About   Help   FAQ
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





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory