Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23395
Gene Symbol: LARS2
LARS2 		0.600 CausalMutation disease CLINVAR First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family. 26657938 2016
Entrez Id: 23395
Gene Symbol: LARS2
LARS2 		0.600 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 23395
Gene Symbol: LARS2
LARS2 		0.600 GeneticVariation disease UNIPROT Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome. 23541342 2013
Entrez Id: 23395
Gene Symbol: LARS2
LARS2 		0.600 Biomarker disease GENOMICS_ENGLAND Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome. 23541342 2013
Entrez Id: 23395
Gene Symbol: LARS2
LARS2 		0.600 Biomarker disease GENOMICS_ENGLAND Human/mouse microcell hybrid based elimination test reduces the putative tumor suppressor region at 3p21.3 to 1.6 cM. 9408748 1997
Entrez Id: 23395
Gene Symbol: LARS2
LARS2 		0.600 GeneticVariation disease CLINVAR
Entrez Id: 8192
Gene Symbol: CLPP
CLPP 		0.200 Biomarker disease MGD Loss of mitochondrial peptidase Clpp leads to infertility, hearing loss plus growth retardation via accumulation of CLPX, mtDNA and inflammatory factors. 23851121 2013