Trait
Irregularly shaped sperm tail
Irregular or changing caliber (diameter) along the tail of the sperm.
Summary
- Also called
- Sperm flagella with irregular caliber, Sperm flagella with irregular calibre
- Body system
- Abnormality of the genitourinary system
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
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page$trait$nameRead the genes linked to Irregularly shaped sperm tail, and the rest of your genome, with one test.
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Get my Genome Test21 genes linked to Irregularly shaped sperm tail
Changes in these genes cause rare conditions in which Irregularly shaped sperm tail 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 |
|---|---|---|
| BRWD1bromodomain and WD repeat domain containing 1 | Always | In 1 condition |
| CCINcalicin | Always | In 1 condition |
| CFAP206cilia and flagella associated protein 206 | Always | In 1 condition |
| CFAP251cilia and flagella associated protein 251 | Always | In 1 condition |
| CFAP47cilia and flagella associated protein 47 | Always | In 1 condition |
| CFAP54cilia and flagella associated protein 54 | Always | In 1 condition |
| CFAP57cilia and flagella associated protein 57 | Always | In 1 condition |
| CFAP61cilia and flagella associated protein 61 | Always | In 1 condition |
| CFAP91cilia and flagella associated protein 91 | Always | In 1 condition |
| DNAH1dynein axonemal heavy chain 1 | Always | In 1 condition |
| DNAH10dynein axonemal heavy chain 10 | Always | In 1 condition |
| DNAH12dynein axonemal heavy chain 12 | Always | In 1 condition |
| DNAH8dynein axonemal heavy chain 8 | Always | In 1 condition |
| DNHD1dynein heavy chain domain 1 | Always | In 1 condition |
| FSIP2fibrous sheath interacting protein 2 | Always | In 1 condition |
| IFT74intraflagellar transport 74 | Always | In 1 condition |
| SSX1SSX family member 1 | Always | In 1 condition |
| STK33serine/threonine kinase 33 | Always | In 1 condition |
| WDR19WD repeat domain 19 | Always | In 1 condition |
| AK9adenylate kinase 9 | Very often (80–99%) | In 1 condition |
| CCDC34coiled-coil domain containing 34 | Often (30–79%) | 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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