CCBE1 and STX11

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

CCBE1

STX11

Gene Name collagen and calcium binding EGF domains 1 syntaxin 11
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 5 interactors: CEP55 KLHL12 SIAH2 STX11 TOX4 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 147372 8676
HPRD ID 08703 09231
Ensembl ID ENSG00000183287
Uniprot IDs Q6UXH8 O75558
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
anomalies  autosomal  boy  bridge  bulb  color  doppler  duodenal  edema  enlargement  facial  fat4  flat  generalized  hennekam  hs  hypertelorism  hypoalbuminemia  lymphangiectasia  lymphangioma  lymphatic  manifestations  manifested  recessive  retardation  superficial  teeth  thriving  unexplained 
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) ?
anomalies  boy  bridge  bulb  color  doppler  duodenal  edema  enlargement  facial  fat4  flat  generalized  hennekam  hs  hypertelorism  hypoalbuminemia  lymphangiectasia  lymphangioma  lymphatic  manifestations  manifested  superficial  teeth  thriving  unexplained 
characterised  defect  done  dysregulation  familial  families  fhl  haemophagocytic  harbour  harbouring  killer  leukaemia  lymphohistiocytosis  milder  mutational  myelogenous  nonsense  perforin  periods  prf1  psychomotor  segregation  syntaxin  uncommon  undertaken  unrelated 
Tagcloud (Intersection) ?
autosomal  recessive  retardation