STXBP1 and NEFH

  • Number of citations of the paper that reports this interaction (PMID 12963086)
  • 9
  • Data Source:
  • HPRD (in vivo)

STXBP1

NEFH

Gene Name syntaxin binding protein 1 neurofilament, heavy polypeptide
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 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 5 interactors: MAPK1 NEFL NEFM PKN1 STXBP1
Entrez ID 6812 4744
HPRD ID 04235 01204
Ensembl ID ENSG00000136854 ENSG00000100285
Uniprot IDs B7Z1V5 P61764 Q68CM6 P12036
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
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 
carriers  certainty  cryb2  d22s268  d22s280  deafness  dominantly  gadolinium  gardner  inherited  linkage  manifestations  manifests  mri  neuro  neurofibromatosis  neurologic  nf2  ophthalmologic  otologic  pedigree  predisposes  presymptomatic  schwannomas  slowly  spine  thoroughly  typically  vestibular 
Tagcloud (Difference) ?
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 
carriers  certainty  cryb2  d22s268  d22s280  deafness  dominantly  gadolinium  gardner  inherited  linkage  manifestations  manifests  mri  neuro  neurofibromatosis  neurologic  nf2  ophthalmologic  otologic  pedigree  predisposes  presymptomatic  schwannomas  slowly  spine  thoroughly  typically  vestibular 
Tagcloud (Intersection) ?