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A genomic fragment encompassing exons 7 through 9 was deleted by cre mediated recombination of an upstream floxed neo cassette and a downstream single loxP site. A single loxP site remains in intron 6. The deleted region encodes residues 707 through 870 of the interferon-inducible form of ADAR. (J:87715, J:142338)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
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
