SHFM1 and PSMD6

  • Number of citations of the paper that reports this interaction (PMID 17563742)
  • 17
  • Data Source:
  • BioGRID (affinity chromatography technology, affinity chromatography technology, two hybrid, affinity chromatography technology, affinity chromatography technology)

SHFM1

PSMD6

Gene Name split hand/foot malformation (ectrodactyly) type 1 proteasome (prosome, macropain) 26S subunit, non-ATPase, 6
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 7 interactors: BRCA1 BRCA2 MAP1LC3B NUDT21 PCID2 PSMD3 PSMD6 4 interactors: SHFM1 TRAF6 UBQLN1 ZFAND5
Entrez ID 7979 9861
HPRD ID 03182 18370
Ensembl ID ENSG00000163636
Uniprot IDs P60896 Q6IBB7 C9IZE4 E9PHI9 Q15008
PDB IDs 1IYJ 1MIU 1MJE 3T5X
Enriched GO Terms of Interacting Partners?
Tagcloud ?
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) ?
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) ?