Gene: DMXL2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23312
Gene Symbol: DMXL2
DMXL2 		0.300 Biomarker disease CLINGEN A dominant variant in DMXL2 is linked to nonsyndromic hearing loss. 27657680 2017
Entrez Id: 23312
Gene Symbol: DMXL2
DMXL2 		0.300 Biomarker disease CLINGEN Rabconnectin3α promotes stable activity of the H+ pump on synaptic vesicles in hair cells. 22875945 2012