hyperthyroidism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A thyroid gland disease that involves an over production of thyroid hormone. (Human Disease Ontology, DOID_7998)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000836
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Genes

24 genes associated with the hyperthyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARVCF armadillo repeat gene deleted in velocardiofacial syndrome
COMT catechol-O-methyltransferase
COX1
COX2
COX3
GNAS GNAS complex locus
GP1BB glycoprotein Ib (platelet), beta polypeptide
HIRA histone cell cycle regulator
MT-ND4 NADH dehydrogenase, subunit 4 (complex I)
MT-ND5 NADH dehydrogenase, subunit 5 (complex I)
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
MT-TF tRNA
MT-TH tRNA
MT-TL1 tRNA
MT-TQ tRNA
MT-TS1 tRNA
MT-TS2 tRNA
MT-TW tRNA
ND1
PTEN phosphatase and tensin homolog
TBX1 T-box 1
THRB thyroid hormone receptor, beta
TSHR thyroid stimulating hormone receptor
UFD1L ubiquitin fusion degradation 1 like (yeast)