GRB7 and DYNC1I1

  • Number of citations of the paper that reports this interaction (PMID 21900206)
  • 27
  • Data Source:
  • BioGRID (two hybrid)

GRB7

DYNC1I1

Gene Name growth factor receptor-bound protein 7 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: A1BG AGAP1 ATP5B CALM1 CAV1 CPNE6 DOCK7 DYNC1I1 EGFR ERBB2 ERBB3 FGB FLAD1 GNB2 GRB2 HADHB INSR KCTD6 KIT KMT2B LAX1 LY6G6F MAP3K14 MSH2 PDGFRB PDHB PHAX PKM PTK2 RET RND1 RPS2 SETDB1 SHC1 TEK TLE1 TMSB4X TRIM36 ZBTB16 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 2886 1780
HPRD ID 03311 04798
Ensembl ID ENSG00000141738 ENSG00000158560
Uniprot IDs Q14451 A4D1I7 B4DME3 F5H050 G5E9K1 O14576 Q8N542 Q8TBF7
PDB IDs 1MW4 1WGR 2L4K 2QMS 3PQZ
Enriched GO Terms of Interacting Partners?
Tagcloud ?
adapter  appears  avidly  bear  bps  conversely  denote  domain  domains  dramatically  existence  grb10  grb14  homology  interact  interaction  interacts  ir  location  loop  obvious  paired  pleckstrin  resemblance  sh2  summary  unidentified  y1150f  y1151f 
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) ?
adapter  appears  avidly  bear  bps  conversely  denote  domain  domains  dramatically  existence  grb10  grb14  homology  interact  interaction  interacts  ir  location  loop  obvious  paired  pleckstrin  resemblance  sh2  summary  unidentified  y1150f  y1151f 
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) ?