Search Results for: MUC1

Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
C1GALT1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1
  • Defective C1GALT1C1 causes Tn polyagglutination syndrome (TNPS)
  • O-linked glycosylation of mucins
C2 complement C2
  • Initial triggering of complement
  • Activation of C3 and C5
  • Regulation of Complement cascade
  • Classic complement pathway component defects, including the following eight diseases: C1q alpha-chain deficiency; C1q beta-chain deficiency; C1q gamma-chain deficiency; C1r deficiency; C1s deficiency; C2 deficiency; C3 deficiency; C4 deficiency
  • Systemic lupus erythematosus
C2CD2L C2CD2 like
C3orf52 chromosome 3 open reading frame 52
CCDC167 coiled-coil domain containing 167
CD47 CD47 molecule
  • Cell surface interactions at the vascular wall
  • Integrin cell surface interactions
  • Signal regulatory protein family interactions
  • Signal regulatory protein family interactions
  • Neutrophil degranulation
CD53 CD53 molecule
  • Neutrophil degranulation
CD68 CD68 molecule
  • Neutrophil degranulation
CLDN19 claudin 19
  • Tight junction interactions
CLDN6 claudin 6
  • Tight junction interactions
CLDND2 claudin domain containing 2
CMTM7 CKLF like MARVEL transmembrane domain containing 7
COL8A2 collagen type VIII alpha 2 chain
  • Collagen degradation
  • Collagen degradation
  • Collagen biosynthesis and modifying enzymes
  • Assembly of collagen fibrils and other multimeric structures
  • Integrin cell surface interactions
  • Collagen chain trimerization
  • Posterior polymorphous corneal dystrophy (PPCD)
  • Fuchs corneal dystrophy (FECD); Fuchs endothelial corneal dystrophy
CSGALNACT2 chondroitin sulfate N-acetylgalactosaminyltransferase 2
  • Chondroitin sulfate biosynthesis
CTNND1 catenin delta 1
  • Adherens junctions interactions
  • VEGFR2 mediated vascular permeability
  • InlA-mediated entry of Listeria monocytogenes into host cells
CTSA cathepsin A
  • Glycosphingolipid metabolism
  • MHC class II antigen presentation
  • Sialic acid metabolism
  • Defective NEU1 causes sialidosis
  • Neutrophil degranulation
  • Galactosialidosis
CXCL16 C-X-C motif chemokine ligand 16
  • Chemokine receptors bind chemokines
  • G alpha (i) signalling events
CXCL9 C-X-C motif chemokine ligand 9
  • Chemokine receptors bind chemokines
  • G alpha (i) signalling events
CYP4F2 cytochrome P450 family 4 subfamily F member 2
  • Fatty acids
  • Miscellaneous substrates
  • Eicosanoids
  • Synthesis of Leukotrienes (LT) and Eoxins (EX)
  • Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE)
EDDM3B epididymal protein 3B

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