Varaico: Literature-Extracted Genetic Variants

Gene:AAAS
Variant:p.W84*
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AAAS

NM_015665.6:p.W84*

Associated Papers

Neurological manifestations of Allgrove syndrome in patients carrying a potentially founder p.Ser263Pro variant in the AAAS gene.

Juścińska E et al.

Neurogenetics, 2026

41498959 (PubMed )
Supplement: 10048_2025_870_MOESM1_ESM.docx

The role of WD40 repeat-containing proteins in endocrine (dys)function.

Hu Y et al.

Journal of Molecular Endocrinology, 2023

Clinical heterogeneity and molecular profile of triple A syndrome: a study of seven cases.

Singh K et al.

Journal of Pediatric Endocrinology & Metabolism : Jpem, 2018

Phenotype-genotype spectrum of AAA syndrome from Western India and systematic review of literature.

Patt H et al.

Endocrine Connections, 2017

29180348 (PubMed )
Supplement: ec-6-901-t002.xls › Combined_Stat

Genetic defects in pediatric-onset adrenal insufficiency in Japan.

Amano N et al.

European Journal of Endocrinology, 2017

The nucleoporin ALADIN regulates Aurora A localization to ensure robust mitotic spindle formation.

Carvalhal S et al.

Molecular Biology of the Cell, 2015

MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing.

Mort M et al.

Genome Biology, 2014

24451234 (PubMed )
Supplement: gb-2014-15-1-r19-S1.pdf

Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndrome.

Toromanovic A et al.

European Journal of Pediatrics, 2009

A Novel V185DfsX4 Mutation of the AAAS Gene in a 2-year-old Boy with Triple A Syndrome.

Huynh T et al.

Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology, 2009

Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430Phe.

Koehler K et al.

European Journal of Human Genetics : Ejhg, 2008

Cellular localization of 17 natural mutant variants of ALADIN protein in triple A syndrome - shedding light on an unexpected splice mutation.

Krumbholz M et al.

Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire, 2006

The triple A syndrome is due to mutations in ALADIN, a novel member of the nuclear pore complex.

Huebner A et al.

Endocrine Research, 2004

Triple-A syndrome with prominent ophthalmic features and a novel mutation in the AAAS gene: a case report.

Brooks BP et al.

Bmc Ophthalmology, 2004

New insights into the molecular basis of the triple A syndrome.

Huebner A et al.

Endocrine Research, 2002

Analysis of the AAAS gene in a Japanese patient with triple A syndrome.

Katsumata N et al.

Endocrine Journal, 2002

Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene.

Handschug K et al.

Human Molecular Genetics, 2001

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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."