Back to discover

WDR26

Gene

WD repeat domain 26

HGNCHGNC:21208EnsemblENSG00000162923NCBI Gene80232
Locus: gene with protein productLocation: 1q42.11-q42.12

Also known as

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

Also known asFLJ21016 · GID7
View full nomenclature history (3)
Alias symbolsFLJ21016, GID7
Alias namesGID complex subunit 7 homolog (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.

Neurodegenerative Diseases
Genetic Diseases, Inborn
Gastritis
Diabetes Mellitus, Type 2
Neurofibromatosis 1

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.

WD repeat domain containingCTLH complex subunitsMicroRNA protein coding host genes

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.