Human Disease and Mouse Model Detail

Human Disease

Term: Glycogen Storage Disease of Heart, Lethal Congenital
OMIM ID: 261740

Synonyms

Glycogen Storage Disease of Heart; Phosphorylase Kinase Deficiency of Heart

Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene

Human Gene

Characteristics of this human disease are associated with mutations in...

PRKAG2

...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene.

Transgenes and
other mutation types

Tg(Myh6-PRKAG2*T400N)1Feah		Characteristics of this human disease are associated with transgenes and other mutation types in mouse.
Tg(Myh6/tetO-PRKAG2*N488I)1Chib
Tg(Myh6-tTA)55Rbns

Mouse Models

Genotype			Ref(s)
Allelic Composition	Note	Genetic Background
Models involving transgenes or other mutation types.¹
Tg(Myh6-PRKAG2*T400N)1Feah/0		involves: FVB/N	J:162180
Tg(Myh6-tTA)55Rbns/0 Tg(Myh6/tetO-PRKAG2*N488I)1Chib/0		Not Specified	J:145090

¹Models involving transgenes or other mutation types may also appear in other sections of the table.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support.	last database update 04/03/2013 MGI 5.12