CARMIL3

Gene

capping protein regulator and myosin 1 linker 3

HGNCHGNC:20272 EnsemblENSG00000186648 NCBI Gene90668

Locus: gene with protein productLocation: 14q11.2

Also known as

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

Also known asC14orf121 · LRRC16B · BC008134 · crml-1

View full nomenclature history (6)

Previous symbolsC14orf121, LRRC16B

Alias symbolsBC008134, crml-1

Previous nameschromosome 14 open reading frame 121, leucine rich repeat containing 16B

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.

Smoking initiation

Helicobacter Infections

Stroke

Ataxia Telangiectasia

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.