RAB39B

Description		RAB39B, member RAS oncogene family
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GO Annotations	Cellular Component	Golgi Membrane Golgi Apparatus Plasma Membrane Cytoplasmic Vesicle Membrane Vesicle Neuron Projection
	Molecular Function	GTPase Activity Protein Binding GTP Binding Myosin V Binding
	Biological Process	Autophagy Regulation Of Autophagy Protein Transport 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		6 interacting genes: GOLGA2 RAB3GAP1 RUFY1 SGSM3 VPS26C ZDHHC17
Entrez ID		116442
HPRD ID		06703
Ensembl ID		ENSG00000155961
Uniprot IDs		Q96DA2
PDB IDs		6S5F
Enriched GO Terms of Interacting Partners?
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