paperKB
coga / coga-kb
Help
Sign in

Chunk #25 — Results — Overlap of Enriched Pathways Between CNV and SNP Data

Source
Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.
Embedded
yes

Text

The exception to this was CHRNA7, which is a member of the Gene Ontology (GO) categories “cation channel activity” (GO:5261; case CNV hits enrichment p=0.0184, GWAS enrichment p=0.042), “channel regulator activity” (GO:16247; p=0.0307, p=0.026), and “regulation of tumor necrosis factor production” (GO:32680; p=0.0088, p=0.014). CHRNA7 was affected by six duplications in case subjects but none in comparison subjects (p=9.08×10–4) and had a Simes-corrected gene-wide p value of 0.0002 from the GWAS.