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Table 3 Genes, which are up- or downregulated in human or model system without functional MECP2

From: Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes

Changes in RTT

Genes

Upregulated [25, 89, 90]

BDNF, FKBP5, IGF2, DLX5, DLX6, SGK1, MPP1, GAMT, FXYD1

Downregulated [25, 83]

UBE3A, GRID1

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172