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MRC2

Gene

mannose receptor C-type 2

HGNCHGNC:16875EnsemblENSG00000011028NCBI Gene9902
Locus: gene with protein productLocation: 17q23.2

Also known as

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

Also known asKIAA0709 · ENDO180 · CLEC13E · CD280
View full nomenclature history (7)
Alias symbolsKIAA0709, ENDO180, CLEC13E, CD280
Previous namesmannose receptor, C type 2
Alias namesC-type lectin domain family 13 member E, endocytic receptor 180

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.

Aneurysm
Aortic Aneurysm
Hypertension
Diabetes Mellitus, Type 2
Coronary Artery Disease
Migraine Disorders
Musculoskeletal Diseases
Neoplasms

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.

CD moleculesC-type lectin domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-04-08.
Open TargetsGene–disease associations from the Open Targets Platform.