SPG21 and CUTC

  • Number of citations of the paper that reports this interaction (PMID 16189514)
  • 699
  • Data Source:
  • HPRD (two hybrid)

SPG21

CUTC

Gene Name spastic paraplegia 21 (autosomal recessive, Mast syndrome) cutC copper transporter
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 37 interactors: AGTRAP AKIRIN2 ARL6IP1 ATPAF2 CCDC102B CCDC33 CD4 CMTM5 CRYAA CTPS2 CUTC DTX2 DTX3L EFHC2 FAM114A1 GGA2 GSK3A IKZF3 INCA1 KRT15 MID2 MTMR9 PRPS1 RABAC1 REEP6 RTN4 S100B SPRED2 TCF12 TCF4 TFG TRAF1 TRAF2 TRIM23 TRIM54 TRIM9 ZNF263 11 interactors: ASCC2 BCL6 CEP76 LNX1 NADSYN1 NIF3L1 NUDT18 PIM2 SDCBP SLC27A6 SPG21
Entrez ID 51324 51076
HPRD ID 10492 13100
Ensembl ID ENSG00000090487 ENSG00000119929
Uniprot IDs Q9NZD8 Q9NTM9
PDB IDs 3IWP
Enriched GO Terms of Interacting Partners?
Tagcloud ?
Tagcloud (Difference) ?
Tagcloud (Intersection) ?