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Symbol
Name
ID

Mrps22
mitochondrial ribosomal protein S22
MGI:1928137

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Retrognathia	Microcephaly	Delayed skeletal maturation
Disease(s) Associated with MRPS22	Retrognathia	Microcephaly	Delayed skeletal maturation
combined oxidative phosphorylation deficiency 5
ovarian dysgenesis 7

Mouse Phenotypes		decreased bone mineral content	decreased bone mineral density
Availability	Mouse Genotype
	Mrps22^{tm1.1(KOMP)Vlcg}/Mrps22⁺

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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