homeostasis/metabolism
• phenobarbital treatment induces increased serum glucose levels in mutant but not wild-type mice
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Allele Symbol Allele Name Allele ID |
Nr1i3tm1Ddm targeted mutation 1, David D Moore MGI:2657124 |
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Summary |
3 genotypes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• phenobarbital treatment induces increased serum glucose levels in mutant but not wild-type mice
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• defective clearance of chronically elevated bilirubin levels
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• resistant to hepatomegaly and induction of DNA synthesis when treated with phenobarbital or TCPOBOP
(J:65416)
• cocaine does not cause acute hepatotoxicity in mutants exposed to phenobarbital or TCPOBOP as it does in wild-type mice
(J:65416)
• zoxazolamine, a muscle relaxant, causes paralysis in mice, however pretreatment with Phenobarbital or TCPOBOP prevents the paralysis in wild-type mice but not in mutants, indicating that mutants have a decreased response to Phenobarbital or TCPOBOP after treatment with zoxazolamine
(J:65416)
• pretreatment with xenobiotic inducers, phenobarbital or TCPOBOP, increases the rate of clearance of an exogenous bilirubin load in wild-type but not mutant mice
(J:82748)
• mice treated with phenobarbital or TCPOBOP plus acetaminophen are resistant to the formation of hepatotoxicity
(J:83102)
• mutants are resistant to toxic doses of acetaminophen
(J:83102)
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• mutants treated with phenobarbital exhibit increased sensitivity to acetaminophen
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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 |
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