beta thalassemia Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A thalassemia characterized by the reduced or absent synthesis of the beta globin chains of hemoglobin. (Human Disease Ontology, DOID_12241)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:12241
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Genes

20 genes associated with the disease beta thalassemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
NPRL3 nitrogen permease regulator-like 3 (S. cerevisiae) 2.45432
BCL11A B-cell CLL/lymphoma 11A (zinc finger protein) 2.35337
OR51B5 olfactory receptor, family 51, subfamily B, member 5 2.29228
HBB hemoglobin, beta 2.14038
UBQLNL ubiquilin-like 1.97129
HBG1 hemoglobin, gamma A 1.94201
HBBP1 hemoglobin, beta pseudogene 1 1.81431
OR51F1 olfactory receptor, family 51, subfamily F, member 1 (gene/pseudogene) 1.7812
OR52I2 olfactory receptor, family 52, subfamily I, member 2 1.68619
CSNK2A1 casein kinase 2, alpha 1 polypeptide 1.51327
OR51E2 olfactory receptor, family 51, subfamily E, member 2 1.49392
OR51I1 olfactory receptor, family 51, subfamily I, member 1 1.45434
RRM1 ribonucleotide reductase M1 1.41484
STIM1 stromal interaction molecule 1 1.39735
OR51B6 olfactory receptor, family 51, subfamily B, member 6 1.37327
PCIF1 PDX1 C-terminal inhibiting factor 1 1.33447
NAP1L4 nucleosome assembly protein 1-like 4 1.32614
CSMD1 CUB and Sushi multiple domains 1 1.29628
HBZ hemoglobin, zeta 1.25348
SYT9 synaptotagmin IX 1.22816