基因ID | taxid | GeneDate LocusTag | Symbol Synonyms | Symbolfna Fullnamefna | dbXrefs | chromosome maplocation | description | genetype fnastatus | Otherdesignations | Featuretype |
266675 | 9606 | 20220522 | BEST4 VMD2L2 | BEST4 bestrophin 4 | MIM:607336|HGNC:HGNC:17106|Ensembl:ENSG00000142959|AllianceGenome:HGNC:17106 | 1 1p34.1 | bestrophin 4 | protein-coding O | bestrophin-4|vitelliform macular dystrophy 2-like 2|vitelliform macular dystrophy 2-like protein 2 | |
266676 | 7955 | 20220519 | dnah9 Lrdr|dnahc11|fj30b09|lrdr1|wu:fj30b09|zgc:63607 | dnah9 dynein, axonemal, heavy chain 9 | ZFIN:ZDB-GENE-020925-1|Ensembl:ENSDARG00000103383|AllianceGenome:ZFIN:ZDB-GENE-020925-1 | 12 | dynein, axonemal, heavy chain 9 | protein-coding O | dynein heavy chain 9, axonemal|dynein, axonemal, heavy chain 11|dynein, axonemal, heavy polypeptide 9 | |
266678 | 9606 | 20191002 | MRX81 | MIM:300433 | X Xp11.2-q12 | mental retardation, X-linked 81 | unknown | |||
266680 | 10116 | 20220623 | St18 Nzf3|r-MyT3 | St18 ST18 C2H2C-type zinc finger transcription factor | RGD:708566|Ensembl:ENSRNOG00000006200|AllianceGenome:RGD:708566 | 5 5q12 | ST18 C2H2C-type zinc finger transcription factor | protein-coding O | suppression of tumorigenicity 18 protein|C2-HC type zinc finger protein r-MyT3|NZF-3|ST18, C2H2C-type zinc finger|neural zinc finger factor 3|suppression of tumorigenicity protein 18 | |
266681 | 10116 | 20220611 | Tmprss5 Amp | Tmprss5 transmembrane serine protease 5 | RGD:628625|Ensembl:ENSRNOG00000008058|AllianceGenome:RGD:628625 | 8 8q23 | transmembrane serine protease 5 | protein-coding O | transmembrane protease serine 5|adrenal mitochondrial protease|transmembrane protease, serine 5 (spinesin) | |
266682 | 10116 | 20220522 | Cyp3a2 Cyp3a11 | Cyp3a2 cytochrome P450, family 3, subfamily a, polypeptide 2 | RGD:708379|Ensembl:ENSRNOG00000032560|AllianceGenome:RGD:708379 | 12 12p11 | cytochrome P450, family 3, subfamily a, polypeptide 2 | protein-coding O | cytochrome P450 3A2|CYPIIIA2|P450-PCN2|P450/6-beta-A|cytochrome P450, family 3, subfamily a, polypeptide 11|cytochrome P450-PCN2|cytochrome P450/6-beta-A|testosterone 6-beta-hydroxylase | |
266683 | 9606 | 20220513 | EIF3MP1 | EIF3MP1 EIF3M pseudogene 1 | HGNC:HGNC:55006|AllianceGenome:HGNC:55006 | X Xq21.1 | EIF3M pseudogene 1 | pseudo O | dendritic cell protein pseudogene|eukaryotic translation initiation factor 3 subunit M pseudogene | |
266684 | 10116 | 20220522 | Cyp2d1 Cyp2d9 | Cyp2d1 cytochrome P450, family 2, subfamily d, polypeptide 1 | RGD:708427|Ensembl:ENSRNOG00000029179|AllianceGenome:RGD:708427 | 7 7q34 | cytochrome P450, family 2, subfamily d, polypeptide 1 | protein-coding O | cytochrome P450 2D1|CYPIID1|P450-CMF1A|P450-DB1|P450-UT-7|cytochrome P450, family 2, subfamily d, polypeptide 9|cytochrome P450-CMF1A|cytochrome P450-DB1|cytochrome P450-UT-7|debrisoquine 4-hydroxylase | |
