abnormality of transition element cation homeostasis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the homeostasis (concentration) of transition element cation. (Human Phenotype Ontology, HP_0011030)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011030
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Genes

24 genes associated with the abnormality of transition element cation homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP7B ATPase, Cu++ transporting, beta polypeptide
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
CP ceruloplasmin (ferroxidase)
FTH1 ferritin, heavy polypeptide 1
FTL ferritin, light polypeptide
GLRX5 glutaredoxin 5
HAMP hepcidin antimicrobial peptide
HBB hemoglobin, beta
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
SLC30A2 solute carrier family 30 (zinc transporter), member 2
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
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
TTC37 tetratricopeptide repeat domain 37
XIAP X-linked inhibitor of apoptosis, E3 ubiquitin protein ligase