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CARMIL1

Gene

capping protein regulator and myosin 1 linker 1

HGNCHGNC:21581EnsemblENSG00000079691NCBI Gene55604
Locus: gene with protein productLocation: 6p22.2

Also known as

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

Also known asLRRC16 · LRRC16A · dJ501N12.1 · FLJ20048 · CARMIL
View full nomenclature history (8)
Previous symbolsLRRC16, LRRC16A
Alias symbolsdJ501N12.1, FLJ20048, CARMIL
Previous namesleucine rich repeat containing 16, leucine rich repeat containing 16A
Alias namescapping protein, Arp2/3, and Myosin-I Linker homolog 1 (Dictyostelium)

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.

Schizophrenia
Graves' Disease
Celiac Disease
Diabetes Mellitus, Type 1
Dentures
Hypertension
Iron Metabolism Disorders
Intelligence
Hypothyroidism
Arthritis, Rheumatoid

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.