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CCDC102B

Gene

coiled-coil domain containing 102B

HGNCHGNC:26295EnsemblENSG00000150636NCBI Gene79839
Locus: gene with protein productLocation: 18q22.1

Also known as

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

Also known asC18orf14 · ACY1L · FLJ23594 · HsT1731 · AN
View full nomenclature history (7)
Previous symbolsC18orf14, ACY1L
Alias symbolsFLJ23594, HsT1731, AN
Previous nameschromosome 18 open reading frame 14, aminoacylase 1-like

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.

Alcohol drinking
Urolithiasis
Parasitic Diseases
Diabetes Mellitus
Liver Diseases
bone Paget's disease
Migraine with Aura

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 2026-02-11.
Open TargetsGene–disease associations from the Open Targets Platform.