|
Symbol Name ID |
Tmem231
transmembrane protein 231 MGI:2685024 |
| Darker colors indicate more annotations |
| Human Phenotypes | Dandy-Walker malformation |
Microcephaly |
Encephalocele |
Oculomotor apraxia |
Hydrocephalus |
Aplasia/Hypoplasia of the corpus callosum |
Anencephaly |
Molar tooth sign on MRI |
Lobar holoprosencephaly |
Absent speech |
Aggressive behavior |
Self-mutilation |
Inability to walk |
Global developmental delay |
| Disease(s) Associated with TMEM231 | ||||||||||||||
| Joubert syndrome 20 | ||||||||||||||
| Meckel syndrome |
| Mouse Phenotypes | abnormal embryonic neuroepithelium morphology |
abnormal nervous system development |
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| Availability | Mouse Genotype | ||
| Tmem231Gt(OST335874)Lex/Tmem231Gt(OST335874)Lex | |||
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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