RHD*D-CE(7-10)
(ISBT table: not listed)
				This entry is an hybrid RHD allele.
						Dav, RHD(1-6)-RHCE(7-10), RHD*D-CE(7-10), 
					
	
				Molecular data
						Nucleotides:
						941G>T; 968C>A; 974G>T; 979A>G; 985GG>CA deletion-insertion; 989A>C; 992A>T; 1025T>C; 1048G>C; 1053C>T; 1057GGA>TGG deletion-insertion; 1060GC>AA deletion-insertion; 1170T>C; 1193A>T; 
					
Amino acids: G314V; P323H; S325I; I327V; G329H; Y330S; N331I; I342T; D350H; T351T; G353W; A354N; L390L; E398V;
						Hybrid allele encompassing at least one  RHCE  exon:
						RHD(1-6)-RHCE(7-10)
					
						Comments on the molecular basis:
						
- allele considered to be at the RHD locus
 - allele considered to be at the RHD locus
 - considered to be at the RHCE locus
 
						Extracellular position of one or more amino acid substitutions: 
						
						Splicing:
						
						Unconventional prediction methods:
						
Phenotype
Main D phenotype: unknown, expected to be D negative (last update: July 28, 2020)Haplotype
Main CcEe phenotype association: cE (last update: March 11, 2020)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: no published cases (last update: July 28, 2020)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: unknown
Reports
Summary: exceptional description(s), in African Americans (last update: March 11, 2020)Detailed reports
- 1/50 (heterozygous with RHef00008) among 50 donors, the majority referred because of ambiguous RH5 antigen typing, found to have RHCE*ceMO (44 with RHef00008, 6 with RHef00442) in the USA population
 - 1 sample investigated for RH5 discrepant typing African American
 
Allele or phenotype frequency
Structure mapping
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| Slab | Ctrl+Second | Not Available | 
References
- Schmid P et al. Specific amino acid substitutions cause distinct expression of JAL (RH48) and JAHK (RH53) antigens in RhCE and not in RhD. Transfusion, 2010. [Citation] [RHeference]
 - C Lomas-Francis et al. Surprising findings with RBCs expressing the low prevalence RH antigen Evans Transfusion, 2011. — Abstract — [RHeference]
 - Westhoff CM et al. RHCE*ceMO is frequently in cis to RHD*DAU0 and encodes a hr(S) -, hr(B) -, RH:-61 phenotype in black persons: clinical significance. Transfusion, 2013. [Citation] [RHeference]
 - Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
 
Last update: June 11, 2020