SPG7 and SPATS1

  • Number of citations of the paper that reports this interaction (PMID 21988832)
  • 14
  • Data Source:
  • BioGRID (two hybrid)

SPG7

SPATS1

Gene Name spastic paraplegia 7 (pure and complicated autosomal recessive) spermatogenesis associated, serine-rich 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 23 interactors: CCNDBP1 HNRNPK KHDRBS2 KRT40 KRTAP10-3 KRTAP10-7 KRTAP10-9 KRTAP4-12 LRIF1 LZTS2 MAPK6 MDFI MTUS2 NOTCH2NL PLSCR1 PNMA1 PSME3 PSTPIP1 RALY RBPMS SPATS1 STAMBP TRIM28 3 interactors: CFLAR GPHN SPG7
Entrez ID 6687 221409
HPRD ID 04149 10248
Ensembl ID ENSG00000197912 ENSG00000249481
Uniprot IDs Q9UQ90 Q496A3
PDB IDs 2QZ4
Enriched GO Terms of Interacting Partners?
Tagcloud ?
ablated  accumulates  axons  biogenesis  corticospinal  defines  exposes  hereditary  implication  isoform  knock  lacks  limbs  lumen  microsomal  name  owing  paraplegia  paraplegin  performs  proteases  recessive  resides  retina  retrograde  spastic  spasticity  usage  weakness 
Tagcloud (Difference) ?
ablated  accumulates  axons  biogenesis  corticospinal  defines  exposes  hereditary  implication  isoform  knock  lacks  limbs  lumen  microsomal  name  owing  paraplegia  paraplegin  performs  proteases  recessive  resides  retina  retrograde  spastic  spasticity  usage  weakness 
Tagcloud (Intersection) ?