Trait
Hypoglycemic seizures
Summary
Reference genomeGRCh38hg38
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Get my Genome Test28 genes linked to Hypoglycemic seizures
Changes in these genes cause rare conditions in which Hypoglycemic seizures 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 |
|---|---|---|
| SLC25A36solute carrier family 25 member 36 | Always | In 1 condition |
| AKT2AKT serine/threonine kinase 2 | Very often (80–99%) | In 1 condition |
| HADHhydroxyacyl-CoA dehydrogenase | Very often (80–99%) | In 3 conditions |
| AAASaladin WD repeat nucleoporin | Often (30–79%) | In 1 condition |
| ABCC8ATP binding cassette subfamily C member 8 | Often (30–79%) | In 2 conditions |
| GCKglucokinase | Often (30–79%) | In 1 condition |
| GMPPAGDP-mannose pyrophosphorylase A | Often (30–79%) | In 1 condition |
| HNF1AHNF1 homeobox A | Often (30–79%) | In 1 condition |
| INSRinsulin receptor | Often (30–79%) | In 1 condition |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Often (30–79%) | In 1 condition |
| MC2Rmelanocortin 2 receptor | Often (30–79%) | In 1 condition |
| MRAPmelanocortin 2 receptor accessory protein | Often (30–79%) | In 1 condition |
| NNTnicotinamide nucleotide transhydrogenase | 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 |
| POGZpogo transposable element derived with ZNF domain | Often (30–79%) | In 1 condition |
| STARsteroidogenic acute regulatory protein | Often (30–79%) | In 1 condition |
| TBX19T-box transcription factor 19 | Often (30–79%) | In 1 condition |
| TRAPPC11trafficking protein particle complex subunit 11 | Often (30–79%) | In 1 condition |
| TXNRD2thioredoxin reductase 2 | Often (30–79%) | In 1 condition |
| PCSK1proprotein convertase subtilisin/kexin type 1 | Sometimes (5–29%) | In 1 condition |
| POMCproopiomelanocortin | Sometimes (5–29%) | In 2 conditions |
| SLC37A4solute carrier family 37 member 4 | Sometimes (5–29%) | In 1 condition |
| TANGO2transport and golgi organization 2 homolog | Sometimes (5–29%) | In 1 condition |
| UCP2uncoupling protein 2 | Sometimes (5–29%) | In 1 condition |
| GLUD1glutamate dehydrogenase 1 | Not recorded | In 1 condition |
| PROP1PROP paired-like homeobox 1 | Not recorded | In 1 condition |
| SLC16A1solute carrier family 16 member 1 | 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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