Varaico: Literature-Extracted Genetic Variants

Gene:RARA
Variant:p.R83H
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RARA

NM_000964.4:p.R83H

Associated Papers

Shared and divergent contribution of vitamin A and oxytocin to the aetiology of autism spectrum disorder.

Wang T et al.

Computational and Structural Biotechnology Journal, 2023

38213898 (PubMed )
Supplement: mmc2.xlsx › DNMs_in_VARGs

Neoantigen-reactive T cells exhibit effective anti-tumor activity against colorectal cancer.

Yu Y et al.

Human Vaccines & Immunotherapeutics, 2022

Exploring the biological role of postzygotic and germinal de novo mutations in ASD.

Alonso-Gonzalez A et al.

Scientific Reports, 2021

33431980 (PubMed )
Supplement: 41598_2020_79412_MOESM1_ESM.xlsx › supplementary_table_14

De novo mutations in folate-related genes associated with common developmental disorders.

Luo T et al.

Computational and Structural Biotechnology Journal, 2021

33777337 (PubMed )
Supplement: mmc6.xlsx › Sheet1

Extracting Complementary Insights from Molecular Phenotypes for Prioritization of Disease-Associated Mutations.

Wierbowski SD et al.

Current Opinion in Systems Biology, 2018

An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders.

Chen S et al.

Nature Genetics, 2018

Molecular determinants of the balance between co-repressor and co-activator recruitment to the retinoic acid receptor.

Benko S et al.

The Journal of Biological Chemistry, 2003

Co-repressor release but not ligand binding is a prerequisite for transcription activation by human retinoid acid receptor alpha ligand-binding domain.

Kao HY et al.

The Journal of Biological Chemistry, 2003

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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."