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 		0.400 Biomarker disease GENOMICS_ENGLAND Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course. 31688942 2019
Entrez Id: 23312
Gene Symbol: DMXL2
DMXL2 		0.400 Biomarker disease GENOMICS_ENGLAND A dominant variant in DMXL2 is linked to nonsyndromic hearing loss. 27657680 2017
Entrez Id: 23312
Gene Symbol: DMXL2
DMXL2 		0.400 Biomarker disease GENOMICS_ENGLAND Haploinsufficiency of Dmxl2, encoding a synaptic protein, causes infertility associated with a loss of GnRH neurons in mouse. 25248098 2014
Entrez Id: 23312
Gene Symbol: DMXL2
DMXL2 		0.400 Biomarker disease GENOMICS_ENGLAND Rabconnectin3α promotes stable activity of the H+ pump on synaptic vesicles in hair cells. 22875945 2012
Entrez Id: 23312
Gene Symbol: DMXL2
DMXL2 		0.400 Biomarker disease HPO