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Symbol Name ID |
B9d1
B9 protein domain 1 MGI:1351471 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcornea |
Sclerocornea |
Cataract |
Aplasia/Hypoplasia of the iris |
Abnormal chorioretinal morphology |
Optic atrophy |
Retinopathy |
Hypertelorism |
Anophthalmia |
Microphthalmia |
Esodeviation |
Oculomotor apraxia |
| Disease(s) Associated with B9D1 | ||||||||||||
| Joubert syndrome 27 | ||||||||||||
| Meckel syndrome |
| Mouse Phenotypes | microphthalmia |
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| Availability | Mouse Genotype | |
| B9d1tm1a(EUCOMM)Wtsi/B9d1tm1a(EUCOMM)Wtsi | ||
| B9d1tm1d(EUCOMM)Wtsi/B9d1tm1d(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 04/16/2024 MGI 6.23 |
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