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Fig. 6 | BMC Medical Genetics

Fig. 6

From: A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family

Fig. 6

Bioinformatic analysis of the HOXD13 duplication variation (c.183_206dup). a, Conservation analysis of HOXD13 using Aminode showed that polyalanine tract (p.57–71) of the HOXD13 protein is conserved among different species. b, Protein structure of HOXD13 wild type (p.57–71) and mutant type (p.57–71 plus 8 aa) showed that duplication variation locally affected the shape and size of HOXD13 protein, the images were created using SWISS-MODEL (www.swissmodel.expasy.org/)

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