SPG7

Gene Name spastic paraplegia 7 (pure and complicated autosomal recessive)
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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
Entrez ID 6687
HPRD ID 04149
Ensembl ID ENSG00000197912
Uniprot IDs Q9UQ90
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