Varaico: Literature-Extracted Genetic Variants

Gene:TGM1
Variant:p.S358R
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TGM1

NM_000359.3:p.S358R

Associated Papers

Identification and In Silico Analysis of a Homozygous Nonsense Variant in TGM1 Gene Segregating with Congenital Ichthyosis in a Consanguineous Family.

Almazroea A et al.

Medicina (kaunas, Lithuania), 2023

36676727 (PubMed )
Supplement: medicina-59-00103-s001.zip › medicina-2007344-supplementary.xlsx › Reported_Variants_in_TGM1_Gene

Molecular profiling of lamellar ichthyosis pathogenic missense mutations on the structural and stability aspects of TGM1 protein.

Nasser KK et al.

Journal of Biomolecular Structure & Dynamics, 2021

High prevalence of autosomal recessive congenital ichthyosis in a Mexican population caused by a new mutation in the TGM1 gene: epidemiological evidence of a founder effect.

González-Del Carmen M et al.

International Journal of Dermatology, 2020

Bathing suit ichthyosis: Two Burmese siblings and a review of the literature.

Li W et al.

Pediatric Dermatology, 2020

Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response?

Zhang H et al.

Experimental Dermatology, 2019

Expanding the Genotypic Spectrum of Bathing Suit Ichthyosis.

Marukian NV et al.

Jama Dermatology, 2017

[Recurrent European missense mutation in a Hungarian pedigree with Papillon-Lefèvre syndrome].

Vályi P et al.

Fogorvosi Szemle, 2014

The expression of epidermal lipoxygenases and transglutaminase-1 is perturbed by NIPAL4 mutations: indications of a common metabolic pathway essential for skin barrier homeostasis.

Li H et al.

The Journal of Investigative Dermatology, 2012

Transglutaminase-1 gene mutations in autosomal recessive congenital ichthyosis: summary of mutations (including 23 novel) and modeling of TGase-1.

Herman ML et al.

Human Mutation, 2009

Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype.

Oji V et al.

Human Molecular Genetics, 2006

Consequences of seven novel mutations on the expression and structure of keratinocyte transglutaminase.

Huber M et al.

The Journal of Biological Chemistry, 1997

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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."