abnormal serum ferritin Gene Set
Genes
17 genes associated with the abnormal serum ferritin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
BCS1L
|
BC1 (ubiquinol-cytochrome c reductase) synthesis-like
|
|
CP
|
ceruloplasmin (ferroxidase)
|
|
FTH1
|
ferritin, heavy polypeptide 1
|
|
FTL
|
ferritin, light polypeptide
|
|
GLRX5
|
glutaredoxin 5
|
|
HFE
|
hemochromatosis
|
|
HFE2
|
hemochromatosis type 2 (juvenile)
|
|
PIEZO1
|
piezo-type mechanosensitive ion channel component 1
|
|
PRF1
|
perforin 1 (pore forming protein)
|
|
PUS1
|
pseudouridylate synthase 1
|
|
SLC25A38
|
solute carrier family 25, member 38
|
|
SLC7A7
|
solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
|
|
STEAP3
|
STEAP family member 3, metalloreductase
|
|
STX11
|
syntaxin 11
|
|
STXBP2
|
syntaxin binding protein 2
|
|
TFR2
|
transferrin receptor 2
|
|
XIAP
|
X-linked inhibitor of apoptosis, E3 ubiquitin protein ligase
|
