PHIP

Gene

PHIP subunit of CUL4-Ring ligase complex

HGNCHGNC:15673 EnsemblENSG00000146247 NCBI Gene55023

Locus: gene with protein productLocation: 6q14.1

Also known as

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

Also known asWDR11 · ndrp · BRWD2 · RepID · DCAF14 · FLJ20705

View full nomenclature history (8)

Previous symbolsWDR11

Alias symbolsndrp, BRWD2, RepID, DCAF14, FLJ20705

Previous namespleckstrin homology domain interacting protein

Alias namesDDB1 and CUL4 associated factor 14

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.

Genetic Diseases, Inborn

Obesity disorder

Obesity due to melanocortin 4 receptor deficiency

Schizophrenia

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.

Bromodomain and WD repeat domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-03-27.

Open TargetsGene–disease associations from the Open Targets Platform.