|
Symbol Name ID |
Tsfm
Ts translation elongation factor, mitochondrial MGI:1913649 |
| Darker colors indicate more annotations |
| Human Phenotypes | Optic atrophy |
Optic neuropathy |
Visual impairment |
| Disease(s) Associated with TSFM | |||
| combined oxidative phosphorylation deficiency 3 |
| Mouse Phenotypes | abnormal retina morphology |
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| Availability | Mouse Genotype | |
| Tsfmtm1a(EUCOMM)Wtsi/Tsfm+ | ||
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 05/07/2024 MGI 6.23 |
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