beta-thalassemia Gene Set
| Dataset |
GAD Gene-Disease Associations
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| Category |
disease or phenotype associations
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| Type |
disease |
| Description |
A thalassemia characterized by the reduced or absent synthesis of the beta globin chains of hemoglobin. (Human Disease Ontology, DOID_12241)
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| Similar Terms |
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| Downloads & Tools |
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Genes
13 genes associated with the disease beta-thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
| Symbol |
Name |
|
F2
|
coagulation factor II (thrombin)
|
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F5
|
coagulation factor V (proaccelerin, labile factor)
|
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HBA1
|
hemoglobin, alpha 1
|
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HBB
|
hemoglobin, beta
|
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HBG1
|
hemoglobin, gamma A
|
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HBG2
|
hemoglobin, gamma G
|
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HBS1L
|
HBS1-like translational GTPase
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MTHFR
|
methylenetetrahydrofolate reductase (NAD(P)H)
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NOS1
|
nitric oxide synthase 1 (neuronal)
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NOS2
|
nitric oxide synthase 2, inducible
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PROCR
|
protein C receptor, endothelial
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TNF
|
tumor necrosis factor
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VDR
|
vitamin D (1,25- dihydroxyvitamin D3) receptor
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