RHCE Chromosome 1

Rh blood group CcEe antigens
5 variants 4 Health Risk 1 Trait

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What This Gene Does
The Rh blood group system is the second most clinically significant of the blood groups, second only to ABO. It is also the most polymorphic of the blood groups, with variations due to deletions, gene conversions, and missense mutations. The Rh blood group includes this gene which encodes both the RhC and RhE antigens on a single polypeptide and a second gene which encodes the RhD protein. The classification of Rh-positive and Rh-negative individuals is determined by the presence or absence of the highly immunogenic RhD protein on the surface of erythrocytes. A mutation in this gene results in amorph-type Rh-null disease. Alternative splicing of this gene results in multiple transcript variants encoding several different isoforms. [provided by RefSeq, Aug 2016]
Gene Info
Gene Group
"Blood group antigens|CD molecules|Solute carrier family 42"
Locus Type
gene with protein product
Location
1p36.11
Ensembl
ENSG00000188672
Associated Conditions (3)
RH-NULL
AMORPH TYPE
altered RhC expression
Key Variants
All Variants (5)
RSID Category Clinical Significance Conditions
RS1553156106 Health Risk Pathogenic RH-NULL, AMORPH TYPE, RH-NULL
RS2124396753 Health Risk Pathogenic RH-NULL, AMORPH TYPE, RH-NULL
RS2124429282 Health Risk Pathogenic RH-NULL, AMORPH TYPE, RH-NULL
RS2523069166 Health Risk Pathogenic RH-NULL, AMORPH TYPE, RH-NULL
RS2124414255 Trait Affects altered RhC expression, altered RhC expression
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