人 FGF13 (NM_001139501) cDNA克隆

基本信息

Accession: NM_001139501
基因名称: FGF13
基因别名: FGF2; FHF2; FHF-2; FGF-13
基因描述: Homo sapiens fibroblast growth factor 13 (FGF13), transcript variant 3, mRNA.
种属: Human
CDS区长度: 681 (查看编码区序列)
翻译后氨基酸长度: 226 (查看氨基酸序列)
Transcript Variant: This variant (3) contains four additional exons at the 5' end compared to transcript variant 1. This results in a slightly shorter isoform (3) with a different N-terminus compared to isoform 1. Variants 3 and 5 encode the same isoform.

订购信息

产品编号 产品名称 载体 规格 价格
G100770 人 FGF13 (NM_001139501) 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 FGF13 (NM_004114) cDNA克隆 transcript variant 1
人 FGF13 (NM_001139500) cDNA克隆 transcript variant 2
人 FGF13 (NM_001139501) cDNA克隆 transcript variant 3
人 FGF13 (NM_001139498) cDNA克隆 transcript variant 4
人 FGF13 (NM_001139502) cDNA克隆 transcript variant 5
人 FGF13 (NM_033642) cDNA克隆 transcript variant 6

基因简介

The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked mental retardation mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini. [provided by RefSeq, Nov 2008]

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