vertebral wedging Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal shape of the vertebral bodies whereby the vertebral bodies are thick on one side and taper to a thin edge at the other. (Human Phenotype Ontology, HP_0008422)
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7 genes associated with the vertebral wedging phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARSB arylsulfatase B
FKBP10 FK506 binding protein 10, 65 kDa
IFITM5 interferon induced transmembrane protein 5
PTCH1 patched 1
PTCH2 patched 2
SEC23A Sec23 homolog A (S. cerevisiae)
SUFU suppressor of fused homolog (Drosophila)