Trait
Motor polyneuropathy
Summary
- Also called
- Peripheral motor neuropathy
- Body system
- Abnormality of the nervous system
Reference genomeGRCh38hg38
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Get my Genome Test27 genes linked to Motor polyneuropathy
Changes in these genes cause rare conditions in which Motor polyneuropathy 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 |
|---|---|---|
| ARHGAP19Rho GTPase activating protein 19 | Always | In 1 condition |
| ARL6IP1ARL6 interacting reticulophagy regulator 1 | Always | In 2 conditions |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Always | In 1 condition |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Always | In 1 condition |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Very often (80–99%) | In 2 conditions |
| TFGtrafficking from ER to golgi regulator | Very often (80–99%) | In 1 condition |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Often (30–79%) | In 1 condition |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Often (30–79%) | In 2 conditions |
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Often (30–79%) | In 1 condition |
| GARS1glycyl-tRNA synthetase 1 | Often (30–79%) | In 1 condition |
| HINT1histidine triad nucleotide binding protein 1 | Often (30–79%) | In 1 condition |
| PPOXprotoporphyrinogen oxidase | Often (30–79%) | In 1 condition |
| REEP1receptor accessory protein 1 | Often (30–79%) | In 1 condition |
| SCO2synthesis of cytochrome C oxidase 2 | Often (30–79%) | In 1 condition |
| ALADaminolevulinate dehydratase | Sometimes (5–29%) | In 1 condition |
| CPOXcoproporphyrinogen oxidase | Sometimes (5–29%) | In 1 condition |
| CPSF3cleavage and polyadenylation specific factor 3 | Sometimes (5–29%) | In 1 condition |
| FLVCR1FLVCR choline and heme transporter 1 | Sometimes (5–29%) | In 1 condition |
| HMBShydroxymethylbilane synthase | Sometimes (5–29%) | In 1 condition |
| LYSTlysosomal trafficking regulator | Sometimes (5–29%) | In 1 condition |
| MPV17mitochondrial inner membrane protein MPV17 | Sometimes (5–29%) | In 1 condition |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Sometimes (5–29%) | In 1 condition |
| UBA1ubiquitin like modifier activating enzyme 1 | Sometimes (5–29%) | In 1 condition |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Rarely (1–4%) | In 1 condition |
| CTDP1CTD phosphatase 1 | Not recorded | In 1 condition |
| SLC12A6solute carrier family 12 member 6 | Not recorded | In 1 condition |
| TRPV4transient receptor potential cation channel subfamily V member 4 | 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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