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Article

Identification of a novel missense mutation (563G>a) in the ABO gene associated with a Bel phenotype.

Transfusion - 1 May 2016

Niwa Reiko, Nakayama Takayuki, Ishii Hiroyuki, Fujita Emi, Ishiyama Kazuki, Matsuo Tomohito, Shimizu Aya, Gao Siqiang, Hayashi Megumi, Katai Akiko, Ando Takanori, Takahashi Miyuki, Takeshita Kyosuke, Takami Akiyoshi, Kato Hidefumi

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Share to ABO Blood-Group System
Share to ABO gene
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mutation, Missense

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Source

Identifiers

PMID: 26841695
DOI: 10.1111/trf.13507

Genes

ABO

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of a novel missense mutation (563G>a) in the ABO gene associated with a Bel phenotype.PMID 26841695Read ↗

A new missense variant c.278C > G on the ABO*B.01 allele associated with a Bel phenotype.Semantic proximity Read ↗

The novel missense variant c.350G>T on the ABO*B.01 allele associated with a Bel phenotype.Semantic proximity Read ↗

c.125_126insT mutation in ABO*B.01 allele responsible for Bel phenotype.Semantic proximity Read ↗

Identification of a novel B allele with missense mutation (c.98G > C) in the ABO gene.Semantic proximity Read ↗

Identification of a novel A allele with a nucleotide deletion c.198delG in the ABO gene associated with Ael phenotype.Semantic proximity Read ↗

A novel B variant allele with c.586T>C (p.Cys196Arg) mutation identified at the ABO locus.Semantic proximity Read ↗

ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype.Semantic proximity Read ↗

c.586T>C mutation on the ABO*A1.02 allele responsible for Ael phenotype.Semantic proximity Read ↗

Identification of novel variant A alleles within the ABO gene.Semantic proximity Read ↗

A novel c.28 + 1G > T mutation in the ABO*A1.02 allele that results in Ael phenotype.Semantic proximity Read ↗

Identification of novel variant B alleles within the ABO gene.Semantic proximity Read ↗

A novel c.29-3C>G variant on the B allele forms the Bel phenotype.Semantic proximity Read ↗

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