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AGRN
Description
agrin
Image
No pdb structure
GO Annotations
Cellular Component
Extracellular Region
Basement Membrane
Golgi Lumen
Plasma Membrane
Integral Component Of Membrane
Lysosomal Lumen
Synapse
Collagen-containing Extracellular Matrix
Extracellular Exosome
Molecular Function
Dystroglycan Binding
Structural Constituent Of Cytoskeleton
Extracellular Matrix Structural Constituent
Calcium Ion Binding
Protein Binding
Sialic Acid Binding
Chondroitin Sulfate Binding
Laminin Binding
Heparan Sulfate Proteoglycan Binding
Biological Process
Retinoid Metabolic Process
Glycosaminoglycan Biosynthetic Process
Glycosaminoglycan Catabolic Process
Cytoskeleton Organization
Signal Transduction
G Protein-coupled Acetylcholine Receptor Signaling Pathway
Neuromuscular Junction Development
Animal Organ Morphogenesis
Tissue Development
Extracellular Matrix Organization
Receptor Clustering
Positive Regulation Of GTPase Activity
Clustering Of Voltage-gated Sodium Channels
Positive Regulation Of Synaptic Growth At Neuromuscular Junction
Positive Regulation Of Transcription By RNA Polymerase II
Synapse Organization
Positive Regulation Of Filopodium Assembly
Pathways
A tetrasaccharide linker sequence is required for GAG synthesis
HS-GAG biosynthesis
HS-GAG biosynthesis
HS-GAG degradation
Integrin cell surface interactions
Non-integrin membrane-ECM interactions
ECM proteoglycans
ECM proteoglycans
Defective B4GALT7 causes EDS, progeroid type
Defective B3GAT3 causes JDSSDHD
Defective EXT2 causes exostoses 2
Defective EXT1 causes exostoses 1, TRPS2 and CHDS
NCAM1 interactions
Defective B3GALT6 causes EDSP2 and SEMDJL1
Retinoid metabolism and transport
Drugs
Diseases
Congenital myasthenic syndrome
GWAS
Interacting Genes
9 interacting genes:
ATN1
ATXN7
BOLL
CACNA1A
DAG1
GFI1B
MAGED1
TEPSIN
UBC
Entrez ID
375790
HPRD ID
10550
Ensembl ID
ENSG00000188157
Uniprot IDs
O00468
PDB IDs
Enriched GO Terms of Interacting Partners
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