Gene Name |
epilepsy, progressive myoclonus type 2A, Lafora disease (laforin) |
NFU1 iron-sulfur cluster scaffold |
Image |
No pdb structure |
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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 |
7 interactors:
EPM2AIP1
NFU1
NHLRC1
PPP1R3D
PRKAA1
PRKAA2
PRKAB2
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8 interactors:
AGTRAP
CALCOCO2
EPM2A
HIRA
NOA1
SH3BP4
TFIP11
TRIM23
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Entrez ID |
7957 |
27247 |
HPRD ID |
06345 |
12163 |
Ensembl ID |
ENSG00000112425
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ENSG00000169599
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Uniprot IDs |
O95278
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Q9UMS0
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PDB IDs |
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2LTM
2M5O
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
arms
autophago
biogenesis
branched
chop
defects
disposal
encode
epilepsy
epm2b
glycogen
hyperphosphorylated
insoluble
knock
lafora
laforin
laforinmalin
lamp1
lc3
lysosomal
malin
myoclonus
overaccumulation
proteasomal
s6
slight
speculate
starvation
ubiquitinated
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Tagcloud (Difference) ? |
arms
autophago
biogenesis
branched
chop
defects
disposal
encode
epilepsy
epm2b
glycogen
hyperphosphorylated
insoluble
knock
lafora
laforin
laforinmalin
lamp1
lc3
lysosomal
malin
myoclonus
overaccumulation
proteasomal
s6
slight
speculate
starvation
ubiquitinated
|
|
Tagcloud (Intersection) ? |
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