thyroid carcinoma Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A thyroid cancer that has_material_basis_in epithelial cells. (Human Disease Ontology, DOID_3963)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002890
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Genes

18 genes associated with the thyroid carcinoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APC adenomatous polyposis coli
CCDC6 coiled-coil domain containing 6
DICER1 dicer 1, ribonuclease type III
GOLGA5 golgin A5
JAG1 jagged 1
MINPP1 multiple inositol-polyphosphate phosphatase 1
NCOA4 nuclear receptor coactivator 4
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PCM1 pericentriolar material 1
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PTEN phosphatase and tensin homolog
RET ret proto-oncogene
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SLC26A4 solute carrier family 26 (anion exchanger), member 4
TG thyroglobulin
TRIM24 tripartite motif containing 24
TRIM33 tripartite motif containing 33