STX11 and CCDC33

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

STX11

CCDC33

Gene Name syntaxin 11 coiled-coil domain containing 33
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 91 interactors: ABCF3 ABLIM3 APP ARIH2 ARMC7 ARNT2 BCCIP BLK BLZF1 BYSL CALCOCO2 CCDC102B CCDC85B CCNH CDCA7L CDKN2B CENPP CHCHD3 DGCR6 DIP2A DVL2 EFEMP2 EHMT2 EMC2 EMD FAM124A FAM161A FXR2 GPATCH2L GRN HGS HNRNPF HNRNPK HOOK2 HOXA1 ING5 KANK2 KCTD19 KCTD9 KHDRBS3 KIFC3 KXD1 LDOC1 LMO2 LMO3 MAGED1 MAPK9 MDFI MIPOL1 MOS NAB2 NCK2 NDOR1 NECAB2 NINL OSGIN1 PID1 PIN1 PLSCR1 PNMA1 PNMA2 POLR1C PPP2R3C PRKAB2 PTGER3 PTK6 RAD54B RBMX RHOXF2 SCNM1 SMAD3 SPAG5 SPG21 SSSCA1 STK16 STX11 TGFB1 TMCC2 TRAF2 TRIM37 TRIM42 TSC22D4 TSGA10 TTC19 TUFT1 UBQLN4 USHBP1 VPS52 ZBTB8A ZGPAT ZNF572
Entrez ID 8676 80125
HPRD ID 09231 09959
Ensembl ID ENSG00000140481
Uniprot IDs O75558 Q8N5R6
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 
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 
Tagcloud (Intersection) ?