266685 | 10116 | 20220522 | Ugt2b15 Rlug38|UDPGT 2B5|Udpgt|Udpgtr-3|Ugt2b17|Ugt2b3|Ugt2b5 | Ugt2b15 UDP glucuronosyltransferase family 2 member B15 | RGD:628623|Ensembl:ENSRNOG00000064466|AllianceGenome:RGD:628623 | 14 14p21 | UDP glucuronosyltransferase family 2 member B15 | protein-coding O | UDP-glucuronosyltransferase 2B17|17-beta-hydroxysteroid specific|17-beta-hydroxysteroid-specific UDPGT|UDP glucuronosyltransferase 2 family, polypeptide B15|UDP glucuronosyltransferase 2 family, polypeptide B17|UDP glucuronosyltransferase 2 family, polypeptide B5|UDP glycosyltransferase 2 family, member 3|UDP-glucuronosyltransferase 2A3-like|UDP-glucuronosyltransferase 2B17-like|UDP-glucuronosyltransferase 2B3 precursor, microsomal|UDP-glucuronosyltransferase 2B5|UDPGT 2B17|UDPGT 2B3|liver 17 beta-hydroxysteroid UDP-glucuronosyltransferase|testosterone, dihydrotestosterone, and beta-estradiol specific|testosterone, dihydrotestosterone, and beta-estradiol-specific UDPGT | |
266686 | 10116 | 20220424 | Dhrs4 PSCD | Dhrs4 dehydrogenase/reductase 4 | RGD:708482|Ensembl:ENSRNOG00000018239|AllianceGenome:RGD:708482 | 15 15p13 | dehydrogenase/reductase 4 | protein-coding O | dehydrogenase/reductase SDR family member 4|CR|DCR-AKL|NADP-retinol dehydrogenase|NADPH-dependent carbonyl reductase|NADPH-dependent carbonyl reductase/NADP-retinol dehydrogenase|NADPH-dependent retinol dehydrogenase/reductase|NDRD|PHCR|carbonyl reductase|dehydrogenase/reductase (SDR family) member 4|peroxisomal short-chain alcohol dehydrogenase|short chain dehydrogenase/reductase family 25C member 2 | |
266687 | 10116 | 20220424 | Slc35e4 | Slc35e4 solute carrier family 35, member E4 | RGD:708484|Ensembl:ENSRNOG00000004168|AllianceGenome:RGD:708484 | 14 14q21 | solute carrier family 35, member E4 | protein-coding O | solute carrier family 35 member E4|putative phosphate-phosphoenolpyruvate translocator | |
266688 | 10116 | 20220522 | Rab8b | Rab8b RAB8B, member RAS oncogene family | RGD:628764|Ensembl:ENSRNOG00000018009|AllianceGenome:RGD:628764 | 8 8q24 | RAB8B, member RAS oncogene family | protein-coding O | ras-related protein Rab-8B|GTPase Rab8b | |
266689 | 10116 | 20220522 | Cyp4f6 | Cyp4f6 cytochrome P450, family 4, subfamily f, polypeptide 6 | RGD:708365|Ensembl:ENSRNOG00000043233|AllianceGenome:RGD:708365 | 7 7q11 | cytochrome P450, family 4, subfamily f, polypeptide 6 | protein-coding O | cytochrome P450 4F6|CYPIVF6 | |
266690 | 10090 | 20220712 | Cyb5r4 2810034J18Rik|B5+B5R|C79736|Cb5cb5r|Ncb5or|b5/b5r|b5b5r | Cyb5r4 cytochrome b5 reductase 4 | MGI:MGI:2386848|Ensembl:ENSMUSG00000032872|AllianceGenome:MGI:2386848 | 9 9|9 E3.1 | cytochrome b5 reductase 4 | protein-coding O | cytochrome b5 reductase 4|N-terminal cytochrome b5 and cytochrome b5 oxidoreductase domain-containing protein|NADPH cytochrome B5 oxidoreductase|cb5/cb5R|cytochrome b-type NAD(P)H oxidoreductase|flavohemoprotein b5/b5R | |
266691 | 9606 | 20191002 | DYX6 DYXQTL18 | MIM:606616 | 18 18p11.2 | dyslexia susceptibility 6 | unknown | Dyslexia QTL on 18 | ||
266692 | 10090 | 20220712 | Cpne1 1810028N16Rik|mKIAA4108 | Cpne1 copine I | MGI:MGI:2386621|Ensembl:ENSMUSG00000074643|AllianceGenome:MGI:2386621 | 2 2|2 H1 | copine I | protein-coding O | copine-1 | |
266693 | 9606 | 20220125 | EZH2P1 | EZH2P1 enhancer of zeste 2 polycomb repressive complex 2 subunit pseudogene 1 | HGNC:HGNC:39918|AllianceGenome:HGNC:39918 | 21 21q22.12 | enhancer of zeste 2 polycomb repressive complex 2 subunit pseudogene 1 | pseudo O | enhancer of zeste homolog 2 pseudogene 1 | |
