abnormal channel response Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomalies in the electrophysiological recordings from ion channels (Mammalian Phenotype Ontology, MP_0003484)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003484
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Genes

24 gene mutations causing the abnormal channel response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARPP21 cAMP-regulated phosphoprotein, 21kDa
BACE1 beta-site APP-cleaving enzyme 1
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CACNA1B calcium channel, voltage-dependent, N type, alpha 1B subunit
CACNA1E calcium channel, voltage-dependent, R type, alpha 1E subunit
CACNA1H calcium channel, voltage-dependent, T type, alpha 1H subunit
CACNA2D1 calcium channel, voltage-dependent, alpha 2/delta subunit 1
CACNB3 calcium channel, voltage-dependent, beta 3 subunit
CHRNA3 cholinergic receptor, nicotinic, alpha 3 (neuronal)
DPP6 dipeptidyl-peptidase 6
GLRA1 glycine receptor, alpha 1
GNAO1 guanine nucleotide binding protein (G protein), alpha activating activity polypeptide O
HCN2 hyperpolarization activated cyclic nucleotide gated potassium channel 2
IL6ST interleukin 6 signal transducer
KCNA2 potassium channel, voltage gated shaker related subfamily A, member 2
KCNA5 potassium channel, voltage gated shaker related subfamily A, member 5
KCND2 potassium channel, voltage gated Shal related subfamily D, member 2
KCNIP3 Kv channel interacting protein 3, calsenilin
NALCN sodium leak channel, non selective
PTPRE protein tyrosine phosphatase, receptor type, E
SCN11A sodium channel, voltage gated, type XI alpha subunit
SLC8A3 solute carrier family 8 (sodium/calcium exchanger), member 3
TRPM1 transient receptor potential cation channel, subfamily M, member 1
TRPM7 transient receptor potential cation channel, subfamily M, member 7