Hyperthyroxinemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0020551
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Genes

13 genes associated with the disease Hyperthyroxinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADH5 alcohol dehydrogenase 5 (class III), chi polypeptide
ALB albumin
ALDH1L1 aldehyde dehydrogenase 1 family, member L1
DIO1 deiodinase, iodothyronine, type I
GC group-specific component (vitamin D binding protein)
HCCS holocytochrome c synthase
OXA1L oxidase (cytochrome c) assembly 1-like
PORCN porcupine homolog (Drosophila)
SACM1L SAC1 suppressor of actin mutations 1-like (yeast)
SERPINA7 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 7
SHBG sex hormone-binding globulin
TTR transthyretin
TXNRD2 thioredoxin reductase 2