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Symbol Name ID |
B9d2
B9 protein domain 2 MGI:2387643 |
| Darker colors indicate more annotations |
| Human Phenotypes | Iris coloboma |
Strabismus |
Nystagmus |
Oculomotor apraxia |
Ptosis |
| Disease(s) Associated with B9D2 | |||||
| Joubert syndrome |
| Mouse Phenotypes | abnormal eye muscle morphology |
abnormal optic chiasm morphology |
aphakia |
abnormal optic cup morphology |
abnormal optic stalk morphology |
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| Availability | Mouse Genotype | |||||
| B9d2tm1a(EUCOMM)Wtsi/B9d2tm1a(EUCOMM)Wtsi | ||||||
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 04/30/2024 MGI 6.23 |
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