Trait
Difficulty in standing
Clinical name: Difficulty standing
Summary
- Also called
- Standing instability
- Body system
- Abnormality of the musculoskeletal system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test23 genes linked to Difficulty in standing
Changes in these genes cause rare conditions in which Difficulty in standing 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 1 condition |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Always | In 1 condition |
| TFGtrafficking from ER to golgi regulator | Always | In 2 conditions |
| GRM1glutamate metabotropic receptor 1 | Very often (80–99%) | In 1 condition |
| TUBA4Atubulin alpha 4a | Very often (80–99%) | In 1 condition |
| CLN8CLN8 transmembrane ER and ERGIC protein | Often (30–79%) | In 1 condition |
| DYSFdysferlin | Often (30–79%) | In 1 condition |
| GPAA1glycosylphosphatidylinositol anchor attachment 1 | Often (30–79%) | In 1 condition |
| KYkyphoscoliosis peptidase | Often (30–79%) | In 1 condition |
| MYOTmyotilin | Often (30–79%) | In 1 condition |
| TBCEtubulin folding cofactor E | Often (30–79%) | In 1 condition |
| TRMT5tRNA methyltransferase 5 | Often (30–79%) | In 1 condition |
| DYMdymeclin | Sometimes (5–29%) | In 1 condition |
| FAR1fatty acyl-CoA reductase 1 | Sometimes (5–29%) | In 1 condition |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | Sometimes (5–29%) | In 1 condition |
| LRP12LDL receptor related protein 12 | Sometimes (5–29%) | In 1 condition |
| SMSspermine synthase | Sometimes (5–29%) | In 1 condition |
| WARS2tryptophanyl tRNA synthetase 2, mitochondrial | Sometimes (5–29%) | In 1 condition |
| ATP2B3ATPase plasma membrane Ca2+ transporting 3 | Not recorded | In 1 condition |
| CYP27B1cytochrome P450 family 27 subfamily B member 1 | Not recorded | In 1 condition |
| CYP2R1cytochrome P450 family 2 subfamily R member 1 | Not recorded | In 1 condition |
| SLC34A3solute carrier family 34 member 3 | Not recorded | In 1 condition |
| VDRvitamin D receptor | 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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