Gene: TJP2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9414
Gene Symbol: TJP2
TJP2 		0.710 Biomarker disease GENOMICS_ENGLAND Genetic analysis of genes related to tight junction function in the Korean population with non-syndromic hearing loss. 24752540 2014
Entrez Id: 9414
Gene Symbol: TJP2
TJP2 		0.710 GermlineCausalMutation disease ORPHANET Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT. 12704386 2003
Entrez Id: 9414
Gene Symbol: TJP2
TJP2 		0.710 GeneticVariation disease UNIPROT Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT. 12704386 2003
Entrez Id: 9414
Gene Symbol: TJP2
TJP2 		0.710 GeneticVariation disease BEFREE Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT. 12704386 2003
Entrez Id: 9414
Gene Symbol: TJP2
TJP2 		0.710 GeneticVariation disease CLINVAR
Entrez Id: 9414
Gene Symbol: TJP2
TJP2 		0.710 CausalMutation disease CLINVAR
Entrez Id: 9414
Gene Symbol: TJP2
TJP2 		0.710 Biomarker disease CTD_human