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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		Myo7a4494SB
shaker 4494SB
MGI:2155421
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
 		Myo7a4494SB/Myo7a4494SB involves: BALB/cRl MGI:3587759


Genotype
MGI:3587759
hm1
Allelic
Composition		 Myo7a4494SB/Myo7a4494SB
Genetic
Background		 involves: BALB/cRl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myo7a4494SB 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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory