TCERG1 and HNRNPU

  • Number of citations of the paper that reports this interaction (PMID 16055720)
  • 52

TCERG1

HNRNPU

Gene Name transcription elongation regulator 1 heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A)
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 52 interactors: ABI1 BARD1 BRD4 CHAF1A CHD3 CPSF6 CYFIP1 CYFIP2 DIAPH1 DIAPH2 DNAJB9 EVL FANCA FANCC FMNL1 GRB2 HNRNPH1 HNRNPK HNRNPM HNRNPU HSPA1A HSPA5 HSPA8 HTT JUNB LUC7L NONO NPM1 NUDT21 PCBP1 PIAS4 POLR2A PSPC1 SETDB1 SF1 SF3A1 SF3A2 SF3A3 SF3B1 SF3B2 SF3B3 SF3B4 SFPQ SRSF1 SUMO1 TPM4 U2AF2 WAS WASF2 WBP4 WIPF2 WWOX 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
Entrez ID 10915 3192
HPRD ID 10393 04185
Ensembl ID ENSG00000113649 ENSG00000153187
Uniprot IDs O14776 Q00839 Q96BA7
PDB IDs 2DK7 2DOD 2DOE 2DOF 2E71 2KIQ 2KIS 2NNT 3HFH 4FQG 1ZRJ
Enriched GO Terms of Interacting Partners?
Tagcloud ?
12p13  12q21  17q11  3q26  5q22  5q32  acgh  bac  balanced  ccnd2  clonality  cnas  concordant  cryptic  cytogenetics  emp1  evi1  evolving  exploratory  hidden  imbalances  karyotypically  karyotyping  kitlg  nf1  platforms  recurring  submicroscopic  unidentified 
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 
Tagcloud (Difference) ?
12p13  12q21  17q11  3q26  5q22  5q32  acgh  bac  balanced  ccnd2  clonality  cnas  concordant  cryptic  cytogenetics  emp1  evi1  evolving  exploratory  hidden  imbalances  karyotypically  karyotyping  kitlg  nf1  platforms  recurring  submicroscopic  unidentified 
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 
Tagcloud (Intersection) ?