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CNTLN

Gene

centlein

HGNCHGNC:23432EnsemblENSG00000044459NCBI Gene54875
Locus: gene with protein productLocation: 9p22.2

Also known as

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

Also known asC9orf101 · C9orf39 · FLJ20276 · bA340N12.1 · OTTHUMG00000019597
View full nomenclature history (8)
Previous symbolsC9orf101, C9orf39
Alias symbolsFLJ20276, bA340N12.1, OTTHUMG00000019597
Previous nameschromosome 9 open reading frame 101, chromosome 9 open reading frame 39, centlein, centrosomal 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.

Major depressive disorder
Smoking initiation
Alcohol drinking
Ovarian Neoplasms
Placental abruption
Empyema, Pleural

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.