ARNT and AIP

  • Number of citations of the paper that reports this interaction (PMID 9111057)
  • 50
  • Data Source:
  • HPRD (in vitro, in vivo)

ARNT

AIP

Gene Name aryl hydrocarbon receptor nuclear translocator aryl hydrocarbon receptor interacting protein
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 37 interactors: ADH5 AHR AHRR AIP ARNT2 BRCA1 CSNK2A1 DIABLO EP300 EPAS1 ESR1 GMNN GTF2F1 GTF2F2 HEY1 HEY2 HIF1A IRAK4 LSM8 MTA3 NCOA1 NCOA2 NCOA7 NCOR2 NPAS4 PML PTGES3 SENP6 SIM1 SIM2 SMAD9 SP1 SRC STRBP TNFAIP1 TRIP11 UBE2I 16 interactors: AHR ARNT CLEC7A CSNK2A1 EGFR GNA13 GNAQ HSP90AA1 IKBKG IRF7 PDE4A PPARA PTGES3 STIP1 TNNI3K TOMM20
Entrez ID 405 9049
HPRD ID 00524 10408
Ensembl ID ENSG00000143437 ENSG00000110711
Uniprot IDs A8K6P0 B0AZM1 F8WAP6 P27540 O00170
PDB IDs 1D7G 1X0O 2A24 2ARN 2B02 2HV1 2K7S 3F1N 3F1O 3F1P 3H7W 3H82 4EQ1 4GHI 4GS9 4H6J 2LKN 4AIF 4APO
Enriched GO Terms of Interacting Partners?
Tagcloud ?
belong  bhlh  cobalt  confers  dimerizes  frame  helix  heterodimer  heterodimeric  heterologous  hif1alpha  hif2alpha  hif3alpha  hifs  hrd1  hre  hypoxia  identity  pas  prototype  reading  recognizes  resultant  shares  superfamily  tacgtg  tension  thymus  transfections 
aminolaevulinate  aspect  autosomal  coproporphyria  counterparts  cutanea  decarboxylase  dehydratase  develops  elucidating  hepatoerythropoietic  hereditary  heteroallelic  homo  inherited  intermittent  mutational  overt  pct  porphyria  porphyrias  puberty  rarely  recessive  tarda  uncommon  uroporphyrinogen  variegate  vp 
Tagcloud (Difference) ?
belong  bhlh  cobalt  confers  dimerizes  frame  helix  heterodimer  heterodimeric  heterologous  hif1alpha  hif2alpha  hif3alpha  hifs  hrd1  hre  hypoxia  identity  pas  prototype  reading  recognizes  resultant  shares  superfamily  tacgtg  tension  thymus  transfections 
aminolaevulinate  aspect  autosomal  coproporphyria  counterparts  cutanea  decarboxylase  dehydratase  develops  elucidating  hepatoerythropoietic  hereditary  heteroallelic  homo  inherited  intermittent  mutational  overt  pct  porphyria  porphyrias  puberty  rarely  recessive  tarda  uncommon  uroporphyrinogen  variegate  vp 
Tagcloud (Intersection) ?