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SLC26A1
Gene Name
solute carrier family 26 (anion exchanger), member 1
Image
No pdb structure
Gene Ontology Annotations
Cellular Component
Plasma Membrane
Integral Component Of Plasma Membrane
Integral Component Of Membrane
Molecular Function
Secondary Active Sulfate Transmembrane Transporter Activity
Chloride Transmembrane Transporter Activity
Sulfate Transmembrane Transporter Activity
Anion:anion Antiporter Activity
Oxalate Transmembrane Transporter Activity
Biological Process
Carbohydrate Metabolic Process
Xenobiotic Metabolic Process
Ion Transport
Chloride Transport
Sulfate Transport
Pathogenesis
Oxalate Transport
Glycosaminoglycan Metabolic Process
Small Molecule Metabolic Process
3'-phosphoadenosine 5'-phosphosulfate Metabolic Process
3'-phosphoadenosine 5'-phosphosulfate Biosynthetic Process
Transmembrane Transport
Sulfate Transmembrane Transport
Chloride Transmembrane Transport
Pathways
Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD)
MPS I - Hurler syndrome
MPS IX - Natowicz syndrome
Transport of inorganic cations/anions and amino acids/oligopeptides
Glycosaminoglycan metabolism
Defective UGT1A4 causes hyperbilirubinemia
Metabolic disorders of biological oxidation enzymes
SLC-mediated transmembrane transport
Defective CHST14 causes EDS, musculocontractural type
Defective UGT1A1 causes hyperbilirubinemia
Myoclonic epilepsy of Lafora
Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD)
MPS IIID - Sanfilippo syndrome D
Glycogen storage diseases
Defective CHST6 causes MCDC1
Defective GSS causes Glutathione synthetase deficiency (GSS deficiency)
Defective OPLAH causes 5-oxoprolinase deficiency (OPLAHD)
Diseases associated with glycosaminoglycan metabolism
Mucopolysaccharidoses
Defective EXT2 causes exostoses 2
Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD)
MPS IV - Morquio syndrome A
Phase II conjugation
Cytosolic sulfonation of small molecules
Transport and synthesis of PAPS
Multifunctional anion exchangers
Transport and synthesis of PAPS
Metabolism of carbohydrates
MPS VI - Maroteaux-Lamy syndrome
MPS IIIB - Sanfilippo syndrome B
Diseases of glycosylation
Defective B4GALT7 causes EDS, progeroid type
Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency)
Defective SLC26A2 causes chondrodysplasias
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
Defective PAPSS2 causes SEMD-PA
MPS IIIA - Sanfilippo syndrome A
Biological oxidations
Defective GGT1 causes Glutathionuria (GLUTH)
Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD)
MPS IIIC - Sanfilippo syndrome C
MPS II - Hunter syndrome
Defective B3GAT3 causes JDSSDHD
Defective CHST3 causes SEDCJD
Defective EXT1 causes exostoses 1, TRPS2 and CHDS
MPS IV - Morquio syndrome B
Defective CHSY1 causes TPBS
MPS VII - Sly syndrome
Drugs
Diseases
GWAS
Protein-protein Interactions
1 interactors:
UBC
Entrez ID
10861
HPRD ID
15361
Ensembl ID
ENSG00000145217
Uniprot IDs
Q9H2B4
PDB IDs
Enriched GO Terms of Interacting Partners
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Viral Protein Processing
Notch Receptor Processing
Virion Assembly
Regulation Of Transcription From RNA Polymerase II Promoter In Response To Hypoxia
Nucleotide-binding Oligomerization Domain Containing Signaling Pathway
Glycogen Biosynthetic Process
Intracellular Transport Of Virus
Cellular Polysaccharide Biosynthetic Process
Nucleotide-binding Domain, Leucine Rich Repeat Containing Receptor Signaling Pathway
Polysaccharide Biosynthetic Process
Negative Regulation Of Type I Interferon Production
Negative Regulation Of Epidermal Growth Factor Receptor Signaling Pathway
Negative Regulation Of ERBB Signaling Pathway
Regulation Of Transcription From RNA Polymerase II Promoter In Response To Stress
Toll-like Receptor 5 Signaling Pathway
Toll-like Receptor 10 Signaling Pathway
Negative Regulation Of Ubiquitin-protein Ligase Activity Involved In Mitotic Cell Cycle
Regulation Of DNA-templated Transcription In Response To Stress
DNA Damage Response, Signal Transduction By P53 Class Mediator Resulting In Cell Cycle Arrest
Signal Transduction Involved In Mitotic G1 DNA Damage Checkpoint
I-kappaB Kinase/NF-kappaB Signaling
Toll-like Receptor TLR6:TLR2 Signaling Pathway
Toll-like Receptor TLR1:TLR2 Signaling Pathway
Positive Regulation Of Ubiquitin-protein Ligase Activity Involved In Regulation Of Mitotic Cell Cycle Transition
Toll-like Receptor 2 Signaling Pathway
Signal Transduction Involved In DNA Damage Checkpoint
Toll-like Receptor 9 Signaling Pathway
Signal Transduction Involved In Cell Cycle Checkpoint
Glycogen Metabolic Process
TRIF-dependent Toll-like Receptor Signaling Pathway
Regulation Of Ubiquitin-protein Ligase Activity Involved In Mitotic Cell Cycle
Negative Regulation Of Ubiquitin-protein Transferase Activity
MyD88-independent Toll-like Receptor Signaling Pathway
Toll-like Receptor 3 Signaling Pathway
Negative Regulation Of Transforming Growth Factor Beta Receptor Signaling Pathway
MyD88-dependent Toll-like Receptor Signaling Pathway
Anaphase-promoting Complex-dependent Proteasomal Ubiquitin-dependent Protein Catabolic Process
Mitotic G1 DNA Damage Checkpoint
Positive Regulation Of Ubiquitin-protein Transferase Activity
Mitotic G1/S Transition Checkpoint
G1 DNA Damage Checkpoint
Positive Regulation Of Cell Cycle Arrest
Regulation Of Epidermal Growth Factor Receptor Signaling Pathway
Positive Regulation Of Ligase Activity
Positive Regulation Of Type I Interferon Production
DNA Damage Response, Signal Transduction By P53 Class Mediator
Toll-like Receptor 4 Signaling Pathway
Regulation Of ERBB Signaling Pathway
Polysaccharide Metabolic Process
Positive Regulation Of Protein Ubiquitination Involved In Ubiquitin-dependent Protein Catabolic Process
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