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CCPG1

Gene

cell cycle progression 1

HGNCHGNC:24227EnsemblENSG00000260916NCBI Gene9236
Locus: gene with protein productLocation: 15q21.3

Also known as

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

Also known asKIAA1254 · CPR8
View full nomenclature history (2)
Alias symbolsKIAA1254, CPR8

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 developmental and epileptic encephalopathy
Genetic Diseases, Inborn
hyperinsulinism due to INSR deficiency
Hereditary chronic pancreatitis
diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
Hyperinsulinemic hypoglycemia, familial, 2

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.

MicroRNA protein coding host genes

Provenance

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