PHF1 and THAP1

  • Number of citations of the paper that reports this interaction (PMID 16189514)
  • 699

PHF1

THAP1

Gene Name PHD finger protein 1 THAP domain containing, apoptosis associated protein 1
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 22 interactors: ATXN7L1 BIRC7 CALCOCO2 EZH2 HIST1H3A HIST1H3B HIST1H3C HIST1H3E HIST1H3F HIST1H3G HIST1H3H HIST1H3I HIST1H3J HSD17B14 NAB2 NEK6 PDLIM7 RBPMS TFCP2 THAP1 TRIM23 VAC14 58 interactors: ACOT7 AKAP17A AKAP9 AP2B1 ARL6IP4 BAG5 BMS1P5 BYSL C11orf57 C1orf35 C7orf50 CHD2 CSNK2A1 DCAF8 DVL2 FAM124A FAM133A FXR2 GPATCH2L HNRNPLL KLF12 KRTAP10-7 LASP1 MORF4L1 MORF4L2 MRPL11 NKAP NUP62 PAWR PHF1 PID1 POLR2L POLR2M PPIG PRKAA1 PRR20A QKI RALYL RBM39 RIPPLY1 RP9P RPS25 SAP30BP SERF2 SLU7 STRBP TCEA2 TPM3 TRAF5 TRIM26 TTLL10 TXN2 U2AF2 WDYHV1 YES1 ZCCHC10 ZNF385C ZNF408
Entrez ID 5252 55145
HPRD ID 04195 15496
Ensembl ID ENSG00000112511 ENSG00000131931
Uniprot IDs O43189 Q9NVV9
PDB IDs 2E5P 2M0O 4HCZ 2JTG 2KO0 2L1G
Enriched GO Terms of Interacting Partners?
Tagcloud ?
12e8  albeit  at180  axon  dendrite  enter  enters  fyn  glutamic  map2  p301l  pseudophosphorylated  pseudophosphorylation  replacements  s235  s262  s356  s396  s404  s422  shaft  shares  spine  spines  synaptosomal  t231  tau  tau1  vastly 
assembled  childhood  compatible  confirms  contiguous  definite  deletions  distinctive  dystonia  dyt1  eighty  gch1  imprinted  ireland  laxity  maternally  microcephaly  myoclonus  nineteen  nkx2  phenotypically  probable  probands  progressing  sequenced  sgce  stature  uk  upper 
Tagcloud (Difference) ?
12e8  albeit  at180  axon  dendrite  enter  enters  fyn  glutamic  map2  p301l  pseudophosphorylated  pseudophosphorylation  replacements  s235  s262  s356  s396  s404  s422  shaft  shares  spine  spines  synaptosomal  t231  tau  tau1  vastly 
assembled  childhood  compatible  confirms  contiguous  definite  deletions  distinctive  dystonia  dyt1  eighty  gch1  imprinted  ireland  laxity  maternally  microcephaly  myoclonus  nineteen  nkx2  phenotypically  probable  probands  progressing  sequenced  sgce  stature  uk  upper 
Tagcloud (Intersection) ?