Trait
Shorter than typical length between neck and abdomen
Clinical name: Short thorax
Reduced inferior to superior extent of the thorax.
Summary
- Body system
- Abnormality of the musculoskeletal system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Shorter than typical length between neck and abdomen, and the rest of your genome, with one test.
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Get my Genome Test51 genes linked to Shorter than typical length between neck and abdomen
Changes in these genes cause rare conditions in which Shorter than typical length between neck and abdomen 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 |
|---|---|---|
| CCDC8coiled-coil domain containing 8 subunit of 3M complex | Always | In 2 conditions |
| DMRT2doublesex and mab-3 related transcription factor 2 | Always | In 1 condition |
| HES7hes family bHLH transcription factor 7 | Always | In 2 conditions |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Always | In 1 condition |
| IFT122intraflagellar transport 122 | Always | In 1 condition |
| IFT52intraflagellar transport 52 | Always | In 1 condition |
| TRIP11thyroid hormone receptor interactor 11 | Always | In 2 conditions |
| ACANaggrecan | Very often (80–99%) | In 1 condition |
| BMPERBMP binding endothelial regulator | Very often (80–99%) | In 1 condition |
| CEP120centrosomal protein 120 | Very often (80–99%) | In 1 condition |
| COL2A1collagen type II alpha 1 chain | Very often (80–99%) | In 2 conditions |
| DLL3delta like canonical Notch ligand 3 | Very often (80–99%) | In 1 condition |
| DYNC2H1dynein cytoplasmic 2 heavy chain 1 | Very often (80–99%) | In 2 conditions |
| DYNC2I1dynein 2 intermediate chain 1 | Very often (80–99%) | In 2 conditions |
| DYNC2I2dynein 2 intermediate chain 2 | Very often (80–99%) | In 2 conditions |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Very often (80–99%) | In 2 conditions |
| EVCEvC ciliary complex subunit 1 | Very often (80–99%) | In 1 condition |
| EVC2EvC ciliary complex subunit 2 | Very often (80–99%) | In 1 condition |
| FGFR3fibroblast growth factor receptor 3 | Very often (80–99%) | In 1 condition |
| FLNAfilamin A | Very often (80–99%) | In 2 conditions |
| GLI1GLI family zinc finger 1 | Very often (80–99%) | In 1 condition |
| IFT140intraflagellar transport 140 | Very often (80–99%) | In 2 conditions |
| IFT172intraflagellar transport 172 | Very often (80–99%) | In 1 condition |
| IFT80intraflagellar transport 80 | Very often (80–99%) | In 2 conditions |
| KIAA0753KIAA0753 | 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 |
| NEU1neuraminidase 1 | Very often (80–99%) | In 1 condition |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Very often (80–99%) | In 1 condition |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Very often (80–99%) | In 1 condition |
| PTH1Rparathyroid hormone 1 receptor | Very often (80–99%) | In 1 condition |
| RIPPLY2ripply transcriptional repressor 2 | Very often (80–99%) | In 1 condition |
| RNU12RNA, U12 small nuclear | Very often (80–99%) | In 1 condition |
| SLC26A2solute carrier family 26 member 2 | Very often (80–99%) | In 1 condition |
| TBX6T-box transcription factor 6 | Very often (80–99%) | In 2 conditions |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Very often (80–99%) | In 1 condition |
| TTC21Btetratricopeptide repeat domain 21B | Very often (80–99%) | In 1 condition |
| WDR19WD repeat domain 19 | Very often (80–99%) | In 1 condition |
| WDR35WD repeat domain 35 | Very often (80–99%) | In 1 condition |
| CUL7cullin 7 | Often (30–79%) | In 2 conditions |
Show 11 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| DYMdymeclin | Often (30–79%) | In 1 condition |
| MBD5methyl-CpG binding domain protein 5 | Often (30–79%) | In 1 condition |
| OBSL1obscurin like cytoskeletal adaptor 1 | Often (30–79%) | In 2 conditions |
| FREM2FRAS1 related extracellular matrix 2 | Sometimes (5–29%) | In 1 condition |
| IHHIndian hedgehog signaling molecule | Sometimes (5–29%) | In 1 condition |
| LTBP1latent transforming growth factor beta binding protein 1 | Sometimes (5–29%) | In 1 condition |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Sometimes (5–29%) | In 1 condition |
| SLC2A1solute carrier family 2 member 1 | Sometimes (5–29%) | In 1 condition |
| NADSYN1NAD synthetase 1 | Not recorded | In 1 condition |
| ORC6origin recognition complex subunit 6 | Not recorded | In 1 condition |
| SLC10A7solute carrier family 10 member 7 | 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 2026.10.16-c6eea6bf.
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