DCX and PPP1R9B

  • Number of citations of the paper that reports this interaction (PMID 17482550)
  • 43
  • Data Source:
  • HPRD (in vitro, in vivo, two hybrid)

DCX

PPP1R9B

Gene Name doublecortin protein phosphatase 1, regulatory subunit 9B
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 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 23 interactors: ACTA1 ADRA1A ADRA1B ADRA2A ADRA2B ADRA2C CCKAR CCKBR CDKN2A CHRM3 DCX DRD2 MAPK1 PPP1CA PPP1CB PPP1CC PPP1R2 PPP1R9A PRKACA RGS2 RPS6KB1 TGOLN2 TIAM1
Entrez ID 1641 84687
HPRD ID 02127 04506
Ensembl ID ENSG00000077279 ENSG00000108819
Uniprot IDs A8K340 B4DM53 O43602 D3DTX6 Q96SB3
PDB IDs 1MJD 2BQQ 2XRP 4ATU
Enriched GO Terms of Interacting Partners?
Tagcloud ?
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 
accn1  ago  arises  cgg  description  disturbed  eef1a2  fmr1  fmrp  fragile  gabrd  hes1  inherited  intelligence  interactive  lending  lymphoblastoid  lymphoblasts  males  microarrays  morphogenesis  neurodevelopment  overrepresentation  retardation  syndrome  transcriptome  trinucleotide  unc13b  untranslated 
Tagcloud (Difference) ?
17p13  classical  deletions  disrupt  epilepsy  frontal  gradient  lis  lis1  lissencephaly  malformation  mutations  occipital  overlapping  parietal  proline  q23  repeats  sequencing  sexes  southern  splice  sporadic  though  truncation  wd40  xlis  xq22 
accn1  ago  arises  cgg  description  disturbed  eef1a2  fmr1  fmrp  fragile  gabrd  hes1  inherited  intelligence  interactive  lending  lymphoblastoid  lymphoblasts  males  microarrays  morphogenesis  neurodevelopment  overrepresentation  syndrome  transcriptome  trinucleotide  unc13b  untranslated 
Tagcloud (Intersection) ?
retardation