人 NPHS1 (NM_004646) cDNA克隆

Accession: NM_004646
基因名称: NPHS1
基因别名: CNF; NPHN; nephrin
基因描述: Homo sapiens nephrosis 1, congenital, Finnish type (nephrin) (NPHS1), mRNA.
种属: Human
CDS区长度: 3726 (查看编码区序列)
翻译后氨基酸长度: 1241 (查看氨基酸序列)
产品编号 产品名称 载体 规格 价格
G152996 人 NPHS1 (NM_004646) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a member of the immunoglobulin family of cell adhesion molecules that functions in the glomerular filtration barrier in the kidney. The gene is primarily expressed in renal tissues, and the protein is a type-1 transmembrane protein found at the slit diaphragm of glomerular podocytes. The slit diaphragm is thought to function as an ultrafilter to exclude albumin and other plasma macromolecules in the formation of urine. Mutations in this gene result in Finnish-type congenital nephrosis 1, characterized by severe proteinuria and loss of the slit diaphragm and foot processes.[provided by RefSeq, Oct 2009]