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GUSB
Gene Name
glucuronidase, beta
Image
Gene Ontology Annotations
Cellular Component
Membrane
Lysosomal Lumen
Intracellular Membrane-bounded Organelle
Extracellular Vesicular Exosome
Molecular Function
Beta-glucuronidase Activity
Receptor Binding
Protein Domain Specific Binding
Biological Process
Carbohydrate Metabolic Process
Glycosaminoglycan Catabolic Process
Pathogenesis
Glycosaminoglycan Metabolic Process
Hyaluronan Metabolic Process
Hyaluronan Catabolic Process
Small Molecule Metabolic Process
Pathways
MPS IIIB - Sanfilippo syndrome B
Diseases of glycosylation
Defective B4GALT7 causes EDS, progeroid type
Heparan sulfate/heparin (HS-GAG) metabolism
MPS I - Hurler syndrome
MPS IX - Natowicz syndrome
Defective SLC26A2 causes chondrodysplasias
Glycosaminoglycan metabolism
Hyaluronan uptake and degradation
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
Hyaluronan metabolism
MPS IIID - Sanfilippo syndrome D
Defective CHST6 causes MCDC1
Glycogen storage diseases
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
MPS IV - Morquio syndrome B
Defective CHSY1 causes TPBS
MPS VII - Sly syndrome
Metabolism of carbohydrates
MPS VI - Maroteaux-Lamy syndrome
HS-GAG degradation
Drugs
Alpha-D-Mannose
Diseases
GWAS
Protein-protein Interactions
3 interactors:
CES1
GIT2
PRKACA
Entrez ID
2990
HPRD ID
02018
Ensembl ID
ENSG00000169919
Uniprot IDs
P08236
PDB IDs
1BHG
3HN3
Enriched GO Terms of Interacting Partners
?
Positive Regulation Of Dense Core Granule Biogenesis
Regulation Of G-protein Coupled Receptor Protein Signaling Pathway
Histone H3-T6 Phosphorylation
Cellular Response To Erythropoietin
Cellular Response To Interleukin-3
Peptidyl-serine Autophosphorylation
Positive Regulation Of Lipopolysaccharide-mediated Signaling Pathway
Cellular Response To Parathyroid Hormone Stimulus
Negative Regulation Of Smoothened Signaling Pathway Involved In Dorsal/ventral Neural Tube Patterning
Cellular Metal Ion Homeostasis
Cellular Cation Homeostasis
Cellular Ion Homeostasis
Desmosome Assembly
Negative Regulation Of Glial Cell Apoptotic Process
Metal Ion Homeostasis
Regulation Of Tight Junction Assembly
Negative Regulation Of Glucose Import
Positive Regulation Of Macrophage Differentiation
Cell Communication By Electrical Coupling Involved In Cardiac Conduction
Cellular Chemical Homeostasis
Response To Parathyroid Hormone
Calcium-mediated Signaling Using Intracellular Calcium Source
Desmosome Organization
Positive Regulation Of Protein Export From Nucleus
Ion Homeostasis
Cell Communication By Electrical Coupling
Activation Of Protein Kinase A Activity
Regulation Of Platelet Aggregation
Negative Regulation Of Glucose Transport
Sperm Capacitation
Cellular Response To Epinephrine Stimulus
Regulation Of Cardiac Muscle Contraction By Regulation Of The Release Of Sequestered Calcium Ion
Induction Of Positive Chemotaxis
Positive Regulation Of Cardiac Muscle Hypertrophy
Response To Epinephrine
Cellular Copper Ion Homeostasis
Cellular Response To Zinc Ion
Positive Regulation Of Blood Vessel Endothelial Cell Migration
Regulation Of Lipopolysaccharide-mediated Signaling Pathway
Cellular Homeostasis
Triglyceride Catabolic Process
Response To Cytokine
Negative Regulation Of Adenylate Cyclase Activity
Behavioral Response To Pain
Copper Ion Homeostasis
Negative Regulation Of Lyase Activity
Regulation Of Cardiac Muscle Contraction By Calcium Ion Signaling
Regulation Of Release Of Sequestered Calcium Ion Into Cytosol By Sarcoplasmic Reticulum
Response To Stress
Regulation Of Rhodopsin Mediated Signaling Pathway
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