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SLX4

Gene

SLX4 structure-specific endonuclease subunit

HGNCHGNC:23845EnsemblENSG00000188827NCBI Gene84464
Locus: gene with protein productLocation: 16p13.3

Also known as

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

Also known asBTBD12 · KIAA1784 · KIAA1987 · FANCP
View full nomenclature history (7)
Previous symbolsBTBD12
Alias symbolsKIAA1784, KIAA1987, FANCP
Previous namesBTB (POZ) domain containing 12, SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae)
Alias namesFanconi anemia, complementation group P

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
Diabetes Mellitus, Type 2
Liver Diseases
Restless Legs Syndrome
Diabetes Mellitus

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 groupsBTB domain containingZinc fingers UBZ4 CCHC-type

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.