HNRNPA2B1 and LIG4

  • Number of citations of the paper that reports this interaction (PMID 22990118)
  • 7
  • Data Source:
  • BioGRID (two hybrid)

HNRNPA2B1

LIG4

Gene Name heterogeneous nuclear ribonucleoprotein A2/B1 ligase IV, DNA, ATP-dependent
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Attention deficit hyperactivity disorder and conduct disorder ( 18951430)
Protein-Protein Interactions 17 interactors: CDKN2A CSNK2A1 CSNK2B ERG HIPK3 HIST3H3 HNRNPL LIG4 MAP4K2 NR4A1 PSMA3 SNRNP70 SREK1 TTF2 VHL YAE1D1 ZMYM2 103 interactors: ACTG1 AFTPH AGAP4 ALMS1 AMZ2P1 ANAPC10 APLF ASPM ATM ATP6V0D1 ATR B9D1 CAP1 CCDC176 CLU COL1A2 COMMD1 COX1 COX2 COX3 CPNE1 CREBBP CTSK DDX19A DGUOK DPP3 EIF2AK1 EIF3I EIF4A1 EIF4G3 ENO1 ETF1 FAM214A FBLL1 FIP1L1 GAPDH GGH GPANK1 GRHPR GUSBP3 GZMK HMGN1 HNRNPA2B1 IPP KDELR1 KIF3A LAP3 MAP2K2 MCM4 MCRS1 MRPS18C ND1 ND4 ND5 NDUFA13 NDUFB10 NEU1 NHEJ1 NOMO3 NPC2 OGFOD1 OSTM1 OXR1 PA2G4 PALLD PEX10 PGP PHF10 PMS2P1 PPIA PRKDC PSMA6 RBM5 RHBDD2 RPL11 RPS19BP1 RUVBL2 SEMA4G SMC2 SNX3 SOWAHC SRSF2 SYCP3 THOC5 TLE4 TOP1 TP53BP1 TPT1 TRAPPC3 TSFM UBB UBE2L3 UFSP2 UNC119 VKORC1 WARS WBP1L WDR20 XRCC4 ZFAND2A ZNF428 ZSCAN18 ZWINT
Entrez ID 3181 3981
HPRD ID 02526 03500
Ensembl ID ENSG00000122566 ENSG00000174405
Uniprot IDs P22626 P49917
PDB IDs 1X4B 1IK9 2E2W 3II6 3VNN 3W1B 3W1G 3W5O 4HTO 4HTP
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 
ageing  ascribes  atm  attrition  brca1  complexity  ctip  ends  fusions  homologous  instability  insufficient  joining  ku70  lig3  mechanistically  nhej  overhang  parp1  rampant  relies  repeats  telomere  telomeres  telomeric  trf2  unanticipated  uncapped  underlining 
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 
ageing  ascribes  atm  attrition  brca1  complexity  ctip  ends  fusions  homologous  instability  insufficient  joining  ku70  lig3  mechanistically  nhej  overhang  parp1  rampant  relies  repeats  telomere  telomeres  telomeric  trf2  unanticipated  uncapped  underlining 
Tagcloud (Intersection) ?