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10947 AP3M2

10947

AP3M2

adaptor related protein complex 3 subunit mu 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition adaptor related protein complex 3 subunit mu 2

研究结论

Date Results Publications
2010-01-21 00:00:00 some AP3M2 mutations still remain candidates for unmapped disorders including epilepsy, febrile seizure, and other neuronal developmental disorders associated with functional abnormalities of GABAergic transmission 17293072
2009-06-24 21:33:00 Observational study of gene-disease association. (HuGE Navigator) 19481122
2008-03-13 09:08:00 Observational study of genotype prevalence. (HuGE Navigator) 17293072

名称对应

Type IDs
Synonymous AP47B, CLA20, P47B
Gene
UniProtKB-ID: AP3M2_HUMAN, A0A384NYL6_HUMAN
UniprotKB: P53677, A0A384NYL6
UniParc: UPI0000125033, UPI00001BB2AC
EMBL: GQ891535, D38293, BC056398, CH471080, AC103724, AK315228, BC056257
Ensembl: ENSG00000070718
KO: hsa:10947
Nucleutide sequences
EMBL-CDS: AAH56398.1, BAG37657.1, BAA07415.1, EAW63236.1, AAH56257.1, EAW63237.1, EAW63238.1, ADO22397.1
Ensembl_TRS: ENST00000174653, ENST00000396926, ENST00000518421, ENST00000530375
Protein sequencees
Ensembl_PRO: ENSP00000174653, ENSP00000431918, ENSP00000380132, ENSP00000428787
RefSeq: NP_001127768.1, XP_016868466.1, NP_006794.1
Others
UniRef100: UniRef100_P53677
UniRef90: UniRef90_P53677
UniRef50: UniRef50_P53677
UniGene: Hs.654529
CCDS: CCDS6125.1

全选

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研究热度

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