人 PLCE1 (NM_001165979) cDNA克隆

Accession: NM_001165979
基因名称: PLCE1
基因别名: PLCE; PPLC; NPHS3
基因描述: Homo sapiens phospholipase C, epsilon 1 (PLCE1), transcript variant 2, mRNA.
种属: Human
CDS区长度: 5985 (查看编码区序列)
翻译后氨基酸长度: 1994 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks two exons and has an additional novel exon at its 5' end, compared to variant 1. These differences produce a unique 5' UTR and cause translation initiation at a novel start codon, compared to variant 1. The encoded protein (isoform 2; also known as PLCepsilon1b) has a shorter and distinct N-terminus, compared to isoform 1.
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G169906 人 PLCE1 (NM_001165979) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a phospholipase enzyme that catalyzes the hydrolysis of phosphatidylinositol-4,5-bisphosphate to generate two second messengers: inositol 1,4,5-triphosphate (IP3) and diacylglycerol (DAG). These second messengers subsequently regulate various processes affecting cell growth, differentiation, and gene expression. This enzyme is regulated by small monomeric GTPases of the Ras and Rho families and by heterotrimeric G proteins. In addition to its phospholipase C catalytic activity, this enzyme has an N-terminal domain with guanine nucleotide exchange (GEF) activity. Mutations in this gene cause early-onset nephrotic syndrome; characterized by proteinuria, edema, and diffuse mesangial sclerosis or focal and segmental glomerulosclerosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Sep 2009]