Varaico: Literature-Extracted Genetic Variants

Gene:PMM2
Variant:p.F122L
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PMM2

NM_000303.3:p.F122L

Associated Papers

Dynamicasome-a molecular dynamics-guided and AI-driven pathogenicity prediction catalogue for all genetic mutations.

Islam NN et al.

Communications Biology, 2025

40624350 (PubMed )
Supplement: 42003_2025_8334_MOESM3_ESM.zip › PMM2-mutation-prediction-with-AI › Latest_AllModel_WithOutSide_Program_May10th_2024.xlsx › Sheet1

In Silico Analysis of Phosphomannomutase-2 Dimer Interface Stability and Heterodimerization with Phosphomannomutase-1.

Hay Mele B et al.

Molecules (basel, Switzerland), 2025

Novel PMM2 missense mutation in a Chinese family with non-syndromic premature ovarian insufficiency.

Peng T et al.

Journal of Assisted Reproduction and Genetics, 2020

A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2.

Chan B et al.

Human Molecular Genetics, 2016

The Effects of PMM2-CDG-Causing Mutations on the Folding, Activity, and Stability of the PMM2 Protein.

Yuste-Checa P et al.

Human Mutation, 2015

Successful prenatal mannose treatment for congenital disorder of glycosylation-Ia in mice.

Schneider A et al.

Nature Medicine, 2011

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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."