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 cognitive disability 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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FGF13BA-20-REGO | 20 (40 μL) | 200 μL |
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| FGF13BA-20-REGR | 20 (40 μL) | 200 μL |
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| FGF13BA-20-ORGR | 20 (40 μL) | 200 μL |
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| FGF13BA-20-GOGR | 20 (40 μL) | 200 μL |
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| FGF13BA-20-GRRE | 20 (40 μL) | 200 μL |
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| FGF13BA-20-GROR | 20 (40 μL) | 200 μL |
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| FGF13BA-20-GRGO | 20 (40 μL) | 200 μL |
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| FGF13BA-20-AQOR | 20 (40 μL) | 200 μL |
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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 cognitive disability 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]
Gene Symbol : FGF13
Gene Name : Fibroblast growth factor 13
Chromosome : CHR X: 139,222,888-138,631,572
Locus : Xq26.3-q27.1
Alt. Genes : KIF20A
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