Myof Phenotype Annotations

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 12/17/2024 MGI 6.24