RHD*D-cE(5-6)-D
(ISBT table: not listed)
This entry is an hybrid RHD allele.
RHD*667G,676C,697C,712A,733C,744T,787A,800T,916A,932G, RHD*D-cE(5-6)-D, RHD-RHcE(5-6)-RHD,
Molecular data
Nucleotides:
667T>G; 676G>C; 697G>C; 712G>A; 733G>C; 744C>T; 787G>A; 800A>T; 916G>A; 932A>G;
Amino acids: F223V; A226P; E233Q; V238M; V245L; S248S; G263R; K267M; V306I; Y311C;
Hybrid allele encompassing at least one RHCE exon:
RHD-RHcE(5-6)-RHD
Comments on the molecular basis:
- The RHCE gene insert is at least 3.868 kb with 5' and 3' breakpoints between IVS4+132–c.667 and IVS6+1960–IVS6+2099, respectively
Extracellular position of one or more amino acid substitutions:
Splicing:
Unconventional prediction methods:
Phenotype
Main D phenotype: variable/discrepant (last update: Nov. 17, 2019)Reports by D phenotype
Other RH phenotypes: RH:-3, 23, -32,
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Rhesus Similarity Index
Haplotype
Main CcEe phenotype association: Ce? (last update: Dec. 9, 2020)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: no published cases (last update: Nov. 17, 2019)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Reports
Summary: exceptional description(s) (last update: Dec. 22, 2019)Structure mapping
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Slab | Ctrl+Second | Not Available |
References
- Lopez GH et al. A D+ blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (D(W) ) characteristic of the partial DVa phenotype. Transfusion, 2016. [Citation] [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
Last update: Aug. 5, 2019