| 基因ID | taxid | GeneDate LocusTag | Symbol Synonyms | Symbolfna Fullnamefna | dbXrefs | chromosome maplocation | description | genetype fnastatus | Otherdesignations | Featuretype |
| 619327 | 10090 | 20220125 | G630093K05Rik | G630093K05Rik RIKEN cDNA G630093K05 gene | MGI:MGI:3588274|Ensembl:ENSMUSG00000114959|AllianceGenome:MGI:3588274 | 13 13|13 A5 | RIKEN cDNA G630093K05 gene | ncRNA O | ||
| 619328 | 10090 | 20220719 | I730028E13Rik | I730028E13Rik RIKEN cDNA I730028E13 gene | MGI:MGI:3588278|Ensembl:ENSMUSG00000110998|AllianceGenome:MGI:3588278 | 9 9 B|9 | RIKEN cDNA I730028E13 gene | ncRNA O | ||
| 619329 | 10090 | 20220125 | F420015M19Rik | F420015M19Rik RIKEN cDNA F420015M19 gene | MGI:MGI:3588283|AllianceGenome:MGI:3588283 | 17 17|17 E3 | RIKEN cDNA F420015M19 gene | protein-coding O | ||
| 619330 | 10090 | 20220125 | F830210D05Rik | F830210D05Rik RIKEN cDNA F830210D05 gene | MGI:MGI:3588228|AllianceGenome:MGI:3588228 | 13 | RIKEN cDNA F830210D05 gene | protein-coding O | ||
| 619331 | 10090 | 20220623 | Zfp551 9630004E07Rik|Znf551 | Zfp551 zinc fingr protein 551 | MGI:MGI:3588205|Ensembl:ENSMUSG00000034071|AllianceGenome:MGI:3588205 | 7 7|7 A1 | zinc fingr protein 551 | protein-coding O | zinc finger protein 551 | |
| 619332 | 10090 | 20220424 | Taf7l2 4933416C03Rik | Taf7l2 Taf7l2 | MGI:MGI:6274337|Ensembl:ENSMUSG00000074734|AllianceGenome:MGI:6274337 | 10 10|10 D2 | Taf7l2 | protein-coding O | uncharacterized protein LOC619332 | |
| 619334 | 10090 | 20220125 | Xlr4e-ps EG667446|Xlr4e | Xlr4e-ps X-linked lymphocyte-regulated 4E, pseudogene | MGI:MGI:3574182|Ensembl:ENSMUSG00000081357|AllianceGenome:MGI:3574182 | X X|X A7.3 | X-linked lymphocyte-regulated 4E, pseudogene | pseudo O | ||
| 619344 | 9606 | 20220513 | LINC01298 C8orf69 | LINC01298 long intergenic non-protein coding RNA 1298 | HGNC:HGNC:32292|Ensembl:ENSG00000253351|AllianceGenome:HGNC:32292 | 8 8q22.1 | long intergenic non-protein coding RNA 1298 | ncRNA O | ||
| 619345 | 10116 | 20220519 | Surf2 | Surf2 surfeit 2 | RGD:1565817|Ensembl:ENSRNOG00000066832|AllianceGenome:RGD:1565817 | 3 3p13 | surfeit 2 | protein-coding I | surfeit locus protein 2|surfeit gene 2|surfeit locus protein 2-like | |
| 619346 | 10116 | 20220424 | Surf4 | Surf4 surfeit 4 | RGD:1561980|Ensembl:ENSRNOG00000060005|AllianceGenome:RGD:1561980 | 3 3p13 | surfeit 4 | protein-coding I | surfeit locus protein 4|surfeit locus protein 4-like | |
| 619349 | 9606 | 20220513 | SETP3 SETP13 | SETP3 SET pseudogene 3 | HGNC:HGNC:31115|AllianceGenome:HGNC:31115 | 17 17q22 | SET pseudogene 3 | pseudo O | SET pseudogene 13|SET translocation, pseudogene 3 | |
| 619351 | 9606 | 20220513 | LINC00589 C8orf75|TSLNC8 | LINC00589 long intergenic non-protein coding RNA 589 | HGNC:HGNC:32299|Ensembl:ENSG00000251191|AllianceGenome:HGNC:32299 | 8 8p12 | long intergenic non-protein coding RNA 589 | ncRNA O | tumor suppressor lncRNA on chromosome 8p12 | |
