Trait
Everted eyelid
Clinical name: Ectropion
An outward turning (eversion) or rotation of the eyelid margin.
Summary
- Also called
- Eyelid folded out, Eyelid turned out
- Body system
- Abnormality of head or neck
Reference genomeGRCh38hg38
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Get my Genome Test63 genes linked to Everted eyelid
Changes in these genes cause rare conditions in which Everted eyelid 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 |
|---|---|---|
| AMOTL1angiomotin like 1 | Always | In 1 condition |
| CERS3ceramide synthase 3 | Always | In 2 conditions |
| GTF2H5general transcription factor IIH subunit 5 | Always | In 2 conditions |
| ABCA12ATP binding cassette subfamily A member 12 | Very often (80–99%) | In 5 conditions |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Very often (80–99%) | In 3 conditions |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Very often (80–99%) | In 4 conditions |
| NIPAL4NIPA like domain containing 4 | Very often (80–99%) | In 3 conditions |
| PNPLA1patatin like domain 1, omega-hydroxyceramide transacylase | Very often (80–99%) | In 1 condition |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | Very often (80–99%) | In 2 conditions |
| SULT2B1sulfotransferase family 2B member 1 | Very often (80–99%) | In 2 conditions |
| TGM1transglutaminase 1 | Very often (80–99%) | In 4 conditions |
| TWIST2twist family bHLH transcription factor 2 | Very often (80–99%) | In 2 conditions |
| ABCA1ATP binding cassette subfamily A member 1 | Often (30–79%) | In 2 conditions |
| ABHD5abhydrolase domain containing 5, lysophosphatidic acid acyltransferase | Often (30–79%) | In 2 conditions |
| ASPRV1aspartic peptidase retroviral like 1 | Often (30–79%) | In 1 condition |
| CCDC47coiled-coil domain containing 47 | 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 2 conditions |
| FOXC2forkhead box C2 | Often (30–79%) | In 2 conditions |
| GBA1glucosylceramidase beta 1 | Often (30–79%) | In 1 condition |
| KRT10keratin 10 | Often (30–79%) | In 1 condition |
| LIPNlipase family member N | Often (30–79%) | In 1 condition |
| RIPK4receptor interacting serine/threonine kinase 4 | Often (30–79%) | In 1 condition |
| SPINK5serine peptidase inhibitor Kazal type 5 | Often (30–79%) | In 1 condition |
| AARS1alanyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| APCAPC regulator of Wnt signaling pathway | Sometimes (5–29%) | In 1 condition |
| CARD14caspase recruitment domain family member 14 | Sometimes (5–29%) | In 1 condition |
| CARS1cysteinyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| CD28CD28 molecule | Sometimes (5–29%) | In 1 condition |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Sometimes (5–29%) | In 1 condition |
| DDB2damage specific DNA binding protein 2 | Sometimes (5–29%) | In 2 conditions |
| EDN1endothelin 1 | Sometimes (5–29%) | In 1 condition |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Sometimes (5–29%) | In 3 conditions |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Sometimes (5–29%) | In 2 conditions |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Sometimes (5–29%) | In 1 condition |
| ERCC5ERCC excision repair 5, endonuclease | Sometimes (5–29%) | In 1 condition |
| FERMT1FERM domain containing kindlin 1 | Sometimes (5–29%) | In 1 condition |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Sometimes (5–29%) | In 1 condition |
| FOXL2forkhead box L2 | Sometimes (5–29%) | In 1 condition |
| GATA1GATA binding protein 1 | Sometimes (5–29%) | In 1 condition |
Show 23 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| GTF2E2general transcription factor IIE subunit 2 | Sometimes (5–29%) | In 1 condition |
| IPO8importin 8 | Sometimes (5–29%) | In 1 condition |
| ITGA6integrin subunit alpha 6 | Sometimes (5–29%) | In 2 conditions |
| ITGB4integrin subunit beta 4 | Sometimes (5–29%) | In 2 conditions |
| LRP4LDL receptor related protein 4 | Sometimes (5–29%) | In 1 condition |
| MPLKIPM-phase specific PLK1 interacting protein | Sometimes (5–29%) | In 1 condition |
| RNF113Aring finger protein 113A | Sometimes (5–29%) | In 1 condition |
| TARS1threonyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| TNFRSF1BTNF receptor superfamily member 1B | Sometimes (5–29%) | In 1 condition |
| URODuroporphyrinogen decarboxylase | Sometimes (5–29%) | In 1 condition |
| UROSuroporphyrinogen III synthase | Sometimes (5–29%) | In 1 condition |
| XPAXPA, DNA damage recognition and repair factor | Sometimes (5–29%) | In 2 conditions |
| XPCXPC complex subunit, DNA damage recognition and repair factor | Sometimes (5–29%) | In 2 conditions |
| ZFXzinc finger protein X-linked | Sometimes (5–29%) | In 1 condition |
| CTCFCCCTC-binding factor | Rarely (1–4%) | In 1 condition |
| PORCNporcupine O-acyltransferase | Rarely (1–4%) | In 1 condition |
| DHODHdihydroorotate dehydrogenase (quinone) | Not recorded | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Not recorded | In 1 condition |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Not recorded | In 1 condition |
| PLECplectin | Not recorded | In 1 condition |
| POLHDNA polymerase eta | Not recorded | In 1 condition |
| POLR3ARNA polymerase III subunit A | Not recorded | In 1 condition |
| RNU12RNA, U12 small nuclear | 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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