rs2445689

This is a downstream gene variant variant in the NEU1 gene.

GWAS Catalog Trait Associations (2)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

heat shock 70 kDa protein 1A measurement

Allele A
OR 0.05
p 2.0e-14
N 47,745
Large GWAS
European

non-receptor tyrosine-protein kinase TYK2 measurement

Allele A
OR 0.20
p 1.0e-11
N 2,935
Large GWAS
Greater Middle Eastern (Middle Eastern, North African or Persian)

About NEU1

The protein encoded by this gene is a lysosomal enzyme that cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids. In the lysosome, this enzyme is part of a heterotrimeric complex together with beta-galactosidase and cathepsin A (the latter is also referred to as 'protective protein'). Mutations in this gene can lead to sialidosis, a lysosomal storage disease that can be type 1 (cherry red spot-myoclonus syndrome or normosomatic type), which is late-onset, or type 2 (the dysmorphic type), which occurs at an earlier age with increased severity. [provided by RefSeq, Jul 2008]

View all NEU1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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