FHL5 and STX11

  • Number of citations of the paper that reports this interaction (PMID 11046156)
  • 37
  • Data Source:
  • BioGRID (two hybrid)

FHL5

STX11

Gene Name four and a half LIM domains 5 syntaxin 11
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 12 interactors: COIL CREB1 CREM DNAL4 FHL2 FHL3 HOXA1 KIF17 SMAD1 SRF STX11 ZNF446 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 9457 8676
HPRD ID 05497 09231
Ensembl ID ENSG00000112214
Uniprot IDs Q5TD97 O75558
PDB IDs 1X68
Enriched GO Terms of Interacting Partners?
Tagcloud ?
1p13  1p36  5x10  6q16  7p14  8q21  affecting  ajap1  apoa1bp  atp5b  c7orf10  candidate  fut9  loci  locus  matched  meta  migraine  mmp16  near  poorly  stat6  subgroup  susceptibility  tbc1d7  trait  tspan2  understood  wide 
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) ?
1p13  1p36  5x10  6q16  7p14  8q21  affecting  ajap1  apoa1bp  atp5b  c7orf10  candidate  fut9  loci  locus  matched  meta  migraine  mmp16  near  poorly  stat6  subgroup  susceptibility  tbc1d7  trait  tspan2  understood  wide 
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) ?