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51475 CABP2

51475

CABP2

calcium binding protein 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition calcium binding protein 2

研究结论

Date Results Publications
2013-03-23 11:09:00 Genetic defects in CABP2 cause moderate-to-severe sensorineural hearing impairment. 22981119

名称对应

Type IDs
Synonymous DFNB93
Gene
UniProtKB-ID: CABP2_HUMAN, F1T0K2_HUMAN
UniprotKB: Q9NPB3, F1T0K2
UniParc: UPI000013E147, UPI0000D49791, UPI000013F23C
EMBL: AB593136, AP001184, AF169154, AF170811, CH471076
Ensembl: ENSG00000167791
KO: hsa:51475
Nucleutide sequences
EMBL-CDS: AAF26283.1, AAF25788.1, BAJ84076.1, EAW74647.1
Gene_ORFName: hCG_21058
Ensembl_TRS: ENST00000353903, ENST00000294288
Protein sequencees
Ensembl_PRO: ENSP00000312037, ENSP00000294288
RefSeq: NP_057450.2, NP_001305425.1
Others
UniRef100: UniRef100_Q9NPB3, UniRef100_F1T0K2
UniRef90: UniRef90_A0A2K6QDI7, UniRef90_Q9NPB3
UniRef50: UniRef50_Q9NPB3
UniGene: Hs.278984
CCDS: CCDS8170.1

全选

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研究热度

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