DNM2 and DYNC1I1

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

DNM2

DYNC1I1

Gene Name dynamin 2 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 52 interactors: AMPH AOC1 AP2A1 APP ATF7IP ATXN3 BIN1 CCDC90B CCR5 CCT7 CDK1 CTTN DDX39B DNM1 DYNC1I1 DYNLL1 EIF3L EPS15 FNBP1 FNBP1L GDF9 GRB2 HCK HMGB1 ITSN1 ITSN2 KDR MAN1B1 MANEA MPHOSPH6 MPP6 PDE6G PFN1 PPIB PSTPIP1 PTK2 RPS2 RWDD2B SH3GL2 SH3GLB1 SHANK1 SHANK2 SNX9 SPRY2 SRC TIAM2 TRIP10 TYK2 VAV1 WBP4 ZBTB16 ZFAND6 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 1785 1780
HPRD ID 03852 04798
Ensembl ID ENSG00000079805 ENSG00000158560
Uniprot IDs P50570 Q8N1K8 A4D1I7 B4DME3 F5H050 G5E9K1 O14576 Q8N542 Q8TBF7
PDB IDs 2YS1
Enriched GO Terms of Interacting Partners?
Tagcloud ?
bcl11b  cadherin  discovered  druggable  exhibitedthe  fat1  fbxw7  frequencies  guide  harboured  herc1  jak  jak3  lymphoblastic  mll2  mutational  notch1  notch2  phf6  recurrent  regulators  reln  secretase  splicing  subclonal  unfavourable  warranted  wt1  zrsr2 
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) ?
bcl11b  cadherin  discovered  druggable  exhibitedthe  fat1  fbxw7  frequencies  guide  harboured  herc1  jak  jak3  lymphoblastic  mll2  mutational  notch1  notch2  phf6  recurrent  regulators  reln  secretase  splicing  subclonal  unfavourable  warranted  wt1  zrsr2 
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) ?