abnormal circulating ferritin level Gene Set
Genes
11 gene mutations causing the abnormal circulating ferritin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Symbol |
Name |
CCKBR
|
cholecystokinin B receptor
|
CP
|
ceruloplasmin (ferroxidase)
|
FOXP2
|
forkhead box P2
|
FTH1
|
ferritin, heavy polypeptide 1
|
HAMP
|
hepcidin antimicrobial peptide
|
HMOX1
|
heme oxygenase 1
|
IREB2
|
iron-responsive element binding protein 2
|
PCMT1
|
protein-L-isoaspartate (D-aspartate) O-methyltransferase
|
SLC40A1
|
solute carrier family 40 (iron-regulated transporter), member 1
|
TFR2
|
transferrin receptor 2
|
UMOD
|
uromodulin
|