All Phenotypes Myo7a<3336SB> MGI Mouse

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Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

Myo7a^3336SB
shaker 3336SB
MGI:2155420

Summary

1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Myo7a^3336SB/Myo7a^3336SB	involves: BALB/cRl	MGI:3587758

Allelic Composition	Myo7a^3336SB/Myo7a^3336SB
Genetic Background	involves: BALB/cRl

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myo7a^3336SB 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)
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