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The Ft mutation is the result of a transgene integration into mouse chromosome 8. The transgene integration event resulted in a deletion of 1.6 Mb of genomic sequences, covering coding regions for six genes. Among these are the genes included in the entire IroquoisB (IrxB) gene cluster. (J:44450, J:76079)
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
