abnormal single cell response Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description altered values from controls obtained upon extra- or intracellular recordings from single cells (Mammalian Phenotype Ontology, MP_0003463)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003463
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Genes

23 gene mutations causing the abnormal single cell response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCY8 adenylate cyclase 8 (brain)
CACNA1B calcium channel, voltage-dependent, N type, alpha 1B subunit
CACNA1G calcium channel, voltage-dependent, T type, alpha 1G subunit
CLOCK clock circadian regulator
CNGB1 cyclic nucleotide gated channel beta 1
CREB1 cAMP responsive element binding protein 1
DAGLA diacylglycerol lipase, alpha
DRD2 dopamine receptor D2
DRD4 dopamine receptor D4
GJD2 gap junction protein, delta 2, 36kDa
GLRA1 glycine receptor, alpha 1
GLRA2 glycine receptor, alpha 2
GRIK2 glutamate receptor, ionotropic, kainate 2
GRIN3A glutamate receptor, ionotropic, N-methyl-D-aspartate 3A
KCNA2 potassium channel, voltage gated shaker related subfamily A, member 2
KCNH3 potassium channel, voltage gated eag related subfamily H, member 3
KCNN2 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 2
MRGPRD MAS-related GPR, member D
P2RX3 purinergic receptor P2X, ligand gated ion channel, 3
SCN10A sodium channel, voltage gated, type X alpha subunit
SCN11A sodium channel, voltage gated, type XI alpha subunit
SLC17A7 solute carrier family 17 (vesicular glutamate transporter), member 7
TRPC1 transient receptor potential cation channel, subfamily C, member 1