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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 (77 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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
01/24/2023
MGI 6.22
The Jackson Laboratory