DYNLL1 and DYNC1H1

  • Number of citations of the paper that reports this interaction (PMID 14760703)
  • 24
  • Data Source:
  • HPRD (in vitro)

DYNLL1

DYNC1H1

Gene Name dynein, light chain, LC8-type 1 dynein, cytoplasmic 1, heavy chain 1
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 77 interactors: ACTB ACTC1 ACTG1 ALDOA AMBRA1 AMOTL2 B3GALT4 BCAS1 BCL2L11 BMF C14orf1 CA2 CACNB1 CCDC36 CLIP2 CS DAZ1 DLG4 DLGAP1 DNAJB9 DNM2 DNM3 DNMT1 DYNC1H1 DYNC1I1 EEF1A1 GAPDH GLUD1 GLUL GNB2L1 GPHN GRIN3A HIP1R HSPA8 INPP1 IQUB KANK2 LDHA MAP1B MARK3 MAST2 ME2 MTA1 MTR MYO10 MYO5A NDUFA4L2 NFKBIA NOS1 NRF1 NTRK1 NTRK2 NTRK3 PAK1 PAN2 PARD3 PAX6 PFKM PFKP PKIA PKIB PKIG POLH RAB4A RGS2 SHROOM3 TERT THAP8 TNFRSF14 TP53BP1 TUBA3C TUBB TXNDC17 VIM ZHX1 ZMYND11 ZNF354A 14 interactors: BRCA1 DISC1 DYNLL1 EGFR FAM46A KATNA1 KATNB1 NDEL1 PRKCD SMAD2 SNCA TNIK YWHAG YWHAQ
Entrez ID 8655 1778
HPRD ID 03334 02524
Ensembl ID ENSG00000088986 ENSG00000197102
Uniprot IDs P63167 Q6FGH9 Q14204
PDB IDs 1CMI 3ZKE 3ZKF 2BOR 2BOT
Enriched GO Terms of Interacting Partners?
Tagcloud ?
1inq53a  250viqd  52gqvd  adapter  attempt  capsid  defective  dynein  hiv  immunodeficiency  integrase  interaction  kd  ma  motifs  mutational  p150glued  particulate  predicts  proper  q252a  replication  requirement  reverse  steps  tctex  transcriptase  uncoating 
200x  customized  dcx  depths  exome  flna  funded  heterotopia  kif5c  kinesin  malformations  megalencephaly  mosaicism  neurodevelopmental  neuropsychiatric  nodular  pachygyria  panels  periventricular  persons  polymicrogyria  read  sanger  somatic  subcloned  subcloning  subcortical  tubb2b  unequal 
Tagcloud (Difference) ?
1inq53a  250viqd  52gqvd  adapter  attempt  capsid  defective  dynein  hiv  immunodeficiency  integrase  interaction  kd  ma  motifs  mutational  p150glued  particulate  predicts  proper  q252a  replication  requirement  reverse  steps  tctex  transcriptase  uncoating 
200x  customized  dcx  depths  exome  flna  funded  heterotopia  kif5c  kinesin  malformations  megalencephaly  mosaicism  neurodevelopmental  neuropsychiatric  nodular  pachygyria  panels  periventricular  persons  polymicrogyria  read  sanger  somatic  subcloned  subcloning  subcortical  tubb2b  unequal 
Tagcloud (Intersection) ?