Search Results for: NR2F2

48 interactions involving NR2F2 - nuclear receptor subfamily 2 group F member 2 found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
PIAS1 protein inhibitor of activated STAT 1
  • SUMOylation of DNA damage response and repair proteins
  • SUMOylation of transcription factors
  • SUMOylation of ubiquitinylation proteins
  • SUMOylation of transcription cofactors
  • SUMOylation of intracellular receptors
  • SUMOylation of intracellular receptors
  • SUMOylation of chromatin organization proteins
  • Formation of Incision Complex in GG-NER
  • Regulation of IFNG signaling
RLBP1 retinaldehyde binding protein 1
  • The retinoid cycle in cones (daylight vision)
  • The retinoid cycle in cones (daylight vision)
  • The canonical retinoid cycle in rods (twilight vision)
  • Defective visual phototransduction due to RDH5 loss of function
  • Newfoundland rod-cone dystrophy (NFRCD)
  • Familial flecked retina syndrome, including: Doyne honeycomb degeneration of retina (DHRD); Basal laminar drusen (BLD); Fundus albipunctatus (FA); Retinitis punctata albescens (RPA); Bietti crystalline corneoretinal dystrophy (BCD)
SETD7 SET domain containing 7, histone lysine methyltransferase
  • PKMTs methylate histone lysines
  • S-adenosyl-L-homocysteine
SQSTM1 sequestosome 1
  • NRIF signals cell death from the nucleus
  • p75NTR recruits signalling complexes
  • NF-kB is activated and signals survival
  • PINK1-PRKN Mediated Mitophagy
  • Neddylation
  • Interleukin-1 signaling
  • Pexophagy
  • Signaling by ALK fusions and activated point mutants
  • KEAP1-NFE2L2 pathway
  • Nuclear events mediated by NFE2L2
  • Paget's disease of bone and related disorders, including: ; Paget's disease of bone (PDB); Familial expansile osteolysis (FEO); Early-onset Paget's disease of bone (PDB2); Expansile skeletal hyperphosphatasia (ESH); Juvenile Paget's disease (JPD)
SYCP3 synaptonemal complex protein 3
  • Meiotic synapsis
  • Azoospermia, including: Azoospermia; Azoospermia due to perturbations of meiosis
TENT5A terminal nucleotidyltransferase 5A
TRIM24 tripartite motif containing 24
  • Signaling by cytosolic FGFR1 fusion mutants
  • Signaling by FGFR1 in disease
  • Signaling by BRAF and RAF1 fusions
TRIP4 thyroid hormone receptor interactor 4
  • ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA

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