Varaico: Literature-Extracted Genetic Variants

Gene:SLC30A8
Variant:p.K34fs
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SLC30A8

NM_173851.3:p.K34fs

Associated Papers

Electrophysiological Characterization of Inducible Pluripotent Stem Cell-Derived Human β-Like Cells and an SLC30A8 Disease Model.

Jaffredo M et al.

Diabetes, 2024

Electrophysiological characterisation of iPSC-derived human β-like cells and an SLC30A8 disease model.

Jaffredo M et al.

Biorxiv : the Preprint Server for Biology, 2023

Toward Precision Medicine with Human Pluripotent Stem Cells for Diabetes.

Memon B et al.

Stem Cells Translational Medicine, 2022

Diabetes and Genetics: A Relationship Between Genetic Risk Alleles, Clinical Phenotypes and Therapeutic Approaches.

Sayed S et al.

Advances in Experimental Medicine and Biology, 2021

Insights into pancreatic islet cell dysfunction from type 2 diabetes mellitus genetics.

Krentz NAJ et al.

Nature Reviews. Endocrinology, 2020

Loss of ZnT8 function protects against diabetes by enhanced insulin secretion.

Dwivedi OP et al.

Nature Genetics, 2019

Association analysis of copy number variations in type 2 diabetes-related susceptible genes in a Chinese population.

Yan YX et al.

Acta Diabetologica, 2018

The Metabolic Syndrome in Men study: a resource for studies of metabolic and cardiovascular diseases.

Laakso M et al.

Journal of Lipid Research, 2017

Genetics of Type 2 Diabetes: the Power of Isolated Populations.

Andersen MK et al.

Current Diabetes Reports, 2016

Genetics of type 2 diabetes-pitfalls and possibilities.

Prasad RB et al.

Genes, 2015

Protein truncating variants of SLC30A8 reduce type 2 diabetes mellitus risk in humans.

Yakala GK

Clinical Genetics, 2014

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.

Flannick J et al.

Nature Genetics, 2014

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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."