organization (ortholog); establishment of mitochondrion localization (ortholog); intracellular signal transduction (ortholog); ASSOCIATED WITH autistic disorder (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); cytoskeleton (ortholog); dendrite (ortholog) NW_004955520 3087581 3205525 - 9068941 102022218 A0A8C2UQJ6 MODEL AGCD01068094;AGCD01068095;AGCD01068096;GBBH01209445;GBDI01178812;XM_005409266 XP_005409323 MAP/microtubule affinity-regulating kinase 1;serine/threonine-protein kinase MARK1 APPROVED protein-coding ENSCLAG00000003109 NW_004955520 3086887 3205525 - 8724977 Gad1 glutamate decarboxylase 1 ENCODES a protein that exhibits glutamate binding (ortholog); glutamate decarboxylase activity (ortholog); identical protein binding (ortholog); INVOLVED IN gamma-aminobutyric acid biosynthetic process (ortholog); glutamate catabolic process (ortholog); locomotory exploration behavior (ortholog); PARTICIPATES IN 2-hydroxyglutaric aciduria pathway; beta-alanine metabolic pathway; Canavan disease pathway; ASSOCIATED WITH anxiety disorder (ortholog); autistic disorder (ortholog); bipolar disorder (ortholog); FOUND IN axon (ortholog); axon terminus (ortholog); cell cortex (ortholog) NW_004955449 3964006 4001850 - 9068941;7240710 102022653 A0A8C2V3I6 MODEL AGCD01041872;GBDF01110754;XM_005393242 XP_005393299 glutamate decarboxylase 1 (brain, 67kDa) APPROVED protein-coding ENSCLAG00000006454 NW_004955449 3963705 4001850 - 8724998 LOC102023080 60S ribosomal protein L13 pseudogene NW_004955443 19809334 19809985 - 102023080 MODEL AGCD01038635 APPROVED pseudo 8724999 Naa11 N-alpha-acetyltransferase 11, NatA catalytic subunit ENCODES a protein that exhibits peptide alpha-N-acetyltransferase activity (ortholog); INVOLVED IN N-terminal protein amino acid acetylation (ortholog); ASSOCIATED WITH genetic disease (ortholog); Kabuki Syndrome 1 (ortholog); FOUND IN centrosome (ortholog); cytosol (ortholog); Golgi apparatus (ortholog) NW_004955433 3653046 3662924 - 9068941 102023729 A0A8C2UX33 MODEL AGCD01031432;GBDF01161781;XM_005388215 XP_005388272 N(alpha)-acetyltransferase 11, NatA catalytic subunit;N-alpha-acetyltransferase 11 APPROVED protein-coding ENSCLAG00000004971 NW_004955433 3662098 3662787 - 8725005 LOC102025149 olfactory receptor 1013-like NW_004955511 1785957 1786877 + 9068941 102025149 MODEL AGCD01066380;XM_005408244 XP_005408301 APPROVED protein-coding 8725008 Slc25a19 solute carrier family 25 member 19 ENCODES a protein that exhibits deoxynucleotide transmembrane transporter activity (ortholog); thiamine pyrophosphate transmembrane transporter activity (ortholog); INVOLVED IN deoxynucleotide transport (ortholog); thiamine diphosphate biosynthetic process (ortholog); thiamine pyrophosphate transmembrane transport (ortholog); ASSOCIATED WITH Amish Lethal Microcephaly (ortholog); genetic disease (ortholog); microcephaly (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrion (ortholog) NW_004955553 2134715 2160777 - 9068941;7240710 102025729 A0A8C2YJQ7 MODEL AGCD01072924;AGCD01072925;AGCD01072926;AGCD01072927;AGCD01072928;AGCD01072929;GBBH01228703;XM_005412291;XM_005412292;XM_013508653 XP_005412348;XP_005412349;XP_013364107 mitochondrial thiamine pyrophosphate carrier;solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 APPROVED protein-coding ENSCLAG00000002668 8725027 Tead4 TEA domain transcription factor 4 ENCODES a protein that exhibits DNA binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); DNA-binding transcription factor activity (ortholog); INVOLVED IN blastocyst formation (ortholog); cell fate commitment (ortholog); cell fate specification (ortholog); ASSOCIATED WITH genetic disease (ortholog); Hyperphosphatemic Familial Tumoral Calcinosis 1 (ortholog); FOUND IN cytoplasm (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955429 18497223 18552504 + 9068941 102025932 A0A8C2VLV9;A0A8C2VS95 MODEL AGCD01028915;GBCB01007409;XM_005387130;XM_013515542;XM_013515543;XM_013515544;XM_013515545;XM_013515546;XM_013515547 XP_005387187;XP_013370996;XP_013370997;XP_013370998;XP_013370999;XP_013371000;XP_013371001 TEA domain family member 4;transcriptional enhancer factor TEF-3 APPROVED protein-coding ENSCLAG00000012070 NW_004955429 18497223 18552504 + 8725053 LOC102026323 serine/threonine-protein kinase Kist pseudogene NW_004955418 11768644 11789023 - 102026323 MODEL AGCD01019013 APPROVED pseudo 8725054 Ap2m1 adaptor related protein complex 2 subunit mu 1 ENCODES a protein that exhibits disordered domain specific binding (ortholog); low-density lipoprotein particle receptor binding (ortholog); signal sequence binding (ortholog); INVOLVED IN clathrin-dependent endocytosis (ortholog); negative regulation of protein localization to plasma membrane (ortholog); positive regulation of receptor internalization (ortholog); PARTICIPATES IN Arf family mediated signaling pathway; clathrin-dependent synaptic vesicle endocytosis; ASSOCIATED WITH 3-Methylcrotonyl-CoA carboxylase 1 deficiency (ortholog); autistic disorder (ortholog); Autosomal Dominant Intellectual Developmental Disorder 60 (ortholog); FOUND IN AP-2 adaptor complex (ortholog); clathrin-coated pit (ortholog); extrinsic component of presynaptic endocytic zone membrane (ortholog) NW_004955420 23281720 23290430 - 9068941 102026752 A0A8C2VXD5;A0A8C2VZ11;A0A8C2W1Q0 MODEL AGCD01021240;GBCB01006751;XM_005383348;XM_005383349 XP_005383405;XP_005383406 AP-2 complex subunit mu;adaptor related protein complex 2 mu 1 subunit;adaptor-related protein complex 2, mu 1 subunit APPROVED protein-coding ENSCLAG00000014315 NW_004955420 23281720 23290430 - 8725075 LOC102027709 uncharacterized LOC102027709 NW_004955404 7575132 7581168 + 102027709 MODEL AGCD01003341;GBDF01145467;XR_259300 ncrna 8725080 Nfatc4 nuclear factor of activated T cells 4 ENCODES a protein that exhibits DNA-binding transcription factor activity (ortholog); DNA-binding transcription factor activity, RNA polymerase II-specific (ortholog); DNA-binding transcription repressor activity, RNA polymerase II-specific (ortholog); INVOLVED IN brain-derived neurotrophic factor receptor signaling pathway (ortholog); branching involved in blood vessel morphogenesis (ortholog); calcineurin-NFAT signaling cascade (ortholog); PARTICIPATES IN calcineurin signaling pathway; nuclear factor of activated T-cells signaling pathway; ASSOCIATED WITH Brain-Lung-Thyroid Syndrome (ortholog); Chemical and Drug Induced Liver Injury (ortholog); dilated cardiomyopathy (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nuclear speck (ortholog) NW_004955409 35931208 35941555 - 9068941 102027821 A0A8C2VKW8 MODEL AGCD01010436;AGCD01010437;GBDK01061586;XM_005377004;XM_005377005 XP_005377061;XP_005377062 nuclear factor of activated T-cells 4;nuclear factor of activated T-cells, cytoplasmic 4;nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 4 APPROVED protein-coding ENSCLAG00000011705 NW_004955409 35931173 35940696 - 8725099 Dbn1 drebrin 1 ENCODES a protein that exhibits actin filament binding (ortholog); cytoskeletal motor inhibitor activity (ortholog); cytoskeletal protein binding (ortholog); INVOLVED IN actin filament organization (ortholog); cell communication by chemical coupling (ortholog); cell communication by electrical coupling (ortholog); ASSOCIATED WITH Alzheimer's disease (ortholog); cognitive disorder (ortholog); Down syndrome (ortholog); FOUND IN actin cytoskeleton (ortholog); actin filament (ortholog); asymmetric synapse (ortholog) NW_004955408 29695442 29705417 - 9068941 102027948 A0A8C2W1Q3;A0A8C2W475 MODEL AGCD01008766;AGCD01008767;GBBH01209235;GBCB01098197;XM_013506526 XP_013361980 drebrin protein-coding ENSCLAG00000015046 NW_004955408 29696266 29705416 - 8725117 Rftn1 raftlin, lipid raft linker 1 ENCODES a protein that exhibits double-stranded RNA binding (ortholog); INVOLVED IN B cell receptor signaling pathway (ortholog); dsRNA transport (ortholog); membrane raft assembly (ortholog); ASSOCIATED WITH 3p deletion syndrome (ortholog); genetic disease (ortholog); glaucoma (ortholog); FOUND IN cytoplasm (ortholog); endosome (ortholog); membrane raft (ortholog) NW_004955430 8605057 8801187 - 9068941 102028668 A0A8C2VGV1 MODEL AGCD01029390;AGCD01029391;AGCD01029392;AGCD01029393;GBDF01187691;GBDJ01316097;XM_013515694 XP_013371148 raftlin protein-coding ENSCLAG00000010603 NW_004955430 8603401 8779896 - 8725131 LOC102029002 uncharacterized LOC102029002 NW_004955435 12846623 12859818 + 102029002 MODEL AGCD01033169;AGCD01033170;GBDF01276953;XR_261683 ncrna 8725136 Ankrd34a ankyrin repeat domain 34A ASSOCIATED WITH Breast Neoplasms (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog) NW_004955568 130062 134841 + 9068941 102029568 A0A8C2UME8 MODEL AGCD01074503;GBCB01063737;XM_005413420;XM_005413421 XP_005413477;XP_005413478 ankyrin repeat domain-containing protein 34A protein-coding ENSCLAG00000000448 NW_004955568 131259 134841 + 8725146 Spef1 sperm flagellar 1 ENCODES a protein that exhibits actin binding (ortholog); microtubule binding (ortholog); INVOLVED IN axonemal central apparatus assembly (ortholog); cilium movement (ortholog); filopodium assembly (ortholog); ASSOCIATED WITH genetic disease (ortholog); Huntington's disease-like 1 (ortholog); Inosine Triphosphatase Deficiency (ortholog); FOUND IN 9+2 motile cilium (ortholog); apical plasma membrane (ortholog); axonemal central apparatus (ortholog) NW_004955415 14620593 14626049 - 9068941 102030067 A0A8C2VTZ7 MODEL AGCD01016301;GBDI01001315;XM_005380802;XM_013512284 XP_005380859;XP_013367738 sperm flagellar protein 1 protein-coding ENSCLAG00000013471 NW_004955415 14620593 14626049 - 8725157 Cenpq centromere protein Q INVOLVED IN metaphase plate congression (ortholog); positive regulation of protein localization to kinetochore (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN actin cytoskeleton (ortholog); nucleoplasm (ortholog) NW_004955410 33463041 33480573 - 9068941 102003524 A0A8C2YNN0 MODEL AGCD01011371;GBDJ01369703;XM_005377535 XP_005377592 protein-coding ENSCLAG00000008256 NW_004955410 33464976 33476609 - 8725170 Tesk2 testis associated actin remodelling kinase 2 ENCODES a protein that exhibits protein serine/threonine kinase activity (ortholog); INVOLVED IN actin cytoskeleton organization (ortholog); focal adhesion assembly (ortholog); protein phosphorylation (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease dominant intermediate C (ortholog); developmental and epileptic encephalopathy (ortholog); early infantile epileptic encephalopathy (ortholog); FOUND IN nuclear body (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955464 12789493 12924077 + 9068941 102003634 A0A8C2V7L3;A0A8C2YNA4;A0A8C2YNA5 MODEL AGCD01050228;AGCD01050229;AGCD01050230;AGCD01050231;AGCD01050232;AGCD01050233;AGCD01050234;AGCD01050235;AGCD01050236;AGCD01050237;AGCD01050238;AGCD01050239;AGCD01050240;GBCQ01123838;GBDF01044666;XM_005398714 XP_005398771 dual specificity testis-specific protein kinase 2;testis-specific kinase 2 APPROVED protein-coding ENSCLAG00000007745 NW_004955464 12815226 12924930 + 8725192 Ttc24 tetratricopeptide repeat domain 24 ASSOCIATED WITH Charcot-Marie-Tooth disease type 2 (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog) NW_004955545 2670629 2679093 + 102003907 A0A8C2UVW6 MODEL AGCD01071915;GBBH01143366;XM_005415343;XM_013508312;XM_013508313;XM_013508314;XM_013508315;XM_013508316;XM_013508317;XM_013508318;XM_013508319;XM_013508320 XP_005415400;XP_013363766;XP_013363767;XP_013363768;XP_013363769;XP_013363770;XP_013363771;XP_013363772;XP_013363773;XP_013363774 tetratricopeptide repeat protein 24 protein-coding ENSCLAG00000002793 8725206 Lrrc30 leucine rich repeat containing 30 ASSOCIATED WITH chromosome 18p deletion syndrome (ortholog); genetic disease (ortholog); intellectual disability (ortholog) NW_004955402 4174990 4178170 - 102004214 A0A8C2W871 MODEL AGCD01000113;GBCB01044200;XM_005372621 XP_005372678 leucine-rich repeat-containing protein 30 protein-coding ENSCLAG00000017849 NW_004955402 4175557 4176462 - 8725211 LOC102005472 CWF19-like protein 2 NW_004955481 1830281 1834787 + 102005472 MODEL AGCD01056855 APPROVED pseudo 8725212 Sugp2 SURP and G-patch domain containing 2 ASSOCIATED WITH genetic disease (ortholog); Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 (ortholog); progressive myoclonus epilepsy 8 (ortholog); FOUND IN nuclear body (ortholog); nucleoplasm (ortholog) NW_004955524 2710656 2731849 + 9068941 102005959 A0A8C2VNI7 