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Trait
Posterior embryotoxon
A posterior embryotoxon is the presence of a prominent and anteriorly displaced line of Schwalbe.
Summary
- Also called
- Embryotoxon
- Body system
- Abnormality of the eye
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This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/posterior-embryotoxon.json"
page <- fromJSON(url)
page$trait$namePosterior embryotoxonHP:0000627
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Get my Genome Test29 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 13 of these genesPEX14PEX1PEX10PEX11BPEX12PEX13About this report →
- Other Inherited LeukodystrophiesReads 13 of these genesPEX14PEX1PEX10PEX11BPEX12PEX13About this report →
- Alagille SyndromeReads 2 of these genesJAG1NOTCH2About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 3 of these genesFOXC1PITX2PAX6About this report →
Show 25 more reports
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
- FHONDA SyndromeReads 1 of these genesSLC38A8About this report →
- Hajdu-Cheney SyndromeReads 1 of these genesNOTCH2About this report →
- PIK3R1-Related DisordersReads 1 of these genesPIK3R1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 14 of these genesJAG1PEX14PEX1PEX10PEX11BPEX12About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 4 of these genesHMX1COX7BHCCSNDUFB11About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 1 of these genesPIK3R1About this report →
- Inherited Neurodegenerative DisordersReads 13 of these genesPEX14PEX1PEX10PEX11BPEX12PEX13About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- GlaucomaReads 1 of these genesFOXC1About this report →
- Inherited Platelet Function DisordersReads 1 of these genesGP1BBAbout this report →
- Kidney CancerReads 1 of these genesPAX6About this report →
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 1 of these genesPIK3R1About this report →
- Urinary and Renal System TumourReads 1 of these genesPAX6About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesPAN2About this report →
- Other Inborn Errors of ImmunityReads 3 of these genesTBX1NCF1PIK3R1About this report →
- Diabetes MellitusReads 1 of these genesPAX6About this report →
- Inherited ThrombocytopeniasReads 1 of these genesGP1BBAbout this report →
- Primary Mitochondrial DiseaseReads 2 of these genesDNAJC30NDUFB11About this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesPEX6About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesJAG1About this report →
- Intellectual DisabilityReads 1 of these genesJMJD1CAbout this report →
Read the genes linked to Posterior embryotoxon, and the rest of your genome, with one test.
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Get my Genome Test60 genes linked to Posterior embryotoxon
Changes in these genes cause rare conditions in which Posterior embryotoxon 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 |
| FOXC1forkhead box C1 | Always | In 3 conditions |
| HMX1H6 family homeobox 1 | Always | In 1 condition |
| JAG1jagged canonical Notch ligand 1 | Always | In 2 conditions |
| PAN2poly(A) specific ribonuclease subunit PAN2 | Always | In 1 condition |
| PEX14peroxisomal biogenesis factor 14 | Always | In 2 conditions |
| PITX2paired like homeodomain 2 | Always | In 2 conditions |
| ARVCFARVCF delta catenin family member | Often (30–79%) | In 1 condition |
| COMTcatechol-O-methyltransferase | Often (30–79%) | In 1 condition |
| GP1BBglycoprotein Ib platelet subunit beta | Often (30–79%) | In 1 condition |
| HIRAhistone cell cycle regulator | Often (30–79%) | In 1 condition |
| JMJD1Cjumonji domain containing 1C | Often (30–79%) | In 1 condition |
| PEX1peroxisomal biogenesis factor 1 | Often (30–79%) | In 1 condition |
