FHAD1

Gene

forkhead associated phosphopeptide binding domain 1

HGNCHGNC:29408 EnsemblENSG00000142621 NCBI Gene114827

Locus: gene with protein productLocation: 1p36.21

Also known as

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

Also known asKIAA1937

View full nomenclature history (2)

Alias symbolsKIAA1937

Previous namesforkhead-associated (FHA) phosphopeptide binding domain 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.

Placental retention

Placental abruption

Ischemic Attack, Transient

Mental Disorders

Ovarian neoplasm

Alcohol drinking

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.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.

Open TargetsGene–disease associations from the Open Targets Platform.