Human Disease and Mouse Model Detail

Human Disease

Term: Cardiomyopathy, Familial Hypertrophic, 14; CMH14
OMIM ID: 613251

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...

Myh6

MYH6

...both mouse and human orthologous genes.

Transgenes and
other mutation types

Tg(Myh6*)131Lnwd		Characteristics of this human disease are associated with transgenes and other mutation types in mouse.
Tg(Myh6*)140Lnwd

Mouse Models

Genotype			Ref(s)
Allelic Composition	Note	Genetic Background
Models with phenotypic similarity to human disease where etiologies involve orthologs.¹
Myh6^tm1Jse/Myh6⁺		129S.129X1-Myh6^tm1Jse	J:104363
Myh6^tm1Jse/Myh6⁺		involves: 129X1/SvJ	J:32960, J:95600
Myh6^tm2Jse/Myh6⁺		involves: 129S1/Sv	J:95600
Myh6^tm3.1Jse/Myh6⁺		involves: 129X1/SvJ	J:165269
Models involving transgenes or other mutation types.²
Tg(Myh6*)131Lnwd/0		involves: C57BL/6 * CBA	J:31537
Tg(Myh6*)140Lnwd/0		involves: C57BL/6 * CBA	J:31537, J:36522

¹Human genes are associated with this disease. Mouse model genotypes include mutations in the orthologs of these human genes.
²Models 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
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