ABCD3 and COL6A2

Data Source:
HPRD (in vivo)

		ABCD3	COL6A2
Description		ATP binding cassette subfamily D member 3	collagen type VI alpha 2 chain
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Mitochondrion Peroxisome Peroxisomal Membrane Peroxisomal Matrix Cytosol Membrane Integral Component Of Membrane Intracellular Membrane-bounded Organelle	Extracellular Region Collagen Trimer Extracellular Space Endoplasmic Reticulum Lumen Protein-containing Complex Sarcolemma Collagen-containing Extracellular Matrix Extracellular Exosome Extracellular Vesicle
	Molecular Function	Long-chain Fatty Acid Transporter Activity Protein Binding ATP Binding ATPase Activity ATPase-coupled Transmembrane Transporter Activity Protein Homodimerization Activity Protein Self-association	Protein Binding Collagen Binding Extracellular Matrix Structural Constituent Conferring Tensile Strength
	Biological Process	Fatty Acid Biosynthetic Process Fatty Acid Beta-oxidation Peroxisome Organization Response To Organic Cyclic Compound Long-chain Fatty Acid Import Into Peroxisome Response To Drug Very Long-chain Fatty Acid Catabolic Process Transmembrane Transport	Cell Adhesion Response To Glucose Extracellular Matrix Organization
Pathways		ABC transporters in lipid homeostasis Class I peroxisomal membrane protein import	Collagen degradation Collagen biosynthesis and modifying enzymes Signaling by PDGF Assembly of collagen fibrils and other multimeric structures Integrin cell surface interactions ECM proteoglycans ECM proteoglycans NCAM1 interactions Collagen chain trimerization
Drugs
Diseases			Congenital muscular dystrophies (CMD/MDC), including: Merosin-deficient CMD (MDC1A); Ullrich CMD (UCMD); Integrin alpha7-deficient CMD; CMD with joint hyperlaxity (CMDH); CMD with epidermolysis bullosa; Walker-Warburg syndrome (WWS); Muscle-eye-brain disease (MEB); Fukuyama CMD (FCMD); CMD with muscle hypertrophy (MDC1C); CMD with severe intellectual impairment and abnormal glycosylation (MDC1D); Rigid spine syndrome (RSS); LMNA-deficient CMD; CMD with respiratory failure and muscle hypertrophy (MDC1B); Bethlem myopathy
GWAS			Central corneal thickness ( 32528159 29760442) Height ( 31562340) Intraocular pressure ( 29235454) Refractive error ( 32231278)
Interacting Genes		6 interacting genes: ABCD1 ABCD2 COL6A2 PEX19 PSMA1 TUFT1	5 interacting genes: ABCD3 COX6A2 FN1 SIRPA SLC38A3
Entrez ID		5825	1292
HPRD ID		01368	02110
Ensembl ID		ENSG00000117528	ENSG00000142173
Uniprot IDs		P28288	A0A384MDP3 P12110
PDB IDs
Enriched GO Terms of Interacting Partners?
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