SQSTM1 and NR2F2

  • Number of citations of the paper that reports this interaction (PMID 8910285)
  • 9
  • Data Source:
  • HPRD (in vitro, two hybrid)

SQSTM1

NR2F2

Gene Name sequestosome 1 nuclear receptor subfamily 2, group F, member 2
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Prostate cancer (gene x gene interaction) ( 22219177)
  • Response to TNF-alpha inhibitors in rheumatoid arthritis ( 22569225)
  • Sex hormone-binding globulin levels ( 22829776)
Protein-Protein Interactions 74 interactors: ATXN3 BCL2 BMPR1B BPTF CALM1 CAMK2A CCNB1 CDC37 CDK1 CSNK2A1 DAZAP2 EEF1D EGLN3 FKBP4 GABARAPL1 GABARAPL2 GABRR1 GABRR2 GEMIN4 GRB14 GRIA1 GRIA2 GRIA3 IRAK1 KCNAB2 KEAP1 LCK LINC00341 MALT1 MAP1LC3A MAP1LC3B MAP2K5 MAP3K3 MAPK14 MBP MEIS2 MLH1 NBR1 NCOR1 NR2F2 NTRK1 NTRK2 NTRK3 OPTN PAWR PIK3CA PPHLN1 PRKCI PRKCZ RAD23A RELN RIPK1 RPL37 SMAD1 SMAD2 SMAD3 SMAD4 SMURF1 SNCA STXBP1 TGFBR1 TKT TOE1 TP53 TRAF6 TRIM55 TRIM63 TTN UBA52 UBB UBC ULK1 ULK2 YWHAZ 19 interactors: BCL11A BCL11B BIK EP300 FAM46A HDAC1 HIPK3 LCK MYOD1 NCOR2 NR2F6 NR3C1 NSD1 PHB2 PIAS1 SETD7 SQSTM1 TRIM24 TRIP4
Entrez ID 8878 7026
HPRD ID 03319 00139
Ensembl ID ENSG00000161011 ENSG00000185551
Uniprot IDs Q13501 F1D8R0 P24468
PDB IDs 1Q02 2JY7 2JY8 2K0B 2KNV 3CJW
Enriched GO Terms of Interacting Partners?
Tagcloud ?
aldh1a1  anxa1  bcar1  cldn1  crmp1  endpoint  folr1  foxm1  il12rb2  il7r  inconclusive  kiaa1524  lox  mcm7  mta1  mtdh  ncoa3  ndrg2  nedd9  nes  overview  pbk  ppm1d  principally  prognostication  qualifying  slc7a5  warranted  wnt1 
akr1c4  anomalies  apparently  array  balanced  bases  cdon  cgh  chrna7  confirming  dd  diagnoses  dock8  gata3  id  indistinguishable  inherited  intellectual  karyotype  karyotyping  mb  mca  overlooked  prenatal  pws  rearrangements  spanning  tier  tp63 
Tagcloud (Difference) ?
aldh1a1  anxa1  bcar1  cldn1  crmp1  endpoint  folr1  foxm1  il12rb2  il7r  inconclusive  kiaa1524  lox  mcm7  mta1  mtdh  ncoa3  ndrg2  nedd9  nes  overview  pbk  ppm1d  principally  prognostication  qualifying  slc7a5  warranted  wnt1 
akr1c4  anomalies  apparently  array  balanced  bases  cdon  cgh  chrna7  confirming  dd  diagnoses  dock8  gata3  id  indistinguishable  inherited  intellectual  karyotype  karyotyping  mb  mca  overlooked  prenatal  pws  rearrangements  spanning  tier  tp63 
Tagcloud (Intersection) ?