abnormal nerve fiber response Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the electrophysiological recordings from a single or several nerve fiber(s) (Mammalian Phenotype Ontology, MP_0003477)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003477
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14 gene mutations causing the abnormal nerve fiber response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
ENTPD2 ectonucleoside triphosphate diphosphohydrolase 2
FMR1 fragile X mental retardation 1
GJD2 gap junction protein, delta 2, 36kDa
GRM5 glutamate receptor, metabotropic 5
HMOX2 heme oxygenase 2
KCNA1 potassium channel, voltage gated shaker related subfamily A, member 1
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
KCNJ16 potassium channel, inwardly rectifying subfamily J, member 16
KCNMA1 potassium channel, calcium activated large conductance subfamily M alpha, member 1
PKD2L1 polycystic kidney disease 2-like 1
SLC32A1 solute carrier family 32 (GABA vesicular transporter), member 1
STOML3 stomatin (EPB72)-like 3
TACR1 tachykinin receptor 1