MODEL AGCD01068830;GBDF01006925;GBDF01006928;XM_013507220 XP_013362674 SURP and G patch domain containing 2;SURP and G-patch domain-containing protein 2 APPROVED protein-coding ENSCLAG00000011375 NW_004955524 2710656 2732203 + 8725229 Slc5a7 solute carrier family 5 member 7 ENCODES a protein that exhibits choline binding (ortholog); choline transmembrane transporter activity (ortholog); choline:sodium symporter activity (ortholog); INVOLVED IN acetylcholine biosynthetic process (ortholog); choline transport (ortholog); in utero embryonic development (ortholog); PARTICIPATES IN acetylcholine signaling pathway via muscarinic acetylcholine receptor; acetylcholine signaling pathway via nicotinic acetylcholine receptor; ASSOCIATED WITH asthma (ortholog); Charcot-Marie-Tooth disease (ortholog); Charcot-Marie-Tooth disease type 2 (ortholog); FOUND IN apical plasma membrane (ortholog); axon (ortholog); clathrin-coated endocytic vesicle (ortholog) NW_004955470 11673491 11694404 + 9068941;7240710 102006334 A0A8C2VCJ5 MODEL AGCD01052897;GBBH01014798;XM_005400796 XP_005400853 high affinity choline transporter 1;solute carrier family 5 (sodium/choline cotransporter), member 7 APPROVED protein-coding ENSCLAG00000009368 NW_004955470 11673465 11697163 + 8725240 Usp32 ubiquitin specific peptidase 32 ENCODES a protein that exhibits cysteine-type deubiquitinase activity (ortholog); ASSOCIATED WITH genetic disease (ortholog); Joubert syndrome (ortholog); megacolon (ortholog); FOUND IN cytosol (ortholog); Golgi apparatus (ortholog) NW_004955451 1511687 1678546 - 9068941 102007490 A0A8C2VS49;A0A8C2VX80 MODEL AGCD01042972;AGCD01042973;AGCD01042974;AGCD01042975;AGCD01042976;GBDK01186069;XM_005393962;XM_013519383 XP_005394019;XP_013374837 ubiquitin carboxyl-terminal hydrolase 32 protein-coding ENSCLAG00000012909 8725278 Kif21b kinesin family member 21B INVOLVED IN brain development (ortholog); corpus callosum development (ortholog); ASSOCIATED WITH familial adult myoclonic epilepsy 5 (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog) NW_004955406 37139168 37187543 - 9068941 102008285 A0A8C2VIK9;A0A8C2VQJ3 MODEL AGCD01006571;GBDF01161913;XM_005375156;XM_005375158;XM_013522093;XR_001236847;XR_001236848;XR_001236849;XR_001236851;XR_001236852 XP_005375213;XP_005375215;XP_013377547 kinesin-like protein KIF21B protein-coding ENSCLAG00000011048 NW_004955406 37139168 37187543 - 8725329 Golph3l golgi phosphoprotein 3 like ENCODES a protein that exhibits phosphatidylinositol-4-phosphate binding (ortholog); INVOLVED IN Golgi organization (ortholog); positive regulation of protein secretion (ortholog); ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); immunodeficiency 42 (ortholog); FOUND IN cytosol (ortholog); Golgi apparatus (ortholog) NW_004955413 154696 183657 + 9068941 102008297 A0A8C2VR32 MODEL AGCD01013440;AGCD01013441;AGCD01013442;AGCD01013443;GBDF01221489;XM_005378663;XM_005378664;XM_013511413 XP_005378720;XP_005378721;XP_013366867 golgi phosphoprotein 3-like APPROVED protein-coding ENSCLAG00000013290 NW_004955413 150864 183657 + 8725341 Qtrt1 queuine tRNA-ribosyltransferase catalytic subunit 1 ENCODES a protein that exhibits protein heterodimerization activity (ortholog); protein homodimerization activity (ortholog); queuine tRNA-ribosyltransferase activity (ortholog); INVOLVED IN tRNA-guanine transglycosylation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); mitochondrion (ortholog); nucleus (ortholog) NW_004955495 1851861 1857599 + 9068941 102008955 A0A8C2VEA1 MODEL AGCD01061735;AGCD01061736;GBCE01028382;XM_005405610 XP_005405667 queuine tRNA-ribosyltransferase;queuine tRNA-ribosyltransferase 1 APPROVED protein-coding ENSCLAG00000009859 NW_004955495 1851995 1857527 + 8725356 LOC102009610 dnaJ homolog subfamily C member 25 NW_004955419 15664786 15684889 - 9068941 102009610 A0A8C2VIQ5 MODEL AGCD01020086;AGCD01020087;GBBH01057437;GBDF01120670;XM_013513302 XP_013368756 Dnajc25 DnaJ (Hsp40) homolog, subfamily C , member 25 APPROVED protein-coding ENSCLAG00000011086 NW_004955419 15662961 15670451 - 8725364 Irx5 iroquois homeobox 5 ENCODES a protein that exhibits sequence-specific double-stranded DNA binding (ortholog); INVOLVED IN cell development (ortholog); embryonic cranial skeleton morphogenesis (ortholog); gonad development (ortholog); ASSOCIATED WITH anodontia (ortholog); Bone Fractures (ortholog); congenital heart disease (ortholog) NW_004955433 12518786 12522744 + 9068941;7240710 102010086 A0A8C2YPS7 MODEL AGCD01031665;AGCD01031666;GBBH01077587;GBDF01227473;XM_013516246 XP_013371700 iroquois-class homeodomain protein IRX-5 protein-coding ENSCLAG00000009884 NW_004955433 12519338 12522118 + 8725372 Samd10 sterile alpha motif domain containing 10 ASSOCIATED WITH developmental and epileptic encephalopathy (ortholog); developmental and epileptic encephalopathy 33 (ortholog); early infantile epileptic encephalopathy (ortholog) NW_004955528 279481 284386 + 102010090 A0A8C2UQK8 MODEL AGCD01069523;AGCD01069524;GBCE01142429;GBDK01284591;XM_013507483 XP_013362937 sterile alpha motif domain-containing protein 10 protein-coding ENSCLAG00000002899 NW_004955528 281932 284386 + 8725381 Coro7 coronin 7 ENCODES a protein that exhibits actin binding (ortholog); INVOLVED IN actin filament organization (ortholog); actin filament polymerization (ortholog); cell migration (ortholog); ASSOCIATED WITH acute megakaryocytic leukemia (ortholog); congenital heart disease (ortholog); epilepsy (ortholog); FOUND IN Golgi apparatus (ortholog); membrane (ortholog); trans-Golgi network (ortholog) NW_004955442 13010032 13084897 + 9068941 102011815 A0A8C2VVH1 MODEL AGCD01037753;AGCD01037754;AGCD01037755;AGCD01037756;AGCD01037757;GBDF01086615;XM_005391296;XM_005391297;XM_005391298 XP_005391353;XP_005391354;XP_005391355 coronin-7 protein-coding ENSCLAG00000013797 NW_004955442 13009977 13084355 + 8725421 Dop1a DOP1 leucine zipper like protein A ASSOCIATED WITH genetic disease (ortholog); hyper IgE syndrome (ortholog); immunodeficiency 23 (ortholog); FOUND IN Golgi-associated vesicle (ortholog) NW_004955411 10836060 10903650 + 9068941 102012294 A0A8C2VL30;A0A8C2VN28;A0A8C2VQR7;A0A8C2VR82 MODEL AGCD01011794;AGCD01011795;AGCD01011796;GBCE01159794;XM_013510756;XM_013510757 XP_013366210;XP_013366211 Dopey1 dopey family member 1 APPROVED protein-coding ENSCLAG00000011249 NW_004955411 10838271 10905256 + 8725467 LOC102012389 PRAME family member 6-like NW_004955618 32981 36268 - 102012389 MODEL AGCD01077283;AGCD01077284;XM_013510147 XP_013365601 protein-coding 8725473 F5 coagulation factor V INVOLVED IN blood circulation (ortholog); blood coagulation (ortholog); proteolysis (ortholog); PARTICIPATES IN acenocoumarol pharmacodynamics pathway; alteplase pharmacodynamics pathway; aminocaproic acid pharmacodynamics pathway; ASSOCIATED WITH 1q24 Deletion Syndrome (ortholog); Acute Liver Failure (ortholog); blood coagulation disease (ortholog); FOUND IN extracellular region (ortholog); extracellular space (ortholog); platelet alpha granule (ortholog) NW_004955462 7695004 7757832 + 9068941;7240710 102012615 A0A8C2VKV0 MODEL AGCD01049309;GBBH01073086;XM_005398188 XP_005398245 coagulation factor V (proaccelerin, labile factor) APPROVED protein-coding ENSCLAG00000011798 NW_004955462 7694939 7757463 + 8725502 Slc22a2 solute carrier family 22 member 2 ENCODES a protein that exhibits acetylcholine transmembrane transporter activity (ortholog); amine transmembrane transporter activity (ortholog); choline transmembrane transporter activity (ortholog); INVOLVED IN acetylcholine transport (ortholog); activation of cysteine-type endopeptidase activity involved in apoptotic process (ortholog); amine transport (ortholog); PARTICIPATES IN amiloride pharmacodynamics pathway; bendroflumethiazide pharmacodynamics pathway; bumetanide pharmacodynamics pathway; ASSOCIATED WITH 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome (ortholog); acute kidney failure (ortholog); end stage renal disease (ortholog); FOUND IN apical plasma membrane (ortholog); basal plasma membrane (ortholog); basolateral plasma membrane (ortholog) NW_004955439 20567241 20608281 + 9068941 102012688 A0A8C2UNR3 MODEL AGCD01036118;AGCD01036119;GBCQ01009150;XM_005390703;XM_005390704 XP_005390760;XP_005390761 solute carrier family 22 (organic cation transporter), member 2 APPROVED protein-coding ENSCLAG00000002562 NW_004955439 20567212 20609105 + 8725521 Cog2 component of oligomeric golgi complex 2 ENCODES a protein that exhibits protein-containing complex binding (ortholog); INVOLVED IN glycosylation (ortholog); Golgi organization (ortholog); intra-Golgi vesicle-mediated transport (ortholog); ASSOCIATED WITH Actin-Accumulation Myopathy (ortholog); congenital disorder of glycosylation type IIq (ortholog); gastrointestinal stromal tumor (ortholog); FOUND IN Golgi stack (ortholog); Golgi transport complex (ortholog) NW_004955492 7879071 7922195 - 9068941 102012767 A0A8C2V2B6 MODEL AGCD01060805;GBCB01056195;XM_005404991 XP_005405048 conserved oligomeric Golgi complex subunit 2 protein-coding ENSCLAG00000005818 NW_004955492 7879548 7922266 - 8725545 LOC102013333 prefoldin subunit 4-like NW_004955530 2262235 2268611 + 102013333 MODEL AGCD01069911 pseudo 8725546 LOC102013444 vomeronasal type-2 receptor 116-like NW_004955524 3567737 3596413 + 102013444 MODEL AGCD01068907;AGCD01068908;AGCD01068909;AGCD01068910;AGCD01068911;AGCD01068912;AGCD01068913;GBDF01116192;XM_005409711 XP_005409768 APPROVED protein-coding 8725555 LOC102015407 uncharacterized protein C12orf45 homolog pseudogene NW_004955419 3283262 3285627 + 102015407 MODEL AGCD01019716 APPROVED pseudo 8725556 LOC102015413 40S ribosomal protein S24 pseudogene NW_004955423 1431836 1432412 + 102015413 MODEL AGCD01023434 APPROVED pseudo 8725557 Eml3 EMAP like 3 ENCODES a protein that exhibits protein self-association (ortholog); INVOLVED IN mitotic metaphase plate congression (ortholog); regulation of mitotic spindle assembly (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual disability (ortholog); leukocyte adhesion deficiency 3 (ortholog); FOUND IN cytoplasm (ortholog); microtubule cytoskeleton (ortholog); midbody (ortholog) NW_004955599 580203 587268 + 9068941 102015584 A0A8C2UNC4 MODEL AGCD01076660;GBCE01002611;XM_013510059;XM_013510060 XP_013365513;XP_013365514 echinoderm microtubule associated protein like 3;echinoderm microtubule-associated protein-like 3 APPROVED protein-coding ENSCLAG00000001662 NW_004955599 580341 587613 + 8725587 Brme1 break repair meiotic recombinase recruitment factor 1 INVOLVED IN double-strand break repair involved in meiotic recombination (ortholog); female meiosis I (ortholog); male meiosis I (ortholog); FOUND IN chromosome (ortholog); site of double-strand break (ortholog) NW_004955415 32652978 32667873 - 9068941 102015838 A0A8C2YTD5 MODEL AGCD01016730;GBBH01138965;XM_013512198;XM_013512199;XM_013512200;XM_013512201;XM_013512202;XM_013512203;XM_013512204;XM_013512205;XM_013512206;XM_013512207 XP_013367652;XP_013367653;XP_013367654;XP_013367655;XP_013367656;XP_013367657;XP_013367658;XP_013367659;XP_013367660;XP_013367661 LOC102015838 chromosome unknown open reading frame, human C19orf57;uncharacterized protein C19orf57 homolog APPROVED protein-coding ENSCLAG00000015002 8725597 Cmtm2 CKLF like MARVEL transmembrane domain containing 2 ASSOCIATED WITH autosomal dominant dyskeratosis congenita 6 (ortholog); cataract 5 multiple types (ortholog); COVID-19 (ortholog) NW_004955433 23140178 23149252 + 9068941 102015883 MODEL AGCD01031952;GBDF01010744;XM_005388510 XP_005388567 CKLF-like MARVEL transmembrane domain containing 2;CKLF-like MARVEL transmembrane domain-containing protein 2 APPROVED protein-coding ENSCLAG00000027341 8725604 Hsph1 heat shock protein family H (Hsp110) member 1 ENCODES a protein that exhibits adenyl-nucleotide exchange factor activity (ortholog); alpha-tubulin binding (ortholog); INVOLVED IN chaperone cofactor-dependent protein refolding (ortholog); negative regulation of apoptotic signaling pathway (ortholog); negative regulation of establishment of protein localization to mitochondrion (ortholog); ASSOCIATED WITH genetic disease (ortholog); human immunodeficiency virus infectious disease (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); microtubule (ortholog) NW_004955431 14680364 14706182 + 9068941 102017369 A0A8C2UWG3;A0A8C2V1P2;A0A8C2YKZ3 MODEL AGCD01030337;AGCD01030338;GBDF01153902;XM_005387734;XM_005387735;XM_013515821;XM_013515822;XM_013515823 