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GENATLAS PHENOTYPE
last update : 5/06/2006
Symbol RH
Location 1p36.1
Name Rhesus blood group
Corresponding gene RHD , RHCE
Main clinical features as determined by RH-D (OMIM111680) and RH C/c-E/e (RH-CE) loci, including hemolytic disease of the newborn (Rhd phenotype)
Genetic determination
Function/system disorder hematology
Type other
Gene product
Name fatty acylated integral red cell membrane protein component (30kD), of the RH antigen multisubunit complex