rickets 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 in children which results_in softening and deformity located_in bone. (Experimental Factor Ontology, EFO_0005583)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003116
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Genes

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

Symbol Name
CASR calcium-sensing receptor
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
PHEX phosphate regulating endopeptidase homolog, X-linked
RGN regucalcin
SIK3 SIK family kinase 3
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor