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Phenotypes Associated with This Genotype
Genotype
MGI:3587744
Allelic
Composition
Myo7a26SB/Myo7a26SB
Genetic
Background
involves: BALB/cRl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myo7a26SB mutation (2 available); any Myo7a mutation (76 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• development abnormal
• no cochlear electrophysiology responses

nervous system
• development abnormal

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
01/12/2022
MGI 6.17
The Jackson Laboratory