vertebral arch anomaly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A morphological abnormality of the vertebral arch, i.e., of the posterior part of a vertebra. (Human Phenotype Ontology, HP_0008438)
External Link
Similar Terms
Downloads & Tools


10 genes associated with the vertebral arch anomaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANKRD11 ankyrin repeat domain 11
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
JAG1 jagged 1
KIF22 kinesin family member 22
NPR2 natriuretic peptide receptor 2
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
RMRP RNA component of mitochondrial RNA processing endoribonuclease
RNU4ATAC RNA, U4atac small nuclear (U12-dependent splicing)
SMAD4 SMAD family member 4