abnormal spleen iron level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the amount of iron present in the spleen tissue (Mammalian Phenotype Ontology, MP_0008739)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008739
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25 gene mutations causing the abnormal spleen iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADD2 adducin 2 (beta)
ANK1 ankyrin 1, erythrocytic
CP ceruloplasmin (ferroxidase)
EPB41 erythrocyte membrane protein band 4.1
EPB42 erythrocyte membrane protein band 4.2
EXOC6 exocyst complex component 6
FBXL5 F-box and leucine-rich repeat protein 5
HAMP hepcidin antimicrobial peptide
HFE hemochromatosis
HFE2 hemochromatosis type 2 (juvenile)
HYAL2 hyaluronoglucosaminidase 2
IL10 interleukin 10
IREB2 iron-responsive element binding protein 2
KCNN4 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 4
KLF1 Kruppel-like factor 1 (erythroid)
LTF lactotransferrin
PRKAG1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
SPIC Spi-C transcription factor (Spi-1/PU.1 related)
SPTA1 spectrin, alpha, erythrocytic 1
TFR2 transferrin receptor 2
TFRC transferrin receptor
TMPRSS6 transmembrane protease, serine 6
TRIB1 tribbles pseudokinase 1
UROS uroporphyrinogen III synthase