ZCCHC10 and THAP1

  • Number of citations of the paper that reports this interaction (PMID 16189514)
  • 699
  • Data Source:
  • HPRD (two hybrid)

ZCCHC10

THAP1

Gene Name zinc finger, CCHC domain containing 10 THAP domain containing, apoptosis associated protein 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 50 interactors: ARGLU1 BEND7 CEP63 CEP70 COIL CTNNBL1 DAB1 DACH1 DHX8 DPPA2 DZIP3 EEF1A1 EPB41 FAM9B FRA10AC1 IK KCTD6 KPNA3 LNX1 LUC7L2 NUDT14 PCBP1 PIN1 PPIG PRPF3 PRPF38A PRPF40A PRR13 PSME3 PTPN3 RBM39 SART1 SDCBP SDCBP2 SF3B2 SF3B4 SFMBT1 SIAH1 SLU7 SNIP1 SNRPD2 STAC3 STX11 TCEB3B TFCP2 THAP1 TP53 U2AF1 ZBTB14 ZBTB8A 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 54819 55145
HPRD ID 15699 15496
Ensembl ID ENSG00000155329 ENSG00000131931
Uniprot IDs D6R9G7 G3XAM1 Q8TBK6 Q9NVV9
PDB IDs 2JTG 2KO0 2L1G
Enriched GO Terms of Interacting Partners?
Tagcloud ?
adcy3  angptl2  annotated  beadchip  bmi  boston  boys  c18orf8  corrected  correction  cpg  dok2  epigenomic  fdr  generational  humanmethylation27  illumina  infant  lends  maternal  mother  offspring  plac1  prepregnancy  prr16  sapcd2  separately  stated  wnt16 
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) ?
adcy3  angptl2  annotated  beadchip  bmi  boston  boys  c18orf8  corrected  correction  cpg  dok2  epigenomic  fdr  generational  humanmethylation27  illumina  infant  lends  maternal  mother  offspring  plac1  prepregnancy  prr16  sapcd2  separately  stated  wnt16 
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) ?