Varaico: Literature-Extracted Genetic Variants

Gene:RPS19
Variant:p.V15F
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RPS19

NM_001022.4:p.V15F

Associated Papers

Genotype-phenotype associations in individuals with Diamond Blackfan anaemia.

Gianferante DM et al.

Ejhaem, 2024

39691264 (PubMed )
Supplement: JHA2-5-1117-s001.pdf

Computational Studies of the Structural Basis of Human RPS19 Mutations Associated With Diamond-Blackfan Anemia.

An K et al.

Frontiers in Genetics, 2021

A functional assay for the clinical annotation of genetic variants of uncertain significance in Diamond-Blackfan anemia.

Aspesi A et al.

Human Mutation, 2018

Drug discovery for Diamond-Blackfan anemia using reprogrammed hematopoietic progenitors.

Doulatov S et al.

Science Translational Medicine, 2017

The ribosomal basis of Diamond-Blackfan Anemia: mutation and database update.

Boria I et al.

Human Mutation, 2010

Study of the effects of proteasome inhibitors on ribosomal protein S19 (RPS19) mutants, identified in patients with Diamond-Blackfan anemia.

Crétien A et al.

Haematologica, 2008

A new database for ribosomal protein genes which are mutated in Diamond-Blackfan Anemia.

Boria I et al.

Human Mutation, 2008

RPS19 mutations in patients with Diamond-Blackfan anemia.

Campagnoli MF et al.

Human Mutation, 2008

Deficient RPS19 protein production induces cell cycle arrest in erythroid progenitor cells.

Kuramitsu M et al.

British Journal of Haematology, 2008

Missense mutations associated with Diamond-Blackfan anemia affect the assembly of ribosomal protein S19 into the ribosome.

Angelini M et al.

Human Molecular Genetics, 2007

Molecular basis of Diamond-Blackfan anemia: structure and function analysis of RPS19.

Gregory LA et al.

Nucleic Acids Research, 2007

Reduced gene expression of clustered ribosomal proteins in Diamond-Blackfan anemia patients without RPS19 gene mutations.

Koga Y et al.

Journal of Pediatric Hematology/oncology, 2006

Diamond Blackfan anaemia in the UK: clinical and genetic heterogeneity.

Orfali KA et al.

British Journal of Haematology, 2004

Nucleolar localization of RPS19 protein in normal cells and mislocalization due to mutations in the nucleolar localization signals in 2 Diamond-Blackfan anemia patients: potential insights into pathophysiology.

Da Costa L et al.

Blood, 2003

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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."