myofibrillar myopathy 10

Summary
Synonym
  • MFM10
Definition
A myofibrillar myopathy characterized by onset of muscle pain, cramping, and exercise fatigue in the first or second decades of life that has_material_basis_in homozygous or compound heterozygous mutation in the SVIL gene on chromosome 10p11.23.
Super Class
autosomal recessive disease myofibrillar myopathy
Disease Ontology
DOID:0112108
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6840 SVIL supervillin
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
O95425 Supervillin

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.2.1

Last updated: April 7, 2025