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HMMR

Gene

hyaluronan mediated motility receptor

HGNCHGNC:5012EnsemblENSG00000072571NCBI Gene3161
Locus: gene with protein productLocation: 5q34

Also known as

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

Also known asRHAMM · CD168
View full nomenclature history (4)
Alias symbolsRHAMM, CD168
Previous nameshyaluronan-mediated motility receptor (RHAMM), hyaluronan-mediated motility receptor

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.

Ovarian Neoplasms
Thyroid gland carcinoma
Ischemic Attack, Transient
Multiple Sclerosis
Alzheimer's Disease
Parkinson's Disease
Lysosomal Storage Diseases
Neurodegenerative Diseases

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 molecules

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.