XP_005387791;XP_005387792;XP_013371275;XP_013371276;XP_013371277 heat shock 105kDa/110kDa protein 1;heat shock protein 105 kDa APPROVED protein-coding ENSCLAG00000004472 NW_004955431 14680498 14706182 + 8725629 Ptges2 prostaglandin E synthase 2 ENCODES a protein that exhibits DNA binding (ortholog); lyase activity (ortholog); prostaglandin-E synthase activity (ortholog); INVOLVED IN lipid metabolic process (ortholog); positive regulation of DNA-templated transcription (ortholog); secretion (ortholog); PARTICIPATES IN prostaglandin biosynthetic pathway; type II interferon signaling pathway; ASSOCIATED WITH autism spectrum disorder (ortholog); Chemical and Drug Induced Liver Injury (ortholog); congenital disorder of glycosylation Iu (ortholog); FOUND IN cytosol (ortholog); Golgi membrane (ortholog); mitochondrion (ortholog) NW_004955419 608313 612813 + 9068941 102017772 A0A8C2VTF7 MODEL AGCD01019598;GBDF01127195;XM_005382381 XP_005382438 protein-coding ENSCLAG00000012409 NW_004955419 608365 612479 + 8725640 LOC102017874 eukaryotic translation initiation factor 4E type 2 pseudogene NW_004955481 6307199 6311302 - 102017874 MODEL AGCD01057023 APPROVED pseudo 8725641 LOC102018118 protein S100-A10 pseudogene NW_004955507 5694303 5694594 + 102018118 MODEL AGCD01065684 APPROVED pseudo 8725642 Rgs7 regulator of G protein signaling 7 ENCODES a protein that exhibits G-protein alpha-subunit binding (ortholog); G-protein beta-subunit binding (ortholog); GTPase activator activity (ortholog); INVOLVED IN G protein-coupled receptor signaling pathway (ortholog); positive regulation of GTPase activity (ortholog); positive regulation of potassium ion transmembrane transport (ortholog); PARTICIPATES IN dopamine signaling pathway via D1 family of receptors; dopamine signaling pathway via D2 family of receptors; G protein mediated signaling pathway via Galphai family; ASSOCIATED WITH Experimental Seizures (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); dendrite terminus (ortholog); glutamatergic synapse (ortholog) NW_004955406 10669127 11127564 + 9068941 102019356 A0A8C2VFZ8;A0A8C2VG20;A0A8C2VG24;A0A8C2VGE1;A0A8C2VLI3;A0A8C2YQ48;A0A8C2YQ49 MODEL AGCD01005869;AGCD01005870;AGCD01005871;AGCD01005872;AGCD01005873;AGCD01005874;AGCD01005875;AGCD01005876;AGCD01005877;AGCD01005878;AGCD01005879;AGCD01005880;AGCD01005881;AGCD01005882;GBCE01084812;GBCE01084814;XM_005374822;XM_005374823;XM_005374824;XM_005374825;XM_005374826;XM_013520541;XM_013520556 XP_005374879;XP_005374880;XP_005374881;XP_005374882;XP_005374883;XP_013375995;XP_013376010 regulator of G-protein signaling 7 APPROVED protein-coding ENSCLAG00000010387 NW_004955406 10670009 11127757 + 8725675 Niban2 niban apoptosis regulator 2 ENCODES a protein that exhibits transcription coactivator activity (ortholog); INVOLVED IN gonadotropin secretion (ortholog); negative regulation of apoptotic process (ortholog); negative regulation of cell population proliferation (ortholog); ASSOCIATED WITH congenital disorder of glycosylation Iu (ortholog); COVID-19 (ortholog); developmental and epileptic encephalopathy (ortholog); FOUND IN adherens junction (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955419 1089602 1119620 + 9068941 102019918 A0A8C2VLL6 MODEL AGCD01019639;AGCD01019640;AGCD01019641;GBBH01034004;XM_013513097 XP_013368551 Fam129b family with sequence similarity 129 member B;family with sequence similarity 129, member B;niban-like protein 1 APPROVED protein-coding ENSCLAG00000011344 NW_004955419 1072243 1119620 + 8725692 Dnah7 dynein axonemal heavy chain 7 INVOLVED IN cilium movement (ortholog); inner dynein arm assembly (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); autistic disorder (ortholog); epilepsy (ortholog); FOUND IN cilium (ortholog); cytosol (ortholog); inner dynein arm (ortholog) NW_004955403 4189887 4426405 + 9068941 102020073 A0A8C2VV16 MODEL AGCD01001780;AGCD01001781;AGCD01001782;AGCD01001783;AGCD01001784;AGCD01001785;AGCD01001786;GBBH01004459;XM_005373280;XR_001233192 XP_005373337 dynein heavy chain 7, axonemal;dynein, axonemal, heavy chain 7 APPROVED protein-coding ENSCLAG00000014436 NW_004955403 4189887 4426399 + 8725768 LOC102021396 uncharacterized LOC102021396 NW_004955550 1116020 1133375 + 102021396 MODEL AGCD01072549;AGCD01072550;GBDF01084147;XR_001232258 ncrna 8725773 Pus7 pseudouridine synthase 7 ENCODES a protein that exhibits enzyme binding (ortholog); pseudouridine synthase activity (ortholog); INVOLVED IN mRNA pseudouridine synthesis (ortholog); negative regulation of translation (ortholog); regulation of hematopoietic stem cell differentiation (ortholog); ASSOCIATED WITH genetic disease (ortholog); intellectual developmental disorder with abnormal behavior, microcephaly, and short stature (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN nucleus (ortholog) NW_004955410 10062768 10119751 - 9068941 102022260 A0A8C2UY82;A0A8C2UYU1;A0A8C2YLI7 MODEL AGCD01010788;AGCD01010789;AGCD01010790;AGCD01010791;GBDJ01004561;XM_005377246;XM_013510649;XM_013510650 XP_005377303;XP_013366103;XP_013366104 pseudouridylate synthase 7;pseudouridylate synthase 7 (putative);pseudouridylate synthase 7 homolog APPROVED protein-coding ENSCLAG00000005275 NW_004955410 10060071 10119757 - 8725796 LOC102023168 melanoma-associated antigen 10-like NW_004955498 4247845 4248615 - 102023168 MODEL AGCD01062979;XM_005406483 XP_005406540 protein-coding 8725799 LOC102023197 septin-11 pseudogene NW_004955438 18236201 18238017 - 102023197 MODEL AGCD01035467;XM_005390398 APPROVED pseudo 8725804 LOC102024443 taste receptor type 2 member 140-like NW_004955413 8151739 8152674 - 102024443 MODEL AGCD01013852;XM_005379630 XP_005379687 protein-coding 8725807 LOC102025172 vasculin pseudogene NW_004955540 1909030 1917626 + 102025172 MODEL AGCD01071308;XR_264822 APPROVED pseudo 8725810 LOC102025288 A-kinase anchor protein 5-like NW_004955543 2222873 2226189 + 102025288 MODEL AGCD01071648;AGCD01071649;XM_013508141 XP_013363595 protein-coding 8725811 LOC102026585 medium-wave-sensitive opsin 1 NW_004955580 774780 781232 + 102026585 A0A8C2ULK0 MODEL AGCD01075622;GBDJ01280073;XM_005414184 XP_005414241 APPROVED protein-coding ENSCLAG00000001715 8725824 Arglu1 arginine and glutamate rich 1 ASSOCIATED WITH Anal Atresia, Hypospadias, and Penoscrotal Inversion (ortholog); genetic disease (ortholog); FOUND IN cytosol (ortholog); mitochondrion (ortholog); nucleoplasm (ortholog) NW_004955404 4962000 4980226 + 9068941 102026596 A0A8C2USR3 MODEL AGCD01003302;GBCE01004218;XM_005374018 XP_005374075 arginine and glutamate-rich protein 1 protein-coding ENSCLAG00000003538 NW_004955404 4962000 4980226 + 8725832 Dydc2 DPY30 domain containing 2 ASSOCIATED WITH genetic disease (ortholog) NW_004955510 337286 348640 + 9068941 102026895 MODEL AGCD01066145;GBDF01053016;XM_013506330 XP_013361784 DPY30 domain-containing protein 2 protein-coding 8725840 Serpini2 serpin family I member 2 ENCODES a protein that exhibits serine-type endopeptidase inhibitor activity (ortholog); ASSOCIATED WITH genetic disease (ortholog); Shwachman-Diamond syndrome (ortholog) NW_004955448 16679885 16694484 - 9068941 102027247 A0A8C2UUP5 MODEL AGCD01041701;GBBH01104730;XM_005393166 XP_005393223 serpin I2;serpin peptidase inhibitor, clade I (pancpin), member 2 APPROVED protein-coding ENSCLAG00000004294 NW_004955448 16679885 16694484 - 8725848 Klhdc1 kelch domain containing 1 ENCODES a protein that exhibits ubiquitin ligase-substrate adaptor activity (ortholog); INVOLVED IN ubiquitin-dependent protein catabolic process via the C-end degron rule pathway (ortholog); ASSOCIATED WITH Brain-Lung-Thyroid Syndrome (ortholog); genetic disease (ortholog); FOUND IN Cul5-RING ubiquitin ligase complex (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955409 12914446 12970266 - 9068941 102027820 A0A8C2VIE2 MODEL AGCD01009577;AGCD01009578;AGCD01009579;AGCD01009580;AGCD01009581;AGCD01009582;GBDK01058373;XM_005376833;XM_005376834;XM_005376835 XP_005376890;XP_005376891;XP_005376892 kelch domain-containing protein 1 protein-coding ENSCLAG00000011115 NW_004955409 12912303 12970474 - 8725871 Tmem59l transmembrane protein 59 like INVOLVED IN branching involved in ureteric bud morphogenesis (ortholog); ASSOCIATED WITH genetic disease (ortholog); Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 (ortholog); ovarian cyst (ortholog) NW_004955524 2983699 2988080 - 9068941 102028010 A0A8C2V2S4 MODEL AGCD01068846;GBBH01034472;GBBH01034473;XM_005409589 XP_005409646 transmembrane protein 59-like APPROVED protein-coding ENSCLAG00000006357 NW_004955524 2981909 2988080 - 8725882 LOC102028369 alanyl-tRNA editing protein Aarsd1 NW_004955451 16692134 16695234 - 9068941 102028369 MODEL AGCD01043697;AGCD01043698;GBDF01047117;GBDF01047120;XM_013519131 XP_013374585 Aarsd1 alanyl-tRNA synthetase domain containing 1 APPROVED protein-coding 8725888 Lyl1 LYL1 basic helix-loop-helix family member ENCODES a protein that exhibits DNA binding (ortholog); INVOLVED IN B cell differentiation (ortholog); blood vessel maturation (ortholog); definitive hemopoiesis (ortholog); ASSOCIATED WITH acute myeloid leukemia (ortholog); alpha-mannosidosis (ortholog); Charcot-Marie-Tooth disease dominant intermediate B (ortholog) NW_004955415 32121808 32124730 - 9068941;7240710 102028743 A0A8C2YT09 MODEL AGCD01016710;GBCQ01177052;XM_005381052 XP_005381109 LYL1, basic helix-loop-helix family member;lymphoblastic leukemia associated hematopoiesis regulator 1;lymphoblastic leukemia derived sequence 1 APPROVED protein-coding ENSCLAG00000014483 NW_004955415 32121808 32124730 - 8725896 LOC102029310 uncharacterized LOC102029310 NW_004955424 23714057 23727836 + 102029310 MODEL AGCD01025018;GBDF01235866;XR_261105 ncrna 8725901 Smco3 single-pass membrane protein with coiled-coil domains 3 ASSOCIATED WITH autosomal dominant intellectual developmental disorder 6 (ortholog); developmental and epileptic encephalopathy 27 (ortholog); genetic disease (ortholog) NW_004955413 11551720 11560566 - 9068941 102029383 A0A8C2YUD7 MODEL AGCD01013964;GBCQ01006581;XM_005379006;XM_005379007;XM_005379010;XM_013511646;XM_013511647;XM_013511648;XM_013511649 XP_005379063;XP_005379064;XP_005379067;XP_013367100;XP_013367101;XP_013367102;XP_013367103 single-pass membrane and coiled-coil domain-containing protein 3 protein-coding ENSCLAG00000016471 NW_004955413 11551720 11560559 - 8725918 LOC102030672 uncharacterized LOC102030672 NW_004955556 917499 934466 + 102030672 MODEL AGCD01073179;GBCB01076510;XR_264974 ncrna 8725928 Arhgap1 Rho GTPase activating protein 1 ENCODES a protein that exhibits GTPase activator activity (ortholog); small GTPase binding (ortholog); INVOLVED IN endosomal transport (ortholog); negative regulation of endocytic recycling (ortholog); regulation of GTPase activity (ortholog); ASSOCIATED WITH congenital disorder of glycosylation type IIc (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN cell leading edge (ortholog); cytoplasm (ortholog); endosome membrane (ortholog) NW_004955422 1378426 1395439 + 9068941 102003771 A0A8C2VUH0;A0A8C2VZ07 MODEL AGCD01022457;GBDF01122966;XM_005384008;XM_013514064 XP_005384065;XP_013369518 rho GTPase-activating protein 1 protein-coding ENSCLAG00000013542 NW_004955422 1378426 1396899 + 8725945 Ccl1 C-C motif chemokine ligand 1 ENCODES a protein that exhibits chemokine activity (ortholog); cytokine activity (ortholog); INVOLVED IN antimicrobial humoral immune response mediated by antimicrobial peptide (ortholog); cellular response to interleukin-17 (ortholog); chemotaxis (ortholog); ASSOCIATED WITH asthma (ortholog); chronic obstructive pulmonary disease (ortholog); endometriosis (ortholog); FOUND IN extracellular space (ortholog) NW_004955481 9085943 9089147 - 9068941 102004708 A0A8C2V282 MODEL AGCD01057094;GBDK01334841;XM_005402841;XM_005402842 XP_005402898;XP_005402899 C-C motif chemokine 1;chemokine (C-C motif) ligand 1 APPROVED protein-coding ENSCLAG00000006411 8725955 Ubl4a ubiquitin like 4A ENCODES a protein that exhibits protein-folding chaperone binding (ortholog); INVOLVED IN post-translational protein targeting to endoplasmic reticulum membrane (ortholog); regulation of protein stability (ortholog); tail-anchored membrane protein insertion into ER membrane (ortholog); ASSOCIATED WITH adrenoleukodystrophy (ortholog); autistic disorder (ortholog); Barth syndrome (ortholog); FOUND IN BAT3 complex (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955580 