STX11 and SMARCE1

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

STX11

SMARCE1

Gene Name syntaxin 11 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1
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 63 interactors: AMOTL2 AR ARID2 BAZ1B BRMS1 CCDC136 CCDC172 CDR2 CEP170P1 CEP63 CEP70 DISC1 EPS8 ESR1 ESR2 EXOC7 GATA1 GOLGA2 ING5 ITCH JAKMIP2 KIFC3 KLF1 KRT15 KRT31 KRT40 KRTAP10-9 MDM2 MED4 MEOX2 MIPOL1 MRFAP1L1 MTUS2 NBPF22P NCOA1 NCOA2 NCOA3 NOTCH2NL NR0B2 NR3C1 NUP62 PGR PRMT5 RALBP1 RARA RCOR1 RELB RINT1 SIN3A SIN3B SMAD1 SMARCA4 SPAG5 SRC STX11 SYCE1 TFE3 TFIP11 TNIK TRIM54 TRIP10 TXLNA USHBP1
Entrez ID 8676 6605
HPRD ID 09231 04382
Ensembl ID ENSG00000073584
Uniprot IDs O75558 Q969G3
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 
acetylase  aldh1a3  belonging  bipotent  cbx6  ccnb1  ccne1  committed  differentiated  disrupt  dysregulation  encode  establishment  gata3  hat1  hdac1  identity  luminal  maintenance  myoepithelial  notch4  pcgf2  polycomb  progenitors  silico  subpopulations  trithorax 
Tagcloud (Difference) ?
autosomal  characterised  defect  done  familial  families  fhl  haemophagocytic  harbour  harbouring  killer  leukaemia  lymphohistiocytosis  milder  mutational  myelogenous  nonsense  perforin  periods  prf1  psychomotor  recessive  retardation  segregation  syntaxin  uncommon  undertaken  unrelated 
acetylase  aldh1a3  belonging  bipotent  cbx6  ccnb1  ccne1  committed  differentiated  disrupt  encode  establishment  gata3  hat1  hdac1  identity  luminal  maintenance  myoepithelial  notch4  pcgf2  polycomb  progenitors  silico  subpopulations  trithorax 
Tagcloud (Intersection) ?
dysregulation