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. Author manuscript; available in PMC: 2018 Aug 10.
Published in final edited form as: Exp Neurol. 2016 Jun 23;283(Pt A):375–395. doi: 10.1016/j.expneurol.2016.06.023

Table 4.

Transcriptional profiline of pain channelopathy genes

Gene name Protein name Pain phenotype(s) Trpv1 Enriched Trpv1 depleted DRG Sciatic DRG Tibial

Mouse     Rat     Human    

SCN10A Nav1.8 Gain of function: painful neuropathy 214.8 59.7 79.2 0.0 26.8 0.0
SCN11A Nav1.9 Gain of function: HSAN7, insensitivity to pain 169.2 16.4 59.5 0.0 91.9 0.3
TRPV1 TRPV1 SNPs correlate with neuropathic pain, migraine.
Loss of function causes insensitivity to capsaicin.
Gain of function painful.
151.2 1.3 31.5 2.5 39.1 0.6
SCN9A Nav1.7 Loss of function: insensitivity to pain
Gain of function: paroxysmal extreme pain disorder, small fiber neuropathy, erythermalgia, HSAN2D
53.9 31.1 44.2 1.7 40.6 3.1
TRPA1 TRPA1 Gain of function: familial episodic pain syndrome 23.6 0.9 14.4 0.2 9.7 0.0

Abbreviations: HSAN - hereditary sensory and autonomic neuropathy; SNP - single nucleotide polymorphism.