PCID2 and SHFM1

  • Number of citations of the paper that reports this interaction (PMID 16189514)
  • 699
  • Data Source:
  • BioGRID (x-ray crystallography, affinity chromatography technology, affinity chromatography technology)
  • HPRD (two hybrid)

PCID2

SHFM1

Gene Name PCI domain containing 2 split hand/foot malformation (ectrodactyly) type 1
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Attention deficit hyperactivity disorder ( 20732625)
  • Immunoglobulin A ( 20694011)
Protein-Protein Interactions 3 interactors: EID1 IKZF3 SHFM1 7 interactors: BRCA1 BRCA2 MAP1LC3B NUDT21 PCID2 PSMD3 PSMD6
Entrez ID 55795 7979
HPRD ID 07749 03182
Ensembl ID ENSG00000126226
Uniprot IDs Q5JVF3 P60896 Q6IBB7
PDB IDs 3T5X 1IYJ 1MIU 1MJE 3T5X
Enriched GO Terms of Interacting Partners?
Tagcloud ?
associates  balance  blastocyst  block  cbp  collectively  degraded  developmental  e3  eid1  embryonic  esc  escs  hallmarks  hat  impede  k48  lethality  ligase  maintenance  mdm2  modulation  pluripotency  renewal  self  suppression  sustain  switch  ubiquitination 
10q24  17p13  cgh  cnvs  congenital  deletions  dlx5  duplications  dync1i1  eexons  encompassing  enhancer  enhancers  exonic  exons  families  foot  fourth  hearing  hs1642  kb  malformation  microdeletions  split  syndromic  telomeric  tp63  unrelated 
Tagcloud (Difference) ?
associates  balance  blastocyst  block  cbp  collectively  degraded  developmental  e3  eid1  embryonic  esc  escs  hallmarks  hat  impede  k48  lethality  ligase  maintenance  mdm2  modulation  pluripotency  renewal  self  suppression  sustain  switch  ubiquitination 
10q24  17p13  cgh  cnvs  congenital  deletions  dlx5  duplications  dync1i1  eexons  encompassing  enhancer  enhancers  exonic  exons  families  foot  fourth  hearing  hs1642  kb  malformation  microdeletions  split  syndromic  telomeric  tp63  unrelated 
Tagcloud (Intersection) ?