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Symbol
Name
ID
Mrps22
mitochondrial ribosomal protein S22
MGI:1928137
Phenotype annotations related to embryo
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
Availability Mouse Genotype
Mrps22tm1.1(KOMP)Vlcg/Mrps22tm1.1(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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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory