Alpha^+^ Thalassemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1456873
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Genes

86 genes associated with the disease Alpha^+^ Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
ADCY9 adenylate cyclase 9
AP5Z1 adaptor-related protein complex 5, zeta 1 subunit
ARR3 arrestin 3, retinal (X-arrestin)
ATAD1 ATPase family, AAA domain containing 1
ATR ATR serine/threonine kinase
ATRX alpha thalassemia/mental retardation syndrome X-linked
BCL11A B-cell CLL/lymphoma 11A (zinc finger protein)
CASR calcium-sensing receptor
CD19 CD19 molecule
CD34 CD34 molecule
CD36 CD36 molecule (thrombospondin receptor)
CD37 CD37 molecule
CEBPD CCAAT/enhancer binding protein (C/EBP), delta
COL9A1 collagen, type IX, alpha 1
COL9A2 collagen, type IX, alpha 2
COL9A3 collagen, type IX, alpha 3
COMP cartilage oligomeric matrix protein
CR1 complement component (3b/4b) receptor 1 (Knops blood group)
CXADR coxsackie virus and adenovirus receptor
DAP death-associated protein
DAXX death-domain associated protein
DOCK11 dedicator of cytokinesis 11
EPGN epithelial mitogen
EPO erythropoietin
F3 coagulation factor III (thromboplastin, tissue factor)
FASTK Fas-activated serine/threonine kinase
FCGRT Fc fragment of IgG, receptor, transporter, alpha
FTMT ferritin mitochondrial
G6PD glucose-6-phosphate dehydrogenase
HAMP hepcidin antimicrobial peptide
HBA1 hemoglobin, alpha 1
HBA2 hemoglobin, alpha 2
HBB hemoglobin, beta
HBG1 hemoglobin, gamma A
HBG2 hemoglobin, gamma G
HBQ1 hemoglobin, theta 1
HBS1L HBS1-like translational GTPase
HBZ hemoglobin, zeta
HFE hemochromatosis
HMOX1 heme oxygenase 1
HP haptoglobin
KLF1 Kruppel-like factor 1 (erythroid)
LMLN leishmanolysin-like (metallopeptidase M8 family)
LMNA lamin A/C
LUC7L LUC7-like (S. cerevisiae)
MSMB microseminoprotein, beta-
MST1 macrophage stimulating 1
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MYB v-myb avian myeloblastosis viral oncogene homolog
NPRL3 nitrogen permease regulator-like 3 (S. cerevisiae)
NR1I3 nuclear receptor subfamily 1, group I, member 3
NSD1 nuclear receptor binding SET domain protein 1
OR10A4 olfactory receptor, family 10, subfamily A, member 4
PGD phosphogluconate dehydrogenase
PKD1 polycystic kidney disease 1 (autosomal dominant)
PMCH pro-melanin-concentrating hormone
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PSMA5 proteasome (prosome, macropain) subunit, alpha type, 5
RAG2 recombination activating gene 2
RASA1 RAS p21 protein activator (GTPase activating protein) 1
RGS6 regulator of G-protein signaling 6
RNGTT RNA guanylyltransferase and 5'-phosphatase
RUNX1 runt-related transcription factor 1
SCLT1 sodium channel and clathrin linker 1
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SEA S13 erythroblastosis (avian) oncogene homolog
SLCO1B1 solute carrier organic anion transporter family, member 1B1
SMARCA2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
TEK TEK tyrosine kinase, endothelial
TFRC transferrin receptor
TGFBR3 transforming growth factor, beta receptor III
TMPRSS13 transmembrane protease, serine 13
TP53 tumor protein p53
TRIM13 tripartite motif containing 13
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1
UGT1A10 UDP glucuronosyltransferase 1 family, polypeptide A10
UGT1A4 UDP glucuronosyltransferase 1 family, polypeptide A4
UGT1A6 UDP glucuronosyltransferase 1 family, polypeptide A6
UGT1A7 UDP glucuronosyltransferase 1 family, polypeptide A7
UGT1A8 UDP glucuronosyltransferase 1 family, polypeptide A8
VCAM1 vascular cell adhesion molecule 1
ZMPSTE24 zinc metallopeptidase STE24
ZNF410 zinc finger protein 410