CLEC4E

Gene

C-type lectin domain family 4 member E

HGNCHGNC:14555 EnsemblENSG00000166523 NCBI Gene26253

Locus: gene with protein productLocation: 12p13.31

Also known as

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

Also known asCLECSF9 · MINCLE

View full nomenclature history (5)

Previous symbolsCLECSF9

Alias symbolsMINCLE

Previous namesC-type (calcium dependent, carbohydrate-recognition domain) lectin, superfamily member 9, C-type lectin domain family 4, member E

Alias namesMacrophage-inducible C-type lectin

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.

Isolated agammaglobulinemia

Autosomal agammaglobulinemia

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.

C-type lectin domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.