SMN2 and GEMIN2

  • Number of citations of the paper that reports this interaction (PMID 9323129)
  • 127
  • Data Source:
  • HPRD (two hybrid, in vitro, in vivo)

SMN2

GEMIN2

Gene Name survival of motor neuron 2, centromeric gem (nuclear organelle) associated protein 2
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 24 interactors: BLOC1S6 BYSL CHTOP DDX20 DHX9 FAM9B FBL GAR1 GEMIN2 HNRNPUL1 POLR1C POLR2A PPIG SMN1 SNRPB SNRPB2 SNRPD1 SNRPD2 SNRPD3 SNRPE SNRPF SNRPG TIAL1 VPS28 21 interactors: DDX20 DHX9 GEMIN5 IKBKG RN7SL1 RNU1-1 RNU2-1 SMN1 SMN2 SNRNP70 SNRPD1 SNRPD2 SNRPD3 SNRPN SRSF1 SRSF2 SRSF3 SRSF4 STXBP2 STXBP3 U2AF2
Entrez ID 6607 8487
HPRD ID 09036 03999
Ensembl ID ENSG00000205571 ENSG00000092208
Uniprot IDs B4DP61 Q16637 O14893
PDB IDs 1G5V 1MHN 2LEH 3S6N 4A4E 4A4G 4GLI 2LEH 3S6N
Enriched GO Terms of Interacting Partners?
Tagcloud ?
atrophy  centromeric  compensate  copies  copy  degeneration  deletions  detectable  display  donor  easily  exon  fails  fatal  harbor  hindering  homozygous  infant  intragenic  italian  modifier  muscular  null  predictable  sma  smn1  splice  unusually  weakness 
associates  atrophy  characterised  efficiently  epitope  epitopes  exists  explain  hela  immunised  immuno  inherited  library  mab  mabs  mansma1  mansma12  mansma3  masked  motor  multimeric  muscular  phage  precipitated  precise  proline  smn  spliceosome  vigorous 
Tagcloud (Difference) ?
centromeric  compensate  copies  copy  degeneration  deletions  detectable  display  donor  easily  exon  fails  fatal  harbor  hindering  homozygous  infant  intragenic  italian  modifier  null  predictable  sma  smn1  splice  unusually  weakness 
associates  characterised  efficiently  epitope  epitopes  exists  explain  hela  immunised  immuno  inherited  library  mab  mabs  mansma1  mansma12  mansma3  masked  motor  multimeric  phage  precipitated  precise  proline  smn  spliceosome  vigorous 
Tagcloud (Intersection) ?
atrophy  muscular