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Trait
Reduced sperm motility
An abnormal reduction in the mobility of ejaculated sperm.
Summary
- Also called
- Asthenospermia, Asthenozoospermia
- Body system
- Abnormality of the genitourinary system
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This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/reduced-sperm-motility.json"
page <- fromJSON(url)
page$trait$nameReduced sperm motilityHP:0012207
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Get my Genome Test15 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Male InfertilityReads 16 of these genesCFAP251CFAP43DNAH1DNAH10DNAH12DNAH17About this report →
- Polycystic Kidney DiseaseReads 8 of these genesALG5ALG9DNAJB11GANABIFT140NEK8About this report →
- Primary Ciliary DyskinesiaReads 10 of these genesCFAP54DNAH1DNAH7HYDINRSPH4ARSPH9About this report →
- IFT140-Related CiliopathyReads 1 of these genesIFT140About this report →
Show 11 more reports
- NEK8-Related Renal-Hepatic-Pancreatic DysplasiaReads 1 of these genesNEK8About this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 1 of these genesHNF1BAbout this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesHNF1BAbout this report →
- Retinitis PigmentosaReads 2 of these genesARL2BPIFT140About this report →
- Neonatal Diabetes MellitusReads 1 of these genesHNF1BAbout this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesNEK8About this report →
- Diabetes MellitusReads 1 of these genesHNF1BAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesGBA2About this report →
- Hearing Loss and DeafnessReads 1 of these genesSTRCAbout this report →
- Congenital Disorders of GlycosylationReads 1 of these genesALG9About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesGBA2About this report →
Read the genes linked to Reduced sperm motility, and the rest of your genome, with one test.
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Get my Genome Test67 genes linked to Reduced sperm motility
Changes in these genes cause rare conditions in which Reduced sperm motility 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 |
|---|---|---|
| AK7adenylate kinase 7 | Always | In 1 condition |
| AK9adenylate kinase 9 | Always | In 1 condition |
| ARL2BPARF like GTPase 2 binding protein | Always | In 1 condition |
| BRDTbromodomain testis associated | Always | In 1 condition |
| BRWD1bromodomain and WD repeat domain containing 1 | Always | In 1 condition |
| CATIPciliogenesis associated TTC17 interacting protein | Always | In 1 condition |
| CATSPER1cation channel sperm associated 1 | Always | In 1 condition |
| CATSPER2cation channel sperm associated 2 | Always | In 2 conditions |
| CCDC146coiled-coil domain containing 146 | Always | In 1 condition |
| CCDC34coiled-coil domain containing 34 | Always | In 1 condition |
| CEP112centrosomal protein 112 | Always | In 1 condition |
| CFAP251cilia and flagella associated protein 251 | Always | In 1 condition |
| CFAP410cilia and flagella associated protein 410 | Always | In 1 condition |
| CFAP43cilia and flagella associated protein 43 | 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 |
| CFAP58cilia and flagella associated protein 58 | Always | In 1 condition |
| CFAP69cilia and flagella associated protein 69 | Always | In 1 condition |
| CFAP91cilia and flagella associated protein 91 | Always | In 1 condition |
| CT55cancer/testis antigen 55 | 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 |
| DNAH17dynein axonemal heavy chain 17 | Always | In 1 condition |
| DNAH2dynein axonemal heavy chain 2 | Always | In 1 condition |
| DNAH7dynein axonemal heavy chain 7 | Always | In 1 condition |
| DNAH8dynein axonemal heavy chain 8 | Always | In 1 condition |
| DNALI1dynein axonemal light intermediate chain 1 | Always | In 1 condition |
| DNHD1dynein heavy chain domain 1 | Always | In 1 condition |
| FSIP2fibrous sheath interacting protein 2 | Always | In 1 condition |
| HYDINHYDIN axonemal central pair apparatus protein | Always | In 1 condition |
| KCNU1potassium calcium-activated channel subfamily U member 1 | Always | In 1 condition |
| RSPH4Aradial spoke head component 4A | Always | In 1 condition |
| RSPH9radial spoke head component 9 | Always | In 1 condition |
| SLC26A8solute carrier family 26 member 8 | Always | In 1 condition |
| SPAG17sperm associated antigen 17 | Always | In 1 condition |
| SSX1SSX family member 1 | Always | In 1 condition |
| STK36serine/threonine kinase 36 | Always | In 1 condition |
| STRCstereocilin | Always | In 2 conditions |
Show 27 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| SUN5Sad1 and UNC84 domain containing 5 | Always | In 2 conditions |
| TTC29tetratricopeptide repeat domain 29 | Always | In 1 condition |
| CFAP61cilia and flagella associated protein 61 | Very often (80–99%) | In 1 condition |
| CCDC39coiled-coil domain 39 molecular ruler complex subunit | Often (30–79%) | In 1 condition |
| KLHL10kelch like family member 10 | Often (30–79%) | In 1 condition |
| LRRC23leucine rich repeat containing 23 | Often (30–79%) | In 1 condition |
| PDHA2pyruvate dehydrogenase E1 subunit alpha 2 | Often (30–79%) | In 1 condition |
| PMFBP1polyamine modulated factor 1 binding protein 1 | Often (30–79%) | In 1 condition |
| SEPTIN12septin 12 | Often (30–79%) | In 1 condition |
| STK33serine/threonine kinase 33 | Often (30–79%) | In 1 condition |
| USP26ubiquitin specific peptidase 26 | Often (30–79%) | In 1 condition |
| ALG5ALG5 dolichyl-phosphate beta-glucosyltransferase | Sometimes (5–29%) | In 1 condition |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Sometimes (5–29%) | In 1 condition |
| BICC1BicC family RNA binding protein 1 | Sometimes (5–29%) | In 1 condition |
| CCINcalicin | Sometimes (5–29%) | In 1 condition |
| DNAJB11DnaJ heat shock protein family (Hsp40) member B11 | Sometimes (5–29%) | In 1 condition |
| GANABglucosidase II alpha subunit | Sometimes (5–29%) | In 1 condition |
| GBA2glucosylceramidase beta 2 | Sometimes (5–29%) | In 1 condition |
| IFT140intraflagellar transport 140 | Sometimes (5–29%) | In 1 condition |
| NEK8NIMA related kinase 8 | Sometimes (5–29%) | In 1 condition |
| PKD1polycystin 1, transient receptor potential channel interacting | Sometimes (5–29%) | In 1 condition |
| PKD2polycystin 2, transient receptor potential cation channel | Sometimes (5–29%) | In 1 condition |
| ARMC2armadillo repeat containing 2 | Not recorded | In 1 condition |
| CFAP298cilia and flagella associated protein 298 | Not recorded | In 1 condition |
| HNF1BHNF1 homeobox B | Not recorded | In 1 condition |
| SPEF2sperm flagellar and cilia associated 2 | Not recorded | In 1 condition |
| ZMYND10zinc finger MYND-type containing 10 | 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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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 2026.10.19-9814e911.
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