A targeting vector was designed to flank exon 2, containing an initiation site and N-terminal 168 amino acids, with loxP sites. Cre expression in the germ line excised exon 2, leaving a single loxP site. Analysis of transcripts suggests that, in the absence of exon 2, exon 1B was replaced by exon 1A, which was spliced to exon 3, thereby allowing translation from an initiation codon in exon 4. The result was a N-terminal truncated transcript. Southern blot confirmed absence of exon 2 in mutant mice with this putatively hypomorphic allele. (J:92058)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129X1/SvJ
Targeted
Intragenic deletion
--
1
6
2

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:
Show/Hide columns
Phenotypes

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top