Symbol Name ID |
Fxn
frataxin MGI:1096879 |
Darker colors indicate more annotations |
Human Phenotypes | Mitochondrial malic enzyme reduced |
Decreased pyruvate carboxylase activity |
Disease(s) Associated with FXN | ||
Friedreich ataxia 1 |
Mouse Phenotypes | abnormal myocardial fiber mitochondrial morphology |
myocardium necrosis |
abnormal mitochondrial morphology |
disorganized mitochondrial cristae |
increased mitochondrial size |
dilated mitochondrion |
increased embryonic tissue cell apoptosis |
embryo tissue necrosis |
abnormal respiratory electron transport chain |
increased mitochondrial fission |
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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) |
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Fxntm2Mkn/Fxntm2.1Mkn Tg(Eno2-cre)39Jme/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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