mitochondrial Gene Set

Dataset GAD High Level Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A mode of inheritance that is observed for traits related to a gene encoded on the mitochondrial genome. Because the mitochondrial genome is essentially always maternally inherited, a mitochondrial condition can only be transmitted by females, although the condition can affect both sexes. The proportion of mutant mitochondria can vary (heteroplasmy). (Human Phenotype Ontology, HP_0001427)
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Genes

1 genes associated with the disease mitochondrial in GWAS and other genetic association datasets from the GAD High Level Gene-Disease Associations dataset.

Symbol Name Standardized Value
TK2 thymidine kinase 2, mitochondrial 0.293278