Symbol Name ID |
Mrps22
mitochondrial ribosomal protein S22 MGI:1928137 |
Darker colors indicate more annotations |
Human Phenotypes | Redundant neck skin |
Ascites |
Delayed puberty |
Growth delay |
Disease(s) Associated with MRPS22 | ||||
combined oxidative phosphorylation deficiency 5 | ||||
ovarian dysgenesis 7 |
Mouse Phenotypes | embryonic growth retardation |
decreased lean body mass |
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Availability | Mouse Genotype | ||
Mrps22tm1.1(KOMP)Vlcg/Mrps22tm1.1(KOMP)Vlcg | |||
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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