Varaico: Literature-Extracted Genetic Variants

Gene:GRM6
Variant:p.P46L
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GRM6

NM_000843.4:p.P46L

Associated Papers

Defective glycosylation and ELFN1 binding of mGluR6 congenital stationary night blindness mutants.

Pindwarawala M et al.

Life Science Alliance, 2025

Congenital Stationary Night Blindness: Structure, Function and Genotype-Phenotype Correlations in a Cohort of 122 Patients.

Katta M et al.

Ophthalmology. Retina, 2024

38522615 (PubMed )
Supplement: mmc11.pdf

Compound heterozygous mutations in GRM6 causing complete Schubert-Bornschein type congenital stationary night blindness.

Bai D et al.

Heliyon, 2024

Z-flipon variants reveal the many roles of Z-DNA and Z-RNA in health and disease.

Umerenkov D et al.

Life Science Alliance, 2023

37164635 (PubMed )
Supplement: LSA-2023-01962_TableS6.xlsx › Experimental_by_OMIM

The mGluR6 ligand-binding domain, but not the C-terminal domain, is required for synaptic localization in retinal ON-bipolar cells.

Agosto MA et al.

The Journal of Biological Chemistry, 2021

34793838 (PubMed )
Supplement: mmc1.pdf

Pseudodominant inheritance of autosomal recessive congenital stationary night blindness in one family with three co-segregating deleterious GRM6 variants identified by next-generation sequencing.

Liu HY et al.

Molecular Genetics & Genomic Medicine, 2019

Characterization of Disease-Associated Mutations in Human Transmembrane Proteins.

Molnár J et al.

Plos One, 2016

26986070 (PubMed )
Supplement: pone.0151760.s001.xlsx › disease

A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene.

Sergouniotis PI et al.

Acta Ophthalmologica, 2012

Altered G-protein coupling in an mGluR6 point mutant associated with congenital stationary night blindness.

Beqollari D et al.

Molecular Pharmacology, 2009

Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein trafficking.

Zeitz C et al.

Human Mutation, 2007

Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.

Zeitz C et al.

Investigative Ophthalmology & Visual Science, 2005

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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."