GYPB, glycophorin B (MNS blood group), 2994

N. diseases: 80; N. variants: 1
Disease: Hereditary spherocytosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		0.020 GeneticVariation disease BEFREE This is because RBCs express a B3 chaperone-like molecule in the form of Glycophorin A that can rescue the majority of B3 mutations that cause dRTA but probably not the majority of HS mutations. 18304844 2008
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		0.020 Biomarker disease BEFREE As an attempt to identify the linking protein(s) between the red cell skeleton and the Rh complex, we analyzed the expression of Rh, RhAG, CD47, LW, and glycophorin B proteins in red cells from patients with hereditary spherocytosis associated with complete protein 4.2 deficiency but normal band 3 (4.2(-)HS). 12393467 2003