266694 | 9606 | 20220513 | EEDP1 | EEDP1 EED pseudogene 1 | HGNC:HGNC:55143|Ensembl:ENSG00000224942|AllianceGenome:HGNC:55143 | X Xq27.1 | EED pseudogene 1 | pseudo O | embryonic ectoderm development pseudogene | |
266695 | 9606 | 20220513 | PHF2P1 | PHF2P1 PHD finger protein 2 pseudogene 1 | HGNC:HGNC:30241|AllianceGenome:HGNC:30241 | 13 13q12.11 | PHD finger protein 2 pseudogene 1 | pseudo O | ||
266697 | 9606 | 20220531 | POM121L4P POM121L1|POM121L1P | POM121L4P POM121 transmembrane nucleoporin like 4, pseudogene | HGNC:HGNC:19326|AllianceGenome:HGNC:19326 | 22 22q11.21 | POM121 transmembrane nucleoporin like 4, pseudogene | pseudo O | POM121 membrane glycoprotein-like 4 pseudogene|Putative POM121-like protein 1 | |
266698 | 9606 | 20220513 | ARHGAP42P3 OPHN1P1 | ARHGAP42P3 ARHGAP42 pseudogene 3 | HGNC:HGNC:19327|AllianceGenome:HGNC:19327 | 22 22q11.1 | ARHGAP42 pseudogene 3 | pseudo O | Rho GTPase activating protein 42 pseudogene 3|oligophrenin 1 pseudogene 1 | |
266699 | 9606 | 20220513 | FABP5P11 FABP5L11|FABP5P1 | FABP5P11 fatty acid binding protein 5 pseudogene 11 | HGNC:HGNC:19328|AllianceGenome:HGNC:19328 | 22 22q11.1 | fatty acid binding protein 5 pseudogene 11 | pseudo O | fatty acid binding protein 5, pseudogene 1|fatty acid binding protein 5-like 11 (pseudogene) | |
266700 | 9606 | 20220513 | BMP6P1 TGF-beta1P|TGFB1P | BMP6P1 bone morphogenetic protein 6 pseudogene 1 | HGNC:HGNC:19329|AllianceGenome:HGNC:19329 | 22 22q11.22 | bone morphogenetic protein 6 pseudogene 1 | pseudo O | transforming growth factor beta 1 pseudogene | |
266701 | 9606 | 20220513 | SOCS2P2 | SOCS2P2 suppressor of cytokine signaling 2 pseudogene 2 | HGNC:HGNC:19330|AllianceGenome:HGNC:19330 | 22 22q11.22 | suppressor of cytokine signaling 2 pseudogene 2 | pseudo O | ||
266703 | 9606 | 20220513 | ASH2LP1 | ASH2LP1 ASH2L pseudogene 1 | HGNC:HGNC:19332|AllianceGenome:HGNC:19332 | 22 22q11.22 | ASH2L pseudogene 1 | pseudo O | ASH2 like histone lysine methyltransferase complex subunit pseudogene 1|ash2 (absent, small, or homeotic)-like pseudogene 1 | |
266704 | 10116 | 20220424 | Gzmf Gzmg|Rnkp7 | Gzmf granzyme F | RGD:628603|Ensembl:ENSRNOG00000028810|AllianceGenome:RGD:628603 | 15 15p12 | granzyme F | protein-coding I | granzyme H|granzyme G|granzyme G-like|natural killer cell protease 7 | |
266705 | 10116 | 20220522 | Ppp1r17 Gsbs | Ppp1r17 protein phosphatase 1, regulatory subunit 17 | RGD:628647|Ensembl:ENSRNOG00000012235|AllianceGenome:RGD:628647 | 4 4q24 | protein phosphatase 1, regulatory subunit 17 | protein-coding O | protein phosphatase 1 regulatory subunit 17|G-substrate | |
266706 | 10116 | 20220424 | Gjc1 Cx45|Cxnq|Gja7 | Gjc1 gap junction protein, gamma 1 | RGD:628889|Ensembl:ENSRNOG00000048838|AllianceGenome:RGD:628889 | 10 10q32.1 | gap junction protein, gamma 1 | protein-coding O | gap junction gamma-1 protein|connexin q|connexin-45|gap junction alpha-7 protein|gap junction channel protein connexin 45|gap junction membrane channel protein alpha 7 | |
266707 | 10116 | 20220522 | Gjd4 Cx39 | Gjd4 gap junction protein, delta 4 | RGD:628621|Ensembl:ENSRNOG00000018407|AllianceGenome:RGD:628621 | 17 17q12.1 | gap junction protein, delta 4 | protein-coding O | gap junction delta-4 protein|connexin 39|gap junction channel protein | |
