FHL2 and RUNX2

  • Number of citations of the paper that reports this interaction (PMID 16079911)
  • 16

FHL2

RUNX2

Gene Name four and a half LIM domains 2 runt-related transcription factor 2
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 92 interactors: ADAM17 AK1 APP AR ARHGAP9 ATXN1 BANP BLZF1 BMPR2 BRCA1 CAPN1 CARD8 CCDC92 CKM CREBBP CSK CSN2 CTNNB1 DCP1A DPF2 DTX2 DUSP10 E2F1 E2F2 E2F3 E2F4 EIF6 EP300 ESR1 FAM129A FAM154A FHL1 FHL3 FHL5 FOXO1 GLYR1 GNG12 HAND1 HIF1A ID3 IGFBP5 IKZF4 INCA1 ITGA3 ITGA7 ITGB1 ITGB2 ITGB5 ITGB6 JUP KANK2 KIAA1217 MCM7 MYBPC1 NRF1 PFKM PHB2 PSEN2 PUF60 RAI2 REL REV1 RFX3 RUNX2 SAP30BP SFPQ SIGLEC6 SLC34A1 SMAD2 SMAD3 SMAD4 SP2 SRF STAT3 TNFRSF11A TRAF6 TRIM55 TRIM63 TTN WT1 ZBTB16 ZFP64 ZFYVE9 ZMYM4 ZNF131 ZNF212 ZNF3 ZNF331 ZNF408 ZNF417 ZNF626 ZNF638 36 interactors: ALYREF AR AXIN1 CBFB CCNB1 CDK1 CEBPB DVL2 EP300 ETS1 FHL2 FOS HDAC3 HDAC4 HDAC6 HIF1A HIVEP3 JUN KAT6B LEF1 MAP3K4 MSX2 PRKCD RB1 RBM14 SMAD2 SMAD3 SMAD6 SMURF2 SOX9 STUB1 TAF1A UBTF XRCC5 XRCC6 YAP1
Entrez ID 2274 860
HPRD ID 04026 02566
Ensembl ID ENSG00000115641 ENSG00000124813
Uniprot IDs J3KNW4 Q14192 Q2XQU9 Q6I9R8 F8W8U5 Q13950 Q32MY8
PDB IDs 1X4K 1X4L 2D8Z
Enriched GO Terms of Interacting Partners?
Tagcloud ?
acted  adapter  converts  cytoplasm  cytoskeleton  deprived  deregulated  direction  e2  ehd2  enrichment  homer3  hydroxytamoxifen  mcf  modulator  oestrogen  oht  organelle  overlap  pf  rationale  remarkable  remodelling  reorganisation  reprogrammed  rhof  transcriptome  uncovered  unexpectedly 
1q22  aml  correlative  cytogenetic  decitabine  demethylating  elucidate  epigenetics  frequent  haematological  hypermethylation  inactivation  inv  leukaemia  leukaemias  lymphocytic  malignancies  methylated  mostly  myelodysplatic  p13  promoters  re  relapse  runx1  runx3  syndromes  unmethylated 
Tagcloud (Difference) ?
acted  adapter  converts  cytoplasm  cytoskeleton  deprived  deregulated  direction  e2  ehd2  enrichment  homer3  hydroxytamoxifen  mcf  modulator  oestrogen  oht  organelle  overlap  pf  rationale  remarkable  remodelling  reorganisation  reprogrammed  rhof  transcriptome  uncovered  unexpectedly 
1q22  aml  correlative  cytogenetic  decitabine  demethylating  elucidate  epigenetics  frequent  haematological  hypermethylation  inactivation  inv  leukaemia  leukaemias  lymphocytic  malignancies  methylated  mostly  myelodysplatic  p13  promoters  re  relapse  runx1  runx3  syndromes  unmethylated 
Tagcloud (Intersection) ?