WDR13

Gene

WD repeat domain 13

HGNCHGNC:14352 EnsemblENSG00000101940 NCBI Gene64743

Locus: gene with protein productLocation: Xp11.23

Also known as

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

No previous or alternative symbols recorded for this gene.

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

Obesity due to melanocortin 4 receptor deficiency

autosomal dominant hyperinsulinism due to Kir6.2 deficiency

MODY

autosomal dominant hyperinsulinism due to SUR1 deficiency

diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency

Hyperinsulinemic hypoglycemia, familial, 2

Hypoinsulinemic hypoglycemia and body hemihypertrophy

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 containing

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.