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FAM13C

Gene

family with sequence similarity 13 member C

HGNCHGNC:19371EnsemblENSG00000148541NCBI Gene220965
Locus: gene with protein productLocation: 10q21.1

Also known as

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

Also known asFAM13C1
View full nomenclature history (3)
Previous symbolsFAM13C1
Previous namesfamily with sequence similarity 13, member C1, family with sequence similarity 13, member C

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.

Kidney transplant
Chronic Kidney Disease-Mineral and Bone Disorder
Influenza, Human
Arthritis
Alcohol drinking
Hypopituitarism
Stroke
Familial prostate cancer
Prostatic Neoplasms

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.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.