Varaico: Literature-Extracted Genetic Variants

Gene:ANKRD26
Variant:p.D158G
Back to variants list

ANKRD26

NM_014915.3:p.D158G

Associated Papers

Moving Beyond Somatic Alterations: Uncovering the Germline Basis of Myeloid Malignancies.

Elbaz Younes I et al.

Cancers, 2026

The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants.

Stefanucci L et al.

Blood, 2023

37647632 (PubMed )
Supplement: BLOOD_BLD-2023-020118-mmc3.xlsx › ST3.3

Analysis of clinical characteristics and treatment efficacy in two pediatric cases of ANKRD26-related thrombocytopenia.

Pang C et al.

Platelets, 2023

Needle in a haystack or elephant in the room? Identifying germline predisposition syndromes in the setting of a new myeloid malignancy diagnosis.

Reinig EF et al.

Leukemia, 2023

ANKRD26-Related Thrombocytopenia and Predisposition to Myeloid Neoplasms.

Sullivan MJ et al.

Current Hematologic Malignancy Reports, 2022

A Rare Big Chinese Family With Thrombocytopenia 2: A Case Report and Literature Review.

Tan C et al.

Frontiers in Genetics, 2020

Genetic predisposition to myelodysplastic syndrome and acute myeloid leukemia in children and young adults.

Babushok DV et al.

Leukemia & Lymphoma, 2016

Inherited predisposition to acute myeloid leukemia.

Godley LA

Seminars in Hematology, 2014

Inherited Thrombocytopenia Caused by Germline ANKRD26 Mutation Should Be Considered in Young Patients With Suspected Myelodysplastic Syndrome.

Kewan T et al.

Journal of Investigative Medicine High Impact Case Reports, 0

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."