Symbol Name ID |
Fars2
phenylalanine-tRNA synthetase 2, mitochondrial MGI:1917205 |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties |
Feeding difficulties in infancy |
Urinary incontinence |
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+ |
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 08/02/2024 MGI 6.24 |
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