A cassette containing lacZ and neo was inserted at the first start codon, located in exon 1a. Deleted sequence included the coding region of exon 1a, intron 1, and the 5' untranslated region of exon 1b. The downstream start codon, located in exon 1b, was left intact. Protein was undetected by Western blot analysis of skin fibroblasts and vascular smooth muscle cells obtained from homozygous mutant mice. (J:86754)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129S6/SvEvTac
Targeted
Insertion, Intragenic deletion
--
1
7
19

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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