SGTA

Gene

small glutamine rich tetratricopeptide repeat co-chaperone alpha

HGNCHGNC:10819 EnsemblENSG00000104969 NCBI Gene6449

Locus: gene with protein productLocation: 19p13.3

Also known as

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

Also known asSGT · UBP · SGT1 · Vpu · hSGT · alphaSGT

View full nomenclature history (10)

Previous symbolsSGT

Alias symbolsUBP, SGT1, Vpu, hSGT, alphaSGT

Previous namessmall glutamine-rich tetratricopeptide repeat (TPR)-containing, small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha, small glutamine rich tetratricopeptide repeat containing alpha

Alias namesviral protein U-binding protein

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.

Neurodegenerative Diseases

Atrial Fibrillation

Asthma

Infections

46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency

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.

Tetratricopeptide repeat domain containingGET4-GET5 transmembrane domain recognition complex subunits

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.