| KEL |
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| Identifiers |
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| Aliases | KEL, Kell Blood Group, CD238, Kell metallo-endopeptidase (Kell blood group), Kell Blood Group Glycoprotein, Kell blood group, metallo-endopeptidase, Kell Blood Group Antigen, EC 3.4.24, Kell Blood Group, Metalloendopeptidase, Kell, ECE3, Kell–Cellano system |
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| External IDs | OMIM: 613883; MGI: 1346053; GeneCards: KEL |
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| Wikidata |
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The Kell blood group glycoprotein also known as CD238 is a protein that in humans is encoded by the KEL gene.[5]
The Kell glycoprotein is a 732-amino-acid, single-pass, glycosylated protein that is expressed in the plasma membrane of red blood cells.[5] It is covalently attached via a disulfide bond to the multipass XK protein.[5] The KEL gene is highly polymorphic and forms the basis of the Kell antigen system.[5] It is responsible for cleaving an inactive endothelin-3 precursor to its active form. The Kell–XK complex is also associated with red blood cell membrane integrity.[5][6]
The Kell protein is clinically important since it strongly immunogenic and can cause life threatening red blood transfusion reactions.[5] In addition, Kell alloimmunization is caused by a direct maternal immune response to fetal KELL antigens or through a prior antigen-positive pregnancy or transfusion.[5][6]
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