Varaico: Literature-Extracted Genetic Variants

Gene:WNT5A
Variant:p.M1I
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WNT5A

NM_003392.7:p.M1I

Associated Papers

A novel homozygous initiation codon variant associated with infantile alpha-Bcrystallinopathy in a Chinese family.

Ma K et al.

Molecular Genetics & Genomic Medicine, 2019

31215171 (PubMed )
Supplement: MGG3-7-e825-s001.docx

Loss-of-function mutations in Rab escort protein 1 (REP-1) affect intracellular transport in fibroblasts and monocytes of choroideremia patients.

Strunnikova NV et al.

Plos One, 2009

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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."