Trait
Cleft nasal tip
Clinical name: Bifid nasal tip
A splitting of the nasal tip. Visually assessable vertical indentation, cleft, or depression of the nasal tip.
Summary
- Also called
- Cleft tip of nose, Notched nasal tip, Notched tip of nose, Bifid tip of nose
- Body system
- Abnormality of head or neck
Read the genes linked to Cleft nasal tip, and the rest of your genome, with one test.
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Get my Genome Test20 genes linked to Cleft nasal tip
Changes in these genes cause rare conditions in which Cleft nasal tip 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 |
|---|---|---|
| ALX4ALX homeobox 4 | Always | In 1 condition |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Always | In 1 condition |
| CPAPcentrosome assembly and centriole elongation protein | Always | In 1 condition |
| H4C3H4 clustered histone 3 | Always | In 1 condition |
| HSPA9heat shock protein family A (Hsp70) member 9 | Always | In 1 condition |
| BCORBCL6 corepressor | Very often (80–99%) | In 2 conditions |
| FREM1FRAS1 related extracellular matrix 1 | Very often (80–99%) | In 2 conditions |
| ZSWIM6zinc finger SWIM-type containing 6 | Very often (80–99%) | In 2 conditions |
| CDH11cadherin 11 | Often (30–79%) | In 1 condition |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Often (30–79%) | In 1 condition |
| NEK1NIMA related kinase 1 | Often (30–79%) | In 1 condition |
| EFNB1ephrin B1 | Sometimes (5–29%) | In 1 condition |
| FRMPD4FERM and PDZ domain containing 4 | Sometimes (5–29%) | In 1 condition |
| KAT6Alysine acetyltransferase 6A | Sometimes (5–29%) | In 1 condition |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Sometimes (5–29%) | In 1 condition |
| RNU4-2RNA, U4 small nuclear 2 | Sometimes (5–29%) | In 1 condition |
| SCNM1sodium channel modifier 1 | Sometimes (5–29%) | In 1 condition |
| ALX3ALX homeobox 3 | Not recorded | In 1 condition |
| FZD2frizzled class receptor 2 | Not recorded | In 1 condition |
| TBC1D32TBC1 domain family member 32 | 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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