Phenotypes for Myo7a MGI:3587642 MGI Mouse

About Help FAQ

Phenotypes Associated with This Genotype

Allelic Composition	Myo7a^sh1-9J/Myo7a^sh1-9J
Genetic Background	involves: C3.MRL-Fas^lpr/J

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myo7a^sh1-9J mutation (1 available); any Myo7a mutation (69 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

behavior/neurological

circling ( J:49039 )

hearing/vestibular/ear

deafness ( J:49039 )

Mouse Models of Human Disease		OMIM ID	Ref(s)
Usher Syndrome, Type I; USH1		276900	J:49039

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 09/20/2016 MGI 6.05