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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Myh14
myosin, heavy polypeptide 14
MGI:1919210
11 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Myh10tm2Rsad/Myh10tm2Rsad
Myh14tm1Rsad/Myh14tm1Rsad
involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6
abnormal centrosome morphology J:168304
abnormal fetal cardiomyocyte morphology J:168304
abnormal microtubule cytoskeleton morphology J:168304
abnormal mitosis J:168304
abnormal mitotic spindle morphology J:168304
cardiomyopathy J:168304
decreased fetal cardiomyocyte number J:168304
heart hypoplasia J:168304
lethality throughout fetal growth and development, complete penetrance J:168304
Myh10tm4Rsad/Myh10tm4Rsad
Myh14tm1Rsad/Myh14tm1Rsad
involves: 129S6/SvEvTac * C57BL/6
abnormal myocardial fiber physiology J:168304
cardiac hypertrophy J:168304
cardiomyopathy J:168304

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory