CCN6

Gene

cellular communication network factor 6

HGNCHGNC:12771 EnsemblENSG00000112761 NCBI Gene8838

Locus: gene with protein productLocation: 6q21

Also known as

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

Also known asWISP3 · WISP-3

View full nomenclature history (3)

Previous symbolsWISP3

Alias symbolsWISP-3

Previous namesWNT1 inducible signaling pathway protein 3

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.

Genetic Diseases, Inborn

Alcohol drinking

Urolithiasis

Amino Acid Metabolism, Inborn Errors

Subarachnoid Hemorrhage

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.

Cellular communication network factors

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.

Open TargetsGene–disease associations from the Open Targets Platform.