RHD*02 - RHD*DII
(ISBT table: RHD partial D v5.0)
				This entry is an RHD allele.
						DII, RHD(A354D), RHD*1061A, RHD*1061A (DII), RHD*1061C>A, 
					
	
				Molecular data
Phenotype
Main D phenotype: variable/discrepant (last update: Nov. 17, 2019)Reports by D phenotype
- Discrepant D phenotype (negative or positive depending on anti-D reagents and techniques)
 - See also "Additional comments" section on the RhesusBase http://www.rhesusbase.info/RHDDII.htm
 
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: March 7, 2020)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: probably allo-anti-D (last update: May 16, 2020)Detailed information
- 
									
										Wagner FF and Flegel WA et al. Online ressource (2011) 
										
											(see also "Additional comments" section on the RhesusBase http://www.rhesusbase.info/RHDDII.htm)
										
										
 - Ab specificity: D (RH1)
 - Number (auto- or allo-):
 - Number listed as allo-:
 - 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:
 
- 
									
										Daniels G et al. Br J Haematol (2013) 
										
											(review; Table I)
										
										
 - Ab specificity: D (RH1)
 - Number (auto- or allo-):
 - Number listed as allo-: no new case detailed (listed as allo-anti-D)
 - Number listed as auto-: NA
 - Number of carriers of the allele assessed: NA
 - DAT: NA
 - Autologuous control: NA
 - Elution: NA
 - Autoadsorption: NA
 - Titer: NA
 - Was anti-LW excluded?: NA
 - Other antibodies detected: NA
 - Cross matches (with Ab and RBCs from different partial types): NA
 - Transfusion history: NA
 - Pregnancy history:
 - Anti-D Ig history: NA
 - Context: NA
 - Hemolytic consequences: NA
 - Comment: list of D variants associated with alloanti-D formation
 
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Reports
Summary: exceptional description(s), Caucasian (last update: March 7, 2020)Detailed reports
Allele or phenotype frequency
Structure mapping
| Movement | Mouse Input | Touch Input | ||
|---|---|---|---|---|
| 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
- Scott M et al. Rh serology--coordinator's report. Transfus Clin Biol, 1996. [Citation] [RHeference]
 - Avent ND et al. Molecular basis of the D variant phenotypes DNU and DII allows localization of critical amino acids required for expression of Rh D epitopes epD3, 4 and 9 to the sixth external domain of the Rh D protein. Br J Haematol, 1997. [Citation] [RHeference]
 - Liu W et al. Site-directed mutagenesis of the human D antigen: definition of D epitopes on the sixth external domain of the D protein expressed on K562 cells. Transfusion, 1999. [Citation] [RHeference]
 - Avent ND et al. The rhesus blood group system: insights from recent advances in molecular biology. Transfus Med Rev, 1999. [Citation] [RHeference]
 - Wagner FF et al. DNB: a partial D with anti-D frequent in Central Europe. Blood, 2002. [Citation] [RHeference]
 - Wagner FF and Flegel WA et al. The Human RhesusBase Online ressource, 2011. — Online ressource — [RHeference]
 - Daniels G et al. Variants of RhD--current testing and clinical consequences. Br J Haematol, 2013. [Citation] [RHeference]
 - Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
 
Last update: March 7, 2020