FHL1 and PDE4DIP

  • Number of citations of the paper that reports this interaction (PMID 21900206)
  • 27
  • Data Source:
  • BioGRID (two hybrid)

FHL1

PDE4DIP

Gene Name four and a half LIM domains 1 phosphodiesterase 4D interacting protein
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 19 interactors: AKAP12 CBX4 DBN1 DEAF1 EED FHL2 HES1 HIVEP3 MYBPC1 PDE4DIP PRNP RBPJ RING1 SRF SRPK1 TTN TXNIP UBE2E2 USP15 64 interactors: ADH1B AEN ANKRD11 ARNT2 BYSL C14orf105 C19orf66 C1orf109 CCDC146 CDC5L CDKN1A CHCHD3 FAM161A FAM74A4 FCHSD2 FES FHL1 GADD45G GFI1B GOLGA8EP GOLGA8F HAUS1 IMMT ITSN2 KDM1A KLC3 KLC4 KRAS KRT18 KRT31 LAMTOR3 LENG1 LMO4 MAPRE1 MIF4GD MTUS2 NAA10 NEFL NEK2 OSGEP PDE4D PFDN1 PIAS4 PPP1R18 PRNP PRPF31 RTP5 SCNM1 SDCBP SH2D4A SMN1 SNCA TFIP11 TK1 TNIK TRAF4 UTP14C VAC14 ZBTB38 ZFYVE21 ZNF408 ZNF512B ZNF581 ZSCAN26
Entrez ID 2273 9659
HPRD ID 02157 10482
Ensembl ID ENSG00000022267 ENSG00000178104
Uniprot IDs B7Z9A1 Q13642 F8WAP3 Q5VU43
PDB IDs 1X63 2CUP 2CUR 2EGQ
Enriched GO Terms of Interacting Partners?
Tagcloud ?
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) ?
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) ?