neoplasm of the thyroid gland Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A tumor (abnormal growth of tissue) of the thyroid gland. (Human Phenotype Ontology, HP_0100031)
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39 genes associated with the neoplasm of the thyroid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
APC adenomatous polyposis coli
CCDC6 coiled-coil domain containing 6
CDC73 cell division cycle 73
DICER1 dicer 1, ribonuclease type III
ECE1 endothelin converting enzyme 1
EDN3 endothelin 3
EDNRB endothelin receptor type B
FLCN folliculin
FOXI1 forkhead box I1
GDNF glial cell derived neurotrophic factor
GNAS GNAS complex locus
GOLGA5 golgin A5
JAG1 jagged 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KLLN killin, p53-regulated DNA replication inhibitor
L1CAM L1 cell adhesion molecule
MINPP1 multiple inositol-polyphosphate phosphatase 1
MLH1 mutL homolog 1
MSH2 mutS homolog 2
MSH6 mutS homolog 6
NCOA4 nuclear receptor coactivator 4
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
NRTN neurturin
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PCM1 pericentriolar material 1
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
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)
SDHC succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
SLC26A4 solute carrier family 26 (anion exchanger), member 4
TG thyroglobulin
TRIM24 tripartite motif containing 24
TRIM33 tripartite motif containing 33
WRN Werner syndrome, RecQ helicase-like