|
Symbol Name ID |
Ocln
occludin MGI:106183 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Increased CSF protein concentration |
Spasticity |
Cerebral calcification |
Ventriculomegaly |
Lissencephaly |
Pachygyria |
Polymicrogyria |
Cerebral cortical atrophy |
Cerebellar hypoplasia |
Intellectual disability, profound |
Abnormality of movement |
Hyperreflexia |
Dystonia |
Global developmental delay |
Seizure |
| Disease(s) Associated with OCLN | ||||||||||||||||
| pseudo-TORCH syndrome 1 |
| Mouse Phenotypes | abnormal basal ganglion morphology |
abnormal cerebellum morphology |
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| Availability | Mouse Genotype | ||
| Oclntm1Sts/Oclntm1Sts | |||
| Oclntm2Sts/Oclntm2Sts | |||
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 04/23/2024 MGI 6.23 |
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