Symbol Name ID |
Mrps22
mitochondrial ribosomal protein S22 MGI:1928137 |
Darker colors indicate more annotations |
Human Phenotypes | Decreased activity of mitochondrial ATP synthase complex |
Decreased activity of mitochondrial complex I |
Decreased activity of mitochondrial complex III |
Decreased activity of mitochondrial complex IV |
Hyperammonemia |
Increased circulating lactate concentration |
Lactic acidosis |
Metabolic acidosis |
Edema |
Ascites |
Elevated circulating follicle stimulating hormone level |
Elevated circulating luteinizing hormone level |
Decreased serum estradiol |
Disease(s) Associated with MRPS22 | |||||||||||||
combined oxidative phosphorylation deficiency 5 | |||||||||||||
ovarian dysgenesis 7 |
Mouse Phenotypes | decreased circulating creatinine level |
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Availability | Mouse Genotype | |
Mrps22tm1.1(KOMP)Vlcg/Mrps22+ |
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 04/23/2024 MGI 6.23 |
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