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FAM194C

Gene

family with sequence similarity 149 member C

HGNCHGNC:25320EnsemblENSG00000131379NCBI Gene84077
Locus: gene with protein productLocation: 3p25.1

Also known as

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

Also known asC3orf20 · DKFZP434N1817
View full nomenclature history (3)
Previous symbolsC3orf20
Alias symbolsDKFZP434N1817
Previous nameschromosome 3 open reading frame 20

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.

Ovarian dysfunction
Alcohol drinking
Fatigue Syndrome, Chronic
Stroke
Gastritis
Non-syndromic male infertility due to sperm motility disorder
Spermatogenic failure

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 2026-05-22.
Open TargetsGene–disease associations from the Open Targets Platform.