RHD*03.04 - RHD*DIII.04
(ISBT table: RHD partial D v5.0)
This entry is an RHD allele.
DIII type 4, DIII type IV, RHD(L62F,A137V,N152T), RHD*186T,410T,455C, RHD*186T,410T,455C (DIII type 4), RHD*DIII.4,
Molecular data
Phenotype
Main D phenotype: D positive (last update: Nov. 17, 2019)Reports by D phenotype
Other RH phenotypes: RH:-3, -4, -30,
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Haplotype
Main CcEe phenotype association: ce (last update: Nov. 11, 2019)ce | Ce | cE | CE | |
---|---|---|---|---|
ce | 0 | 0 | 0 | 0 |
Ce | 0 | 0 | 0 | |
cE | 0 | 0 | ||
CE | 0 |
Reports by CcEe phenotype
- with Ce 0 samples (Figure 2; presented as a general association, no sample count) (Figure 2; presented as a general association, no sample count)
- with ce 0 samples (not counted, but 16 samples could be RHef00442 associated with RHef00058 or, less likely, RHef00313 associated with RHef00056)
- with Ccee 0 samples (not counted, but 3 samples could be RHef00442 associated with RHef00058 or, less likely, RHef00313 associated with RHef00056)
- with ccEe 0 samples (not counted, but 2 samples could be RHef00442 associated with RHef00058 or, less likely, RHef00313 associated with RHef00056)
Reports by allele association
Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: allo-anti-D (last update: Nov. 17, 2019)Detailed information
-
Wagner FF et al. Transfus Med Hemother (2014)
(RIR n°12)
- Ab specificity: D (RH1)
- Number (auto- or allo-): 1
- Number listed as allo-: 1
- Number listed as auto-:
- Number of carriers of the allele assessed:
- 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:
Wagner FF et al. Blood (2000)
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Reports
Summary: exceptional description(s) (last update: Feb. 22, 2020)Detailed reports
- 0/167 (1 could be RHef00442 associated with RHef00058 or, less likely, RHef00313 associated with RHef00056) among 1702 samples tested for the combined presence of RHD c.602G and c.667G (700 Dutch White, 310 South African Black, 319 South African Asians, 197 Curacao Black, 176 Ethiopian Black) Ethiopian (Black)
- 0/310 (but 20 samples could be RHef00442 associated with RHef00058 or, less likely, RHef00313 associated with RHef00056) among 1702 samples tested for the combined presence of RHD c.602G and c.667G (700 Dutch White, 310 South African Black, 319 South African Asians, 197 Curacao Black, 176 Ethiopian Black) South African (Black)
- 0 or 1/10 (1 sample could be RHef00008 in trans with RHef00317 or RHef00313 with RHef00056) individuals with D positive phenotype Bantu, subgroup Teke, Boma from villages in the north of Léfini river
- 1 sample reported by a Swiss lab (RIR n°12)
- 1 heterozygote 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
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References
- Wagner FF et al. Weak D alleles express distinct phenotypes. Blood, 2000. [Citation] [RHeference]
- Wagner FF et al. The DAU allele cluster of the RHD gene. Blood, 2002. [Citation] [RHeference]
- Chen Q et al. Random survey for RHD alleles among D+ European persons. Transfusion, 2005. [Citation] [RHeference]
- Grootkerk-Tax MG et al. RHD(T201R, F223V) cluster analysis in five different ethnic groups and serologic characterization of a new Ethiopian variant DARE, the DIII type 6, and the RHD(F223V). Transfusion, 2006. [Citation] [RHeference]
- Touinssi M et al. Molecular analysis of inactive and active RHD alleles in native Congolese cohorts. Transfusion, 2009. [Citation] [RHeference]
- Flegel WA et al. D variants at the RhD vestibule in the weak D type 4 and Eurasian D clusters. Transfusion, 2009. [Citation] [RHeference]
- 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]
- Lomas-Francis C et al. DIII Type 7 is likely the original serologically defined DIIIb. Transfusion, 2012. [Citation] [RHeference]
- von Zabern I et al. D category IV: a group of clinically relevant and phylogenetically diverse partial D. Transfusion, 2013. [Citation] [RHeference]
- Reid ME et al. Genomic analyses of RH alleles to improve transfusion therapy in patients with sickle cell disease. Blood Cells Mol Dis, 2014. [Citation] [RHeference]
- Wagner FF et al. The Rhesus Site. Transfus Med Hemother, 2014. [Citation] [RHeference]
- Srivastava K et al. The DAU cluster: a comparative analysis of 18 RHD alleles, some forming partial D antigens. Transfusion, 2016. [Citation] [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
- Stef M et al. RH genotyping by nonspecific quantitative next-generation sequencing. Transfusion, 2020. [Citation] [RHeference]
Last update: Jan. 11, 2021