Trait
Glucose in urine
Clinical name: Glycosuria
An increased concentration of glucose in the urine.
Summary
- Also called
- Glucosuria
Reference genomeGRCh38hg38
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Get my Genome Test54 genes linked to Glucose in urine
Changes in these genes cause rare conditions in which Glucose in urine 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 |
|---|---|---|
| ABCC8ATP binding cassette subfamily C member 8 | Always | In 3 conditions |
| CTNScystinosin, lysosomal cystine transporter | Always | In 3 conditions |
| GATMglycine amidinotransferase | Always | In 2 conditions |
| HNF4Ahepatocyte nuclear factor 4 alpha | Always | In 3 conditions |
| IFT140intraflagellar transport 140 | Always | In 1 condition |
| SLC2A2solute carrier family 2 member 2 | Always | In 2 conditions |
| SLC34A1solute carrier family 34 member 1 | Always | In 2 conditions |
| SLC5A2solute carrier family 5 member 2 | Always | In 2 conditions |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | Always | In 1 condition |
| WASWASP actin nucleation promoting factor | Always | In 1 condition |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Very often (80–99%) | In 2 conditions |
| GCKglucokinase | Very often (80–99%) | In 2 conditions |
| INSinsulin | Very often (80–99%) | In 2 conditions |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Very often (80–99%) | In 2 conditions |
| LMNAlamin A/C | Very often (80–99%) | In 1 condition |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Very often (80–99%) | In 2 conditions |
| PDX1pancreatic and duodenal homeobox 1 | Very often (80–99%) | In 2 conditions |
| STAT3signal transducer and activator of transcription 3 | Very often (80–99%) | In 1 condition |
| APPL1adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1 | Often (30–79%) | In 1 condition |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Often (30–79%) | In 1 condition |
| CELcarboxyl ester lipase | Often (30–79%) | In 1 condition |
| COA8cytochrome c oxidase assembly factor 8 | Often (30–79%) | In 1 condition |
| FAN1FANCD2 and FANCI associated nuclease 1 | Often (30–79%) | In 1 condition |
| GYS2glycogen synthase 2 | Often (30–79%) | In 1 condition |
| HNF1AHNF1 homeobox A | Often (30–79%) | In 1 condition |
| HNF1BHNF1 homeobox B | Often (30–79%) | In 1 condition |
| KLF11KLF transcription factor 11 | Often (30–79%) | In 1 condition |
| NEUROD1neuronal differentiation 1 | Often (30–79%) | In 1 condition |
| PAX4paired box 4 | Often (30–79%) | In 1 condition |
| SLC16A12solute carrier family 16 member 12 | Often (30–79%) | In 1 condition |
| TRMT5tRNA methyltransferase 5 | Often (30–79%) | In 1 condition |
| PAX2paired box 2 | Sometimes (5–29%) | In 1 condition |
| PBX1PBX homeobox 1 | Sometimes (5–29%) | In 1 condition |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sometimes (5–29%) | In 1 condition |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Rarely (1–4%) | In 1 condition |
| ALDOBaldolase, fructose-bisphosphate B | Not recorded | In 1 condition |
| ATP7BATPase copper transporting beta | Not recorded | In 1 condition |
| CLCN5Cl-/H+ antiporter 5 | Not recorded | In 2 conditions |
| COX10cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 | Not recorded | In 1 condition |
| COX15cytochrome c oxidase assembly factor COX15 | Not recorded | In 1 condition |
Show 14 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| COX6B1cytochrome c oxidase subunit 6B1 | Not recorded | In 1 condition |
| ETFAelectron transfer flavoprotein subunit alpha | Not recorded | In 1 condition |
| ETFBelectron transfer flavoprotein subunit beta | Not recorded | In 1 condition |
| ETFDHelectron transfer flavoprotein dehydrogenase | Not recorded | In 1 condition |
| FASTKD2FASTK mitochondrial RNA regulator 2 | Not recorded | In 1 condition |
| GATA6GATA binding protein 6 | Not recorded | In 1 condition |
| MT-TNmitochondrially encoded tRNA-Asn (AAU/C) | Not recorded | In 1 condition |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Not recorded | In 1 condition |
| NSMCE2NSE2 SUMO ligase component of SMC5/6 complex | Not recorded | In 1 condition |
| SCO1synthesis of cytochrome C oxidase 1 | Not recorded | In 1 condition |
| SCO2synthesis of cytochrome C oxidase 2 | Not recorded | In 1 condition |
| SLC5A1solute carrier family 5 member 1 | Not recorded | In 1 condition |
| SURF1SURF1 cytochrome c oxidase assembly factor | Not recorded | In 1 condition |
| TACO1translational activator of cytochrome c oxidase I | 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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