Symbol
Name
ID

Rab39b
RAB39B, member RAS oncogene family
MGI:1915040

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes

Lewy bodies

Megalencephaly

Bradykinesia

Parkinsonism

Parkinsonism with favorable response to dopaminergic medication

Resting tremor

Dysarthria

Poor speech

Autistic behavior

Hyperactivity

Motor stereotypy

Dementia

Intellectual disability

Intellectual disability, mild

Dyskinesia

Shuffling gait

Postural instability

Global developmental delay

Seizure

Disease(s) Associated with RAB39B

non-syndromic X-linked intellectual disability 72

Waisman syndrome

Mouse Phenotypes		increased brain weight	increased brain size	abnormal cerebral cortex morphology	increased cerebral cortex cell number	abnormal dendritic spine morphology	increased dendritic spine density
Availability	Mouse Genotype	increased brain weight	increased brain size	abnormal cerebral cortex morphology	increased cerebral cortex cell number	abnormal dendritic spine morphology	increased dendritic spine density
	Rab39b^em1Jfch/Rab39b^em1Jfch
	Rab39b^em1Jfch/Y
	Rab39b^tm1Pdad/Y

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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