人 ATP6V1B1 (NM_001692) cDNA克隆

Accession: NM_001692
基因名称: ATP6V1B1
基因别名: VATB; VMA2; VPP3; RTA1B; ATP6B1
基因描述: Homo sapiens ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1 (ATP6V1B1), mRNA.
种属: Human
CDS区长度: 1542 (查看编码区序列)
翻译后氨基酸长度: 513 (查看氨基酸序列)
产品编号 产品名称 载体 规格 价格
G117462 人 ATP6V1B1 (NM_001692) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c'', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This encoded protein is one of two V1 domain B subunit isoforms and is found in the kidney. Mutations in this gene cause distal renal tubular acidosis associated with sensorineural deafness. [provided by RefSeq, Jul 2008]