|
Symbol Name ID |
Tmem237
transmembrane protein 237 MGI:2138365 |
| Darker colors indicate more annotations |
| Human Phenotypes | Intracranial hemorrhage |
Dandy-Walker malformation |
Encephalocele |
Aganglionic megacolon |
Oculomotor apraxia |
Hypoplasia of the brainstem |
Hydrocephalus |
Polymicrogyria |
Aplasia/Hypoplasia of the corpus callosum |
Hypoplasia of the corpus callosum |
Agenesis of cerebellar vermis |
Cerebellar vermis hypoplasia |
Molar tooth sign on MRI |
Meningocele |
Abnormality of neuronal migration |
Ataxia |
Tremor |
Irritability |
Intellectual disability |
Intellectual disability, severe |
Gait disturbance |
Global developmental delay |
Seizure |
| Disease(s) Associated with TMEM237 | |||||||||||||||||||||||
| Joubert syndrome | |||||||||||||||||||||||
| Joubert syndrome 14 |
| Mouse Phenotypes | abnormal brain morphology |
increased brain size |
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| Availability | Mouse Genotype | ||
| Tmem237tm1b(EUCOMM)Hmgu/Tmem237+ | |||
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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