CEP41

Gene

centrosomal protein 41

HGNCHGNC:12370 EnsemblENSG00000106477 NCBI Gene95681

Locus: gene with protein productLocation: 7q32.2

Also known as

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

Also known asTSGA14 · DKFZp762H1311 · FLJ22445 · JBTS15

View full nomenclature history (6)

Previous symbolsTSGA14

Alias symbolsDKFZp762H1311, FLJ22445, JBTS15

Previous namestestis specific, 14, centrosomal protein 41kDa

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 Diseases, Inborn

Autism Spectrum Disorder

Ciliopathy

Kidney transplant

Hereditary cerebral hemorrhage with amyloidosis, Piedmont type

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.