SUPT4H1

Gene

SPT4 homolog, DSIF elongation factor subunit

HGNCHGNC:11467 EnsemblENSG00000213246 NCBI Gene6827

Locus: gene with protein productLocation: 17q22

Also known as

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

Also known asSUPT4H · SPT4H · Spt4 · Supt4a

View full nomenclature history (6)

Previous symbolsSUPT4H

Alias symbolsSPT4H, Spt4, Supt4a

Previous namessuppressor of Ty (S.cerevisiae) 4 homolog 1, suppressor of Ty 4 homolog 1 (S. cerevisiae)

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.

HIV Infections

Prostate carcinoma

Hypertension

Neurodegenerative Diseases

Disorder of lipid metabolism

Familial hypercholesterolemia

Metabolic Diseases

Major depressive disorder

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.