Gene: TPRKB ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51002
Gene Symbol: TPRKB
TPRKB 		0.600 Biomarker disease GENOMICS_ENGLAND A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report. 30053862 2018
Entrez Id: 51002
Gene Symbol: TPRKB
TPRKB 		0.600 Biomarker disease GENOMICS_ENGLAND Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly. 28805828 2017
Entrez Id: 51002
Gene Symbol: TPRKB
TPRKB 		0.600 GeneticVariation disease UNIPROT Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly. 28805828 2017
Entrez Id: 51002
Gene Symbol: TPRKB
TPRKB 		0.600 CausalMutation disease CLINVAR