C14orf93

Gene

chromosome 14 open reading frame 93

HGNCHGNC:20162 EnsemblENSG00000100802 NCBI Gene60686

Locus: gene with protein productLocation: 14q11.2

Also known as

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

Also known asFLJ12154 · RTFC

View full nomenclature history (3)

Alias symbolsFLJ12154, RTFC

Alias namesregulator of thyroid function and cancer

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.

hypothyroidism due to TSH receptor mutations

Selective pituitary resistance to thyroid hormone

Familial gestational hyperthyroidism

Glaucoma, Open-Angle

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 2023-03-09.

Open TargetsGene–disease associations from the Open Targets Platform.