人 ATP6V1H (NM_213619) cDNA克隆

Accession: NM_213619
基因名称: ATP6V1H
基因别名: SFD; NBP1; VMA13; CGI-11; MSTP042; SFDbeta; SFDalpha
基因描述: Homo sapiens ATPase, H+ transporting, lysosomal 50/57kDa, V1 subunit H (ATP6V1H), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1398 (查看编码区序列)
翻译后氨基酸长度: 465 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks an exon in the coding region, but maintains the reading frame, compared to variant 1. The encoded isoform (2) is shorter than isoform 1.
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G154034 人 ATP6V1H (NM_213619) 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 intracellular organelles. V-ATPase-dependent organelle acidification is necessary for multiple processes including protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. The encoded protein is the regulatory H subunit of the V1 domain of V-ATPase, which is required for catalysis of ATP but not the assembly of V-ATPase. Decreased expression of this gene may play a role in the development of type 2 diabetes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]