Varaico: Literature-Extracted Genetic Variants

Gene:FOXP1
Variant:p.V445Fs
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FOXP1

NM_001349338.3:p.V445Fs

Associated Papers

Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+).

Rivera-Munoz EA et al.

European Journal of Human Genetics : Ejhg, 2025

40913078 (PubMed )
Supplement: NIHMS2114636-supplement-Supplemental_Table_S1.xlsx › Table_S1

Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms.

Trelles MP et al.

Molecular Autism, 2021

34588003 (PubMed )
Supplement: 13229_2021_469_MOESM1_ESM.pdf

Prospective investigation of FOXP1 syndrome.

Siper PM et al.

Molecular Autism, 2017

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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."