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Fig. 5 | Hereditas

Fig. 5

From: An Axin2 mutation and perinatal risk factors contribute to sagittal craniosynostosis: evidence from a Chinese female monochorionic diamniotic twin family

Fig. 5

modified by H3K4Me3 or H3K27Ac in seven cell lines by ChIP-Seq assay. b Location of Arg394 residues within the GSK3β binding domain of AXIN2. c Location of the His 394 residues within the GSK3β binding domain of AXIN2. Arrowheads indicate the hydrogen bond in the domain

Functional annotation and structural analysis and of AXIN2 (c.1181G > A: p.R394H, rs200899695). a UCSC database predicted that wild type AXIN2 (c.1181G) loci locates in the region

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Hereditas

ISSN: 1601-5223

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