Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

RhD variant caused by an in-frame triplet duplication in the RHD gene.

Transfusion - 1 Mar 2011

Pereira Janet C, Rodrigues Maria J, Tilley Louise, Poole Joyce, Chabert Teresa, Ribeiro Maria L

Abstract excerpt

BACKGROUND: The RHD gene is highly polymorphic and a large number of D variants have already been detected. Several mechanisms are involved in the origin of D variants. In-frame deletions, resulting in a single-amino-acid deletion, have been described associated with RhD and RhCE variants. No in-frame duplications and/or insertions have been reported in the RH genes to date. STUDY DESIGN AND METHODS: Blood...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Exons
Share to Gene Duplication
Share to RHD gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Immunoglobulin G

Share to Immunoglobulin M

Share to Rh-Hr Blood-Group System

Source

Identifiers

PMID: 20738827
DOI: 10.1111/j.1537-2995.2010.02856.x

Genes

RHD

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

RhD variant caused by an in-frame triplet duplication in the RHD gene.PMID 20738827Read ↗

In-frame triplet deletions in RHD alter the D antigen phenotype.Semantic proximity Read ↗

Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanisms.Semantic proximity Read ↗

[Blood Typing and Pedigree Analysis of a Novel RHD Allele with c.179T>C and c.1154-31T>C Mutations].Semantic proximity Read ↗

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

A new RHD variant allele is caused by a RHD 662C>G mutation.Semantic proximity Read ↗

Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare alleles.Semantic proximity Read ↗

The Significance of RHD Genotyping and Characteristic Analysis in Chinese RhD Variant Individuals.Semantic proximity Read ↗

A new RHD variant allele (RHD Gly339Val) shows weakened D expression compared to RHD Gly339Glu and Gly339Arg mutants.Semantic proximity Read ↗

[Gene Mutation Analysis of an Individual with a RHD Variant RHD*DV.5 and RHD Negative Gene Heterozygote].Semantic proximity Read ↗

Characterization of novel RHD alleles: relationship between phenotype, genotype, and trimeric architecture.Semantic proximity Read ↗

Two new RHD alleles with deletions spanning multiple exons.Semantic proximity Read ↗

Functional analysis of novel RHD variants: splicing disruption is likely to be a common mechanism of variant D phenotypeSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.