osteomalacia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A bone remodeling disease that has_material_basis_in a vitamin D deficiency which results_in softening located_in bone. (Human Disease Ontology, DOID_10573)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009445
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Genes

5 gene mutations causing the osteomalacia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANO6 anoctamin 6
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
FGF23 fibroblast growth factor 23
PHEX phosphate regulating endopeptidase homolog, X-linked
PHOSPHO1 phosphatase, orphan 1