Varaico: Literature-Extracted Genetic Variants

Gene:RTN4R
Variant:p.R196H
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RTN4R

NM_023004.6:p.R196H

Associated Papers

Genomic and Reverse Translational Analysis Discloses a Role for Small GTPase RhoA Signaling in the Pathogenesis of Schizophrenia: Rho-Kinase as a Novel Drug Target.

Tanaka R et al.

International Journal of Molecular Sciences, 2023

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

Tracking Neoantigens by Personalized Circulating Tumor DNA Sequencing during Checkpoint Blockade Immunotherapy in Non-Small Cell Lung Cancer.

Jia Q et al.

Advanced Science (weinheim, Baden-wurttemberg, Germany), 2020

32382482 (PubMed )
Supplement: ADVS-7-1903410-s005.xlsx › P7

A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility.

Kimura H et al.

Translational Psychiatry, 2017

Genetic variants in Nogo receptor signaling pathways may be associated with early life adversity in schizophrenia susceptibility.

Andrews JL et al.

Bba Clinical, 2015

Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.

Budel S et al.

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience, 2008

Nogo Receptor 1 (RTN4R) as a candidate gene for schizophrenia: analysis using human and mouse genetic approaches.

Hsu R et al.

Plos One, 2007

Structural analysis of leucine-rich-repeat variants in proteins associated with human diseases.

Matsushima N et al.

Cellular and Molecular Life Sciences : Cmls, 2005

Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia.

Sinibaldi L et al.

Human Mutation, 2004

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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."