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Symbol
Name
ID

Mrps22
mitochondrial ribosomal protein S22
MGI:1928137

Phenotype annotations related to mortality/aging

Darker colors indicate more annotations

Human Phenotypes	Death in infancy
Disease(s) Associated with MRPS22	Death in infancy
combined oxidative phosphorylation deficiency 5

Mouse Phenotypes		embryonic lethality prior to organogenesis	embryonic lethality, complete penetrance	prenatal lethality, complete penetrance	preweaning lethality, complete penetrance
Availability	Mouse Genotype
	Mrps22^{tm1.1(KOMP)Vlcg}/Mrps22^{tm1.1(KOMP)Vlcg}

Contributing Projects: 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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