RAB39B and VPS26C

Data Source:
BioGRID (two hybrid)

		RAB39B	VPS26C
Description		RAB39B, member RAS oncogene family	VPS26 endosomal protein sorting factor C
Image			No pdb structure
GO Annotations	Cellular Component	Golgi Membrane Golgi Apparatus Plasma Membrane Cytoplasmic Vesicle Membrane Vesicle Neuron Projection	Nucleus Endosome
	Molecular Function	GTPase Activity Protein Binding GTP Binding Myosin V Binding	Molecular_function Protein Binding
	Biological Process	Autophagy Regulation Of Autophagy Protein Transport Vesicle-mediated Transport Rab Protein Signal Transduction Synapse Organization	Intracellular Protein Transport Endocytic Recycling Retrograde Transport, Endosome To Plasma Membrane
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	14 interacting genes: CBLB DECR2 INCA1 LRIF1 MAML3 MAPK6 MDM4 MEI4 MEOX2 PTPN21 RAB39B TEPSIN XPA ZNF655
Entrez ID		116442	10311
HPRD ID		06703	10390
Ensembl ID		ENSG00000155961	ENSG00000157538
Uniprot IDs		Q96DA2	A8MTY9 A8MY26 O14972
PDB IDs		6S5F
Enriched GO Terms of Interacting Partners?
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