abnormality of thyroid morphology Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A structural abnormality of the thyroid gland. (Human Phenotype Ontology, HP_0011772)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0011772
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Genes

7 genes associated with the abnormality of thyroid morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
CAPZB capping protein (actin filament) muscle Z-line, beta 1.66286
FGF7 fibroblast growth factor 7 1.60335
FOXE1 forkhead box E1 0.836224
DIRC3 disrupted in renal carcinoma 3 0.43266
NRG1 neuregulin 1 0.416272
CARD9 caspase recruitment domain family, member 9 0.329663
TMOD1 tropomodulin 1 0.296411