RHD*59
(ISBT table: RHD partial D v5.0)
This entry is an RHD allele.
RHD(F175F), RHD*525C>T, RHD*525T, RHD*525T (RHD*59),
Molecular data
Nucleotides:
525C>T;
Amino acids: F175F;
Hybrid allele encompassing at least one RHCE exon:
no
Comments on the molecular basis:
- see also "Additional comments" section on the RhesusBase http://www.rhesusbase.info/RHDRHD(F175L).htm
- nucleotide and amino acid substitutions from the description are incompatible, respectively: c.525C>T and p.F175L, we considered the latter to be the typo
- RHD c.525C>T is reported in the 1000 Genomes project with a prevalence of: Africa: 0.15%. America: 0.14%. East Asia: 0.20%.
Extracellular position of one or more amino acid substitutions:
Splicing:
Unconventional prediction methods:
Phenotype
Main D phenotype: variable/discrepant (last update: May 4, 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 (last update: Aug. 15, 2020)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: no published cases (last update: Nov. 17, 2019)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Reports
Summary: exceptional description(s), probably in the Dutch population (last update: Aug. 27, 2020)Structure mapping
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References
- Wagner FF and Flegel WA et al. The Human RhesusBase Online ressource, 2011. — Online ressource — [RHeference]
- Haer-Wigman L et al. RHD and RHCE variant and zygosity genotyping via multiplex ligation-dependent probe amplification. Transfusion, 2013. [Citation] [RHeference]
- Möller M et al. Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project. Blood Adv, 2016. [Citation] [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
Last update: May 4, 2020