Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3035
Gene Symbol: HARS1
HARS1
CUI: C3281066
Disease: USHER SYNDROME, TYPE IIIB
USHER SYNDROME, TYPE IIIB 		0.710 GeneticVariation BEFREE The Usher Syndrome Type IIIB Histidyl-tRNA Synthetase Mutation Confers Temperature Sensitivity. 28632987

2017
Entrez Id: 3035
Gene Symbol: HARS1
HARS1
CUI: C3281066
Disease: USHER SYNDROME, TYPE IIIB
USHER SYNDROME, TYPE IIIB 		0.710 GeneticVariation UNIPROT Genetic mapping and exome sequencing identify variants associated with five novel diseases. 22279524

2012
Entrez Id: 3035
Gene Symbol: HARS1
HARS1
CUI: C3281066
Disease: USHER SYNDROME, TYPE IIIB
USHER SYNDROME, TYPE IIIB 		0.710 Biomarker GENOMICS_ENGLAND Genetic mapping and exome sequencing identify variants associated with five novel diseases. 22279524

2012
Entrez Id: 3035
Gene Symbol: HARS1
HARS1
CUI: C3281066
Disease: USHER SYNDROME, TYPE IIIB
USHER SYNDROME, TYPE IIIB 		0.710 Biomarker GENOMICS_ENGLAND A novel gene oriented in a head-to-head configuration with the human histidyl-tRNA synthetase (HRS) gene encodes an mRNA that predicts a polypeptide homologous to HRS. 7755634

1995
Entrez Id: 3035
Gene Symbol: HARS1
HARS1
CUI: C3281066
Disease: USHER SYNDROME, TYPE IIIB
USHER SYNDROME, TYPE IIIB 		0.710 CausalMutation CLINVAR

Entrez Id: 3035
Gene Symbol: HARS1
HARS1
CUI: C3281066
Disease: USHER SYNDROME, TYPE IIIB
USHER SYNDROME, TYPE IIIB 		0.710 Biomarker CTD_human

Entrez Id: 3035
Gene Symbol: HARS1
HARS1
CUI: C3281066
Disease: USHER SYNDROME, TYPE IIIB
USHER SYNDROME, TYPE IIIB 		0.710 GeneticVariation CLINVAR

Entrez Id: 23438
Gene Symbol: HARS2
HARS2
CUI: C3281066
Disease: USHER SYNDROME, TYPE IIIB
USHER SYNDROME, TYPE IIIB 		0.010 GeneticVariation BEFREE The Usher Syndrome Type IIIB Histidyl-tRNA Synthetase Mutation Confers Temperature Sensitivity. 28632987

2017