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Browse result for Epileptic encephalopathy
※ introduction Encephalopathy (; from Ancient Greek: ?¦Í¦Ê?¦Õ¦Á¦Ë¦Ï? "brain" + ¦Ð?¦È¦Ï? "suffering") means any disorder or disease of the brain, especially chronic degenerative conditions. In modern usage, encephalopathy does not refer to a single disease, but rather to a syndrome of overall brain dysfunction; this syndrome has many possible organic and inorganic causes.
Reference
Wiki: Epileptic encephalopathy
Reference
Wiki: Epileptic encephalopathy
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD01433 | O60701 | 7358 | UGDH | UDP-glucose 6-dehydrogenase | Homo sapiens |
| PTMD01577 | P28472 | 2562 | GABRB3 | Gamma-aminobutyric acid receptor subunit beta-3 receptor subunit beta-3) | Homo sapiens |
| PTMD02403 | O14647 | 1106 | CHD2 | Chromodomain-helicase-DNA-binding protein 2 | Homo sapiens |
| PTMD03208 | O75899 | 9568 | GABBR2 | Gamma-aminobutyric acid type B receptor subunit 2 | Homo sapiens |
| PTMD03328 | O94966 | 10869 | USP19 | Ubiquitin carboxyl-terminal hydrolase 19 | Homo sapiens |
| PTMD05293 | P49327 | 2194 | FASN | Fatty acid synthase [Includes: [Acyl-carrier-protein] S-acetyltransferase ; [Acyl-carrier-protein] S-malonyltransferase ; 3-oxoacyl-[acyl-carrier-protein] synthase ; 3-oxoacyl-[acyl-carrier-protein] reductase ; 3-hydroxyacyl-[acyl-carrier-protein] dehydratase ; Enoyl-[acyl-carrier-protein] reductase ; Acyl-[acyl-carrier-protein] hydrolase ] | Homo sapiens |
| PTMD05821 | P61764 | 6812 | STXBP1 | Syntaxin-binding protein 1 | Homo sapiens |
| PTMD06959 | Q15413 | 6263 | RYR3 | Ryanodine receptor 3 | Homo sapiens |
| PTMD09291 | Q8IVS8 | 13215 | GLYCTK | Glycerate kinase | Homo sapiens |