FIGURE
FIGURE 1
- ID
- ZDB-FIG-221211-34
- Publication
- Solman et al., 2022 - Modeling (not so) rare developmental disorders associated with mutations in the protein-tyrosine phosphatase SHP2
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FIGURE 1
Distribution of PTPN11 genetic variants associated with rare diseases. Schematic overview of the exonic structure of PTPN11, consisting of 15 exons (above) and the encoded protein SHP2 (below) with two SH2 domains and the catalytic PTP domain. Frequently occurring mutations are indicated color-coded corresponding to the boxes with the 2–4 most frequently occurring mutations highlighted. Created using BioRender (BioRender.com). |
Expression Data
Expression Detail
Antibody Labeling
Phenotype Data
Phenotype Detail
Acknowledgments
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Full text @ Front Cell Dev Biol