abnormal brain wave pattern Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the standard pattern of rhythmic and rapid fluctuation of electrical potential between parts of the brain, often visualized on an electroencephalogram (EEG); the pattern is often measured to diagnose neurological conditions such as seizure disorders (epilepsy) (Mammalian Phenotype Ontology, MP_0004994)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004994
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Genes

43 gene mutations causing the abnormal brain wave pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH5A1 aldehyde dehydrogenase 5 family, member A1
AP3D1 adaptor-related protein complex 3, delta 1 subunit
ARX aristaless related homeobox
BSN bassoon presynaptic cytomatrix protein
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CACNA2D2 calcium channel, voltage-dependent, alpha 2/delta subunit 2
CACNB4 calcium channel, voltage-dependent, beta 4 subunit
CACNG2 calcium channel, voltage-dependent, gamma subunit 2
CHRM3 cholinergic receptor, muscarinic 3
CHRNA4 cholinergic receptor, nicotinic, alpha 4 (neuronal)
CNTNAP2 contactin associated protein-like 2
CSTB cystatin B (stefin B)
ELAVL3 ELAV like neuron-specific RNA binding protein 3
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
FOXO6 forkhead box O6
GABBR2 gamma-aminobutyric acid (GABA) B receptor, 2
GABRG2 gamma-aminobutyric acid (GABA) A receptor, gamma 2
GAD1 glutamate decarboxylase 1 (brain, 67kDa)
GIT1 G protein-coupled receptor kinase interacting ArfGAP 1
GJD2 gap junction protein, delta 2, 36kDa
KCNA1 potassium channel, voltage gated shaker related subfamily A, member 1
KCNA2 potassium channel, voltage gated shaker related subfamily A, member 2
KCNC2 potassium channel, voltage gated Shaw related subfamily C, member 2
LGI1 leucine-rich, glioma inactivated 1
MECP2 methyl CpG binding protein 2
NEUROD1 neuronal differentiation 1
NOS1 nitric oxide synthase 1 (neuronal)
NOS2 nitric oxide synthase 2, inducible
NPAS2 neuronal PAS domain protein 2
PCMT1 protein-L-isoaspartate (D-aspartate) O-methyltransferase
PER1 period circadian clock 1
PER3 period circadian clock 3
RAI1 retinoic acid induced 1
RYR2 ryanodine receptor 2 (cardiac)
S1PR2 sphingosine-1-phosphate receptor 2
SCN10A sodium channel, voltage gated, type X alpha subunit
SCN1A sodium channel, voltage gated, type I alpha subunit
SCN1B sodium channel, voltage gated, type I beta subunit
SLC17A8 solute carrier family 17 (vesicular glutamate transporter), member 8
SLC2A3 solute carrier family 2 (facilitated glucose transporter), member 3
SSTR1 somatostatin receptor 1
SSTR2 somatostatin receptor 2
UBE3A ubiquitin protein ligase E3A