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CCDC68

Gene

coiled-coil domain containing 68

HGNCHGNC:24350EnsemblENSG00000166510NCBI Gene80323
Locus: gene with protein productLocation: 18q21.2

Also known as

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

Also known asSE57-1
View full nomenclature history (2)
Alias symbolsSE57-1
Alias namescutaneous T-cell lymphoma associated antigen

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.

Presbycusis
Schizophrenia
Corneal Dystrophies, Hereditary
Major depressive disorder
Smoking initiation
Exocrine pancreatic carcinoma
Fuchs' Endothelial Dystrophy

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.