人 BEST1 (NM_004183) cDNA克隆

Accession: NM_004183
基因名称: BEST1
基因别名: ARB; BMD; BEST; RP50; VMD2; TU15B
基因描述: Homo sapiens bestrophin 1 (BEST1), transcript variant 1, mRNA.
种属: Human
CDS区长度: 1758 (查看编码区序列)
翻译后氨基酸长度: 585 (查看氨基酸序列)
Transcript Variant: This variant (1) represents the shorter transcript and encodes the shorter isoform (1).
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G111738 人 BEST1 (NM_004183) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a member of the bestrophin gene family. This small gene family is characterized by proteins with a highly conserved N-terminus with four to six transmembrane domains. Bestrophins may form chloride ion channels or may regulate voltage-gated L-type calcium-ion channels. Bestrophins are generally believed to form calcium-activated chloride-ion channels in epithelial cells but they have also been shown to be highly permeable to bicarbonate ion transport in retinal tissue. Mutations in this gene are responsible for juvenile-onset vitelliform macular dystrophy (VMD2), also known as Best macular dystrophy, in addition to adult-onset vitelliform macular dystrophy (AVMD) and other retinopathies. Alternative splicing results in multiple variants encoding distinct isoforms.[provided by RefSeq, Nov 2008]