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- accession：NM_004114
- 基因别名：FGF13
- 基因描述：Homo sapiens fibroblast growth factor 13 (FGF13), transcript variant 1, mRNA.
- 载体：现货载体
- CDS区长度：738
- 翻译后氨基酸长度：245
- TranscriptVariant：This variant (1) represents the most predominant transcript and encodes isoform 1.
- 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]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
