人 ABCA4 (NM_000350) cDNA克隆

Accession: NM_000350
基因名称: ABCA4
基因别名: FFM; RMP; ABCR; RP19; STGD; ABC10; ARMD2; CORD3; STGD1
基因描述: Homo sapiens ATP-binding cassette, sub-family A (ABC1), member 4 (ABCA4), mRNA.
种属: Human
CDS区长度: 6822 (查看编码区序列)
翻译后氨基酸长度: 2273 (查看氨基酸序列)
产品编号 产品名称 载体 规格 价格
G141462 人 ABCA4 (NM_000350) cDNA克隆 pDONR223 2ug质粒 点击询价

The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This protein is a retina-specific ABC transporter with N-retinylidene-PE as a substrate. It is expressed exclusively in retina photoreceptor cells, indicating the gene product mediates transport of an essental molecule across the photoreceptor cell membrane. Mutations in this gene are found in patients diagnosed with Stargardt disease, a form of juvenile-onset macular degeneration. Mutations in this gene are also associated with retinitis pigmentosa-19, cone-rod dystrophy type 3, early-onset severe retinal dystrophy, fundus flavimaculatus, and macular degeneration age-related 2. [provided by RefSeq, Jul 2008]