Trait
Common atrium
Complete absence of the interatrial septum with common atrioventricular valve and two atrioventricular connections.
Summary
- Also called
- Single atrium
- Body system
- Abnormality of the cardiovascular system
This page as data
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Get my Genome Test6 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.
- Heterotaxy & Laterality DefectsReads 6 of these genesGDF1ACVR2BCFAP53CIROPMMP21ZIC3About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 2 of these genesEVCEVC2About this report →
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesTBX5About this report →
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Get my Genome Test14 genes linked to Common atrium
Changes in these genes cause rare conditions in which Common atrium 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 |
|---|---|---|
| GDF1growth differentiation factor 1 | Always | In 1 condition |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Always | In 1 condition |
| ACVR2Bactivin A receptor type 2B | Often (30–79%) | In 1 condition |
| CFAP53cilia and flagella associated protein 53 | Often (30–79%) | In 1 condition |
| CLXNcalaxin | Often (30–79%) | In 1 condition |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Often (30–79%) | In 1 condition |
| CIROPciliated left-right organizer metallopeptidase | Sometimes (5–29%) | In 1 condition |
| IFT56intraflagellar transport 56 | Sometimes (5–29%) | In 1 condition |
| WT1WT1 transcription factor | Sometimes (5–29%) | In 1 condition |
| TBX5T-box transcription factor 5 | Rarely (1–4%) | In 1 condition |
| EVCEvC ciliary complex subunit 1 | Not recorded | In 1 condition |
| EVC2EvC ciliary complex subunit 2 | Not recorded | In 1 condition |
| MMP21matrix metallopeptidase 21 | Not recorded | In 1 condition |
| ZIC3Zic family zinc finger 3 | 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 2026.10.17-8666dff2.
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