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A A-to-G point mutation at nucleotide 3126 was induced by ENU mutagenesis. The mutation results in an aspartate to glycine substitution at codon 1040, which lies within the eighth cadherin repeat of the extracellular domain. Western blot analysis indicates no difference in abundance of protein. (J:84285, J:216413)
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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References Literature
Title
PMID
Journal
Year
IF
