Varaico: Literature-Extracted Genetic Variants

Gene:CALR
Variant:p.L367_A382delFs
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CALR

NM_004343.4:p.L367_A382delFs

Associated Papers

Diagnosis- and Prognosis-Related Gene Alterations in BCR::ABL1-Negative Myeloproliferative Neoplasms.

Morishita S et al.

International Journal of Molecular Sciences, 2023

37629188 (PubMed )
Supplement: ijms-24-13008-s001.zip › ijms-2555672-supplementary.pdf

A rare CALR variant mutation and efficient peginterferon alfa-2a response in a patient with essential thrombocythemia.

Ciftciler R et al.

Cancer Genetics, 2023

Effects of CALR-Mutant Type and Burden on the Phenotype of Myeloproliferative Neoplasms.

Kim HY et al.

Diagnostics (basel, Switzerland), 2022

Mutation Profile in BCR-ABL1-Negative Myeloproliferative Neoplasms: A Single-Center Experience From India.

Maddali M et al.

Hematology/oncology and Stem Cell Therapy, 2022

SmMIP-tools: a computational toolset for processing and analysis of single-molecule molecular inversion probes-derived data.

Medeiros JJF et al.

Bioinformatics (oxford, England), 2022

35150236 (PubMed )
Supplement: btac081_supplementary_data.zip › Table_S4.xlsx › Clinically_reported_Indels

Myeloproliferative neoplasm-driving Calr frameshift promotes the development of pulmonary hypertension in mice.

Minakawa K et al.

Journal of Hematology & Oncology, 2021

33785036 (PubMed )
Supplement: 13045_2021_1064_MOESM7_ESM.pdf

Clinical and Hematological Relevance of JAK2V617F, CALR, and MPL Mutations in Vietnamese Patients with Essential Thrombocythemia.

Vu HA et al.

Asian Pacific Journal of Cancer Prevention : Apjcp, 2019

Coexistence of JAK2 or CALR mutation is a rare but clinically important event in chronic myeloid leukemia patients treated with tyrosine kinase inhibitors.

Lewandowski K et al.

International Journal of Laboratory Hematology, 2018

A novel molecular assay using hybridisation probes and melt curve analysis for CALR exon 9 mutation detection in myeloproliferative neoplasms.

Keaney T et al.

Journal of Clinical Pathology, 2017

Detection of CALR and MPL Mutations in Low Allelic Burden JAK2 V617F Essential Thrombocythemia.

Usseglio F et al.

The Journal of Molecular Diagnostics : Jmd, 2017

Coexistence of JAK2 and CALR mutations and their clinical implications in patients with essential thrombocythemia.

Kang MG et al.

Oncotarget, 2016

Coexisting JAK2V617F and CALR Exon 9 Mutations in Myeloproliferative Neoplasms - Do They Designate a New Subtype?

Ahmed RZ et al.

Asian Pacific Journal of Cancer Prevention : Apjcp, 2016

Mutations and long-term outcome of 217 young patients with essential thrombocythemia or early primary myelofibrosis.

Palandri F et al.

Leukemia, 2015

Calreticulin mutations in myeloproliferative neoplasms and new methodology for their detection and monitoring.

Chi J et al.

Annals of Hematology, 2015

Calreticulin mutations and long-term survival in essential thrombocythemia.

Tefferi A et al.

Leukemia, 2014

Frequencies, clinical characteristics, and outcome of somatic CALR mutations in JAK2-unmutated essential thrombocythemia.

Chen CC et al.

Annals of Hematology, 2014

Analysis of calreticulin mutations in Chinese patients with essential thrombocythemia: clinical implications in diagnosis, prognosis and treatment.

Fu R et al.

Leukemia, 2014

Distinct clinical characteristics of myeloproliferative neoplasms with calreticulin mutations.

Andrikovics H et al.

Haematologica, 2014

Somatic mutations of calreticulin in myeloproliferative neoplasms.

Klampfl T et al.

The New England Journal of Medicine, 2013

24325356 (PubMed )
Supplement: nejmoa1311347_appendix.pdf
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