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DOK7

Gene

docking protein 7

HGNCHGNC:26594EnsemblENSG00000175920NCBI Gene285489
Locus: gene with protein productLocation: 4p16.3

Also known as

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

Also known asC4orf25 · FLJ33718 · FLJ39137 · Dok-7
View full nomenclature history (5)
Previous symbolsC4orf25
Alias symbolsFLJ33718, FLJ39137, Dok-7
Previous nameschromosome 4 open reading frame 25

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.

Congenital myasthenic syndromes
Genetic Diseases, Inborn
Coronary Artery Disease

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.

Docking protein 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.