人 TRPV4 (NM_147204) cDNA克隆

基本信息

Accession: NM_147204
基因名称: TRPV4
基因别名: SMAL; VRL2; CMT2C; SPSMA; TRP12; VROAC; HMSN2C; OTRPC4; SSQTL1
基因描述: Homo sapiens transient receptor potential cation channel, subfamily V, member 4 (TRPV4), transcript variant 2, mRNA.
种属: Human
CDS区长度: 2436 (查看编码区序列)
翻译后氨基酸长度: 811 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks an alternate in-frame exon compared to variant 1, resulting in an isoform (b) that lacks an internal segment compared to isoform a.

订购信息

产品编号 产品名称 载体 规格 价格
G122366 人 TRPV4 (NM_147204) 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 TRPV4 (NM_021625) cDNA克隆 transcript variant 1
人 TRPV4 (NM_147204) cDNA克隆 transcript variant 2
人 TRPV4 (NM_001177433) cDNA克隆 transcript variant 3
人 TRPV4 (NM_001177431) cDNA克隆 transcript variant 4
人 TRPV4 (NM_001177428) cDNA克隆 transcript variant 5

基因简介

This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2010]

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