Rlbp1 - retinaldehyde binding protein 1-BMKCloudï½ç¾è¿å®¢äº

例如："NBL1", "4681", "drought"

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293049 Rlbp1

基因描述

Type	Description
Definition	retinaldehyde binding protein 1

名称对应

Type	IDs
Gene	UniProtKB-ID: D3Z956_RAT UniprotKB: D3Z956 UniParc: UPI0000500793 EMBL: AABR07004395, CH473980 Ensembl: ENSRNOG00000016897 KO: rno:293049
Nucleutide sequences	EMBL-CDS: EDM08576.1, EDM08575.1 Gene_ORFName: rCG_24761 Ensembl_TRS: ENSRNOT00000022962
Protein sequencees	Ensembl_PRO: ENSRNOP00000022962 RefSeq: NP_001099744.1, XP_006229458.1, XP_017444427.1
Others	UniRef100: UniRef100_D3Z956 UniRef90: UniRef90_Q9Z275 UniRef50: UniRef50_Q9Z275 UniGene: Rn.41007

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mRNA

Protein

UniprotKB

Description

Refseq

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Pubmed编号	文献信息	发表日期	相关基因
23701314	Genes and mutations causing retinitis pigmentosa. Clin. Genet. S P Daiger , L S Sullivan , S J Bowne	2013-08-01	Rbp3, Rho, Prph2, Sag, Clrn1, Prpf8, Ush2a, Pde6b, Prpf31, Rlbp1, Best1, Pde6a, Tulp1, Abca4, Rdh12, Guca1b, Rpgr, Crx, Lrat, Rp1, Pde6g, Cngb1, Cnga1, Rpe65
21873635	Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Brief. Bioinformatics Pascale Gaudet , Michael S Livstone , Suzanna E Lewis , Paul D Thomas	2011-09-01	-
20188572	The biochemical and structural basis for trans-to-cis isomerization of retinoids in the chemistry of vision. Trends Biochem. Sci. Johannes von Lintig , Philip D Kiser , Marcin Golczak , Krzysztof Palczewski	2010-07-01	Rlbp1
20212494	Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait. Nat. Rev. Genet. Alan F Wright , Christina F Chakarova , Mai M Abd El-Aziz , Shomi S Bhattacharya	2010-04-01	-
19180257	Localizations of visual cycle components in retinal pigment epithelium. Mol Vis Jing Huang , Daniel E Possin , John C Saari	2009-01-01	-
11453974	Fundus albipunctatus and retinitis punctata albescens in a pedigree with an R150Q mutation in RLBP1. Clin. Genet. N Katsanis , N F Shroyer , R A Lewis , J C Cavender , A A Al-Rajhi , M Jabak , J R Lupski	2001-06-01	-
11176989	Ocular phenotype of bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene. Arch. Ophthalmol. M S Burstedt , K Forsman-Semb , I Golovleva , T Janunger , L Wachtmeister , O Sandgren	2001-02-01	Rlbp1, RLBP1
9326942	Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa. Nat. Genet. M A Maw , B Kennedy , A Knight , R Bridges , K E Roth , E J Mani , J K Mukkadan , D Nancarrow , J W Crabb , M J Denton	1997-10-01	Rlbp1, RLBP1

研究热度

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