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CEP19

Gene

centrosomal protein 19

HGNCHGNC:28209EnsemblENSG00000174007NCBI Gene84984
Locus: gene with protein productLocation: 3q29

Also known as

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

Also known asC3orf34 · MGC14126
View full nomenclature history (4)
Previous symbolsC3orf34
Alias symbolsMGC14126
Previous namescentrosomal protein 19kDa, chromosome 3 open reading frame 34

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.

Bardet-Biedl Syndrome
Obesity, Morbid
Optic Atrophy
Obesity due to melanocortin 4 receptor deficiency
Hypersensitivity
MODY
Hypoinsulinemic hypoglycemia and body hemihypertrophy

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.