Gene: PTPRQ ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 374462
Gene Symbol: PTPRQ
PTPRQ 		0.020 GeneticVariation disease BEFREE Autosomal Recessive Congenital Sensorineural Hearing Loss due to a Novel Compound Heterozygous PTPRQ Mutation in a Chinese Family. 29849575 2018
Entrez Id: 374462
Gene Symbol: PTPRQ
PTPRQ 		0.020 GeneticVariation disease BEFREE We present 3 patients with congenital sensorineural hearing loss (SNHL) caused by novel PTPRQ mutations, including clinical manifestations and phenotypic features. 25788564 2015