POU3F4 and HNRNPU

  • Number of citations of the paper that reports this interaction (PMID 9105675)
  • 1
  • Data Source:
  • BioGRID (far western blotting)
  • HPRD (two hybrid, in vitro)

POU3F4

HNRNPU

Gene Name POU class 3 homeobox 4 heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A)
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 4 interactors: HNRNPU POU3F1 POU3F2 POU3F3 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 5456 3192
HPRD ID 02076 04185
Ensembl ID ENSG00000196767 ENSG00000153187
Uniprot IDs P49335 Q00839 Q96BA7
PDB IDs 1ZRJ
Enriched GO Terms of Interacting Partners?
Tagcloud ?
abnormality  accordingly  acgh  anomaly  asian  attempted  causative  counseling  de  deletions  dfnx2  ear  east  etiologic  homogeneity  iii  incomplete  inheritance  ip  korean  koreans  look  novo  partition  referral  sanger  siblings  striking  verify 
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) ?
abnormality  accordingly  acgh  anomaly  asian  attempted  causative  counseling  de  deletions  dfnx2  ear  east  etiologic  homogeneity  iii  incomplete  inheritance  ip  korean  koreans  look  novo  partition  referral  sanger  siblings  striking  verify 
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) ?