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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
AmfrGt(IST12797A11)Tigm
gene trap IST12797A11, Texas A&M Institute for Genomic Medicine
MGI:4093875
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
AmfrGt(IST12797A11)Tigm/AmfrGt(IST12797A11)Tigm C57BL/6-AmfrGt(IST12797A11)Tigm MGI:5699972


Genotype
MGI:5699972
hm1
Allelic
Composition
AmfrGt(IST12797A11)Tigm/AmfrGt(IST12797A11)Tigm
Genetic
Background
C57BL/6-AmfrGt(IST12797A11)Tigm
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
AmfrGt(IST12797A11)Tigm mutation (2 available); any Amfr mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• more than 70% of mice grow fat with abdominal obesity at around 1 year of age

immune system
• hepatic inflammation, characterized by the infiltration of inflammatory cells in which lymphocytes infiltrate, gather, and interface among liver lobules regardless of fat accumulation
• hepatitis is likely to be independent of steatohepatitis progression

liver/biliary system
• hepatic inflammation, characterized by the infiltration of inflammatory cells in which lymphocytes infiltrate, gather, and interface among liver lobules regardless of fat accumulation
• hepatitis is likely to be independent of steatohepatitis progression
• liver of obese aged mice develops simple steatosis and/or hepatic inflammation to varying degrees indicating the development of nonalcoholic steatohepatitis
• hepatocytes are enlarged and distended by large single or multiple well-defined droplets of fat
• accumulation of lipids in the liver
• mice injected with tunicamycin in the liver at 6 months of age to induce acute ER stress show greater steatosis in the entire liver compared to local and partial areas of steatosis in wild-type mice
• mice injected with tunicamycin in the liver at 11 days of age exhibit persistent steatosis and progression of fibrosis while wild-type mice recover fully
• 6 of 25 mice develop liver tumors; aged mice have dysplastic foci but no tumors in other organs
• irregular distribution of collagen fibers in the liver, indicative of liver injury and fibrosis
• 2 of 6 mice with liver tumors have severe fibrosis in another liver lobe distant from the tumor region

neoplasm
• 6 of 25 mice develop liver tumors; aged mice have dysplastic foci but no tumors in other organs

homeostasis/metabolism
• MEFs are more sensitive to tunicamycin treatment, showing reduced survival rate compared to wild-type MEFs
• mice injected with tunicamycin in the liver at 6 months of age to induce acute ER stress show greater steatosis in the entire liver compared to local and partial areas of steatosis in wild-type mice
• mice injected with tunicamycin in the liver at 11 days of age exhibit persistent steatosis and progression of fibrosis while wild-type mice recover fully





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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
12/10/2024
MGI 6.24
The Jackson Laboratory