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CAMSAP2

Gene

calmodulin regulated spectrin associated protein family member 2

HGNCHGNC:29188EnsemblENSG00000118200NCBI Gene23271
Locus: gene with protein productLocation: 1q32.1

Also known as

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

Also known asCAMSAP1L1 · KIAA1078
View full nomenclature history (4)
Previous symbolsCAMSAP1L1
Alias symbolsKIAA1078
Previous namescalmodulin regulated spectrin-associated protein 1-like 1, calmodulin regulated spectrin-associated protein family, member 2

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.

Hypothyroidism
Ovarian neoplasm
COVID-19
Gastrointestinal Neoplasms
Myxedema
Cardiomyopathy, Hypertrophic
Thyroid Diseases
Diabetes Mellitus, Type 1

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.

CAMSAP family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.