人 PRCD (NM_001077620) cDNA克隆

基本信息

Accession: NM_001077620
基因名称: PRCD
基因别名: RP36
基因描述: Homo sapiens progressive rod-cone degeneration (PRCD), transcript variant 1, mRNA.
种属: Human
CDS区长度: 165 (查看编码区序列)
翻译后氨基酸长度: 54 (查看氨基酸序列)
Transcript Variant: This variant (1) represents the protein coding transcript.

订购信息

产品编号 产品名称 载体 规格 价格
G164667 人 PRCD (NM_001077620) cDNA克隆 pDONR223 2ug质粒 点击询价

载体信息

pDONR223载体图谱

相关转录本

人 PRCD (NM_001077620) cDNA克隆 transcript variant 1

基因简介

This gene is predominantly expressed in the retina, and mutations in this gene are the cause of autosomal recessive retinal degeneration in both humans and dogs. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010]