FAM3C

Gene

FAM3 metabolism regulating signaling molecule C

HGNCHGNC:18664 EnsemblENSG00000196937 NCBI Gene10447

Locus: gene with protein productLocation: 7q31.31

Also known as

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

Also known asGS3876 · ILEI

View full nomenclature history (6)

Alias symbolsGS3876, ILEI

Previous namesfamily with sequence similarity 3 member C

Alias namesinterleukin-like epithelial-mesenchymal transition inducer, predicted osteoblast protein, interleukin-like EMT inducer

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.

Ventricular Fibrillation

Amyotrophic Lateral Sclerosis

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.