Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Rib segmentation abnormalities, and the rest of your genome, with one test.
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Get my Genome Test13 genes linked to Rib segmentation abnormalities
Changes in these genes cause rare conditions in which Rib segmentation abnormalities 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 |
|---|---|---|
| DLL3delta like canonical Notch ligand 3 | Very often (80–99%) | In 1 condition |
| HES7hes family bHLH transcription factor 7 | Very often (80–99%) | In 1 condition |
| LFNGLFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Very often (80–99%) | In 1 condition |
| MESP2mesoderm posterior bHLH transcription factor 2 | Very often (80–99%) | In 1 condition |
| RIPPLY2ripply transcriptional repressor 2 | Very often (80–99%) | In 1 condition |
| TBX6T-box transcription factor 6 | Very often (80–99%) | In 1 condition |
| CPLX1complexin 1 | Often (30–79%) | In 2 conditions |
| CTBP1C-terminal binding protein 1 | Often (30–79%) | In 2 conditions |
| FGFRL1fibroblast growth factor receptor like 1 | Often (30–79%) | In 1 condition |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Often (30–79%) | In 2 conditions |
| NELFAnegative elongation factor complex member A | Often (30–79%) | In 1 condition |
| NSD2nuclear receptor binding SET domain protein 2 | Often (30–79%) | In 2 conditions |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Often (30–79%) | 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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