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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Agr2tm1.1Lex
targeted mutation 1.1, Lexicon Genetics
MGI:5494472
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Agr2tm1.1Lex/Agr2tm1.1Lex involves: 129S5/SvEvBrd * BALB/cJ * C57BL/6 MGI:5494479


Genotype
MGI:5494479
hm1
Allelic
Composition
Agr2tm1.1Lex/Agr2tm1.1Lex
Genetic
Background
involves: 129S5/SvEvBrd * BALB/cJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Agr2tm1.1Lex mutation (0 available); any Agr2 mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Mucosal hyperplasia in glandular stomach of Agr2tm1.1Lex/Agr2tm1.1Lex mice

mortality/aging
• progressive morbidity necessitates euthanasia

reproductive system

digestive/alimentary system
• decreased expression of enteroendocrine cell markers in the antrum
• enlarged
• 2-fold increase in weight at 24 weeks
• maturation defect of chief cells
• loss of parietal cells by 16 weeks
• thickened in the corpus and antrum
• progressive in the corpus and antrum at 6 to 16 weeks
• with retention of large amounts of food due to gastric obstruction
• stomach weight is increased 5 times at 18 weeks
• reduced mucin production by the small intestine
• increased cell proliferation

cellular
• 3.8- and 2.5-fold in the corpus and antrum, respectively
• in the small and large intestine
• however, no increase in proliferation of parietal, pit and chief cell cells

growth/size/body
• after 12 weeks of age

adipose tissue
• due to poor nutrition

hematopoietic system
• due to poor nutrition

homeostasis/metabolism

endocrine/exocrine glands
• decreased expression of enteroendocrine cell markers in the antrum
• maturation defect of chief cells
• loss of parietal cells by 16 weeks





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last database update
11/05/2024
MGI 6.24
The Jackson Laboratory