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Symbol
Name
ID
Cars2
cysteinyl-tRNA synthetase 2, mitochondrial
MGI:1919191
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Nonimmune hydrops fetalis
Disease(s) Associated with CARS2
combined oxidative phosphorylation deficiency 27

Mouse Phenotypes
abnormal embryo turning
embryonic growth retardation
abnormal embryo size
abnormal placenta size
Availability Mouse Genotype
Cars2em1(IMPC)Bay/Cars2em1(IMPC)Bay
Cars2em1(IMPC)Bay/Cars2+

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