mitochondrial myopathy

Summary
Synonym
  • mitochondrial cytopathy
Definition
A myopathy that is characterized by mitochondrial dysfunction.
Super Class
myopathy
External Links
Disease Ontology
DOID:699
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 20 of 26 in total
Gene ID Gene Symbol Description Source
2632 GBE1 1,4-alpha-glucan branching enzyme 1
2678 GGT1 gamma-glutamyltransferase 1
2876 GPX1 glutathione peroxidase 1
3155 HMGCL 3-hydroxy-3-methylglutaryl-CoA lyase
4968 OGG1 8-oxoguanine DNA glycosylase
5160 PDHA1 pyruvate dehydrogenase E1 subunit alpha 1
6389 SDHA succinate dehydrogenase complex flavoprotein subunit A
6390 SDHB succinate dehydrogenase complex iron sulfur subunit B
6391 SDHC succinate dehydrogenase complex subunit C
6646 SOAT1 sterol O-acyltransferase 1
Related Glycoprotein
Displaying entries 21 - 22 of 22 in total
UniProt ID Protein Name Source
Q6ZMG9 Ceramide synthase 6
Q9C0K1 Metal cation symporter ZIP8

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 v4.0.0

Last updated: August 19, 2024