Symbol Name ID |
Rab39b
RAB39B, member RAS oncogene family MGI:1915040 |
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 |
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Availability | Mouse Genotype | ||||||
Rab39bem1Jfch/Rab39bem1Jfch | |||||||
Rab39bem1Jfch/Y | |||||||
Rab39btm1Pdad/Y |
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 07/05/2024 MGI 6.24 |
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