Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 374462
Gene Symbol: PTPRQ
PTPRQ 		0.710 Biomarker disease GENOMICS_ENGLAND Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunction. 20346435 2010
Entrez Id: 374462
Gene Symbol: PTPRQ
PTPRQ 		0.710 Biomarker disease BEFREE Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84. 20472657 2010
Entrez Id: 374462
Gene Symbol: PTPRQ
PTPRQ 		0.710 GeneticVariation disease UNIPROT Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunction. 20346435 2010
Entrez Id: 374462
Gene Symbol: PTPRQ
PTPRQ 		0.710 GeneticVariation disease UNIPROT Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84. 20472657 2010
Entrez Id: 374462
Gene Symbol: PTPRQ
PTPRQ 		0.710 CausalMutation disease CLINVAR
Entrez Id: 374462
Gene Symbol: PTPRQ
PTPRQ 		0.710 Biomarker disease CTD_human
Entrez Id: 64072
Gene Symbol: CDH23
CDH23 		0.100 CausalMutation disease CLINVAR