U2AF2 and THAP1

  • Number of citations of the paper that reports this interaction (PMID 16189514)
  • 699
  • Data Source:
  • BioGRID (two hybrid, two hybrid)
  • HPRD (two hybrid)

U2AF2

THAP1

Gene Name U2 small nuclear RNA auxiliary factor 2 THAP domain containing, apoptosis associated protein 1
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 51 interactors: AES APBB1 ATXN1 BEND7 CCAR1 CHERP CHIC2 CPSF7 DACH1 DDX17 DDX6 DPPA2 DVL2 EPB41 GEMIN2 GLIS2 HLA-DMA HNRNPA0 HNRNPD HNRNPK IL7R KHDRBS1 KHDRBS3 KIAA0907 LURAP1 MAP1B PIN1 POLR2A PRPF3 PRPF40A PUF60 QKI RBFOX2 RBM39 RBM4 SAP30BP SCAF11 SF1 SMAD5 SNRPA SRPK1 SRPK2 SRSF1 SRSF11 SUGP1 TCERG1 THAP1 TOP1 U2AF1 WT1 ZRSR2 58 interactors: ACOT7 AKAP17A AKAP9 AP2B1 ARL6IP4 BAG5 BMS1P5 BYSL C11orf57 C1orf35 C7orf50 CHD2 CSNK2A1 DCAF8 DVL2 FAM124A FAM133A FXR2 GPATCH2L HNRNPLL KLF12 KRTAP10-7 LASP1 MORF4L1 MORF4L2 MRPL11 NKAP NUP62 PAWR PHF1 PID1 POLR2L POLR2M PPIG PRKAA1 PRR20A QKI RALYL RBM39 RIPPLY1 RP9P RPS25 SAP30BP SERF2 SLU7 STRBP TCEA2 TPM3 TRAF5 TRIM26 TTLL10 TXN2 U2AF2 WDYHV1 YES1 ZCCHC10 ZNF385C ZNF408
Entrez ID 11338 55145
HPRD ID 01872 15496
Ensembl ID ENSG00000063244 ENSG00000131931
Uniprot IDs P26368 Q9NVV9
PDB IDs 1JMT 1O0P 1OPI 1U2F 2G4B 2HZC 2M0G 2U2F 2YH0 2YH1 3VAF 3VAG 3VAH 3VAI 3VAJ 3VAK 3VAL 3VAM 4FXW 2JTG 2KO0 2L1G
Enriched GO Terms of Interacting Partners?
Tagcloud ?
acceptor  accessory  advance  alters  codons  corroborated  cytidine  doi  junctions  leu  missense  november  novo  online  publication  q157  q157p  q157r  s34  s34f  s34y  seq  snrnp  speckles  splice  splicing  u2af1  uridine 
assembled  childhood  compatible  confirms  contiguous  definite  deletions  distinctive  dystonia  dyt1  eighty  gch1  imprinted  ireland  laxity  maternally  microcephaly  myoclonus  nineteen  nkx2  phenotypically  probable  probands  progressing  sequenced  sgce  stature  uk  upper 
Tagcloud (Difference) ?
acceptor  accessory  advance  alters  codons  corroborated  cytidine  doi  junctions  leu  missense  november  novo  online  publication  q157  q157p  q157r  s34  s34f  s34y  seq  snrnp  speckles  splice  splicing  u2af1  uridine 
assembled  childhood  compatible  confirms  contiguous  definite  deletions  distinctive  dystonia  dyt1  eighty  gch1  imprinted  ireland  laxity  maternally  microcephaly  myoclonus  nineteen  nkx2  phenotypically  probable  probands  progressing  sequenced  sgce  stature  uk  upper 
Tagcloud (Intersection) ?