Gene: SLC12A6 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9990
Gene Symbol: SLC12A6
SLC12A6 		0.220 Biomarker group BEFREE Among them, KCC3 has been the subject of great attention in view of its important role in the nervous system and its association with a rare hereditary sensorimotor neuropathy (called Andermann syndrome) that affects many individuals in Quebec province (Canada). 28814402 2017
Entrez Id: 9990
Gene Symbol: SLC12A6
SLC12A6 		0.220 GeneticVariation group BEFREE We hypothesize that mutations of the KCC3 gene may result in non-syndromic childhood onset HMSN. 20020398 2009
Entrez Id: 9990
Gene Symbol: SLC12A6
SLC12A6 		0.220 Biomarker group MGD Loss of K-Cl co-transporter KCC3 causes deafness, neurodegeneration and reduced seizure threshold. 14532115 2003
Entrez Id: 9990
Gene Symbol: SLC12A6
SLC12A6 		0.220 Biomarker group MGD The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum. 12368912 2002