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myol
Spontaneous Allele Detail
Nomenclature
Symbol: myol
Name: myotonia-like
MGI ID: MGI:5790669
Gene: myol  Location: unknown  Genetic Position: Chr6, Syntenic
Mutation
origin
Strain of Origin:  C3.Cg-H2p hael/GrsrJ
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Not Specified
 
Mutation detailsThis 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
Phenotypes
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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 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)

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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last database update
11/30/2021
MGI 6.17
The Jackson Laboratory