blood group antigen abnormality Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of an erythrocyte cell surface molecule. (Human Phenotype Ontology, HP_0010970)
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2 genes associated with the blood group antigen abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GCNT2 glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group)
KLF1 Kruppel-like factor 1 (erythroid)