PSMD3 and SHFM1

  • Number of citations of the paper that reports this interaction (PMID 24515614)
  • 1
  • Data Source:
  • BioGRID (two hybrid, affinity chromatography technology)

PSMD3

SHFM1

Gene Name proteasome (prosome, macropain) 26S subunit, non-ATPase, 3 split hand/foot malformation (ectrodactyly) type 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Attention deficit hyperactivity disorder ( 20732625)
  • Immunoglobulin A ( 20694011)
Protein-Protein Interactions 4 interactors: BLM CEP44 SHFM1 ZBTB43 7 interactors: BRCA1 BRCA2 MAP1LC3B NUDT21 PCID2 PSMD3 PSMD6
Entrez ID 5709 7979
HPRD ID 10170 03182
Ensembl ID ENSG00000108344
Uniprot IDs O43242 P60896 Q6IBB7
PDB IDs 1IYJ 1MIU 1MJE 3T5X
Enriched GO Terms of Interacting Partners?
Tagcloud ?
annotations  atlas  canx  cascade  combinatorial  constrained  dataset  distinguishing  dnm1  dysregulated  exhaustively  exhibiting  gbm  glioblastoma  hspa9  label  mapk1  multiforme  outlines  ppi  ppis  programmed  proteomics  signature  signatures  subnetwork  survivor  tcga  translatable 
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) ?
annotations  atlas  canx  cascade  combinatorial  constrained  dataset  distinguishing  dnm1  dysregulated  exhaustively  exhibiting  gbm  glioblastoma  hspa9  label  mapk1  multiforme  outlines  ppi  ppis  programmed  proteomics  signature  signatures  subnetwork  survivor  tcga  translatable 
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) ?