Gene: SCN11A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 11280
Gene Symbol: SCN11A
SCN11A 		0.040 Biomarker disease BEFREE Gain-of-function variants in Nav1.9, which cause smaller depolarizations of RMP, have been identified in patients with familial episodic pain type 3 (FEPS3) and the more common pain disorder small fiber neuropathy. 31551682 2019
Entrez Id: 11280
Gene Symbol: SCN11A
SCN11A 		0.040 GeneticVariation disease BEFREE The mouse model developed here will be useful for drug screening for familial episodic pain syndrome associated with SCN11A mutations. 27224030 2016
Entrez Id: 11280
Gene Symbol: SCN11A
SCN11A 		0.040 GeneticVariation disease BEFREE Gain-of-function mutations in the human SCN11A-encoded voltage-gated Na(+) channel NaV1.9 cause severe pain disorders ranging from neuropathic pain to congenital pain insensitivity. 26645915 2015
Entrez Id: 11280
Gene Symbol: SCN11A
SCN11A 		0.040 GeneticVariation disease BEFREE Taken together, our results suggest that gain-of-function mutations in SCN11A can be causative of an autosomal-dominant episodic pain disorder. 24207120 2013