|
Symbol Name ID |
Megf8
multiple EGF-like-domains 8 MGI:2446294 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Aplasia/Hypoplasia of the corpus callosum |
Cerebral atrophy |
Spina bifida occulta |
Intellectual disability |
Global developmental delay |
Delayed ability to walk |
Generalized non-motor (absence) seizure |
| Disease(s) Associated with MEGF8 | |||||||
| Carpenter syndrome |
| Mouse Phenotypes | nervous system phenotype |
abnormal axon extension |
abnormal axon fasciculation |
abnormal nervous system morphology |
exencephaly |
abnormal glossopharyngeal nerve morphology |
abnormal trigeminal nerve morphology |
abnormal maxillary nerve morphology |
abnormal ophthalmic nerve morphology |
abnormal vagus nerve morphology |
abnormal spinal nerve morphology |
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| Availability | Mouse Genotype | |||||||||||
| Megf8m687Ddg/Megf8m687Ddg | ||||||||||||
| Megf8tm1.1Ddg/Megf8tm1.1Ddg | ||||||||||||
| Megf8Gt(G037A09)Wrst/Megf8m687Ddg | ||||||||||||
| Megf8tm1.2Ddg/Megf8tm1.2Ddg H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
* | |||||||||||
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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