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WDR11

Gene

WD repeat domain 11

HGNCHGNC:13831EnsemblENSG00000120008NCBI Gene55717
Locus: gene with protein productLocation: 10q26.12

Also known as

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

Also known asBRWD2 · KIAA1351 · FLJ10506 · WDR15 · HH14 · DR11 · SRI1
View full nomenclature history (9)
Previous symbolsBRWD2
Alias symbolsKIAA1351, FLJ10506, WDR15, HH14, DR11, SRI1
Previous namesbromodomain and WD repeat domain containing 2
Alias namessensitization to ricin complex subunit 1

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.

Kallmann syndrome
Microcephaly
Hypogonadism
Diabetes Mellitus, Type 2
Prostate carcinoma
Benign prostatic hyperplasia

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 2024-08-08.
Open TargetsGene–disease associations from the Open Targets Platform.