CNMD

Gene

chondromodulin

HGNCHGNC:17005 EnsemblENSG00000136110 NCBI Gene11061

Locus: gene with protein productLocation: 13q14.3

Also known as

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

Also known asMYETS1 · LECT1 · CHM-I · CHM1 · BRICD3

View full nomenclature history (8)

Previous symbolsMYETS1, LECT1

Alias symbolsCHM-I, CHM1, BRICD3

Previous namesmultiple myeloma tumor suppressor 1, leukocyte cell derived chemotaxin 1

Alias namesBRICHOS domain containing 3

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.

Sleep Apnea Syndromes

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.

BRICHOS 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.