CAV1 and GJB2

  • Number of citations of the paper that reports this interaction (PMID 11980479)
  • 46
  • Data Source:
  • BioGRID (affinity chromatography technology)
  • HPRD (in vivo, in vitro)

CAV1

GJB2

Gene Name caveolin 1, caveolae protein, 22kDa gap junction protein, beta 2, 26kDa
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 81 interactors: ABCB1 ABL1 ADRBK1 AKAP1 APP AR BMX BSG BST1 BTK CAV2 CD40 CSK CSNK2A1 CSNK2A2 DAG1 DNM1 EDNRB EGFR ERBB2 ESR1 FLNA FLOT2 FYN GJA1 GJA3 GJB2 GNAI2 GRB7 GRK1 GRK5 HRAS HTR1F IGF1R IGFBP3 ILK INSR IRS1 KDR LATS1 LRP1 MALL MAPK1 MAPK3 MMP14 NEU3 NGFR NOS2 NOS3 NTRK1 PDGFRA PDGFRB PLD1 PLD2 PPP1CA PPP2CA PRNP PTEN PTGS2 PTPN1 PTPN11 PTPN6 PTPRF RAC1 RCVRN RHOA RHOC S1PR1 SCP2 SNCA SOS1 SRC STOML3 STRN STRN4 TGFBR1 TNFRSF1B TRAF2 TRAF6 TRPC1 VCP 5 interactors: CAV1 CD14 CNST GJB1 GJB6
Entrez ID 857 2706
HPRD ID 03028 00413
Ensembl ID ENSG00000105974 ENSG00000165474
Uniprot IDs A9XTE5 Q03135 Q2TNI1 Q59E85 Q7Z4F3 H9U1J4 P29033
PDB IDs 1XIR 2ZW3 3IZ1 3IZ2
Enriched GO Terms of Interacting Partners?
Tagcloud ?
17beta  caveolae  caveolin  cgg  cingulate  copyright  coupling  demonstration  electrophysiological  eralpha  facilitation  fear  fmr1  fmrp  fragile  fxs  glua1  inherited  interacted  ko  plasticity  potentiation  raft  recording  rescued  reserved  retardation  rights  shrna 
12s  audiometry  brainstem  clinics  counseling  deaf  deafness  del  etiologies  gjb3  guidance  hearing  hereditary  heterozygous  homozygous  hot  liaoning  mutation  occupies  profound  questionnaires  rrna  slc26a4  spot  syndromic  templates  theoretical  tone  tympanometry 
Tagcloud (Difference) ?
17beta  caveolae  caveolin  cgg  cingulate  copyright  coupling  demonstration  electrophysiological  eralpha  facilitation  fear  fmr1  fmrp  fragile  fxs  glua1  inherited  interacted  ko  plasticity  potentiation  raft  recording  rescued  reserved  retardation  rights  shrna 
12s  audiometry  brainstem  clinics  counseling  deaf  deafness  del  etiologies  gjb3  guidance  hearing  hereditary  heterozygous  homozygous  hot  liaoning  mutation  occupies  profound  questionnaires  rrna  slc26a4  spot  syndromic  templates  theoretical  tone  tympanometry 
Tagcloud (Intersection) ?