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FGF13

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Protein-coding gene in the species Homo sapiens
FGF13
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

3HBW, 4DCK, 4JPZ

Identifiers
AliasesFGF13, FGF-13, FGF2, FHF-2, FHF2, fibroblast growth factor 13
External IDsOMIM: 300070; MGI: 109178; HomoloGene: 3036; GeneCards: FGF13; OMA:FGF13 - orthologs
Gene location (Human)
X chromosome (human)
Chr.X chromosome (human)
X chromosome (human)Genomic location for FGF13Genomic location for FGF13
BandXq26.3-q27.1Start138,614,727 bp
End139,222,777 bp
Gene location (Mouse)
X chromosome (mouse)
Chr.X chromosome (mouse)
X chromosome (mouse)Genomic location for FGF13Genomic location for FGF13
BandX A6|X 33.31 cMStart58,107,505 bp
End58,613,431 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • endothelial cell

  • spinal ganglia

  • Region I of hippocampus proper

  • pars reticulata

  • orbitofrontal cortex

  • trigeminal ganglion

  • middle temporal gyrus

  • Brodmann area 46

  • postcentral gyrus

  • superior frontal gyrus
Top expressed in
  • ventral tegmental area

  • substantia nigra

  • subiculum

  • medial geniculate nucleus

  • medial dorsal nucleus

  • dentate gyrus of hippocampal formation granule cell

  • prefrontal cortex

  • anterior amygdaloid area

  • habenula

  • lateral geniculate nucleus
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

2258

14168

Ensembl

ENSG00000129682

ENSMUSG00000031137

UniProt

Q92913

P70377

RefSeq (mRNA)
NM_001139498
NM_001139500
NM_001139501
NM_001139502
NM_004114

NM_033642

NM_001290414
NM_001290415
NM_010200
NM_001356335

RefSeq (protein)
NP_001132970
NP_001132972
NP_001132973
NP_001132974
NP_004105

NP_378668

NP_001277343
NP_001277344
NP_034330
NP_001343264

Location (UCSC)Chr X: 138.61 – 139.22 MbChr X: 58.11 – 58.61 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Fibroblast growth factor 13 is a protein that in humans is encoded by the FGF13 gene.

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, invasion, and neuronal physiology. This gene is located to a region associated with Börjeson-Forssman-Lehmann syndrome (BFLS), a syndromal X-linked intellectual disability, which suggests it may be a candidate gene for familial cases of the BFL syndrome. The function of this gene has not yet been determined. Several alternatively spliced transcripts encoding different isoforms have been described for this gene. FGF13 isoform 1 (FGF13A) binds to the leucine-rich repeats of the hominid-specific receptor LRRC37B. In human pyramidal neurons of the cerebral cortex, this interaction leads to a lower excitability, a divergent cellular property of human pyramidal neurons compared to other mammals.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000129682Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000031137Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Smallwood PM, Munoz-Sanjuan I, Tong P, Macke JP, Hendry SH, Gilbert DJ, Copeland NG, Jenkins NA, Nathans J (Oct 1996). "Fibroblast growth factor (FGF) homologous factors: new members of the FGF family implicated in nervous system development". Proc Natl Acad Sci U S A. 93 (18): 9850–7. Bibcode:1996PNAS...93.9850S. doi:10.1073/pnas.93.18.9850. PMC 38518. PMID 8790420.
  6. ^ "Entrez Gene: FGF13 fibroblast growth factor 13".
  7. ^ Libé-Philippot B, Lejeune A, Wierda K, Louros N, Erkol E, Vlaeminck I, Beckers S, Gaspariunaite V, Bilheu A, Konstantoulea K, Nyitrai H, De Vleeschouwer M, Vennekens KM, Vidal N, Bird TW (2023-12-21). "LRRC37B is a human modifier of voltage-gated sodium channels and axon excitability in cortical neurons". Cell. 186 (26): 5766–5783.e25. doi:10.1016/j.cell.2023.11.028. ISSN 0092-8674. PMC 10754148. PMID 38134874.

Further reading

Growth factors
Fibroblast
FGF receptor ligands:
KGF
FGF homologous factors:
hormone-like: FGF15/19
EGF-like domain
TGFβ pathway
Insulin/IGF/
Relaxin family
Insulin and Insulin-like growth factor
Relaxin family peptide hormones
Platelet-derived
Vascular endothelial
Other
Growth factor receptor modulators
Angiopoietin
CNTF
EGF (ErbB)
EGF
(ErbB1/HER1)
ErbB2/HER2
  • Agonists: Unknown/none
ErbB3/HER3
ErbB4/HER4
FGF
FGFR1
FGFR2
FGFR3
FGFR4
Unsorted
HGF (c-Met)
IGF
IGF-1
IGF-2
Others
LNGF (p75)
PDGF
RET (GFL)
GFRα1
GFRα2
GFRα3
GFRα4
Unsorted
SCF (c-Kit)
TGFβ
Trk
TrkA
  • Negative allosteric modulators: VM-902A
TrkB
TrkC
VEGF
Others
  • Additional growth factor receptor modulators: Cerebrolysin (neurotrophin mixture)


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