Search Results for: MUC1

146 interactions involving MUC1 - mucin 1, cell surface associated found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
AQP1 aquaporin 1 (Colton blood group)
  • Erythrocytes take up carbon dioxide and release oxygen
  • Erythrocytes take up oxygen and release carbon dioxide
  • Vasopressin regulates renal water homeostasis via Aquaporins
  • Passive transport by Aquaporins
  • Acetazolamide
  • B-nonylglucoside
  • Mersalyl
AQP2 aquaporin 2
  • Vasopressin regulates renal water homeostasis via Aquaporins
  • Passive transport by Aquaporins
  • Congenital nephrogenic diabetes insipidus (NDI)
AQP3 aquaporin 3 (Gill blood group)
  • Vasopressin regulates renal water homeostasis via Aquaporins
  • Passive transport by Aquaporins
  • Sennosides
ARV1 ARV1 homolog, fatty acid homeostasis modulator
  • Cholesterol biosynthesis
BCL2L2 BCL2 like 2
  • Navitoclax
BMI1 BMI1 proto-oncogene, polycomb ring finger
  • Oxidative Stress Induced Senescence
  • SUMOylation of DNA damage response and repair proteins
  • SUMOylation of transcription cofactors
  • SUMOylation of chromatin organization proteins
  • SUMOylation of RNA binding proteins
  • SUMOylation of DNA methylation proteins
  • RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known
  • Regulation of PTEN gene transcription
  • Regulation of PTEN gene transcription
  • Transcriptional Regulation by E2F6
  • Penile cancer
BRICD5 BRICHOS domain containing 5
BTN2A2 butyrophilin subfamily 2 member A2
  • Butyrophilin (BTN) family interactions
C14orf180 chromosome 14 open reading frame 180
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
CACNG1 calcium voltage-gated channel auxiliary subunit gamma 1
  • Ergocalciferol
  • Enflurane
  • Ibutilide
  • Diltiazem
  • Spironolactone
  • Lercanidipine
  • Ethanol
  • Fluspirilene
  • Butamben
  • Bioallethrin
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

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