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CRIPSR/cas9 mediated recombination created 3 nucleotide changes (GAAG to CGAA) resulting in a substitution mutation of lysine 117 to glutamic acid. The homologous mutation in humans is associated with maturity-onset diabetes of the young 3. (J:342895)
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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References Literature
Title
PMID
Journal
Year
IF
