atlantoaxial dislocation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Partial dislocation of the atlantoaxial joint. (Human Phenotype Ontology, HP_0003414)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003414
Similar Terms
Downloads & Tools

Genes

3 genes associated with the atlantoaxial dislocation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COMP cartilage oligomeric matrix protein
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
NFIX nuclear factor I/X (CCAAT-binding transcription factor)