Varaico: Literature-Extracted Genetic Variants

Gene:CD36
Variant:p.Y409_I413del0
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CD36

NM_001001548.3:p.Y409_I413del0

Associated Papers

Full-length haplotype reconstruction of CD36 by long-read sequencing: uncovers a novel structural variant.

Liang S et al.

Bmc Genomics, 2026

Comparative genetic analysis of blood and semen samples in sperm donors from Hunan, China.

Huang C et al.

Annals of Medicine, 2025

Two novel mutations (c.878T>C and c.1316delA) in CD36 alleles lead to CD36 antigen deficiency.

He H et al.

Transfusion, 2025

Haplotypes analysis reveals the genetic basis of type I CD36 deficiency.

Xia W et al.

Scientific Reports, 2024

The polymorphism analysis for CD36 among platelet donors.

Lyu Q et al.

Scientific Reports, 2024

High-Throughput CD36 Phenotyping on Human Platelets Based on Sandwich ELISA and Mutant Gene Analysis.

He H et al.

Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2024

Frequency and molecular basis of CD36 deficiency among platelet donors in Kunming, China.

Lyu Q et al.

Platelets, 2023

Analysis of clinically relevant variants from ancestrally diverse Asian genomes.

Chan SH et al.

Nature Communications, 2022

36335097 (PubMed )
Supplement: 41467_2022_34116_MOESM4_ESM.zip › NCOMMS-22-14716A_SupplementaryData › NCOMM-22-14716A_SupplementaryData_2.xlsx › SuppData_2

A synergetic effect of BARD1 mutations on tumorigenesis.

Li W et al.

Nature Communications, 2021

33623049 (PubMed )
Supplement: 41467_2021_21519_MOESM6_ESM.xlsx › Sheet1

New molecular basis associated with CD36-negative phenotype in the sub-Saharan African population.

Le Toriellec E et al.

Transfusion, 2020

Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgrades.

Xiang J et al.

Scientific Reports, 2020

31942019 (PubMed )
Supplement: 41598_2019_57335_MOESM1_ESM.xlsx › Sup_table_1

Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants.

Chen X et al.

Bmc Medical Genetics, 2019

31146700 (PubMed )
Supplement: 12881_2019_813_MOESM1_ESM.xls › CHD7_ChenXiang_query_Report_Fil
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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."