Myo6<sv> Spontaneous Allele Detail MGI Mouse (MGI:1856555)

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:

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

Phenotypes

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

Disease models

Expression

In Structures Affected by this Mutation:

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)

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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