998953 1001368 - 9068941 102004869 A0A8C2UNU9 MODEL AGCD01075637;GBCE01076715;XM_005414205 XP_005414262 ubiquitin-like 4A;ubiquitin-like protein 4A APPROVED protein-coding ENSCLAG00000002161 NW_004955580 997204 1001368 - 8725963 Irak1bp1 interleukin 1 receptor associated kinase 1 binding protein 1 INVOLVED IN I-kappaB kinase/NF-kappaB signaling (ortholog); ASSOCIATED WITH autistic disorder (ortholog); DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES (ortholog); genetic disease (ortholog) NW_004955502 6800532 6811214 + 9068941 102005063 A0A8C2YKP8 MODEL AGCD01064421;GBCQ01069000;XM_005406903 XP_005406960 interleukin-1 receptor-associated kinase 1 binding protein 1;interleukin-1 receptor-associated kinase 1-binding protein 1 APPROVED protein-coding ENSCLAG00000004073 NW_004955502 6800595 6810880 + 8725972 LOC102005075 uncharacterized LOC102005075 NW_004955433 12925114 12937990 - 102005075 MODEL AGCD01031673;XR_261590 ncrna 8725977 Mef2a myocyte enhancer factor 2A ENCODES a protein that exhibits chromatin binding (ortholog); DNA binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); INVOLVED IN cardiac conduction (ortholog); cellular response to calcium ion (ortholog); cellular response to glucose stimulus (ortholog); ASSOCIATED WITH chromosome 15q26-qter deletion syndrome (ortholog); Coronary Artery Disease, Autosomal Dominant 1 (ortholog); dilated cardiomyopathy (ortholog); FOUND IN chromatin (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955416 26926753 27051171 + 9068941;7240710 102005139 A0A8C2VHN9;A0A8C2VJQ1;A0A8C2VMF3 MODEL AGCD01017607;AGCD01017608;AGCD01017609;GBDI01059219;XM_005381629;XM_005381630;XM_005381631;XM_005381632;XM_013512516;XM_013512517;XM_013512518;XM_013512519 XP_005381686;XP_005381687;XP_005381688;XP_005381689;XP_013367970;XP_013367971;XP_013367972;XP_013367973 myocyte-specific enhancer factor 2A protein-coding ENSCLAG00000010314 NW_004955416 26953798 27051171 + 8725998 LOC102006589 uncharacterized LOC102006589 NW_004955495 6548347 6552199 + 102006589 MODEL AGCD01062085;GBDF01303427;XR_264164 ncrna 8726005 Asnsd1 asparagine synthetase domain containing 1 ASSOCIATED WITH genetic disease (ortholog); immunodeficiency 31B (ortholog); Neurodevelopmental Disorders (ortholog) NW_004955403 9176425 9184310 - 9068941 102007394 A0A8C2VNE9 MODEL AGCD01001901;GBDF01123988;GBDI01173372;XM_005373320;XM_013512372 XP_005373377;XP_013367826 asparagine synthetase domain-containing protein 1 protein-coding ENSCLAG00000010450 8726016 LOC102007689 DNA-3-methyladenine glycosylase pseudogene NW_004955516 1140332 1141187 + 102007689 MODEL AGCD01067413 APPROVED pseudo 8726017 Nckap5l NCK associated protein 5 like INVOLVED IN microtubule bundle formation (ortholog); microtubule depolymerization (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN centrosome (ortholog); microtubule plus-end (ortholog) NW_004955547 381338 416658 - 9068941 102007942 A0A8C2UIK8;A0A8C2YIA0 MODEL AGCD01072153;AGCD01072154;GBDJ01280139;XM_005411849;XM_005411850;XM_013508476;XM_013508477;XM_013508478 XP_005411906;XP_005411907;XP_013363930;XP_013363931;XP_013363932 NCK-associated protein 5-like APPROVED protein-coding ENSCLAG00000000530 NW_004955547 379440 417284 - 8726040 LOC102008328 uncharacterized LOC102008328 NW_004955423 11498337 11509824 - 102008328 MODEL AGCD01023701;GBDF01306799;XR_260965;XR_260966 ncrna 8726053 Cnga2 cyclic nucleotide gated channel subunit alpha 2 ENCODES a protein that exhibits cGMP binding (ortholog); identical protein binding (ortholog); intracellular cAMP-activated cation channel activity (ortholog); INVOLVED IN membrane depolarization (ortholog); sensory perception of smell (ortholog); PARTICIPATES IN calcium transport pathway; calcium/calcium-mediated signaling pathway; ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); syndromic X-linked intellectual disability Lubs type (ortholog); FOUND IN ciliary membrane (ortholog); intracellular cyclic nucleotide activated cation channel complex (ortholog); perikaryon (ortholog) NW_004955498 7250514 7257701 + 9068941 102009400 A0A8C2UKE6 MODEL AGCD01063146;GBBH01223843;XM_013505548 XP_013361002 cyclic nucleotide gated channel alpha 2;cyclic nucleotide-gated olfactory channel APPROVED protein-coding ENSCLAG00000001030 NW_004955498 7250514 7257701 + 8726064 Bfsp1 beaded filament structural protein 1 ENCODES a protein that exhibits structural constituent of eye lens (ortholog); INVOLVED IN cell maturation (ortholog); intermediate filament organization (ortholog); lens fiber cell development (ortholog); ASSOCIATED WITH cataract (ortholog); cataract 33 (ortholog); coloboma (ortholog); FOUND IN cytoplasm (ortholog); intermediate filament (ortholog); plasma membrane (ortholog) NW_004955415 26507381 26535545 - 9068941;7240710 102009495 A0A8C2VT60 MODEL AGCD01016596;AGCD01016597;AGCD01016598;GBCE01168540;XM_005380906;XM_013512110 XP_005380963;XP_013367564 beaded filament structural protein 1, filensin;filensin APPROVED protein-coding ENSCLAG00000013897 NW_004955415 26507528 26535551 - 8726076 Kmt2a lysine methyltransferase 2A ENCODES a protein that exhibits chromatin binding (ortholog); DNA binding (ortholog); DNA-binding transcription factor binding (ortholog); INVOLVED IN anterior/posterior pattern specification (ortholog); cellular response to transforming growth factor beta stimulus (ortholog); circadian regulation of gene expression (ortholog); PARTICIPATES IN DNA modification pathway; histone modification pathway; ASSOCIATED WITH Acute Erythroleukemia (ortholog); acute lymphoblastic leukemia (ortholog); acute monocytic leukemia (ortholog); FOUND IN cytosol (ortholog); histone methyltransferase complex (ortholog); MLL1 complex (ortholog) NW_004955412 19586435 19670149 + 9068941;7240710 102010237 A0A8C2W0V1;A0A8C2YU51 MODEL AGCD01012966;AGCD01012967;AGCD01012968;GBBH01208480;GBCE01008536;XM_005378244 XP_005378301 histone-lysine N-methyltransferase 2A;lysine (K)-specific methyltransferase 2A APPROVED protein-coding ENSCLAG00000016132 NW_004955412 19586141 19665527 + 8726125 Cdk5rap3 CDK5 regulatory subunit associated protein 3 ENCODES a protein that exhibits cyclin binding (ortholog); MDM2/MDM4 family protein binding (ortholog); mitogen-activated protein kinase binding (ortholog); INVOLVED IN apoptotic nuclear changes (ortholog); cell population proliferation (ortholog); definitive erythrocyte differentiation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN centrosome (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955451 13160811 13170012 - 9068941 102010329 A0A8C2VPZ5;A0A8C2VT09 MODEL AGCD01043455;AGCD01043456;GBDJ01011824;XM_005394252 XP_005394309 CDK5 regulatory subunit-associated protein 3 protein-coding ENSCLAG00000012292 NW_004955451 13120761 13170073 - 8726146 Prdx5 peroxiredoxin 5 ENCODES a protein that exhibits antioxidant activity (ortholog); cysteine-type endopeptidase inhibitor activity involved in apoptotic process (ortholog); identical protein binding (ortholog); INVOLVED IN cellular response to reactive oxygen species (ortholog); hydrogen peroxide catabolic process (ortholog); NADPH oxidation (ortholog); ASSOCIATED WITH alopecia areata (ortholog); brucellosis (ortholog); Chronic Hepatitis C (ortholog); FOUND IN cytoplasm (ortholog); cytoplasmic vesicle (ortholog); cytosol (ortholog) NW_004955422 20763822 20766976 - 9068941 102010595 A0A8C2YUU0 MODEL AGCD01023086;GBCB01004546;XM_005384597 XP_005384654 peroxiredoxin-5, mitochondrial protein-coding ENSCLAG00000017097 NW_004955422 20761495 20766976 - 8726162 Notch3 notch receptor 3 ENCODES a protein that exhibits enzyme binding (ortholog); identical protein binding (ortholog); signaling receptor activity (ortholog); INVOLVED IN artery morphogenesis (ortholog); forebrain development (ortholog); glomerular capillary formation (ortholog); PARTICIPATES IN altered Notch signaling pathway involving the main players; CADASIL pathway; Notch signaling pathway; ASSOCIATED WITH acute lymphoblastic leukemia (ortholog); autism spectrum disorder (ortholog); breast ductal carcinoma (ortholog); FOUND IN actin cytoskeleton (ortholog); cytosol (ortholog); nucleoplasm (ortholog) NW_004955495 8012370 8048616 + 9068941;7240710 102010599 A0A8C2YQ42 MODEL AGCD01062175;AGCD01062176;AGCD01062177;GBBH01119449;GBDK01129547;XM_013505128 XP_013360582 neurogenic locus notch homolog protein 3;notch 3 APPROVED protein-coding ENSCLAG00000010364 NW_004955495 8012502 8047710 + 8726199 LOC102011238 uncharacterized LOC102011238 NW_004955435 16675032 16735309 - 102011238 MODEL AGCD01033336;AGCD01033337;GBDF01045771;XR_001234857;XR_001234858;XR_261711;XR_261713 ncrna 8726211 Aurka aurora kinase A ENCODES a protein that exhibits histone H3S10 kinase activity (ortholog); molecular function activator activity (ortholog); protein heterodimerization activity (ortholog); INVOLVED IN anterior/posterior axis specification (ortholog); apoptotic process (ortholog); centrosome cycle (ortholog); ASSOCIATED WITH Aneuploidy (ortholog); Breast Neoplasms (ortholog); Chromosomal Instability (ortholog); FOUND IN axon hillock (ortholog); basolateral plasma membrane (ortholog); centrosome (ortholog) NW_004955445 2831073 2853151 + 9068941;7240710 102011371 A0A8C2VIE4 MODEL AGCD01039369;GBDF01083611;XM_005392275;XM_013518333 XP_005392332;XP_013373787 protein-coding ENSCLAG00000009511 NW_004955445 2831157 2853357 + 8726228 LOC102013501 uncharacterized LOC102013501 NW_004955473 5281173 5291335 + 102013501 MODEL AGCD01053974;GBDI01312184;XR_001237117;XR_263581 ncrna 8726235 LOC102014181 olfactory receptor 4K14-like NW_004955550 359157 360092 + 9068941 102014181 MODEL AGCD01072495;XM_005412030 XP_005412087 protein-coding 8726239 Maea macrophage erythroblast attacher, E3 ubiquitin ligase ENCODES a protein that exhibits actin binding (ortholog); INVOLVED IN cell adhesion (ortholog); cytoskeleton organization (ortholog); enucleate erythrocyte development (ortholog); ASSOCIATED WITH cherubism (ortholog); genetic disease (ortholog); type 2 diabetes mellitus (ortholog); FOUND IN actin cytoskeleton (ortholog); actomyosin contractile ring (ortholog); cytoskeleton (ortholog) NW_004955514 689867 722779 + 9068941 102014934 A0A8C2VYZ7 MODEL AGCD01067019;GBCE01030158;XM_005408696;XM_005408697 XP_005408753;XP_005408754 macrophage erythroblast attacher APPROVED protein-coding ENSCLAG00000013403 NW_004955514 689868 722779 + 8726261 Qrfp pyroglutamylated RFamide peptide ENCODES a protein that exhibits G protein-coupled receptor binding (ortholog); neuropeptide hormone activity (ortholog); orexigenic neuropeptide QRFP receptor binding (ortholog); INVOLVED IN grooming behavior (ortholog); locomotory behavior (ortholog); neuropeptide signaling pathway (ortholog); ASSOCIATED WITH autosomal recessive limb-girdle muscular dystrophy type 2K (ortholog); genetic disease (ortholog); primary coenzyme Q10 deficiency 7 (ortholog) NW_004955513 802809 805835 - 9068941 102017901 A0A8C2VY48 MODEL AGCD01066832;GBCE01009059;XM_005408349 XP_005408406 orexigenic neuropeptide QRFP protein-coding ENSCLAG00000015339 NW_004955513 803630 804034 - 8726272 Otud7b OTU deubiquitinase 7B ENCODES a protein that exhibits cysteine-type deubiquitinase activity (ortholog); cysteine-type peptidase activity (ortholog); K48-linked deubiquitinase activity (ortholog); INVOLVED IN in utero embryonic development (ortholog); mucosal immune response (ortholog); negative regulation of I-kappaB kinase/NF-kappaB signaling (ortholog); ASSOCIATED WITH gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); immunodeficiency 42 (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog) NW_004955413 758098 812605 + 9068941 102019900 A0A8C2VZB6 MODEL AGCD01013490;AGCD01013491;GBDF01086853;XM_005378701;XM_005378702;XM_005378703;XM_005378704 XP_005378758;XP_005378759;XP_005378760;XP_005378761 OTU domain containing 7B;OTU domain-containing protein 7B APPROVED protein-coding ENSCLAG00000015021 NW_004955413 751546 812605 + 8726297 Nsun4 NOP2/Sun RNA methyltransferase 4 ENCODES a protein that exhibits methyltransferase activity (ortholog); rRNA (cytosine-C5-)-methyltransferase activity (ortholog); small ribosomal subunit rRNA binding (ortholog); INVOLVED IN cytosolic ribosome assembly (ortholog); positive regulation of mitochondrial translation (ortholog); rRNA methylation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN mitochondrial large ribosomal subunit (ortholog); mitochondrion (ortholog) NW_004955464 11934146 11962513 - 9068941 102019989 A0A8C2UXZ9 MODEL AGCD01050168;AGCD01050169;GBCE01032888;XM_005398675;XM_005398676;XM_013521590;XM_013521591 XP_005398732;XP_005398733;XP_013377044;XP_013377045 5-methylcytosine rRNA methyltransferase NSUN4;NOP2/Sun RNA methyltransferase family member 4;NOP2/Sun domain family, member 4 APPROVED protein-coding ENSCLAG00000005205 NW_004955464 11932429 11967414 - 8726313 Ube2e3 ubiquitin conjugating enzyme E2 E3 ENCODES a protein that exhibits ubiquitin conjugating enzyme activity (ortholog); ubiquitin-protein transferase activity (ortholog); INVOLVED IN protein K11-linked ubiquitination (ortholog); protein K48-linked ubiquitination (ortholog); protein K63-linked ubiquitination (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN nucleus (ortholog) NW_004955403 16151629 16239855 - 9068941 102020511 A0A8C2YS53 MODEL AGCD01002061;AGCD01002062;GBBH01093741;GBCB01003070;XM_005373356;XM_013512545 XP_005373413;XP_013367999 ubiquitin-conjugating enzyme E2 E3;ubiquitin-conjugating enzyme E2E 3 APPROVED protein-coding ENSCLAG00000013235 NW_004955403 16151629 16239855 - 8726326 Bola2b bolA family member 2B INVOLVED IN [2Fe-2S] cluster assembly (ortholog); cell redox homeostasis (ortholog); iron-sulfur cluster assembly (ortholog); ASSOCIATED WITH 16p11.2 Deletion Syndrome (ortholog); autism spectrum disorder (ortholog); autistic disorder (ortholog); FOUND IN cytoplasm (ortholog); iron-sulfur cluster assembly complex (ortholog); nucleus (ortholog) NW_004955493 6812208 6812932 + 9068941 102020575 A0A8C2VWU7 MODEL AGCD01061141;GBDF01002632;XM_005405183 XP_005405240 bolA homolog 2B;bolA-like protein 2 APPROVED protein-coding ENSCLAG00000014934 8726338 Anapc4 anaphase promoting complex subunit 4 ENCODES a protein that exhibits protein phosphatase binding (ortholog); INVOLVED IN protein K11-linked ubiquitination (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN anaphase-promoting complex (ortholog); nucleus (ortholog) NW_004955443 19620480 19653179 - 9068941 102021287 A0A8C2USS4 MODEL AGCD01038631;GBBH01141916;XM_005392036;XM_005392037 XP_005392093;XP_005392094 anaphase-promoting complex subunit 4 protein-coding ENSCLAG00000003544 NW_004955443 19620480 19653200 - 8726374 LOC102022613 uncharacterized LOC102022613 NW_004955494 2980579 2986183 - 102022613 MODEL AGCD01061458;GBDF01238692;XM_005405425 XP_005405482 uncharacterized protein LOC102022613 protein-coding ENSCLAG00000026745 8726389 LOC102023948 histone acetyltransferase KAT2B pseudogene NW_004955525 2539956 2542715 + 102023948 MODEL AGCD01069098 APPROVED pseudo 8726390 Majin membrane anchored junction protein INVOLVED IN double-strand break repair involved in meiotic recombination (ortholog); homologous chromosome pairing at meiosis (ortholog); meiotic attachment of telomere to nuclear envelope (ortholog); ASSOCIATED WITH Bardet-Biedl syndrome (ortholog); genetic disease (ortholog); glycogen storage disease V (ortholog); FOUND IN chromosome, telomeric region (ortholog); nuclear envelope (ortholog); nuclear inner membrane (ortholog) NW_004955422 20216773 20249042 + 9068941 102024019 MODEL AGCD01023070;AGCD01023071;AGCD01023072;GBBH01078059;XM_005384541 XP_005384598 LOC102024019 chromosome unknown open reading frame, human C11orf85;uncharacterized protein C11orf85 homolog APPROVED protein-coding 8726410 LOC102024891 sodium-dependent multivitamin transporter NW_004955469 9182247 9194557 - 102024891 A0A8C2YP59 MODEL AGCD01052496;GBDF01222601;XM_005400472;XM_005400474;XM_013522641;XM_013522642 XP_005400529;XP_005400531;XP_013378095;XP_013378096 Slc5a6 solute carrier family 5 (sodium/multivitamin and iodide cotransporter), member 6 APPROVED protein-coding ENSCLAG00000008994 NW_004955469 9182247 9194557 - 8726437 Lhx2 LIM homeobox 2 ENCODES a protein that exhibits chromatin binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); RNA polymerase II cis-regulatory region sequence-specific DNA binding (ortholog); INVOLVED IN anatomical structure formation involved in morphogenesis (ortholog); axon extension (ortholog); axon guidance (ortholog); ASSOCIATED WITH genetic disease (ortholog); rheumatoid arthritis (ortholog); FOUND IN nucleus (ortholog) NW_004955419 3999364 4019543 - 9068941 102025581 A0A8C2VJL0 MODEL AGCD01019745;AGCD01019746;AGCD01019747;GBBH01168279;GBDF01257508;XM_005382498 XP_005382555 LIM/homeobox protein Lhx2 protein-coding ENSCLAG00000010277 NW_004955419 3998242 4018875 - 8726453 LOC102025642 lanC-like protein 1 pseudogene NW_004955450 3209756 3227293 - 102025642 MODEL AGCD01042426 APPROVED pseudo 8726454 LOC102026006 UDP-N-acetylglucosamine transporter-like NW_004955481 1573638 1578463 - 102026006 MODEL AGCD01056837;AGCD01056838 pseudo 8726455 LOC102026345 chromosome unknown open reading frame, human C19orf44 ASSOCIATED WITH genetic disease (ortholog) NW_004955524 1235137 1245526 - 9068941 102026345 A0A8C2V1D4 MODEL AGCD01068740;GBDF01049996;XM_005409496;XM_005409497;XM_005409498;XM_005409499 XP_005409553;XP_005409554;XP_005409555;XP_005409556 uncharacterized protein C19orf44 homolog protein-coding ENSCLAG00000005950 8726475 LOC102026391 testis-specific serine/threonine-protein kinase 2 NW_004955455 3456753 3458084 + 102026391 A0A8C2WDA2 MODEL AGCD01045628;GBDF01006455;XM_005396176 XP_005396233 APPROVED protein-coding ENSCLAG00000017852 8726480 Dck deoxycytidine kinase ENCODES a protein that exhibits ATP binding (ortholog); cytidine kinase activity (ortholog); deoxyadenosine kinase activity (ortholog); INVOLVED IN dAMP salvage (ortholog); deoxycytidine metabolic process (ortholog); nucleoside phosphate biosynthetic process (ortholog); PARTICIPATES IN gemcitabine pharmacodynamics pathway; gemcitabine pharmacokinetics pathway; lamivudine pharmacokinetics pathway; ASSOCIATED WITH genetic disease (ortholog); Kabuki Syndrome 1 (ortholog); FOUND IN nucleoplasm (ortholog) NW_004955447 2031851 2067005 - 9068941 102026689 A0A8C2UWV8 MODEL AGCD01040526;AGCD01040527;AGCD01040528;GBDJ01304367;GBDJ01336545;XM_005392943 XP_005393000 protein-coding ENSCLAG00000004592 NW_004955447 2031258 2067210 - 8726489 LOC102027155 septin-7-like NW_004955463 14303925 14306398 + 102027155 MODEL AGCD01049906 pseudo 8726490 Mblac1 metallo-beta-lactamase domain containing 1 ENCODES a protein that exhibits metal ion binding (ortholog); RNA endonuclease activity (ortholog); INVOLVED IN histone mRNA metabolic process (ortholog); mRNA 3'-end processing (ortholog); positive regulation of G1/S transition of mitotic cell cycle (ortholog); ASSOCIATED WITH genetic disease (ortholog); pleomorphic xanthoastrocytoma (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog) NW_004955573 745202 747402 - 9068941 102027585 A0A8C2UL84 MODEL AGCD01075004;GBCE01000285;XM_005413741 XP_005413798 metallo-beta-lactamase domain-containing protein 1 protein-coding ENSCLAG00000001302 NW_004955573 745202 747402 - 8726496 Krtcap2 keratinocyte associated protein 2 ENCODES a protein that exhibits enzyme activator activity (ortholog); INVOLVED IN protein N-linked glycosylation (ortholog); protein N-linked glycosylation via arginine (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease type 2 (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN oligosaccharyltransferase complex (ortholog) NW_004955545 1642578 1645699 - 9068941 102027681 A0A8C2UWN3 MODEL AGCD01071864;GBDF01000034;XM_005411578;XM_013508306 XP_005411635;XP_013363760 keratinocyte-associated protein 2 protein-coding ENSCLAG00000004535 NW_004955545 1642578 1645698 - 8726505 LOC102028472 uncharacterized LOC102028472 NW_004955547 2291235 2304297 - 102028472 MODEL AGCD01072266;AGCD01072267;AGCD01072268;GBDF01132937;XR_264906;XR_264907 ncrna 8726512 Rps27l ribosomal protein S27 like ENCODES a protein that exhibits cysteine-type endopeptidase activator activity involved in apoptotic process (ortholog); translation activator activity (ortholog); INVOLVED IN activation of cysteine-type endopeptidase activity involved in apoptotic process (ortholog); DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator (ortholog); intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator (ortholog); PARTICIPATES IN ribosome biogenesis pathway; ASSOCIATED WITH Bloom syndrome (ortholog); colorectal cancer (ortholog); genetic disease (ortholog); FOUND IN nucleus (ortholog) NW_004955450 12122948 12126167 + 9068941 102028485 A0A8C2VHM0 MODEL AGCD01042688;AGCD01042689;GBDI01001525;GBDK01022916;XM_005393794 XP_005393851 40S ribosomal protein S27-like;ribosomal protein S27-like APPROVED protein-coding ENSCLAG00000010811 NW_004955450 12122921 12128101 + 8726520 Mlf2 myeloid leukemia factor 2 ASSOCIATED WITH genetic disease (ortholog); Hyperphosphatemic Familial Tumoral Calcinosis 1 (ortholog); lymphoproliferative syndrome 2 (ortholog); FOUND IN nucleus (ortholog) NW_004955413 4359936 4364284 - 9068941 102028519 A0A8C2VSM2;A0A8C2VXV6 MODEL AGCD01013610;GBDJ01003878;XM_005378824 XP_005378881 protein-coding ENSCLAG00000013739 NW_004955413 4359936 4364284 - 8726536 LOC102028658 growth factor receptor-bound protein 2 pseudogene NW_004955504 385030 385794 - 102028658 MODEL AGCD01064819 APPROVED pseudo 8726541 LOC102029670 dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 4-like NW_004955442 12689424 12691146 - 102029670 MODEL AGCD01037745;XM_005391260 XP_005391317 protein-coding 8726546 Rbm17 RNA binding motif protein 17 INVOLVED IN alternative mRNA splicing, via spliceosome (ortholog); ASSOCIATED WITH genetic disease (ortholog); hypoparathyroidism-deafness-renal disease syndrome (ortholog); schizophrenia (ortholog); FOUND IN nucleoplasm (ortholog); nucleus (ortholog); protein-containing complex (ortholog) NW_004955421 22732757 22745926 + 9068941 102030537 A0A8C2VMD3 MODEL AGCD01022147;AGCD01022148;GBDF01086381;XM_005383861 XP_005383918 splicing factor 45 protein-coding ENSCLAG00000012195 NW_004955421 22732757 22746014 + 8726565 LOC102003182 protamine-2 NW_004955442 7306731 7307449 + 9068941;11556220 10911401 102003182 MODEL AGCD01037623;GBDF01007122;XM_005391168 XP_005391225 Prm2 protamine 2 APPROVED protein-coding 8726571 LOC102003484 RNA-binding protein 25 pseudogene NW_004955437 14612893 14618799 - 102003484 MODEL AGCD01034678 APPROVED pseudo 8726572 LOC102003988 PEST proteolytic signal-containing nuclear protein pseudogene NW_004955505 1483191 1484367 + 102003988 MODEL AGCD01064974;XM_005407108 APPROVED pseudo 8726577 Arih2 ariadne RBR E3 ubiquitin protein ligase 2 ENCODES a protein that exhibits ubiquitin conjugating enzyme binding (ortholog); ubiquitin-protein transferase activity (ortholog); INVOLVED IN developmental cell growth (ortholog); hematopoietic stem cell proliferation (ortholog); positive regulation of protein targeting to mitochondrion (ortholog); ASSOCIATED WITH Aicardi-Goutieres Syndrome 1 (ortholog); genetic disease (ortholog); myoepithelioma (ortholog); FOUND IN Cul5-RING ubiquitin ligase complex (ortholog); cytoplasm (ortholog); nucleoplasm (ortholog) NW_004955532 933749 1008619 + 9068941 102004200 A0A8C2V6X0;A0A8C2V9M1 MODEL AGCD01070159;AGCD01070160;GBDF01043720;XM_005410170;XM_013507578 XP_005410227;XP_013363032 E3 ubiquitin-protein ligase ARIH2;ariadne homolog 2 APPROVED protein-coding ENSCLAG00000007056 NW_004955532 933749 1008619 + 8726600 Serpina7 serpin family A member 7 ENCODES a protein that exhibits hormone binding (ortholog); INVOLVED IN post-embryonic development (ortholog); response to corticosterone (ortholog); response to nutrient levels (ortholog); ASSOCIATED WITH autistic disorder (ortholog); diabetes mellitus (ortholog); diabetic ketoacidosis (ortholog); FOUND IN extracellular space (ortholog) NW_004955548 2855377 2861946 - 9068941;7240710 102006287 A0A8C2YI03 MODEL AGCD01072411;GBDF01025901;XM_005412013 XP_005412070 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 7;thyroxine-binding globulin APPROVED protein-coding ENSCLAG00000000119 NW_004955548 2855111 2861952 - 8726609 Pwwp3b PWWP domain containing 3B ASSOCIATED WITH autistic disorder (ortholog); genetic disease (ortholog); syndromic X-linked intellectual disability Lubs type (ortholog) NW_004955548 2904964 2951956 + 9068941 102006614 A0A8C2W9S6 MODEL AGCD01072411;AGCD01072412;GBDF01125244;XM_005412014;XM_005412015;XM_005412016;XM_013508513;XM_013508514;XM_013508515 XP_005412071;XP_005412072;XP_005412073;XP_013363967;XP_013363968;XP_013363969 LOC102006614;Mum1l1 MUM1 like 1;PWWP domain-containing protein MUM1L1 APPROVED protein-coding