PFN2 and RPS10

  • Number of citations of the paper that reports this interaction (PMID 16169070)
  • 531

PFN2

RPS10

Gene Name profilin 2 ribosomal protein S10
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 31 interactors: ACTB ACTG1 CCDC113 DDX11 DLST DNM1 EEF1A1 EVL FAM173A FHOD1 FLT3LG FMNL1 GOLGB1 HTT IK IVNS1ABP MYPOP NDUFB8 PLAUR PTPRS RAP1GAP RNF146 ROCK1 RPS10 SEPT5 SGTA SNTA1 SYN1 TERF1 VASP WDR33 15 interactors: APP DMPK DNMT3B DVL3 EED FBXO25 HAP1 HIP1 KAT7 PFN2 PTTG1 SYK TCF25 WIZ XRCC6
Entrez ID 5217 6204
HPRD ID 01451 04697
Ensembl ID ENSG00000070087 ENSG00000124614
Uniprot IDs G5E9Q6 P35080 P46783
PDB IDs 1D1J 3J3A
Enriched GO Terms of Interacting Partners?
Tagcloud ?
actn1  candidates  clonogenic  gap  gy  hcls1  integration  integrin  itgb5  junction  junctions  microarray  microarrays  nci  overrepresented  platforms  postgenome  profiling  ptprc  rab13  radiosensitive  radiosensitivity  radiosensitization  radiotherapy  reanalyzed  sam  set  sf2  signature 
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) ?
actn1  candidates  clonogenic  gap  gy  hcls1  integration  integrin  itgb5  junction  junctions  microarray  microarrays  nci  overrepresented  platforms  postgenome  profiling  ptprc  rab13  radiosensitive  radiosensitivity  radiosensitization  radiotherapy  reanalyzed  sam  set  sf2  signature 
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) ?