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Symbol
Name
ID
Fars2
phenylalanine-tRNA synthetase 2 (mitochondrial)
MGI:1917205
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties
Feeding difficulties in infancy
Urinary incontinence
Insomnia
Disease(s) Associated with FARS2
combined oxidative phosphorylation deficiency 14
hereditary spastic paraplegia 77

Mouse Phenotypes
decreased grip strength
Availability Mouse Genotype
Fars2em1(IMPC)J/Fars2+

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
09/15/2020
MGI 6.15
The Jackson Laboratory