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Symbol Name ID |
Fars2
phenylalanine-tRNA synthetase 2, mitochondrial MGI:1917205 |
| Darker colors indicate more annotations |
| Human Phenotypes | Retrognathia |
Microcephaly |
Hip dysplasia |
Kyphoscoliosis |
| Disease(s) Associated with FARS2 | ||||
| combined oxidative phosphorylation deficiency 14 | ||||
| hereditary spastic paraplegia 77 |
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 |
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