RHD*35 - RHD*DMA
(ISBT table: RHD partial D v5.0)
This entry is an RHD allele.
DMA, RHD(L207F), RHD*621C, RHD*621C (DMA, RHD*35), RHD*621G>C,
Molecular data
Nucleotides:
621G>C;
Amino acids: L207F;
Hybrid allele encompassing at least one RHCE exon:
no
Comments on the molecular basis:
- additional intronic IVS5+12G>A mutation in one sample heterozygous with RHef00442; initial proband is heterozyguous
Extracellular position of one or more amino acid substitutions:
- none of the mutations are predicted to affect an extracellular amino acid
- mutation predicted to be in a transmembrane domain
Splicing:
Unconventional prediction methods:
Phenotype
Main D phenotype: (last update: Dec. 28, 2020)Reports by D phenotype
Other RH phenotypes: RH:-2,
- RH:-2 inferred from the reported RHCE phenotypes of the carriers
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Rhesus Similarity Index
Haplotype
Main CcEe phenotype association: ce (last update: Dec. 28, 2020)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: no published cases (last update: Dec. 28, 2020)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Reports
Summary: exceptional description(s), in individuals of African descent or compatible with such descent (last update: Dec. 28, 2020)Structure mapping
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References
- Wagner FF et al. RHD allele distribution in Africans of Mali. BMC Genet, 2003. [Citation] [RHeference]
- S Vege et al. RHD Genotyping of Discrepant or Weak D Samples: Over a Year’s Experience. Transfusion, 2017. — Abstract — [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
- Vege S et al. Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles. Transfusion, 2021. [Citation] [RHeference]
Last update: Dec. 28, 2020