RHD*66 (provisional)
(ISBT table: not listed)
This entry is an RHD allele.
RHD(T109A), RHD*325A>G, RHD*325G, RHD*325G (RHD*66),
Molecular data
Phenotype
Main D phenotype: variable/discrepant (last update: Dec. 10, 2020)Reports by D phenotype
Other RH phenotypes: RH:-3, -4,
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: probably allo-anti-D (last update: Nov. 17, 2019)Detailed information
-
L Castilho et al. Vox Sanguinis (2019)
- Ab specificity: D (RH1)
- Number (auto- or allo-): 1
- Number listed as allo-:
- Number listed as auto-:
- Number of carriers of the allele assessed:
- DAT: ND
- Autologuous control: ND
- Elution: ND
- Autoadsorption: ND
- Titer: ND
- Was anti-LW excluded?: ND
- Other antibodies detected: ND
- Cross matches (with Ab and RBCs from different partial types): ND
- Transfusion history: ND, probable
- Pregnancy history:
- Anti-D Ig history: ND, probably none
- Context: SCD patient
- Hemolytic consequences: ND
- Comment:
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Reports
Summary: rare descriptions, in South African individuals (last update: Dec. 10, 2020)Structure mapping
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References
- L Castilho et al. From genotyping to the functional and clinical interpretation of variations in blood group genes by 3D-protein structure investigation: two novel variant alleles in the RHD gene Vox Sanguinis, 2019. — Abstract — [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
- Mufarrege N et al. The novel RHD c.325A>G single nucleotide variation found in Argentineans leads to a partial D phenotype. Transfusion, 2020. [Citation] [RHeference]
Last update: Nov. 13, 2019