abnormal kidney 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 kidney tissue (Mammalian Phenotype Ontology, MP_0008742)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008742
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12 gene mutations causing the abnormal kidney iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADD2 adducin 2 (beta)
ANK1 ankyrin 1, erythrocytic
EPB41 erythrocyte membrane protein band 4.1
HFE2 hemochromatosis type 2 (juvenile)
HK1 hexokinase 1
HP haptoglobin
HPX hemopexin
HYAL2 hyaluronoglucosaminidase 2
KLF1 Kruppel-like factor 1 (erythroid)
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
SPTA1 spectrin, alpha, erythrocytic 1
SPTB spectrin, beta, erythrocytic