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Symbol Name ID |
Snrpb
small nuclear ribonucleoprotein B MGI:98342 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Cerebral calcification |
Hydranencephaly |
Porencephalic cyst |
Meningocele |
Myelomeningocele |
Spina bifida |
Intellectual disability |
| Disease(s) Associated with SNRPB | ||||||||
| cerebrocostomandibular syndrome |
| Mouse Phenotypes | hindbrain hypoplasia |
midbrain hypoplasia |
enlarged lateral ventricles |
abnormal forebrain morphology |
thin cerebral cortex |
abnormal cranial ganglia morphology |
abnormal geniculate ganglion morphology |
abnormal vestibular ganglion morphology |
abnormal glossopharyngeal nerve morphology |
abnormal trigeminal nerve morphology |
abnormal mandibular nerve morphology |
abnormal maxillary nerve morphology |
abnormal ophthalmic nerve morphology |
abnormal vagus nerve morphology |
small dorsal root ganglion |
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| Availability | Mouse Genotype | |||||||||||||||
| E2f1Tg(Wnt1-cre)2Sor/E2f1+ Snrpbem1Lajm/Snrpb+ (conditional) |
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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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