Genetic variation features of neonatal hyperbilirubinemia caused by inherited diseases

Figure 1 Results for the percentage of mutated genes in 105 patients. UGT1A1: Uridine 5'-diphospho-glucuronosyltransferase 1A1; SLC10A1: Na+/taurocholate cotransporting polypeptide Ntcp; SLC25A13: Heterozygous 851del4 mutation; ATP7B: Adenosine triphosphatase 7B; JAG1: Jagged 1; NPC1: Niemann-Pick type C 1; ABCC2: Adenosine triphosphatase-binding cassette subfamily C member 2; G6PD: Glucose-6-phosphate dehydrogenase.

Figure 2 Analysis of the percentage of genes between the high and low total serum bilirubin groups. The blue bars represent the high-risk group with a total bilirubin level greater than 342 μmol/L. The orange bars correspond to the high-risk group with a total bilirubin level of less than 342 μmol/L. UGT1A1: Uridine 5'-diphospho-glucuronosyltransferase 1A1; SLC10A1: Na+/taurocholate cotransporting polypeptide Ntcp; SLC25A13: Heterozygous 851del4 mutation; ATP7B: Adenosine triphosphatase 7B; G6PD: Glucose-6-phosphate dehydrogenase.