RHD*186T,410T,455C,602G,667G
(ISBT table: not listed)
This entry is an RHD allele.
DIIIa [819G], DIIIa(819G), RHD(L62F,A137V,N152T,T201R,F223V), RHD*186G>T,410C>T,455A>C,602C>G,667T>G, RHD*186T,410T,455C,602G,667G, RHD*DIIIa(819G),
Molecular data
Phenotype
Main D phenotype: unknown (last update: Nov. 17, 2019)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 (last update: Jan. 8, 2021)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: allo-anti-D (last update: Nov. 17, 2019)Detailed information
-
Westhoff CM et al. Transfusion (2010)
- Ab specificity: D (RH1)
- Number (auto- or allo-): 2
- Number listed as allo-:
- Number listed as auto-:
- Number of carriers of the allele assessed: 4
- DAT:
- Autologuous control:
- Elution:
- Autoadsorption:
- Titer:
- Was anti-LW excluded?:
- Other antibodies detected:
- Cross matches (with Ab and RBCs from different partial types):
- Transfusion history:
- Pregnancy history:
- Anti-D Ig history:
- Context:
- Hemolytic consequences:
- Comment: for patients with anti-D, 1 had RHef00058 in trans, 1 was hemizygous; for patients without anti-D, 1 had a RHef00446 in trans, 1 was heterozygous for RHef00163; see article for multiple antibodies in these patients; in Discussion: "Sixteen of 37 (43%) of the pregnant or transfused patients in this report had anti-D.", grouping RHef00058 and RHef00672
Antibodies in D negative recipients
Alloimmunization in recipients: unknown
Reports
Summary: few descriptions, expected to be in individuals of African descent (last update: Dec. 22, 2019)Detailed reports
- 5/67 among 67 DIIIa alleles in the USA population (inferred African American)
- 5/60 (1/21 donors, hemizygous; 4/39 patients, 1 heterozygous with RHef00058, 1 with RHef00452, 1 with RHef00163, 1 hemizygous) among 60 individuals (21 donors, 39 patients) phenotyped as RH:54 and/or submitted for investigation to determine the RH genotype in the USA population (inferred African American)
- 2 heterozygotes among 278 samples selected for the development of nonspecific quantitative next-generation sequencing. (non-random samples, may have been reported in other studies)
Allele or phenotype frequency
Structure mapping
Movement | Mouse Input | Touch Input | ||
---|---|---|---|---|
Rotation | Primary Mouse Button | Single touch | ||
Translation | Middle Mouse Button or Ctrl+Primary | Triple touch | ||
Zoom | Scroll Wheel or Second Mouse Button or Shift+Primary | Pinch (double touch) | ||
Slab | Ctrl+Second | Not Available |
References
- Westhoff CM et al. DIIIa and DIII Type 5 are encoded by the same allele and are associated with altered RHCE*ce alleles: clinical implications. Transfusion, 2010. [Citation] [RHeference]
- Stef M et al. RH genotyping by nonspecific quantitative next-generation sequencing. Transfusion, 2020. [Citation] [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
Last update: Jan. 8, 2021