266708 | 10116 | 20220522 | Gzma | Gzma granzyme A | RGD:628640|Ensembl:ENSRNOG00000010603|AllianceGenome:RGD:628640 | 2 2q14 | granzyme A | protein-coding O | ||
266709 | 10116 | 20220522 | Pkig | Pkig cAMP-dependent protein kinase inhibitor gamma | RGD:628775|AllianceGenome:RGD:628775 | 3 3q42 | cAMP-dependent protein kinase inhibitor gamma | protein-coding O | cAMP-dependent protein kinase inhibitor gamma|protein kinase (cAMP-dependent, catalytic) inhibitor gamma|protein kinase inhibitor, gamma | |
266710 | 9606 | 20190816 | COMA | MIM:257550 | 2 2q13 | Cogan-type congential oculomotor apraxia | unknown | |||
266711 | 10116 | 20220522 | Lzts1 Psdzip70 | Lzts1 leucine zipper tumor suppressor 1 | RGD:708565|Ensembl:ENSRNOG00000011826|AllianceGenome:RGD:708565 | 16 16p14 | leucine zipper tumor suppressor 1 | protein-coding O | leucine zipper putative tumor suppressor 1|PSD-Zip70|leucine zipper, putative tumor suppressor 1 | |
266712 | 10116 | 20220424 | Rnf40 | Rnf40 ring finger protein 40 | RGD:628638|Ensembl:ENSRNOG00000018840|AllianceGenome:RGD:628638 | 1 1q37 | ring finger protein 40 | protein-coding O | E3 ubiquitin-protein ligase BRE1B|BRE1-B|RING-type E3 ubiquitin transferase BRE1B|protein staring|ring finger protein 40, E3 ubiquitin protein ligase|staring protein|syntaxin-1-interacting RING finger protein | |
266713 | 10116 | 20220623 | Mnat1 | Mnat1 MNAT1 component of CDK activating kinase | RGD:628874|Ensembl:ENSRNOG00000007267|AllianceGenome:RGD:628874 | 6 6q24 | MNAT1 component of CDK activating kinase | protein-coding O | CDK-activating kinase assembly factor MAT1|MNAT CDK-activating kinase assembly factor 1|MNAT1, CDK activating kinase assembly factor|menage a trois 1|menage a trois homolog 1, cyclin H assembly factor | |
266714 | 10116 | 20220522 | Myo7a | Myo7a myosin VIIA | RGD:628830|Ensembl:ENSRNOG00000013641|AllianceGenome:RGD:628830 | 1 1q32 | myosin VIIA | protein-coding O | unconventional myosin-VIIa|myosin VIIA (Usher syndrome 1B (autosomal recessive, severe))|myosin-VIIa | |
266715 | 10116 | 20220522 | Fzd3 | Fzd3 frizzled class receptor 3 | RGD:628814|Ensembl:ENSRNOG00000047211|AllianceGenome:RGD:628814 | 15 15p11 | frizzled class receptor 3 | protein-coding O | frizzled-3|frizzled family receptor 3 | |
266716 | 10116 | 20220514 | Zscan12 Zfp96 | Zscan12 zinc finger and SCAN domain containing 12 | RGD:628738|Ensembl:ENSRNOG00000052959|AllianceGenome:RGD:628738 | 17 17p11 | zinc finger and SCAN domain containing 12 | protein-coding O | zinc finger and SCAN domain-containing protein 12|zinc finger protein 96 | |
266717 | 10116 | 20220424 | Krt9 Krt1-9 | Krt9 keratin 9 | RGD:628785|Ensembl:ENSRNOG00000014370|AllianceGenome:RGD:628785 | 10 10q31 | keratin 9 | protein-coding O | keratin, type I cytoskeletal 9|CK-9|K9|cytokeratin-9|keratin 9 (epidermolytic palmoplantar keratoderma)|keratin 9, type I|keratin complex 1, acidic, gene 9|spermatid perinuclear ring manchette protein K9 | |
266719 | 9606 | 20190816 | RRDX | MIM:300378 | X Xq24-q25 | Radial ray deficiency | unknown | |||
