THOC5

Gene

THO complex subunit 5

HGNCHGNC:19074 EnsemblENSG00000100296 NCBI Gene8563

Locus: gene with protein productLocation: 22q12.2

Also known as

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

Also known asC22orf19 · PK1.3 · KIAA0983 · Fmip · fSAP79

View full nomenclature history (8)

Previous symbolsC22orf19

Alias symbolsPK1.3, KIAA0983, Fmip, fSAP79

Previous nameschromosome 22 open reading frame 19, THO complex 5

Alias namesfunctional spliceosome-associated protein 79

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

Neurodegenerative Diseases

Carcinoma, Hepatocellular

Radiculopathy

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.

THO complex

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.