Symbol Name ID |
Mrps22
mitochondrial ribosomal protein S22 MGI:1928137 |
Darker colors indicate more annotations |
Human Phenotypes | Fetal skin edema |
Disease(s) Associated with MRPS22 | |
combined oxidative phosphorylation deficiency 5 |
Mouse Phenotypes | failure to gastrulate |
embryonic growth arrest |
embryonic growth retardation |
failure of primitive streak formation |
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Availability | Mouse Genotype | ||||
Mrps22tm1.1(KOMP)Vlcg/Mrps22tm1.1(KOMP)Vlcg |
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 08/02/2024 MGI 6.24 |
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