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Allele : myol myotonia-like
Primary Identifier  MGI:5790669 Allele Type  Spontaneous
Attribute String  Not Specified Gene  myol
Inheritance Mode  Recessive Strain of Origin  C3.Cg-H2<p> hael/GrsrJ
Is Recombinase  false Is Wild Type  false
molecularNote  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.
  • mutations:
  • Not Specified
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

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1 Carried By

Trail: Allele

0 Driven By

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Trail: Allele




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