RAB39B

Description		RAB39B, member RAS oncogene family
Image		No pdb structure
GO Annotations	Cellular Component	Intracellular Golgi Apparatus Plasma Membrane Endomembrane System Cytoplasmic Vesicle Membrane Vesicle Neuron Projection
	Molecular Function	GTPase Activity Protein Binding GTP Binding Myosin V Binding
	Biological Process	Intracellular Protein Transport Autophagy Regulation Of Autophagy Vesicle-mediated Transport Rab Protein Signal Transduction Synapse Organization
Pathways		RAB geranylgeranylation RAB GEFs exchange GTP for GDP on RABs
Drugs
Diseases		Syndromic X-linked mental retardation with epilepsy or seizures, including: West syndrome (WS); Partington syndrome (PRTS); Proud syndrome (ACCAG); XMR and epilepsy (XMRE); MRXHF1; XMR OPHN1-related (MRXSO) ; XELBD; XMR, Christianson type (MRXSC); Creatine deficiency syndrome (XL-CDS); Renpenning syndrome (RENS1); Epilepsy and mental retardation limited to females (EFMR); Periventricular nodular heterotopia (PVNH); Hydrocephalus (XLH); XMR, JARID1C related (MRXSJ); Boerjeson-Forssman syndrome (BFLS); CK syndrome (CKS)
GWAS
Interacting Genes		5 interacting genes: GOLGA2 RAB3GAP1 RUFY1 SGSM3 ZDHHC17
Entrez ID		116442
HPRD ID		06703
Ensembl ID		ENSG00000155961
Uniprot IDs		Q96DA2
PDB IDs
Enriched GO Terms of Interacting Partners?
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