deformed rib cage Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Malformation of the rib cage. (Human Phenotype Ontology, HP_0000886)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000886
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Genes

4 genes associated with the deformed rib cage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
CYP2R1 cytochrome P450, family 2, subfamily R, polypeptide 1
SLC34A3 solute carrier family 34 (type II sodium/phosphate cotransporter), member 3
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor