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102724652 CRYAA2

102724652

CRYAA2

crystallin alpha A2

protein-coding

Homo sapiens

基因描述

Type Description
Definition crystallin alpha A2

研究结论

Date Results Publications
2017-07-22 10:25:00 CRISPR/Cas9-mediated mutation of the alphaA-crystallin gene in rabbits recapitulates phenotypes of congenital cataracts, microphthalmia, obscurity, and early atrophy of the lens, and failed differentiation of lens fibers. 28475701

名称对应

Type IDs
Synonymous CRYAA
Gene
UniProtKB-ID: CRYA2_HUMAN, CRYAA_HUMAN
UniprotKB: A0A140G945, P02489
UniParc: UPI0000128380, UPI0000206C2B
EMBL: BC113598, FP236240, M35629, X14789, KM220588, U05569, KM220590, KM220591, BC069528, AP001631, CR407691, CH471079, M35628, AP001748, U66584, KM220592, KM220589
Ensembl: ENSG00000160202, ENSG00000276076
KO: hsa:1409, hsa:102724652
Nucleutide sequences
EMBL-CDS: AMM63586.1, AMM63585.1, AMM63587.1, AMM63583.1, AMM63584.1, AAA97523.1, AAH69528.1, EAX09497.1, AAC50900.1, CAG28619.1, AAA52105.1, EAX09498.1, AAA52106.1, AAI13599.1, BAA95535.1, CAA32891.1
Ensembl_TRS: ENST00000624932, ENST00000619537, ENST00000291554
Protein sequencees
Ensembl_PRO: ENSP00000482816, ENSP00000485302, ENSP00000291554
RefSeq: NP_001300979.1, NP_001307648.1
Others
UniRef100: UniRef100_A0A140G945
UniRef90: UniRef90_A0A140G945
UniRef50: UniRef50_P24622
CCDS: CCDS82651.1, CCDS82652.1, CCDS13695.1

全选

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