Myo6^sv
Spontaneous Allele Detail

Summary

• Symbol: Myo6^sv
• Name: myosin VI; Snell's waltzer
• MGI ID: MGI:1856555
• Synonyms: sv
• Gene: Myo6 Location: Chr9:80072313-80219011 bp, + strand Genetic Position: Chr9, 43.98 cM
• Alliance: Myo6^sv page

Mutation origin

• Strain of Origin: B10.HA/(33NX)Sn

Mutation description

• Allele Type: Spontaneous
• Mutation: Intragenic deletion
• Mutation details: On 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

Disease models

Expression

In Structures Affected by this Mutation:

12 anatomical structure(s)

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: 91 strains or lines available

References

• Original: J:26342 Green MC, New mutant - Snell's waltzer - sv. Mouse News Lett. 1960;23:34
• All: 35 reference(s)