myol
Spontaneous Allele Detail

Summary

• Symbol: myol
• Name: myotonia-like
• MGI ID: MGI:5790669
• Gene: myol Location: unknown Genetic Position: Chr6, Syntenic
• Alliance: myol page

Mutation origin

• Strain of Origin: C3.Cg-H2^p hael/GrsrJ

Mutation description

• Allele Type: Spontaneous (Not Specified)
• Mutation: Not Specified
• Mutation details: This heritable phenotypic marker arose spontaneously at The Jackson Laboratory and was mapped to Chromosome 6 between rs3702975 at 12,199,651 bp and rs3023069 at 52,243,142 bp, an interval that includes the candidate gene Clcn1. (J:234691)
• Inheritance: Recessive

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 myol Mutation: 1 strain or line available

References

• Original: J:234691 Harris BS, et al., Myotonia-like: a recessive neuromuscular mutation on Chromosome 6. MGI Direct Data Submission. 2016
• All: 1 reference(s)