About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:3587758
Allelic
Composition
Myo7a3336SB/Myo7a3336SB
Genetic
Background
involves: BALB/cRl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myo7a3336SB mutation (2 available); any Myo7a mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• abnormal hair cell development
• no cochlear electrophysiology responses

nervous system
• abnormal hair cell development

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Usher syndrome type 1 DOID:0110826 OMIM:276900
J:42644


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
06/20/2017
MGI 6.10
The Jackson Laboratory