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This mutation, discovered among G3 progeny of an ENU mutagenized male mouse, was mapped to Chr 10. It has been identified as a deletion spanning exons 27 through 29 of the 39 exons of Pcdh15 (based on the longest cDNA sequences), from nucleotide position 685,325 to 779,172 (Genbank accession NC_000076; genomic DNA sequence). (J:140625)
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
