Symbol Name ID |
Rac1
Rac family small GTPase 1 MGI:97845 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Hypoplasia of the brainstem |
Dilated fourth ventricle |
Lateral ventricle dilatation |
Polymicrogyria |
Hypoplasia of the corpus callosum |
Cerebellar vermis hypoplasia |
Dysgenesis of the cerebellar vermis |
Cerebellar hypoplasia |
Cerebellar dysplasia |
Absent speech |
Autistic behavior |
Hyperactivity |
Motor stereotypy |
Intellectual disability |
Sleep abnormality |
Seizure |
Disease(s) Associated with RAC1 | |||||||||||||||||
autosomal dominant intellectual developmental disorder 48 |
Mouse Phenotypes | abnormal neural tube closure |
abnormal brain commissure morphology |
abnormal corpus callosum morphology |
decreased hippocampal commissure size |
decreased anterior commissure size |
abnormal dentate gyrus morphology |
abnormal hippocampus pyramidal cell layer |
small hippocampus |
abnormal telencephalon morphology |
abnormal barrel cortex morphology |
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Availability | Mouse Genotype | ||||||||||
Rac1tm1Tyb/Rac1tm2Tyb Edil3Tg(Sox2-cre)1Amc/Edil3+ (conditional) |
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Emx1tm1(cre)Ito/Emx1+ Rac1tm1Atai/Rac1tm1Jms (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 04/16/2024 MGI 6.23 |
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