Trait
Functional motor deficit
Summary
- Also called
- Functional motor problems
- Body system
- Abnormality of the musculoskeletal system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Functional motor deficit, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test67 genes linked to Functional motor deficit
Changes in these genes cause rare conditions in which Functional motor deficit 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 |
|---|---|---|
| ASAH1N-acylsphingosine amidohydrolase 1 | Very often (80–99%) | In 1 condition |
| ASPAaspartoacylase | Very often (80–99%) | In 1 condition |
| CDKL5cyclin dependent kinase like 5 | Very often (80–99%) | In 1 condition |
| GABBR2gamma-aminobutyric acid type B receptor subunit 2 | Very often (80–99%) | In 1 condition |
| GALCgalactosylceramidase | Very often (80–99%) | In 3 conditions |
| KCNQ2potassium voltage-gated channel subfamily Q member 2 | Very often (80–99%) | In 1 condition |
| KCNT1potassium sodium-activated channel subfamily T member 1 | Very often (80–99%) | In 1 condition |
| MECP2methyl-CpG binding protein 2 | Very often (80–99%) | In 1 condition |
| NTNG1netrin G1 | Very often (80–99%) | In 1 condition |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Very often (80–99%) | In 1 condition |
| PLCB1phospholipase C beta 1 | Very often (80–99%) | In 1 condition |
| PSAPprosaposin | Very often (80–99%) | In 1 condition |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Very often (80–99%) | In 1 condition |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Very often (80–99%) | In 1 condition |
| SH3TC2SH3 domain and tetratricopeptide repeats 2 | Very often (80–99%) | In 1 condition |
| SLC12A5solute carrier family 12 member 5 | Very often (80–99%) | In 1 condition |
| SLC25A22solute carrier family 25 member 22 | Very often (80–99%) | In 1 condition |
| SMC1Astructural maintenance of chromosomes 1A | Very often (80–99%) | In 1 condition |
| TBC1D24TBC1 domain family member 24 | Very often (80–99%) | In 1 condition |
| ABCD1ATP binding cassette subfamily D member 1 | Often (30–79%) | In 2 conditions |
| BRCC3BRCA1/BRCA2-containing complex subunit 3 | Often (30–79%) | In 1 condition |
| CCDC88Ccoiled-coil and HOOK domain protein 88C | Often (30–79%) | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Often (30–79%) | In 1 condition |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Often (30–79%) | In 1 condition |
| EXT1exostosin glycosyltransferase 1 | Often (30–79%) | In 1 condition |
| EXT2exostosin glycosyltransferase 2 | Often (30–79%) | In 1 condition |
| GRID2glutamate ionotropic receptor delta type subunit 2 | Often (30–79%) | In 1 condition |
| GRM1glutamate metabotropic receptor 1 | Often (30–79%) | In 1 condition |
| MFFmitochondrial fission factor | Often (30–79%) | In 1 condition |
| MORC2MORC family CW-type zinc finger 2 | Often (30–79%) | In 1 condition |
| OCA2OCA2 melanosomal transmembrane protein | Often (30–79%) | In 1 condition |
| PLP1proteolipid protein 1 | Often (30–79%) | In 1 condition |
| SPASTspastin | Often (30–79%) | In 1 condition |
| UBE3Aubiquitin protein ligase E3A | Often (30–79%) | In 1 condition |
| AKT1AKT serine/threonine kinase 1 | Sometimes (5–29%) | In 1 condition |
| AKT3AKT serine/threonine kinase 3 | Sometimes (5–29%) | In 1 condition |
| ALADaminolevulinate dehydratase | Sometimes (5–29%) | In 1 condition |
| BAP1BRCA1 associated deubiquitinase 1 | Sometimes (5–29%) | In 1 condition |
| COX7Bcytochrome c oxidase subunit 7B | Sometimes (5–29%) | In 1 condition |
| DLATdihydrolipoamide S-acetyltransferase | Sometimes (5–29%) | In 1 condition |
Show 27 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| HCCSholocytochrome c synthase | Sometimes (5–29%) | In 1 condition |
| JPH3junctophilin 3 | Sometimes (5–29%) | In 1 condition |
| LMNB1lamin B1 | Sometimes (5–29%) | In 1 condition |
| MTORmechanistic target of rapamycin kinase | Sometimes (5–29%) | In 1 condition |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Sometimes (5–29%) | In 1 condition |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Sometimes (5–29%) | In 1 condition |
| NTRK1neurotrophic receptor tyrosine kinase 1 | Sometimes (5–29%) | In 1 condition |
| PDGFBplatelet derived growth factor subunit B | Sometimes (5–29%) | In 1 condition |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Sometimes (5–29%) | In 2 conditions |
| PRF1perforin 1 | Sometimes (5–29%) | In 1 condition |
| SELENOIselenoprotein I | Sometimes (5–29%) | In 1 condition |
| SLC19A3solute carrier family 19 member 3 | Sometimes (5–29%) | In 1 condition |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Sometimes (5–29%) | In 1 condition |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Sometimes (5–29%) | In 1 condition |
| SMOsmoothened, frizzled class receptor | Sometimes (5–29%) | In 1 condition |
| STX11syntaxin 11 | Sometimes (5–29%) | In 1 condition |
| STXBP2syntaxin binding protein 2 | Sometimes (5–29%) | In 1 condition |
| SUFUSUFU negative regulator of hedgehog signaling | Sometimes (5–29%) | In 1 condition |
| TBK1TANK binding kinase 1 | Sometimes (5–29%) | In 1 condition |
| TERTtelomerase reverse transcriptase | Sometimes (5–29%) | In 1 condition |
| TICAM1TIR domain containing adaptor molecule 1 | Sometimes (5–29%) | In 1 condition |
| TLR3toll like receptor 3 | Sometimes (5–29%) | In 1 condition |
| TRAF3TNF receptor associated factor 3 | Sometimes (5–29%) | In 1 condition |
| TRAF7TNF receptor associated factor 7 | Sometimes (5–29%) | In 1 condition |
| UNC13Dunc-13 homolog D | Sometimes (5–29%) | In 1 condition |
| UNC93B1unc-93B1 regulator of TLR signaling | Sometimes (5–29%) | In 1 condition |
| VPS13Avacuolar protein sorting 13 homolog A | Sometimes (5–29%) | 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.
Narrower traits
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.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks