SLC13A4 and CBLIF

Data Source:
BioGRID (two hybrid)

		SLC13A4	CBLIF
Description		solute carrier family 13 member 4	cobalamin binding intrinsic factor
Image		No pdb structure
GO Annotations	Cellular Component	Plasma Membrane Integral Component Of Plasma Membrane Integral Component Of Membrane	Extracellular Region Extracellular Space Endosome Microvillus Apical Plasma Membrane Lysosomal Lumen
	Molecular Function	Protein Binding Sodium:sulfate Symporter Activity	Protein Binding Cobalamin Binding
	Biological Process	Sodium Ion Transport Sulfate Transport Anion Transmembrane Transport Sulfate Transmembrane Transport	Cobalt Ion Transport Cobalamin Metabolic Process Cobalamin Transport
Pathways		Sodium-coupled sulphate, di- and tri-carboxylate transporters	Cobalamin (Cbl, vitamin B12) transport and metabolism Defective GIF causes intrinsic factor deficiency Defective AMN causes hereditary megaloblastic anemia 1 Defective CUBN causes hereditary megaloblastic anemia 1
Drugs
Diseases
GWAS		Alcoholic chronic pancreatitis ( 28754779) Diverticular disease ( 30177863)
Interacting Genes		26 interacting genes: ACKR2 CBLIF CD79A CDS1 CERS4 DEFB108B DERL3 EFNA5 EOGT ERMP1 FCER1G GJA5 GPR152 GPR61 IER3 IGFBP5 MS4A13 OPRD1 OTOP3 SLC35A4 SLC35E4 SLC38A1 SLC41A1 TMEM147 TMEM60 TRARG1	8 interacting genes: CBL CUBN FFAR2 SLC13A4 SLC22A23 SLC7A1 SLC7A14 TMEM237
Entrez ID		26266	2694
HPRD ID		10372	02024
Ensembl ID		ENSG00000164707	ENSG00000134812
Uniprot IDs		Q59HF0 Q9UKG4	P27352
PDB IDs			2CKT 2PMV 3KQ4
Enriched GO Terms of Interacting Partners?
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