SMARCD2

Gene

SWI/SNF related BAF chromatin remodeling complex subunit D2

HGNCHGNC:11107 EnsemblENSG00000108604 NCBI Gene6603

Locus: gene with protein productLocation: 17q23.3

Also known as

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

Also known asBAF60B · Rsc6p · CRACD2 · PRO2451

View full nomenclature history (9)

Alias symbolsBAF60B, Rsc6p, CRACD2, PRO2451

Previous namesSWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2

Alias namesmammalian chromatin remodeling complex BRG1-associated factor 60B, Swp73-like protein, chromatin remodeling complex BAF60B subunit, SWI/SNF complex 60 kDa subunit B

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.

Genetic Diseases, Inborn

Metabolic Syndrome

Non-alcoholic Fatty Liver Disease

Fatty Liver

Neuroblastoma

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.

BAF complex subunitsPBAF complex subunitsGBAF complex subunits

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-09-19.

Open TargetsGene–disease associations from the Open Targets Platform.