| 619353 | 9598 | 20210724 | DEFA7 DEFA7P | 8 | defensin, alpha 7 | protein-coding | defensin-7|alpha-defensin 7|defensin, alpha 7 pseudogene | |||
| 619354 | 9598 | 20200627 CK820_G0046882 | DEFA6 | DEFA6 defensin alpha 6 | VGNC:VGNC:50325|Ensembl:ENSPTRG00000051516 | 8 | defensin alpha 6 | protein-coding O | defensin-6|alpha-defensin 6 | |
| 619355 | 10090 | 20220125 | Gm6083 | Gm6083 predicted gene 6083 | MGI:MGI:3779550|AllianceGenome:MGI:3779550 | 5 5 B1|5 | developmental pluripotency associated 5 pseudogene | pseudo O | ||
| 619357 | 8364 | 20220719 | becn1 atg6|beclin1|vps30 | becn1 beclin 1, autophagy related | Xenbase:XB-GENE-999318|Ensembl:ENSXETG00000012613 | 10 | beclin 1, autophagy related | protein-coding O | beclin-1|beclin 1 (coiled-coil, myosin-like BCL2 interacting protein) | |
| 619358 | 8364 | 20220719 | xkr5 xrg5 | xkr5 X-linked Kx blood group related 5 | Xenbase:XB-GENE-5870731|Ensembl:ENSXETG00000042442 | 5 | X-linked Kx blood group related 5 | protein-coding O | XK-related protein 5|XK, Kell blood group complex subunit-related family, member 5 | |
| 619359 | 8364 | 20220719 | xkr6 xrg6 | xkr6 X-linked Kx blood group related 6 | Xenbase:XB-GENE-983572|Ensembl:ENSXETG00000000686 | 5 | X-linked Kx blood group related 6 | protein-coding O | XK-related protein 6|XK, Kell blood group complex subunit-related family, member 6 | |
| 619360 | 8364 | 20220719 | xkr8 xrg8 | xkr8 X-linked Kx blood group related 8 | Xenbase:XB-GENE-940182|Ensembl:ENSXETG00000030874 | 2 | X-linked Kx blood group related 8 | protein-coding O | XK-related protein 8|XK, Kell blood group complex subunit-related family, member 8 | |
| 619361 | 8364 | 20220719 | xkr9 xrg9 | xkr9 X-linked Kx blood group related 9 | Xenbase:XB-GENE-5841541|Ensembl:ENSXETG00000032634 | 6 | X-linked Kx blood group related 9 | protein-coding O | XK-related protein 9|XK, Kell blood group complex subunit-related family, member 9 | |
| 619362 | 8364 | 20220719 | mogs gcs1 | mogs mannosyl-oligosaccharide glucosidase | Xenbase:XB-GENE-5911793|Ensembl:ENSXETG00000002403 | 1 | mannosyl-oligosaccharide glucosidase | protein-coding O | mannosyl-oligosaccharide glucosidase|glucosidase 1 | |
| 619363 | 8364 | 20220719 | bmp7.2 bmp7|op-1 | bmp7.2 bone morphogenetic protein 7, gene 2 | Xenbase:XB-GENE-855954|Ensembl:ENSXETG00000016386 | 3 | bone morphogenetic protein 7, gene 2 | protein-coding O | bone morphogenetic protein 7, gene 2|bone morphogenetic protein 7 (osteogenic protein 1) gene 2|bone morphogenetic protein 7 (osteogenic protein 1), gene 2|bone morphogenetic protein 7.2 | |
| 619364 | 8364 | 20220719 | sh3gl1 | sh3gl1 SH3-domain GRB2-like 1 | Xenbase:XB-GENE-951561|Ensembl:ENSXETG00000015811 | 1 | SH3-domain GRB2-like 1 | protein-coding O | endophilin-A2 | |
| 619366 | 8364 | 20220719 | igfbp1 afbp|higfbp-1|ibp1|igf-bp25|igfbp1-a|igfbp1-b|pp12 | igfbp1 insulin like growth factor binding protein 1 | Xenbase:XB-GENE-485497|Ensembl:ENSXETG00000015656 | 6 | insulin like growth factor binding protein 1 | protein-coding O | insulin-like growth factor-binding protein 1 | |
