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Myoclonic encephalopathy
Myoclonic encephalopathy
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
EARLY MYOCLONIC ENCEPHALOPATHY
C0270855
MONDO:0016022
JMJD1C
Unknown
—
Disgenet
Transcriptional misregulation in cancer
Factors involved in megakaryocyte development and platelet production
SIK1
Unknown
25839329
CTD
Glucagon signaling pathway
TUBA1A
Unknown
—
Disgenet
Phagosome
Apoptosis
Tight junction
Gap junction
Motor proteins
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Pathogenic Escherichia coli infection
Salmonella infection
Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane
MHC class II antigen presentation
Separation of Sister Chromatids
Resolution of Sister Chromatid Cohesion
Regulation of PLK1 Activity at G2/M Transition
HSP90 chaperone cycle for steroid hormone receptors (SHR)
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
Recycling pathway of L1
Hedgehog 'off' state
Cilium Assembly
Anchoring of the basal body to the plasma membrane
Intraflagellar transport
RHO GTPases activate IQGAPs
RHO GTPases Activate Formins
COPI-mediated anterograde transport
COPI-dependent Golgi-to-ER retrograde traffic
COPI-independent Golgi-to-ER retrograde traffic
Mitotic Prometaphase
The role of GTSE1 in G2/M progression after G2 checkpoint
AURKA Activation by TPX2
Carboxyterminal post-translational modifications of tubulin
HCMV Early Events
Aggrephagy
EML4 and NUDC in mitotic spindle formation
Sealing of the nuclear envelope (NE) by ESCRT-III
Kinesins
+39 more
All
5
Causal
2
Unknown
3
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
2
CTD
1
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Related Diseases
Diseases that share the most curated genes with Myoclonic encephalopathy.
5
View disease cluster →
KCND2-related neurodevelopmental disorder with or without seizures
1 shared gene
KCND2
Related via 1 shared gene including KCND2.
Tubulinopathy
1 shared gene
TUBA1A
Related via 1 shared gene including TUBA1A.
22q11.2 deletion syndrome
1 shared gene
JMJD1C
Related via 1 shared gene including JMJD1C.
Epilepsy of infancy with migrating focal seizures
1 shared gene
SLC25A22
Related via 1 shared gene including SLC25A22.
Malignant migrating partial seizures of infancy
1 shared gene
SLC25A22
Related via 1 shared gene including SLC25A22.
1
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