Varaico: Literature-Extracted Genetic Variants

Gene:HCRTR1
Variant:p.D332N
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HCRTR1

NM_001525.3:p.D332N

Associated Papers

Unraveling the function and structure impact of deleterious missense SNPs in the human OX1R receptor by computational analysis.

Farajzadeh-Dehkordi M et al.

Scientific Reports, 2024

38191899 (PubMed )
Supplement: 41598_2023_49809_MOESM5_ESM.xlsx › Table_S2

Integrative analysis prioritised oxytocin-related biomarkers associated with the aetiology of autism spectrum disorder.

Wang T et al.

Ebiomedicine, 2022

35665681 (PubMed )
Supplement: mmc24.xlsx › Sheet1

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
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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."