HAP1 and RPS10

  • Number of citations of the paper that reports this interaction (PMID 16169070)
  • 531
  • Data Source:
  • BioGRID (two hybrid, two hybrid)
  • HPRD (two hybrid)

HAP1

RPS10

Gene Name huntingtin-associated protein 1 ribosomal protein S10
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Esophageal cancer (squamous cell) ( 22960999)
Protein-Protein Interactions 68 interactors: APLP1 ATP5J2 BARD1 BRD7 C7orf25 C8orf33 CBX8 CCDC113 CDC73 CDK5RAP2 COL9A2 CRIP1 DCTN1 DDX49 DEFB1 EIF3E FAM173A FEZ1 GADD45G GIT1 GLTSCR2 GPRASP2 HGS HMOX2 HSPA4 HTT IMMT ING5 KAT5 KAT7 KATNBL1 KBTBD7 KPNA2 LRIF1 LUC7L2 MPP3 MRPS9 NAP1L5 NDUFB9 NEUROD1 NIPSNAP3A PABPC4 PCM1 PDCD7 PFDN1 PPID PPOX PSMD11 RER1 RIF1 RPS10 RPS25 SNAPIN SRSF4 STX5 TAF1D TBP TIMM17A TNNT1 TNNT3 TOMM20 TSPYL1 UTP3 VIM ZNF20 ZNF24 ZNF33B ZNF691 15 interactors: APP DMPK DNMT3B DVL3 EED FBXO25 HAP1 HIP1 KAT7 PFN2 PTTG1 SYK TCF25 WIZ XRCC6
Entrez ID 9001 6204
HPRD ID 02972 04697
Ensembl ID ENSG00000173805 ENSG00000124614
Uniprot IDs P54257 P46783
PDB IDs 3J3A
Enriched GO Terms of Interacting Partners?
Tagcloud ?
autism  axons  cognition  elucidated  hippocampal  huntingtin  impairs  knockdown  morphogenesis  mtorc1  neurons  partner  phenotypes  polarity  positioning  profoundly  proteomics  pyramidal  recapitulate  reflected  s6  specification  supernumerary  suppresses  tsc  tsc1  tsc2  tuberous  uncover 
26t  2a  aberrations  anemia  blackfan  cgh  congenital  copy  dba  deletions  diamond  fourfold  haploinsufficiency  heterozygous  hyperactivation  hypoproliferative  korean  malformations  predisposition  reductions  rpl11  rpl35a  rpl5  rps17  rps19  rps24  rps26  supports  variations 
Tagcloud (Difference) ?
autism  axons  cognition  elucidated  hippocampal  huntingtin  impairs  knockdown  morphogenesis  mtorc1  neurons  partner  phenotypes  polarity  positioning  profoundly  proteomics  pyramidal  recapitulate  reflected  s6  specification  supernumerary  suppresses  tsc  tsc1  tsc2  tuberous  uncover 
26t  2a  aberrations  anemia  blackfan  cgh  congenital  copy  dba  deletions  diamond  fourfold  haploinsufficiency  heterozygous  hyperactivation  hypoproliferative  korean  malformations  predisposition  reductions  rpl11  rpl35a  rpl5  rps17  rps19  rps24  rps26  supports  variations 
Tagcloud (Intersection) ?