266721 | 7955 | 20220424 | trh Pro-TRH|zgc:110168 | trh thyrotropin-releasing hormone | ZFIN:ZDB-GENE-020930-1|Ensembl:ENSDARG00000006868|AllianceGenome:ZFIN:ZDB-GENE-020930-1 | 8 | thyrotropin-releasing hormone | protein-coding O | pro-thyrotropin-releasing hormone|prepro-thyrotropin-releasing hormone|prothyroliberin | |
266722 | 9606 | 20220522 | HS6ST3 HS6ST-3 | HS6ST3 heparan sulfate 6-O-sulfotransferase 3 | MIM:609401|HGNC:HGNC:19134|Ensembl:ENSG00000185352|AllianceGenome:HGNC:19134 | 13 13q32.1 | heparan sulfate 6-O-sulfotransferase 3 | protein-coding O | heparan-sulfate 6-O-sulfotransferase 3 | |
266723 | 9606 | 20220513 | PSMC6P1 PSMC6P | PSMC6P1 proteasome 26S subunit, ATPase, 6 pseudogene 1 | HGNC:HGNC:20634|AllianceGenome:HGNC:20634 | 8 8q12.1 | proteasome 26S subunit, ATPase, 6 pseudogene 1 | pseudo O | proteasome (prosome, macropain) 26S subunit, ATPase, 6 pseudogene|proteasome 26S ATPase subunit 6 pseudogene | |
266724 | 9606 | 20220513 | HSPA9P1 HSPA9BP|HSPA9P | HSPA9P1 heat shock protein family A (Hsp70) member 9 pseudogene 1 | HGNC:HGNC:24915|AllianceGenome:HGNC:24915 | 2 2q36.1 | heat shock protein family A (Hsp70) member 9 pseudogene 1 | pseudo O | heat shock 70kDa protein 9 (mortalin) pseudogene|heat shock 70kDa protein 9 pseudogene 1 | |
266725 | 6239 | 20220707 CELE_F10C1.8 | F10C1.8 | WormBase:WBGene00017327|AllianceGenome:WB:WBGene00017327 | II | LTD domain-containing protein | protein-coding | |||
266727 | 9606 | 20220513 | MDGA1 GPIM|MAMDC3 | MDGA1 MAM domain containing glycosylphosphatidylinositol anchor 1 | MIM:609626|HGNC:HGNC:19267|Ensembl:ENSG00000112139|AllianceGenome:HGNC:19267 | 6 6p21.2 | MAM domain containing glycosylphosphatidylinositol anchor 1 | protein-coding O | MAM domain-containing glycosylphosphatidylinositol anchor protein 1|GPI and MAM protein|MAM domain-containing protein 3|glycosylphosphatidylinositol-MAM | |
266729 | 10116 | 20220522 | Dab1 | Dab1 DAB adaptor protein 1 | RGD:628770|Ensembl:ENSRNOG00000007410|AllianceGenome:RGD:628770 | 5 5q33-q34 | DAB adaptor protein 1 | protein-coding O | disabled homolog 1|DAB1, reelin adaptor protein|Dab, reelin signal transducer, homolog 1 | |
266730 | 10116 | 20220424 | Slc17a3 Rnpt4 | Slc17a3 solute carrier family 17 member 3 | RGD:628815|Ensembl:ENSRNOG00000032745|AllianceGenome:RGD:628815 | 17 17p11 | solute carrier family 17 member 3 | protein-coding O | sodium-dependent phosphate transport protein 4|Na/Pi cotransporter 4|sodium-phosphate cotransporter|solute carrier family 17 (organic anion transporter), member 3|solute carrier family 17 (sodium phosphate), member 3 | |
266732 | 10116 | 20220522 | Npc1 Cdig2|SLC66A1 | Npc1 NPC intracellular cholesterol transporter 1 | RGD:628693|Ensembl:ENSRNOG00000012016|AllianceGenome:RGD:628693 | 18 18p13 | NPC intracellular cholesterol transporter 1 | protein-coding O | NPC intracellular cholesterol transporter 1|Niemann-Pick disease, type C1|solute carrier family 66 member 1 | |
266733 | 10116 | 20220522 | Slc12a8 Ccc9 | Slc12a8 solute carrier family 12, member 8 | RGD:628730|Ensembl:ENSRNOG00000001792|AllianceGenome:RGD:628730 | 11 11q22 | solute carrier family 12, member 8 | protein-coding O | solute carrier family 12 member 8|cation-chloride cotransporter 9|solute carrier family 12 (potassium/chloride transporters), member 8 |
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