abnormality of thyroid morphology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A structural abnormality of the thyroid gland. (Human Phenotype Ontology, HP_0011772)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011772
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Genes

83 genes associated with the abnormality of thyroid morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADA adenosine deaminase
AKT1 v-akt murine thymoma viral oncogene homolog 1
ALMS1 Alstrom syndrome protein 1
APC adenomatous polyposis coli
C1S complement component 1, s subcomponent
CCBE1 collagen and calcium binding EGF domains 1
CCDC6 coiled-coil domain containing 6
CDC73 cell division cycle 73
CHD7 chromodomain helicase DNA binding protein 7
COX1
COX2
COX3
DCLRE1C DNA cross-link repair 1C
DICER1 dicer 1, ribonuclease type III
DIO1 deiodinase, iodothyronine, type I
DUOX2 dual oxidase 2
DUOXA2 dual oxidase maturation factor 2
ECE1 endothelin converting enzyme 1
EDN3 endothelin 3
EDNRB endothelin receptor type B
EYA1 EYA transcriptional coactivator and phosphatase 1
FLCN folliculin
FOXE1 forkhead box E1
FOXI1 forkhead box I1
GDNF glial cell derived neurotrophic factor
GLI3 GLI family zinc finger 3
GNAS GNAS complex locus
GOLGA5 golgin A5
IDH1 isocitrate dehydrogenase 1 (NADP+), soluble
IDH2 isocitrate dehydrogenase 2 (NADP+), mitochondrial
IL2RG interleukin 2 receptor, gamma
IL7R interleukin 7 receptor
IYD iodotyrosine deiodinase
JAG1 jagged 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KLLN killin, p53-regulated DNA replication inhibitor
L1CAM L1 cell adhesion molecule
LIG4 ligase IV, DNA, ATP-dependent
MINPP1 multiple inositol-polyphosphate phosphatase 1
MLH1 mutL homolog 1
MSH2 mutS homolog 2
MSH6 mutS homolog 6
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
NCOA4 nuclear receptor coactivator 4
ND1
NKX2-1 NK2 homeobox 1
NKX2-5 NK2 homeobox 5
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
NRTN neurturin
NSDHL NAD(P) dependent steroid dehydrogenase-like
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PAX8 paired box 8
PCM1 pericentriolar material 1
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PLCG2 phospholipase C, gamma 2 (phosphatidylinositol-specific)
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PTEN phosphatase and tensin homolog
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2
RET ret proto-oncogene
RMRP RNA component of mitochondrial RNA processing endoribonuclease
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
SLC5A5 solute carrier family 5 (sodium/iodide cotransporter), member 5
TG thyroglobulin
THRB thyroid hormone receptor, beta
TPO thyroid peroxidase
TRIM24 tripartite motif containing 24
TRIM33 tripartite motif containing 33
TSHR thyroid stimulating hormone receptor
WRN Werner syndrome, RecQ helicase-like