AKTIP and C10orf2

  • Number of citations of the paper that reports this interaction (PMID 16169070)
  • 531

AKTIP

C10orf2

Gene Name AKT interacting protein chromosome 10 open reading frame 2
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 23 interactors: AKT1 ASS1 C10orf2 CTBP2 DZIP3 EXOC7 FAM160A2 GTF3C1 HOOK1 HOOK2 HOOK3 IMMT KIAA1377 MARCH5 PDPK1 POLA2 RPA1 TRIM23 TRIM41 UTP14A VPS16 VPS18 VPS41 2 interactors: AKTIP SMAD9
Entrez ID 64400 56652
HPRD ID 07467 05830
Ensembl ID ENSG00000166971 ENSG00000107815
Uniprot IDs Q9H8T0 E5KSY5 Q96RR1 Q9H6V3
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
apoa1bp  apolipoprotein  behaves  biophysical  cathepsin  cellulo  characterisation  ctsb  differently  forkhead  foxe3  implication  initiating  milieu  modules  mrnas  naturally  neighbouring  pg4  qrt  quadruplex  quadruplexes  recognises  render  scans  though  untranslated  utr  works 
autosomal  cofactor  controversial  dguok  dysmotility  efficacious  encephalomyopathic  encephalopathy  hepatocerebral  heterogeneous  hypotonia  infancy  mngie  mpv17  mtdna  myopathic  neurogastrointestinal  neurological  neuropathy  phenotypically  polg  recessive  rrm2b  sucla2  suclg1  tk2  tymp  typically  weakness 
Tagcloud (Difference) ?
apoa1bp  apolipoprotein  behaves  biophysical  cathepsin  cellulo  characterisation  ctsb  differently  forkhead  foxe3  implication  initiating  milieu  modules  mrnas  naturally  neighbouring  pg4  qrt  quadruplex  quadruplexes  recognises  render  scans  though  untranslated  utr  works 
autosomal  cofactor  controversial  dguok  dysmotility  efficacious  encephalomyopathic  encephalopathy  hepatocerebral  heterogeneous  hypotonia  infancy  mngie  mpv17  mtdna  myopathic  neurogastrointestinal  neurological  neuropathy  phenotypically  polg  recessive  rrm2b  sucla2  suclg1  tk2  tymp  typically  weakness 
Tagcloud (Intersection) ?