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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Mrps22
mitochondrial ribosomal protein S22
MGI:1928137
16 phenotypes from 1 allele in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Mrps22tm1.1(KOMP)Vlcg/Mrps22+
C57BL/6N-Mrps22tm1.1(KOMP)Vlcg/J
decreased bone mineral content J:211773
decreased bone mineral density J:211773
decreased circulating creatinine level J:211773
decreased lean body mass J:211773
hyperactivity J:211773
increased leukocyte cell number J:211773
increased mean corpuscular hemoglobin concentration J:211773
increased total body fat amount J:211773
Mrps22tm1.1(KOMP)Vlcg/Mrps22tm1.1(KOMP)Vlcg
B6N(Cg)-Mrps22tm1.1(KOMP)Vlcg/J
embryonic growth arrest J:279207
embryonic growth retardation J:279207
embryonic lethality prior to organogenesis J:279207
embryonic lethality, complete penetrance J:279207
failure of primitive streak formation J:279207
failure to gastrulate J:279207
prenatal lethality, complete penetrance J:261971
Mrps22tm1.1(KOMP)Vlcg/Mrps22tm1.1(KOMP)Vlcg
C57BL/6N-Mrps22tm1.1(KOMP)Vlcg/J
embryonic lethality prior to organogenesis J:211773
preweaning lethality, complete penetrance J:211773

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
04/23/2024
MGI 6.23
The Jackson Laboratory