HNRNPU and POLR2A

  • Number of citations of the paper that reports this interaction (PMID 18710935)
  • 27

HNRNPU

POLR2A

Gene Name heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A) polymerase (RNA) II (DNA directed) polypeptide A, 220kDa
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 35 interactors: ACTB BTRC CASP3 CD5 CDKN2A CR2 ELL EP300 ERG GAS7 GRIN1 GRIN2D GTF2H1 HNRNPD HNRNPH3 IL7R KAT2B NDN NDRG1 NEDD4 NR3C1 PIN1 POLR2A POU3F4 PRMT1 PRPF40A PTPN11 SMN1 SREK1 STAU1 SYK TCERG1 WBP4 YAP1 ZNF689 100 interactors: ABL1 ACTB ACTL6A ATM BARD1 BRCA1 CASP10 CCNH CCNK CCNL2 CCNT1 CDC14A CDK12 CDK7 CDK8 CDK9 CPSF1 CPSF2 CPSF3 CREBBP CSH2 CSNK2A1 CSTF1 CSTF2 CTCF CTD CTDP1 CTDSP1 CTDSP2 DHX9 ELL ERCC5 ERCC6 ERG FCP1 FUS GRB2 GTF2B GTF2E1 GTF2H4 HIST1H1C HNRNPF HNRNPU HTATSF1 ITCH IWS1 KAT2B KLK2 KMT2D LEO1 MCM3 MED21 MNAT1 MYC NEDD4 NELFA NONO NR0B2 PCIF1 PHF8 PIN1 POLR2B POLR2C POLR2D POLR2E POLR2F POLR2G POLR2H POLR2I POLR2K POLR2L PPIG PPP1CA PQBP1 PRPF19 RECQL5 SAFB SETD2 SMN1 SMN2 SMURF1 SND1 SUB1 SUPT5H TAF10 TBP TCEA1 TCEB3 TCERG1 TRAK1 TRAM2 U2AF2 UBC UBE2L3 UPF1 WAC WWP2 XAB2 XRCC5 ZNF74
Entrez ID 3192 5430
HPRD ID 04185 08916
Ensembl ID ENSG00000153187 ENSG00000181222
Uniprot IDs Q00839 Q96BA7 P24928
PDB IDs 1ZRJ 2GHQ 2GHT 2LTO 3D9K 3D9L 3D9M 3D9N 3D9O 3D9P
Enriched GO Terms of Interacting Partners?
Tagcloud ?
17p13  1q21  1q44  2q23  2q31  agilent  annotations  asd  autism  backgrounds  cgh  cnv  cnvs  disabilities  dissect  encephalopathy  epileptic  exome  expand  hallux  implicates  infantile  intellectual  lissencephaly  mbd5  microcephaly  pafah1b1  pathogenicity  spasms 
actb  appropriately  benchmark  chosen  confounding  gapdh  hormonal  hprt1  hyperglycemia  hyperglycemic  lean  myocardium  normalization  normalized  obesity  ppia  predisposition  reference  reproducibility  rpl13a  scrutiny  sdha  select  stably  tbp  tfrc  underline  ywhag  zucker 
Tagcloud (Difference) ?
17p13  1q21  1q44  2q23  2q31  agilent  annotations  asd  autism  backgrounds  cgh  cnv  cnvs  disabilities  dissect  encephalopathy  epileptic  exome  expand  hallux  implicates  infantile  intellectual  lissencephaly  mbd5  microcephaly  pafah1b1  pathogenicity  spasms 
actb  appropriately  benchmark  chosen  confounding  gapdh  hormonal  hprt1  hyperglycemia  hyperglycemic  lean  myocardium  normalization  normalized  obesity  ppia  predisposition  reference  reproducibility  rpl13a  scrutiny  sdha  select  stably  tbp  tfrc  underline  ywhag  zucker 
Tagcloud (Intersection) ?