Table 2

Summary of the P/GLOB-related blood group genetic and serologic findings in the rare persons whose cells were used in this study

Sample ID in this studyGenetic change
Cellular antigens*
Antibodies in serumPhenotypeOriginal description of the allele causing phenotype
A4GALTB3GALNT1P1PPk
p1 657delG No change − − − P, P1, Pk Hellberg et al14  (2003) 
p2 548T>A No change − − − P, P1, Pk Steffensen et al13  (2000) 
p3 548T>A No change − − − P, P1, Pk Steffensen et al13  (2000) 
P1k-a No change 811G>A − P1k Hellberg et al (2002) 
P1k-b No change 538insA − P1k Hellberg et al (2002) 
Sample ID in this studyGenetic change
Cellular antigens*
Antibodies in serumPhenotypeOriginal description of the allele causing phenotype
A4GALTB3GALNT1P1PPk
p1 657delG No change − − − P, P1, Pk Hellberg et al14  (2003) 
p2 548T>A No change − − − P, P1, Pk Steffensen et al13  (2000) 
p3 548T>A No change − − − P, P1, Pk Steffensen et al13  (2000) 
P1k-a No change 811G>A − P1k Hellberg et al (2002) 
P1k-b No change 538insA − P1k Hellberg et al (2002) 

+ indicates present; and −, absent.

*

The P1 antigen is present in P1 and P1k phenotype samples, detectable with anti-P1 but absent in P2 and P2k and p.

Anti-PP1Pk is also known as anti-Tja and is only found in individuals having the p phenotype.

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