rs6494223

This variant is located in the CHRNA7 gene.

Research that mentions this SNP (1)

Sex and ESR1 genotype may influence the response to treatment with donepezil and rivastigmine in patients with Alzheimer's disease
ReviewRenato Scacchi et al.(2014)· International Journal of Geriatric Psychiatry

This is a comprehensive review of genetic and biological determinants of acetylcholinesterase inhibitor (ChEI) response in Alzheimer's disease and other neurodegenerative diseases. The paper discusses how genetic variants in APOE (particularly the ε4 allele, which increases LOAD risk 3-15-fold), cholinergic system genes (CHRNA7, CHRFAM7A), and drug-metabolizing enzymes (CYP2D6, CYP3A4) influence both cholinergic homeostasis and clinical response to ChEI therapy, with emphasis on precision medicine approaches for patient stratification.

Traits studied:Acetylcholinesterase inhibitor responseAlzheimer's diseaseCognitive declineDementia with Lewy bodiesFrontotemporal lobar degenerationLate-onset Alzheimer's disease (LOAD)Mild cognitive impairmentParkinson's disease dementia

About CHRNA7

The nicotinic acetylcholine receptors (nAChRs) are members of a superfamily of ligand-gated ion channels that mediate fast signal transmission at synapses. The nAChRs are thought to be hetero-pentamers composed of homologous subunits. The proposed structure for each subunit is a conserved N-terminal extracellular domain followed by three conserved transmembrane domains, a variable cytoplasmic loop, a fourth conserved transmembrane domain, and a short C-terminal extracellular region. The protein encoded by this gene forms a homo-oligomeric channel, displays marked permeability to calcium ions and is a major component of brain nicotinic receptors that are blocked by, and highly sensitive to, alpha-bungarotoxin. Once this receptor binds acetylcholine, it undergoes an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. This gene is located in a region identified as a major susceptibility locus for juvenile myoclonic epilepsy and a chromosomal location involved in the genetic transmission of schizophrenia. An evolutionarily recent partial duplication event in this region results in a hybrid containing sequence from this gene and a novel FAM7A gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]

View all CHRNA7 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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