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BGN
Gene Name
biglycan
Image
No pdb structure
Gene Ontology Annotations
Cellular Component
Extracellular Region
Proteinaceous Extracellular Matrix
Golgi Lumen
Cell Surface
Transport Vesicle
Extracellular Matrix
Sarcolemma
Lysosomal Lumen
Extracellular Vesicular Exosome
Molecular Function
Extracellular Matrix Structural Constituent
Glycosaminoglycan Binding
Extracellular Matrix Binding
Biological Process
Blood Vessel Remodeling
Carbohydrate Metabolic Process
Biological_process
Pathogenesis
Peptide Cross-linking Via Chondroitin 4-sulfate Glycosaminoglycan
Extracellular Matrix Organization
Glycosaminoglycan Metabolic Process
Chondroitin Sulfate Metabolic Process
Chondroitin Sulfate Biosynthetic Process
Chondroitin Sulfate Catabolic Process
Dermatan Sulfate Biosynthetic Process
Small Molecule Metabolic Process
Pathways
MPS IIIB - Sanfilippo syndrome B
Diseases of glycosylation
Heparan sulfate/heparin (HS-GAG) metabolism
Defective B4GALT7 causes EDS, progeroid type
MPS I - Hurler syndrome
MPS IX - Natowicz syndrome
Chondroitin sulfate/dermatan sulfate metabolism
CS/DS degradation
Defective SLC26A2 causes chondrodysplasias
Glycosaminoglycan metabolism
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
Defective CHST14 causes EDS, musculocontractural type
Defective PAPSS2 causes SEMD-PA
MPS IIIA - Sanfilippo syndrome A
Myoclonic epilepsy of Lafora
ECM proteoglycans
Defective CHST6 causes MCDC1
Glycogen storage diseases
MPS IIID - Sanfilippo syndrome D
A tetrasaccharide linker sequence is required for GAG synthesis
Chondroitin sulfate biosynthesis
MPS IIIC - Sanfilippo syndrome C
Diseases associated with glycosaminoglycan metabolism
Mucopolysaccharidoses
Defective EXT2 causes exostoses 2
MPS II - Hunter syndrome
Defective B3GAT3 causes JDSSDHD
Defective CHST3 causes SEDCJD
Defective EXT1 causes exostoses 1, TRPS2 and CHDS
MPS IV - Morquio syndrome A
Dermatan sulfate biosynthesis
Defective CHSY1 causes TPBS
MPS IV - Morquio syndrome B
MPS VII - Sly syndrome
Metabolism of carbohydrates
MPS VI - Maroteaux-Lamy syndrome
Drugs
Diseases
GWAS
Protein-protein Interactions
16 interactors:
APOB
APP
BMP4
COL1A1
COL1A2
COL2A1
COL4A2
DAG1
ELN
HDL3
JPH3
MFAP2
PLA2G1B
TGFB1
TNF
WISP1
Entrez ID
633
HPRD ID
02359
Ensembl ID
ENSG00000182492
Uniprot IDs
B4DNL4
P21810
Q8NAB7
PDB IDs
Enriched GO Terms of Interacting Partners
?
Extracellular Matrix Organization
Extracellular Structure Organization
Locomotion
Anatomical Structure Morphogenesis
Multicellular Organismal Metabolic Process
Movement Of Cell Or Subcellular Component
Extracellular Matrix Disassembly
Response To External Stimulus
Organ Morphogenesis
Protein Localization To Nucleus
Collagen Catabolic Process
Cell Morphogenesis Involved In Differentiation
Collagen Metabolic Process
Multicellular Organismal Macromolecule Metabolic Process
Leukocyte Migration
System Development
Response To Organic Substance
Cellular Response To Organic Substance
Negative Regulation Of Myoblast Differentiation
Response To Hormone
Cellular Response To Growth Factor Stimulus
Bone Morphogenesis
Chemotaxis
Multicellular Organismal Development
Response To Growth Factor
Immune System Process
Anatomical Structure Development
Cell Morphogenesis
Organ Development
Salivary Gland Morphogenesis
Endochondral Ossification
Gland Morphogenesis
Regulation Of Myoblast Differentiation
Salivary Gland Development
Negative Regulation Of Muscle Cell Differentiation
Cellular Response To Acid Chemical
Cellular Response To Lipid
Cellular Response To Transforming Growth Factor Beta Stimulus
Blood Coagulation
Hemostasis
Developmental Process
Exocrine System Development
Response To Transforming Growth Factor Beta
Platelet Activation
Cartilage Development
Common-partner SMAD Protein Phosphorylation
Cell Migration
Cellular Response To Amino Acid Stimulus
Collagen Fibril Organization
Cardiovascular System Development
Tagcloud
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bambara
bean
beverage
bgnm
bgns
boiled
cow
cowpea
crop
crops
drought
eaten
fermented
groundnut
irritable
legume
legumes
neglected
nutritious
probiotic
probiotics
relish
roasted
salted
snack
subterraenea
traced
verdc
vigna