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MYORG

Gene

myogenesis regulating glycosidase

HGNCHGNC:19918EnsemblENSG00000164976NCBI Gene57462
Locus: gene with protein productLocation: 9p13.3

Also known as

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

Also known asNET37
View full nomenclature history (3)
Alias symbolsNET37
Previous namesKIAA1161, myogenesis regulating glycosidase (putative)

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.

Bilateral striopallidodentate calcinosis
Genetic Diseases, Inborn
Osteoarthritis, Hip
Osteoarthritis, Knee
Total joint arthroplasty
Diabetes Mellitus, Type 2

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.

Glycoside hydrolase family 31

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-07-09.
Open TargetsGene–disease associations from the Open Targets Platform.