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Using DNA markers D15Mit28 and D15Mit68, Krt71Ca-15J mapped to the location of Krt71. This mutation was identified as an allele of Krt71Ca-14J by a non-complementation test. The molecular lesion that defines this allele has not been determined.
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
