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Symbol Name ID |
Tctn3
tectonic family member 3 MGI:1914840 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Occipital encephalocele |
Cerebral cortical atrophy |
Cerebral cortical hemiatrophy |
Agenesis of corpus callosum |
Cerebral atrophy |
Subcortical cerebral atrophy |
Porencephalic cyst |
Arrhinencephaly |
Agenesis of cerebellar vermis |
Molar tooth sign on MRI |
Intellectual disability |
Global developmental delay |
Specific learning disability |
| Disease(s) Associated with TCTN3 | ||||||||||||||
| Joubert syndrome 18 | ||||||||||||||
| orofaciodigital syndrome IV |
| Mouse Phenotypes | decreased embryonic neuroepithelium primary cilium number |
absent floor plate |
holoprosencephaly |
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| Availability | Mouse Genotype | |||
| Tctn3tm1.2Blnw/Tctn3tm1.2Blnw | ||||
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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