Gene: RBP4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5950
Gene Symbol: RBP4
RBP4 		0.320 GeneticVariation disease BEFREE Bi-allelic mutations in RBP4 were identified (c.248+1G>A), consistent with a diagnosis of inherited vitamin A deficiency. 27892788 2017
Entrez Id: 5950
Gene Symbol: RBP4
RBP4 		0.320 Biomarker disease BEFREE Ret heterozygosity increases the incidence and severity of distal bowel aganglionosis induced by vitamin A deficiency in Rbp4(-/-) animals. 20110328 2010
Entrez Id: 5950
Gene Symbol: RBP4
RBP4 		0.320 Biomarker disease CTD_human Biochemical basis for retinol deficiency induced by the I41N and G75D mutations in human plasma retinol-binding protein. 16157297 2005