early myoclonic encephalopathy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

22 genes co-occuring with the disease early myoclonic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SLC25A22 solute carrier family 25 (mitochondrial carrier: glutamate), member 22 1.62157
STXBP1 syntaxin binding protein 1 1.50623
SLC1A6 solute carrier family 1 (high affinity aspartate/glutamate transporter), member 6 1.24428
GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1 1.20137
GLDC glycine dehydrogenase (decarboxylating) 1.17894
SPTAN1 spectrin, alpha, non-erythrocytic 1 1.11141
SPTBN2 spectrin, beta, non-erythrocytic 2 1.09965
SUOX sulfite oxidase 1.069
ITPR3 inositol 1,4,5-trisphosphate receptor, type 3 1.04251
ERBB4 erb-b2 receptor tyrosine kinase 4 0.979268
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1 0.973801
CDKL5 cyclin-dependent kinase-like 5 0.954108
SLC1A3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 0.808129
CYLD cylindromatosis (turban tumor syndrome) 0.784345
TPH1 tryptophan hydroxylase 1 0.656837
NRG1 neuregulin 1 0.644192
POMC proopiomelanocortin 0.632777
MNX1 motor neuron and pancreas homeobox 1 0.531928
PIGA phosphatidylinositol glycan anchor biosynthesis, class A 0.458619
NPY neuropeptide Y 0.354499
TH tyrosine hydroxylase 0.230409
TRH thyrotropin-releasing hormone 0.214975