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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