FIGURE

Fig. 1

ID

ZDB-FIG-200429-15

Publication

Tessadori et al., 2019 - A de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorder

Other Figures

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Fig. 1

De novo missense variant identified in HIST1H4J. a Pedigree and photographs of the proband. The tilted square refers to unspecified sex. b Location of the de novo missense variant at gene and protein level and alignment of H4 residues demonstrating that K91 as well as surrounding residues are highly conserved across species. At the genomic level, this A > G substitution is located at chr6:27792176 (hg19). See main text for more information on the nomenclature

Expression Data

Expression Detail

Antibody Labeling

Phenotype Data

Phenotype Detail

Acknowledgments

This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Eur. J. Hum. Genet.