FIGURE

Fig. 5

ID

ZDB-FIG-220623-67

Publication

Silvennoinen et al., 2022 - SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility

Other Figures

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7

All Figure Page

Back to All Figure Page

Fig. 5

a Transcription start sites (TSSs) identified by the FANTOM5 project, located upstream of the SCN1A gene body. Six TSSs fell within two of the three SCN1A promoters and one TSS was located 981 bp away from rs7587026. b X-axis: genetic positions on chromosome 2, Y-axis: genetic elements that were considered

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 @ Acta Neuropathol.