ENSCLAG00000017384 NW_004955548 2948340 2950403 + 8726625 LOC102006814 cysteine-rich PDZ-binding protein pseudogene NW_004955433 2469951 2470255 - 102006814 MODEL AGCD01031393 APPROVED pseudo 8726626 Ptn pleiotrophin ENCODES a protein that exhibits carbohydrate binding (ortholog); chondroitin sulfate binding (ortholog); chondroitin sulfate proteoglycan binding (ortholog); INVOLVED IN bone mineralization (ortholog); cellular response to hypoxia (ortholog); cellular response to organic cyclic compound (ortholog); PARTICIPATES IN syndecan signaling pathway; ASSOCIATED WITH adrenal carcinoma (ortholog); Animal Mammary Neoplasms (ortholog); Body Weight (ortholog); FOUND IN basement membrane (ortholog); cell surface (ortholog); endoplasmic reticulum (ortholog) NW_004955494 5580264 5681848 + 9068941 102006927 A0A8C2YJ06 MODEL AGCD01061522;AGCD01061523;GBCE01001843;XM_013505031;XM_013505032 XP_013360485;XP_013360486 protein-coding ENSCLAG00000001593 NW_004955494 5580422 5684190 + 8726639 Grhpr glyoxylate and hydroxypyruvate reductase ENCODES a protein that exhibits carboxylic acid binding (ortholog); glycerate dehydrogenase activity (ortholog); glyoxylate reductase (NADP+) activity (ortholog); INVOLVED IN dicarboxylic acid metabolic process (ortholog); glyoxylate metabolic process (ortholog); PARTICIPATES IN Leigh disease pathway; primary hyperoxaluria type 2 pathway; pyruvate decarboxylase deficiency pathway; ASSOCIATED WITH acromesomelic dysplasia, Maroteaux type (ortholog); COVID-19 (ortholog); distal arthrogryposis type 1A (ortholog); FOUND IN catalytic complex (ortholog); cytoplasm (ortholog) NW_004955419 29032591 29044046 - 9068941;7240710 102008319 A0A8C2W3V4;A0A8C2W3X5 MODEL AGCD01020484;GBDI01225270;XM_005382885 XP_005382942 glyoxylate reductase/hydroxypyruvate reductase APPROVED protein-coding ENSCLAG00000017032 NW_004955419 29032600 29044257 - 8726655 Slc28a1 solute carrier family 28 member 1 ENCODES a protein that exhibits azole transmembrane transporter activity (ortholog); pyrimidine nucleobase transmembrane transporter activity (ortholog); pyrimidine- and adenosine-specific:sodium symporter activity (ortholog); INVOLVED IN azole transmembrane transport (ortholog); cytidine transport (ortholog); import across plasma membrane (ortholog); PARTICIPATES IN capecitabine pharmacodynamics pathway; capecitabine pharmacokinetics pathway; gemcitabine pharmacodynamics pathway; ASSOCIATED WITH Bloom syndrome (ortholog); Breast Neoplasms (ortholog); colorectal cancer (ortholog); FOUND IN apical plasma membrane (ortholog); brush border membrane (ortholog); cytosol (ortholog) NW_004955416 14226411 14267962 - 9068941 102009715 A0A8C2V6E7;A0A8C2YN46 MODEL AGCD01017248;AGCD01017249;GBCQ01101688;XM_005381488;XM_013512686;XM_013512687 XP_005381545;XP_013368140;XP_013368141 sodium/nucleoside cotransporter 1;solute carrier family 28 (concentrative nucleoside transporter), member 1 APPROVED protein-coding ENSCLAG00000007489 NW_004955416 14226278 14268350 - 8726679 LOC102010047 nucleolar and spindle-associated protein 1 pseudogene NW_004955413 13435713 13437079 - 102010047 MODEL AGCD01014015 APPROVED pseudo 8726680 Mrps5 mitochondrial ribosomal protein S5 ASSOCIATED WITH Animal Disease Models (ortholog); genetic disease (ortholog); lung adenocarcinoma (ortholog); FOUND IN mitochondrial small ribosomal subunit (ortholog); mitochondrion (ortholog) NW_004955470 3419052 3443481 - 9068941 102010893 A0A8C2YM70 MODEL AGCD01052700;AGCD01052701;GBBH01114876;XM_005400641 XP_005400698 28S ribosomal protein S5, mitochondrial protein-coding ENSCLAG00000006224 NW_004955470 3416731 3443298 - 8726704 Gna12 G protein subunit alpha 12 ENCODES a protein that exhibits D5 dopamine receptor binding (ortholog); protein phosphatase 2A binding (ortholog); protein phosphatase regulator activity (ortholog); INVOLVED IN cell differentiation (ortholog); embryonic digit morphogenesis (ortholog); G protein-coupled receptor signaling pathway (ortholog); PARTICIPATES IN eicosanoid signaling pathway; endothelin signaling pathway; sphingosine 1-phosphate signaling pathway; ASSOCIATED WITH genetic disease (ortholog); immunodeficiency 11A (ortholog); Myocardial Ischemia (ortholog); FOUND IN brush border membrane (ortholog); lateral plasma membrane (ortholog); neuron projection (ortholog) NW_004955460 12534210 12628090 + 9068941 102011512 A0A8C2VEK7 MODEL AGCD01048660;AGCD01048661;GBCB01042795;GBCQ01096239;XM_005397862 XP_005397919 guanine nucleotide binding protein (G protein) alpha 12;guanine nucleotide-binding protein subunit alpha-12 APPROVED protein-coding ENSCLAG00000009938 NW_004955460 12534168 12622537 + 8726712 Magoh mago homolog, exon junction complex subunit INVOLVED IN nuclear-transcribed mRNA catabolic process, nonsense-mediated decay (ortholog); regulation of alternative mRNA splicing, via spliceosome (ortholog); regulation of mRNA processing (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN catalytic step 2 spliceosome (ortholog); exon-exon junction complex (ortholog); exon-exon junction subcomplex mago-y14 (ortholog) NW_004955464 5919289 5929152 + 9068941 102011517 A0A8C2VA61 MODEL AGCD01050015;GBDJ01188614;XM_005398559;XM_013521687 XP_005398616;XP_013377141 mago homolog, exon junction complex core component;mago-nashi homolog, proliferation-associated APPROVED protein-coding ENSCLAG00000008005 8726721 LOC102011840 uncharacterized LOC102011840 NW_004955407 35818286 35827944 - 102011840 MODEL AGCD01007751;GBCQ01178585;XR_001231235;XR_001231237;XR_001231238;XR_259614 ncrna 8726727 Ptpn18 protein tyrosine phosphatase non-receptor type 18 ENCODES a protein that exhibits non-membrane spanning protein tyrosine phosphatase activity (ortholog); protein tyrosine phosphatase activity (ortholog); INVOLVED IN blastocyst formation (ortholog); ASSOCIATED WITH Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (ortholog); nucleus (ortholog) NW_004955459 65191 90459 + 9068941 102012407 A0A8C2UST9 MODEL AGCD01047924;GBDK01194260;XM_005397542;XM_005397543;XM_005397544 XP_005397599;XP_005397600;XP_005397601 tyrosine-protein phosphatase non-receptor type 18 APPROVED protein-coding ENSCLAG00000003389 NW_004955459 65612 91545 + 8726752 Ppil4 peptidylprolyl isomerase like 4 ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytosol (ortholog); nucleoplasm (ortholog) NW_004955439 11705096 11745478 + 9068941 102012687 A0A8C2UUV0 MODEL AGCD01035919;AGCD01035920;AGCD01035921;AGCD01035922;GBDF01189460;XM_005390608 XP_005390665 peptidyl-prolyl cis-trans isomerase-like 4;peptidylprolyl isomerase (cyclophilin)-like 4 APPROVED protein-coding ENSCLAG00000003991 NW_004955439 11704834 11746548 + 8726769 LOC102013037 solute carrier organic anion transporter family member 5A1-like NW_004955655 54988 70910 - 102013037 MODEL AGCD01077842;GBCB01004342;GBDF01097203;XM_013510175 XP_013365629 protein-coding 8726778 LOC102014755 B-cell CLL/lymphoma 7 protein family member C pseudogene NW_004955411 3209581 3210469 - 102014755 MODEL AGCD01011541 APPROVED pseudo 8726779 Acaa2 acetyl-CoA acyltransferase 2 ENCODES a protein that exhibits acetyl-CoA C-acetyltransferase activity (ortholog); acetyl-CoA C-acyltransferase activity (ortholog); acyl-CoA hydrolase activity (ortholog); INVOLVED IN acetyl-CoA metabolic process (ortholog); cellular response to hypoxia (ortholog); fatty acid beta-oxidation (ortholog); PARTICIPATES IN 3-hydroxy-3-methylglutaryl-CoA lyase deficiency pathway; 3-hydroxyacyl-CoA dehydrogenase deficiency pathway; 3-hydroxyisobutyric aciduria pathway; ASSOCIATED WITH adult respiratory distress syndrome (ortholog); genetic disease (ortholog); intellectual disability (ortholog); FOUND IN mitochondrial matrix (ortholog); mitochondrion (ortholog) NW_004955402 34857317 34885169 - 9068941 102014845 A0A8C2VDJ3 MODEL AGCD01000872;AGCD01000873;GBDJ01085210;XM_005372912;XM_013510632 XP_005372969;XP_013366086 3-ketoacyl-CoA thiolase, mitochondrial protein-coding ENSCLAG00000008998 NW_004955402 34857317 34885169 - 8726793 Tmed5 transmembrane p24 trafficking protein 5 INVOLVED IN Golgi ribbon formation (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cis-Golgi network (ortholog); endoplasmic reticulum exit site (ortholog); endoplasmic reticulum-Golgi intermediate compartment (ortholog) NW_004955423 1436628 1456970 + 9068941 102014917 A0A8C2YMS7 MODEL AGCD01023434;AGCD01023435;GBDF01193843;XM_005385018;XM_005385019 XP_005385075;XP_005385076 transmembrane emp24 domain-containing protein 5;transmembrane emp24 protein transport domain containing 5 APPROVED protein-coding ENSCLAG00000007030 NW_004955423 1436628 1456970 + 8726807 Fancd2 FA complementation group D2 ENCODES a protein that exhibits DNA polymerase binding (ortholog); INVOLVED IN brain morphogenesis (ortholog); cellular response to oxidative stress (ortholog); DNA damage response (ortholog); ASSOCIATED WITH Atrioventricular Septal Defect 2 (ortholog); breast cancer (ortholog); Candidiasis, Familial, 9 (ortholog); FOUND IN condensed chromosome (ortholog); cytosol (ortholog); DNA repair complex (ortholog) NW_004955561 1460080 1538026 + 9068941;7240710 102015783 A0A8C2UUN3;A0A8C2UY88 MODEL AGCD01073855;AGCD01073856;GBDF01081668;XM_005413059;XM_005413060;XM_005413062;XM_013509097;XM_013509098;XM_013509099 XP_005413116;XP_005413117;XP_005413119;XP_013364551;XP_013364552;XP_013364553 Fanconi anemia complementation group D2;Fanconi anemia, complementation group D2 APPROVED protein-coding ENSCLAG00000003572 NW_004955561 1464869 1538045 + 8726862 LOC102017346 polyadenylate-binding protein-interacting protein 1-like NW_004955420 15919327 15926645 + 102017346 MODEL AGCD01020984 pseudo 8726863 LOC102018153 protein phosphatase 1A pseudogene NW_004955405 7689040 7690265 - 102018153 MODEL AGCD01004721 APPROVED pseudo 8726864 Nfatc2 nuclear factor of activated T cells 2 ENCODES a protein that exhibits 14-3-3 protein binding (ortholog); chromatin binding (ortholog); DNA-binding transcription activator activity, RNA polymerase II-specific (ortholog); INVOLVED IN B cell receptor signaling pathway (ortholog); calcineurin-NFAT signaling cascade (ortholog); cell migration (ortholog); PARTICIPATES IN calcineurin signaling pathway; nuclear factor of activated T-cells signaling pathway; Wnt signaling, non-canonical pathway; ASSOCIATED WITH dilated cardiomyopathy 1A (ortholog); genetic disease (ortholog); JOINT CONTRACTURES, OSTEOCHONDROMAS, AND B-CELL LYMPHOMA (ortholog); FOUND IN chromatin (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955445 7035876 7153199 + 9068941 102018867 A0A8C2V3K9;A0A8C2V5Y7;A0A8C2V8H9;A0A8C2V912 MODEL AGCD01039533;AGCD01039534;GBCB01092874;GBDF01234651;XM_005392294 XP_005392351 nuclear factor of activated T-cells 2;nuclear factor of activated T-cells, cytoplasmic 2;nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2 APPROVED protein-coding ENSCLAG00000006467 NW_004955445 7035876 7153237 + 8726896 LOC102020043 MICAL-like protein 1 NW_004955517 2041415 2043518 - 102020043 MODEL AGCD01067614;GBBH01168608;XM_005409030 XP_005409087 APPROVED protein-coding 8726903 LOC102020262 olfactory receptor 10T2-like NW_004955495 8104546 8109731 + 102020262 MODEL AGCD01062183;AGCD01062184;XM_013505150 XP_013360604 protein-coding 8726904 Eloc elongin C ENCODES a protein that exhibits protein-containing complex binding (ortholog); transcription corepressor binding (ortholog); INVOLVED IN positive regulation of transcription elongation by RNA polymerase II (ortholog); protein ubiquitination (ortholog); target-directed miRNA degradation (ortholog); PARTICIPATES IN hypoxia inducible factor pathway; ASSOCIATED WITH Charcot-Marie-Tooth disease axonal type 2K (ortholog); renal cell carcinoma (ortholog); Renal Cell Carcinoma 1 (ortholog); FOUND IN Cul5-RING ubiquitin ligase complex (ortholog); elongin complex (ortholog); VCB complex (ortholog) NW_004955444 6400721 6415881 + 9068941 102020296 A0A8C2US58 MODEL AGCD01038864;AGCD01038865;GBDF01004742;XM_005392079;XM_005392080 XP_005392136;XP_005392137 Tceb1 transcription elongation factor B (SIII), polypeptide 1 (15kDa, elongin C);transcription elongation factor B polypeptide 1;transcription elongation factor B subunit 1 APPROVED protein-coding ENSCLAG00000002529 NW_004955444 6400832 6415881 + 8726919 LOC102020390 uncharacterized LOC102020390 NW_004955445 12888527 12928600 + 102020390 MODEL AGCD01039764;AGCD01039765;GBDF01222119;XR_262332 ncrna 8726923 LOC102020496 long-chain-fatty-acid--CoA