This allele was derived by crossing mice bearing Muctm1(cre/ERT2)Lcm to Gt(ROSA)26Sortm1(FLP1)Dym mice to delete the frt site-flanked neomycin resistance cassette in the germline. The present, neo-, allele contains, downstream of the termination codon of the endogenous gene, an internal ribosomal entry site (IRES) followed by DNA encoding Cre recombinase joined to ERT2 and a single frt site (IRES-CreERT2-FRT). ERT2 is a triply mutated (G400V, M543A, L544A) human estrogen receptor ligand-binding domain (LBD) that renders the fusion protein highly sensitive to activation by 4-hydroxytamoxifen, but unresponsive to the receptor's native ligands. The cre/ERT2 fusion protein is expressed under control of the endogenous promoter without disrupting expression of the endogenous gene. Tamoxifen-induced Cre activity has been demonstrated in acinar and ductal cells of the adult pancreas and in their embryonic precursors. (J:159445)

Basic Information

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

References Literature

Title
PMID
Journal
Year
IF
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