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References OMIM Gene GeneReviews HGMD HGNC
last update : 7/09/2006
Symbol RHNR
Location 6p21.1-p11
Name RH-null syndrome
Corresponding gene RHAG
Other symbol(s) RHNR
Main clinical features
  • regulator or mod (translation initiator) phenotype, associated with chronic hemolytic anemia,stomatocytosis and spherocytosis
  • Genetic determination
    Function/system disorder hematology
    Gene product
    Name glycoprotein (RHAG)(mutation in RHAG of the structure interaction and processing in the RH-mod) phenotype