hypertrophic cardiomyopathy 6

Summary
Synonym
  • CMH6
  • cardiomyopathy, familial hypertrophic 6
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2).
Super Class
familial hypertrophic cardiomyopathy
Disease Ontology
DOID:0110312
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
51422 PRKAG2 protein kinase AMP-activated non-catalytic subunit gamma 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
108099 Prkag2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit

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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


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Last updated: December 9, 2024