SLC34A3 and TMEM167B

Data Source:
BioGRID (two hybrid)

		SLC34A3	TMEM167B
Description		solute carrier family 34 member 3	transmembrane protein 167B
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Plasma Membrane Brush Border Integral Component Of Membrane Apical Plasma Membrane Brush Border Membrane Vesicle	Golgi Membrane Golgi Apparatus Integral Component Of Membrane
	Molecular Function	Sodium:phosphate Symporter Activity Protein Binding	Molecular_function Protein Binding
	Biological Process	Sodium Ion Transport Phosphate Ion Transport Cellular Phosphate Ion Homeostasis Sodium Ion Transmembrane Transport Sodium-dependent Phosphate Transport	Constitutive Secretory Pathway
Pathways		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			Apolipoprotein B levels ( 32203549)
Interacting Genes		4 interacting genes: CLRN1 GPX8 TMEM167B TMEM234	33 interacting genes: ACKR2 AGPAT3 APOL3 AQP10 AQP6 ASPH C14orf180 CD300C CD47 CTXN3 EBP FXYD6-FXYD2 HSD17B11 HSD17B13 LETMD1 LSS MFSD14B MGST2 PLLP REEP4 SACM1L SEC22B SERINC2 SLC34A3 SMPD2 STX12 STX1B TAS2R19 TM4SF19 TMEM100 TMEM107 UNC50 ZDHHC21
Entrez ID		142680	56900
HPRD ID		10236	16474
Ensembl ID		ENSG00000198569	ENSG00000215717
Uniprot IDs		Q8N130	A0A024R096 A0A494C0V7 Q9NRX6
PDB IDs
Enriched GO Terms of Interacting Partners?
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