Search Results for: COMT

73 interactions involving COMT - catechol-O-methyltransferase found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
REEP4 receptor accessory protein 4
RGS2 regulator of G protein signaling 2
  • G alpha (q) signalling events
RHBDD2 rhomboid domain containing 2
RHBDL1 rhomboid like 1
S1PR3 sphingosine-1-phosphate receptor 3
  • G alpha (i) signalling events
  • Lysosphingolipid and LPA receptors
  • Extra-nuclear estrogen signaling
  • Fingolimod
SELENOK selenoprotein K
SLC10A6 solute carrier family 10 member 6
  • SLC-mediated bile acid transport
SLC16A7 solute carrier family 16 member 7
  • Proton-coupled monocarboxylate transport
  • Pyruvic acid
SLC2A5 solute carrier family 2 member 5
  • Neutrophil degranulation
  • Intestinal hexose absorption
SLC35A4 solute carrier family 35 member A4
  • Matriglycan biosynthesis on DAG1
SLC35F1 solute carrier family 35 member F1
SLC39A1 solute carrier family 39 member 1
  • Zinc influx into cells by the SLC39 gene family
SLC39A2 solute carrier family 39 member 2
  • Zinc influx into cells by the SLC39 gene family
SLC48A1 solute carrier family 48 member 1
SLC71A2 solute carrier family 71 member 2
SLC7A8 solute carrier family 7 member 8
  • Basigin interactions
  • Amino acid transport across the plasma membrane
  • Phenylalanine
  • Alanine
SMIM1 small integral membrane protein 1 (Vel blood group)
THSD7A thrombospondin type 1 domain containing 7A
  • Defective B3GALTL causes PpS
  • O-glycosylation of TSR domain-containing proteins
TLCD4 TLC domain containing 4
TMEM100 transmembrane protein 100

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