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This mutation was discovered at generation F6 of inbreeding at MRC Harwell of STOCK Myo15sh2 mice obtained from The Jackson Laboratory. It is reported as an allele of Eda based on its X-linkage and multiple phenotypic characteristics. (J:169366)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
