COL6A2 and ABCD3

Number of citations of the paper that reports this interaction (PubMedID 12176987)
14

Data Source:
HPRD (in vivo)

		COL6A2	ABCD3
Description		collagen type VI alpha 2 chain	ATP binding cassette subfamily D member 3
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Extracellular Region Collagen Trimer Extracellular Space Endoplasmic Reticulum Lumen Extracellular Matrix Protein-containing Complex Sarcolemma Collagen-containing Extracellular Matrix Extracellular Exosome Extracellular Vesicle	Mitochondrion Peroxisome Peroxisomal Membrane Peroxisomal Matrix Cytosol Membrane Integral Component Of Membrane Intracellular Membrane-bounded Organelle
	Molecular Function	Protein Binding Collagen Binding Extracellular Matrix Structural Constituent Conferring Tensile Strength	Long-chain Fatty Acid Transporter Activity Protein Binding ATP Binding ATPase Activity ATPase Activity, Coupled To Transmembrane Movement Of Substances Protein Homodimerization Activity Protein Self-association
	Biological Process	Growth Plate Cartilage Chondrocyte Morphogenesis Cell Adhesion Response To Glucose Extracellular Matrix Organization	Fatty Acid Biosynthetic Process Fatty Acid Beta-oxidation Peroxisome Organization Response To Organic Cyclic Compound Peroxisomal Long-chain Fatty Acid Import Response To Drug Very Long-chain Fatty Acid Catabolic Process Transmembrane Transport
Pathways		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	ABC transporters in lipid homeostasis Class I peroxisomal membrane protein import
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 ( 29760442) Height ( 31562340) Intraocular pressure ( 29235454)
Interacting Genes		6 interacting genes: ABCD3 COL6A1 COX6A2 FN1 SIRPA SLC38A3	7 interacting genes: ABCD1 ABCD2 ACADM COL6A2 PEX19 PSMA1 TUFT1
Entrez ID		1292	5825
HPRD ID		02110	01368
Ensembl ID		ENSG00000142173	ENSG00000117528
Uniprot IDs		A0A384MDP3 P12110	P28288
PDB IDs
Enriched GO Terms of Interacting Partners?
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