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10692 RRH

10692

RRH

retinal pigment epithelium-derived rhodopsin homolog

protein-coding

Homo sapiens

基因描述

Type Description
Definition retinal pigment epithelium-derived rhodopsin homolog

研究结论

Date Results Publications
2019-09-21 12:09:00 By using chimeric mutant peropsins, it was found that peropsin potentially generates an "active form" that drives G-protein signalling in the dark by binding to all-trans-retinal, and that the active form photo-converts to an inactive form containing 11-cis-retinal. 29476064
2010-06-30 22:04:00 Observational study of gene-disease association. (HuGE Navigator) 20332099
2010-01-21 00:00:00 Peropsin gene is not a common cause of retinitis pigmentosa or some related retinal degenerations, at least in the set of patients we analyzed. 17167409

名称对应

Type IDs
Gene
UniProtKB-ID: OPSX_HUMAN
UniprotKB: O14718
UniParc: UPI000005043C
EMBL: BC128120, CH471057, BC128121, AF012270, BK000958, BC128401
Ensembl: ENSG00000180245
KO: hsa:10692
Nucleutide sequences
EMBL-CDS: AAC51757.1, EAX06255.1, AAI28122.1, AAI28121.1, DAA00976.1, AAI28402.1
Ensembl_TRS: ENST00000317735
Protein sequencees
Ensembl_PRO: ENSP00000314992
RefSeq: NP_006574.1
Others
UniRef100: UniRef100_O14718
UniRef90: UniRef90_O14718
UniRef50: UniRef50_O14718
UniGene: Hs.658310
CCDS: CCDS3687.1

全选

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研究热度

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