About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:3587760
Allelic
Composition		 Myo7a816SB/Myo7a816SB
Genetic
Background		 involves: BALB/cRl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myo7a816SB 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 )
• abnormal hair cell development
abnormal hearing physiology ( J:49926 )
• no cochlear electrophysiology responses

nervous system
abnormal hair cell morphology ( J:49926 )
• 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory