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Focal epilepsy
Focal epilepsy
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
FOCAL EPILEPSY
MONDO:0005384
CLASP1
Unknown
—
GenCC
Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal
Separation of Sister Chromatids
Resolution of Sister Chromatid Cohesion
Regulation of PLK1 Activity at G2/M Transition
Loss of Nlp from mitotic centrosomes
Recruitment of mitotic centrosome proteins and complexes
Loss of proteins required for interphase microtubule organization from the centrosome
Recruitment of NuMA to mitotic centrosomes
Anchoring of the basal body to the plasma membrane
RHO GTPases Activate Formins
Mitotic Prometaphase
AURKA Activation by TPX2
EML4 and NUDC in mitotic spindle formation
+10 more
NPRL2
Unknown
26505888
27173016
28199897
29281825
30093711
31835056
34376795
37259768
ClinGen
,
GWAS catalog
mTOR signaling pathway
Amino acids regulate mTORC1
NPRL3
Unknown
26285051
26505888
26786403
27173016
34868250
35136953
ClinGen
,
GWAS catalog
mTOR signaling pathway
Amino acids regulate mTORC1
All
4
Causal
1
Unknown
3
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
2
GenCC
1
ClinGen
2
Related Diseases
Diseases that share the most curated genes with Focal epilepsy.
5
View disease cluster →
Familial focal epilepsy with variable foci
3 shared genes
DEPDC5, NPRL2, NPRL3
Related via 3 shared genes including DEPDC5, NPRL2, NPRL3.
Roifman syndrome
1 shared gene
CLASP1
Related via 1 shared gene including CLASP1.
Epilepsy with auditory features
1 shared gene
DEPDC5
Related via 1 shared gene including DEPDC5.
Lateral temporal lobe epilepsy
1 shared gene
DEPDC5
Related via 1 shared gene including DEPDC5.
Progressive myoclonic epilepsy
3 shared genes
DEPDC5, NPRL2, NPRL3
Related via 3 shared genes including DEPDC5, NPRL2, NPRL3.
1
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