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