Target intelligence / Profile preview

Glycophorin B (GYPB)

Target
GYPB
Molecular classification
Single-pass transmembrane glycoprotein, Blood group antigen (carrier), Red blood cell membrane protein (erythrocyte sialoglycoprotein), Cluster of differentiation marker (CD235b)
01

Overview

Glycophorin B is a major **red blood cell (erythrocyte) membrane glycoprotein** encoded by the *GYPB* gene, part of the MNS blood group system and designated as **CD235b**[3][5][6]. It carries the **S and s blood group antigens** and is heavily glycosylated, contributing to the negative charge and non-adherent properties of RBCs[1][6][5]. Glycophorin B is involved in immune and infection biology: genetic variants like the Dantu allele (DUP4) protect against malaria by altering red cell membrane tension[1][3]. It also acts as a **receptor for pathogens** (*Plasmodium falciparum*, viruses), but its precise physiological function remains only partly understood since its absence does not cause disease in healthy individuals[1][6]. Glycophorin B is clinically significant in transfusion medicine due to its role in blood group compatibility and risk for hemolytic disease of the newborn and transfusion reactions mediated by antibodies against S, s, or U antigens[6][3]. The gene is prone to structural variation and recombination, producing hybrid proteins and rare antigenic variants[1][4][6].

Other names
Glycophorin-BGPBCD235bSS-active sialoglycoproteinSialoglycoprotein deltaSs sialoglycoproteinblood group system MNSsblood group system SsPAS-3St(a)Miltenberger (Mi)Stones (St^a^)DantuHenshaw (He)MgMNS antigen systemU antigenGYPB-A fusionGYPB/GYPA fusionglycophorin A/B hybridSsS-s-U-Mit+En[a]
02

Mechanism of action

Monoclonal antibodies bind Glycophorin B to detect specific Ss antigens for blood typing, transfusion compatibility, and prevent hemolytic complications Screening for genetic variants (e.g., DUP4) in malaria-endemic regions for predictive medicine

03

Biological functions

Carrier of Ss blood group antigensProvides the red blood cell surface with a negatively charged glycan coat (glycosylation substrate)Acts as a receptor for pathogens (notably *Plasmodium falciparum* malaria parasite and viruses)May be involved in immune response interactions and cellular recognition
04

Disease associations

Hemolytic transfusion reactions and hemolytic disease of the newborn (HDN) due to anti-S, anti-s, or anti-U antibodiesInfection (malaria, *Plasmodium falciparum*)—variation in GYPB confers resistance to malaria (e.g., DUP4 allele for Dantu blood type)Rare blood types (S-s-U-, En[a]-) can impact transfusion compatibility and disease susceptibilityNo established links to cancer, cardiovascular, or neurodegenerative disease
05

Safety considerations

Potential for transfusion reactions (mild to severe) if anti-S, anti-s, or anti-U antibodies are present in recipientsRisk of hemolytic disease of the newborn (HDN)Genetic variation (deletion or fusion events) may affect blood compatibility; rare null phenotypes like S-s-U-, En[a]-No evidence for toxicity or off-target effects since individuals lacking Glycophorin B are usually healthy
06

Interacting drugs

No approved drugs directly target Glycophorin B as a therapeutic receptor; however, monoclonal antibodies are used for blood typing and transfusion compatibility

1 more in the full profile.

07

Biomarkers

Ss antigen positivity or negativity (S, s, U antigens) guides transfusion strategies and risk of HDNDantu (DUP4) allele as a genetic biomarker for malaria resistance in endemic populations

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