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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 (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• development abnormal (J:49926)
• development abnormal (J:49926)
• no cochlear electrophysiology responses (J:49926)
• no cochlear electrophysiology responses (J:49926)

nervous system
• development abnormal (J:49926)
• development abnormal (J:49926)

Mouse Models of Human Disease
OMIM ID Ref(s)
Usher Syndrome, Type I; USH1 276900 J:42644


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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last database update
01/26/2016
MGI 6.02
The Jackson Laboratory