abnormal intestinal calcium 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 calcium into the blood by absorption from the small intestine (Mammalian Phenotype Ontology, MP_0011219)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011219
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2 gene mutations causing the abnormal intestinal calcium absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
PHEX phosphate regulating endopeptidase homolog, X-linked
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor