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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 (118 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
hearing/vestibular/ear
abnormal hair cell morphology ( J:49926 )
• development abnormal
abnormal hearing physiology ( J:49926 )
• no cochlear electrophysiology responses

nervous system
abnormal hair cell morphology ( J:49926 )
• 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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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory