A loxP site was inserted between exons 7 and 8 and a loxP and frt-flanked neomycin selection cassette was inserted between exons 13 and 14. After FLP and Cre-mediated recombination, a deletion of exons 8-13 was created, with a single loxP and a single frt site remaining at the deletion site. This deletion removes K homology (KH) motifs 2, 3 and the amino terminal half of KH4, yielding an allele that is incapable of expressing a protein that binds properly with single-strand nucleic acids. Immunoblot analysis confirmed the absence of protein expression in primary MEFs derived from E13.5 homozygous mutant embryos. (J:229985)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129
Targeted
Insertion, Intragenic deletion
--
1
--
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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