GTPBP6

Gene

GTP binding protein 6

HGNCHGNC:30189 EnsemblENSG00000178605 NCBI Gene8225

Locus: gene with protein productLocation: Xp22.33 and Yp11.32

Also known as

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

Also known asPGPL · FLJ20977

View full nomenclature history (4)

Alias symbolsPGPL, FLJ20977

Previous namesGTP binding protein 6 (putative)

Alias namespseudoautosomal GTP binding protein-like

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.

Klinefelter Syndrome

Mitral valve 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.

Gene family

HGNC gene-group membership.

Pseudoautosomal region 1

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-08-07.

Open TargetsGene–disease associations from the Open Targets Platform.