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This deletion of the majority (~9/10) of the male-specific region of the long arm (MSYq) arose in a mouse carrying the 11 kb Srydl1Rob short arm deletion that removes Sry. The deleted region on the long arm included most or all copies of the Ssty gene family. The Rbmy gene family on the short arm and the pseudoautosomal region were left intact. (J:89616)
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
