STX11 and ZCCHC10

  • Number of citations of the paper that reports this interaction (PMID 25416956)
  • 0
  • Data Source:
  • BioGRID (two hybrid)

STX11

ZCCHC10

Gene Name syntaxin 11 zinc finger, CCHC domain containing 10
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 62 interactors: AES APP BLOC1S6 BYSL C1orf109 CARD9 CCBE1 CCDC184 CCDC33 CCNK CDCA7L CTBP2 CWF19L2 EIF1AD FAM110A FAM161A FAM74A4 FAM90A1 FARS2 FHL5 GOLGA8EP GOLGA8F HAUS1 IKBKG IKZF3 KAT5 KCTD9 KDM1A KLC3 KXD1 LENG1 LONRF1 MBIP MEOX2 MFAP1 MID2 NDC80 PPP1R18 PRKAB2 PRPF31 PSMA3 PSMC3 RUNX1T1 SH2D4A SLC38A2 SMARCE1 SNAP23 SNAP25 SNX3 STXBP1 SUV39H1 TAF6L TBK1 TCF4 TNFRSF21 USHBP1 VAMP2 VPS52 WDYHV1 ZCCHC10 ZNF417 ZNF587 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
Entrez ID 8676 54819
HPRD ID 09231 15699
Ensembl ID ENSG00000155329
Uniprot IDs O75558 D6R9G7 G3XAM1 Q8TBK6
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
autosomal  characterised  defect  done  dysregulation  familial  families  fhl  haemophagocytic  harbour  harbouring  killer  leukaemia  lymphohistiocytosis  milder  mutational  myelogenous  nonsense  perforin  periods  prf1  psychomotor  recessive  retardation  segregation  syntaxin  uncommon  undertaken  unrelated 
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 
Tagcloud (Difference) ?
autosomal  characterised  defect  done  dysregulation  familial  families  fhl  haemophagocytic  harbour  harbouring  killer  leukaemia  lymphohistiocytosis  milder  mutational  myelogenous  nonsense  perforin  periods  prf1  psychomotor  recessive  retardation  segregation  syntaxin  uncommon  undertaken  unrelated 
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 
Tagcloud (Intersection) ?