Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Hyperactive deep tendon reflexes, and the rest of your genome, with one test.
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Get my Genome Test29 genes linked to Hyperactive deep tendon reflexes
Changes in these genes cause rare conditions in which Hyperactive deep tendon reflexes 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 |
|---|---|---|
| RETREG1reticulophagy regulator 1 | Always | In 1 condition |
| MECP2methyl-CpG binding protein 2 | Very often (80–99%) | In 1 condition |
| UROC1urocanate hydratase 1 | Very often (80–99%) | In 1 condition |
| ATP6AP2ATPase H+ transporting accessory protein 2 | Often (30–79%) | In 1 condition |
| GALCgalactosylceramidase | Often (30–79%) | In 2 conditions |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Often (30–79%) | In 1 condition |
| PRRT2proline rich transmembrane protein 2 | Often (30–79%) | In 1 condition |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Often (30–79%) | In 1 condition |
| SDHAF1succinate dehydrogenase complex assembly factor 1 | Often (30–79%) | In 1 condition |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Often (30–79%) | In 1 condition |
| SDHDsuccinate dehydrogenase complex subunit D | Often (30–79%) | In 1 condition |
| SLC2A1solute carrier family 2 member 1 | Often (30–79%) | In 1 condition |
| TIMM8Atranslocase of inner mitochondrial membrane 8A | Often (30–79%) | In 1 condition |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Sometimes (5–29%) | In 1 condition |
| ATXN1ataxin 1 | Sometimes (5–29%) | In 1 condition |
| ATXN2ataxin 2 | Sometimes (5–29%) | In 1 condition |
| BEAN1brain expressed associated with NEDD4 1 | Sometimes (5–29%) | In 1 condition |
| DNM1Ldynamin 1L | Sometimes (5–29%) | In 1 condition |
| KCNC3potassium voltage-gated channel subfamily C member 3 | Sometimes (5–29%) | In 1 condition |
| MRE11MRE11 double strand break repair nuclease | Sometimes (5–29%) | In 1 condition |
| PRNPprion protein (Kanno blood group) | Sometimes (5–29%) | In 1 condition |
| STUB1STIP1 homology and U-box containing protein 1 | Sometimes (5–29%) | In 1 condition |
| PMP22peripheral myelin protein 22 | Rarely (1–4%) | In 1 condition |
| GJA1gap junction protein alpha 1 | Not recorded | In 1 condition |
| MAB21L1mab-21 like 1 | Not recorded | In 1 condition |
| PRSS12serine protease 12 | Not recorded | In 1 condition |
| SAMD9Lsterile alpha motif domain containing 9 like | Not recorded | In 1 condition |
| SMG9SMG9 nonsense mediated mRNA decay factor | Not recorded | In 1 condition |
| TANGO2transport and golgi organization 2 homolog | 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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