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 05/28/2024 MGI 6.13 |
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