Gene Name |
epilepsy, progressive myoclonus type 2A, Lafora disease (laforin) |
EPM2A (laforin) interacting protein 1 |
Image |
No pdb structure |
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 |
7 interactors:
EPM2AIP1
NFU1
NHLRC1
PPP1R3D
PRKAA1
PRKAA2
PRKAB2
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16 interactors:
ACTN1
C1orf50
CCNB1IP1
CPSF7
EMP2
EPM2A
FHL3
KCTD1
MEOX2
PRTFDC1
REL
SERPINF1
TNFAIP1
TRIM54
VPS52
ZBTB14
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Entrez ID |
7957 |
9852 |
HPRD ID |
06345 |
07445 |
Ensembl ID |
ENSG00000112425
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ENSG00000178567
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Uniprot IDs |
O95278
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Q7L775
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PDB IDs |
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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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