PAFAH1B1 and DCX

  • Number of citations of the paper that reports this interaction (PMID 11001923)
  • 25
  • Data Source:
  • HPRD (in vitro, in vivo)

PAFAH1B1

DCX

Gene Name platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa) doublecortin
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 22 interactors: CLIP1 CSNK2A1 DAB1 DCTN1 DCTN2 DCX DISC1 DNAI1 HSPH1 KARS KATNA1 KATNB1 MAP1B MAP2 NDE1 NDEL1 NUDC PAFAH1B2 PAFAH1B3 PDE4D TNIK TUBA1A 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 5048 1641
HPRD ID 03329 02127
Ensembl ID ENSG00000007168 ENSG00000077279
Uniprot IDs P43034 A8K340 B4DM53 O43602
PDB IDs 1MJD 2BQQ 2XRP 4ATU
Enriched GO Terms of Interacting Partners?
Tagcloud ?
acetylhydrolase  alleles  autonomous  bulb  cerebellar  defects  delayed  developmental  die  disorganization  display  dosage  embryogenesis  heterozygous  hippocampal  homozygous  implantation  inactive  lis1  lissencephaly  migration  neuronal  null  olfactory  participates  phenotypes  soon  thought  understand 
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) ?
acetylhydrolase  alleles  autonomous  bulb  cerebellar  defects  delayed  developmental  die  disorganization  display  dosage  embryogenesis  heterozygous  hippocampal  homozygous  implantation  inactive  migration  neuronal  null  olfactory  participates  phenotypes  soon  thought  understand 
17p13  classical  deletions  disrupt  epilepsy  frontal  gradient  lis  malformation  mutations  occipital  overlapping  parietal  proline  q23  repeats  retardation  sequencing  sexes  southern  splice  sporadic  though  truncation  wd40  xlis  xq22 
Tagcloud (Intersection) ?
lis1  lissencephaly