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This allele is a derivative of the t6 haplotype, missing the proximal end but retaining the distal end including the recessive lethal factor of t6 and is linked to the Chr 17 breakpoint in the reciprocal translocation T(1;17)190Ca. The breakpoint is within a crossover-suppression region therefore th17 can not be separated from the translocation. (J:5889)
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
