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Trait
Short columella
Reduced distance from the anterior border of the naris to the subnasale.
Summary
- Also called
- Columella, short, Decreased length of columella
- Body system
- Abnormality of head or neck
Short columellaHP:0002000
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Read the genes linked to Short columella, and the rest of your genome, with one test.
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Get my Genome Test36 genes linked to Short columella
Changes in these genes cause rare conditions in which Short 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 |
|---|---|---|
| ASXL3ASXL transcriptional regulator 3 | Always | In 1 condition |
| CHST14carbohydrate sulfotransferase 14 | Always | In 1 condition |
| CREBBPCREB binding lysine acetyltransferase | Always | In 3 conditions |
| DNMT3ADNA methyltransferase 3 alpha | Always | In 2 conditions |
| ELFN1extracellular leucine rich repeat and fibronectin type III domain containing 1 | Always | In 1 condition |
| EP300EP300 lysine acetyltransferase | Always | In 1 condition |
| NALCNsodium leak channel, non-selective | Always | In 2 conditions |
| TAF4TATA-box binding protein associated factor 4 | Always | In 1 condition |
| THOC2THO complex subunit 2 | Always | In 1 condition |
| ACTBactin beta | Very often (80–99%) | In 1 condition |
| ACTG1actin gamma 1 | Very often (80–99%) | In 1 condition |
| B3GLCTbeta 3-glucosyltransferase | Very often (80–99%) | In 1 condition |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Very often (80–99%) | In 1 condition |
| KDM6Alysine demethylase 6A | Very often (80–99%) | In 2 conditions |
| KMT2Dlysine methyltransferase 2D | Very often (80–99%) | In 1 condition |
| AHDC1AT-hook DNA binding motif containing 1 | Often (30–79%) | In 1 condition |
| ARSLarylsulfatase L | Often (30–79%) | In 1 condition |
| KMT2Alysine methyltransferase 2A | Often (30–79%) | In 1 condition |
| LMBR1limb development membrane protein 1 | Often (30–79%) | In 1 condition |
| MAN2C1mannosidase alpha class 2C member 1 | Often (30–79%) | In 1 condition |
| MBD5methyl-CpG binding domain protein 5 | Often (30–79%) | In 1 condition |
| NOS3nitric oxide synthase 3 | Often (30–79%) | In 1 condition |
| PPP2R3Cprotein phosphatase 2 regulatory subunit B''gamma | Often (30–79%) | In 1 condition |
| TWIST1twist family bHLH transcription factor 1 | Often (30–79%) | In 1 condition |
| CTCFCCCTC-binding factor | Sometimes (5–29%) | In 1 condition |
| FILIP1filamin A interacting protein 1 | Sometimes (5–29%) | In 1 condition |
| KCTD1potassium channel tetramerization domain containing 1 | Sometimes (5–29%) | In 1 condition |
| MAB21L1mab-21 like 1 | Sometimes (5–29%) | In 1 condition |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Sometimes (5–29%) | In 2 conditions |
| SCNM1sodium channel modifier 1 | Sometimes (5–29%) | In 1 condition |
| CNTNAP2contactin associated protein 2 | Rarely (1–4%) | In 1 condition |
| ALX3ALX homeobox 3 | Not recorded | In 1 condition |
| CENPFcentromere protein F | Not recorded | In 1 condition |
| ERFETS2 repressor factor | Not recorded | In 1 condition |
| SHHsonic hedgehog signaling molecule | Not recorded | In 1 condition |
| THUMPD1THUMP domain 1 NAT10 acetyltransferase adaptor | 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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