Atlantoaxial Instability Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Abnormally increased movement at the junction between the first cervical (atlas) and the second cervical (axis) vertebrae as a result of either a bony or ligamentous anomaly. (Human Phenotype Ontology, HP_0003467)
External Link https://www.disgenet.org/browser/0/1/0/C0410653
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Genes

6 genes associated with the disease Atlantoaxial Instability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
DDR2 discoidin domain receptor tyrosine kinase 2
DYM dymeclin
FKBP14 FK506 binding protein 14, 22 kDa
GATA1 GATA binding protein 1 (globin transcription factor 1)
PCYT1A phosphate cytidylyltransferase 1, choline, alpha
SRC SRC proto-oncogene, non-receptor tyrosine kinase