Symbol Name ID |
Fxn
frataxin MGI:1096879 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Mitochondrial malic enzyme reduced |
Decreased pyruvate carboxylase activity |
Diabetes mellitus |
Type II diabetes mellitus |
Insulin resistance |
Disease(s) Associated with FXN | |||||
Friedreich ataxia 1 | |||||
type 2 diabetes mellitus |
Mouse Phenotypes | homeostasis/metabolism phenotype |
increased heart iron level |
abnormal iron homeostasis |
abnormal enzyme/coenzyme activity |
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Availability | Mouse Genotype | ||||
Fxntm1Mkn/Fxntm1Mkn | * | ||||
Gt(ROSA)26Sortm1(H1/tetO-RNAi:Fxn)Dhg/Gt(ROSA)26Sor+ | |||||
Fxntm2Mkn/Fxntm2.1Mkn Tg(Ckmm-cre)1Lrsn/0 (conditional) |
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 04/30/2024 MGI 6.23 |
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