decreased circulating iron level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than the normal concentration of iron in the blood (Mammalian Phenotype Ontology, MP_0004151)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004151
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Genes

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

Symbol Name
AP4E1 adaptor-related protein complex 4, epsilon 1 subunit
ATP4A ATPase, H+/K+ exchanging, alpha polypeptide
CAND2 cullin-associated and neddylation-dissociated 2 (putative)
CP ceruloplasmin (ferroxidase)
DDHD1 DDHD domain containing 1
EHD1 EH-domain containing 1
FAM132B family with sequence similarity 132, member B
FBXO7 F-box protein 7
GAST gastrin
HMOX1 heme oxygenase 1
HNF4A hepatocyte nuclear factor 4, alpha
IL10 interleukin 10
JAK2 Janus kinase 2
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
KDM7A lysine (K)-specific demethylase 7A
MAPKAPK2 mitogen-activated protein kinase-activated protein kinase 2
MYO10 myosin X
PITX3 paired-like homeodomain 3
PRDM4 PR domain containing 4
SLC25A4 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
TFRC transferrin receptor
TMEM189 transmembrane protein 189
TMPRSS6 transmembrane protease, serine 6
UMOD uromodulin