HNRNPK and DIDO1

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

HNRNPK

DIDO1

Gene Name heterogeneous nuclear ribonucleoprotein K death inducer-obliterator 1
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 107 interactors: ABI2 APBB1 AQP5 BTRC C6orf226 CBLB CCAR1 CCDC33 CDKN1A CEBPB CIRBP CNNM3 CSK CTNNBL1 DALRD3 DDX1 DDX17 DDX5 DHX9 DIDO1 DOCK2 EIF3F ELAVL1 FBXL18 FYN GFI1B GRAP2 GRB2 GZMA GZMK HCK HIST3H3 HMGB1 HNRNPA0 HNRNPD HNRNPL HNRNPLL ITK ITSN2 KHDRBS1 KHDRBS2 KHDRBS3 LYN MAPK10 MARK4 MATR3 NCK2 NEDD4 NPDC1 PABPC1 PCBP1 PCBP2 PCDHB14 PELI2 PIN1 PPP1R10 PRKCD PRMT1 PRPF31 PRPF40A PRR3 PTBP1 QKI RALY RASD1 RBFOX2 RBM10 RBM3 RBM4 RBM41 RBM42 RBM7 RBMX RBMY1A1 RBMY1F RNA18S5 RNA28S5 RTP5 SAFB SF1 SMAD3 SNRPA SORBS3 SPG7 SRC SREK1 SRRT SRSF3 SUMO1 SYNCRIP TBP TCERG1 TERF2IP TYK2 U2AF1 U2AF2 UBE2I VAV1 WBP4 WWOX YBX1 YTHDC1 YWHAQ ZFC3H1 ZNF385C ZNF792 ZNRF2P1 9 interactors: APP ARAF DVL3 HIST3H3 HNRNPK KCNK4 SRSF1 WWP1 WWP2
Entrez ID 3190 11083
HPRD ID 02834 10363
Ensembl ID ENSG00000165119 ENSG00000101191
Uniprot IDs B4DFF1 B4DUQ1 P61978 Q6IBN1 Q9BTC0
PDB IDs 1J5K 1KHM 1ZZI 1ZZJ 1ZZK 2M3H 4L7X
Enriched GO Terms of Interacting Partners?
Tagcloud ?
associates  boosted  consequently  cpg  dnmt1  facilitated  h3k9  h3k9me3  heterochromatin  impairs  insight  instead  intergenic  lincrna  link  lncrnas  methyltransferase  noncoding  notably  p21  pluripotency  prevents  profiling  promoters  reprogramming  rnas  setdb1  somatic  sustaining 
20q  20q11  abnormality  amplification  arm  band  breakpoints  chromosome  consistently  del  deleted  distal  explain  favourable  hck  hybridization  ider  interstitial  isochromosome  material  myelodysplastic  possibly  proximal  regions  retained  tnfrsf6b  tumour  variable  variant 
Tagcloud (Difference) ?
associates  boosted  consequently  cpg  dnmt1  facilitated  h3k9  h3k9me3  heterochromatin  impairs  insight  instead  intergenic  lincrna  link  lncrnas  methyltransferase  noncoding  notably  p21  pluripotency  prevents  profiling  promoters  reprogramming  rnas  setdb1  somatic  sustaining 
20q  20q11  abnormality  amplification  arm  band  breakpoints  chromosome  consistently  del  deleted  distal  explain  favourable  hck  hybridization  ider  interstitial  isochromosome  material  myelodysplastic  possibly  proximal  regions  retained  tnfrsf6b  tumour  variable  variant 
Tagcloud (Intersection) ?