Mouse Genome Informatics
hm
    Myo7a816SB/Myo7a816SB
involves: BALB/cRl
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
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
OMIM IDRef(s)
Usher Syndrome, Type I; USH1 276900 J:42644