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Symbol Name ID |
Ptcd3
pentatricopeptide repeat domain 3 MGI:1917206 |
| Darker colors indicate more annotations |
| Human Phenotypes | Optic atrophy |
Nystagmus |
| Disease(s) Associated with PTCD3 | ||
| combined oxidative phosphorylation deficiency 51 |
| Mouse Phenotypes | impaired pupillary reflex |
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| Availability | Mouse Genotype | |
| Ptcd3tm1.1(KOMP)Vlcg/Ptcd3+ | ||
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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