RHD*602G,667G,697C,733C,1136T
(ISBT table: not listed)
This entry is an RHD allele.
RHD(T201R,F223V,E233Q,V245L,T379M), RHD*602C>G,667T>G,697G>C,733G>C,1136C>T, RHD*602G,667G,697C,733C,1136T, RHD*602G,667G,697C,733C,1136T (DAU),
Molecular data
Phenotype
Main D phenotype: variable/discrepant (last update: Aug. 9, 2020)Reports by D phenotype
Other RH phenotypes: RH:
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Rhesus Similarity Index
Haplotype
Main CcEe phenotype association: ce expected (last update: Dec. 9, 2020)ce | Ce | cE | CE | |
---|---|---|---|---|
ce | 0 | 0 | 0 | 0 |
Ce | 0 | 0 | 0 | |
cE | 0 | 0 | ||
CE | 0 |
Reports by CcEe phenotype
Reports by allele association
Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: maybe allo-anti-D? (last update: Aug. 9, 2020)Detailed information
-
Trina Horn et al. Transfusion (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: 2
- 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
- Pregnancy history:
- Anti-D Ig history: ND, probably none
- Context: African American female patient
- Hemolytic consequences: ND
- Comment:
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Reports
Summary: exceptional description(s), in African American (last update: Aug. 9, 2020)Structure mapping
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References
- Trina Horn et al. Two New RHD*Dau family Alleles Found in Three African American Patients Transfusion, 2019. — Abstract — [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
Last update: Nov. 3, 2020