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FAM13A

Gene

family with sequence similarity 13 member A

HGNCHGNC:19367EnsemblENSG00000138640NCBI Gene10144
Locus: gene with protein productLocation: 4q22.1

Also known as

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

Also known asFAM13A1 · KIAA0914 · ARHGAP48
View full nomenclature history (5)
Previous symbolsFAM13A1
Alias symbolsKIAA0914, ARHGAP48
Previous namesfamily with sequence similarity 13, member A1, family with sequence similarity 13, member A

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.

Pulmonary Disease, Chronic Obstructive
Idiopathic Pulmonary Fibrosis
Osteoarthritis, Knee
Respiratory Tract Diseases
Carcinoma, Squamous Cell
Lung Diseases, Interstitial
Metabolic Syndrome

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.

Rho GTPase activating proteins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2026-05-11.
Open TargetsGene–disease associations from the Open Targets Platform.