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FAAP24

Gene

FA core complex associated protein 24

HGNCHGNC:28467EnsemblENSG00000131944NCBI Gene91442
Locus: gene with protein productLocation: 19q13.11

Also known as

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

Also known asC19orf40 · FLJ46828 · MGC32020
View full nomenclature history (6)
Previous symbolsC19orf40
Alias symbolsFLJ46828, MGC32020
Previous nameschromosome 19 open reading frame 40, Fanconi anemia core complex associated protein 24
Alias namesFanconi anemia-associated protein, 24kDa

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.

Vitiligo
Leukemia, Myeloid, Acute
Gout
Neoplasms
Pre-Eclampsia
Fanconi Anemia
Friedreich Ataxia
Anemia

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 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.