| 619367 | 8364 | 20220719 | ncf2 noxa2|p67-phox|p67phox | ncf2 neutrophil cytosolic factor 2 | Xenbase:XB-GENE-482959|Ensembl:ENSXETG00000012530 | 4 | neutrophil cytosolic factor 2 | protein-coding O | neutrophil cytosol factor 2|neutrophil cytosolic factor 2 (65kDa, chronic granulomatous disease, autosomal 2) | |
| 619368 | 8364 | 20220719 | ddi2 | ddi2 DNA damage inducible 1 homolog 2 | Xenbase:XB-GENE-6073016|Ensembl:ENSXETG00000013448 | 7 | DNA damage inducible 1 homolog 2 | protein-coding O | protein DDI1 homolog 2 | |
| 619369 | 9598 | 20210319 CK820_G0039824 | CHRNA5 | CHRNA5 cholinergic receptor nicotinic alpha 5 subunit | VGNC:VGNC:10796|Ensembl:ENSPTRG00000007346 | 15 | cholinergic receptor nicotinic alpha 5 subunit | protein-coding O | neuronal acetylcholine receptor subunit alpha-5|cholinergic receptor neuronal nicotinic alpha protein 5|cholinergic receptor, nicotinic, alpha 5 (neuronal) | |
| 619371 | 10090 | 20220519 | Stxbp3-ps Munc18c(L)|Stxbp3-1|Stxbp3b | Stxbp3-ps syntaxin-binding protein 3, pseudogene | MGI:MGI:3586869|AllianceGenome:MGI:3586869 | 19 19|19 A | syntaxin-binding protein 3, pseudogene | pseudo O | syntaxin-binding protein 3-1|syntaxin-binding protein 3B | |
| 619372 | 10090 | 20220125 | Klra17c Ly49q3 | Klra17c killer cell lectin-like receptor, subfamily A, member 17C | MGI:MGI:3588585|AllianceGenome:MGI:3588585 | killer cell lectin-like receptor, subfamily A, member 17C | protein-coding O | |||
| 619373 | 9606 | 20220513 | MBOAT4 FKSG89|GOAT|OACT4 | MBOAT4 membrane bound O-acyltransferase domain containing 4 | MIM:611940|HGNC:HGNC:32311|Ensembl:ENSG00000177669|AllianceGenome:HGNC:32311 | 8 8p12 | membrane bound O-acyltransferase domain containing 4 | protein-coding O | ghrelin O-acyltransferase|O-acyltransferase (membrane bound) domain containing 4|O-acyltransferase domain-containing protein 4|membrane-bound O-acyltransferase domain-containing protein 4 | |
| 619374 | 10116 | 20220522 | Jam2 | Jam2 junctional adhesion molecule 2 | RGD:1561692|Ensembl:ENSRNOG00000042848|AllianceGenome:RGD:1561692 | 11 11q11 | junctional adhesion molecule 2 | protein-coding O | junctional adhesion molecule B|junction adhesion molecule 2 | |
| 619376 | 13616 | 20190324 | ZNFX | zinc finger protein, X-linked | protein-coding | |||||
| 619379 | 9606 | 20191002 | SPG29 | MIM:609727 | 1 1p31.1-p21.1 | spastic paraplegia 29 (autosomal dominant) | unknown | |||
| 619382 | 10116 | 20220424 | Acap2 Centb2|cnt-b2 | Acap2 ArfGAP with coiled-coil, ankyrin repeat and PH domains 2 | RGD:1562939|Ensembl:ENSRNOG00000001730|AllianceGenome:RGD:1562939 | 11 11q22 | ArfGAP with coiled-coil, ankyrin repeat and PH domains 2 | protein-coding O | arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2|centaurin-beta-2 | |
