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EN
This cytologically detectable Y Chromosome (Chr) deletion resulted from asymmetric recombination during male meiosis between the short arm of a Y Chr (Yp) of SWR origin and an X Chr carrying Tp(Y)1CtSxr-a, which originally occurred in the RIII inbred strain. (J:194031)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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
