abnormality of the cervical spine Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Any abnormality of the cervical vertebral column. (Human Phenotype Ontology, HP_0003319)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0003319
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Genes

11 genes associated with the abnormality of the cervical spine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
EXOC1 exocyst complex component 1 1.40061
HLA-DPB1 major histocompatibility complex, class II, DP beta 1 1.10701
CTNNA3 catenin (cadherin-associated protein), alpha 3 1.02868
HLA-B major histocompatibility complex, class I, B 0.731489
MAGI2 membrane associated guanylate kinase, WW and PDZ domain containing 2 0.652869
NELFE negative elongation factor complex member E 0.522136
CGN cingulin 0.481126
EGFR epidermal growth factor receptor 0.446211
HLA-DPA1 major histocompatibility complex, class II, DP alpha 1 0.440194
FANCL Fanconi anemia, complementation group L 0.43316
NFYC nuclear transcription factor Y, gamma 0.426101