ligase 4 pseudogene NW_004955567 204423 206599 - 102020496 MODEL AGCD01074386 APPROVED pseudo 8726924 Eif3d eukaryotic translation initiation factor 3 subunit D ENCODES a protein that exhibits mRNA cap binding (ortholog); RNA binding (ortholog); translation initiation factor activity (ortholog); INVOLVED IN cap-dependent translational initiation (ortholog); formation of cytoplasmic translation initiation complex (ortholog); IRES-dependent viral translational initiation (ortholog); PARTICIPATES IN translation initiation pathway; ASSOCIATED WITH adenylosuccinase lyase deficiency (ortholog); genetic disease (ortholog); pre-eclampsia (ortholog); FOUND IN eukaryotic translation initiation factor 3 complex (ortholog); eukaryotic translation initiation factor 3 complex, eIF3m (ortholog); synapse (ortholog) NW_004955413 23096440 23110312 - 9068941 102020790 A0A8C2W277;A0A8C2W295 MODEL AGCD01014327;GBBH01030582;GBCE01030924;XM_013511591 XP_013367045 eukaryotic translation initiation factor 3, subunit D APPROVED protein-coding ENSCLAG00000016545 NW_004955413 23092749 23110312 - 8726943 LOC102021437 E3 SUMO-protein ligase PIAS2 pseudogene NW_004955415 14409004 14410892 - 102021437 MODEL AGCD01016298 APPROVED pseudo 8726944 Rab28 RAB28, member RAS oncogene family ENCODES a protein that exhibits GDP binding (ortholog); GTP binding (ortholog); ASSOCIATED WITH cone-rod dystrophy (ortholog); cone-rod dystrophy 18 (ortholog); fundus dystrophy (ortholog); FOUND IN ciliary basal body (ortholog); ciliary rootlet (ortholog) NW_004955480 10220811 10374021 + 9068941;7240710 102021555 A0A8C2UN91;A0A8C2UR30 MODEL AGCD01056760;AGCD01056761;AGCD01056762;AGCD01056763;AGCD01056764;AGCD01056765;AGCD01056766;GBCE01031034;XM_005402540;XM_005402541;XM_013503323;XM_013503324;XM_013503325;XM_013503326;XR_001230910 XP_005402597;XP_005402598;XP_013358777;XP_013358778;XP_013358779;XP_013358780 ras-related protein Rab-28 protein-coding ENSCLAG00000002201 NW_004955480 10258028 10374021 + 8726959 Sox2 SRY-box transcription factor 2 ENCODES a protein that exhibits chromatin binding (ortholog); chromatin DNA binding (ortholog); DNA binding (ortholog); INVOLVED IN adenohypophysis development (ortholog); anatomical structure formation involved in morphogenesis (ortholog); cell fate commitment (ortholog); ASSOCIATED WITH amenorrhea (ortholog); aniridia (ortholog); Anophthalmia (ortholog); FOUND IN chromatin (ortholog); cytoplasm (ortholog); cytosol (ortholog) NW_004955420 10671888 10674080 + 9068941;7240710 102023039 A0A8C2W911 MODEL AGCD01020783;GBBH01034135;XM_005383075 XP_005383132 SRY (sex determining region Y)-box 2;SRY-box 2;transcription factor SOX-2 APPROVED protein-coding ENSCLAG00000017978 NW_004955420 10671978 10672934 + 8726965 Klk10 kallikrein related peptidase 10 ASSOCIATED WITH Breast Neoplasms (ortholog); ductal carcinoma in situ (ortholog); genetic disease (ortholog) NW_004955558 1466162 1471112 + 9068941 102023205 A0A8C2ULU3 MODEL AGCD01073444;GBCQ01176836;XM_005412720 XP_005412777 kallikrein-10;kallikrein-related peptidase 10 APPROVED protein-coding ENSCLAG00000001547 NW_004955558 1466717 1471368 + 8726975 LOC102023270 fibrillin-3-like NW_004955489 7357305 7439090 - 102023270 MODEL AGCD01059983;GBDF01188439;GBDK01150101;XM_013504457 XP_013359911 APPROVED protein-coding 8726987 LOC102023558 elongation factor 1-alpha 1 pseudogene NW_004955457 3190550 3192322 + 102023558 MODEL AGCD01046765 APPROVED pseudo 8726988 Ncoa4 nuclear receptor coactivator 4 INVOLVED IN intracellular iron ion homeostasis (ortholog); protein targeting to lysosome (ortholog); response to hormone (ortholog); PARTICIPATES IN iron homeostasis pathway; ASSOCIATED WITH genetic disease (ortholog); invasive ductal carcinoma (ortholog); megacolon (ortholog); FOUND IN autolysosome (ortholog) NW_004955556 392412 413643 + 9068941 102024513 A0A8C2UM06 MODEL AGCD01073175;GBCQ01033190;XM_005412555;XM_005412556;XM_013508789 XP_005412612;XP_005412613;XP_013364243 protein-coding ENSCLAG00000001026 NW_004955556 392398 412166 + 8727016 LOC102024656 uracil-DNA glycosylase pseudogene NW_004955462 1209532 1210412 - 102024656 MODEL AGCD01049103 APPROVED pseudo 8727017 Padi2 peptidyl arginine deiminase 2 ENCODES a protein that exhibits histone H3R26 arginine deiminase activity (ortholog); nuclear estrogen receptor binding (ortholog); protein homodimerization activity (ortholog); INVOLVED IN cellular response to leukemia inhibitory factor (ortholog); intracellular estrogen receptor signaling pathway (ortholog); negative regulation of chemokine-mediated signaling pathway (ortholog); ASSOCIATED WITH chromosome 1p36 deletion syndrome (ortholog); COVID-19 (ortholog); gastrointestinal stromal tumor (ortholog); FOUND IN cytoplasm (ortholog); euchromatin (ortholog) NW_004955527 1709307 1751332 + 9068941 102024948 A0A8C2UPK5 MODEL AGCD01069414;GBCB01005607;XM_005409821 XP_005409878 peptidyl arginine deiminase, type II;protein-arginine deiminase type-2 APPROVED protein-coding ENSCLAG00000002391 NW_004955527 1709444 1752783 + 8727037 Ccdc142 coiled-coil domain containing 142 ASSOCIATED WITH congenital disorder of glycosylation type IIb (ortholog); dystonia (ortholog); genetic disease (ortholog) NW_004955424 11304968 11312679 + 102025263 A0A8C2YST4 MODEL AGCD01024561;GBDK01233807;XM_005385496 XP_005385553 coiled-coil domain-containing protein 142 protein-coding ENSCLAG00000014185 NW_004955424 11304988 11317294 + 8727052 Mroh2b maestro heat like repeat family member 2B INVOLVED IN protein kinase A signaling (ortholog); ASSOCIATED WITH genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); FOUND IN acrosomal vesicle (ortholog); cytoplasm (ortholog); sperm flagellum (ortholog) NW_004955426 25245920 25311757 - 102026237 A0A8C2V9E1;A0A8C2YNN6 MODEL AGCD01026710;AGCD01026711;AGCD01026712;GBDF01002540;XM_005386245;XM_005386246;XM_013514925;XM_013514927 XP_005386302;XP_005386303;XP_013370379;XP_013370381 maestro heat-like repeat family member 2B;maestro heat-like repeat-containing protein family member 2B APPROVED protein-coding ENSCLAG00000008282 NW_004955426 25237272 25312082 - 8727100 Ubald2 UBA like domain containing 2 ASSOCIATED WITH genetic disease (ortholog) NW_004955506 6018472 6027133 - 102026772 A0A8C2VB57 MODEL AGCD01065398;GBCB01006590;XM_005407438;XM_005407439;XM_013506126 XP_005407495;XP_005407496;XP_013361580 UBA-like domain containing 2;UBA-like domain-containing protein 2 APPROVED protein-coding ENSCLAG00000007176 NW_004955506 6015245 6024283 - 8727115 LOC102026962 DNA dC->dU-editing enzyme APOBEC-3H NW_004955413 25056223 25059761 + 9068941 102026962 A0A8C2W5A7 MODEL AGCD01014392;GBBH01087809;XM_013511480 XP_013366934 Apobec3h apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3H APPROVED protein-coding ENSCLAG00000016615 8727125 LOC102027013 uncharacterized LOC102027013 NW_004955438 14888310 14894069 - 102027013 MODEL AGCD01035354;XR_001235151;XR_261934;XR_261935 ncrna 8727140 Carm1 coactivator associated arginine methyltransferase 1 ENCODES a protein that exhibits DNA-binding transcription factor binding (ortholog); histone arginine N-methyltransferase activity (ortholog); histone H3R17 methyltransferase activity (ortholog); INVOLVED IN cell population proliferation (ortholog); endochondral bone morphogenesis (ortholog); intracellular estrogen receptor signaling pathway (ortholog); PARTICIPATES IN androgen signaling pathway; estrogen signaling pathway; histone modification pathway; ASSOCIATED WITH alpha-mannosidosis (ortholog); asthma (ortholog); Charcot-Marie-Tooth disease dominant intermediate B (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nuclear replication fork (ortholog) NW_004955495 1983599 2002174 + 9068941 102028553 A0A8C2VI21;A0A8C2VI82 MODEL AGCD01061743;AGCD01061744;GBDF01009004;XM_005406133 XP_005406190 coactivator-associated arginine methyltransferase 1;histone-arginine methyltransferase CARM1 APPROVED protein-coding ENSCLAG00000011012 NW_004955495 1983599 2002174 + 8727158 Ripk3 receptor interacting serine/threonine kinase 3 ENCODES a protein that exhibits identical protein binding (ortholog); NF-kappaB-inducing kinase activity (ortholog); protein kinase activity (ortholog); INVOLVED IN activation of protein kinase activity (ortholog); amyloid fibril formation (ortholog); cellular response to hydrogen peroxide (ortholog); ASSOCIATED WITH Acute-On-Chronic Liver Failure (ortholog); adult respiratory distress syndrome (ortholog); avian influenza (ortholog); FOUND IN cytoplasm (ortholog); cytosol (ortholog); nucleus (ortholog) NW_004955409 35961604 35965477 + 9068941 102028620 A0A8C2VTP3;A0A8C2YSM7;A0A8C2YSN0 MODEL AGCD01010437;GBDF01271691;XM_005377007;XM_005377010;XM_013510393;XM_013510394;XM_013510395;XM_013510396 XP_005377064;XP_005377067;XP_013365847;XP_013365848;XP_013365849;XP_013365850 receptor-interacting serine-threonine kinase 3;receptor-interacting serine/threonine-protein kinase 3 APPROVED protein-coding ENSCLAG00000013944 NW_004955409 35937880 35965712 + 8727183 LOC102029293 olfactory receptor 139-like NW_004955481 63565 64511 - 102029293 A0A8C2V9G2 MODEL AGCD01056778;XM_013503346 XP_013358800 protein-coding ENSCLAG00000008299 8727184 LOC102029340 UDP-glucuronosyltransferase 2B17-like NW_004955447 3892500 3921299 + 102029340 MODEL AGCD01040684;AGCD01040685;AGCD01040686;AGCD01040687;GBDJ01074834;XM_005392950 XP_005393007 protein-coding 8727192 Ppil3 peptidylprolyl isomerase like 3 PARTICIPATES IN spliceosome pathway; ASSOCIATED WITH genetic disease (ortholog); Neurodevelopmental Disorders (ortholog); Pulmonary Arterial Hypertension (ortholog); FOUND IN catalytic step 2 spliceosome (ortholog) NW_004955403 640956 648498 + 9068941 102029462 A0A8C2VY35 MODEL AGCD01001700;GBCQ01038792;XM_005373232;XM_005373233;XM_005373234;XM_005373235 XP_005373289;XP_005373290;XP_005373291;XP_005373292 peptidyl-prolyl cis-trans isomerase-like 3;peptidylprolyl isomerase (cyclophilin)-like 3 APPROVED protein-coding ENSCLAG00000014050 NW_004955403 640956 648604 + 8727212 Pdxdc1 pyridoxal dependent decarboxylase domain containing 1 ASSOCIATED WITH autistic disorder (ortholog); epilepsy (ortholog); genetic disease (ortholog); FOUND IN Golgi apparatus (ortholog); intracellular membrane-bounded organelle (ortholog) NW_004955442 187983 238586 - 9068941 102029673 A0A8C2VQN9;A0A8C2VW24 MODEL AGCD01037414;AGCD01037415;AGCD01037416;GBBH01063606;GBDJ01382967;XM_005391842 XP_005391899 pyridoxal-dependent decarboxylase domain containing 1;pyridoxal-dependent decarboxylase domain-containing protein 1 APPROVED protein-coding ENSCLAG00000013191 NW_004955442 185615 222956 - 8727236 Dok3 docking protein 3 INVOLVED IN Ras protein signal transduction (ortholog); ASSOCIATED WITH colorectal adenocarcinoma (ortholog); Ehlers-Danlos syndrome dermatosparaxis type (ortholog); Ehlers-Danlos syndrome spondylodysplastic type 2 (ortholog); FOUND IN cytoplasm (ortholog) NW_004955408 29740606 29747986 - 9068941 102029831 A0A8C2W0E9 MODEL AGCD01008770;GBDK01360031;XM_005376448;XM_013506590;XM_013506594 XP_005376505;XP_013362044;XP_013362048 protein-coding ENSCLAG00000015994 NW_004955408 29740449 29747986 - 8727246 Thbs3 thrombospondin 3 ENCODES a protein that exhibits heparin binding (ortholog); INVOLVED IN bone trabecula formation (ortholog); growth plate cartilage development (ortholog); ossification involved in bone maturation (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease type 2 (ortholog); gastrointestinal stromal tumor (ortholog); genetic disease (ortholog); FOUND IN perinuclear region of cytoplasm (ortholog) NW_004955545 1664372 1675810 - 9068941 102003381 A0A8C2UVU7;A0A8C2V0W4 MODEL AGCD01071865;AGCD01071866;GBDK01058843;XM_005411591;XM_005411593;XM_005411594;XM_013508309;XM_013508310 XP_005411648;XP_005411650;XP_005411651;XP_013363763;XP_013363764 thrombospondin-3 protein-coding ENSCLAG00000004613 NW_004955545 1664372 1675810 - 8727280 Loxl4 lysyl oxidase like 4 ENCODES a protein that exhibits protein-lysine 6-oxidase activity (ortholog); ASSOCIATED WITH autism spectrum disorder (ortholog); genetic disease (ortholog); urinary bladder cancer (ortholog); FOUND IN extracellular region (ortholog); receptor complex (ortholog) NW_004955507 4229284 4260005 - 9068941 102004405 A0A8C2UTA6 MODEL AGCD01065642;AGCD01065643;AGCD01065644;AGCD01065645;GBDI01328500;GBDK01396522;XM_013506211 XP_013361665 lysyl oxidase homolog 4;lysyl oxidase-like 4 APPROVED protein-coding ENSCLAG00000002846 NW_004955507 4231792 