| PEX10peroxisomal biogenesis factor 10 | Often (30–79%) | In 1 condition |
| PEX11Bperoxisomal biogenesis factor 11 beta | Often (30–79%) | In 1 condition |
| PEX12peroxisomal biogenesis factor 12 | Often (30–79%) | In 1 condition |
| PEX13peroxisomal biogenesis factor 13 | Often (30–79%) | In 1 condition |
| PEX16peroxisomal biogenesis factor 16 | Often (30–79%) | In 1 condition |
| PEX19peroxisomal biogenesis factor 19 | Often (30–79%) | In 1 condition |
| PEX2peroxisomal biogenesis factor 2 | Often (30–79%) | In 1 condition |
| PEX26peroxisomal biogenesis factor 26 | Often (30–79%) | In 1 condition |
| PEX3peroxisomal biogenesis factor 3 | Often (30–79%) | In 1 condition |
| PEX5peroxisomal biogenesis factor 5 | Often (30–79%) | In 1 condition |
| PEX6peroxisomal biogenesis factor 6 | Often (30–79%) | In 1 condition |
| RREB1ras responsive element binding protein 1 | Often (30–79%) | In 1 condition |
| SEC24CSEC24 homolog C, COPII component | Often (30–79%) | In 1 condition |
| TBX1T-box transcription factor 1 | Often (30–79%) | In 3 conditions |
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Often (30–79%) | In 1 condition |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Sometimes (5–29%) | In 1 condition |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Sometimes (5–29%) | In 1 condition |
| CLIP2CAP-Gly domain containing linker protein 2 | Sometimes (5–29%) | In 1 condition |
| COX7Bcytochrome c oxidase subunit 7B | Sometimes (5–29%) | In 1 condition |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Sometimes (5–29%) | In 1 condition |
| EIF4Heukaryotic translation initiation factor 4H | Sometimes (5–29%) | In 1 condition |
| ELNelastin | Sometimes (5–29%) | In 1 condition |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Sometimes (5–29%) | In 1 condition |
| GTF2Igeneral transcription factor IIi | Sometimes (5–29%) | In 1 condition |
| GTF2IRD1GTF2I repeat domain containing 1 | Sometimes (5–29%) | In 1 condition |
| GTF2IRD2GTF2I repeat domain containing 2 | Sometimes (5–29%) | In 1 condition |
| HCCSholocytochrome c synthase | Sometimes (5–29%) | In 1 condition |
Show 20 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| HS2ST1heparan sulfate 2-O-sulfotransferase 1 | Sometimes (5–29%) | In 1 condition |
| KDM5Alysine demethylase 5A | Sometimes (5–29%) | In 1 condition |
| LIMK1LIM domain kinase 1 | Sometimes (5–29%) | In 1 condition |
| METTL27methyltransferase like 27 | Sometimes (5–29%) | In 1 condition |
| NCF1neutrophil cytosolic factor 1 | Sometimes (5–29%) | In 1 condition |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Sometimes (5–29%) | In 1 condition |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sometimes (5–29%) | In 1 condition |
| RFC2replication factor C subunit 2 | Sometimes (5–29%) | In 1 condition |
| SLC38A8solute carrier family 38 member 8 | Sometimes (5–29%) | In 1 condition |
| STX1Asyntaxin 1A | Sometimes (5–29%) | In 1 condition |
| TBL2transducin beta like 2 | Sometimes (5–29%) | In 1 condition |
| TMEM270transmembrane protein 270 | Sometimes (5–29%) | In 1 condition |
| VPS37DVPS37D subunit of ESCRT-I | Sometimes (5–29%) | In 1 condition |
| YAP1Yes1 associated transcriptional regulator | Sometimes (5–29%) | In 1 condition |
| DGCR2DiGeorge syndrome critical region gene 2 | Not recorded | In 1 condition |
| DGCR6DiGeorge syndrome critical region gene 6 | Not recorded | In 1 condition |
| DGCR8DGCR8 microprocessor complex subunit | Not recorded | In 1 condition |
| ESS2ess-2 spliceosome associated protein | Not recorded | In 1 condition |
| NOTCH2notch receptor 2 | Not recorded | In 1 condition |
| PAX6paired box 6 | 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 2026.10.19-9814e911.
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