Varaico: Literature-Extracted Genetic Variants

Gene:TRNT1
Variant:p.D163V
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TRNT1

NM_182916.3:p.D163V

Associated Papers

Alternative start codon selection shapes mitochondrial function and rare human diseases.

Ly J et al.

Molecular Cell, 2025

41205602 (PubMed )
Supplement: NIHMS2117943-supplement-MMMC1.pdf

Thalidomide as an Effective Treatment in Sideroblastic Anemia, Immunodeficiency, Periodic Fevers, and Developmental Delay (SIFD).

Li Y et al.

Journal of Clinical Immunology, 2023

Clinical and Therapeutic Aspects of Sideroblastic Anaemia with B-Cell Immunodeficiency, Periodic Fever and Developmental Delay (SIFD) Syndrome: a Systematic Review.

Maccora I et al.

Journal of Clinical Immunology, 2023

Case report: Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay: Three cases and a literature review.

Chen X et al.

Frontiers in Pediatrics, 2023

A phenotypic expansion of TRNT1 associated sideroblastic anemia with immunodeficiency, fevers, and developmental delay.

Odom J et al.

American Journal of Medical Genetics. Part A, 2022

Etanercept as a successful therapy in autoinflammatory syndrome related to TRNT1 mutations: a case-based review.

Orlando F et al.

Clinical Rheumatology, 2021

Diseases Associated with Defects in tRNA CCA Addition.

Slade A et al.

International Journal of Molecular Sciences, 2020

Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors.

Giannelou A et al.

Annals of the Rheumatic Diseases, 2018

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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."