人 ATP2C1 (NM_001001486) cDNA克隆

基本信息

Accession: NM_001001486
基因名称: ATP2C1
基因别名: HHD; BCPM; PMR1; SPCA1; hSPCA1; ATP2C1A
基因描述: Homo sapiens ATPase, Ca++ transporting, type 2C, member 1 (ATP2C1), transcript variant 4, mRNA.
种属: Human
CDS区长度: 2850 (查看编码区序列)
翻译后氨基酸长度: 949 (查看氨基酸序列)
Transcript Variant: This variant (4) has an alternate 5' exon and an alternate splice site in the last splice junction, as compared to variant 6. The resulting isoform (1d) has a shorter and distinct N-terminus and an additional segment in the C-terminal region, as compared to isoform 2a.

订购信息

产品编号 产品名称 载体 规格 价格
G104474 人 ATP2C1 (NM_001001486) 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 ATP2C1 (NM_014382) cDNA克隆 transcript variant 1
人 ATP2C1 (NM_001199184) cDNA克隆 transcript variant 10
人 ATP2C1 (NM_001199185) cDNA克隆 transcript variant 11
人 ATP2C1 (NM_001001487) cDNA克隆 transcript variant 2
人 ATP2C1 (NM_001001485) cDNA克隆 transcript variant 3
人 ATP2C1 (NM_001001486) cDNA克隆 transcript variant 4
人 ATP2C1 (NM_001199179) cDNA克隆 transcript variant 5
人 ATP2C1 (NM_001199180) cDNA克隆 transcript variant 6
人 ATP2C1 (NM_001199181) cDNA克隆 transcript variant 7
人 ATP2C1 (NM_001199182) cDNA克隆 transcript variant 8
人 ATP2C1 (NM_001199183) cDNA克隆 transcript variant 9

基因简介

The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium ions. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]

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