Myo7a<sh1-8J> Spontaneous Allele Detail MGI Mouse (MGI:2182918)

Myo7a^sh1-8J
Spontaneous Allele Detail

Summary

Symbol:	Myo7a^sh1-8J
Name:	myosin VIIA; shaker 1, 8 Jackson
MGI ID:	MGI:2182918
Gene:	Myo7a Location: Chr7:97700267-97768731 bp, - strand Genetic Position: Chr7, 53.57 cM
Alliance:	Myo7a^sh1-8J page

Mutation
origin

Strain of Origin:

B6;SJL-Tg(c177-lacZ)226Bri/J

Mutation
description

Allele Type:		Spontaneous
Mutation:		Intragenic deletion
		Mutation details: Two genomic regions encompassing a total of about 6.4 kb was deleted n this mutation. One region spans about 3.6 kb and covers exons 38 through 40. The other region spans about 2.8 kb and covers exons 46 and 47. Immunoblot analysis failed to detect protein in extracts from homozygous mice. (J:77937, J:183898)

Phenotypes

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

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 Myo7a Mutation:	118 strains or lines available

Notes

Genetic Background:

The 266Bri stock on which Myo7a^sh1-8J arose was homozygous for a lacZ transgene. The mutation was not the result of the transgene integration, as not all animals exhibited the neurological phenotype.

References

Original:	J:77937 Samples RM, et al., A new shaker 1 mutation of the Myo7 gene in the mouse. MGI Direct Data Submission. 2002;
All:	7 reference(s)

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