RAB23

Description		RAB23, member RAS oncogene family
Image		No pdb structure
GO Annotations	Cellular Component	Cytoplasm Autophagosome Centrosome Cytosol Plasma Membrane Endosome Membrane Endomembrane System Cell Junction Phagocytic Vesicle Membrane Phagocytic Vesicle
	Molecular Function	GTPase Activity Protein Binding GTP Binding
	Biological Process	Autophagosome Assembly Intracellular Protein Transport Cellular Defense Response Negative Regulation Of Protein Import Into Nucleus GTP Metabolic Process 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		Coronary artery disease ( 30104761) Systemic lupus erythematosus ( 28714469)
Interacting Genes		2 interacting genes: ARFGAP1 CREB3
Entrez ID		51715
HPRD ID		05850
Ensembl ID		ENSG00000112210
Uniprot IDs		A0A024RD41 Q9ULC3
PDB IDs
Enriched GO Terms of Interacting Partners?
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