M1
(ISBT table: not listed)
This entry is not counted as an allele.
Molecular data
Nucleotides:
intronic 149C>A; intronic 802>; intronic 939>; intronic 940>;
Hybrid allele encompassing at least one RHCE exon:
no
Comments on the molecular basis:
- There were no mutations detected in exons and promoter, RNA was not available for testing
- relevance of the mutations? Should this sequence really be considered as an allele?
Extracellular position of one or more amino acid substitutions:
Splicing:
Unconventional prediction methods:
Phenotype
Main D phenotype: D negative (DEL excluded) (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: NA (last update: Aug. 15, 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: not relevant (last update: Aug. 25, 2020)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: not expected, see phenotype data
Reports
Summary: exceptional description(s), Moroccan (last update: Dec. 22, 2019)Structure mapping
Movement | Mouse Input | Touch Input | ||
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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
- El Wafi M et al. Novel intronic RHD variants identified in serologically D-negative blood donors. Vox Sang, 2017. [Citation] [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
Last update: July 30, 2019