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Symbol Name ID |
B9d2
B9 protein domain 2 MGI:2387643 |
| Darker colors indicate more annotations |
| Human Phenotypes | Biparietal narrowing |
Encephalocele |
Hand polydactyly |
Foot polydactyly |
Scoliosis |
Abnormal form of the vertebral bodies |
| Disease(s) Associated with B9D2 | ||||||
| Joubert syndrome |
| Mouse Phenotypes | abnormal incisor morphology |
absent upper incisors |
abnormal maxilla morphology |
abnormal rib morphology |
abnormal vertebral arch morphology |
fusion of vertebral arches |
abnormal vertebral body 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 04/16/2024 MGI 6.23 |
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