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Trait
Low hanging columella
Columella extending inferior to the level of the nasal base, when viewed from the side.
Summary
- Also called
- Columella, low, Columella, low hanging, Extension of the columella below the ala nasi, Low-hanging columella
- Body system
- Abnormality of head or neck
Low hanging columellaHP:0009765
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Read the genes linked to Low hanging columella, and the rest of your genome, with one test.
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Get my Genome Test68 genes linked to Low hanging columella
Changes in these genes cause rare conditions in which Low hanging columella 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 |
|---|---|---|
| CLP1cleavage factor polyribonucleotide kinase subunit 1 | Always | In 1 condition |
| CREBBPCREB binding lysine acetyltransferase | Always | In 3 conditions |
| EP300EP300 lysine acetyltransferase | Always | In 3 conditions |
| ITCHitchy E3 ubiquitin protein ligase | Always | In 1 condition |
| KNL1kinetochore scaffold 1 | Always | In 1 condition |
| LIFRLIF receptor subunit alpha | Always | In 1 condition |
| PPP1R21protein phosphatase 1 regulatory subunit 21 | Always | In 1 condition |
| PUM1pumilio RNA binding family member 1 | Always | In 1 condition |
| RBSNrabenosyn, RAB effector | Always | In 1 condition |
| RYR1ryanodine receptor 1 | Always | In 1 condition |
| SRCAPSnf2 related CREBBP activator protein | Always | In 2 conditions |
| THOC6THO complex subunit 6 | Always | In 2 conditions |
| TOP2BDNA topoisomerase II beta | Always | In 1 condition |
| ZEB2zinc finger E-box binding homeobox 2 | Always | In 3 conditions |
| UBE2Aubiquitin conjugating enzyme E2 A | Very often (80–99%) | In 1 condition |
| AFF3ALF transcription elongation factor 3 | Often (30–79%) | In 1 condition |
| AIMP2aminoacyl tRNA synthetase complex interacting multifunctional protein 2 | Often (30–79%) | In 1 condition |
| CEP295centrosomal protein 295 | Often (30–79%) | In 1 condition |
| EDEM3ER degradation enhancing alpha-mannosidase like protein 3 | Often (30–79%) | In 1 condition |
| HNRNPH2heterogeneous nuclear ribonucleoprotein H2 | Often (30–79%) | In 1 condition |
| HNRNPRheterogeneous nuclear ribonucleoprotein R | Often (30–79%) | In 1 condition |
| KDM3Blysine demethylase 3B | Often (30–79%) | In 1 condition |
| KDM5Blysine demethylase 5B | Often (30–79%) | In 1 condition |
| KICS2KICSTOR subunit 2 | Often (30–79%) | In 1 condition |
| NOGnoggin | Often (30–79%) | In 1 condition |
| SETD2SET domain containing 2, histone lysine methyltransferase | Often (30–79%) | In 1 condition |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Often (30–79%) | In 1 condition |
| SOX11SRY-box transcription factor 11 | Often (30–79%) | In 1 condition |
| TAF6TATA-box binding protein associated factor 6 | Often (30–79%) | In 1 condition |
| TWIST1twist family bHLH transcription factor 1 | Often (30–79%) | In 1 condition |
| AHDC1AT-hook DNA binding motif containing 1 | Sometimes (5–29%) | In 1 condition |
| ASXL3ASXL transcriptional regulator 3 | Sometimes (5–29%) | In 1 condition |
| BICRABRD4 interacting chromatin remodeling complex associated protein | Sometimes (5–29%) | In 1 condition |
| BORCS8BLOC-1 related complex subunit 8 | Sometimes (5–29%) | In 1 condition |
| CAPN15calpain 15 | Sometimes (5–29%) | In 1 condition |
| CAPRIN1cell cycle associated protein 1 | Sometimes (5–29%) | In 1 condition |
| CDC42BPBCDC42 binding protein kinase beta | Sometimes (5–29%) | In 1 condition |
| CLCN3Cl-/H+ antiporter 3 | Sometimes (5–29%) | In 1 condition |
| CTNNB1catenin beta 1 | Sometimes (5–29%) | In 1 condition |
| FEM1Bfem-1 homolog B | Sometimes (5–29%) | In 1 condition |
Show 28 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| GJA5gap junction protein alpha 5 | Sometimes (5–29%) | In 1 condition |
| GJA8gap junction protein alpha 8 | Sometimes (5–29%) | In 1 condition |
| H3-3BH3.3 histone B | Sometimes (5–29%) | In 1 condition |
| HIVEP2HIVEP zinc finger 2 | Sometimes (5–29%) | In 1 condition |
| KAT6Alysine acetyltransferase 6A | Sometimes (5–29%) | In 1 condition |
| KMT2Dlysine methyltransferase 2D | Sometimes (5–29%) | In 1 condition |
| KMT5Blysine methyltransferase 5B | Sometimes (5–29%) | In 1 condition |
| MGAT2alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Sometimes (5–29%) | In 2 conditions |
| PCDHGC4protocadherin gamma subfamily C, 4 | Sometimes (5–29%) | In 1 condition |
| POC1APOC1 centriolar protein A | Sometimes (5–29%) | In 1 condition |
| PQBP1polyglutamine binding protein 1 | Sometimes (5–29%) | In 1 condition |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Sometimes (5–29%) | In 1 condition |
| RAC1Rac family small GTPase 1 | Sometimes (5–29%) | In 2 conditions |
| RNU4-2RNA, U4 small nuclear 2 | Sometimes (5–29%) | In 1 condition |
| SEPHS1selenophosphate synthetase 1 | Sometimes (5–29%) | In 1 condition |
| TBCDtubulin folding cofactor D | Sometimes (5–29%) | In 1 condition |
| TRIOtrio Rho guanine nucleotide exchange factor | Sometimes (5–29%) | In 1 condition |
| TRIP12thyroid hormone receptor interactor 12 | Sometimes (5–29%) | In 1 condition |
| ZFXzinc finger protein X-linked | Sometimes (5–29%) | In 1 condition |
| ZNF148zinc finger protein 148 | Sometimes (5–29%) | In 1 condition |
| CNTNAP2contactin associated protein 2 | Rarely (1–4%) | In 1 condition |
| CTCFCCCTC-binding factor | Rarely (1–4%) | In 1 condition |
| MED16mediator complex subunit 16 | Rarely (1–4%) | In 1 condition |
| ATN1atrophin 1 | Not recorded | In 1 condition |
| CDH11cadherin 11 | Not recorded | In 1 condition |
| CKAP2Lcytoskeleton associated protein 2L | Not recorded | In 1 condition |
| GJA1gap junction protein alpha 1 | Not recorded | In 1 condition |
| ZMIZ1zinc finger MIZ-type containing 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.
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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