FGF13

Gene

fibroblast growth factor 13

HGNCHGNC:3670 EnsemblENSG00000129682 NCBI Gene2258

Locus: gene with protein productLocation: Xq26.3-q27.1

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asLINC00889 · FHF2 · FGF2 · FLJ30672

View full nomenclature history (6)

Previous symbolsLINC00889

Alias symbolsFHF2, FGF2, FLJ30672

Previous nameslong intergenic non-protein coding RNA 889

Alias namesfibroblast growth factor homologous factor 2

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Atrial Fibrillation

Genetic developmental and epileptic encephalopathy

Neurodevelopmental Disorders

Generalized epilepsy with febrile seizures-plus

Neurodegenerative Diseases

Genetic Diseases, Inborn

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

MicroRNA protein coding host genesFibroblast growth factor family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-06-19.

Open TargetsGene–disease associations from the Open Targets Platform.