CUTC and SPG21

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

CUTC

SPG21

Gene Name cutC copper transporter spastic paraplegia 21 (autosomal recessive, Mast syndrome)
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 11 interactors: ASCC2 BCL6 CEP76 LNX1 NADSYN1 NIF3L1 NUDT18 PIM2 SDCBP SLC27A6 SPG21 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
Entrez ID 51076 51324
HPRD ID 13100 10492
Ensembl ID ENSG00000119929 ENSG00000090487
Uniprot IDs Q9NTM9 Q9NZD8
PDB IDs 3IWP
Enriched GO Terms of Interacting Partners?
Tagcloud ?
Tagcloud (Difference) ?
Tagcloud (Intersection) ?