| 619383 | 9606 | 20220513 | SCARNA9 Z32|mgU2-19/30 | SCARNA9 small Cajal body-specific RNA 9 | HGNC:HGNC:32566|Ensembl:ENSG00000254911|AllianceGenome:HGNC:32566 | 11 11q21 | small Cajal body-specific RNA 9 | ncRNA O | lncC11orf54-1|mgU2-19/30 scaRNA | |
| 619384 | 13616 | 20220708 | FGF2 BFGF|FGF-2|HBGF2 | Ensembl:ENSMODG00000018899 | 5 | fibroblast growth factor 2 | protein-coding | fibroblast growth factor 2|HBGF-2|basic fibroblast growth factor|fibroblast growth factor 2 (basic)|heparin-binding growth factor 2|prostatropin | ||
| 619385 | 10116 | 20220623 | Ncoa4 | Ncoa4 nuclear receptor coactivator 4 | RGD:1563014|Ensembl:ENSRNOG00000019768|Ensembl:ENSRNOG00000063221|AllianceGenome:RGD:1563014 | 16 16p16 | nuclear receptor coactivator 4 | protein-coding O | ||
| 619390 | 13616 | 20220708 | UCP3 | Ensembl:ENSMODG00000007461 | 4 | mitochondrial uncoupling protein 3 | protein-coding | mitochondrial uncoupling protein 3|uncoupling protein 3 (mitochondrial, proton carrier) | ||
| 619391 | 7955 | 20220519 | il10rb IL10R2|crfb5|il10rbl|zgc:153823 | il10rb interleukin 10 receptor, beta | ZFIN:ZDB-GENE-050909-1|Ensembl:ENSDARG00000078042|AllianceGenome:ZFIN:ZDB-GENE-050909-1 | 9 | interleukin 10 receptor, beta | protein-coding O | interleukin-10 receptor subunit beta|interferon alpha/beta receptor 1|cytokine receptor family member b5 | |
| 619393 | 10116 | 20220424 | Dnajc12 Jdp1 | Dnajc12 DnaJ heat shock protein family (Hsp40) member C12 | RGD:1591898|Ensembl:ENSRNOG00000051960|AllianceGenome:RGD:1591898 | 20 20p11 | DnaJ heat shock protein family (Hsp40) member C12 | protein-coding O | dnaJ homolog subfamily C member 12|DnaJ (Hsp40) homolog, subfamily C, member 12|J domain protein 1|j domain-containing protein 1 | |
| 619394 | 9606 | 20200625 | SPOAN | MIM:609541 | 11 | spastic paraplegia, optic atrophy, and neuropathy | unknown | |||
| 619397 | 9606 | 20191002 | FEB6 | MIM:609253 | 18 18p11.2 | febrile convulsions 6 | unknown | |||
| 619398 | 9606 | 20191002 | FEB5 | MIM:609255 | 6 6q22-q24 | febrile convulsions 5 | unknown | |||
| 619399 | 9606 | 20170408 | ETL2 FTLE | MIM:608096 | 12 12q22-q23.3 | epilepsy, familial temporal lobe | unknown | |||
| 619402 | 9606 | 20170408 | HPC5 | MIM:609299 | 3 3p26 | prostate cancer, hereditary, 5 | unknown | |||
| 619404 | 9606 | 20170408 | CTRCT35 CATCN1 | MIM:609376 | 19 19q13 | cataract, congenital nuclear, autosomal recessive | unknown | |||
| 619405 | 9606 | 20170408 | AIS4 VAMAS5 | MIM:609400 | 4 4q13-q21 | autoimmune disease, susceptibility to, 4 | unknown | |||
| 619406 | 9606 | 20170408 | HPE8 | MIM:609408 | 14 14q13 | holoprosencephaly 8 | unknown | |||
| 619407 | 9606 | 20170402 | MSSD | MIM:609432 | 17 17p13.3 | syndactyly, mesoaxial synostotic, with phalangeal reduction | unknown | syntactyly, type IX | ||
| 619408 | 9606 | 20170408 | PSNP2 | MIM:609454 | 1 1q31.1 | supranuclear palsy, progressive, 2 | unknown |
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