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| Nomenclature |
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Symbol:
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Myo6sv
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Name:
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myosin VI;
Snell's waltzer
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MGI ID: |
MGI:1856555 |
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Synonyms: |
sv |
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Gene:
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Myo6
Location:
Chr9:80012838-80159536 bp, + strand
Genetic Position: Chr9,
44.0 cM
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Mutation
origin |
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Strain of Origin:
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B10.HA/(33NX)Sn
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Mutation
description |
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Allele
Type: |
Spontaneous |
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Mutation: |
Intragenic deletion |
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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) |
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Inheritance: |
Recessive |
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Phenotype
summary
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Phenotype Summary by Mammalian Phenotype terms
(show or
hide all annotated terms)
Genotypes are listed in the next section.
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Key:
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| hm |
homozygous |
ht |
heterozygous |
| cn |
conditional genotype |
cx |
complex: > 1 genome feature |
| tg |
involves transgenes |
ot |
other: hemizygous, indeterminate,... |
| N |
normal phenotype |
 |
expected model not found |
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Phenotypic
data by
genotype
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Phenotypic Data by Genotype
(show or
hide all phenotypic details)
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Disease
models
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| References |
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Original: |
J:26342
Green MC,
"New mutant - Snell's waltzer - sv"
Mouse News Lett 1960;23():34
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All: |
13 reference(s)
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