ABO Chromosome 9

ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase
8 variants 4 Health Risk 4 Trait

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What This Gene Does
This gene encodes proteins related to the first discovered blood group system, ABO. Variation in the ABO gene (chromosome 9q34.2) is the basis of the ABO blood group, thus the presence of an allele determines the blood group in an individual. The 'O' blood group is caused by a deletion of guanine-258 near the N-terminus of the protein which results in a frameshift and translation of an almost entirely different protein. Individuals with the A, B, and AB alleles express glycosyltransferase activities that convert the H antigen into the A or B antigen. Other minor alleles have been found for this gene. [provided by RefSeq, Apr 2022]
Gene Info
Gene Group
"Glycosyltransferase family 6|Blood group antigens"
Locus Type
gene with protein product
Location
9q34.2
Ensembl
ENSG00000175164
Associated Conditions (2)
ABO blood group system
Severely weakened expression of A on erythrocytes
Key Variants
All Variants (8)
RSID Category Clinical Significance Conditions
RS1554760445 Health Risk association ABO blood group system, ABO blood group system
RS2519093 Health Risk association ABO blood group system, ABO blood group system
RS507666 Health Risk association ABO blood group system, ABO blood group system
RS532436 Health Risk association ABO blood group system, ABO blood group system
RS2490441566 Trait Affects ABO blood group system, ABO blood group system
RS55722397 Trait Affects ABO blood group system, ABO blood group system
RS56392308 Trait Affects ABO blood group system, ABO blood group system
RS782544248 Trait Benign; Affects ABO blood group system, Severely weakened expression of A on erythrocytes, ABO blood group system
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