EPM2A and NHLRC1

  • Number of citations of the paper that reports this interaction (PMID 22578008)
  • 1

EPM2A

NHLRC1

Gene Name epilepsy, progressive myoclonus type 2A, Lafora disease (laforin) NHL repeat containing E3 ubiquitin protein ligase 1
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 7 interactors: EPM2AIP1 NFU1 NHLRC1 PPP1R3D PRKAA1 PRKAA2 PRKAB2 9 interactors: AGL EPM2A NNAT PPP1R3C UBE2D1 UBE2D2 UBE2D3 UBE2E1 UBE2H
Entrez ID 7957 378884
HPRD ID 06345 06995
Ensembl ID ENSG00000112425 ENSG00000187566
Uniprot IDs O95278 Q6VVB1
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
arms  autophago  biogenesis  branched  chop  defects  disposal  encode  epilepsy  epm2b  glycogen  hyperphosphorylated  insoluble  knock  lafora  laforin  laforinmalin  lamp1  lc3  lysosomal  malin  myoclonus  overaccumulation  proteasomal  s6  slight  speculate  starvation  ubiquitinated 
accepted  apparently  asses  ataxia  autosomal  bodies  cerebral  characterizing  codifying  cortex  dysregulation  epm2a  epm2b  gabaergic  glycogen  imply  lafora  laforin  malin  myoclonic  myoclonus  neurodegeneration  neurodevelopment  neurotrophins  operate  p75ntr  recessive  seizures  want 
Tagcloud (Difference) ?
arms  autophago  biogenesis  branched  chop  defects  disposal  encode  epilepsy  hyperphosphorylated  insoluble  knock  laforinmalin  lamp1  lc3  lysosomal  overaccumulation  proteasomal  s6  slight  speculate  starvation  ubiquitinated 
accepted  apparently  asses  ataxia  autosomal  bodies  cerebral  characterizing  codifying  cortex  dysregulation  gabaergic  imply  myoclonic  neurodegeneration  neurodevelopment  neurotrophins  operate  p75ntr  recessive  seizures  want 
Tagcloud (Intersection) ?
epm2a  epm2b  glycogen  lafora  laforin  malin  myoclonus