SLC34A3 and MRPS2

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