Skip to main content
Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: A recurrent ABCC2 p.G693R mutation resulting in loss of function of MRP2 and hyperbilirubinemia in Dubin-Johnson syndrome in China

Fig. 1

Mutation analysis of the two DJS cases with ABCC2 p.G693R. a Sequencing of the heterozygous missense mutation c.2190G > A, p.G693R in exon 16 in both cases. b Aligned amino acid sequences of human, rhesus, mouse, dog, elephant, chicken, xenopus tropicalis, zebrafish, and lamprey MRP2 with mutation p.G693R flanking regions. The position of the p.G693R mutation is indicated by the red box. Alignment was performed by http://genome.ucsc.edu/

Back to article page

Orphanet Journal of Rare Diseases

ISSN: 1750-1172