CBARP

Gene

CACN subunit beta associated regulatory protein

HGNCHGNC:28617 EnsemblENSG00000099625 NCBI Gene255057

Locus: gene with protein productLocation: 19p13.3

Also known as

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

Also known asC19orf26 · MGC40084 · DOS · BARP

View full nomenclature history (9)

Previous symbolsC19orf26

Alias symbolsMGC40084, DOS, BARP

Previous nameschromosome 19 open reading frame 26, calcium channel, voltage-dependent, beta subunit associated regulatory protein, CACN beta subunit associated regulatory protein

Alias namesdownstream of STK11, VGCC beta-anchoring and -regulatory protein

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.

Diabetes Mellitus, Type 2

Diabetes Mellitus

Peutz-Jeghers Syndrome

Bilateral striopallidodentate calcinosis

Familial focal epilepsy with variable foci

Genetic central nervous system malformation

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.

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.