Search Results for: PVR

77 interactions involving PVR - PVR cell adhesion molecule found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
SYS1 SYS1 golgi trafficking protein
  • Retrograde transport at the Trans-Golgi-Network
TAS2R19 taste 2 receptor member 19
  • G alpha (i) signalling events
  • Class C/3 (Metabotropic glutamate/pheromone receptors)
TIGIT T cell immunoreceptor with Ig and ITIM domains
TM6SF2 transmembrane 6 superfamily member 2
TMBIM6 transmembrane BAX inhibitor motif containing 6
TMEM147 transmembrane protein 147
TMEM229B transmembrane protein 229B
TMEM54 transmembrane protein 54
TMEM65 transmembrane protein 65
TMEM79 transmembrane protein 79
TSPO translocator protein
  • Pregnenolone biosynthesis
  • Chlormezanone
  • Zopiclone
VAMP5 vesicle associated membrane protein 5
VTN vitronectin
  • Molecules associated with elastic fibres
  • Integrin cell surface interactions
  • Syndecan interactions
  • ECM proteoglycans
  • ECM proteoglycans
  • Regulation of Complement cascade
  • Abciximab
  • Zinc
  • Copper
  • Zinc acetate
  • Zinc chloride
  • Zinc sulfate, unspecified form
WNK1 WNK lysine deficient protein kinase 1
  • Stimuli-sensing channels
  • Hyperkalemic distal renal tubular acidosis (RTA type 4), including the following two diseases: Pseudohypoaldosteronism type I (PHA1); Pseudohypoaldosteronism type II (Gordon's syndrome)
ZDHHC15 zinc finger DHHC-type palmitoyltransferase 15
  • Syndromic X-linked mental retardation with epilepsy or seizures, including: West syndrome (WS); Partington syndrome (PRTS); Proud syndrome (ACCAG); XMR and epilepsy (XMRE); MRXHF1; XMR OPHN1-related (MRXSO) ; XELBD; XMR, Christianson type (MRXSC); Creatine deficiency syndrome (XL-CDS); Renpenning syndrome (RENS1); Epilepsy and mental retardation limited to females (EFMR); Periventricular nodular heterotopia (PVNH); Hydrocephalus (XLH); XMR, JARID1C related (MRXSJ); Boerjeson-Forssman syndrome (BFLS); CK syndrome (CKS)
ZDHHC22 zinc finger DHHC-type palmitoyltransferase 22
ZFPL1 zinc finger protein like 1

Page 4 out of 4 pages