Trait
Delayed ability to roll over
Delayed achievement of the ability to roll front to back and back to front.
Summary
- Body system
- Abnormality of the nervous system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test24 genes linked to Delayed ability to roll over
Changes in these genes cause rare conditions in which Delayed ability to roll over 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 |
|---|---|---|
| ADCY5adenylate cyclase 5 | Always | In 1 condition |
| KLHL20kelch like family member 20 | Always | In 1 condition |
| LMNAlamin A/C | Always | In 1 condition |
| MECP2methyl-CpG binding protein 2 | Always | In 1 condition |
| MED16mediator complex subunit 16 | Always | In 1 condition |
| MOCS3molybdenum cofactor synthesis 3 | Always | In 1 condition |
| MRPS25mitochondrial ribosomal protein S25 | Always | In 1 condition |
| NAV3neuron navigator 3 | Always | In 1 condition |
| NDUFA8NADH:ubiquinone oxidoreductase subunit A8 | Always | In 1 condition |
| PGAP1post-GPI attachment to proteins inositol deacylase 1 | Always | In 1 condition |
| RNU2-2RNA, U2 small nuclear 2 | Always | In 1 condition |
| RNU5B-1RNA, U5B small nuclear 1 | Always | In 1 condition |
| SLC25A12solute carrier family 25 member 12 | Always | In 1 condition |
| SLC31A1solute carrier family 31 member 1 | Always | In 1 condition |
| SONSON DNA and RNA binding protein | Always | In 1 condition |
| TAF8TATA-box binding protein associated factor 8 | Always | In 1 condition |
| UBR5ubiquitin protein ligase E3 component n-recognin 5 | Always | In 1 condition |
| VPS35LVPS35 endosomal protein sorting factor like | Always | In 1 condition |
| YWHAZtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta | Always | In 1 condition |
| YIF1BYip1 interacting factor homolog B, membrane trafficking protein | Very often (80–99%) | In 1 condition |
| ACTA1actin alpha 1, skeletal muscle | Often (30–79%) | In 1 condition |
| ATP6V0A1ATPase H+ transporting V0 subunit a1 | Often (30–79%) | In 1 condition |
| CELF2CUGBP Elav-like family member 2 | Often (30–79%) | In 1 condition |
| VRK1VRK serine/threonine kinase 1 | 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.
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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