The insertion of sequence encoding GFP into exon 3 resulted in the generation of a hypomorphic allele lacking exon 3. Though the floxed neo cassette used for selection was excised, inverted repeats at the insertion site of the remaining loxP site may be the reason for the aberrant splicing. Mutant transcript was detected by Northern blot, RT-PCR, and RNase protection. Sequence analysis of the RT-PCR products showed that exon 2 spliced directly to exon 4, producing a transcript lacking exon 3 similar to a splice variant found at low levels in wild-type mice. The transcript putatively encodes protein lacking 154 residues from the N-terminal domain, but containing the nuclear localization signal and DNA-binding and C-terminal acidic activation domains. (J:86255)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Not Specified
Targeted
Insertion
--
1
4
5

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

References Literature

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PMID
Journal
Year
IF
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