4256227 - 8727298 Cdc42 cell division cycle 42 ENCODES a protein that exhibits apolipoprotein A-I receptor binding (ortholog); GBD domain binding (ortholog); GTP binding (ortholog); INVOLVED IN actin cytoskeleton organization (ortholog); actin filament branching (ortholog); actin filament organization (ortholog); PARTICIPATES IN adenosine signaling pathway; c-Jun N-terminal kinases MAPK signaling pathway; E-cadherin signaling pathway; ASSOCIATED WITH 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (ortholog); Adrenal Gland Neoplasms (ortholog); Alzheimer's disease (ortholog); FOUND IN apical part of cell (ortholog); cell leading edge (ortholog); cell periphery (ortholog) NW_004955452 2255940 2299042 + 9068941;7240710 102005099 A0A8C2VJ29;A0A8C2VJ40 MODEL AGCD01043886;AGCD01043887;AGCD01043888;AGCD01043889;AGCD01043890;GBBH01031197;XM_005394731;XM_005394732;XM_005394733;XM_013519580 XP_005394788;XP_005394789;XP_005394790;XP_013375034 cell division control protein 42 homolog protein-coding ENSCLAG00000011266 NW_004955452 2255117 2299042 + 8727317 LOC102005703 double-strand break repair protein MRE11A-like NW_004955414 105311 171913 + 102005703 MODEL AGCD01014702;AGCD01014703;AGCD01014704;AGCD01014705;AGCD01014706;GBCE01032230;GBDF01042621;XM_013512034 XP_013367488 protein-coding 8727318 Ppy pancreatic polypeptide ENCODES a protein that exhibits G protein-coupled receptor binding (ortholog); ASSOCIATED WITH genetic disease (ortholog); FOUND IN cytoplasm (ortholog); extracellular space (ortholog) NW_004955451 17155681 17156829 - 9068941 102005767 A0A8C2W0Z6 MODEL AGCD01043724;XM_013519200 XP_013374654 pancreatic prohormone protein-coding ENSCLAG00000014670 NW_004955451 17155876 17156214 - 8727323 LOC102005943 myoD family inhibitor domain-containing protein-like NW_004955421 17734841 17752220 + 102005943 A0A8C2UUE6 MODEL AGCD01022030;XM_005383926 XP_005383983 protein-coding ENSCLAG00000003152 NW_004955421 17742878 17752220 + 8727328 Eif4e3 eukaryotic translation initiation factor 4E family member 3 ASSOCIATED WITH COVID-19 (ortholog); Experimental Liver Cirrhosis (ortholog); genetic disease (ortholog) NW_004955421 16354282 16520422 + 9068941 102006921 A0A8C2UVE4;A0A8C2UZ18 MODEL AGCD01021999;AGCD01022000;AGCD01022001;AGCD01022002;AGCD01022003;AGCD01022004;GBBH01218978;GBCE01142138;XM_005383789;XM_013513679 XP_005383846;XP_013369133 eukaryotic translation initiation factor 4E type 3 protein-coding ENSCLAG00000003818 NW_004955421 16354282 16419304 + 8727339 Qrsl1 glutaminyl-tRNA amidotransferase subunit QRSL1 ENCODES a protein that exhibits glutaminyl-tRNA synthase (glutamine-hydrolyzing) activity (ortholog); INVOLVED IN glutaminyl-tRNAGln biosynthesis via transamidation (ortholog); mitochondrial translation (ortholog); regulation of protein stability (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease type 4 (ortholog); combined oxidative phosphorylation deficiency 40 (ortholog); Developmental Disabilities (ortholog); FOUND IN glutamyl-tRNA(Gln) amidotransferase complex (ortholog); mitochondrion (ortholog) NW_004955411 31950727 31981522 + 9068941 102006992 A0A8C2W531;A0A8C2YUZ6 MODEL AGCD01012289;AGCD01012290;GBDF01157003;XM_005377831 XP_005377888 QRSL1, glutaminyl-tRNA amidotransferase subunit A;glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1;glutamyl-tRNA(Gln) amidotransferase subunit A, mitochondrial APPROVED protein-coding ENSCLAG00000017367 NW_004955411 31950828 31981468 + 8727354 Sowahc sosondowah ankyrin repeat domain family member C ASSOCIATED WITH genetic disease (ortholog) NW_004955470 12699007 12702332 + 102007004 MODEL AGCD01052937;GBDF01250483;GBDK01218176;XM_013522810 XP_013378264 ankyrin repeat domain-containing protein SOWAHC protein-coding 8727359 Rapgef5 Rap guanine nucleotide exchange factor 5 ENCODES a protein that exhibits GTP-dependent protein binding (ortholog); guanyl-nucleotide exchange factor activity (ortholog); ASSOCIATED WITH amphetamine abuse (ortholog); dilated cardiomyopathy 1A (ortholog); genetic disease (ortholog); FOUND IN nuclear body (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955410 24525748 24716151 - 9068941 102007634 A0A8C2VHU3 MODEL AGCD01011131;AGCD01011132;AGCD01011133;AGCD01011134;GBBH01203298;XM_005377379 XP_005377436 Rap guanine nucleotide exchange factor (GEF) 5 APPROVED protein-coding ENSCLAG00000009347 NW_004955410 24525748 24716372 - 8727392 LOC102007742 probable C-mannosyltransferase DPY19L2 NW_004955460 7871421 7960495 + 102007742 A0A8C2V029 MODEL AGCD01048500;AGCD01048501;AGCD01048502;AGCD01048503;AGCD01048504;AGCD01048505;AGCD01048506;AGCD01048507;AGCD01048508;GBDF01196111;XM_013521290;XM_013521291;XM_013521292 XP_013376744;XP_013376745;XP_013376746 APPROVED protein-coding ENSCLAG00000005564 8727393 Caps2 calcyphosine 2 ASSOCIATED WITH genetic disease (ortholog) NW_004955405 14658335 14761708 - 9068941 102008053 A0A8C2UV91 MODEL AGCD01004931;AGCD01004932;AGCD01004933;GBDI01163209;XM_005374329;XM_005374330;XM_005374331;XM_005374332;XM_013517679;XM_013517680;XM_013517683;XM_013517685;XM_013517689 XP_005374386;XP_005374387;XP_005374388;XP_005374389;XP_013373133;XP_013373134;XP_013373137;XP_013373139;XP_013373143 calcyphosin-2 protein-coding ENSCLAG00000004453 8727424 Tatdn1 TatD DNase domain containing 1 ASSOCIATED WITH genetic disease (ortholog); hepatocellular carcinoma (ortholog); trichorhinophalangeal syndrome type I (ortholog); FOUND IN nucleoplasm (ortholog) NW_004955540 3154273 3198140 - 9068941 102008147 A0A8C2UMU4 MODEL AGCD01071335;AGCD01071336;GBBH01177239;XM_013507914;XM_013507915;XM_013507917;XR_001232123;XR_001232124;XR_001232125;XR_001232126 XP_013363368;XP_013363369;XP_013363371 putative deoxyribonuclease TATDN1 protein-coding ENSCLAG00000000573 NW_004955540 3157902 3198064 - 8727444 Ammecr1 AMMECR nuclear protein 1 ASSOCIATED WITH autistic disorder (ortholog); Dwarfism (ortholog); genetic disease (ortholog); FOUND IN mitochondrion (ortholog); nucleoplasm (ortholog); nucleus (ortholog) NW_004955490 5538445 5657959 + 9068941 102008632 A0A8C2UYB1 MODEL AGCD01060205;AGCD01060206;AGCD01060207;GBDI01339138;XM_005404657 XP_005404714 Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 APPROVED protein-coding ENSCLAG00000005053 NW_004955490 5538415 5658097 + 8727457 Ripk2 receptor interacting serine/threonine kinase 2 ENCODES a protein that exhibits CARD domain binding (ortholog); caspase binding (ortholog); identical protein binding (ortholog); INVOLVED IN activation of cysteine-type endopeptidase activity (ortholog); adaptive immune response (ortholog); apoptotic process (ortholog); PARTICIPATES IN interleukin-12 signaling pathway; nuclear factor kappa B signaling pathway; ASSOCIATED WITH genetic disease (ortholog); leprosy (ortholog); ulcerative colitis (ortholog); FOUND IN cytoplasm (ortholog); cytoskeleton (ortholog); cytosol (ortholog) NW_004955417 6669675 6698142 + 9068941 102008942 A0A8C2YMK0 MODEL AGCD01017988;GBCE01045721;GBDI01182180;XM_013512753 XP_013368207 receptor-interacting serine-threonine kinase 2;receptor-interacting serine/threonine-protein kinase 2 APPROVED protein-coding ENSCLAG00000006724 NW_004955417 6669675 6702228 + 8727472 LOC102009764 keratin, type II cytoskeletal 75 NW_004955547 2773524 2784448 - 9068941;7240710 102009764 A0A8C2UHM9;A0A8C2UHN0 MODEL AGCD01072294;GBCB01107480;XM_005411943 XP_005412000 Krt75 keratin 75 APPROVED protein-coding ENSCLAG00000000837 NW_004955547 2773523 2932609 - 8727485 Tspyl2 TSPY like 2 INVOLVED IN negative regulation of cell growth (ortholog); negative regulation of DNA replication (ortholog); regulation of protein kinase activity (ortholog); ASSOCIATED WITH autistic disorder (ortholog); Endometrial Neoplasms (ortholog); genetic disease (ortholog); FOUND IN nucleolus (ortholog); nucleus (ortholog) NW_004955475 160768 167359 + 9068941 102010477 A0A8C2US85 MODEL AGCD01054680;GBBH01208279;XM_005401476 XP_005401533 TSPY-like 2;testis-specific Y-encoded-like protein 2 APPROVED protein-coding ENSCLAG00000003149 NW_004955475 160964 167440 + 8727496 LOC102010963 uncharacterized LOC102010963 NW_004955450 6116015 6122123 - 102010963 MODEL AGCD01042519;GBDF01296262;XR_262533 ncrna 8727505 Pink1 PTEN induced kinase 1 ENCODES a protein that exhibits ATP binding (ortholog); C3HC4-type RING finger domain binding (ortholog); calcium-dependent protein kinase activity (ortholog); INVOLVED IN autophagy of mitochondrion (ortholog); catecholamine secretion (ortholog); cellular response to hydrogen sulfide (ortholog); PARTICIPATES IN altered mitochondrial autophagy pathway; mitochondria dynamics pathway; mitochondrial autophagy pathway; ASSOCIATED WITH 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (ortholog); congenital disorder of glycosylation (ortholog); congenital disorder of glycosylation Ir (ortholog); FOUND IN astrocyte projection (ortholog); axon (ortholog); cell body (ortholog) NW_004955452 1171115 1186338 + 9068941;7240710 102011271 A0A8C2VHF6 MODEL AGCD01043834;AGCD01043835;GBBH01034979;GBDF01010551;XM_013519660 XP_013375114 PTEN induced putative kinase 1;serine/threonine-protein kinase PINK1, mitochondrial APPROVED protein-coding ENSCLAG00000008925 NW_004955452 1171205 1185125 + 8727518 Tlcd5 TLC domain containing 5 ASSOCIATED WITH CD3epsilon deficiency (ortholog); Chromosome 11, Partial Trisomy 11q (ortholog); Dwarfism (ortholog) NW_004955412 21344464 21350675 + 9068941 102011421 A0A8C2W0E0 MODEL AGCD01013021;GBCE01163283;XM_005378348;XM_005378349;XM_005378350 XP_005378405;XP_005378406;XP_005378407 Tmem136 transmembrane protein 136 APPROVED protein-coding ENSCLAG00000016010 NW_004955412 21344261 21352074 + 8727530 Laptm4a lysosomal protein transmembrane 4 alpha ASSOCIATED WITH genetic disease (ortholog); FOUND IN Golgi apparatus (ortholog); late endosome membrane (ortholog); lysosomal membrane (ortholog) NW_004955469 2604464 2626835 - 9068941 102012419 A0A8C2V9C7 MODEL AGCD01052279;AGCD01052280;GBBH01004233;XM_005400342 XP_005400399 lysosomal-associated transmembrane protein 4A protein-coding ENSCLAG00000006983 NW_004955469 2604464 2627043 - 8727541 Vsig2 V-set and immunoglobulin domain containing 2 ASSOCIATED WITH Chromosome 11, Partial Trisomy 11q (ortholog); Dwarfism (ortholog); genetic disease (ortholog) NW_004955412 25818501 25823393 - 9068941 102013400 A0A8C2W2C1 MODEL AGCD01013174;GBBH01046285;XM_005378438;XM_005378441 XP_005378495;XP_005378498 V-set and immunoglobulin domain-containing protein 2 protein-coding ENSCLAG00000015241 NW_004955412 25818566 25823224 - 8727567 Tab2 TGF-beta activated kinase 1 (MAP3K7) binding protein 2 ENCODES a protein that exhibits K63-linked polyubiquitin modification-dependent protein binding (ortholog); molecular adaptor activity (ortholog); protein serine/threonine kinase activator activity (ortholog); INVOLVED IN heart development (ortholog); inflammatory response (ortholog); NIK/NF-kappaB signaling (ortholog); PARTICIPATES IN Bone morphogenetic proteins signaling pathway; interleukin-1 signaling pathway; nuclear factor kappa B signaling pathway; ASSOCIATED WITH brain disease (ortholog); cardiomyopathy (ortholog); chronic obstructive pulmonary disease (ortholog); FOUND IN cytoplasm (ortholog) NW_004955439 11826469 11903103 - 9068941;7240710 102014175 A0A8C2URK7 MODEL AGCD01035924;AGCD01035925;GBCB01022887;XM_005390614;XM_005390615;XM_005390616;XM_013517374;XM_013517375;XM_013517376 XP_005390671;XP_005390672;XP_005390673;XP_013372828;XP_013372829;XP_013372830 TGF-beta activated kinase 1/MAP3K7 binding protein 2;TGF-beta-activated kinase 1 and MAP3K7-binding protein 2 APPROVED protein-coding ENSCLAG00000002977 NW_004955439 11826469 11903103 - 8727583 Pygl glycogen phosphorylase L ENCODES a protein that exhibits AMP binding (ortholog); ATP binding (ortholog); bile acid binding (ortholog); INVOLVED IN 5-phosphoribose 1-diphosphate biosynthetic process (ortholog); glucose homeostasis (ortholog); glycogen catabolic process (ortholog); PARTICIPATES IN congenital sucrase-isomaltase deficiency pathway; glycogen degradation pathway; glycogen metabolic pathway; ASSOCIATED WITH Chemical and Drug Induced Liver Injury (ortholog); genetic disease (ortholog); glycogen storage disease (ortholog) NW_004955409 11970112 12007102 + 9068941;7240710 102014538 A0A8C2VHX7 MODEL AGCD01009530;GBBH01062062;XM_005376795 XP_005376852 glycogen phosphorylase, liver form;phosphorylase, glycogen, liver APPROVED protein-coding ENSCLAG00000010968 NW_004955409 11970112