SREK1 and HNRNPA1

  • Number of citations of the paper that reports this interaction (PMID 14559993)
  • 9
  • Data Source:
  • HPRD (in vitro, in vivo, two hybrid)

SREK1

HNRNPA1

Gene Name splicing regulatory glutamine/lysine-rich protein 1 heterogeneous nuclear ribonucleoprotein A1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 55 interactors: CD8A CSNK2A1 DDX17 DDX39B DDX3X DGKA DGKD EFTUD2 ELAVL1 GNB2L1 HNRNPA1 HNRNPA2B1 HNRNPA3 HNRNPC HNRNPD HNRNPH1 HNRNPK HNRNPU ILF2 MDM2 NCL NPM1 PABPC1 PABPC4 PARP1 PIN1 RBM10 RBMX SAFB SF3A3 SF3B3 SFPQ SH3GLB2 SNRPD1 SNRPD3 SRPK1 SRPK2 SRPK3 SRSF1 SRSF10 SRSF11 SRSF2 SRSF3 SRSF4 SRSF5 SRSF6 SRSF7 SRSF8 SSRP1 SUPT16H TARBP1 THRAP3 TRA2B YBX1 ZRANB2 32 interactors: ABHD16A APP ERG FEN1 HIPK3 HIST3H3 HMGA1 HNRNPH3 KHSRP NFKBIA NR0B2 NR3C1 PABPN1 PHYHIP PPIL1 PRKDC PRMT1 PRMT2 PRMT3 PRRC2A RNF14 RPL21 SAFB SREK1 SRPK1 SUFU TFEC TNPO1 TRA2B TTF2 XRN1 YWHAQ
Entrez ID 140890 3178
HPRD ID 18043 01242
Ensembl ID ENSG00000153914 ENSG00000135486
Uniprot IDs E5RFV3 Q8WXA9 P09651
PDB IDs 1HA1 1L3K 1PGZ 1PO6 1U1K 1U1L 1U1M 1U1N 1U1O 1U1P 1U1Q 1U1R 1UP1 2H4M 2LYV 2UP1
Enriched GO Terms of Interacting Partners?
Tagcloud ?
amyotrophic  autosomal  carriers  coding  conserved  equivocal  et  ewsr1  exons  export  familial  frontotemporal  fus  genotyped  genotyping  lobar  nes  neurodegeneration  pathogenicity  r471c  relatives  sequenced  subject  substitution  taf15  tardbp  tdp43  tremor 
Tagcloud (Difference) ?
amyotrophic  autosomal  carriers  coding  conserved  equivocal  et  ewsr1  exons  export  familial  frontotemporal  fus  genotyped  genotyping  lobar  nes  neurodegeneration  pathogenicity  r471c  relatives  sequenced  subject  substitution  taf15  tardbp  tdp43  tremor 
Tagcloud (Intersection) ?