ACD and DCX

  • Number of citations of the paper that reports this interaction (PMID 21044950)
  • 9
  • Data Source:
  • BioGRID (two hybrid)

ACD

DCX

Gene Name adrenocortical dysplasia homolog (mouse) doublecortin
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 59 interactors: ACTB ADPRH AFAP1L2 AIPL1 ANKMY2 APOBEC3F BAG3 CKB CTTN DBN1 DBNL DCX DPYSL3 EIF3G EIF4B ENO2 ENSA FAM131B FKBP6 GAPDH HSP90AB1 IPO5 IVL LASP1 LDHA LGALSL LLGL1 LRRC25 NCDN NUDC NUDCD2 PAGE2 PDLIM2 PEX5 PFKP PGM2 POT1 RBKS RECQL4 RGS3 RPSA SBDS STIP1 STUB1 SULT1C2 TAGLN TBC1D10A TBCD TINF2 TOMM34 TRIM15 TRIM16 TUBB2A TUBB4B USP7 XRCC6 YWHAE ZFP36L1 ZNF790 29 interactors: ACD AP1M1 AP2M1 APP CALCOCO2 CDK5 FBXO25 GOLGA2 IKZF1 KIFC3 KRT40 KRTAP10-8 MEOX1 MID2 NFASC PAFAH1B1 POT1 PPP1CA PPP1R9B RINT1 SPAG5 SPP1 TERF1 TINF2 TRIM23 TRIM27 TRIM39 USP9X ZBTB5
Entrez ID 65057 1641
HPRD ID 12417 02127
Ensembl ID ENSG00000102977 ENSG00000077279
Uniprot IDs Q96AP0 A8K340 B4DM53 O43602
PDB IDs 2I46 1MJD 2BQQ 2XRP 4ATU
Enriched GO Terms of Interacting Partners?
Tagcloud ?
acpra  apng1  arg52  betaherpesvirus  capsid  carboxy  carboxyl  ccd  corroborated  counterparts  cytomegalovirus  deleting  gal4  gammaherpesvirus  hcmv  his34  homologs  maturational  mcp  pap  proteinase  replace  scmv  simian  substituting  transporting  ul80  ul80a  ul86 
17p13  classical  deletions  disrupt  epilepsy  frontal  gradient  lis  lis1  lissencephaly  malformation  mutations  occipital  overlapping  parietal  proline  q23  repeats  retardation  sequencing  sexes  southern  splice  sporadic  though  truncation  wd40  xlis  xq22 
Tagcloud (Difference) ?
acpra  apng1  arg52  betaherpesvirus  capsid  carboxy  carboxyl  ccd  corroborated  counterparts  cytomegalovirus  deleting  gal4  gammaherpesvirus  hcmv  his34  homologs  maturational  mcp  pap  proteinase  replace  scmv  simian  substituting  transporting  ul80  ul80a  ul86 
17p13  classical  deletions  disrupt  epilepsy  frontal  gradient  lis  lis1  lissencephaly  malformation  mutations  occipital  overlapping  parietal  proline  q23  repeats  retardation  sequencing  sexes  southern  splice  sporadic  though  truncation  wd40  xlis  xq22 
Tagcloud (Intersection) ?