beta-Thalassemia Gene Set

Dataset CTD Gene-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://ctdbase.org/detail.go?type=disease&acc=MESH:D017086
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Genes

10 genes/proteins associated with the disease beta-Thalassemia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
LCN2 lipocalin 2 2.88009
UMPS uridine monophosphate synthetase 2.88009
CAD carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase 2.88009
TFR2 transferrin receptor 2 2.88009
TFRC transferrin receptor 2.88009
HBB hemoglobin, beta 2.88009
DHODH dihydroorotate dehydrogenase (quinone) 2.88009
EPO erythropoietin 2.88009
HAMP hepcidin antimicrobial peptide 2.88009
HBA2 hemoglobin, alpha 2 2.88009