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GTR Home > Conditions/Phenotypes > BLOOD GROUP, EMM SYSTEM

BLOOD GROUP, EMM SYSTEM

Summary

The Emm red blood cell antigen is assigned number 901008 in the International Society of Blood Transfusion (ISBY) 901 series of high incidence antigens. Emm has been designated the 42nd blood group system. Rare individuals have an Emm- phenotype due to homozygous loss-of-function mutations in the PIGG gene. These individuals often have naturally occurring anti-Emm antibodies that are identified during routine blood type and crossing. These antibodies have the potential to cause acute hemolytic transfusion reactions (summary by Lane et al., 2021). [from OMIM]

Available tests

2 tests are in the database for this condition.

Clinical tests (2 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: EMM, GPI7, LAS21, MRT53, NEDHSCA, PRO4405, RLGS1930, PIGG
    Summary: phosphatidylinositol glycan anchor biosynthesis class G (EMM blood group)

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