Trait
High urine lactic acid levels
Clinical name: Lacticaciduria
An increased concentration of lactic acid in the urine.
Summary
- Also called
- Increased urine lactate
Reference genomeGRCh38hg38
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Get my Genome Test38 genes linked to High urine lactic acid levels
Changes in these genes cause rare conditions in which High urine lactic acid 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 |
|---|---|---|
| ATPAF2ATP synthase mitochondrial F1 complex assembly factor 2 | Always | In 1 condition |
| CA5Acarbonic anhydrase 5A | Always | In 1 condition |
| FBXL4F-box and leucine rich repeat protein 4 | Always | In 1 condition |
| LIPT1lipoyltransferase 1 | Always | In 1 condition |
| LYRM4LYR motif containing 4 | Always | In 1 condition |
| MPV17mitochondrial inner membrane protein MPV17 | Always | In 1 condition |
| NDUFA9NADH:ubiquinone oxidoreductase subunit A9 | Always | In 1 condition |
| NDUFB10NADH:ubiquinone oxidoreductase subunit B10 | Always | In 1 condition |
| NFU1NFU1 iron-sulfur cluster scaffold | Always | In 2 conditions |
| SCO2synthesis of cytochrome C oxidase 2 | Always | In 1 condition |
| SDHDsuccinate dehydrogenase complex subunit D | Always | In 1 condition |
| SLC25A21solute carrier family 25 member 21 | Always | In 1 condition |
| SUCLG1succinate-CoA ligase GDP/ADP-forming subunit alpha | Always | In 1 condition |
| TEFMtranscription elongation factor, mitochondrial | Always | In 1 condition |
| TRMUtRNA mitochondrial 2-thiouridylase | Always | In 1 condition |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Very often (80–99%) | In 1 condition |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Often (30–79%) | In 1 condition |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Often (30–79%) | In 1 condition |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Often (30–79%) | In 1 condition |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Often (30–79%) | In 1 condition |
| MT-ND3mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 | Often (30–79%) | In 1 condition |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Often (30–79%) | In 1 condition |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Often (30–79%) | In 1 condition |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Often (30–79%) | In 1 condition |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Often (30–79%) | In 1 condition |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Often (30–79%) | In 1 condition |
| MT-TVmitochondrially encoded tRNA-Val (GUN) | Often (30–79%) | In 1 condition |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Often (30–79%) | In 1 condition |
| NDUFS4NADH:ubiquinone oxidoreductase subunit S4 | Often (30–79%) | In 1 condition |
| NFS1NFS1 cysteine desulfurase | Often (30–79%) | In 1 condition |
| PCK1phosphoenolpyruvate carboxykinase 1 | Often (30–79%) | In 1 condition |
| PCK2phosphoenolpyruvate carboxykinase 2, mitochondrial | Often (30–79%) | In 1 condition |
| PDP1pyruvate dehydrogenase phosphatase catalytic subunit 1 | Often (30–79%) | In 1 condition |
| TAMM41TAM41 mitochondrial translocator assembly and maintenance homolog | Often (30–79%) | In 1 condition |
| TMEM126Btransmembrane protein 126B | Often (30–79%) | In 1 condition |
| GATMglycine amidinotransferase | Not recorded | In 1 condition |
| LDHDlactate dehydrogenase D | Not recorded | In 1 condition |
| PET117PET117 cytochrome c oxidase chaperone | 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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