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Symbol Name ID |
Rrm2b
ribonucleotide reductase M2 B (TP53 inducible) MGI:2155865 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased activity of mitochondrial complex IV |
Multiple mitochondrial DNA deletions |
Increased CSF lactate |
Lactic acidosis |
Severe lactic acidosis |
Aminoaciduria |
Exercise intolerance |
| Disease(s) Associated with RRM2B | |||||||
| autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5 | |||||||
| mitochondrial DNA depletion syndrome 8a |
| Mouse Phenotypes | increased circulating creatinine level |
abnormal blood homeostasis |
decreased circulating glucose level |
increased circulating cholesterol level |
increased circulating triglyceride level |
hyperlipidemia |
increased circulating phosphate level |
decreased circulating alkaline phosphatase level |
decreased circulating serum albumin level |
increased blood urea nitrogen level |
increased urine protein level |
abnormal urine homeostasis |
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| Availability | Mouse Genotype | ||||||||||||
| Rrm2bGt(OST85254)Lex/Rrm2bGt(OST85254)Lex | |||||||||||||
| Rrm2btm1Ynak/Rrm2btm1Ynak | |||||||||||||
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 09/08/2026 MGI 6.24 |
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