Approximately 3.1 kb of upstream sequence was replaced with the equivalent region upstream of the human insulin gene but with a -331C>G mutation (relative to the translation start site) that disrupts a CC dinucleotide and that is found in some diabetes patients. IRES sequence and an EGFP reporter gene cassette were inserted into the 3' UTR. The loxP site flanked neomycin resistance gene cassette that was also inserted was removed through subsequent cre-mediated recombination. In this allele the mutated human INS promoter fails to drive expression of the mouse Ins2 gene and the EGFP reporter. (J:308553)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6J
Targeted
Insertion, Intergenic deletion
--
1
9
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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