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Exon 12 was replaced with a floxed neo cassette and a modified exon 12 containing nucleotide substitutions that result in the amino acid substitution of phenylalanine for tyrosine at position 1325 (Y1325F). The neo cassette was removed by cre mediated recombination. (J:155360)
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
