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Myo7ash1-8J
Spontaneous Allele Detail
Summary
Symbol: Myo7ash1-8J
Name: myosin VIIA; shaker 1, 8 Jackson
MGI ID: MGI:2182918
Gene: Myo7a  Location: Chr7:97700267-97768731 bp, - strand  Genetic Position: Chr7, 53.57 cM
Alliance: Myo7ash1-8J page
Mutation
origin
Strain of Origin:  B6;SJL-Tg(c177-lacZ)226Bri/J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation detailsTwo genomic regions encompassing a total of about 6.4 kb was deleted n this mutation. One region spans about 3.6 kb and covers exons 38 through 40. The other region spans about 2.8 kb and covers exons 46 and 47. Immunoblot analysis failed to detect protein in extracts from homozygous mice. (J:77937, J:183898)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Myo7a Mutation:  118 strains or lines available
Notes

Genetic Background:

The 266Bri stock on which Myo7ash1-8J arose was homozygous for a lacZ transgene. The mutation was not the result of the transgene integration, as not all animals exhibited the neurological phenotype.
References
Original:  J:77937 Samples RM, et al., A new shaker 1 mutation of the Myo7 gene in the mouse. MGI Direct Data Submission. 2002;
All:  7 reference(s)

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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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory