Trait
Increased methionine in blood
Clinical name: Hypermethioninemia
An increased concentration of methionine in the blood.
Summary
- Also called
- Methioninemia
- Body system
- Laboratory abnormality
Reference genomeGRCh38hg38
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Get my Genome Test9 genes linked to Increased methionine in blood
Changes in these genes cause rare conditions in which Increased methionine in blood is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ADKadenosine kinase | Always | In 1 condition |
| AHCYadenosylhomocysteinase | Always | In 2 conditions |
| CBScystathionine beta-synthase | Always | In 1 condition |
| SLC25A13solute carrier family 25 member 13 | Always | In 2 conditions |
| TFAMtranscription factor A, mitochondrial | Always | In 1 condition |
| FAHfumarylacetoacetate hydrolase | Not recorded | In 1 condition |
| GNMTglycine N-methyltransferase | Not recorded | In 1 condition |
| MAT1Amethionine adenosyltransferase 1A | Not recorded | In 1 condition |
| SKIC3SKI3 subunit of superkiller complex | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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