Trait
Myoglobinuria
Presence of myoglobin in the urine.
Summary
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test24 genes linked to Myoglobinuria
Changes in these genes cause rare conditions in which Myoglobinuria 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 |
|---|---|---|
| ATP2A2ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 | Always | In 1 condition |
| FDX2ferredoxin 2 | Always | In 1 condition |
| LPIN1lipin 1 | Always | In 1 condition |
| TANGO2transport and golgi organization 2 homolog | Always | In 1 condition |
| CPT2carnitine palmitoyltransferase 2 | Very often (80–99%) | In 4 conditions |
| DMDdystrophin | Very often (80–99%) | In 1 condition |
| PGAM2phosphoglycerate mutase 2 | Often (30–79%) | In 2 conditions |
| PGK1phosphoglycerate kinase 1 | Often (30–79%) | In 1 condition |
| PYGMglycogen phosphorylase, muscle associated | Often (30–79%) | In 1 condition |
| ALDOAaldolase, fructose-bisphosphate A | Sometimes (5–29%) | In 1 condition |
| ANO5anoctamin 5 | Sometimes (5–29%) | In 1 condition |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Sometimes (5–29%) | In 1 condition |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Sometimes (5–29%) | In 1 condition |
| PHKA1phosphorylase kinase regulatory subunit alpha 1 | Sometimes (5–29%) | In 1 condition |
| PHKA2phosphorylase kinase regulatory subunit alpha 2 | Sometimes (5–29%) | In 1 condition |
| PHKG1phosphorylase kinase catalytic subunit gamma 1 | Sometimes (5–29%) | In 1 condition |
| PHKG2phosphorylase kinase catalytic subunit gamma 2 | Sometimes (5–29%) | In 1 condition |
| RYR1ryanodine receptor 1 | Sometimes (5–29%) | In 2 conditions |
| SGCBsarcoglycan beta | Sometimes (5–29%) | In 1 condition |
| HADHhydroxyacyl-CoA dehydrogenase | Rarely (1–4%) | In 2 conditions |
| PHKBphosphorylase kinase regulatory subunit beta | Rarely (1–4%) | In 1 condition |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Not recorded | In 1 condition |
| ISCUiron-sulfur cluster assembly enzyme | Not recorded | In 1 condition |
| LDHAlactate dehydrogenase A | 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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