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Table 3 Candidate genes identified in multi-omics analysis of patients with RTT and with a concordant alteration at the protein level in patients with RTT-like phenotypes

From: Identification of molecular signatures and pathways involved in Rett syndrome using a multi-omics approach

Gene

Direction

Biological process

Potential TF

ARMC9

Upregulated

Cytoskeletal processes

SRF

DDX31

Downregulated

RNA processing

CREB1, SRF

DDX54

Downregulated

RNA processing

SRF

MYBBP1A

Downregulated

RNA processing

SRF

COMT

Downregulated

Metabolism

CREB1

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Human Genomics

ISSN: 1479-7364