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Myo6sv
Spontaneous Allele Detail
Nomenclature
Symbol: Myo6sv
Name: myosin VI; Snell's waltzer
MGI ID: MGI:1856555
Synonyms: sv
Gene: Myo6  Location: Chr9:80165031-80311729 bp, + strand  Genetic Position: Chr9, 43.98 cM
Mutation
origin
Strain of Origin:  B10.HA/(33NX)Sn
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation detailsOn the basis of a series of southern blots, this mutation appears to involve a 1.1 kb intragenic deletion. Gene transcripts could be detected by RT-PCR. Sequence analysis of these transcripts identified a 150 bp deletion corresponding to nucleotides 2456-2585. The deletion results in a frame shift which introduces a stop codon at the beginning of the neck region. (J:29898)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 11 anatomical structures
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 Myo6 Mutation:  12 strains or lines available
References
Original:  J:26342 Green MC, New mutant - Snell's waltzer - sv. Mouse News Lett. 1960;23:34
All:  27 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
11/05/2019
MGI 6.14
The Jackson Laboratory