HNRNPU and POU3F4

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

HNRNPU

POU3F4

Gene Name heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A) POU class 3 homeobox 4
Image No pdb structure
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 4 interactors: HNRNPU POU3F1 POU3F2 POU3F3
Entrez ID 3192 5456
HPRD ID 04185 02076
Ensembl ID ENSG00000153187 ENSG00000196767
Uniprot IDs Q00839 Q96BA7 P49335
PDB IDs 1ZRJ
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 
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 
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 
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 
Tagcloud (Intersection) ?