STX11 and PRPF31

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

STX11

PRPF31

Gene Name syntaxin 11 pre-mRNA processing factor 31
Image 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 55 interactors: AES C1QTNF1 CALCOCO2 CCDC136 CCDC57 CDCA7L CEP70 FANCA GNB2L1 GOLGA2 HNRNPH2 HNRNPK JAKMIP2 KCTD6 KHDRBS2 KHDRBS3 KRT15 KRT40 KRTAP10-1 KRTAP10-3 KRTAP10-8 KRTAP10-9 LDOC1 LURAP1 MID2 MIPOL1 MKRN3 MTUS2 NHP2L1 NOTCH2NL PDE4DIP PHC2 PHF5A PNMA1 PNMA2 PPIH PRICKLE1 PRPF3 PRPF4 PSTPIP1 RBM25 RBM4 RBMY1A1 RBMY1F SIAH1 SSX2IP STX11 TADA2A TFIP11 TMCC2 TP53BP2 TRIM27 TSGA10 ZNF250 ZNF587
Entrez ID 8676 26121
HPRD ID 09231 05917
Ensembl ID ENSG00000105618
Uniprot IDs O75558 E7ESA8 F1T0A4 F1T0A5 Q8WWY3
PDB IDs 2OZB 3SIU 3SIV
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 
ala78leufsx99  amplified  autosomal  chinese  exons  families  frequencies  harbor  heterozygous  hong  kong  missense  modify  nonpathogenic  phe262serfsx59  pigmentosa  pro347leu  prph2  retina  retinitis  rho  screen  screened  simplex  stranded  thirteen  truncating  woman 
Tagcloud (Difference) ?
characterised  defect  done  dysregulation  familial  fhl  haemophagocytic  harbour  harbouring  killer  leukaemia  lymphohistiocytosis  milder  mutational  myelogenous  nonsense  perforin  periods  prf1  psychomotor  recessive  retardation  segregation  syntaxin  uncommon  undertaken  unrelated 
ala78leufsx99  amplified  chinese  exons  frequencies  harbor  heterozygous  hong  kong  missense  modify  nonpathogenic  phe262serfsx59  pigmentosa  pro347leu  prph2  retina  retinitis  rho  screen  screened  simplex  stranded  thirteen  truncating  woman 
Tagcloud (Intersection) ?
autosomal  families