Varaico: Literature-Extracted Genetic Variants

Gene:SLC6A8
Variant:p.V539I
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SLC6A8

NM_005629.4:p.V539I

Associated Papers

Structural insights into the substrate uptake and inhibition of the human creatine transporter (hCRT).

Yuan X et al.

Proceedings of the National Academy of Sciences of the United States of America, 2025

ProteoMutaMetrics: machine learning approaches for solute carrier family 6 mutation pathogenicity prediction.

Huang J et al.

Rsc Advances, 2024

SIGMA leverages protein structural information to predict the pathogenicity of missense variants.

Zhao H et al.

Cell Reports Methods, 2024

38211594 (PubMed )
Supplement: mmc2.xlsx › Sheet1

Experimental and Computational Analysis of Newly Identified Pathogenic Mutations in the Creatine Transporter SLC6A8.

Ferrada E et al.

Journal of Molecular Biology, 2024

Rare disease variant curation from literature: assessing gaps with creatine transport deficiency in focus.

Lyons EL et al.

Bmc Genomics, 2023

Rescue by 4-phenylbutyrate of several misfolded creatine transporter-1 variants linked to the creatine transporter deficiency syndrome.

El-Kasaby A et al.

Neuropharmacology, 2019

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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."