Gene: HARS2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23438
Gene Symbol: HARS2
HARS2 		0.700 GeneticVariation disease UNIPROT Novel HARS2 missense variants identified in individuals with sensorineural hearing impairment and Perrault syndrome. 31449985 2020
Entrez Id: 23438
Gene Symbol: HARS2
HARS2 		0.700 Biomarker disease CLINGEN Laser-capture micro dissection combined with next-generation sequencing analysis of cell type-specific deafness gene expression in the mouse cochlea. 28263850 2017
Entrez Id: 23438
Gene Symbol: HARS2
HARS2 		0.700 Biomarker disease CLINGEN An Application of NGS for Molecular Investigations in Perrault Syndrome: Study of 14 Families and Review of the Literature. 27650058 2016
Entrez Id: 23438
Gene Symbol: HARS2
HARS2 		0.700 Biomarker disease GENOMICS_ENGLAND An Application of NGS for Molecular Investigations in Perrault Syndrome: Study of 14 Families and Review of the Literature. 27650058 2016
Entrez Id: 23438
Gene Symbol: HARS2
HARS2 		0.700 GeneticVariation disease UNIPROT Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. 21464306 2011
Entrez Id: 23438
Gene Symbol: HARS2
HARS2 		0.700 GeneticVariation disease CLINVAR Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. 21464306 2011
Entrez Id: 23438
Gene Symbol: HARS2
HARS2 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. 21464306 2011
Entrez Id: 23438
Gene Symbol: HARS2
HARS2 		0.700 Biomarker disease CLINGEN Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. 21464306 2011
Entrez Id: 23438
Gene Symbol: HARS2
HARS2 		0.700 CausalMutation disease CLINVAR