RAB23

Description		RAB23, member RAS oncogene family
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GO Annotations	Cellular Component	Cytoplasm Endosome Autophagosome Centrosome Cytosol Plasma Membrane Cilium Endosome Membrane Endomembrane System Membrane Cell Junction Phagocytic Vesicle Membrane Cytoplasmic Vesicle Ciliary Basal Body Phagocytic Vesicle
	Molecular Function	Nucleotide Binding GTPase Activity Protein Binding GTP Binding Hydrolase Activity Metal Ion Binding
	Biological Process	Autophagosome Assembly Intracellular Protein Transport Cellular Defense Response Anatomical Structure Morphogenesis Protein Transport Negative Regulation Of Protein Import Into Nucleus GTP Metabolic Process System Development Cilium Assembly Craniofacial Suture Morphogenesis
Pathways		RAB geranylgeranylation
Drugs
Diseases		Craniosynostosis, including: Pfeiffer syndrome; Apert syndrome; Crouzon syndrome; Jackson-Weiss syndrome; Beare-Stevenson syndrome; Muenke craniosynostosis; Saethre-Chotzen syndrome; Craniosynostosis Boston type; Antley-Bixler syndrome; Carpenter syndrome; Craniofrontonasal dysplasia; Noonan syndrome; Baller-Gerold syndrome
GWAS		Systemic lupus erythematosus ( 28714469)
Interacting Genes		2 interacting genes: ARFGAP1 CREB3
Entrez ID		51715
HPRD ID		05850
Ensembl ID		ENSG00000112210
Uniprot IDs		Q9ULC3
PDB IDs		8YIM 8YL3 8YNR 8YO0 8YP0
Enriched GO Terms of Interacting Partners?		Positive Regulation Of Deacetylase Activity CCR1 Chemokine Receptor Binding Release From Viral Latency Golgi Membrane CAMP Response Element Binding Protein Binding Induction Of Positive Chemotaxis Positive Regulation Of Monocyte Chemotaxis Negative Regulation Of Endoplasmic Reticulum Stress-induced Intrinsic Apoptotic Signaling Pathway Positive Regulation Of Positive Chemotaxis Regulation Of ARF Protein Signal Transduction
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