MRPS2 and SLC34A3

		MRPS2	SLC34A3
Description		mitochondrial ribosomal protein S2	solute carrier family 34 member 3
Image			No pdb structure
GO Annotations	Cellular Component	Mitochondrion Mitochondrial Inner Membrane Mitochondrial Small Ribosomal Subunit	Cell Plasma Membrane Brush Border Integral Component Of Membrane Apical Plasma Membrane Brush Border Membrane Vesicle
	Molecular Function	Structural Constituent Of Ribosome	Sodium:phosphate Symporter Activity
	Biological Process	Mitochondrial Translation Mitochondrial Ribosome Assembly Mitochondrial Translational Elongation Mitochondrial Translational Termination	Sodium Ion Transport Phosphate Ion Transport Cellular Phosphate Ion Homeostasis Sodium Ion Transmembrane Transport Sodium-dependent Phosphate Transport
Pathways		Mitochondrial translation initiation Mitochondrial translation elongation Mitochondrial translation elongation Mitochondrial translation termination	Type II Na+/Pi cotransporters Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH)
Drugs
Diseases			Hypophosphatemic rickets; X-Linked dominant hypophosphatemia (XLH); Autosomal dominant hypophosphatemic rickets (ADHR); Autosomal recessive hypophosphatemic rickets (ARHR); Hereditary hypophophatemic rickets with hypercalciuria (HHRH)
GWAS
Interacting Genes		4 interacting genes: APP OBP2A SLC34A3 TOR1B	1 interacting genes: MRPS2
Entrez ID		51116	142680
HPRD ID		14783	10236
Ensembl ID		ENSG00000122140	ENSG00000198569
Uniprot IDs		Q9Y399	Q8N130
PDB IDs		3J9M 6NU2 6NU3
Enriched GO Terms of Interacting Partners?
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