Trait
Abnormal sperm development
Clinical name: Abnormal spermatogenesis
Incomplete maturation or aberrant formation of the male gametes.
Summary
- Also called
- Impaired spermatogenesis
- Body system
- Abnormality of the genitourinary system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test64 genes linked to Abnormal sperm development
Changes in these genes cause rare conditions in which Abnormal sperm development 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 |
|---|---|---|
| CATSPER2cation channel sperm associated 2 | Always | In 1 condition |
| STRCstereocilin | Always | In 1 condition |
| CATIPciliogenesis associated TTC17 interacting protein | Very often (80–99%) | In 1 condition |
| CCDC34coiled-coil domain containing 34 | Very often (80–99%) | In 1 condition |
| CFTRCF transmembrane conductance regulator | Very often (80–99%) | In 1 condition |
| CT55cancer/testis antigen 55 | Very often (80–99%) | In 1 condition |
| DAZ1deleted in azoospermia 1 | Very often (80–99%) | In 1 condition |
| DAZ2deleted in azoospermia 2 | Very often (80–99%) | In 1 condition |
| DAZ3deleted in azoospermia 3 | Very often (80–99%) | In 1 condition |
| DAZ4deleted in azoospermia 4 | Very often (80–99%) | In 1 condition |
| DCAF17DDB1 and CUL4 associated factor 17 | Very often (80–99%) | In 1 condition |
| DDX3YDEAD-box helicase 3 Y-linked | Very often (80–99%) | In 1 condition |
| DNAH10dynein axonemal heavy chain 10 | Very often (80–99%) | In 1 condition |
| DNHD1dynein heavy chain domain 1 | Very often (80–99%) | In 1 condition |
| FANCMFA complementation group M | Very often (80–99%) | In 1 condition |
| FBXO43F-box protein 43 | Very often (80–99%) | In 2 conditions |
| GCNAgerm cell nuclear acidic peptidase | Very often (80–99%) | In 1 condition |
| KLHL10kelch like family member 10 | Very often (80–99%) | In 1 condition |
| MEIOBmeiosis specific with OB-fold | Very often (80–99%) | In 1 condition |
| MOV10L1Mov10 like RNA helicase 1 | Very often (80–99%) | In 1 condition |
| MSH5mutS homolog 5 | Very often (80–99%) | In 1 condition |
| NANOS1nanos C2HC-type zinc finger 1 | Very often (80–99%) | In 1 condition |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Very often (80–99%) | In 1 condition |
| PDHA2pyruvate dehydrogenase E1 subunit alpha 2 | Very often (80–99%) | In 1 condition |
| PNLDC1PARN like ribonuclease domain containing exonuclease 1 | Very often (80–99%) | In 1 condition |
| RBBP7RB binding protein 7, chromatin remodeling factor | Very often (80–99%) | In 1 condition |
| RBMY1A1RNA binding motif protein Y-linked family 1 member A1 | Very often (80–99%) | In 1 condition |
| RNF212ring finger protein 212 | Very often (80–99%) | In 1 condition |
| RPL10Lribosomal protein L10 like | Very often (80–99%) | In 1 condition |
| SHOC1shortage in chiasmata 1 | Very often (80–99%) | In 1 condition |
| SOHLH1spermatogenesis and oogenesis specific basic helix-loop-helix 1 | Very often (80–99%) | In 1 condition |
| SPAG17sperm associated antigen 17 | Very often (80–99%) | In 1 condition |
| SPINK2serine peptidase inhibitor Kazal type 2 | Very often (80–99%) | In 1 condition |
| STAG3STAG3 cohesin complex component | Very often (80–99%) | In 1 condition |
| SYCE1synaptonemal complex central element protein 1 | Very often (80–99%) | In 1 condition |
| SYCP3synaptonemal complex protein 3 | Very often (80–99%) | In 1 condition |
| TAF4BTATA-box binding protein associated factor 4b | Very often (80–99%) | In 1 condition |
| TDRD9tudor domain containing 9 | Very often (80–99%) | In 1 condition |
| TERB1telomere repeat binding bouquet formation protein 1 | Very often (80–99%) | In 1 condition |
| TERB2telomere repeat binding bouquet formation protein 2 | Very often (80–99%) | In 1 condition |
Show 24 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| TEX11testis expressed 11 | Very often (80–99%) | In 1 condition |
| TEX14testis expressed 14, intercellular bridge forming factor | Very often (80–99%) | In 1 condition |
| TEX15testis expressed 15, meiosis and synapsis associated | Very often (80–99%) | In 1 condition |
| TSPY1testis specific protein Y-linked 1 | Very often (80–99%) | In 1 condition |
| USP9Yubiquitin specific peptidase 9 Y-linked | Very often (80–99%) | In 1 condition |
| XRCC2X-ray repair cross complementing 2 | Very often (80–99%) | In 1 condition |
| ZMYND15zinc finger MYND-type containing 15 | Very often (80–99%) | In 1 condition |
| ZSWIM7zinc finger SWIM-type containing 7 | Very often (80–99%) | In 1 condition |
| ATMATM serine/threonine kinase | Not recorded | In 1 condition |
| CDC20cell division cycle 20 | Not recorded | In 1 condition |
| CHEK1checkpoint kinase 1 | Not recorded | In 1 condition |
| KPNA7karyopherin subunit alpha 7 | Not recorded | In 1 condition |
| LHBluteinizing hormone subunit beta | Not recorded | In 1 condition |
| MOSMOS proto-oncogene, serine/threonine kinase | Not recorded | In 1 condition |
| NLRP2NLR family pyrin domain containing 2 | Not recorded | In 1 condition |
| NLRP5NLR family pyrin domain containing 5 | Not recorded | In 1 condition |
| NLRP7NLR family pyrin domain containing 7 | Not recorded | In 1 condition |
| PADI6peptidyl arginine deiminase 6 | Not recorded | In 1 condition |
| PANX1pannexin 1 | Not recorded | In 1 condition |
| PATL2PAT1 homolog 2 | Not recorded | In 1 condition |
| TLE6TLE family member 6, subcortical maternal complex member | Not recorded | In 1 condition |
| TUBB8tubulin beta 8 class VIII | Not recorded | In 1 condition |
| WEE2WEE2 oocyte meiosis inhibiting kinase | Not recorded | In 1 condition |
| ZFP36L2ZFP36 like 2 zinc finger CCCH-type | 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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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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