Hemoglobin F Disease Gene Set
Genes
23 genes associated with the disease Hemoglobin F Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
BCL11A
|
B-cell CLL/lymphoma 11A (zinc finger protein)
|
|
CACNA1H
|
calcium channel, voltage-dependent, T type, alpha 1H subunit
|
|
CAD
|
carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase
|
|
DHODH
|
dihydroorotate dehydrogenase (quinone)
|
|
DLL1
|
delta-like 1 (Drosophila)
|
|
EPO
|
erythropoietin
|
|
GATA1
|
GATA binding protein 1 (globin transcription factor 1)
|
|
HAMP
|
hepcidin antimicrobial peptide
|
|
HBA1
|
hemoglobin, alpha 1
|
|
HBA2
|
hemoglobin, alpha 2
|
|
HBB
|
hemoglobin, beta
|
|
HBD
|
hemoglobin, delta
|
|
HBG1
|
hemoglobin, gamma A
|
|
HBG2
|
hemoglobin, gamma G
|
|
KLF1
|
Kruppel-like factor 1 (erythroid)
|
|
LCN2
|
lipocalin 2
|
|
POU2F1
|
POU class 2 homeobox 1
|
|
PSMB6
|
proteasome (prosome, macropain) subunit, beta type, 6
|
|
TFR2
|
transferrin receptor 2
|
|
TFRC
|
transferrin receptor
|
|
UMPS
|
uridine monophosphate synthetase
|
|
YY1
|
YY1 transcription factor
|
|
ZBTB7A
|
zinc finger and BTB domain containing 7A
|
