A loxP site, a mutated exon 2 containing a G to C change at position 423 resulting in a lysine to asparagine mutation at amino acid 141 (K141N), an FRT-flanked neomycin selection cassette, and a loxP site replaced exon 2. Cre-mediated recombination removed the mutated exon 2 and the neomycin gene resulting in a null allele. Western blot analysis confirmed absence of protein. (J:284796)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
(129S6/SvEvTac x C57BL/6NCrl)F1
Targeted
Insertion, Intragenic deletion
--
1
5
1

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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