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Symbol
Name
ID
Rac1
Rac family small GTPase 1
MGI:97845
Phenotype annotations related to nervous system
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
Availability Mouse Genotype
Rac1tm1Tyb/Rac1tm2Tyb
Edil3Tg(Sox2-cre)1Amc/Edil3+  (conditional)
Emx1tm1(cre)Ito/Emx1+
Rac1tm1Atai/Rac1tm1Jms  (conditional)

Contributing Projects:
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
The Jackson Laboratory