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Gene: FGF13 (fibroblast growth factor 13) Homo sapiens
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Symbol: FGF13
Name: fibroblast growth factor 13
Description: 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]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: FGF-13; FGF2; FHF-2; FHF2; fibroblast growth factor homologous factor 2; FLJ30672; LINC00889; long intergenic non-protein coding RNA 889
Orthologs:
Mus musculus (house mouse) : Fgf13 (fibroblast growth factor 13)  MGI  Alliance
Rattus norvegicus (Norway rat) : Fgf13 (fibroblast growth factor 13)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Fgf13 (fibroblast growth factor 13)
Pan paniscus (bonobo/pygmy chimpanzee) : FGF13 (fibroblast growth factor 13)
Canis lupus familiaris (dog) : FGF13 (fibroblast growth factor 13)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Fgf13 (fibroblast growth factor 13)
Sus scrofa (pig) : FGF13 (fibroblast growth factor 13)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X138,631,573 - 139,222,889 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X137,713,734 - 138,305,051 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X137,541,401 - 137,649,181 (-)NCBINCBI36hg18NCBI36
Build 34X137,439,254 - 137,547,035NCBI
CeleraX138,079,723 - 138,653,021 (-)NCBI
Cytogenetic MapXq26.3-q27.1NCBI
HuRefX126,980,049 - 127,553,217 (-)NCBIHuRef
CHM1_1X137,624,856 - 138,198,651 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FGF13
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 733500
Created: 2004-01-12
Species: Homo sapiens
Last Modified: 2019-07-16
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.