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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pdx1tm1.1Stof
targeted mutation 1.1, Doris Stoffers
MGI:4359453
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Pdx1tm1.1Stof/Pdx1tm1.1Stof involves: 129/Sv * C57BL/6 MGI:4359482
ht2
Pdx1tm1.1Stof/Pdx1+ involves: 129/Sv * C57BL/6 MGI:4359483
ht3
Pdx1tm1Cvw/Pdx1tm1.1Stof involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:4359484


Genotype
MGI:4359482
hm1
Allelic
Composition
Pdx1tm1.1Stof/Pdx1tm1.1Stof
Genetic
Background
involves: 129/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdx1tm1.1Stof mutation (0 available); any Pdx1 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Reduction in Ngn3+ pancreatic endocrine progenitor cells in Pdx1tm1.1Stof/Pdx1+ and Pdx1tm1.1Stof/Pdx1tm1.1Stof mice

endocrine/exocrine glands
N
• pancreatic weight and appearance are normal
• at E17.5, PP cells occupy less pancreatic area than in wild-type mice
• at E17.5, alpha cells occupy less pancreatic area than in wild-type mice
• at E17.5, beta cells occupy less pancreatic area than in wild-type mice
• at E17.5, delta cells occupy less pancreatic area than in wild-type mice
• at E17.5, epsilon cells occupy less pancreatic area than in wild-type mice
• at E17.5, endocrine lineage cells are reduced compared to in wild-type mice with beta and alpha cells most severely affected
• from E13.5, Ngn3+ endocrine progenitor cells are decreased in number and staining intensity compared to in wild-type mice
• at E19.5, apoptosis of Ngn3+ endocrine progenitor cells is increased compared to in wild-type mice
• however, the number of Ngn3+ endocrine progenitor cells at E11.5 is normal and progenitor cell proliferation is normal

homeostasis/metabolism
• hypoglycemia is mild at birth but progressively worsens with age
• in fasting mice or following glucose stimulation
• at 3 to 4 weeks, mice are diabetic unlike wild-type mice




Genotype
MGI:4359483
ht2
Allelic
Composition
Pdx1tm1.1Stof/Pdx1+
Genetic
Background
involves: 129/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdx1tm1.1Stof mutation (0 available); any Pdx1 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Reduction in Ngn3+ pancreatic endocrine progenitor cells in Pdx1tm1.1Stof/Pdx1+ and Pdx1tm1.1Stof/Pdx1tm1.1Stof mice

endocrine/exocrine glands
• at E17.5, beta cells occupy less pancreatic area than in wild-type mice
• at E19.5, apoptosis of Ngn3+ endocrine progenitor cells is increased compared to in wild-type mice
• however, the number of Ngn3+ endocrine progenitor cells at E17.5 is normal

homeostasis/metabolism
• unlike similarly treated wild-type mice, glucose-stimulated male mice fail to exhibit an increase in plasma insulin levels while female mice exhibit reduced fasting insulin levels
• at 3 to 4 weeks, male mice are glucose intolerant unlike wild-type mice
• however, female mice exhibit normal glucose tolerance at 3 to 4 weeks of age




Genotype
MGI:4359484
ht3
Allelic
Composition
Pdx1tm1Cvw/Pdx1tm1.1Stof
Genetic
Background
involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdx1tm1.1Stof mutation (0 available); any Pdx1 mutation (35 available)
Pdx1tm1Cvw mutation (1 available); any Pdx1 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Pancreatic hypoplasia in Pdx1tm1Cvw/Pdx1tm1.1Stof mice

endocrine/exocrine glands
• small compared to in wild-type mice but not as small as in Pdx1tm1Cvw homozygotes
• decreased weight compared to in wild-type mice but not as much as in Pdx1tm1Cvw homozygotes

homeostasis/metabolism
• at birth





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory