FHL2 and FHL1

  • Number of citations of the paper that reports this interaction (PMID 12432079)
  • 54
  • Data Source:
  • HPRD (in vitro)

FHL2

FHL1

Gene Name four and a half LIM domains 2 four and a half LIM domains 1
Image
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 19 interactors: AKAP12 CBX4 DBN1 DEAF1 EED FHL2 HES1 HIVEP3 MYBPC1 PDE4DIP PRNP RBPJ RING1 SRF SRPK1 TTN TXNIP UBE2E2 USP15
Entrez ID 2274 2273
HPRD ID 04026 02157
Ensembl ID ENSG00000115641 ENSG00000022267
Uniprot IDs J3KNW4 Q14192 Q2XQU9 Q6I9R8 B7Z9A1 Q13642
PDB IDs 1X4K 1X4L 2D8Z 1X63 2CUP 2CUR 2EGQ
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 
764g  atrophy  biopsy  bodies  boy  cardiomyopathy  distal  dreifuss  dystrophy  echocardiogram  emery  exon  hemizygous  hypertrophic  linked  missense  muscle  muscular  myopathy  occurring  pathology  postural  predominantly  reducing  scapuloperoneal  sequencing  vacuolar  wasting  weakness 
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 
764g  atrophy  biopsy  bodies  boy  cardiomyopathy  distal  dreifuss  dystrophy  echocardiogram  emery  exon  hemizygous  hypertrophic  linked  missense  muscle  muscular  myopathy  occurring  pathology  postural  predominantly  reducing  scapuloperoneal  sequencing  vacuolar  wasting  weakness 
Tagcloud (Intersection) ?