FMOD

Description		fibromodulin
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GO Annotations	Cellular Component	Extracellular Region Extracellular Space Golgi Lumen Extracellular Matrix Lysosomal Lumen Collagen-containing Extracellular Matrix
	Molecular Function	Extracellular Matrix Structural Constituent Conferring Compression Resistance
	Biological Process	Transforming Growth Factor Beta Receptor Complex Assembly Collagen Fibril Organization
Pathways		Keratan sulfate biosynthesis Keratan sulfate degradation ECM proteoglycans Defective CHST6 causes MCDC1 Defective ST3GAL3 causes MCT12 and EIEE15 Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
Drugs
Diseases
GWAS		Attention deficit hyperactivity disorder (inattention symptoms) ( 32595297) Blood protein levels ( 30072576) Obesity-related traits ( 23251661)
Interacting Genes		4 interacting genes: FBXO7 TGFB1 TGFB2 TGFB3
Entrez ID		2331
HPRD ID		02591
Ensembl ID		ENSG00000122176
Uniprot IDs		A0A024R971 B3KS64 Q06828 Q12833
PDB IDs		5MX0
Enriched GO Terms of Interacting Partners?
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