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Most of the coding sequence was replaced with the corresponding human sequence with a single nucleotide polymorphism of asparagine at position 36 (36N). This variant is associated with increased risk for acute myeloid leukemia in humans. Cre-mediated recombination removed a floxed neo cassette inserted upstream of the last coding exon. (J:192927)
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
