STAU1 and DYNC1I1

  • Number of citations of the paper that reports this interaction (PMID 15121898)
  • 40
  • Data Source:
  • BioGRID (affinity chromatography technology)
  • HPRD (in vitro)

STAU1

DYNC1I1

Gene Name staufen double-stranded RNA binding protein 1 dynein, cytoplasmic 1, intermediate chain 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Immune reponse to smallpox (secreted IL-10) ( 22610502)
  • Obesity-related traits ( 23251661)
Protein-Protein Interactions 39 interactors: APP CASC3 CDC42 CSNK2B DHX9 DYNC1I1 FMR1 GLRX3 HNRNPU INA IQGAP1 KIF2B LONRF1 MAP1B MAPT MYH1 NCBP1 NCL NXT1 PABPC1 PABPN1 PPP1CA PPP1CC RAC1 RASA1 ROCK2 RPL28 RPL6 RPL7A RPLP0 RPS6 SPP1 SRPK1 TAX1BP3 TUBB TUBB4A UBE2D3 UPF1 ZMAT3 31 interactors: ANXA7 BICD1 C2orf44 CADM4 CDKN1A DNM2 DYNLL1 DYNLL2 DYNLRB1 DYNLT1 DYNLT3 EMILIN1 FAM110A FAM83D FBP1 GRB7 GSK3B KAT7 MCC NAGK NUDT21 PIN1 RAP1GAP RCC1 RUNDC3B SMN1 STAU1 TAOK1 TK1 TRIM58 UBC
Entrez ID 6780 1780
HPRD ID 03422 04798
Ensembl ID ENSG00000124214 ENSG00000158560
Uniprot IDs B3KRE0 O95793 Q6PJX3 A4D1I7 B4DME3 F5H050 G5E9K1 O14576 Q8N542 Q8TBF7
PDB IDs 4DKK
Enriched GO Terms of Interacting Partners?
Tagcloud ?
activators  anaphase  apc  arrested  asynchronous  cdc20  cdh1  code  consistently  cyclosome  e3  fluctuates  hct116  impairs  ligase  messenger  mitosis  mitotic  mrnas  participates  precedes  prometaphase  ribonucleic  rnas  transit  u2os  underscored 
10q24  17p13  cgh  cnvs  congenital  deletions  dlx5  duplications  eexons  encompassing  enhancer  enhancers  exonic  exons  families  foot  fourth  hearing  hs1642  kb  malformation  microdeletions  shfm  shfm1  split  syndromic  telomeric  tp63  unrelated 
Tagcloud (Difference) ?
activators  anaphase  apc  arrested  asynchronous  cdc20  cdh1  code  consistently  cyclosome  e3  fluctuates  hct116  impairs  ligase  messenger  mitosis  mitotic  mrnas  participates  precedes  prometaphase  ribonucleic  rnas  transit  u2os  underscored 
10q24  17p13  cgh  cnvs  congenital  deletions  dlx5  duplications  eexons  encompassing  enhancer  enhancers  exonic  exons  families  foot  fourth  hearing  hs1642  kb  malformation  microdeletions  shfm  shfm1  split  syndromic  telomeric  tp63  unrelated 
Tagcloud (Intersection) ?