This t haplotype resulted from a rare recombination event between haplotype tw5 and a wild-type chromosome. DNA probes obtained by microdissection and microcloning of fragments of mouse Chromosome 17 show that this allele comprises a deletion of D17Leh54, 94, 180 and 443, and a duplication of D17Leh89, 467,and 525. This haplotype is a member of the t9 complementation group and, although derived from tw5, it is not found in wild mouse populations. (J:8922)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
STOCK T Itpr3tf/tw5+
Spontaneous
Other
Recessive
--
--
3

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

References Literature

Title
PMID
Journal
Year
IF
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