DHMii (obsolete) - phenotypic description
(ISBT table: not listed)
This entry is a phenotypic characterization.
DHMii (obsolete) - phenotypic description, HMii,
Molecular data
Nucleotides:
Amino acids:
Hybrid allele encompassing at least one RHCE exon:
NA
Comments on the molecular basis:
- see also "Additional comments" section on the RhesusBase http://www.rhesusbase.info/RHDDHMii.htm
- see also "Additional comments" section on the RhesusBase http://www.rhesusbase.info/RHDDVItype4.htm
Extracellular position of one or more amino acid substitutions:
Splicing:
Unconventional prediction methods:
Phenotype
Main D phenotype: variable/discrepant (last update: May 2, 2020)Reports by D phenotype
Other RH phenotypes: RH:-23, -30, -32, -33, -35, -36, -40, -48, -50,
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Rhesus Similarity Index
Haplotype
Main CcEe phenotype association: cE (last update: Feb. 26, 2020)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: not relevant, see types or alleles (last update: Aug. 25, 2020)Detailed information
-
Jones J et al. Vox Sang (1995)
- Ab specificity: D (RH1)
- Number (auto- or allo-):
- Number listed as allo-: 1
- Number listed as auto-:
- Number of carriers of the allele assessed:
- DAT: ND
- Autologuous control: negative
- Elution: ND
- Autoadsorption: ND
- Titer: 128 (by AGT on R2r cells)
- Was anti-LW excluded?: ND
- Other antibodies detected: ND
- Cross matches (with Ab and RBCs from different partial types): "This anti-D reacted with untreated and papain-treated cells from DIIIc, DIVa, D+ and the group 2 patient fs, but not with those from DIVb, DVa, DVI, DVII, and Du group 1 cells"
- Transfusion history: ND
- Pregnancy history:
- Anti-D Ig history: ND, probably none
- Context: ND
- Hemolytic consequences: ND
- Comment:
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Structure mapping
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References
- Jones J et al. Identification of two new D variants, DHMi and DHMii using monoclonal anti-D. Vox Sang, 1995. [Citation] [RHeference]
- Jones JW et al. Quantitation of Rh D antigen sites on weak D and D variant red cells by flow cytometry. Vox Sang, 1996. [Citation] [RHeference]
- Cartron JP et al. Tentative model for the mapping of D epitopes on the RhD polypeptide. Transfus Clin Biol, 1996. [Citation] [RHeference]
- Jones J et al. Selection of monoclonal antibodies for the identification of D variants: ability to detect weak D and to split epD2, epD5 and epD6/7. Vox Sang, 1996. [Citation] [RHeference]
- Flegel WA et al. RHD epitope density profiles of RHD variant red cells analyzed by flow cytometry. Transfus Clin Biol, 1996. [Citation] [RHeference]
- Liu et al. Molecular analysis of two D-variants, DHMi and DHMii. Transfusion Medicine, 1996. — Abstract — [RHeference]
- Avent ND et al. Evidence of genetic diversity underlying Rh D-, weak D (Du), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene. Blood, 1997. [Citation] [RHeference]
- Wagner FF and Flegel WA et al. The Human RhesusBase Online ressource, 2011. — Online ressource — [RHeference]
Last update: Feb. 26, 2020