Trait
Outward turned lips
Clinical name: Eclabion
A turning outward of the lip or lips, that is, eversion of the lips.
Summary
- Also called
- Eclabium, Everted lips
- Body system
- Abnormality of head or neck
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test30 genes linked to Outward turned lips
Changes in these genes cause rare conditions in which Outward turned lips 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 |
|---|---|---|
| CERS3ceramide synthase 3 | Always | In 1 condition |
| GTF2H5general transcription factor IIH subunit 5 | Always | In 1 condition |
| RIN2Ras and Rab interactor 2 | Always | In 1 condition |
| ABCA12ATP binding cassette subfamily A member 12 | Often (30–79%) | In 2 conditions |
| ABHD5abhydrolase domain containing 5, lysophosphatidic acid acyltransferase | Often (30–79%) | In 1 condition |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Often (30–79%) | In 1 condition |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Often (30–79%) | In 2 conditions |
| ASPRV1aspartic peptidase retroviral like 1 | Often (30–79%) | In 1 condition |
| CYP4F22cytochrome P450 family 4 subfamily F member 22 | Often (30–79%) | In 1 condition |
| DBR1debranching RNA lariats 1 | Often (30–79%) | In 1 condition |
| LIPNlipase family member N | Often (30–79%) | In 1 condition |
| NFIXnuclear factor I X | Often (30–79%) | In 1 condition |
| NIPAL4NIPA like domain containing 4 | Often (30–79%) | In 1 condition |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | Often (30–79%) | In 1 condition |
| SULT2B1sulfotransferase family 2B member 1 | Often (30–79%) | In 1 condition |
| TGM1transglutaminase 1 | Often (30–79%) | In 2 conditions |
| EDAectodysplasin A | Sometimes (5–29%) | In 1 condition |
| EDARADDEDAR associated via death domain | Sometimes (5–29%) | In 1 condition |
| FGFR1fibroblast growth factor receptor 1 | Sometimes (5–29%) | In 1 condition |
| GREM2gremlin 2, DAN family BMP antagonist | Sometimes (5–29%) | In 1 condition |
| H4C5H4 clustered histone 5 | Sometimes (5–29%) | In 1 condition |
| IRF6interferon regulatory factor 6 | Sometimes (5–29%) | In 1 condition |
| LRP6LDL receptor related protein 6 | Sometimes (5–29%) | In 1 condition |
| MSX1msh homeobox 1 | Sometimes (5–29%) | In 1 condition |
| PAX9paired box 9 | Sometimes (5–29%) | In 1 condition |
| SUMO1small ubiquitin like modifier 1 | Sometimes (5–29%) | In 1 condition |
| TGFAtransforming growth factor alpha | Sometimes (5–29%) | In 1 condition |
| WNT10AWnt family member 10A | Sometimes (5–29%) | In 1 condition |
| WNT10BWnt family member 10B | Sometimes (5–29%) | In 1 condition |
| MAN1B1mannosidase alpha class 1B member 1 | Rarely (1–4%) | 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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