RUBCNL

Gene

rubicon like autophagy enhancer

HGNCHGNC:20420 EnsemblENSG00000102445 NCBI Gene80183

Locus: gene with protein productLocation: 13q14.13

Also known as

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

Also known asC13orf18 · KIAA0226L · FLJ21562 · PACER

View full nomenclature history (7)

Previous symbolsC13orf18, KIAA0226L

Alias symbolsFLJ21562, PACER

Previous nameschromosome 13 open reading frame 18, KIAA0226 like, RUN and cysteine rich domain containing beclin 1 interacting protein 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.

Diabetes Mellitus, Type 1

Familial prostate cancer

Prostatic Neoplasms

Alcohol drinking

Stroke

Urinary Tract Infections

Cardiomyopathies

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.

PIK3C3 complex subunits

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.