benign familial infantile epilepsy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An infancy electroclinical syndrome that is characterized by convulsions, with onset at age 3 to 12 months. (Human Disease Ontology, DOID_0060169)
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Genes

15 genes co-occuring with the disease benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PRRT2 proline-rich transmembrane protein 2 3.17639
TMEM2 transmembrane protein 2 1.91734
SCN2A sodium channel, voltage gated, type II alpha subunit 1.72958
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2 1.62336
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3 1.55336
KCNT1 potassium channel, sodium activated subfamily T, member 1 1.32629
VRK2 vaccinia related kinase 2 1.24645
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide 1.13966
PNPO pyridoxamine 5'-phosphate oxidase 1.13374
PNKD paroxysmal nonkinesigenic dyskinesia 1.02566
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide 0.998658
SCN3A sodium channel, voltage gated, type III alpha subunit 0.986849
SCN8A sodium channel, voltage gated, type VIII alpha subunit 0.926692
SCN1A sodium channel, voltage gated, type I alpha subunit 0.494648
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1 0.406051