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Symbol Name ID |
Pibf1
progesterone immunomodulatory binding factor 1 MGI:1261910 |
| Darker colors indicate more annotations |
| Human Phenotypes | Oculomotor apraxia |
Delayed CNS myelination |
Molar tooth sign on MRI |
Ataxia |
Global developmental delay |
| Disease(s) Associated with PIBF1 | |||||
| Joubert syndrome 33 |
| Mouse Phenotypes | abnormal neural tube morphology |
abnormal neural tube closure |
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| Availability | Mouse Genotype | ||
| Pibf1tm1.1(KOMP)Vlcg/Pibf1tm1.1(KOMP)Vlcg | |||
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 04/16/2024 MGI 6.23 |
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