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Article

A new genetic background for the Jr(a-) blood group phenotype caused by the ABCG2*439T allele encoding a p.Arg147Trp change.

Transfusion - 1 Dec 2017

Wieckhusen Carola, Rink Gabi, Scharberg Erwin A, Rothenberger Sina, Stürtzel Annette, Richter Ekkehard, Bugert Peter

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Topics

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Share to Amino Acid Substitution
Share to ATP Binding Cassette Transporter, Subfamily G, Member 2
Share to Blood Group Antigens

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Mutation, Missense

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Source

Identifiers

PMID: 29106709
DOI: 10.1111/trf.14375

Genes

ABCG2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

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A new genetic background for the Jr(a-) blood group phenotype caused by the ABCG2*439T allele encoding a p.Arg147Trp change.PMID 29106709Read ↗

A review of the JR blood group system.Semantic proximity Read ↗

A novel ABCG2 variant causing Jr(a-) phenotype.Semantic proximity Read ↗

Two novel ABCG2 alleles resulting in a Jr(a-) phenotype.Semantic proximity Read ↗

The JR blood group system (ISBT 032): molecular characterization of three new null alleles.Semantic proximity Read ↗

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A Peruvian patient carrying the novel RHCE*cE(c.382G > C) missense allele in the RH blood group system.Semantic proximity Read ↗

Novel A group allele with a 556A>G substitution previously found in a B subgroup allele.Semantic proximity Read ↗

RHCE null allele causing D-- phenotype in a Latin-American blood donor.Semantic proximity Read ↗

A new ABCG2 null allele with a 27-kb deletion including the promoter region causing the Jr(a-) phenotype.Semantic proximity Read ↗

Defining the Jr(a-) phenotype in the Japanese population.Semantic proximity Read ↗

A novel B allele with c.736T>C, c.738C>A, and c.930A>G variations identified in a Chinese individual with Bw phenotype.Semantic proximity Read ↗

A novel RHD allele caused by c.687_689delAAG variant.Semantic proximity Read ↗

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