人 FHL1 (NM_001159704) cDNA克隆

基本信息

Accession: NM_001159704
基因名称: FHL1
基因别名: KYOT; SLIM; FHL-1; FHL1A; FHL1B; FLH1A; SLIM1; XMPMA; SLIM-1; SLIMMER
基因描述: Homo sapiens four and a half LIM domains 1 (FHL1), transcript variant 4, mRNA.
种属: Human
CDS区长度: 843 (查看编码区序列)
翻译后氨基酸长度: 280 (查看氨基酸序列)
Transcript Variant: This variant (4) differs in the 5' UTR, 3' UTR, and 3' coding region compared to variant 1. The encoded protein (isoform 2) has a distinct C-terminus and is shorter than isoform 1. Variants 2, 3, 4 and 9 encode the same protein (isoform 2).

订购信息

产品编号 产品名称 载体 规格 价格
G108987 人 FHL1 (NM_001159704) 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 FHL1 (NM_001159702) cDNA克隆 transcript variant 1
人 FHL1 (NM_001449) cDNA克隆 transcript variant 2
人 FHL1 (NM_001159700) cDNA克隆 transcript variant 3
人 FHL1 (NM_001159704) cDNA克隆 transcript variant 4
人 FHL1 (NM_001159701) cDNA克隆 transcript variant 5
人 FHL1 (NM_001159703) cDNA克隆 transcript variant 6
人 FHL1 (NM_001159699) cDNA克隆 transcript variant 7
人 FHL1 (NM_001167819) cDNA克隆 transcript variant 9

基因简介

This gene encodes a member of the four-and-a-half-LIM-only protein family. Family members contain two highly conserved, tandemly arranged, zinc finger domains with four highly conserved cysteines binding a zinc atom in each zinc finger. Expression of these family members occurs in a cell- and tissue-specific mode and these proteins are involved in many cellular processes. Mutations in this gene have been found in patients with Emery-Dreifuss muscular dystrophy. Multiple alternately spliced transcript variants which encode different protein isoforms have been described.[provided by RefSeq, Nov 2009]

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