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Symbol Name ID |
Ocln
occludin MGI:106183 |
| Darker colors indicate more annotations |
| Human Phenotypes | Splenomegaly |
Hepatomegaly |
Umbilical hernia |
Failure to thrive |
| Disease(s) Associated with OCLN | ||||
| pseudo-TORCH syndrome 1 |
| Mouse Phenotypes | postnatal growth retardation |
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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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