FANCL

Gene

FA complementation group L

HGNCHGNC:20748 EnsemblENSG00000115392 NCBI Gene55120

Locus: gene with protein productLocation: 2p16.1

Also known as

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

Also known asPHF9 · FLJ10335 · FAAP43 · Pog

View full nomenclature history (6)

Previous symbolsPHF9

Alias symbolsFLJ10335, FAAP43, Pog

Previous namesPHD finger protein 9, Fanconi anemia complementation group L

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

Myelodysplastic syndrome

Genetic Diseases, Inborn

Hypertension

Head and Neck 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.

PHD finger proteinsFA complementation groupsFA core complex

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.