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NEBL

Gene

nebulette

HGNCHGNC:16932EnsemblENSG00000078114NCBI Gene10529
Locus: gene with protein productLocation: 10p12.31

Also known as

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

Also known asC10orf113 · LNEBL · LASP2 · bA165O3.1
View full nomenclature history (7)
Previous symbolsC10orf113
Alias symbolsLNEBL, LASP2, bA165O3.1
Previous nameschromosome 10 open reading frame 113
Alias namesLIM and SH3 protein 2, LIM-nebulette

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.

Atrial Fibrillation
Neurodegenerative Diseases
Smoking initiation
Cardiomyopathy, Dilated
Arrhythmias, Cardiac
Cardiomyopathy, Hypertrophic
Mental Disorders
Alcohol drinking

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.

LIM domain containingNebulin family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.