abnormal intestinal mineral absorption Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the ability of the body to take up inorganic substances that have importance in body functions into the blood by absorption from the small intestine (Mammalian Phenotype Ontology, MP_0001670)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001670
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Genes

6 gene mutations causing the abnormal intestinal mineral absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
KRT8 keratin 8, type II
PHEX phosphate regulating endopeptidase homolog, X-linked
SLC30A7 solute carrier family 30 (zinc transporter), member 7
TFRC transferrin receptor
TMPRSS6 transmembrane protease, serine 6
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor