Exon 17 was flanked with a loxP site and a floxed neo cassette via homologous recombination. The neo cassette and exon 17 were subsequently removed via in vivo Cre-mediated recombination. This results in a frameshift, premature termination codon and truncated protein. PCR analysis confirmed the presence of a 0.4 kb truncated transcript in mice carrying this allele. (J:131043)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
(129X1/SvJ x 129S1/Sv)F1-Kitl+
Targeted
Intragenic deletion
--
1
3
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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