Trait
Elevated blood glycine levels
Clinical name: Hyperglycinemia
An elevated concentration of glycine in the blood.
Summary
- Also called
- Hyperglycinaemia
- Body system
- Laboratory abnormality
Reference genomeGRCh38hg38
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Get my Genome Test28 genes linked to Elevated blood glycine levels
Changes in these genes cause rare conditions in which Elevated blood glycine levels 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 |
|---|---|---|
| BOLA3bolA family member 3 | Always | In 2 conditions |
| COX8Acytochrome c oxidase subunit 8A | Always | In 1 condition |
| GCSHglycine cleavage system protein H | Always | In 1 condition |
| GLRX5glutaredoxin 5 | Always | In 1 condition |
| IBA57iron-sulfur cluster assembly factor IBA57 | Always | In 2 conditions |
| NFS1NFS1 cysteine desulfurase | Always | In 1 condition |
| NFU1NFU1 iron-sulfur cluster scaffold | Very often (80–99%) | In 2 conditions |
| PSAT1phosphoserine aminotransferase 1 | Very often (80–99%) | In 1 condition |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Often (30–79%) | In 1 condition |
| ATP5F1AATP synthase F1 subunit alpha | Often (30–79%) | In 1 condition |
| GLYCTKglycerate kinase | Often (30–79%) | In 1 condition |
| LIPT2lipoyl(octanoyl) transferase 2 | Often (30–79%) | In 1 condition |
| PET117PET117 cytochrome c oxidase chaperone | Often (30–79%) | In 1 condition |
| SLC7A7solute carrier family 7 member 7 | Often (30–79%) | In 1 condition |
| ISCA2iron-sulfur cluster assembly 2 | Sometimes (5–29%) | In 1 condition |
| SLC30A10solute carrier family 30 member 10 | Sometimes (5–29%) | In 1 condition |
| GLDCglycine decarboxylase | Not recorded | In 1 condition |
| MMAAmetabolism of cobalamin associated A | Not recorded | In 1 condition |
| MMABmetabolism of cobalamin associated B | Not recorded | In 1 condition |
| MMUTmethylmalonyl-CoA mutase | Not recorded | In 1 condition |
| PCCApropionyl-CoA carboxylase subunit alpha | Not recorded | In 1 condition |
| PCCBpropionyl-CoA carboxylase subunit beta | Not recorded | In 1 condition |
| SLC36A2solute carrier family 36 member 2 | Not recorded | In 1 condition |
| SLC6A18solute carrier family 6 member 18 | Not recorded | In 1 condition |
| SLC6A19solute carrier family 6 member 19 | Not recorded | In 1 condition |
| SLC6A20solute carrier family 6 member 20 | Not recorded | In 1 condition |
| SLC6A9solute carrier family 6 member 9 | Not recorded | In 1 condition |
| SUCLG1succinate-CoA ligase GDP/ADP-forming subunit alpha | 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.
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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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