CBX4 and FHL1

  • Number of citations of the paper that reports this interaction (PMID 15710417)
  • 4
  • Data Source:
  • HPRD (two hybrid, in vivo, in vitro)

CBX4

FHL1

Gene Name chromobox homolog 4 four and a half LIM domains 1
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 18 interactors: CBS CSNK2B CTBP1 CTBP2 FHL1 HIST3H3 KMT2A LNX2 MBD1 MED9 RB1 RING1 RNF2 SATB1 SKIL SUV39H1 UBE2I ZEB2 19 interactors: AKAP12 CBX4 DBN1 DEAF1 EED FHL2 HES1 HIVEP3 MYBPC1 PDE4DIP PRNP RBPJ RING1 SRF SRPK1 TTN TXNIP UBE2E2 USP15
Entrez ID 8535 2273
HPRD ID 04357 02157
Ensembl ID ENSG00000141582 ENSG00000022267
Uniprot IDs O00257 B7Z9A1 Q13642
PDB IDs 2K28 3I8Z 1X63 2CUP 2CUR 2EGQ
Enriched GO Terms of Interacting Partners?
Tagcloud ?
3p  accordingly  bodies  brachyury  cbx7  chemicals  ectodermal  embryoid  endodermal  fgf5  foxa2  ideal  markers  meanwhile  mebs  mesodermal  nanog  nestin  oct4  pcg  perfluorooctane  pfos  pluripotency  polycomb  poses  sma  sox17  sox2  sulfonate 
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) ?
3p  accordingly  brachyury  cbx7  chemicals  ectodermal  embryoid  endodermal  fgf5  foxa2  ideal  markers  meanwhile  mebs  mesodermal  nanog  nestin  oct4  pcg  perfluorooctane  pfos  pluripotency  polycomb  poses  sma  sox17  sox2  sulfonate 
764g  atrophy  biopsy  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) ?
bodies