Myof Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Myof
myoferlin
MGI:1919192

7 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Hprt1^{tm2(CAG-Myof)Isrd}/Y involves: 129 * C57BL/6	normal muscle phenotype	J:187293
Hprt1^{tm2(CAG-Myof)Isrd}/Hprt1^{tm2(CAG-Myof)Isrd} involves: 129 * C57BL/6	normal muscle phenotype	J:187293
Myof^tm1Mcn/Myof^tm1Mcn involves: 129X1/SvJ	abnormal myogenesis	J:163585
	abnormal soleus morphology	J:163585
	decreased body size	J:163585
	decreased skeletal muscle fiber density	J:163585
	skeletal muscle fiber degeneration	J:163585
Myof^tm1Mcn/Myof^tm1Mcn Not Specified	decreased vascular permeability	J:163126

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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