SPG7 and KHDRBS2

  • Number of citations of the paper that reports this interaction (PMID 25416956)
  • 0
  • Data Source:
  • BioGRID (two hybrid)

SPG7

KHDRBS2

Gene Name spastic paraplegia 7 (pure and complicated autosomal recessive) KH domain containing, RNA binding, signal transduction associated 2
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Protein quantitative trait loci ( 18464913)
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 29 interactors: AEN CATSPER1 CHTOP CIRBP DOCK2 EWSR1 GRB2 HBZ HNRNPK HNRNPR KHDRBS3 LINC01018 MTA1 NABP1 NCOA5 NPDC1 PRMT1 PRPF31 PRR3 PTK6 RBM3 RBMX SDCBP SPG7 SULT1A3 TYK2 TYMSOS YTHDC1 ZFC3H1
Entrez ID 6687 202559
HPRD ID 04149 13775
Ensembl ID ENSG00000197912 ENSG00000112232
Uniprot IDs Q9UQ90 Q5VWX1
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) ?