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 study . | Genetic change .  | Cellular antigens* .  | Antibodies in serum† . | Phenotype . | Original description of the allele causing phenotype . | |||
|---|---|---|---|---|---|---|---|---|
| A4GALT . | B3GALNT1 . | P1 . | P . | Pk . | ||||
| p1 | 657delG | No change | − | − | − | P, P1, Pk | P | Hellberg et al14 (2003) | 
| p2 | 548T>A | No change | − | − | − | P, P1, Pk | P | Steffensen et al13 (2000) | 
| p3 | 548T>A | No change | − | − | − | P, P1, Pk | P | Steffensen et al13 (2000) | 
| P1k-a | No change | 811G>A | + | − | + | P | P1k | Hellberg et al9 (2002) | 
| P1k-b | No change | 538insA | + | − | + | P | P1k | Hellberg et al9 (2002) | 
| Sample ID in this study . | Genetic change .  | Cellular antigens* .  | Antibodies in serum† . | Phenotype . | Original description of the allele causing phenotype . | |||
|---|---|---|---|---|---|---|---|---|
| A4GALT . | B3GALNT1 . | P1 . | P . | Pk . | ||||
| p1 | 657delG | No change | − | − | − | P, P1, Pk | P | Hellberg et al14 (2003) | 
| p2 | 548T>A | No change | − | − | − | P, P1, Pk | P | Steffensen et al13 (2000) | 
| p3 | 548T>A | No change | − | − | − | P, P1, Pk | P | Steffensen et al13 (2000) | 
| P1k-a | No change | 811G>A | + | − | + | P | P1k | Hellberg et al9 (2002) | 
| P1k-b | No change | 538insA | + | − | + | P | P1k | Hellberg et al9 (2002) |