Anemia, Iron-Deficiency Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

32 genes associated with the Anemia, Iron-Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
ARHGEF3 Rho guanine nucleotide exchange factor (GEF) 3
BMP2 bone morphogenetic protein 2
BTBD9 BTB (POZ) domain containing 9
CACNA2D3 calcium channel, voltage-dependent, alpha 2/delta subunit 3
COPZ1 coatomer protein complex, subunit zeta 1
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
DRD2 dopamine receptor D2
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
GSTM1 glutathione S-transferase mu 1
GSTT1 glutathione S-transferase theta 1
HBB hemoglobin, beta
HBE1 hemoglobin, epsilon 1
HFE hemochromatosis
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
JAK2 Janus kinase 2
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
RFC1 replication factor C (activator 1) 1, 145kDa
SLC11A1 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 1
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
TCN2 transcobalamin II
TF transferrin
TFR2 transferrin receptor 2
TMPRSS6 transmembrane protease, serine 6
TNF tumor necrosis factor
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor