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COLEC11

Gene

collectin subfamily member 11

HGNCHGNC:17213EnsemblENSG00000118004NCBI Gene78989
Locus: gene with protein productLocation: 2p25.3

Also known as

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

Also known asMGC3279 · CL-K1 · CL-11
View full nomenclature history (4)
Alias symbolsMGC3279, CL-K1, CL-11
Alias namesCollectin K1

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.

Genetic Diseases, Inborn
Metabolic Syndrome
Non-alcoholic Fatty Liver Disease
Kidney transplant

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.

CollectinsC-type lectin domain containingComplement system activation components

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-11-26.
Open TargetsGene–disease associations from the Open Targets Platform.