Summary | Mutation origin | Mutation description | Expression | Phenotypes | Disease models | Find Mice (IMSR) | References

Symbol:	Myo6sv
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:	Myo6sv page

Strain of Origin:

B10.HA/(33NX)Sn

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

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

12 anatomical structure(s)

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:	90 strains or lines available

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