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FANCD2

Gene

FA complementation group D2

HGNCHGNC:3585EnsemblENSG00000144554NCBI Gene2177
Locus: gene with protein productLocation: 3p25.3

Also known as

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

Also known asFACD · FANCD · FAD · FA-D2
View full nomenclature history (5)
Previous symbolsFACD, FANCD
Alias symbolsFAD, FA-D2
Previous namesFanconi anemia complementation group D2

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.

Fanconi Anemia
Leukemia, Myeloid, Acute
Genetic Diseases, Inborn
Leukemia
Myelodysplastic syndrome
Ovarian Neoplasms

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.

FA complementation groupsArmadillo like helical 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.