RP2

Gene Name		retinitis pigmentosa 2 (X-linked recessive)
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Gene Ontology Annotations	Cellular Component	Cytoplasm Golgi Apparatus Centriole Plasma Membrane Cytoplasmic Vesicle Ciliary Basal Body Extracellular Vesicular Exosome Primary Cilium Periciliary Membrane Compartment
	Molecular Function	Actin Binding Nucleoside Diphosphate Kinase Activity GTPase Activator Activity Protein Binding ATP Binding GTP Binding Unfolded Protein Binding
	Biological Process	Cell Morphogenesis Nucleoside Diphosphate Phosphorylation GTP Biosynthetic Process UTP Biosynthetic Process CTP Biosynthetic Process Protein Folding Post-Golgi Vesicle-mediated Transport Organelle Organization Cytoskeleton Organization Post-chaperonin Tubulin Folding Pathway Visual Perception Protein Transport Positive Regulation Of GTPase Activity
Pathways		Cargo trafficking to the periciliary membrane Organelle biogenesis and maintenance Trafficking of myristoylated proteins to the cilium Assembly of the primary cilium
Drugs
Diseases
GWAS
Protein-protein Interactions		1 interactors: ARL3
Entrez ID		6102
HPRD ID		02424
Ensembl ID		ENSG00000102218
Uniprot IDs		O75695
PDB IDs		2BX6 3BH6 3BH7
Enriched GO Terms of Interacting Partners?		Intraciliary Transport Photoreceptor Cell Development Post-Golgi Vesicle-mediated Transport Cytokinesis Smoothened Signaling Pathway Microtubule-based Transport Cytoskeleton-dependent Intracellular Transport
Tagcloud ?		challenges combinations consequences deal dichotomized diphosphate displaying face great hetero hexamers highlight motility ndpk ndpks nm23 nme nme1 nmes nucleoside oligomers perhaps redundancy span spread surprising taxonomically typically uncertainty