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DST

Gene

dystonin

HGNCHGNC:1090EnsemblENSG00000151914NCBI Gene667
Locus: gene with protein productLocation: 6p12.1

Also known as

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

Also known asBPAG1 · BP240 · KIAA0728 · FLJ21489 · FLJ13425 · FLJ32235 · FLJ30627 · CATX-15 · BPA · MACF2
View full nomenclature history (11)
Previous symbolsBPAG1
Alias symbolsBP240, KIAA0728, FLJ21489, FLJ13425, FLJ32235, FLJ30627, CATX-15, BPA, MACF2
Previous namesbullous pemphigoid antigen 1, 230/240kDa

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.

Cardiomyopathies
Genetic Diseases, Inborn
Multiple Sclerosis

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.

EF-hand domain containingPlakinsSpectrin repeat containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2026-01-09.
Open TargetsGene–disease associations from the Open Targets Platform.