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Symbol
Name
ID
Aars2
alanyl-tRNA synthetase 2, mitochondrial
MGI:2681839
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Feeding difficulties
Feeding difficulties in infancy
Poor eye contact
Psychomotor retardation
Disease(s) Associated with AARS2
combined oxidative phosphorylation deficiency

Mouse Phenotypes
impaired pupillary reflex
Availability Mouse Genotype
Aars2tm1(KOMP)Wtsi/Aars2+

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
08/13/2019
MGI 6.14
The Jackson Laboratory