RHD*Ex2del
(ISBT table: not listed)
This entry is an RHD allele.
RHD*Ex2del, RHD*delEx2, RHDex 2del,
Molecular data
Nucleotides:
exon deletion(s);
Amino acids: exon deletion(s) 2;
Hybrid allele encompassing at least one RHCE exon:
RHD(1)-del(Ex2)-RHD(3-10)
Comments on the molecular basis:
Extracellular position of one or more amino acid substitutions:
Splicing:
Unconventional prediction methods:
Phenotype
Main D phenotype: D negative (DEL not excluded) (last update: May 19, 2020)Reports by D phenotype
Other RH phenotypes: RH:-2, -3,
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Rhesus Similarity Index
Haplotype
Main CcEe phenotype association: ce (last update: Nov. 11, 2019)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: D negative, at risk for anti-D (last update: Aug. 25, 2020)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: not expected, see phenotype data
Reports
Summary: exceptional description(s), in the Swiss population (last update: Dec. 22, 2019)Structure mapping
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Slab | Ctrl+Second | Not Available |
References
- Gowland P et al. Molecular RHD screening of RhD negative donors can replace standard serological testing for RhD negative donors. Transfus Apher Sci, 2014. [Citation] [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
- Matteocci A et al. Two new RHD alleles with deletions spanning multiple exons. Transfusion, 2021. [Citation] [RHeference]
Last update: Jan. 11, 2021