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Symbol Name ID |
Mboat7
membrane bound O-acyltransferase domain containing 7 MGI:1924832 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Polymicrogyria |
Absent speech |
Autistic behavior |
Intellectual disability |
Hyperreflexia |
Inability to walk |
Global developmental delay |
Delayed ability to walk |
Seizure |
Focal-onset seizure |
Generalized-onset seizure |
Generalized myoclonic seizure |
Febrile seizure (within the age range of 3 months to 6 years) |
| Disease(s) Associated with MBOAT7 | ||||||||||||||
| autosomal recessive intellectual developmental disorder 57 |
| Mouse Phenotypes | nervous system phenotype |
increased neuron apoptosis |
abnormal neuron differentiation |
abnormal neuronal migration |
hydrocephaly |
forebrain hypoplasia |
dilated lateral ventricle |
dilated third ventricle |
abnormal hippocampus morphology |
small hippocampus |
abnormal cerebral cortex morphology |
abnormal neurite morphology |
|
| Availability | Mouse Genotype | ||||||||||||
| Mboat7tm1Arai/Mboat7tm1Arai | * | ||||||||||||
| Mboat7tm1Lex/Mboat7tm1Lex | |||||||||||||
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 05/21/2024 MGI 6.23 |
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