Skip to main content
Fig. 4 | Journal of Neurodevelopmental Disorders

Fig. 4

From: Transcriptomic profiling of unmethylated full mutation carriers implicates TET3 in FMR1 CGG repeat expansion methylation dynamics in fragile X syndrome

Fig. 4

TET3 variants and expression in the general population. (a) Genomic variants for TET3 for both UFM cell lines in the TET3 locus ~ 600 kb showing the genes, TET3 eQTLs and SNPs found in both UFM carriers with a MAF < 0.01 (b) The 4 SNPs in or adjacent to TET3, showing 2 in the introns, one in the 3’UTR and one just downstream. The Genotypes for UFM1/UFM2 are written below the SNP names (e.g. T/C, T/C)

Back to article page

Journal of Neurodevelopmental Disorders

ISSN: 1866-1955

Contact us