increased circulating iron level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description elevation in the concentration of iron in the blood (Mammalian Phenotype Ontology, MP_0008810)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008810
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Genes

22 gene mutations causing the increased circulating iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AP2A2 adaptor-related protein complex 2, alpha 2 subunit
BTBD9 BTB (POZ) domain containing 9
DDHD1 DDHD domain containing 1
EXOC6 exocyst complex component 6
HAMP hepcidin antimicrobial peptide
HFE hemochromatosis
HFE2 hemochromatosis type 2 (juvenile)
LTF lactotransferrin
MAPKAPK2 mitogen-activated protein kinase-activated protein kinase 2
NGFR nerve growth factor receptor
NPTN neuroplastin
PRDM4 PR domain containing 4
RHAG Rh-associated glycoprotein
RHCE Rh blood group, CcEe antigens
SLC38A10 solute carrier family 38, member 10
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
SPTA1 spectrin, alpha, erythrocytic 1
SPTB spectrin, beta, erythrocytic
TF transferrin
TFR2 transferrin receptor 2
TRPC3 transient receptor potential cation channel, subfamily C, member 3
TTC7A tetratricopeptide repeat domain 7A