Hemoglobin H Disease Gene Set
Genes
27 genes associated with the disease Hemoglobin H Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
AHSP
|
alpha hemoglobin stabilizing protein
|
|
AP5Z1
|
adaptor-related protein complex 5, zeta 1 subunit
|
|
ATR
|
ATR serine/threonine kinase
|
|
ATRX
|
alpha thalassemia/mental retardation syndrome X-linked
|
|
CDAN1
|
codanin 1
|
|
COL9A1
|
collagen, type IX, alpha 1
|
|
COL9A2
|
collagen, type IX, alpha 2
|
|
COL9A3
|
collagen, type IX, alpha 3
|
|
COMP
|
cartilage oligomeric matrix protein
|
|
EPO
|
erythropoietin
|
|
FASTK
|
Fas-activated serine/threonine kinase
|
|
HAMP
|
hepcidin antimicrobial peptide
|
|
HBA1
|
hemoglobin, alpha 1
|
|
HBA2
|
hemoglobin, alpha 2
|
|
HBB
|
hemoglobin, beta
|
|
HBG2
|
hemoglobin, gamma G
|
|
HBZ
|
hemoglobin, zeta
|
|
HFE
|
hemochromatosis
|
|
HP
|
haptoglobin
|
|
KLF1
|
Kruppel-like factor 1 (erythroid)
|
|
PMCH
|
pro-melanin-concentrating hormone
|
|
PSMA5
|
proteasome (prosome, macropain) subunit, alpha type, 5
|
|
SCN8A
|
sodium channel, voltage gated, type VIII alpha subunit
|
|
SEA
|
S13 erythroblastosis (avian) oncogene homolog
|
|
TFR2
|
transferrin receptor 2
|
|
TPMT
|
thiopurine S-methyltransferase
|
|
TSPYL2
|
TSPY-like 2
|
