centronuclear myopathy

Summary
Synonym
  • myotubular myopathy
Definition
A congenital structural myopathy characterized by abnormally located nuclei in skeletal muscle cells. The nuclei are located in the center of the cell, instead of their normal location at the periphery.
Super Class
congenital structural myopathy
External Links
Disease Ontology
DOID:14717
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 11 - 20 of 26 in total
Gene ID Gene Symbol Description Source
6517 SLC2A4 solute carrier family 2 member 4
8776 MTMR1 myotubularin related protein 1
8898 MTMR2 myotubularin related protein 2
9107 MTMR6 myotubularin related protein 6
9108 MTMR7 myotubularin related protein 7
9200 HACD1 3-hydroxyacyl-CoA dehydratase 1
9215 LARGE1 LARGE xylosyl- and glucuronyltransferase 1
10462 CLEC10A C-type lectin domain containing 10A
10585 POMT1 protein O-mannosyltransferase 1
11041 B4GAT1 beta-1,4-glucuronyltransferase 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024