Exon 22 and 23a were replaced with a segment containing exon 22, a floxed neo cassette and exon 23 containing a nucleotide substitution that results in an amino acid substitution of an alanine for a serine at position 727 (S727A), a site within the transactivation domain. The neo cassette was removed by germ-line, cre-mediated recombination. Protein expression and the absence of phosphorylation was confirmed by western blot analysis. (J:130622)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129P2/OlaHsd
Targeted
Insertion, Nucleotide substitutions
--
1
8
6

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

Title
PMID
Journal
Year
IF
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