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Symbol Name ID |
Pibf1
progesterone immunomodulatory binding factor 1 MGI:1261910 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cone/cone-rod dystrophy |
Oculomotor apraxia |
| Disease(s) Associated with PIBF1 | ||
| Joubert syndrome 33 |
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 04/09/2024 MGI 6.23 |
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