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CADPS

Gene

calcium dependent secretion activator

HGNCHGNC:1426EnsemblENSG00000163618NCBI Gene8618
Locus: gene with protein productLocation: 3p14.2

Also known as

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

Also known asCAPS · KIAA1121 · CAPS1 · UNC-31 · CADPS1
View full nomenclature history (7)
Alias symbolsCAPS, KIAA1121, CAPS1, UNC-31, CADPS1
Previous namesCa++-dependent secretion activator, Ca2+ dependent secretion activator

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.

Liver Diseases
Diabetes Mellitus, Type 2
Obesity disorder
Diabetes Mellitus
Osteoarthritis
Hearing Loss
Placental retention
Ovarian dysfunction

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.

Pleckstrin homology domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-05-09.
Open TargetsGene–disease associations from the Open Targets Platform.