rs7177008

This is a downstream gene variant variant in the LINGO1 gene.

Research that mentions this SNP (2)

Role of LINGO1 polymorphisms in Parkinson's disease
AssociationN=694Dietrich Haubenberger et al.(2009)· Movement Disorders

This case-control study examined whether LINGO1 gene variants (rs9652490, rs11856808, rs7177008) associated with essential tremor also confer risk for Parkinson's disease in an Austrian population of 349 PD patients and 345 controls. No significant associations were found between any LINGO1 SNP genotypes or alleles and PD (rs9652490 p=0.61), nor in the subgroup of tremor-dominant PD patients (n=34, p=0.76). The findings argue against a major role of LINGO1 variants in PD susceptibility despite the documented clinical overlap between the two disorders.

Traits studied:Essential tremorParkinson's disease
Alpha‐synuclein polymorphisms are associated with Parkinson's disease in a Saskatchewan population
AssociationN=694Alex Rajput et al.(2009)· Movement Disorders

This case-control study investigated whether LINGO1 gene polymorphisms associated with essential tremor also confer risk for Parkinson's disease (PD). Three SNPs (rs9652490, rs11856808, rs7177008) were genotyped in 349 PD patients and 345 controls from Austria. No significant associations were found between any LINGO1 variants and PD risk overall (p=0.61 for rs9652490) or in tremor-dominant PD patients, arguing against a major role of LINGO1 variants in PD susceptibility.

Traits studied:Essential tremorParkinson's diseaseTremor-dominant Parkinson's disease

About LINGO1

Predicted to enable epidermal growth factor receptor binding activity. Predicted to act upstream of or within negative regulation of oligodendrocyte differentiation; negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction; and neuron development. Predicted to be located in plasma membrane. Predicted to be active in several cellular components, including extracellular space; glutamatergic synapse; and presynapse. Implicated in autosomal recessive intellectual developmental disorder 64 and glaucoma. [provided by Alliance of Genome Resources, Jul 2025]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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