| Gene Symbol | ME2 | ||
|---|---|---|---|
| Ensembl ID | ENSG00000082212 | Entrez | 4200 |
| Gene Alias | - | Subcellular Locations | Mitochondria Mitochondrial-matrix |
| Map Position | 6p25-p24|18q21 | Subcell PMIDs | 1993674 15532013 |
| OMIM Gene | 154270 | Protein Complex | |
| Swissprot ID | P23368 | Swissprot Description | NAD-dependent malic enzyme, mitochondrial precursor |
| OMIM Disease | Idiopathic generalized epilepsy (IGE) [600669] | ||
Gene-Feature associations that are associated with 1 Gene
| Gene | OMIM Disease | Phenotypic Feature | Phenotype Annotation | Clinical Category | PMIDs |
|---|---|---|---|---|---|
| ME2 | 600669 | Nervous-system-diseases | neurologic | #15532013 | |
| ME2 | 600669 | Central-nervous-system-diseases | neurologic | #15532013 | |
| ME2 | 600669 | Brain-diseases | neurologic | #15532013 | |
| ME2 | 600669 | Seizures | generalized epilepsy; epilepsy; convulsions | neurologic | 15532013 |
| ME2 | 600669 | Electroencephalogram-abnormal | generalized; bilateral; synchronous; symmetrical discharge; spikes; multispike waves | neurologic | 15532013 |
| ME2 | 600669 | Neurologic-manifestations | neurologic | #15532013 | |
| ME2 | 600669 | Neurobehavioral-manifestations | neurologic | #15532013 | |
| ME2 | 600669 | Consciousness-disorders | absence seizures; staring spells with loss of consciousness | neurologic | 15532013 |
