STX11 and STXBP1

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

STX11

STXBP1

Gene Name syntaxin 11 syntaxin binding protein 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 27 interactors: APBA1 APBA2 APP CDK5 CDK5R1 DOC2A DOC2B DYT10 HGS MAPT NEFH NEFM PLD1 PLD2 PRKCA PRKCB PRKCG SQSTM1 STX11 STX19 STX1A STX1B STX2 STX3 SYTL4 TRIM38 USO1
Entrez ID 8676 6812
HPRD ID 09231 04235
Ensembl ID ENSG00000136854
Uniprot IDs O75558 B7Z1V5 P61764 Q68CM6
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 
16p12  2q24  5q14  9q34  aetiology  caln1  cdkl5  cgh  cnv  cnvs  counselling  ehmt1  encephalopathies  encompassing  epileptic  etiological  grin2a  hypsarrhythmia  infantile  intronic  iss  kcnq2  magi2  mef2c  microdeletions  microduplications  scn2a  spasms  xq28 
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 
16p12  2q24  5q14  9q34  aetiology  caln1  cdkl5  cgh  cnv  cnvs  counselling  ehmt1  encephalopathies  encompassing  epileptic  etiological  grin2a  hypsarrhythmia  infantile  intronic  iss  kcnq2  magi2  mef2c  microdeletions  microduplications  scn2a  spasms  xq28 
Tagcloud (Intersection) ?