Back to discover

CEP104

Gene

centrosomal protein 104

HGNCHGNC:24866EnsemblENSG00000116198NCBI Gene9731
Locus: gene with protein productLocation: 1p36.32

Also known as

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

Also known asGlyBP · RP1-286D6.4 · CFAP256 · ROC22 · JBTS25
View full nomenclature history (8)
Alias symbolsGlyBP, RP1-286D6.4, CFAP256, ROC22, JBTS25
Previous namesKIAA0562, centrosomal protein 104kDa
Alias namesglycine, glutamate, thienylcyclohexylpiperidine binding protein

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.

Ciliopathy
Autosomal recessive non-syndromic intellectual disability
Cerebellar Ataxia
Dystonic Disorders

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.

Cilia and flagella associatedTOG domain containing

Provenance

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