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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Hes1tm1(cre/ERT2)Lcm
targeted mutation 1, L Charles Murtaugh
MGI:4412375
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Hes1tm1(cre/ERT2)Lcm/Hes1tm1(cre/ERT2)Lcm involves: 129S1/Sv * 129X1/SvJ MGI:4943522
ht2
Hes1tm1(cre/ERT2)Lcm/Hes1+ involves: 129S1/Sv * 129X1/SvJ MGI:4415725
cn3
Rbpjtm1Hon/Rbpjtm1.1Hon
Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+
Hes1tm1(cre/ERT2)Lcm/Hes1+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ MGI:5310799
cn4
Gt(ROSA)26Sortm1(Notch1)Dam/Gt(ROSA)26Sor+
Hes1tm1(cre/ERT2)Lcm/Hes1+
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ MGI:4943527


Genotype
MGI:4943522
hm1
Allelic
Composition
Hes1tm1(cre/ERT2)Lcm/Hes1tm1(cre/ERT2)Lcm
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hes1tm1(cre/ERT2)Lcm mutation (0 available); any Hes1 mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos die between E12.5 and E13.5, similar to published Hes1tm1Fgu knockouts




Genotype
MGI:4415725
ht2
Allelic
Composition
Hes1tm1(cre/ERT2)Lcm/Hes1+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hes1tm1(cre/ERT2)Lcm mutation (0 available); any Hes1 mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• heterozygotes are viable and fertile




Genotype
MGI:5310799
cn3
Allelic
Composition
Rbpjtm1Hon/Rbpjtm1.1Hon
Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+
Hes1tm1(cre/ERT2)Lcm/Hes1+
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1(EYFP)Cos mutation (12 available); any Gt(ROSA)26Sor mutation (968 available)
Hes1tm1(cre/ERT2)Lcm mutation (0 available); any Hes1 mutation (21 available)
Rbpjtm1.1Hon mutation (1 available); any Rbpj mutation (193 available)
Rbpjtm1Hon mutation (2 available); any Rbpj mutation (193 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
N
• tamoxifen-treated mice exhibit normal pancreatic ductal morphology and pancreata mass
• tamoxifen-treated mice exhibit a decrease in YFP+ centroacinar cells compared with control mice
• tamoxifen-treated mice exhibit an increase in YFP+ acinar cells compared with control mice
• tamoxifen-treated mice exhibit a rapid transformation of YFP+ centroacinar cells into acinar cells compared with control mice
• however, tamoxifen-treated mice exhibit normal centroacinar and acinar cells proliferation and apoptosis

digestive/alimentary system
• tamoxifen-treated mice exhibit a decrease in YFP+ centroacinar cells compared with control mice
• tamoxifen-treated mice exhibit an increase in YFP+ acinar cells compared with control mice




Genotype
MGI:4943527
cn4
Allelic
Composition
Gt(ROSA)26Sortm1(Notch1)Dam/Gt(ROSA)26Sor+
Hes1tm1(cre/ERT2)Lcm/Hes1+
Genetic
Background
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1(Notch1)Dam mutation (1 available); any Gt(ROSA)26Sor mutation (968 available)
Hes1tm1(cre/ERT2)Lcm mutation (0 available); any Hes1 mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• pancreatic progenitor cells (GFP +ve) form cystic structures, not narrow, branched structures, that lack endocrine or acinar marker expression with tamoxifen treatment (2 mg) at E9.5 or 11.5
• treatment at E13.5 or 15.5 blocks islet differentiation, but some exocrine differentiation occurs, with labeled cells integrating into normal acini and ducts
• treatment with 0.5 mg tamoxifen at E9.5 still results in formation of abnormal cystic tubules as seen with the higher dose
• Notch 1 activation at E13.5 results in most GFP +ve cells adopting a ductal, rather than acinar, fate; activation at E15.5 reverses the proportions with most cells taking an acinar fate





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last database update
06/12/2024
MGI 6.13
The Jackson Laboratory