Varaico: Literature-Extracted Genetic Variants

Gene:PRICKLE2
Variant:p.V153I
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PRICKLE2

NM_198859.4:p.V153I

Associated Papers

PRICKLE2 revisited-further evidence implicating PRICKLE2 in neurodevelopmental disorders.

Bayat A et al.

European Journal of Human Genetics : Ejhg, 2021

Protein-protein interactions underlying the behavioral and psychological symptoms of dementia (BPSD) and Alzheimer's disease.

Mao Y et al.

Plos One, 2020

31951614 (PubMed )
Supplement: pone.0226021.s001.xlsx › Sheet2

Precision Health Resource of Control iPSC Lines for Versatile Multilineage Differentiation.

Hildebrandt MR et al.

Stem Cell Reports, 2019

31813827 (PubMed )
Supplement: mmc3.xlsx › SNVs

Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction.

Sowers LP et al.

Molecular Psychiatry, 2013

Mutations in prickle orthologs cause seizures in flies, mice, and humans.

Tao H et al.

American Journal of Human Genetics, 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."