alpha-Thalassemia Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Alpha thalassemia is a thalassemia involving the genes HBA1and HBA2 hemoglobin genes. (Human Disease Ontology, DOID_1099)
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Genes

21 genes associated with the alpha-Thalassemia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABO ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase)
BCL11A B-cell CLL/lymphoma 11A (zinc finger protein)
CD36 CD36 molecule (thrombospondin receptor)
G6PD glucose-6-phosphate dehydrogenase
HBA1 hemoglobin, alpha 1
HBA2 hemoglobin, alpha 2
HBB hemoglobin, beta
HBG2 hemoglobin, gamma G
HBS1L HBS1-like translational GTPase
HFE hemochromatosis
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
HP haptoglobin
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MYB v-myb avian myeloblastosis viral oncogene homolog
NOS3 nitric oxide synthase 3 (endothelial cell)
TFR2 transferrin receptor 2
TMPRSS6 transmembrane protease, serine 6
TNF tumor necrosis factor
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1
VCAM1 vascular cell adhesion molecule 1