Trait
Short ribs
Reduced rib length.
Summary
- Also called
- Hypoplastic ribs, Rib hypoplasia
- Body system
- Abnormality of the musculoskeletal system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test69 genes linked to Short ribs
Changes in these genes cause rare conditions in which Short ribs 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 |
|---|---|---|
| CEP120centrosomal protein 120 | Always | In 1 condition |
| COL11A2collagen type XI alpha 2 chain | Always | In 2 conditions |
| DMRT2doublesex and mab-3 related transcription factor 2 | Always | In 1 condition |
| FGF4fibroblast growth factor 4 | Always | In 1 condition |
| FGFR3fibroblast growth factor receptor 3 | Always | In 3 conditions |
| IFT140intraflagellar transport 140 | Always | In 2 conditions |
| LBRlamin B receptor | Always | In 1 condition |
| MYF5myogenic factor 5 | Always | In 1 condition |
| PAM16presequence translocase associated motor 16 | Always | In 1 condition |
| PLCB3phospholipase C beta 3 | Always | In 1 condition |
| PTH1Rparathyroid hormone 1 receptor | Always | In 3 conditions |
| TRIP11thyroid hormone receptor interactor 11 | Always | In 1 condition |
| CHD6chromodomain helicase DNA binding protein 6 | Very often (80–99%) | In 1 condition |
| COL11A1collagen type XI alpha 1 chain | Very often (80–99%) | In 2 conditions |
| 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 1 condition |
| IFT80intraflagellar transport 80 | Very often (80–99%) | In 1 condition |
| INPPL1inositol polyphosphate phosphatase like 1 | Very often (80–99%) | In 1 condition |
| SLC35D1solute carrier family 35 member D1 | Very often (80–99%) | In 2 conditions |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Very often (80–99%) | In 1 condition |
| WDR35WD repeat domain 35 | Very often (80–99%) | In 3 conditions |
| COL2A1collagen type II alpha 1 chain | Often (30–79%) | In 3 conditions |
| DYNLT2Bdynein light chain Tctex-type 2B | Often (30–79%) | In 1 condition |
| GPC3glypican 3 | Often (30–79%) | In 1 condition |
| IFT43intraflagellar transport 43 | Often (30–79%) | In 1 condition |
| IFT81intraflagellar transport 81 | Often (30–79%) | In 1 condition |
| KIAA0586KIAA0586 | Often (30–79%) | In 2 conditions |
| LAMA5laminin subunit alpha 5 | Often (30–79%) | In 1 condition |
| SLC26A2solute carrier family 26 member 2 | Often (30–79%) | In 2 conditions |
| UBA1ubiquitin like modifier activating enzyme 1 | Often (30–79%) | In 1 condition |
| CSPP1centrosome and spindle pole associated protein 1 | Sometimes (5–29%) | In 2 conditions |
| DHCR2424-dehydrocholesterol reductase | Sometimes (5–29%) | In 1 condition |
| DLK1delta like non-canonical Notch ligand 1 | Sometimes (5–29%) | In 1 condition |
| FIG4FIG4 phosphoinositide 5-phosphatase | Sometimes (5–29%) | In 1 condition |
| HSPG2heparan sulfate proteoglycan 2 | Sometimes (5–29%) | In 1 condition |
| MEG3maternally expressed 3 | Sometimes (5–29%) | In 1 condition |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Sometimes (5–29%) | In 1 condition |
| RTL1retrotransposon Gag like 1 | Sometimes (5–29%) | In 1 condition |
| SCARF2scavenger receptor class F member 2 | Sometimes (5–29%) | In 1 condition |
Show 29 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| TRPV6transient receptor potential cation channel subfamily V member 6 | Sometimes (5–29%) | In 1 condition |
| VAC14VAC14 component of PIKFYVE complex | Sometimes (5–29%) | In 1 condition |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Not recorded | In 1 condition |
| ALPLalkaline phosphatase, biomineralization associated | Not recorded | In 1 condition |
| C2CD3C2 domain containing 3 centriole elongation regulator | Not recorded | In 1 condition |
| CUL7cullin 7 | Not recorded | In 1 condition |
| DDR2discoidin domain receptor tyrosine kinase 2 | Not recorded | In 1 condition |
| DDRGK1DDRGK domain containing 1 | Not recorded | In 1 condition |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Not recorded | In 1 condition |
| EVCEvC ciliary complex subunit 1 | Not recorded | In 1 condition |
| EVC2EvC ciliary complex subunit 2 | Not recorded | In 1 condition |
| EZH2enhancer of zeste 2 polycomb repressive complex 2 subunit | Not recorded | In 1 condition |
| FLNAfilamin A | Not recorded | In 1 condition |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Not recorded | In 1 condition |
| GPX4glutathione peroxidase 4 | Not recorded | In 1 condition |
| IFT122intraflagellar transport 122 | Not recorded | In 1 condition |
| IFT172intraflagellar transport 172 | Not recorded | In 1 condition |
| IHHIndian hedgehog signaling molecule | Not recorded | In 1 condition |
| INTUinturned planar cell polarity protein | Not recorded | In 1 condition |
| NEK1NIMA related kinase 1 | Not recorded | In 1 condition |
| NKX3-2NK3 homeobox 2 | Not recorded | In 1 condition |
| ORC1origin recognition complex subunit 1 | Not recorded | In 1 condition |
| ORC6origin recognition complex subunit 6 | Not recorded | In 1 condition |
| PORCNporcupine O-acyltransferase | Not recorded | In 1 condition |
| PTCH1patched 1 | Not recorded | In 1 condition |
| RNU12RNA, U12 small nuclear | Not recorded | In 1 condition |
| RUNX2RUNX family transcription factor 2 | Not recorded | In 1 condition |
| SMOsmoothened, frizzled class receptor | Not recorded | In 1 condition |
| TAPT1transmembrane anterior posterior transformation 1 | 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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