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Exons 12 and 13 were fused and a G to A point mutation in exon 13 results in the amino acid substitution of threonine for alanine at position 324 (A324T). An FRT-flanked neomycin resistance cassette with a 5' loxP site was inserted upstream of exon 12. (J:224431)
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
