|
Symbol Name ID |
B9d2
B9 protein domain 2 MGI:2387643 |
| Darker colors indicate more annotations |
| Human Phenotypes | Encephalocele |
Aganglionic megacolon |
Oculomotor apraxia |
Hydrocephalus |
Polymicrogyria |
Aplasia/Hypoplasia of the corpus callosum |
Cerebellar vermis hypoplasia |
Abnormality of neuronal migration |
Ataxia |
Tremor |
Intellectual disability |
Gait disturbance |
Global developmental delay |
Seizure |
| Disease(s) Associated with B9D2 | ||||||||||||||
| Joubert syndrome |
| Mouse Phenotypes | anastomosis between internal carotid artery and basilar artery |
absent segment of anterior cerebral artery |
absent segment of posterior cerebral artery |
abnormal brain vasculature morphology |
abnormal adenohypophysis morphology |
absent adenohypophysis |
abnormal neurohypophysis morphology |
small superior cervical ganglion |
reduced sympathetic cervical ganglion size |
abnormal brain morphology |
enlarged brain ventricles |
abnormal choroid plexus morphology |
abnormal brain internal capsule morphology |
abnormal forebrain morphology |
abnormal olfactory bulb morphology |
abnormal hindbrain morphology |
small superior vagus ganglion |
abnormal hypoglossal nerve topology |
absent oculomotor nerve |
thin oculomotor nerve |
abnormal optic chiasm morphology |
thin motoric part of trigeminal nerve |
abnormal intrathoracic topology of vagus nerve |
abnormal spinal cord 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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