MMRN1

Gene

multimerin 1

HGNCHGNC:7178 EnsemblENSG00000138722 NCBI Gene22915

Locus: gene with protein productLocation: 4q22.1

Also known as

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

Also known asMMRN · ECM · EMILIN4 · GPIa*

View full nomenclature history (7)

Previous symbolsMMRN

Alias symbolsECM, EMILIN4, GPIa*

Previous namesmultimerin

Alias namesglycoprotein Ia*, endothelial cell multimerin

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.

Irritable Bowel Syndrome

Neoplasms

REM Sleep Behavior Disorder

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.

EMI domain containingC1q domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-08-07.

Open TargetsGene–disease associations from the Open Targets Platform.