thyroiditis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Updating to more specific UMLS_CUI from C0029495 to C0040147. (Human Disease Ontology, DOID_7166)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100646
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Genes

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

Symbol Name
ADA adenosine deaminase
C1S complement component 1, s subcomponent
CHD7 chromodomain helicase DNA binding protein 7
COX1
COX2
COX3
DCLRE1C DNA cross-link repair 1C
IL2RG interleukin 2 receptor, gamma
IL7R interleukin 7 receptor
LIG4 ligase IV, DNA, ATP-dependent
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
PLCG2 phospholipase C, gamma 2 (phosphatidylinositol-specific)
PTEN phosphatase and tensin homolog
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2
RMRP RNA component of mitochondrial RNA processing endoribonuclease