人 RPGR (NM_001034853) cDNA克隆

Accession: NM_001034853
基因名称: RPGR
基因别名: CRD; RP3; COD1; PCDX; RP15; XLRP3; orf15; CORDX1
基因描述: Homo sapiens retinitis pigmentosa GTPase regulator (RPGR), transcript variant C, mRNA.
种属: Human
CDS区长度: 3459 (查看编码区序列)
翻译后氨基酸长度: 1152 (查看氨基酸序列)
Transcript Variant: This variant (C) encodes the longest isoform (C).
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G111528 人 RPGR (NM_001034853) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a protein with a series of six RCC1-like domains (RLDs), characteristic of the highly conserved guanine nucleotide exchange factors. The encoded protein is found in the Golgi body and interacts with RPGRIP1. This protein localizes to the outer segment of rod photoreceptors and is essential for their viability. Mutations in this gene have been associated with X-linked retinitis pigmentosa (XLRP). Multiple alternatively spliced transcript variants that encode different isoforms of this gene have been reported, but the full-length natures of only some have been determined. [provided by RefSeq, Dec 2008]