SNX3 and STX11

  • Number of citations of the paper that reports this interaction (PMID 16169070)
  • 531
  • Data Source:
  • HPRD (two hybrid)

SNX3

STX11

Gene Name sorting nexin 3 syntaxin 11
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 9 interactors: ARL6IP1 BARD1 BRCA1 LIG4 PAXIP1 SCNN1A STX11 USP10 VPS35 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
Entrez ID 8724 8676
HPRD ID 09333 09231
Ensembl ID ENSG00000112335
Uniprot IDs O60493 O75558
PDB IDs 2YPS
Enriched GO Terms of Interacting Partners?
Tagcloud ?
altogether  biogenesis  degradative  depends  detachment  endocytic  endocytosis  endosomal  endosomes  find  homology  intralumenal  knockdown  lysosomes  maturation  multivesicular  nexin  phosphoinositides  prevents  px  recycling  redundant  restores  retrograde  shares  snx12  sorting  turn  vesicles 
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 
Tagcloud (Difference) ?
altogether  biogenesis  degradative  depends  detachment  endocytic  endocytosis  endosomal  endosomes  find  homology  intralumenal  knockdown  lysosomes  maturation  multivesicular  nexin  phosphoinositides  prevents  px  recycling  redundant  restores  retrograde  shares  snx12  sorting  turn  vesicles 
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 
Tagcloud (Intersection) ?