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Article

Study of the D-- phenotype reveals erythrocyte membrane alterations in the absence of RHCE.

British journal of haematology - 1 Jul 2012

Flatt Joanna F, Musa Rozi H, Ayob Yasmin, Hassan Afifah, Asidin Norhanim, Yahya Nurul M, Mathlouthi Rosalind, Thornton Nicole, Anstee David J, Bruce Lesley J

Abstract excerpt

Red cells with the D-- phenotype do not express the RHCE protein because of mutations in both alleles of the RHCE gene. At present, little is known of the effect this has on the normal function of erythrocytes. In this study a group of five families belonging to a nomadic tribe in Malaysia were identified as carriers of the D-- haplotype. Analysis of homozygous individuals' genomic DNA showed two separate novel...

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Source

Identifiers

PMID: 22571328
DOI: 10.1111/j.1365-2141.2012.09149.x

Genes

RHCE
RHAG
RHD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 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

Study of the D-- phenotype reveals erythrocyte membrane alterations in the absence of RHCE.PMID 22571328Read ↗

Molecular characterization of rare D--/D-- variants in individuals of Indian origin.Semantic proximity Read ↗

Molecular characterization of a new D- - haplotype in a Comorian man.Semantic proximity Read ↗

New RHCE variant alleles encoding the D- - phenotype.Semantic proximity Read ↗

Two new alleles of the RHCE gene in Black individuals: the RHce allele ceMO and the RHcE allele cEMI.Semantic proximity Read ↗

Molecular characterization of a rare Rh phenotype Dc-from the Indian subcontinent.Semantic proximity Read ↗

Identification of a partial internal deletion in the RH locus causing the human erythrocyte D--phenotype.Semantic proximity Read ↗

Integrated analyses reveal unexpected complex inversion and recombination in RH genes.Semantic proximity Read ↗

RHCE*cE734C allele encodes an altered c antigen and a suppressed E antigen not detected with standard reagents.Semantic proximity Read ↗

D-- phenotype caused by a novel RHCE null allele.Semantic proximity Read ↗

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

Heterogeneous molecular background of the weak C, VS+, hr B-, Hr B- phenotype in black persons.Semantic proximity Read ↗

The serological profile and molecular basis of a new partial D phenotype, DHR.Semantic proximity Read ↗

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