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Exons 2 and 3 were replaced by an EGFP with a floxed pgk neo. A stop codon was created in exon 4 by the deletion, resulting in the prevention of a transcript through alternative splicing. Mutants expressed EGFP as a fusion protein with the N-terminal part of exon 2. (J:112168)
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
