Varaico: Literature-Extracted Genetic Variants

Gene:GPR37
Variant:p.R558Q
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GPR37

NM_005302.5:p.R558Q

Associated Papers

Role and regulatory mechanism of GPR37 in neurological diseases.

Liu S et al.

Frontiers in Cellular Neuroscience, 2025

Single nucleotide variations encoding missense mutations in G protein-coupled receptors may contribute to autism.

van der Westhuizen ET

British Journal of Pharmacology, 2024

Intragenic CNTNAP2 Deletions: A Bridge Too Far?

Poot M

Molecular Syndromology, 2017

CASPR2 forms a complex with GPR37 via MUPP1 but not with GPR37(R558Q), an autism spectrum disorder-related mutation.

Tanabe Y et al.

Journal of Neurochemistry, 2015

Mutation in Parkinson disease-associated, G-protein-coupled receptor 37 (GPR37/PaelR) is related to autism spectrum disorder.

Fujita-Jimbo E et al.

Plos One, 2012

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."