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Symbol Name ID |
Fat4
FAT atypical cadherin 4 MGI:3045256 |
| Darker colors indicate more annotations |
| Human Phenotypes | Pachygyria |
Subcortical band heterotopia |
Hypoplasia of the corpus callosum |
Spina bifida occulta |
Gray matter heterotopia |
Periventricular nodular heterotopia |
Benign neoplasm of the central nervous system |
Hyperactivity |
Intellectual disability |
Intellectual disability, mild |
Global developmental delay |
Delayed gross motor development |
Seizure |
| Disease(s) Associated with FAT4 | |||||||||||||
| Hennekam syndrome | |||||||||||||
| Van Maldergem syndrome 2 |
| Mouse Phenotypes | abnormal neural tube morphology |
abnormal orientation of cochlear hair cell stereociliary bundles |
abnormal orientation of outer hair cell stereociliary bundles |
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| Availability | Mouse Genotype | |||
| Fat4tm1.1Hmc/Fat4tm1.1Hmc | ||||
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 04/30/2024 MGI 6.23 |
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