MNAB |
MNCC-SEA |
Podoplanin |
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[MN blood group antigens]
[MN sialoglycoprotein] This blood group antigen is caused by mutations in the Glycophorin A gene, which has two codominant alleles, termed M antigen and N antigen. These are caused by point mutations. The M antigen and N antigen phenotypes differ from each other by one amino acid at positions 1 and 5 in the extracellular N-terminal domain.
In the nomenclature of CD antigens this protein has been given the designation CD235a. See also: blood group antigens.
For additional information on CD antigens see also:
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