人 FHL1 (NM_001159699) cDNA克隆

基本信息

Accession: NM_001159699
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 7, mRNA.
种属: Human
CDS区长度: 891 (查看编码区序列)
翻译后氨基酸长度: 296 (查看氨基酸序列)
Transcript Variant: This variant (7) differs in the 5' UTR, 3' UTR, and 3' coding region and initiates translation at an alternate start codon, compared to variant 1. The encoded protein (isoform 5) has distinct N- and C-termini and is shorter than isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G108982 人 FHL1 (NM_001159699) 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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