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SMARCE1

Gene

SWI/SNF related BAF chromatin remodeling complex subunit E1

HGNCHGNC:11109EnsemblENSG00000073584NCBI Gene6605
Locus: gene with protein productLocation: 17q21.2

Also known as

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

Also known asBAF57
View full nomenclature history (2)
Alias symbolsBAF57
Previous namesSWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1

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.

Inherited cancer-predisposing syndrome
Neoplastic Syndromes, Hereditary
Neurodegenerative Diseases
Meningioma

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 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.