Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5087
Gene Symbol: PBX1
PBX1 		0.410 GeneticVariation disease BEFREE PBX1 is an essential developmental transcription factor, mutations in which have recently been associated with CAKUTHED syndrome, characterised by multiple congenital defects including congenital heart disease. 31625560 2019
Entrez Id: 5087
Gene Symbol: PBX1
PBX1 		0.410 Biomarker disease GENOMICS_ENGLAND PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans. 28270404 2017
Entrez Id: 5087
Gene Symbol: PBX1
PBX1 		0.410 CausalMutation disease CLINVAR
Entrez Id: 5087
Gene Symbol: PBX1
PBX1 		0.410 GeneticVariation disease CLINVAR